This is a Validated Antibody Database (VAD) review about chicken ELAVL4, based on 297 published articles (read how Labome selects the articles), using ELAVL4 antibody in all methods. It is aimed to help Labome visitors find the most suited ELAVL4 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
ELAVL4 synonym: HUD

Invitrogen
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; loading ...; fig 4c
Invitrogen ELAVL4 antibody (Thermo Fisher, A-21271) was used in immunohistochemistry on zebrafish samples (fig 4c). Am J Hum Genet (2022) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:300; loading ...; fig 7f
Invitrogen ELAVL4 antibody (Thermo Fisher Scientific, A-21271) was used in immunohistochemistry on mouse samples at 1:300 (fig 7f). Front Cell Dev Biol (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 1c
Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on mouse samples (fig 1c). Invest Ophthalmol Vis Sci (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:50; loading ...; fig e3d
Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:50 (fig e3d). EMBO Rep (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; loading ...; fig s12j
Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on mouse samples (fig s12j). iScience (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:300; loading ...; fig 4d
Invitrogen ELAVL4 antibody (INVITROGEN, A21271) was used in immunohistochemistry on zebrafish samples at 1:300 (fig 4d). Sci Rep (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500; loading ...; fig 6f
Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on chicken samples at 1:500 (fig 6f). Development (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:200; loading ...; fig 1a
Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry - frozen section on pigs samples at 1:200 (fig 1a). Animals (Basel) (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; fig 1b
Invitrogen ELAVL4 antibody (Thermo-Fisher Scientific, A21271) was used in immunohistochemistry on mouse samples (fig 1b). Cell Mol Gastroenterol Hepatol (2021) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:50; loading ...; fig 3a
Invitrogen ELAVL4 antibody (Thermo Fisher Scientific, A21271) was used in immunohistochemistry on human samples at 1:50 (fig 3a). Front Physiol (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:500; loading ...; fig s3b
Invitrogen ELAVL4 antibody (LifeTech, A21271) was used in immunohistochemistry on human samples at 1:500 (fig s3b). Science (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; rat; 1:200; loading ...; fig 2a1
Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - free floating section on rat samples at 1:200 (fig 2a1). Int J Mol Sci (2020) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; loading ...; fig 3a
Invitrogen ELAVL4 antibody (Thermofisher, A21271) was used in immunocytochemistry on human samples (fig 3a). J Neuroinflammation (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:35; loading ...; fig 4, 5
Invitrogen ELAVL4 antibody (Thermo Fisher, A-21271) was used in immunohistochemistry on rat samples at 1:35 (fig 4, 5). J Neuroendocrinol (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:250; loading ...; fig 6d
Invitrogen ELAVL4 antibody (ThermoFisher, A21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:250 (fig 6d). Development (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:300; loading ...; fig 2d
Invitrogen ELAVL4 antibody (Thermo Fischer, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:300 (fig 2d). PLoS Biol (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; chicken; loading ...; fig 1e
Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - frozen section on chicken samples (fig 1e). J Comp Neurol (2020) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:1000; loading ...; fig 2o
Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:1000 (fig 2o). elife (2019) ncbi
mouse monoclonal (16A11)
Invitrogen ELAVL4 antibody (Thermo Fisher Scientific, A21271) was used . J Comp Neurol (2019) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:200; loading ...; fig 4s1b
Invitrogen ELAVL4 antibody (Thermo Fisher, A-21271) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig 4s1b). elife (2018) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:400; loading ...; fig s4d
In order to identify the organizing features of the mammalian enteric nervous system, Invitrogen ELAVL4 antibody (Thermo Fisher Scientific, A21271) was used in immunohistochemistry - frozen section on mouse samples at 1:400 (fig s4d). Science (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:500; loading ...; tbl 2
In order to conduct tracing experiments for dlx1a/2a and dlx5a/6a expressing cells in the developing zebrafish brain, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:500 (tbl 2). Dev Biol (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1 ug/ml; loading ...; fig 5a
  • western blot; mouse; 1 ug/ml; loading ...; fig 1c
In order to determine the effect of CPT-11 on the enteric glial and neuronal cells and assess the role of mast cells in the CPT-11-induced intestinal mucositis, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on mouse samples at 1 ug/ml (fig 5a) and in western blot on mouse samples at 1 ug/ml (fig 1c). J Neuroinflammation (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500; loading ...; fig 10d
In order to compare the organization of cerebrospinal fluid-contacting cells in chicken, Xenopus, and zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on chicken samples at 1:500 (fig 10d). J Comp Neurol (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:500; loading ...; fig 3a
In order to evaluate the influences of S100B synthesis in enteric nervous system development, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on mouse samples at 1:500 (fig 3a). Front Cell Neurosci (2017) ncbi
mouse monoclonal (16A11)
In order to analyze the role of the microRNA miR-29 in limiting neuronal iron accumulation, Invitrogen ELAVL4 antibody (Thermo Fisher, A-21271) was used . BMC Biol (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; zebrafish ; 1:200; loading ...; fig 3h
In order to propose that neurodevelopmental disorders and brain tumors may arise from changes in oncogenes, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry - paraffin section on zebrafish samples at 1:200 (fig 3h). Dis Model Mech (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; chicken; 1:500; loading ...; fig 5a
In order to discuss the roles of proneural genes and their effectors during differentiation of the neuronal populations, Invitrogen ELAVL4 antibody (molecular probes, A21271) was used in immunohistochemistry - paraffin section on chicken samples at 1:500 (fig 5a). Neural Dev (2016) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; mouse; 1:400; fig s5a
In order to discuss factors that impact the migratory behavior of neural crest cells, Invitrogen ELAVL4 antibody (ThermoFisher Scientific, A21271) was used in immunocytochemistry on mouse samples at 1:400 (fig s5a). BMC Biol (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:200; fig 6b
In order to study the contractility of the detrusor muscle and the morphology and code of the vesical plexus from Octodon degus, Invitrogen ELAVL4 antibody (Mol Probes, A-21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:200 (fig 6b). J Physiol Biochem (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:50; fig 2
In order to use CLARITY and PACT to visualize the intestinal architecture, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:50 (fig 2). Sci Rep (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:500; fig 1
In order to evaluate the effect of dietary l-glutamine on the development of experimental cachexia, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples at 1:500 (fig 1). PLoS ONE (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:400; fig 1
In order to demonstrate that stroke results in central and peripheral galectin-3 release causing enteric neuronal loss through a TLR4-mediated mechanism, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on mouse samples at 1:400 (fig 1). Sci Rep (2016) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; fig 1
In order to describe a protocol for retinal ganglion cell differentiation, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunocytochemistry on human samples (fig 1). Sci Rep (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; loading ...; fig 8
In order to investigate non-neuronal proopiomelanocortin expression, Invitrogen ELAVL4 antibody (molecular Probes, A21271) was used in immunohistochemistry on rat samples (fig 8). J Comp Neurol (2017) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:500; loading ...; fig 2a
In order to compare the effects of supplementation with l-glutamine and l-glutathione on neurons and enteric glial cells in ileum of diabetic rats, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on rat samples at 1:500 (fig 2a). Acta Histochem (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:50; fig 2
In order to characterize the action of administered ciliary neurotrophic factor the dorsal vagal complex in mice, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on mouse samples at 1:50 (fig 2). Front Neurosci (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; chicken; 1:400; fig s7
In order to assess pools of neural stem/progenitor cells regulated by Sox2 and the novel role of hindbrain boundaries, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on chicken samples at 1:400 (fig s7). BMC Biol (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:20; loading ...; fig 2g
In order to study brain-derived neurotrophic factor in zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on zebrafish samples at 1:20 (fig 2g). PLoS ONE (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; zebrafish ; 1:200; fig 3
In order to investigate mediation by the GAP-related domain in the synergy between loss of NF1 and overexpression of MYCN in neuroblastoma, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - paraffin section on zebrafish samples at 1:200 (fig 3). elife (2016) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; fig 1
In order to assess activation during congenital cytomegalovirus infection of PPAR-gamma that inhibits neuronogenesis from human neural stem cells, Invitrogen ELAVL4 antibody (Life technologies, 16A11) was used in immunocytochemistry on human samples (fig 1). PLoS Pathog (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:200; fig s3b
In order to study neocrotical development and promotion of astrocytogenesis by Zbtb20, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig s3b). Nat Commun (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; rat; 1:500; fig 5
In order to study the anatomy of the satiety network by focusing on connectivity of the parabrachial nucleus in the adult rat, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on rat samples at 1:500 (fig 5). J Comp Neurol (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:50; fig 2
In order to study contribution to spinal cord regeneration in adult zebrafish by L1.2, the zebrafish paralog of L1.1 and ortholog of the mammalian cell adhesion molecule L1, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:50 (fig 2). Restor Neurol Neurosci (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:600; fig 2
In order to compare differences in mouse and chicken development in spatiotemporal expression and epistatic gene regulation of the mesodiencephalic dopaminergic precursor marker PITX3, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on chicken samples at 1:600 (fig 2). Development (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; tbl 1
In order to elucidate the zebrafish model and congenital enteric neuropathies, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples (tbl 1). Neurogastroenterol Motil (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100; loading ...; fig s10a
In order to identify that a cerebral vascularization deficit of the no food for thought gene is caused by an inactivating lesion in reversion-inducing cysteine-rich protein with Kazal motifs, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on zebrafish samples at 1:100 (fig s10a). Development (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 5 ug/ml; fig 4
In order to characterize Huntington's disease through a zebrafrish model where the N17 domain mitigates nuclear toxicity, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry - frozen section on zebrafish samples at 5 ug/ml (fig 4). Mol Neurodegener (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:50; fig 1,b,e
In order to assess histological changes in the distal ileum and intestinal motor function in a rat model of irritable bowel syndrome with diarrhea, Invitrogen ELAVL4 antibody (Mol Probes, A-21271) was used in immunohistochemistry on rat samples at 1:50 (fig 1,b,e). J Neurogastroenterol Motil (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:50; fig 1
In order to discuss the molecular mechanism for endogenous regeneration of the adult zebrafish spinal cord, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:50 (fig 1). PLoS ONE (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; fig 7
In order to assess the impact of central dopaminergic denervation on distal colonic excitatory cholinergic neuromotor activity in rats, Invitrogen ELAVL4 antibody (Molecular probes, A21271) was used in immunohistochemistry on rat samples (fig 7). J Pharmacol Exp Ther (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; zebrafish ; 1:100; fig 2
In order to examine how increasing amounts of urea affect the olfactory organs, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on zebrafish samples at 1:100 (fig 2). J Anat (2016) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; 1:500; fig 3d
In order to identify mutations that contribute North Carolina macular dystrophy, Invitrogen ELAVL4 antibody (Thermo Fisher Scientific, A-21271) was used in immunocytochemistry on human samples at 1:500 (fig 3d). Ophthalmology (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:5000; fig 2
In order to study galaninergic innervation, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:5000 (fig 2). Histochem Cell Biol (2016) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:400
In order to study the luteinizing hormone receptor in rat myenteric neurons, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunocytochemistry on rat samples at 1:400. Auton Neurosci (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Xenopus laevis
In order to examine the role of asporin in the early stages of eye development in Xenopus embryos, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on Xenopus laevis samples . Development (2015) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:100
  • immunohistochemistry; zebrafish ; 1:100
In order to describe neuronal patterns in the spinal cord of adult zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on zebrafish samples at 1:100 and in immunohistochemistry on zebrafish samples at 1:100. Dev Neurobiol (2016) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat
In order to determine the effect of LPS-induced inflammation on the expression of LAT1 and LAT2, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on rat samples . Fluids Barriers CNS (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; fig 2a
In order to create a mathematical model that predicts the average rates of proliferative and differentiative divisions in stem cell population, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on chicken samples (fig 2a). Sci Rep (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; pigs ; 1:1000
In order to test the effect of streptozotocin-induced diabetes on the cocaine- and amphetamine-regulated transcript-like immunoreactive enteric nervous structures, Invitrogen ELAVL4 antibody (Invitrogene, A-21271) was used in immunohistochemistry on pigs samples at 1:1000. J Mol Neurosci (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; pigs ; 1:200; fig 4
In order to determine the expression and co-localization of different neurotransmitters and neuronal markers in the inner submucous plexus, the outer submucous plexus and neuronal fibers, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on pigs samples at 1:200 (fig 4). PLoS ONE (2015) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:100
In order to examine the neurogenic potential of the adult hypothalamus using zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunocytochemistry on zebrafish samples at 1:100. Biol Open (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500
In order to study the maturation of neurogenic placodes, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunohistochemistry on chicken samples at 1:500. J Anat (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Japanese rice fish; fig s1
In order to analyze the spatiotemporal dynamics of microglia during tissue repair in the irradiated embryonic medaka brain, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on Japanese rice fish samples (fig s1). PLoS ONE (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:400; fig 1
In order to assess dorsal root avulsion injury and how human embryonic stem cell-derived progenitors assist functional sensory axo regeneration, Invitrogen ELAVL4 antibody (Novex (Life Technologies), A21271) was used in immunohistochemistry on human samples at 1:400 (fig 1). Sci Rep (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; chicken; 1:200
In order to test if nutrition-related developmental stress impacts neurogenesis in HVC in song birds, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - free floating section on chicken samples at 1:200. Dev Neurobiol (2016) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish
In order to examine the role of 1q21.1 genes in neurogenesis, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunocytochemistry on zebrafish samples . J Neurosci (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to correlate the presence of ciliopathy genes to clinical phenotypes, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on zebrafish samples at 1:500. Am J Hum Genet (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; rat; 1:200
In order to study prototypic and arkypallidal neurons in dopamine-intact rats, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - free floating section on rat samples at 1:200. J Neurosci (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to investigate the role of Wnt/beta-catenin signaling in spinal cord regeneration, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:500. Dev Biol (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human; 1:800
In order to investigate the role of doublecortin during neurogenesis using fishes, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - paraffin section on human samples at 1:800. Exp Eye Res (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100
In order to demonstrate that semaphorin 3C/3D signaling is an evolutionarily conserved regulator of the enteric nervous system development, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:100. Am J Hum Genet (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:2000; fig 4
In order to study the localization of flotillin-1 in the rat visual cortex during development, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on rat samples at 1:2000 (fig 4). Neuroscience (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:200
In order to characterize the long term effects of diabetic enteric neuropathy using mouse models, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on mouse samples at 1:200. Cell Tissue Res (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:1000
In order to determine role of IKBKAP in the development of enteric nervous system and Hirschsprung disease, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:1000. World J Gastroenterol (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:200
In order to elucidate the innervation of the heart using zebrafish, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on zebrafish samples at 1:200. J Comp Neurol (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; fig 2
In order to determine the efficiency, tropism, spread, and immunogenicity of adeno-associated virus transduction in the enteric nervous system, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on rat samples (fig 2). Mol Ther (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic horse; 1:400
In order to study the lower esophageal sphincter of horses, Invitrogen ELAVL4 antibody (Molecular Probes, 833294) was used in immunohistochemistry on domestic horse samples at 1:400. Histochem Cell Biol (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:200; fig 1
In order to test if brain-derived neurotrophic factor in the paraventricular nucleus of the hypothalamus contributes to increases in blood pressure, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on rat samples at 1:200 (fig 1). Am J Physiol Heart Circ Physiol (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500
In order to study downstream Notch targets needed for neuronal specification, Invitrogen ELAVL4 antibody (molecular probes, A21271) was used in immunohistochemistry on chicken samples at 1:500. Front Neuroanat (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:250
In order to assess tissue and cellular changes in the colonic wall upon induction of colitis, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples at 1:250. J Cell Mol Med (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human
In order to discuss cytogenetically visible chromosomal translocations, Invitrogen ELAVL4 antibody (life technologies, cat #A21271) was used in immunohistochemistry - paraffin section on human samples . J Med Genet (2015) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:100; fig s3
In order to examine the contribution of the von Hippel-Lindau gene to sympathoadrenal homeostasis, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:100 (fig s3). EMBO Mol Med (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:25
In order to determine the enteric nervous system transduction following systemic AAV9 administration, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:25. Front Mol Neurosci (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:1000
In order to describe a method to study adult neurogenesis using avian brains, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunohistochemistry on mouse samples at 1:1000. Cold Spring Harb Protoc (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:10; fig S2
In order to show that fibroblast growth factors and bone morphogenetic proteins contribute to astrocyte development, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunocytochemistry on rat samples at 1:10 (fig S2). PLoS ONE (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500; fig 6
In order to characterize sequencing, repair, stuttering, and basal ganglia function in adult songbirds, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on chicken samples at 1:500 (fig 6). Sci Rep (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:1000
In order to examine the transcriptional networks that CHD8 regulates in neural progenitor cells, Invitrogen ELAVL4 antibody (invitrogen, A21271) was used in immunohistochemistry on zebrafish samples at 1:1000. Proc Natl Acad Sci U S A (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1 ug/ml
In order to test if diet and hormonal status modulate hypothalamic neurogenesis in the adult female mouse, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunohistochemistry - frozen section on mouse samples at 1 ug/ml. J Neuroendocrinol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human
In order to examine cavitation and differentiation of human dental pulp stem cells, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunohistochemistry - paraffin section on human samples . Biol Cell (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Japanese rice fish; 1:100
In order to explore the differential susceptibilities of early retinal progenitor cells to Atoh7 in vivo, Invitrogen ELAVL4 antibody (invitrogen, A-21271) was used in immunohistochemistry on Japanese rice fish samples at 1:100. Mech Dev (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; Japanese rice fish; 1:200
In order to develop a clonal labeling and non-invasive fate tracking system and study post-embryonic stem cells in the retina, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunocytochemistry on Japanese rice fish samples at 1:200. Development (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; 1:300
In order to demonstrate that growth factor depletion in human neural progenitor cells induces mitochondrial ROS production, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunocytochemistry on human samples at 1:300. J Biol Chem (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100; fig 3
In order to determine the effects pf estrogen in adult brain proliferation zones, Invitrogen ELAVL4 antibody (Molecular Probes, .A-21271) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 3). Neuroscience (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to characterize mpz gene expression during development and axonal injury in zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:500. J Biol Chem (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; mouse; 1:750
In order to describe the development a neurosphere culture method that results in highly proliferative stem/progenitor cell population, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on mouse samples at 1:750. Int J Dev Neurosci (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:500
In order to identify CHD8 disruptions in a distinct autism spectrum disorder subtype and reveal comorbidities between brain development and enteric innervation, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunocytochemistry on zebrafish samples at 1:500. Cell (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 20 ug/ml
In order to establish a model to study the effects of opioids on the gut development and peristalsis using zebrafish, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunocytochemistry on zebrafish samples at 20 ug/ml. Sci Rep (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500; fig 1
In order to report that beta-catenin controls the cell fate and polarity of neuroblasts by modulating the expression and localization of aPKC, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on chicken samples at 1:500 (fig 1). Nat Commun (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:2000
In order to discuss Ewing sarcoma, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on human samples at 1:2000. Histopathology (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:500; fig s7
In order to investigate the impact of the BAF complex and SOX11 transcriptional network in brain development, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on mouse samples at 1:500 (fig s7). Nat Commun (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:500
In order to investigate the role of Dbx1 in neurogenesis in zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:500. Exp Neurol (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; chicken
In order to study the mechanisms that regulate the acquisition and maintenance germ cell character, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunocytochemistry on chicken samples . Stem Cells Dev (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human
In order to study the effects of increased MECP2 on development of the nervous system, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunocytochemistry on human samples . Neurobiol Dis (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human
In order to identify QARS (encoding glutaminyl-tRNA synthetase [QARS]) mutations in two unrelated families affected by progressive microcephaly, Invitrogen ELAVL4 antibody (Life Technologies, A-21271) was used in immunocytochemistry on human samples . Am J Hum Genet (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic horse; 1:100
In order to study the equine intestinal expression of PAR2, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on domestic horse samples at 1:100. Res Vet Sci (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; 1:50
In order to study the role of PTEN in neurite outgrowth in human embryonic stem cell-derived neuronal progenitor cells, Invitrogen ELAVL4 antibody (Invitrogen, A 21271) was used in immunocytochemistry on human samples at 1:50. J Comp Neurol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:1000
In order to identify the characteristics of morphology, distribution, and phenoype of polycystin kidney disease 2-like 1-positive cerebrospinal fluid that contacts neurons in the brainstem of mice, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on mouse samples at 1:1000. PLoS ONE (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; Apteronotus leptorhynchus
In order to identify proteins involved in the development of a sexually dimorphic behavior using the brown ghost knifefish, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry - frozen section on Apteronotus leptorhynchus samples . J Neurophysiol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human; 1:160; fig 4
In order to characterize two patients with multinodular and vacuolating neuronal tumors, Invitrogen ELAVL4 antibody (Molecular probes, A-21271) was used in immunohistochemistry - paraffin section on human samples at 1:160 (fig 4). Acta Neuropathol Commun (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; true eels; 1:400; fig 2, 3
In order to use European eels to understand the adaptive changes of the enteric nervous system to modified salinity and starvation, Invitrogen ELAVL4 antibody (Molecular Probes, 833294) was used in immunohistochemistry - frozen section on true eels samples at 1:400 (fig 2, 3). J Anat (2014) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:500; fig 3
In order to describe a brainstem culture model to study axonal growth, neurogenesis, and regeneration of the adult zebrafish central nervous system, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on zebrafish samples at 1:500 (fig 3). J Neurosci Methods (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Apteronotus leptorhynchus; fig 3
In order to assess the age-related changes associated with adult neurogenesis in the brain of brown ghost knifefish, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on Apteronotus leptorhynchus samples (fig 3). Dev Neurobiol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; fig 1
In order to test if nongenetic factors might contribute to Hirschsprung disease using a zebrafish model, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples (fig 1). J Clin Invest (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; chicken; fig 3
In order to investigate what defines the neural crest and the origin of the ectomesenchyme in mice and chickens, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry - frozen section on chicken samples (fig 3). Development (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:1000; fig 3
In order to report the contribution of Tal1 and Tal2 to GABAergic neurogenesis in the midbrain, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:1000 (fig 3). Biol Open (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:800
In order to determine the neuronal distribution of CART in porcine dorsal root ganglia, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on pigs samples at 1:800. Acta Histochem (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:500; fig 1
In order to elucidate the role of transforming growth factor beta during neurogenesis, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:500 (fig 1). J Cell Sci (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500; fig 5
In order to investigate the role of matrix metalloproteinase 17b to neural crest cell migration in zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on zebrafish samples at 1:500 (fig 5). PLoS ONE (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:800; fig 1, 2
In order to investigate calbindin expression in the pig gastrointestinal tract, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on pigs samples at 1:800 (fig 1, 2). Pol J Vet Sci (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; bank vole; 1:150; tbl 1
In order to describe the phenotype of ileal myenteric plexus neuronal cells and fibers of the bank vole, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on bank vole samples at 1:150 (tbl 1). Res Vet Sci (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; domestic horse; 1:200; fig 2
In order to study adrenergic receptors in the horse intestine, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on domestic horse samples at 1:200 (fig 2). Res Vet Sci (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse
In order to study the function of cerebellins in the cerebellum and striatum, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on mouse samples . J Comp Neurol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; goldfish; 1:100; tbl 1
In order to report the innervation patterns in the heart of the goldfish, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on goldfish samples at 1:100 (tbl 1). J Comp Neurol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; smaller spotted dogfish; 1:100
In order to study the cerebellar connections in shark embryos and juveniles, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on smaller spotted dogfish samples at 1:100. J Comp Neurol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human; fig 7
In order to study the dynamics, cell distribution, molecular profiles, and neuronal/osteogenic potential of spheroids generated from human dental pulp, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - paraffin section on human samples (fig 7). J Cell Biochem (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; zebrafish ; 1:500
In order to investigate the effect of aging on neurogenesis and its mechanism in zebrafish telencephalon, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry - free floating section on zebrafish samples at 1:500. J Comp Neurol (2013) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1 ug/ml; fig 8
In order to test if the Z-gene contributes to sexual differentiation of the song system, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunocytochemistry on zebrafish samples at 1 ug/ml (fig 8). Neuroscience (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:200; fig 4
In order to report that mucosal glia cell damage occurs during diabetic symptoms, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on mouse samples at 1:200 (fig 4). Auton Neurosci (2013) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; mouse; fig 2
In order to elucidate the BMP antimitotic mechanism, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunocytochemistry on mouse samples (fig 2). Mol Cell Biol (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:250; fig 5
In order to examine the diverse neural stem and progenitor cell types in the teleost fish brain, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:250 (fig 5). Neural Dev (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; fig 3
In order to develop an inducible system to control the timing of transgene expression in zebrafish and chicks, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples (fig 3). Development (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; fig 3
In order to assess the use of stem cell therapy for Parkinson's disease using rhesus monkeys, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples (fig 3). Cell Transplant (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:200; fig 4
  • immunohistochemistry; pigs ; 1:200; fig 4
In order to study the role of serotonin on enteric mast cells, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on human samples at 1:200 (fig 4) and in immunohistochemistry on pigs samples at 1:200 (fig 4). Am J Physiol Gastrointest Liver Physiol (2013) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; mouse; 1:250; fig 1
In order to examine neurons in the mouse distal colon during aging, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunocytochemistry on mouse samples at 1:250 (fig 1). Neurogastroenterol Motil (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:800
In order to study the distribution patterns of cocaine- and amphetamine-regulated transcript in the stomach of the pig and wild boar, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on pigs samples at 1:800. Anat Histol Embryol (2014) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:200; fig 1
In order to examine the expression of Runx1 and Runx3 in the mouse dorsal root ganglion during embryonic and postnatal development, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig 1). Dev Neurobiol (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:20
In order to study the generation of motor neurons and oligodendrocytes, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples at 1:20. J Neurosci (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:1000; fig 6
In order to show a causal role of AUTS2 in neurocognitive disorders, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on zebrafish samples at 1:1000 (fig 6). Am J Hum Genet (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500; fig 3
In order to investigate the role of Delta/notch-like epidermal growth factor-related receptor in the developing Drosophilia nervous system, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples at 1:500 (fig 3). Dev Biol (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:10,000; fig 2
In order to develop tools to study fluorescent enteric neurons in zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:10,000 (fig 2). Zebrafish (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to study how to restrict transgene expression to the nervous system in zebrafish larvae, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples at 1:500. Front Neural Circuits (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; smaller spotted dogfish; 1:100
In order to study the development of the olfactory system in Scyliorhinus canicula, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on smaller spotted dogfish samples at 1:100. Brain Struct Funct (2014) ncbi
mouse monoclonal (16A11)
  • western blot; zebrafish ; 1:100; fig 3
In order to show that MCT8 deficient zebrafish exhibit a neurological phenotype, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in western blot on zebrafish samples at 1:100 (fig 3). J Biol Chem (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Apteronotus leptorhynchus; fig 3
In order to assess the proliferation and survival of cells following complete spinal cord transection using teleost fish, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on Apteronotus leptorhynchus samples (fig 3). Brain Behav Evol (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:10,000; fig s2
In order to examine the roles of Mnx family transcription factors in specifying the subtypes of individually identified zebrafish primary motoneurons, Invitrogen ELAVL4 antibody (Life Technologies, A21271) was used in immunohistochemistry on zebrafish samples at 1:10,000 (fig s2). Neural Dev (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; tbl 2
In order to examine if sex differences in cell proliferation represents a conserved feature of adult brain plasticity, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples (tbl 2). Neuroscience (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:800; fig 6
In order to study the fate of GABAergic neurons in different diencephalic prosomeres and the transcriptional mechanisms involved, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on mouse samples at 1:800 (fig 6). Development (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Caucasian squirrel; 1:150
In order to study the enteric nervous system of wild or 'unconventional' rodents, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on Caucasian squirrel samples at 1:150. Anat Histol Embryol (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:500; fig 3
In order to compare electrophysiological events in rats and zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:500 (fig 3). PLoS ONE (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:400; fig 1
In order to test if treatment with red kidney bean lectin influences the chemical code of the small intestine nervous system of suckling pigs, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on pigs samples at 1:400 (fig 1). Acta Histochem (2013) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100; fig 7
In order to determine the molecular and cellular factors involved in NF1 disease pathogenesis in vivo, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 7). Dis Model Mech (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:200; fig 5
In order to investigate how fgf20a-expressing neurons in segment centers cluster, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on zebrafish samples at 1:200 (fig 5). Development (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:20; fig 1
In order to elucidate mechanisms underlying oligodendrocyte differentiation, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples at 1:20 (fig 1). J Neurosci (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Japanese quail; 1:1000; tbl 1
In order to investigate the ontogeny of diencephalic brain nuclei using quail, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on Japanese quail samples at 1:1000 (tbl 1). J Comp Neurol (2012) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; fig 1
In order to investigate mechanisms underlying the enteric neurochemical plasticity events evoked by disruption of the normal brain-gut cross-talk, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on rat samples (fig 1). Auton Neurosci (2012) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:1000; tbl 1
In order to assess the role of galanin in developing zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunocytochemistry on zebrafish samples at 1:1000 (tbl 1). J Comp Neurol (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Hawaiian perch; 1:20; fig 10
In order to study the generation, migration, and differentiation of new neurons and glial cells in the Mozambique tilapia, Invitrogen ELAVL4 antibody (Molecular Probe, A-21271) was used in immunohistochemistry on Hawaiian perch samples at 1:20 (fig 10). J Comp Physiol A Neuroethol Sens Neural Behav Physiol (2012) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:400; fig 1
In order to assess the neuroprotective effects of vasoactive intestinal peptide and glucagon-like peptide 1 and 2, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on rat samples at 1:400 (fig 1). BMC Gastroenterol (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; rat; 1:5000; fig 5
In order to study interactions between macrophages and the autonomic innervation of gastrointestinal tract smooth muscle, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry - free floating section on rat samples at 1:5000 (fig 5). Auton Neurosci (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:400
In order to investigate neurogenic periventricular zones in the adult zebrafish forebrain, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry - frozen section on zebrafish samples at 1:400. J Comp Neurol (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100; fig 3
In order to show that olig2 function contributes to the migration of facial motor neurons, Invitrogen ELAVL4 antibody (Molecular Probes, 16a11) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 3). Dev Dyn (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 10 ug/ml
In order to examine the contribution of nitric oxide synthase-immunoreactive neurons to pancreatitis-induced ileus, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples at 10 ug/ml. BMC Gastroenterol (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:600; fig 7
In order to study glial responses using an invasive stab wound model, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:600 (fig 7). Glia (2012) ncbi
mouse monoclonal (16A11)
  • western blot; rat; fig 4
In order to elucidate the role of Ser129 phosphorylation in alpha-syn neurotoxicity, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in western blot on rat samples (fig 4). J Neurosci (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:300; fig 4
In order to investigate brain regeneration mechanisms in adult zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:300 (fig 4). Development (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; fig 3
In order to determine the role of neuroepithelial cells cohesion in facial branchiomotor neuron migration, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples (fig 3). Development (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; fig 2
In order to elucidate mechanisms that regulate the maturation of enteric neurons in postnatal life, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on mouse samples (fig 2). J Neurosci (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; fig 3
In order to study upbeat nystagmus in a female patient with pancreatic cancer, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples (fig 3). Ann N Y Acad Sci (2011) ncbi
mouse monoclonal (16A11)
  • western blot; society finch; 1:200
In order to elucidate the molecular mechanisms that regulate avian vocal development, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in western blot on society finch samples at 1:200. PLoS ONE (2011) ncbi
mouse monoclonal (16A11)
  • western blot; mouse; fig 3
In order to identify pathways that can functionally replace CD28-mediated costimulation in normal T cells, Invitrogen ELAVL4 antibody (Zymed, A-21271) was used in western blot on mouse samples (fig 3). PLoS ONE (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500; fig 5
In order to assess the contribution of sec61al1 in the formation of bilaterally symmetric habenular nuclei, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:500 (fig 5). Dev Biol (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Trachemys dorbigni; 1:100; fig 9
In order to study the action of GABA around the central canal of the turtle spinal cord, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on Trachemys dorbigni samples at 1:100 (fig 9). J Physiol (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:100; fig 7
In order to determine the origin of hypertrophic GFAP(+)/vimentin(+)/nestin(+) "reactive" astroglia, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on mouse samples at 1:100 (fig 7). J Neurosci (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:50; fig 1
In order to discuss paraneoplastic upbeat nystagmus, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:50 (fig 1). Neurology (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100; fig 4
In order to investigate the assembly of the cerebral vasculature, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 4). Dev Biol (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:1500; fig 2
In order to discuss the inhibitory functions of members of the Hairy/Enhancer of Split family of bHLH-Orange transcription factors, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on zebrafish samples at 1:1500 (fig 2). BMC Dev Biol (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:500; fig 4
In order to examine expression of toll-like receptors in the neonatal brain and their regulation after hypoxic-ischemic brain injury, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on mouse samples at 1:500 (fig 4). J Neuroinflammation (2011) ncbi
mouse monoclonal (16A11)
  • western blot; human; 1:1000; fig s1
In order to investigate the role of HuR in brain tumor growth, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in western blot on human samples at 1:1000 (fig s1). Mol Cancer Res (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:400; fig s4
In order to use a zebrafish model to examine the impact of altered dopamine signaling on brain development and larval motor behavior, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on zebrafish samples at 1:400 (fig s4). J Neurosci (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:250; fig s3
In order to study the different subtypes of glutamatergic OB interneurons, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunohistochemistry on mouse samples at 1:250 (fig s3). Neural Dev (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human; 1:1250; fig 3
In order to examine the gastrointestinal neuromuscular pathology in patients with Alpers disease, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - paraffin section on human samples at 1:1250 (fig 3). Am J Surg Pathol (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:100; fig 2
In order to examine the neural-glial components of myenteric ganglia and interstitial cells of Cajal in patients with ulcerative colitis, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:100 (fig 2). J Cell Mol Med (2012) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; chicken; 1:120; fig 8
In order to report the distribution of chicken aquaporin-4, Invitrogen ELAVL4 antibody (Invitrogen, clone 16A11) was used in immunohistochemistry - frozen section on chicken samples at 1:120 (fig 8). Cell Tissue Res (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100-1:200; fig 2
In order to study calbindin in the gut of adult and larval zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on zebrafish samples at 1:100-1:200 (fig 2). Cell Tissue Res (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:100; tbl 1
In order to determine the cellular distribution of alpha1, alpha2 and alpha3 GABA(A) receptor subunits in the striatopallidal and pallidopallidal synapses, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples at 1:100 (tbl 1). Eur J Neurosci (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; rat; fig 5
In order to investigate the therapeutic potential of enteric neural crest stem cells in Hirschsprung disease, Invitrogen ELAVL4 antibody (Moleculer Probes, A21271) was used in immunohistochemistry - frozen section on rat samples (fig 5). Neurogastroenterol Motil (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic sheep; 1:400; fig 1
In order to determine the localization of aquaporin 1 in the sheep duodenum, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on domestic sheep samples at 1:400 (fig 1). Ann Anat (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:1000; fig 3
In order to determine the origin of new neurons in the hippocampus, Invitrogen ELAVL4 antibody (Molecular probes, A21271) was used in immunohistochemistry on rat samples at 1:1000 (fig 3). Neurosci Res (2011) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; 1:250; fig 12
  • immunohistochemistry; human; 1:250; fig 12
In order to discuss neural crest stem cells, Invitrogen ELAVL4 antibody (Invitrogen, A-21271) was used in immunocytochemistry on human samples at 1:250 (fig 12) and in immunohistochemistry on human samples at 1:250 (fig 12). PLoS ONE (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; fig 5
In order to characterize cells expressing IP3 receptor type 3 in the olfactory epithelium, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on mouse samples (fig 5). Eur J Neurosci (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish
In order to investigate the neurochemical coding of enteric neurons in zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes Inc., A-21271) was used in immunohistochemistry - frozen section on zebrafish samples . J Comp Neurol (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:20; fig 2
In order to use teleost fish to test if inhibition of apoptosis after injury enhances spinal cord regeneration, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:20 (fig 2). Neuroscience (2010) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:400; fig 1
In order to study the localization of corticotropin releasing factor in rat small and large intestines and study its role in nerve survival, Invitrogen ELAVL4 antibody (Molecular Probes, code A-21271) was used in immunocytochemistry on rat samples at 1:400 (fig 1). Regul Pept (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:100-1:200; fig 1
In order to examine calbindin immunoreactivity in the enteric nervous system of the teleost shorthorn sculpin, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on human samples at 1:100-1:200 (fig 1). Auton Neurosci (2011) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:100; fig 1
In order to determine the localization of glial fibrillary acidic protein immunoreactivity in adult and developing fish, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:100 (fig 1). Cell Tissue Res (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; chicken; 1:100
In order to identify cerebellin2 in chick and study its expression pattern, Invitrogen ELAVL4 antibody (Molecular Probes, A- 21271) was used in immunohistochemistry - paraffin section on chicken samples at 1:100. J Comp Neurol (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; pigs ; tbl 1
In order to discuss neurotransmission to the longitudinal muscle in neonatal and adult guinea pig ileum, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on pigs samples (tbl 1). Neurogastroenterol Motil (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:800; fig 4
In order to study the distinct involvement of Asc11 in the development of different midbrain GABAergic neurone sub-populations, Invitrogen ELAVL4 antibody (Molecular probes, A21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:800 (fig 4). Dev Biol (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 4 ug/ml; fig 2
In order to study the contribution of sodium channels to mechanosensory responses in zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on zebrafish samples at 4 ug/ml (fig 2). Development (2010) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:100; fig 3
In order to determine the expression and function of protogenin in the developing nervous system, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunocytochemistry on rat samples at 1:100 (fig 3). J Neurosci (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; Atlantic canary; 1:40
In order to study neuronal migration and recruitment in the adult songbird brain, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - free floating section on Atlantic canary samples at 1:40. J Comp Neurol (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:100
In order to localize beta2-adrenoceptors in the adult zebrafish brain, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on zebrafish samples at 1:100. J Comp Neurol (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:3000; fig 4
In order to create tools to help make inducible knockout zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on zebrafish samples at 1:3000 (fig 4). Nat Methods (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; mouse; 1:100; fig 1
In order to investigate how astrocyte-like progenitors differentiate into neuron-committed progenitors, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry - free floating section on mouse samples at 1:100 (fig 1). Neuroscience (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; pigs ; 1:50; fig 9
In order to test if urocortins in the enteric nervous system regulate colonic motor behavior, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on pigs samples at 1:50 (fig 9). Br J Pharmacol (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:200; fig 1
In order to test if transplanted embryonic retinal cells from various stages of development influence the survival of mature ganglion cells, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on chicken samples at 1:200 (fig 1). Invest Ophthalmol Vis Sci (2010) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:750; fig 4
In order to study the brain-endocrine interactions in the mediobasal hypothalamus, Invitrogen ELAVL4 antibody (Probes, A21271) was used in immunohistochemistry on rat samples at 1:750 (fig 4). Endocrinology (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; zebrafish ; 1:200
In order to discuss methods for antigen retrieval, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry - paraffin section on zebrafish samples at 1:200. Zebrafish (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:500
In order to suggest that retinal pigment epithelium morphogenesis and cytodifferentiation requires SoxB1 downregulation and an absence of FGF-like signal, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on chicken samples at 1:500. Development (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; guinea pig; 1:300; fig 4
In order to examine age-associated changes in the guinea-pig ileum, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on guinea pig samples at 1:300 (fig 4). Neurogastroenterol Motil (2009) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:500; fig 4
In order to develop and characterize a zebrafish model for Parkin deficiency, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunocytochemistry on zebrafish samples at 1:500 (fig 4). Brain (2009) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; chicken; 1:50
In order to study the development of microglia in the spinal cord and characterize their changes in response to naturally occurring and pathological death of motoneurons, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunocytochemistry on chicken samples at 1:50. J Neurosci Res (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to elucidate the exact roles of canonical Wnt signaling in neurogenesis, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on zebrafish samples at 1:500. Zebrafish (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebra finch
In order to compare estrogen and ribosomal protein expression in juvenile male and female zebra finches, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on zebra finch samples . Dev Neurobiol (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; human; 1:100; tbl 1
In order to find a method to detect and count myenteric neurons and glial cells in paraffin sections of human colon, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on human samples at 1:100 (tbl 1). Cell Tissue Res (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:20
In order to characterize nuclear aberrations present in zebrafish brains, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:20. Neuroscience (2009) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; zebrafish ; 1:800; fig 3
In order to develop a method for visualizing intestinal transit in larval zebrafish, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunocytochemistry on zebrafish samples at 1:800 (fig 3). Neurogastroenterol Motil (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; 1:500; fig 2
In order to study the role of the Gata2 transcription factor in midbrain GABAergic neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - paraffin section on mouse samples at 1:500 (fig 2). Development (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; fig 2
In order to identify the gene impacted in the "flotte lotte" zebrafish mutant, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on zebrafish samples (fig 2). Gastroenterology (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100; fig 4
In order to describe the first mutation in the human AP1S1 gene, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 4). PLoS Genet (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic horse; fig 5
In order to develop a method for the carbocyanine triple fluorescence labelling of neuronal, vascular, and glial markers and use this technique to study a mouse model of Alzheimer's disease, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry on domestic horse samples (fig 5). J Chem Neuroanat (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:700; fig 4
In order to demonstrate that the neural crest population that gives rise to dorsal root ganglion neurons becomes fate restricted to a neuronal/glial precursor before the onset of neurog1 function using transgenic zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on zebrafish samples at 1:700 (fig 4). J Neurosci (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:200; fig 1
  • western blot; mouse; fig 3
In order to determine the localization of HuR and HuD RNA-binding proteins after seizure or cocaine treatment, Invitrogen ELAVL4 antibody (Molecular Probes, clone 16A11) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig 1) and in western blot on mouse samples (fig 3). J Neurochem (2008) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:400
In order to examine the impact of mast cells on neuronal survival and plasticity of myenteric neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on rat samples at 1:400. Neuropharmacology (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; domestic sheep; 1:300
In order to determine the distribution patterns of cocaine- and amphetamine-regulated transcript-immunoreactive nerve fibers and enteric neurons present in the rumen, reticulum, omasum, and abomasum of the sheep, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on domestic sheep samples at 1:300. Anat Histol Embryol (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat
  • immunohistochemistry; human
In order to determine the expression of glutathione peroxidase in control, Parkinson's disease, and dementia with Lewy bodies tissues, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples and in immunohistochemistry on human samples . Acta Neuropathol (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; chicken; 1:200
In order to determine the roles of the mitogen-activated protein kinase pathway in regulating the activity of Muller glia in the chicken retina, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry - frozen section on chicken samples at 1:200. Glia (2009) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to investigate the role of FGF in stem cell maintenance and neurogenesis in zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on zebrafish samples at 1:500. J Comp Neurol (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic sheep; 1:1000; fig 2
In order to examine the enteric nervous system innervating the pyloric sphincter of the lamb abomasum, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on domestic sheep samples at 1:1000 (fig 2). J Chem Neuroanat (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; 1:50; fig 2h
In order to investigate the timing of maturation of the leptin signal transduction system, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on mouse samples at 1:50 (fig 2h). Brain Res (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; river trout ; fig 2
In order to study the appearance and distribution of calretinin in the olfactory system of developing and adult brown trout, Invitrogen ELAVL4 antibody (Invitrogen, Molecular Probes, A21271) was used in immunohistochemistry - paraffin section on river trout samples (fig 2). J Chem Neuroanat (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; domestic sheep; 1:200
In order to study enteric neuroinvasion by scrapie prions, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on domestic sheep samples at 1:200. Acta Neuropathol (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; 1:100; tbl 1
In order to investigate the functions of nNOS in mouse small intestinal smooth muscle, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (tbl 1). J Cell Mol Med (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:500
In order to identify Zic2a as a novel regulator of prethalamic development in zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:500. Dev Biol (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:100
In order to localize alpha(2A)-adrenoceptors in the adult zebrafish brain, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry - frozen section on zebrafish samples at 1:100. J Comp Neurol (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - free floating section; mouse; 1:50
In order to study the contribution of Nkx2.1 lineages to neurons in the mature telencephalon, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - free floating section on mouse samples at 1:50. J Comp Neurol (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; guinea pig; 1:50
In order to examine the effects of tegaserod on mucosal secretion and secretomotor neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on guinea pig samples at 1:50. Neurogastroenterol Motil (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic sheep; 1:1000; fig 8
In order to characterize myenteric plexus neurons of the sheep ileum, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on domestic sheep samples at 1:1000 (fig 8). Anat Rec (Hoboken) (2007) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:800
In order to assess the effects of lipopolysaccharide on enteric neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on rat samples at 1:800. Regul Pept (2008) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; guinea pig; fig 6
In order to determine the localization of the Na(v)1.7 alpha subunit in the guinea pig myenteric ganglia, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on guinea pig samples (fig 6). J Comp Neurol (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; fig 3
In order to study the role of FnTm2 (Phantom 2) in learned song, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in immunohistochemistry on human samples (fig 3). J Comp Neurol (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; Xenopus laevis; 1:250
In order to study the regeneration of the neural crest derivatives in the Xenopus tadpole tail, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - paraffin section on Xenopus laevis samples at 1:250. BMC Dev Biol (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebra finch; 1:50; fig 6
In order to study implication in avian vocal learning by characterizing CaMKII-expressing neurons within a striatal region, Invitrogen ELAVL4 antibody (Molecular Probes, noca) was used in immunohistochemistry on zebra finch samples at 1:50 (fig 6). Brain Res (2007) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:1000
In order to study Notch signaling in neural stem cells, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunocytochemistry on rat samples at 1:1000. Mol Cell Biol (2007) ncbi
mouse monoclonal (16A11)
In order to investigate the central gelatinosa in the turtle spinal cord, Invitrogen ELAVL4 antibody (Molecular Probes, A 21271) was used . J Comp Neurol (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100-1:200; fig 4
In order to analyze the roles of intrinsic and extrinsic innervation for initiating and propagating the spontaneous contractions in the developing zebrafish gut, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on zebrafish samples at 1:100-1:200 (fig 4). J Exp Biol (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; rat; 1:400; tbl 1
In order to count the rat colonic myenteric neuronal cells that express calcitonin gene-related peptide, galanin, neuropeptide Y, somatostatin, vasoactive intestinal peptide, and nitric oxide synthase, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on rat samples at 1:400 (tbl 1). Regul Pept (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:1000; tbl 1
In order to characterize myenteric neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on human samples at 1:1000 (tbl 1). Neurogastroenterol Motil (2007) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:100
In order to identify mitral cells in the olfactory bulb of adult zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:100. J Comp Neurol (2006) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; mouse; fig 3
In order to identify the cells infected by FrCasE and Moloney MLV-ts1 viruses, Invitrogen ELAVL4 antibody (Invitrogen, 16A11) was used in immunohistochemistry - paraffin section on mouse samples (fig 3). Am J Pathol (2006) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human
In order to determine how human embryonic stem cells are efficiently generated from retinal progenitor cells, Invitrogen ELAVL4 antibody (Molecular Probes, noca) was used in immunocytochemistry on human samples . Proc Natl Acad Sci U S A (2006) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; chicken; 1:250
In order to study the development of avian auditory system, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on chicken samples at 1:250. J Comp Neurol (2006) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; mouse; 1:200
In order to study the role of Hedgehog signaling in the differentiation of the neurectoderm and vascular cell types, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on mouse samples at 1:200. Methods Mol Biol (2006) ncbi
mouse monoclonal (16A11)
  • western blot; guinea pig; fig 2
In order to compare the extrinsic efferent innervation of the distal colon and rectum of guinea pigs, Invitrogen ELAVL4 antibody (Invitrogen, A21271) was used in western blot on guinea pig samples (fig 2). J Comp Neurol (2006) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:50; fig 1
In order to characterized human myenteric neurons co-immunoreactive for neuronal nitric oxide synthase and vasoactive intestinal peptide, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:50 (fig 1). Histochem Cell Biol (2006) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:50; tbl 2
In order to compare panneuronal markers in the enteric nervous system, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:50 (tbl 2). Histol Histopathol (2006) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; domestic sheep; 1:1000
In order to examine the extrinsic origins of calcitonin gene-related peptide immunoreactive nerve fibers in the sheep ileum, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on domestic sheep samples at 1:1000. Cell Tissue Res (2006) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:400
In order to study the effects of LPS on the survival and neurotransmitter expression of cultured porcine myenteric neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on pigs samples at 1:400. Dig Dis Sci (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; fig 2
In order to study the effects of nerve growth factor on enteric nerves, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on human samples (fig 2). J Comp Neurol (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; mouse; fig 3
In order to study PEPT2 in the gastrointestinal tract, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on mouse samples (fig 3). J Comp Neurol (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; tbl 1
In order to assess the distribution and fate of cocaine- and amphetamine-regulated transcript peptide-immunoreactive structures in the neonatal and adult rat urinary bladder, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples (tbl 1). J Comp Neurol (2005) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; chicken
In order to define a novel Nogo-A-specific domain in Amino-Nogo that binds the Nogo-66 receptor, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on chicken samples . J Neurosci (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; rat; 1:800
In order to examine the enteric nervous system and intestinal mobility of rats that received total parenteral nutrition, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on rat samples at 1:800. J Surg Res (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:50; fig 6
In order to characterize leu-enkephalin positive neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:50 (fig 6). Histochem Cell Biol (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; fig 4
In order to study the development of the caudal neural tube, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on chicken samples (fig 4). Dev Biol (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:300
In order to elucidate the molecular bases for lateral intervening zone formation, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:300. Development (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; pigs ; 1:400
In order to examine the roles of galanin and vasoactive intestinal peptide on small intestinal porcine myenteric neuron survival, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - frozen section on pigs samples at 1:400. Regul Pept (2005) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; human; 1:500
In order to assess the ability of human embryonic stem cells to differentiate into dopamine-producing neurons in a simple serum-free suspension culture system, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on human samples at 1:500. Stem Cells (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:1000
In order to discuss methods to study neural cell migration, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on chicken samples at 1:1000. Methods Mol Biol (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; rat; fig 3
In order to determine the occurrence of neurogenesis in the dorsal vagal complex of adult rats, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry - frozen section on rat samples (fig 3). Neuroscience (2005) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; rat; 1:1000; fig 1
  • immunohistochemistry; guinea pig; 1:1000; fig 1
  • immunohistochemistry; mouse; 1:1000; fig 1
In order to determine the expression and localization of hyperpolarisation-activated nucleotide-gated isoforms in the enteric nervous systems of mice, rats and guinea-pigs, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on rat samples at 1:1000 (fig 1), in immunohistochemistry on guinea pig samples at 1:1000 (fig 1) and in immunohistochemistry on mouse samples at 1:1000 (fig 1). Neuroscience (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; zebrafish ; 1:500
In order to study the requirement for retinal expression during optic nerve regeneration by an element in the alpha1-tubulin promoter and not after eye injury in the adult zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, noca) was used in immunohistochemistry - frozen section on zebrafish samples at 1:500. J Neurosci (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; domestic sheep; 1:1000
In order to test if CALB-IR expressed in sheep Dogiel type II cells, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on domestic sheep samples at 1:1000. Cell Tissue Res (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; rat; 1:800; fig 2
In order to determine the expression of VIP and NOS in cultured submucous neurons from adult rat large intestine, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry - paraffin section on rat samples at 1:800 (fig 2). Auton Neurosci (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse
In order to assess the contribution to interneuron generation in the postnatal hippocampus by NG2-expression cells in the subventricular zone that are type C-like cells, Invitrogen ELAVL4 antibody (Molecular Probes, noca) was used in immunohistochemistry - frozen section on mouse samples . J Cell Biol (2004) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; mouse; fig 3
In order to analyze ectopic expression of Rx/rax, a homeobox gene, that specifies the retinal fate of mouse embryonic stem cells, Invitrogen ELAVL4 antibody (Molecular Probes, noca) was used in immunocytochemistry on mouse samples (fig 3). Mol Cell Biol (2004) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:200; fig 3
  • immunohistochemistry; rat; 1:800; fig 2
In order to assess the efficacy of four putative pan-neuronal markers for the enteric nervous system, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunocytochemistry on rat samples at 1:200 (fig 3) and in immunohistochemistry on rat samples at 1:800 (fig 2). J Neurosci Methods (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:1000; fig 2
In order to describe methods to observe antibody localization in zebrafish whole mount preparations, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:1000 (fig 2). Methods Cell Sci (2003) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; guinea pig; 1:200
In order to use microelectrodes to study actions of bradykinin on electrical behavior of morphologically identified neurons and determine the localization of BK receptors in the submucosal plexus of guinea pig small intestine, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on guinea pig samples at 1:200. J Pharmacol Exp Ther (2004) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; chicken; fig 2
In order to identify the first population of post-mitotic neurons in the developing nervous system of the chick embryo, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry - paraffin section on chicken samples (fig 2). Neuroscience (2003) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish
In order to characterize tfap2a mutant zebrafish, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry on zebrafish samples . Development (2003) ncbi
mouse monoclonal (16A11)
  • western blot; zebrafish ; 1:500
In order to demonstrate that Smn contributes to motor axon development, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in western blot on zebrafish samples at 1:500. J Cell Biol (2003) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:800; fig 1
In order to investigate vasoactive intestinal polypeptide and nitric oxide synthase in cultured myenteric ganglia and dissociated neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on rat samples at 1:800 (fig 1). Auton Neurosci (2003) ncbi
mouse monoclonal (16A11)
  • immunocytochemistry; rat; 1:800
In order to test if vasoactive intestinal peptide and nitric oxide affect the survival of cultured, dissociated myenteric neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunocytochemistry on rat samples at 1:800. J Neurosci Res (2003) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; guinea pig; 1:50
In order to investigate the actions of bradykinin in neurons of the myenteric plexus of guinea-pig small intestine in vitro, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on guinea pig samples at 1:50. Br J Pharmacol (2003) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; guinea pig; 1:100
In order to compare peripheral ChAT distribution with that of the common form of ChAT, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on guinea pig samples at 1:100. Cell Tissue Res (2003) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; human; 1:800; fig 2
In order to determine if ghrelin is expressed in human pancreas, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on human samples at 1:800 (fig 2). Regul Pept (2002) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; pigs ; 1:50; fig 5
In order to investigate the role of P2X(7) receptors in the enteric nervous system, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on pigs samples at 1:50 (fig 5). J Comp Neurol (2001) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; chicken; fig 4
In order to study migration of cells from the olfactory neuroepithelium in chickens, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry - paraffin section on chicken samples (fig 4). Neuroscience (2001) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - paraffin section; rat; 1:200; fig 1
In order to determine the cellular distribution of HuC/D RNA-binding proteins in adult rat primary sensory neurons, Invitrogen ELAVL4 antibody (Molecular Probes,, A21271) was used in immunohistochemistry - paraffin section on rat samples at 1:200 (fig 1). Ann Anat (2001) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; mouse; fig 6
In order to analyze the inheritance pattern of asymmetry by radial glial fibers by cortical neurons, Invitrogen ELAVL4 antibody (Molecular Probes, 16A11) was used in immunohistochemistry - frozen section on mouse samples (fig 6). Neuron (2001) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; zebrafish ; 1:400
In order to investigate the role of zebrafish lakritz (lak) locus in the developing retina, Invitrogen ELAVL4 antibody (Molecular Probes, A-21271) was used in immunohistochemistry on zebrafish samples at 1:400. Neuron (2001) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; chicken; 1:200; fig 6
In order to show that the retina of postnatal chickens can generate new neurons, Invitrogen ELAVL4 antibody (Molecular Probes, A21271) was used in immunohistochemistry on chicken samples at 1:200 (fig 6). Nat Neurosci (2001) ncbi
mouse monoclonal (16A11)
  • ELISA; human
  • western blot; human; fig 1
In order to correlate the immunoreactivity of all four Hu antigens in sera from 75 patients with ANNA-1 autoantibodies with clinical parameters, Invitrogen ELAVL4 antibody (noco, A21271) was used in ELISA on human samples and in western blot on human samples (fig 1). J Autoimmun (1999) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry; Atlantic canary; fig 3
  • western blot; Atlantic canary; fig 1
In order to follow the commitment of newborn cells to neuronal lineage in the avian forebrain, Invitrogen ELAVL4 antibody (noco, 16A 1 I) was used in immunohistochemistry on Atlantic canary samples (fig 3) and in western blot on Atlantic canary samples (fig 1). J Neurobiol (1995) ncbi
mouse monoclonal (16A11)
  • immunohistochemistry - frozen section; human
  • western blot; human
In order to use antibody-associated paraneoplastic encephalomyelitis patient sera to identify a neuronal antigen HuD, Invitrogen ELAVL4 antibody (noco, noca) was used in immunohistochemistry - frozen section on human samples and in western blot on human samples . Cell (1991) ncbi
Articles Reviewed
  1. Coolen M, Altin N, Rajamani K, Pereira E, Siquier Pernet K, Puig Lombardi E, et al. Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation. Am J Hum Genet. 2022;109:909-927 pubmed publisher
  2. Völkner M, Kurth T, Schor J, Ebner L, Bardtke L, Kavak C, et al. Mouse Retinal Organoid Growth and Maintenance in Longer-Term Culture. Front Cell Dev Biol. 2021;9:645704 pubmed publisher
  3. Deng X, Iwagawa T, Fukushima M, Suzuki Y, Watanabe S. Setd1a Plays Pivotal Roles for the Survival and Proliferation of Retinal Progenitors via Histone Modifications of Uhrf1. Invest Ophthalmol Vis Sci. 2021;62:1 pubmed publisher
  4. Jamadagni P, Breuer M, Schmeisser K, Cardinal T, Kassa B, Parker J, et al. Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression. EMBO Rep. 2021;22:e50958 pubmed publisher
  5. Yoshinaga S, Shin M, Kitazawa A, Ishii K, Tanuma M, Kasai A, et al. Comprehensive characterization of migration profiles of murine cerebral cortical neurons during development using FlashTag labeling. iScience. 2021;24:102277 pubmed publisher
  6. Sulliman N, Ghaddar B, Gence L, Patche J, Rastegar S, Meilhac O, et al. HDL biodistribution and brain receptors in zebrafish, using HDLs as vectors for targeting endothelial cells and neural progenitors. Sci Rep. 2021;11:6439 pubmed publisher
  7. Gandhi S, Li Y, Tang W, Christensen J, Urrutia H, Vieceli F, et al. A single-plasmid approach for genome editing coupled with long-term lineage analysis in chick embryos. Development. 2021;148: pubmed publisher
  8. Toschi A, Galiazzo G, Piva A, Tagliavia C, Mazzuoli Weber G, Chiocchetti R, et al. Cannabinoid and Cannabinoid-Related Receptors in the Myenteric Plexus of the Porcine Ileum. Animals (Basel). 2021;11: pubmed publisher
  9. Wright C, Schneider S, Smith Edwards K, Mafra F, Leembruggen A, Gonzalez M, et al. scRNA-Seq Reveals New Enteric Nervous System Roles for GDNF, NRTN, and TBX3. Cell Mol Gastroenterol Hepatol. 2021;11:1548-1592.e1 pubmed publisher
  10. Mohsin M, Souza L, Aliabadi S, Worker C, Cooper S, Afrin S, et al. Increased (Pro)renin Receptor Expression in the Hypertensive Human Brain. Front Physiol. 2020;11:606811 pubmed publisher
  11. Pellegrini L, Bonfio C, Chadwick J, Begum F, Skehel M, Lancaster M. Human CNS barrier-forming organoids with cerebrospinal fluid production. Science. 2020;: pubmed publisher
  12. Bombardi C, Delicata F, Tagliavia C, Pierucci M, Deidda G, Casarrubea M, et al. Acute and Chronic Nicotine Exposures Differentially Affect Central Serotonin 2A Receptor Function: Focus on the Lateral Habenula. Int J Mol Sci. 2020;21: pubmed publisher
  13. Fares M, Cochet Bernoin M, Gonzalez G, Montero Menei C, Blanchet O, Benchoua A, et al. Pathological modeling of TBEV infection reveals differential innate immune responses in human neurons and astrocytes that correlate with their susceptibility to infection. J Neuroinflammation. 2020;17:76 pubmed publisher
  14. Plaisier F, Hume C, Menzies J. Neural connectivity between the hypothalamic supramammillary nucleus and appetite- and motivation-related regions of the rat brain. J Neuroendocrinol. 2020;32:e12829 pubmed publisher
  15. Lange C, Rost F, Machate A, Reinhardt S, Lesche M, Weber A, et al. Single cell sequencing of radial glia progeny reveals the diversity of newborn neurons in the adult zebrafish brain. Development. 2020;147: pubmed publisher
  16. Bhattarai P, Cosacak M, Mashkaryan V, Demir S, Popova S, Govindarajan N, et al. Neuron-glia interaction through Serotonin-BDNF-NGFR axis enables regenerative neurogenesis in Alzheimer's model of adult zebrafish brain. PLoS Biol. 2020;18:e3000585 pubmed publisher
  17. Margarido A, Le Guen L, Falco A, Faure S, Chauvet N, de Santa Barbara P. PROX1 is a specific and dynamic marker of sacral neural crest cells in the chicken intestine. J Comp Neurol. 2020;528:879-889 pubmed publisher
  18. Yu S, He J. Stochastic cell-cycle entry and cell-state-dependent fate outputs of injury-reactivated tectal radial glia in zebrafish. elife. 2019;8: pubmed publisher
  19. Kawaguchi M, Hagio H, Yamamoto N, Matsumoto K, Nakayama K, Akazome Y, et al. Atlas of the telencephalon based on cytoarchitecture, neurochemical markers, and gene expressions in Rhinogobius flumineus [Mizuno, 1960]. J Comp Neurol. 2019;527:874-900 pubmed publisher
  20. Kaczmarek Hájek K, Zhang J, Kopp R, Grosche A, Rissiek B, Saul A, et al. Re-evaluation of neuronal P2X7 expression using novel mouse models and a P2X7-specific nanobody. elife. 2018;7: pubmed publisher
  21. Lasrado R, Boesmans W, Kleinjung J, Pin C, Bell D, Bhaw L, et al. Lineage-dependent spatial and functional organization of the mammalian enteric nervous system. Science. 2017;356:722-726 pubmed publisher
  22. Solek C, Feng S, Perin S, Weinschutz Mendes H, Ekker M. Lineage tracing of dlx1a/2a and dlx5a/6a expressing cells in the developing zebrafish brain. Dev Biol. 2017;427:131-147 pubmed publisher
  23. Nogueira L, Costa D, Gomes A, Martins C, Silva A, Coelho Aguiar J, et al. The involvement of mast cells in the irinotecan-induced enteric neurons loss and reactive gliosis. J Neuroinflammation. 2017;14:79 pubmed publisher
  24. Xavier A, Fontaine R, Bloch S, Affaticati P, Jenett A, Demarque M, et al. Comparative analysis of monoaminergic cerebrospinal fluid-contacting cells in Osteichthyes (bony vertebrates). J Comp Neurol. 2017;525:2265-2283 pubmed publisher
  25. Hao M, Capoccia E, Cirillo C, Boesmans W, Vanden Berghe P. Arundic Acid Prevents Developmental Upregulation of S100B Expression and Inhibits Enteric Glial Development. Front Cell Neurosci. 2017;11:42 pubmed publisher
  26. Ripa R, Dolfi L, Terrigno M, Pandolfini L, Savino A, Arcucci V, et al. MicroRNA miR-29 controls a compensatory response to limit neuronal iron accumulation during adult life and aging. BMC Biol. 2017;15:9 pubmed publisher
  27. Mayrhofer M, Gourain V, Reischl M, Affaticati P, Jenett A, Joly J, et al. A novel brain tumour model in zebrafish reveals the role of YAP activation in MAPK- and PI3K-induced malignant growth. Dis Model Mech. 2017;10:15-28 pubmed publisher
  28. Ware M, Hamdi Rozé H, Le Friec J, David V, Dupé V. Regulation of downstream neuronal genes by proneural transcription factors during initial neurogenesis in the vertebrate brain. Neural Dev. 2016;11:22 pubmed
  29. Konstantinidou C, Taraviras S, Pachnis V. Geminin prevents DNA damage in vagal neural crest cells to ensure normal enteric neurogenesis. BMC Biol. 2016;14:94 pubmed
  30. Martin Cano F, Caso Agundez M, Camello Almaraz C, Santos F, Espin M, Madrid J, et al. Octodon degus, a new model to study the agonist and plexus-induced response in the urinary bladder. J Physiol Biochem. 2017;73:77-87 pubmed publisher
  31. Neckel P, Mattheus U, Hirt B, Just L, Mack A. Large-scale tissue clearing (PACT): Technical evaluation and new perspectives in immunofluorescence, histology, and ultrastructure. Sci Rep. 2016;6:34331 pubmed publisher
  32. Vicentini G, Fracaro L, de Souza S, Martins H, Guarnier F, Zanoni J. Experimental Cancer Cachexia Changes Neuron Numbers and Peptide Levels in the Intestine: Partial Protective Effects after Dietary Supplementation with L-Glutamine. PLoS ONE. 2016;11:e0162998 pubmed publisher
  33. Cheng X, Boza Serrano A, Turesson M, Deierborg T, Ekblad E, Voss U. Galectin-3 causes enteric neuronal loss in mice after left sided permanent middle cerebral artery occlusion, a model of stroke. Sci Rep. 2016;6:32893 pubmed publisher
  34. Gill K, Hung S, Sharov A, Lo C, Needham K, Lidgerwood G, et al. Enriched retinal ganglion cells derived from human embryonic stem cells. Sci Rep. 2016;6:30552 pubmed publisher
  35. Wittmann G, Farkas E, Szilvásy Szabó A, Gereben B, Fekete C, Lechan R. Variable proopiomelanocortin expression in tanycytes of the adult rat hypothalamus and pituitary stalk. J Comp Neurol. 2017;525:411-441 pubmed publisher
  36. Panizzon C, Zanoni J, Hermes Uliana C, Trevizan A, Sehaber C, Pereira R, et al. Desired and side effects of the supplementation with l-glutamine and l-glutathione in enteric glia of diabetic rats. Acta Histochem. 2016;118:625-631 pubmed publisher
  37. Senzacqua M, Severi I, Perugini J, Acciarini S, Cinti S, Giordano A. Action of Administered Ciliary Neurotrophic Factor on the Mouse Dorsal Vagal Complex. Front Neurosci. 2016;10:289 pubmed publisher
  38. Peretz Y, Eren N, Kohl A, Hen G, Yaniv K, Weisinger K, et al. A new role of hindbrain boundaries as pools of neural stem/progenitor cells regulated by Sox2. BMC Biol. 2016;14:57 pubmed publisher
  39. Cacialli P, Gueguen M, Coumailleau P, D angelo L, Kah O, Lucini C, et al. BDNF Expression in Larval and Adult Zebrafish Brain: Distribution and Cell Identification. PLoS ONE. 2016;11:e0158057 pubmed publisher
  40. He S, Mansour M, Zimmerman M, Ki D, Layden H, Akahane K, et al. Synergy between loss of NF1 and overexpression of MYCN in neuroblastoma is mediated by the GAP-related domain. elife. 2016;5: pubmed publisher
  41. Rolland M, Li X, Sellier Y, Martin H, Pérez Berezo T, Rauwel B, et al. PPARγ Is Activated during Congenital Cytomegalovirus Infection and Inhibits Neuronogenesis from Human Neural Stem Cells. PLoS Pathog. 2016;12:e1005547 pubmed publisher
  42. Nagao M, Ogata T, Sawada Y, Gotoh Y. Zbtb20 promotes astrocytogenesis during neocortical development. Nat Commun. 2016;7:11102 pubmed publisher
  43. Zséli G, Vida B, Martinez A, Lechan R, Khan A, Fekete C. Elucidation of the anatomy of a satiety network: Focus on connectivity of the parabrachial nucleus in the adult rat. J Comp Neurol. 2016;524:2803-27 pubmed publisher
  44. Chen T, Yu Y, Hu C, Schachner M. L1.2, the zebrafish paralog of L1.1 and ortholog of the mammalian cell adhesion molecule L1 contributes to spinal cord regeneration in adult zebrafish. Restor Neurol Neurosci. 2016;34:325-35 pubmed publisher
  45. Klafke R, Prem Anand A, Wurst W, Prakash N, Wizenmann A. Differences in the spatiotemporal expression and epistatic gene regulation of the mesodiencephalic dopaminergic precursor marker PITX3 during chicken and mouse development. Development. 2016;143:691-702 pubmed publisher
  46. Uyttebroek L, Shepherd I, Vanden Berghe P, Hubens G, Timmermans J, van Nassauw L. The zebrafish mutant lessen: an experimental model for congenital enteric neuropathies. Neurogastroenterol Motil. 2016;28:345-57 pubmed publisher
  47. Ulrich F, Carretero Ortega J, Menendez J, Narvaez C, Sun B, Lancaster E, et al. Reck enables cerebrovascular development by promoting canonical Wnt signaling. Development. 2016;143:147-59 pubmed publisher
  48. Veldman M, Rios Galdamez Y, Lu X, Gu X, Qin W, Li S, et al. The N17 domain mitigates nuclear toxicity in a novel zebrafish Huntington's disease model. Mol Neurodegener. 2015;10:67 pubmed publisher
  49. Li S, Fei G, Fang X, Yang X, Sun X, Qian J, et al. Changes in Enteric Neurons of Small Intestine in a Rat Model of Irritable Bowel Syndrome with Diarrhea. J Neurogastroenterol Motil. 2016;22:310-20 pubmed publisher
  50. Hui S, Nag T, Ghosh S. Characterization of Proliferating Neural Progenitors after Spinal Cord Injury in Adult Zebrafish. PLoS ONE. 2015;10:e0143595 pubmed publisher
  51. Fornai M, Pellegrini C, Antonioli L, Segnani C, Ippolito C, Barocelli E, et al. Enteric Dysfunctions in Experimental Parkinson's Disease: Alterations of Excitatory Cholinergic Neurotransmission Regulating Colonic Motility in Rats. J Pharmacol Exp Ther. 2016;356:434-44 pubmed publisher
  52. Bettini S, Lazzari M, Ferrando S, Gallus L, Franceschini V. Histopathological analysis of the olfactory epithelium of zebrafish (Danio rerio) exposed to sublethal doses of urea. J Anat. 2016;228:59-69 pubmed publisher
  53. Small K, DeLuca A, Whitmore S, Rosenberg T, Silva Garcia R, Udar N, et al. North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13. Ophthalmology. 2016;123:9-18 pubmed publisher
  54. Podlasz P, Jakimiuk A, Chmielewska Krzesinska M, Kasica N, Nowik N, Kaleczyc J. Galanin regulates blood glucose level in the zebrafish: a morphological and functional study. Histochem Cell Biol. 2016;145:105-17 pubmed publisher
  55. Sand E, Voss U, Ohlsson B, Ekblad E. Luteinizing hormone receptors are expressed in rat myenteric neurons and mediate neuronal loss. Auton Neurosci. 2015;193:104-7 pubmed publisher
  56. Luehders K, Sasai N, Davaapil H, Kurosawa Yoshida M, Hiura H, Brah T, et al. The small leucine-rich repeat secreted protein Asporin induces eyes in Xenopus embryos through the IGF signalling pathway. Development. 2015;142:3351-61 pubmed publisher
  57. Stil A, Drapeau P. Neuronal labeling patterns in the spinal cord of adult transgenic Zebrafish. Dev Neurobiol. 2016;76:642-60 pubmed publisher
  58. Wittmann G, Mohácsik P, Balkhi M, Gereben B, Lechan R. Endotoxin-induced inflammation down-regulates L-type amino acid transporter 1 (LAT1) expression at the blood-brain barrier of male rats and mice. Fluids Barriers CNS. 2015;12:21 pubmed publisher
  59. Míguez D. A Branching Process to Characterize the Dynamics of Stem Cell Differentiation. Sci Rep. 2015;5:13265 pubmed publisher
  60. Bulc M, Gonkowski S, Całka J. Expression of Cocaine and Amphetamine Regulated Transcript (CART) in the Porcine Intramural Neurons of Stomach in the Course of Experimentally Induced Diabetes Mellitus. J Mol Neurosci. 2015;57:376-85 pubmed publisher
  61. Petto C, Gäbel G, Pfannkuche H. Architecture and Chemical Coding of the Inner and Outer Submucous Plexus in the Colon of Piglets. PLoS ONE. 2015;10:e0133350 pubmed publisher
  62. Cortés Campos C, Letelier J, Ceriani R, Whitlock K. Zebrafish adult-derived hypothalamic neurospheres generate gonadotropin-releasing hormone (GnRH) neurons. Biol Open. 2015;4:1077-86 pubmed publisher
  63. Smith A, Fleenor S, Begbie J. Changes in gene expression and cell shape characterise stages of epibranchial placode-derived neuron maturation in the chick. J Anat. 2015;227:89-102 pubmed publisher
  64. Yasuda T, Oda S, Hibi Y, Satoh S, Nagata K, Hirakawa K, et al. Embryonic Medaka Model of Microglia in the Developing CNS Allowing In Vivo Analysis of Their Spatiotemporal Recruitment in Response to Irradiation. PLoS ONE. 2015;10:e0127325 pubmed publisher
  65. Hoeber J, Trolle C, König N, Du Z, Gallo A, Hermans E, et al. Human Embryonic Stem Cell-Derived Progenitors Assist Functional Sensory Axon Regeneration after Dorsal Root Avulsion Injury. Sci Rep. 2015;5:10666 pubmed publisher
  66. Honarmand M, Thompson C, Schatton A, Kipper S, Scharff C. Early developmental stress negatively affects neuronal recruitment to avian song system nucleus HVC. Dev Neurobiol. 2016;76:107-18 pubmed publisher
  67. Mao H, Pilaz L, McMahon J, Golzio C, Wu D, Shi L, et al. Rbm8a haploinsufficiency disrupts embryonic cortical development resulting in microcephaly. J Neurosci. 2015;35:7003-18 pubmed publisher
  68. Migliavacca E, Golzio C, Männik K, Blumenthal I, Oh E, Harewood L, et al. A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology. Am J Hum Genet. 2015;96:784-96 pubmed publisher
  69. Abdi A, Mallet N, Mohamed F, Sharott A, Dodson P, Nakamura K, et al. Prototypic and arkypallidal neurons in the dopamine-intact external globus pallidus. J Neurosci. 2015;35:6667-88 pubmed publisher
  70. Briona L, Poulain F, Mosimann C, Dorsky R. Wnt/ß-catenin signaling is required for radial glial neurogenesis following spinal cord injury. Dev Biol. 2015;403:15-21 pubmed publisher
  71. Sánchez Farías N, Candal E. Doublecortin is widely expressed in the developing and adult retina of sharks. Exp Eye Res. 2015;134:90-100 pubmed publisher
  72. Jiang Q, Arnold S, Heanue T, Kilambi K, Doan B, Kapoor A, et al. Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability. Am J Hum Genet. 2015;96:581-96 pubmed publisher
  73. Nakadate K. Developmental changes in the flotillin-1 expression pattern of the rat visual cortex. Neuroscience. 2015;292:101-11 pubmed publisher
  74. Stenkamp Strahm C, Nyavor Y, Kappmeyer A, Horton S, Gericke M, Balemba O. Prolonged high fat diet ingestion, obesity, and type 2 diabetes symptoms correlate with phenotypic plasticity in myenteric neurons and nerve damage in the mouse duodenum. Cell Tissue Res. 2015;361:411-26 pubmed publisher
  75. Cheng W, Tang C, Gui H, So M, Lui V, Tam P, et al. Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype. World J Gastroenterol. 2015;21:2040-6 pubmed publisher
  76. Stoyek M, Croll R, Smith F. Intrinsic and extrinsic innervation of the heart in zebrafish (Danio rerio). J Comp Neurol. 2015;523:1683-700 pubmed publisher
  77. Benskey M, Kuhn N, Galligan J, García J, Boye S, Hauswirth W, et al. Targeted gene delivery to the enteric nervous system using AAV: a comparison across serotypes and capsid mutants. Mol Ther. 2015;23:488-500 pubmed publisher
  78. Chiocchetti R, Giancola F, Mazzoni M, Sorteni C, Romagnoli N, Pietra M. Excitatory and inhibitory enteric innervation of horse lower esophageal sphincter. Histochem Cell Biol. 2015;143:625-35 pubmed publisher
  79. Erdos B, Backes I, McCowan M, Hayward L, Scheuer D. Brain-derived neurotrophic factor modulates angiotensin signaling in the hypothalamus to increase blood pressure in rats. Am J Physiol Heart Circ Physiol. 2015;308:H612-22 pubmed publisher
  80. Ratié L, Ware M, Jagline H, David V, Dupé V. Dynamic expression of Notch-dependent neurogenic markers in the chick embryonic nervous system. Front Neuroanat. 2014;8:158 pubmed publisher
  81. Ippolito C, Segnani C, Errede M, Virgintino D, Colucci R, Fornai M, et al. An integrated assessment of histopathological changes of the enteric neuromuscular compartment in experimental colitis. J Cell Mol Med. 2015;19:485-500 pubmed publisher
  82. Hofmeister W, Nilsson D, Topa A, Anderlid B, Darki F, Matsson H, et al. CTNND2-a candidate gene for reading problems and mild intellectual disability. J Med Genet. 2015;52:111-22 pubmed publisher
  83. Macías D, Fernández Agüera M, Bonilla Henao V, López Barneo J. Deletion of the von Hippel-Lindau gene causes sympathoadrenal cell death and impairs chemoreceptor-mediated adaptation to hypoxia. EMBO Mol Med. 2014;6:1577-92 pubmed publisher
  84. Gombash S, Cowley C, Fitzgerald J, Hall J, Mueller C, CHRISTOFI F, et al. Intravenous AAV9 efficiently transduces myenteric neurons in neonate and juvenile mice. Front Mol Neurosci. 2014;7:81 pubmed publisher
  85. Asik K, Rao J, Kirn J. A method for exploring adult neurogenesis in the songbird brain. Cold Spring Harb Protoc. 2014;2014:1259-66 pubmed publisher
  86. Scholze A, Foo L, Mulinyawe S, Barres B. BMP signaling in astrocytes downregulates EGFR to modulate survival and maturation. PLoS ONE. 2014;9:e110668 pubmed publisher
  87. Kubikova L, Bosíková E, Cviková M, Lukacova K, Scharff C, Jarvis E. Basal ganglia function, stuttering, sequencing, and repair in adult songbirds. Sci Rep. 2014;4:6590 pubmed publisher
  88. Sugathan A, Biagioli M, Golzio C, Erdin S, Blumenthal I, Manavalan P, et al. CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. Proc Natl Acad Sci U S A. 2014;111:E4468-77 pubmed publisher
  89. Bless E, Reddy T, Acharya K, Beltz B, Tetel M. Oestradiol and diet modulate energy homeostasis and hypothalamic neurogenesis in the adult female mouse. J Neuroendocrinol. 2014;26:805-16 pubmed publisher
  90. Xiao L, Kumazawa Y, Okamura H. Cell death, cavitation and spontaneous multi-differentiation of dental pulp stem cells-derived spheroids in vitro: a journey to survival and organogenesis. Biol Cell. 2014;106:405-19 pubmed publisher
  91. Sinn R, Peravali R, Heermann S, Wittbrodt J. Differential responsiveness of distinct retinal domains to Atoh7. Mech Dev. 2014;133:218-29 pubmed publisher
  92. Centanin L, Ander J, Hoeckendorf B, Lust K, Kellner T, Kraemer I, et al. Exclusive multipotency and preferential asymmetric divisions in post-embryonic neural stem cells of the fish retina. Development. 2014;141:3472-82 pubmed publisher
  93. Rharass T, Lemcke H, Lantow M, Kuznetsov S, Weiss D, Panàkovà D. Ca2+-mediated mitochondrial reactive oxygen species metabolism augments Wnt/?-catenin pathway activation to facilitate cell differentiation. J Biol Chem. 2014;289:27937-51 pubmed publisher
  94. Makantasi P, Dermon C. Estradiol treatment decreases cell proliferation in the neurogenic zones of adult female zebrafish (Danio rerio) brain. Neuroscience. 2014;277:306-20 pubmed publisher
  95. Bai Q, Parris R, Burton E. Different mechanisms regulate expression of zebrafish myelin protein zero (P0) in myelinating oligodendrocytes and its induction following axonal injury. J Biol Chem. 2014;289:24114-28 pubmed publisher
  96. Torrado E, Gomes C, Santos G, Fernandes A, Brites D, Falcão A. Directing mouse embryonic neurosphere differentiation toward an enriched neuronal population. Int J Dev Neurosci. 2014;37:94-9 pubmed publisher
  97. Bernier R, Golzio C, Xiong B, Stessman H, Coe B, Penn O, et al. Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 2014;158:263-276 pubmed publisher
  98. Shi Y, Zhang Y, Zhao F, Ruan H, Huang H, Luo L, et al. Acetylcholine serves as a derepressor in Loperamide-induced Opioid-Induced Bowel Dysfunction (OIBD) in zebrafish. Sci Rep. 2014;4:5602 pubmed publisher
  99. Herrera A, Saade M, Menendez A, Marti E, Pons S. Sustained Wnt/?-catenin signalling causes neuroepithelial aberrations through the accumulation of aPKC at the apical pole. Nat Commun. 2014;5:4168 pubmed publisher
  100. Milione M, Gasparini P, Sozzi G, Mazzaferro V, Ferrari A, Casali P, et al. Ewing sarcoma of the small bowel: a study of seven cases, including one with the uncommonly reported EWSR1-FEV translocation. Histopathology. 2014;64:1014-26 pubmed publisher
  101. Tsurusaki Y, Koshimizu E, Ohashi H, Phadke S, Kou I, Shiina M, et al. De novo SOX11 mutations cause Coffin-Siris syndrome. Nat Commun. 2014;5:4011 pubmed publisher
  102. Briona L, Dorsky R. Radial glial progenitors repair the zebrafish spinal cord following transection. Exp Neurol. 2014;256:81-92 pubmed publisher
  103. Lu Y, West F, Jordan B, Jordan E, West R, Yu P, et al. Induced pluripotency in chicken embryonic fibroblast results in a germ cell fate. Stem Cells Dev. 2014;23:1755-64 pubmed publisher
  104. Petazzi P, Akizu N, Garcia A, Estarás C, Martinez de Paz A, Rodríguez Paredes M, et al. An increase in MECP2 dosage impairs neural tube formation. Neurobiol Dis. 2014;67:49-56 pubmed publisher
  105. Zhang X, Ling J, Barcia G, Jing L, Wu J, Barry B, et al. Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. Am J Hum Genet. 2014;94:547-58 pubmed publisher
  106. Zannoni A, Bombardi C, Dondi F, Morini M, Forni M, Chiocchetti R, et al. Proteinase-activated receptor 2 expression in the intestinal tract of the horse. Res Vet Sci. 2014;96:464-71 pubmed publisher
  107. Wyatt L, Filbin M, Keirstead H. PTEN inhibition enhances neurite outgrowth in human embryonic stem cell-derived neuronal progenitor cells. J Comp Neurol. 2014;522:2741-55 pubmed publisher
  108. Orts Del Immagine A, Kastner A, Tillement V, Tardivel C, Trouslard J, Wanaverbecq N. Morphology, distribution and phenotype of polycystin kidney disease 2-like 1-positive cerebrospinal fluid contacting neurons in the brainstem of adult mice. PLoS ONE. 2014;9:e87748 pubmed publisher
  109. Zupanc G, Ilieş I, Sîrbulescu R, Zupanc M. Large-scale identification of proteins involved in the development of a sexually dimorphic behavior. J Neurophysiol. 2014;111:1646-54 pubmed publisher
  110. Bodi I, Curran O, Selway R, Elwes R, Burrone J, Laxton R, et al. Two cases of multinodular and vacuolating neuronal tumour. Acta Neuropathol Commun. 2014;2:7 pubmed publisher
  111. Sorteni C, Clavenzani P, De Giorgio R, Portnoy O, Sirri R, Mordenti O, et al. Enteric neuroplasticity in seawater-adapted European eel (Anguilla anguilla). J Anat. 2014;224:180-91 pubmed publisher
  112. Tapanes Castillo A, Shabazz F, Mboge M, Vajn K, Oudega M, Plunkett J. Characterization of a novel primary culture system of adult zebrafish brainstem cells. J Neurosci Methods. 2014;223:11-9 pubmed publisher
  113. Traniello I, Sîrbulescu R, Ilieş I, Zupanc G. Age-related changes in stem cell dynamics, neurogenesis, apoptosis, and gliosis in the adult brain: a novel teleost fish model of negligible senescence. Dev Neurobiol. 2014;74:514-30 pubmed publisher
  114. Lake J, Tusheva O, Graham B, Heuckeroth R. Hirschsprung-like disease is exacerbated by reduced de novo GMP synthesis. J Clin Invest. 2013;123:4875-87 pubmed
  115. Lee R, Nagai H, Nakaya Y, Sheng G, Trainor P, Weston J, et al. Cell delamination in the mesencephalic neural fold and its implication for the origin of ectomesenchyme. Development. 2013;140:4890-902 pubmed publisher
  116. Achim K, Peltopuro P, Lahti L, Tsai H, Zachariah A, Astrand M, et al. The role of Tal2 and Tal1 in the differentiation of midbrain GABAergic neuron precursors. Biol Open. 2013;2:990-7 pubmed publisher
  117. Zacharko Siembida A, Kulik P, Szalak R, Lalak R, Arciszewski M. Co-expression patterns of cocaine- and amphetamine-regulated transcript (CART) with neuropeptides in dorsal root ganglia of the pig. Acta Histochem. 2014;116:390-8 pubmed publisher
  118. Miguez D, Gil Guiñón E, Pons S, Marti E. Smad2 and Smad3 cooperate and antagonize simultaneously in vertebrate neurogenesis. J Cell Sci. 2013;126:5335-43 pubmed publisher
  119. Leigh N, Schupp M, Li K, Padmanabhan V, Gastonguay A, Wang L, et al. Mmp17b is essential for proper neural crest cell migration in vivo. PLoS ONE. 2013;8:e76484 pubmed publisher
  120. Zacharko Siembida A, Piedra J, Arciszewski M. Changes in expression of calbindin 28 kDa in the small intestine of red kidney bean (Phaseolus vulgaris) lectin-treated suckling piglets. Pol J Vet Sci. 2013;16:201-9 pubmed
  121. Sadeghinezhad J, Sorteni C, Di Guardo G, D Agostino C, Agrimi U, Nonno R, et al. Neurochemistry of myenteric plexus neurons of bank vole (Myodes glareolus) ileum. Res Vet Sci. 2013;95:846-53 pubmed publisher
  122. Bombardi C, Grandis A, Gardini A, Sorteni C, Clavenzani P, Chiocchetti R. Expression of ?2 adrenoceptors within enteric neurons of the horse ileum. Res Vet Sci. 2013;95:837-45 pubmed publisher
  123. Cagle M, Honig M. Parcellation of cerebellins 1, 2, and 4 among different subpopulations of dorsal horn neurons in mouse spinal cord. J Comp Neurol. 2014;522:479-97 pubmed publisher
  124. Newton C, Stoyek M, Croll R, Smith F. Regional innervation of the heart in the goldfish, Carassius auratus: a confocal microscopy study. J Comp Neurol. 2014;522:456-78 pubmed publisher
  125. Pose Méndez S, Candal E, Adrio F, Rodriguez Moldes I. Development of the cerebellar afferent system in the shark Scyliorhinus canicula: insights into the basal organization of precerebellar nuclei in gnathostomes. J Comp Neurol. 2014;522:131-68 pubmed publisher
  126. Xiao L, Tsutsui T. Characterization of human dental pulp cells-derived spheroids in serum-free medium: stem cells in the core. J Cell Biochem. 2013;114:2624-36 pubmed publisher
  127. Edelmann K, Glashauser L, Sprungala S, Hesl B, Fritschle M, Ninkovic J, et al. Increased radial glia quiescence, decreased reactivation upon injury and unaltered neuroblast behavior underlie decreased neurogenesis in the aging zebrafish telencephalon. J Comp Neurol. 2013;521:3099-115 pubmed publisher
  128. Qi L, Wade J. Sexually dimorphic and developmentally regulated expression of tubulin-specific chaperone protein A in the LMAN of zebra finches. Neuroscience. 2013;247:182-90 pubmed publisher
  129. Stenkamp Strahm C, Patterson S, Boren J, Gericke M, Balemba O. High-fat diet and age-dependent effects on enteric glial cell populations of mouse small intestine. Auton Neurosci. 2013;177:199-210 pubmed publisher
  130. Berenguer J, Herrera A, Vuolo L, Torroba B, Llorens F, Sumoy L, et al. MicroRNA 22 regulates cell cycle length in cerebellar granular neuron precursors. Mol Cell Biol. 2013;33:2706-17 pubmed publisher
  131. Kaslin J, Kroehne V, Benato F, Argenton F, Brand M. Development and specification of cerebellar stem and progenitor cells in zebrafish: from embryo to adult. Neural Dev. 2013;8:9 pubmed publisher
  132. Gerety S, Breau M, Sasai N, Xu Q, Briscoe J, Wilkinson D. An inducible transgene expression system for zebrafish and chick. Development. 2013;140:2235-43 pubmed publisher
  133. Emborg M, Zhang Z, Joers V, Brunner K, Bondarenko V, Ohshima S, et al. Intracerebral transplantation of differentiated human embryonic stem cells to hemiparkinsonian monkeys. Cell Transplant. 2013;22:831-8 pubmed publisher
  134. Wang G, Wang X, Zou F, Qu M, Liu S, Fei G, et al. Mast cell expression of the serotonin1A receptor in guinea pig and human intestine. Am J Physiol Gastrointest Liver Physiol. 2013;304:G855-63 pubmed publisher
  135. Gamage P, Ranson R, Patel B, Yeoman M, Saffrey M. Myenteric neuron numbers are maintained in aging mouse distal colon. Neurogastroenterol Motil. 2013;25:e495-e505 pubmed
  136. Zacharko Siembida A, Arciszewski M. Immunoreactivity to cocaine- and amphetamine-regulated transcript in the enteric nervous system of the pig and wild boar stomach. Anat Histol Embryol. 2014;43:48-55 pubmed publisher
  137. Yoshikawa M, Murakami Y, Senzaki K, Masuda T, Ozaki S, Ito Y, et al. Coexpression of Runx1 and Runx3 in mechanoreceptive dorsal root ganglion neurons. Dev Neurobiol. 2013;73:469-79 pubmed publisher
  138. Chung A, Kim S, Kim E, Kim D, Jeong I, Cha Y, et al. Indian hedgehog B function is required for the specification of oligodendrocyte progenitor cells in the zebrafish CNS. J Neurosci. 2013;33:1728-33 pubmed publisher
  139. Beunders G, Voorhoeve E, Golzio C, Pardo L, Rosenfeld J, Talkowski M, et al. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. Am J Hum Genet. 2013;92:210-20 pubmed publisher
  140. Hsieh F, Ma T, Shih H, Lin S, Huang C, Wang H, et al. Dner inhibits neural progenitor proliferation and induces neuronal and glial differentiation in zebrafish. Dev Biol. 2013;375:1-12 pubmed publisher
  141. Simonson L, Ganz J, Melancon E, Eisen J. Characterization of enteric neurons in wild-type and mutant zebrafish using semi-automated cell counting and co-expression analysis. Zebrafish. 2013;10:147-53 pubmed publisher
  142. Bergeron S, Hannan M, Codore H, Fero K, Li G, Moak Z, et al. Brain selective transgene expression in zebrafish using an NRSE derived motif. Front Neural Circuits. 2012;6:110 pubmed publisher
  143. Quintana Urzainqui I, Rodriguez Moldes I, Candal E. Developmental, tract-tracing and immunohistochemical study of the peripheral olfactory system in a basal vertebrate: insights on Pax6 neurons migrating along the olfactory nerve. Brain Struct Funct. 2014;219:85-104 pubmed publisher
  144. Vatine G, Zada D, Lerer Goldshtein T, Tovin A, Malkinson G, Yaniv K, et al. Zebrafish as a model for monocarboxyl transporter 8-deficiency. J Biol Chem. 2013;288:169-80 pubmed publisher
  145. Allen A, Smith G. Spinal transection induces widespread proliferation of cells along the length of the spinal cord in a weakly electric fish. Brain Behav Evol. 2012;80:269-80 pubmed publisher
  146. Seredick S, Van Ryswyk L, Hutchinson S, Eisen J. Zebrafish Mnx proteins specify one motoneuron subtype and suppress acquisition of interneuron characteristics. Neural Dev. 2012;7:35 pubmed publisher
  147. Ampatzis K, Makantasi P, Dermon C. Cell proliferation pattern in adult zebrafish forebrain is sexually dimorphic. Neuroscience. 2012;226:367-81 pubmed publisher
  148. Virolainen S, Achim K, Peltopuro P, Salminen M, Partanen J. Transcriptional regulatory mechanisms underlying the GABAergic neuron fate in different diencephalic prosomeres. Development. 2012;139:3795-805 pubmed
  149. Sadeghinezhad J, Tootian Z, Latorre R, Sorteni C, Chiocchetti R. Intrinsic innervation of the Persian squirrel (Sciurus anomalus) ileum. Anat Histol Embryol. 2013;42:201-12 pubmed publisher
  150. Won Y, Ono F, Ikeda S. Characterization of Na+ and Ca2+ channels in zebrafish dorsal root ganglion neurons. PLoS ONE. 2012;7:e42602 pubmed publisher
  151. Zacharko Siembida A, Valverde Piedra J, Szymańczyk S, Arciszewski M. Immunolocalization of NOS, VIP, galanin and SP in the small intestine of suckling pigs treated with red kidney bean (Phaseolus vulgaris) lectin. Acta Histochem. 2013;115:219-25 pubmed publisher
  152. Shin J, Padmanabhan A, de Groh E, Lee J, Haidar S, Dahlberg S, et al. Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development. Dis Model Mech. 2012;5:881-94 pubmed publisher
  153. Terriente J, Gerety S, Watanabe Asaka T, Gonzalez Quevedo R, Wilkinson D. Signalling from hindbrain boundaries regulates neuronal clustering that patterns neurogenesis. Development. 2012;139:2978-87 pubmed publisher
  154. Kim S, Kim J, Chung A, Kim H, Kim Y, Kim M, et al. Antagonistic regulation of PAF1C and p-TEFb is required for oligodendrocyte differentiation. J Neurosci. 2012;32:8201-7 pubmed publisher
  155. Bardet S, Mouriec K, Balthazart J. Birth of neural progenitors during the embryonic period of sexual differentiation in the Japanese quail brain. J Comp Neurol. 2012;520:4226-53 pubmed publisher
  156. Colucci M, Cervio M, Faniglione M, De Angelis S, Pajoro M, Levandis G, et al. Intestinal dysmotility and enteric neurochemical changes in a Parkinson's disease rat model. Auton Neurosci. 2012;169:77-86 pubmed publisher
  157. Podlasz P, Sallinen V, Chen Y, Kudo H, Fedorowska N, Panula P. Galanin gene expression and effects of its knock-down on the development of the nervous system in larval zebrafish. J Comp Neurol. 2012;520:3846-62 pubmed publisher
  158. Teles M, Sîrbulescu R, Wellbrock U, Oliveira R, Zupanc G. Adult neurogenesis in the brain of the Mozambique tilapia, Oreochromis mossambicus. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2012;198:427-49 pubmed publisher
  159. Voss U, Sand E, Hellstrom P, Ekblad E. Glucagon-like peptides 1 and 2 and vasoactive intestinal peptide are neuroprotective on cultured and mast cell co-cultured rat myenteric neurons. BMC Gastroenterol. 2012;12:30 pubmed publisher
  160. Phillips R, Powley T. Macrophages associated with the intrinsic and extrinsic autonomic innervation of the rat gastrointestinal tract. Auton Neurosci. 2012;169:12-27 pubmed publisher
  161. Lindsey B, Darabie A, Tropepe V. The cellular composition of neurogenic periventricular zones in the adult zebrafish forebrain. J Comp Neurol. 2012;520:2275-316 pubmed publisher
  162. Zannino D, SAGERSTROM C, Appel B. olig2-Expressing hindbrain cells are required for migrating facial motor neurons. Dev Dyn. 2012;241:315-26 pubmed publisher
  163. Lin Z, Liu Y, Zheng Q, Hu Q. Increased proportion of nitric oxide synthase immunoreactive neurons in rat ileal myenteric ganglia after severe acute pancreatitis. BMC Gastroenterol. 2011;11:127 pubmed publisher
  164. Baumgart E, Barbosa J, Bally Cuif L, Gotz M, Ninkovic J. Stab wound injury of the zebrafish telencephalon: a model for comparative analysis of reactive gliosis. Glia. 2012;60:343-57 pubmed publisher
  165. Sato H, Arawaka S, Hara S, Fukushima S, Koga K, Koyama S, et al. Authentically phosphorylated ?-synuclein at Ser129 accelerates neurodegeneration in a rat model of familial Parkinson's disease. J Neurosci. 2011;31:16884-94 pubmed publisher
  166. Kroehne V, Freudenreich D, Hans S, Kaslin J, Brand M. Regeneration of the adult zebrafish brain from neurogenic radial glia-type progenitors. Development. 2011;138:4831-41 pubmed publisher
  167. Stockinger P, Maître J, Heisenberg C. Defective neuroepithelial cell cohesion affects tangential branchiomotor neuron migration in the zebrafish neural tube. Development. 2011;138:4673-83 pubmed publisher
  168. CHALAZONITIS A, Tang A, Shang Y, Pham T, Hsieh I, Setlik W, et al. Homeodomain interacting protein kinase 2 regulates postnatal development of enteric dopaminergic neurons and glia via BMP signaling. J Neurosci. 2011;31:13746-57 pubmed publisher
  169. Wray S, Dalmau J, Chen A, King S, Leigh R. Paraneoplastic disorders of eye movements. Ann N Y Acad Sci. 2011;1233:279-84 pubmed publisher
  170. Matsunaga E, Suzuki K, Kato S, Kurotani T, Kobayashi K, Okanoya K. Dynamic expression of cadherins regulates vocal development in a songbird. PLoS ONE. 2011;6:e25272 pubmed publisher
  171. Janardhan S, Praveen K, Marks R, Gajewski T. Evidence implicating the Ras pathway in multiple CD28 costimulatory functions in CD4+ T cells. PLoS ONE. 2011;6:e24931 pubmed publisher
  172. Doll C, Burkart J, Hope K, Halpern M, Gamse J. Subnuclear development of the zebrafish habenular nuclei requires ER translocon function. Dev Biol. 2011;360:44-57 pubmed publisher
  173. Reali C, Fernandez A, Radmilovich M, TRUJILLO CENOZ O, RUSSO R. GABAergic signalling in a neurogenic niche of the turtle spinal cord. J Physiol. 2011;589:5633-47 pubmed publisher
  174. Guo F, Maeda Y, Ma J, Delgado M, Sohn J, Miers L, et al. Macroglial plasticity and the origins of reactive astroglia in experimental autoimmune encephalomyelitis. J Neurosci. 2011;31:11914-28 pubmed publisher
  175. Wray S, Martinez Hernandez E, Dalmau J, Maheshwari A, Chen A, King S, et al. Paraneoplastic upbeat nystagmus. Neurology. 2011;77:691-3 pubmed publisher
  176. Ulrich F, Ma L, Baker R, Torres Vazquez J. Neurovascular development in the embryonic zebrafish hindbrain. Dev Biol. 2011;357:134-51 pubmed publisher
  177. Webb K, Coolen M, Gloeckner C, Stigloher C, Bahn B, Topp S, et al. The Enhancer of split transcription factor Her8a is a novel dimerisation partner for Her3 that controls anterior hindbrain neurogenesis in zebrafish. BMC Dev Biol. 2011;11:27 pubmed publisher
  178. Stridh L, Smith P, Naylor A, Wang X, Mallard C. Regulation of toll-like receptor 1 and -2 in neonatal mice brains after hypoxia-ischemia. J Neuroinflammation. 2011;8:45 pubmed publisher
  179. Filippova N, Yang X, Wang Y, Gillespie G, Langford C, King P, et al. The RNA-binding protein HuR promotes glioma growth and treatment resistance. Mol Cancer Res. 2011;9:648-59 pubmed publisher
  180. Souza B, Romano Silva M, Tropepe V. Dopamine D2 receptor activity modulates Akt signaling and alters GABAergic neuron development and motor behavior in zebrafish larvae. J Neurosci. 2011;31:5512-25 pubmed publisher
  181. Winpenny E, Lebel Potter M, Fernandez M, Brill M, Gotz M, Guillemot F, et al. Sequential generation of olfactory bulb glutamatergic neurons by Neurog2-expressing precursor cells. Neural Dev. 2011;6:12 pubmed publisher
  182. Kapur R, Fligner C, Maghsoodi B, Jaffe R. Gastrointestinal neuromuscular pathology in alpers disease. Am J Surg Pathol. 2011;35:714-22 pubmed publisher
  183. Bernardini N, Segnani C, Ippolito C, De Giorgio R, Colucci R, Faussone Pellegrini M, et al. Immunohistochemical analysis of myenteric ganglia and interstitial cells of Cajal in ulcerative colitis. J Cell Mol Med. 2012;16:318-27 pubmed publisher
  184. Yoshimura K, Sugiura K, Ohmori Y, Aste N, Saito N. Immunolocalization of aquaporin-4 in the brain, kidney, skeletal muscle, and gastro-intestinal tract of chicken. Cell Tissue Res. 2011;344:51-61 pubmed publisher
  185. Olsson C. Calbindin immunoreactivity in the enteric nervous system of larval and adult zebrafish (Danio rerio). Cell Tissue Res. 2011;344:31-40 pubmed publisher
  186. Gross A, Sims R, Swinny J, Sieghart W, Bolam J, Stanford I. Differential localization of GABA(A) receptor subunits in relation to rat striatopallidal and pallidopallidal synapses. Eur J Neurosci. 2011;33:868-78 pubmed publisher
  187. Tsai Y, Murakami N, Gariepy C. Postnatal intestinal engraftment of prospectively selected enteric neural crest stem cells in a rat model of Hirschsprung disease. Neurogastroenterol Motil. 2011;23:362-9 pubmed publisher
  188. Arciszewski M, Stefaniak M, Zacharko Siembida A, Ca ka J. Aquaporin 1 water channel is expressed on submucosal but not myenteric neurons from the ovine duodenum. Ann Anat. 2011;193:81-5 pubmed publisher
  189. Yokose J, Ishizuka T, Yoshida T, Aoki J, Koyanagi Y, Yawo H. Lineage analysis of newly generated neurons in organotypic culture of rat hippocampus. Neurosci Res. 2011;69:223-33 pubmed publisher
  190. Curchoe C, Maurer J, McKeown S, Cattarossi G, Cimadamore F, Nilbratt M, et al. Early acquisition of neural crest competence during hESCs neuralization. PLoS ONE. 2010;5:e13890 pubmed publisher
  191. Hegg C, Jia C, Chick W, Restrepo D, Hansen A. Microvillous cells expressing IP3 receptor type 3 in the olfactory epithelium of mice. Eur J Neurosci. 2010;32:1632-45 pubmed publisher
  192. Uyttebroek L, Shepherd I, Harrisson F, Hubens G, Blust R, Timmermans J, et al. Neurochemical coding of enteric neurons in adult and embryonic zebrafish (Danio rerio). J Comp Neurol. 2010;518:4419-38 pubmed publisher
  193. Sîrbulescu R, Zupanc G. Inhibition of caspase-3-mediated apoptosis improves spinal cord repair in a regeneration-competent vertebrate system. Neuroscience. 2010;171:599-612 pubmed publisher
  194. Sand E, Themner Persson A, Ekblad E. Corticotropin releasing factor-distribution in rat intestine and role in neuroprotection. Regul Pept. 2011;166:68-75 pubmed publisher
  195. Olsson C. Calbindin-immunoreactive cells in the fish enteric nervous system. Auton Neurosci. 2011;159:7-14 pubmed publisher
  196. Hagström C, Olsson C. Glial cells revealed by GFAP immunoreactivity in fish gut. Cell Tissue Res. 2010;341:73-81 pubmed publisher
  197. Yang M, Cagle M, Honig M. Identification of cerebellin2 in chick and its preferential expression by subsets of developing sensory neurons and their targets in the dorsal horn. J Comp Neurol. 2010;518:2818-40 pubmed publisher
  198. Patel B, Dai X, Burda J, Zhao H, Swain G, Galligan J, et al. Inhibitory neuromuscular transmission to ileal longitudinal muscle predominates in neonatal guinea pigs. Neurogastroenterol Motil. 2010;22:909-18, e236-7 pubmed publisher
  199. Peltopuro P, Kala K, Partanen J. Distinct requirements for Ascl1 in subpopulations of midbrain GABAergic neurons. Dev Biol. 2010;343:63-70 pubmed publisher
  200. Nakano Y, Fujita M, Ogino K, Saint Amant L, Kinoshita T, Oda Y, et al. Biogenesis of GPI-anchored proteins is essential for surface expression of sodium channels in zebrafish Rohon-Beard neurons to respond to mechanosensory stimulation. Development. 2010;137:1689-98 pubmed publisher
  201. Wong Y, Lu A, Wang Y, Cheng H, Chang C, Chen P, et al. Protogenin defines a transition stage during embryonic neurogenesis and prevents precocious neuronal differentiation. J Neurosci. 2010;30:4428-39 pubmed publisher
  202. Vellema M, Van der Linden A, Gahr M. Area-specific migration and recruitment of new neurons in the adult songbird brain. J Comp Neurol. 2010;518:1442-59 pubmed publisher
  203. Ampatzis K, Dermon C. Regional distribution and cellular localization of beta2-adrenoceptors in the adult zebrafish brain (Danio rerio). J Comp Neurol. 2010;518:1418-41 pubmed publisher
  204. Collins R, Linker C, Lewis J. MAZe: a tool for mosaic analysis of gene function in zebrafish. Nat Methods. 2010;7:219-23 pubmed publisher
  205. Liu Y, Namba T, Liu J, Suzuki R, Shioda S, Seki T. Glial fibrillary acidic protein-expressing neural progenitors give rise to immature neurons via early intermediate progenitors expressing both glial fibrillary acidic protein and neuronal markers in the adult hippocampus. Neuroscience. 2010;166:241-51 pubmed publisher
  206. Liu S, Ren W, Qu M, Bishop G, Wang G, Wang X, et al. Differential actions of urocortins on neurons of the myenteric division of the enteric nervous system in guinea pig distal colon. Br J Pharmacol. 2010;159:222-36 pubmed publisher
  207. Stanke J, Fischer A. Embryonic retinal cells and support to mature retinal neurons. Invest Ophthalmol Vis Sci. 2010;51:2208-18 pubmed publisher
  208. Ciofi P, Garret M, Lapirot O, Lafon P, Loyens A, Prevot V, et al. Brain-endocrine interactions: a microvascular route in the mediobasal hypothalamus. Endocrinology. 2009;150:5509-19 pubmed publisher
  209. Akhtar T, Li J, Olden T, Wallace K. Use of phospholipase A2 for antigen retrieval in zebrafish whole-mount immunohistochemistry. Zebrafish. 2009;6:223-7 pubmed publisher
  210. Ishii Y, Weinberg K, Oda Ishii I, Coughlin L, Mikawa T. Morphogenesis and cytodifferentiation of the avian retinal pigmented epithelium require downregulation of Group B1 Sox genes. Development. 2009;136:2579-89 pubmed publisher
  211. Peck C, Samsuria S, Harrington A, King S, Hutson J, Southwell B. Fall in density, but not number of myenteric neurons and circular muscle nerve fibres in guinea-pig colon with ageing. Neurogastroenterol Motil. 2009;21:1075-e90 pubmed publisher
  212. Flinn L, Mortiboys H, Volkmann K, Köster R, Ingham P, Bandmann O. Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). Brain. 2009;132:1613-23 pubmed publisher
  213. Caldero J, Brunet N, Ciutat D, Hereu M, Esquerda J. Development of microglia in the chick embryo spinal cord: implications in the regulation of motoneuronal survival and death. J Neurosci Res. 2009;87:2447-66 pubmed publisher
  214. Wang X, Lee J, Dorsky R. Identification of Wnt-responsive cells in the zebrafish hypothalamus. Zebrafish. 2009;6:49-58 pubmed publisher
  215. Tang Y, Wade J. Effects of estradiol on incorporation of new cells in the developing zebra finch song system: potential relationship to expression of ribosomal proteins L17 and L37. Dev Neurobiol. 2009;69:462-75 pubmed publisher
  216. Ippolito C, Segnani C, De Giorgio R, Blandizzi C, Mattii L, Castagna M, et al. Quantitative evaluation of myenteric ganglion cells in normal human left colon: implications for histopathological analysis. Cell Tissue Res. 2009;336:191-201 pubmed publisher
  217. Zupanc G, Wellbrock U, Sîrbulescu R, Rajendran R. Generation, long-term persistence, and neuronal differentiation of cells with nuclear aberrations in the adult zebrafish brain. Neuroscience. 2009;159:1338-48 pubmed publisher
  218. Field H, Kelley K, Martell L, Goldstein A, Serluca F. Analysis of gastrointestinal physiology using a novel intestinal transit assay in zebrafish. Neurogastroenterol Motil. 2009;21:304-12 pubmed publisher
  219. Kala K, Haugas M, Lilleväli K, Guimera J, Wurst W, Salminen M, et al. Gata2 is a tissue-specific post-mitotic selector gene for midbrain GABAergic neurons. Development. 2009;136:253-62 pubmed publisher
  220. de Jong Curtain T, Parslow A, Trotter A, Hall N, Verkade H, Tabone T, et al. Abnormal nuclear pore formation triggers apoptosis in the intestinal epithelium of elys-deficient zebrafish. Gastroenterology. 2009;136:902-11 pubmed publisher
  221. Montpetit A, Cote S, Brustein E, Drouin C, Lapointe L, Boudreau M, et al. Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord. PLoS Genet. 2008;4:e1000296 pubmed publisher
  222. Hartig W, Reichenbach A, Voigt C, Boltze J, Bulavina L, Schuhmann M, et al. Triple fluorescence labelling of neuronal, glial and vascular markers revealing pathological alterations in various animal models. J Chem Neuroanat. 2009;37:128-38 pubmed publisher
  223. McGraw H, Nechiporuk A, Raible D. Zebrafish dorsal root ganglia neural precursor cells adopt a glial fate in the absence of neurogenin1. J Neurosci. 2008;28:12558-69 pubmed publisher
  224. Tiruchinapalli D, Caron M, Keene J. Activity-dependent expression of ELAV/Hu RBPs and neuronal mRNAs in seizure and cocaine brain. J Neurochem. 2008;107:1529-43 pubmed publisher
  225. Sand E, Themner Persson A, Ekblad E. Mast cells reduce survival of myenteric neurons in culture. Neuropharmacology. 2009;56:522-30 pubmed publisher
  226. Arciszewski M, Barabasz S, Skobowiat C, Maksymowicz W, Majewski M. Immunodetection of cocaine- and amphetamine-regulated transcript in the rumen, reticulum, omasum and abomasum of the sheep. Anat Histol Embryol. 2009;38:62-7 pubmed publisher
  227. Power J, Blumbergs P. Cellular glutathione peroxidase in human brain: cellular distribution, and its potential role in the degradation of Lewy bodies in Parkinson's disease and dementia with Lewy bodies. Acta Neuropathol. 2009;117:63-73 pubmed publisher
  228. Fischer A, Scott M, Tuten W. Mitogen-activated protein kinase-signaling stimulates Müller glia to proliferate in acutely damaged chicken retina. Glia. 2009;57:166-81 pubmed publisher
  229. Topp S, Stigloher C, Komisarczuk A, Adolf B, Becker T, Bally Cuif L. Fgf signaling in the zebrafish adult brain: association of Fgf activity with ventricular zones but not cell proliferation. J Comp Neurol. 2008;510:422-39 pubmed publisher
  230. Mazzuoli G, Lucherini M, Russo D, Clavenzani P, Chiocchetti R. Intrinsic neuronal control of the pyloric sphincter of the lamb. J Chem Neuroanat. 2008;36:98-106 pubmed publisher
  231. Frontini A, Bertolotti P, Tonello C, Valerio A, Nisoli E, Cinti S, et al. Leptin-dependent STAT3 phosphorylation in postnatal mouse hypothalamus. Brain Res. 2008;1215:105-15 pubmed publisher
  232. Castro A, Becerra M, Anadón R, Manso M. Distribution of calretinin during development of the olfactory system in the brown trout, Salmo trutta fario: Comparison with other immunohistochemical markers. J Chem Neuroanat. 2008;35:306-16 pubmed publisher
  233. Schneider D, Yan H, Fry L, Alverson J, White S, O Rourke K. Myenteric neurons of the ileum that express somatostatin are a target of prion neuroinvasion in an alimentary model of sheep scrapie. Acta Neuropathol. 2008;115:651-61 pubmed publisher
  234. El Yazbi A, Cho W, Cena J, Schulz R, Daniel E. Smooth muscle NOS, colocalized with caveolin-1, modulates contraction in mouse small intestine. J Cell Mol Med. 2008;12:1404-15 pubmed publisher
  235. Sanek N, Grinblat Y. A novel role for zebrafish zic2a during forebrain development. Dev Biol. 2008;317:325-35 pubmed publisher
  236. Ampatzis K, Kentouri M, Dermon C. Neuronal and glial localization of alpha(2A)-adrenoceptors in the adult zebrafish (Danio rerio) brain. J Comp Neurol. 2008;508:72-93 pubmed publisher
  237. Xu Q, Tam M, Anderson S. Fate mapping Nkx2.1-lineage cells in the mouse telencephalon. J Comp Neurol. 2008;506:16-29 pubmed
  238. Fang X, Liu S, Wang X, Gao N, Hu H, Wang G, et al. Neurogastroenterology of tegaserod (HTF 919) in the submucosal division of the guinea-pig and human enteric nervous system. Neurogastroenterol Motil. 2008;20:80-93 pubmed
  239. Mazzuoli G, Mazzoni M, Albanese V, Clavenzani P, Lalatta Costerbosa G, Lucchi M, et al. Morphology and neurochemistry of descending and ascending myenteric plexus neurons of sheep ileum. Anat Rec (Hoboken). 2007;290:1480-91 pubmed
  240. Arciszewski M, Sand E, Ekblad E. Vasoactive intestinal peptide rescues cultured rat myenteric neurons from lipopolysaccharide induced cell death. Regul Pept. 2008;146:218-23 pubmed
  241. Sage D, Salin P, Alcaraz G, Castets F, Giraud P, Crest M, et al. Na(v)1.7 and Na(v)1.3 are the only tetrodotoxin-sensitive sodium channels expressed by the adult guinea pig enteric nervous system. J Comp Neurol. 2007;504:363-78 pubmed
  242. Agate R, Hertel M, Nottebohm F. FnTm2, a novel brain-specific transcript, is dynamically expressed in the song learning circuit of the zebra finch. J Comp Neurol. 2007;504:127-48 pubmed
  243. Lin G, Chen Y, Slack J. Regeneration of neural crest derivatives in the Xenopus tadpole tail. BMC Dev Biol. 2007;7:56 pubmed
  244. Hein A, Sridharan A, Nordeen K, Nordeen E. Characterization of CaMKII-expressing neurons within a striatal region implicated in avian vocal learning. Brain Res. 2007;1155:125-33 pubmed
  245. Nagao M, Sugimori M, Nakafuku M. Cross talk between notch and growth factor/cytokine signaling pathways in neural stem cells. Mol Cell Biol. 2007;27:3982-94 pubmed
  246. TRUJILLO CENOZ O, Fernandez A, Radmilovich M, Reali C, RUSSO R. Cytological organization of the central gelatinosa in the turtle spinal cord. J Comp Neurol. 2007;502:291-308 pubmed
  247. Holmberg A, Olsson C, Hennig G. TTX-sensitive and TTX-insensitive control of spontaneous gut motility in the developing zebrafish (Danio rerio) larvae. J Exp Biol. 2007;210:1084-91 pubmed
  248. Kristensson E, Themner Persson A, Ekblad E. Survival and neurotransmitter plasticity in cultured rat colonic myenteric neurons. Regul Pept. 2007;140:109-16 pubmed
  249. Murphy E, Defontgalland D, Costa M, Brookes S, Wattchow D. Quantification of subclasses of human colonic myenteric neurons by immunoreactivity to Hu, choline acetyltransferase and nitric oxide synthase. Neurogastroenterol Motil. 2007;19:126-34 pubmed
  250. Fuller C, Yettaw H, Byrd C. Mitral cells in the olfactory bulb of adult zebrafish (Danio rerio): morphology and distribution. J Comp Neurol. 2006;499:218-30 pubmed
  251. Clase A, Dimcheff D, Favara C, Dorward D, McAtee F, Parrie L, et al. Oligodendrocytes are a major target of the toxicity of spongiogenic murine retroviruses. Am J Pathol. 2006;169:1026-38 pubmed
  252. Lamba D, Karl M, Ware C, Reh T. Efficient generation of retinal progenitor cells from human embryonic stem cells. Proc Natl Acad Sci U S A. 2006;103:12769-74 pubmed
  253. Hendricks S, Rubel E, Nishi R. Formation of the avian nucleus magnocellularis from the auditory anlage. J Comp Neurol. 2006;498:433-42 pubmed
  254. Becker S, Grabel L. The use of embryonic stem cells to study hedgehog signaling. Methods Mol Biol. 2006;329:171-85 pubmed
  255. Olsson C, Chen B, Jones S, Chataway T, Costa M, Brookes S. Comparison of extrinsic efferent innervation of guinea pig distal colon and rectum. J Comp Neurol. 2006;496:787-801 pubmed
  256. Brehmer A, Schrodl F, Neuhuber W. Morphology of VIP/nNOS-immunoreactive myenteric neurons in the human gut. Histochem Cell Biol. 2006;125:557-65 pubmed
  257. Ganns D, Schrodl F, Neuhuber W, Brehmer A. Investigation of general and cytoskeletal markers to estimate numbers and proportions of neurons in the human intestine. Histol Histopathol. 2006;21:41-51 pubmed publisher
  258. Chiocchetti R, Grandis A, Bombardi C, Lucchi M, Dal Lago D, Bortolami R, et al. Extrinsic and intrinsic sources of calcitonin gene-related peptide immunoreactivity in the lamb ileum: a morphometric and neurochemical investigation. Cell Tissue Res. 2006;323:183-96 pubmed
  259. Arciszewski M, Pierzynowski S, Ekblad E. Lipopolysaccharide induces cell death in cultured porcine myenteric neurons. Dig Dis Sci. 2005;50:1661-8 pubmed
  260. Lin A, Lourenssen S, Stanzel R, Blennerhassett M. Nerve growth factor sensitivity is broadly distributed among myenteric neurons of the rat colon. J Comp Neurol. 2005;490:194-206 pubmed
  261. Ruhl A, Hoppe S, Frey I, Daniel H, Schemann M. Functional expression of the peptide transporter PEPT2 in the mammalian enteric nervous system. J Comp Neurol. 2005;490:1-11 pubmed
  262. Zvarova K, Vizzard M. Distribution and fate of cocaine- and amphetamine-regulated transcript peptide (CARTp)-expressing cells in rat urinary bladder: a developmental study. J Comp Neurol. 2005;489:501-17 pubmed
  263. Hu F, Liu B, Budel S, Liao J, Chin J, Fournier A, et al. Nogo-A interacts with the Nogo-66 receptor through multiple sites to create an isoform-selective subnanomolar agonist. J Neurosci. 2005;25:5298-304 pubmed
  264. Ekelund M, Ekelund M, Qader S, Hallén M, Ekblad E. Effects of total parenteral nutrition on rat enteric nervous system, intestinal morphology, and motility. J Surg Res. 2005;124:187-93 pubmed
  265. Brehmer A, Lindig T, Schrodl F, Neuhuber W, Ditterich D, Rexer M, et al. Morphology of enkephalin-immunoreactive myenteric neurons in the human gut. Histochem Cell Biol. 2005;123:131-8 pubmed
  266. Afonso N, Catala M. Sonic hedgehog and retinoic acid are not sufficient to induce motoneuron generation in the avian caudal neural tube. Dev Biol. 2005;279:356-67 pubmed
  267. Ninkovic J, Tallafuss A, Leucht C, Topczewski J, Tannhäuser B, Solnica Krezel L, et al. Inhibition of neurogenesis at the zebrafish midbrain-hindbrain boundary by the combined and dose-dependent activity of a new hairy/E(spl) gene pair. Development. 2005;132:75-88 pubmed
  268. Arciszewski M, Ekblad E. Effects of vasoactive intestinal peptide and galanin on survival of cultured porcine myenteric neurons. Regul Pept. 2005;125:185-92 pubmed
  269. Schulz T, Noggle S, Palmarini G, Weiler D, Lyons I, Pensa K, et al. Differentiation of human embryonic stem cells to dopaminergic neurons in serum-free suspension culture. Stem Cells. 2004;22:1218-38 pubmed
  270. Elena de Bellard M, Bronner Fraser M. Neural crest migration methods in the chicken embryo. Methods Mol Biol. 2005;294:247-67 pubmed
  271. Bauer S, Hay M, Amilhon B, Jean A, Moyse E. In vivo neurogenesis in the dorsal vagal complex of the adult rat brainstem. Neuroscience. 2005;130:75-90 pubmed
  272. Xiao J, Nguyen T, Ngui K, Strijbos P, Selmer I, Neylon C, et al. Molecular and functional analysis of hyperpolarisation-activated nucleotide-gated (HCN) channels in the enteric nervous system. Neuroscience. 2004;129:603-14 pubmed
  273. Senut M, Gulati Leekha A, Goldman D. An element in the alpha1-tubulin promoter is necessary for retinal expression during optic nerve regeneration but not after eye injury in the adult zebrafish. J Neurosci. 2004;24:7663-73 pubmed
  274. Chiocchetti R, Grandis A, Bombardi C, Clavenzani P, Costerbosa G, Lucchi M, et al. Characterisation of neurons expressing calbindin immunoreactivity in the ileum of the unweaned and mature sheep. Cell Tissue Res. 2004;318:289-303 pubmed
  275. Lin Z, Sandgren K, Ekblad E. Increased expression of nitric oxide synthase in cultured neurons from adult rat colonic submucous ganglia. Auton Neurosci. 2004;114:29-38 pubmed
  276. Aguirre A, Chittajallu R, Belachew S, Gallo V. NG2-expressing cells in the subventricular zone are type C-like cells and contribute to interneuron generation in the postnatal hippocampus. J Cell Biol. 2004;165:575-89 pubmed
  277. Tabata Y, Ouchi Y, Kamiya H, Manabe T, Arai K, Watanabe S. Specification of the retinal fate of mouse embryonic stem cells by ectopic expression of Rx/rax, a homeobox gene. Mol Cell Biol. 2004;24:4513-21 pubmed
  278. Phillips R, Hargrave S, Rhodes B, Zopf D, Powley T. Quantification of neurons in the myenteric plexus: an evaluation of putative pan-neuronal markers. J Neurosci Methods. 2004;133:99-107 pubmed
  279. Novak A, Ribera A. Immunocytochemistry as a tool for zebrafish developmental neurobiology. Methods Cell Sci. 2003;25:79-83 pubmed
  280. Hu H, Gao N, Liu S, Ren J, Wang X, Xia Y, et al. Action of bradykinin in the submucosal plexus of guinea pig small intestine. J Pharmacol Exp Ther. 2004;309:320-7 pubmed
  281. Fornaro M, Geuna S, Fasolo A, Giacobini Robecchi M. HuC/D confocal imaging points to olfactory migratory cells as the first cell population that expresses a post-mitotic neuronal phenotype in the chick embryo. Neuroscience. 2003;122:123-8 pubmed
  282. Holzschuh J, Barrallo Gimeno A, Ettl A, Durr K, Knapik E, Driever W. Noradrenergic neurons in the zebrafish hindbrain are induced by retinoic acid and require tfap2a for expression of the neurotransmitter phenotype. Development. 2003;130:5741-54 pubmed
  283. McWhorter M, Monani U, Burghes A, Beattie C. Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. J Cell Biol. 2003;162:919-31 pubmed
  284. Lin Z, Sandgren K, Ekblad E. Increased expression of vasoactive intestinal polypeptide in cultured myenteric neurons from adult rat small intestine. Auton Neurosci. 2003;107:9-19 pubmed
  285. Sandgren K, Lin Z, Fex Svenningsen A, Ekblad E. Vasoactive intestinal peptide and nitric oxide promote survival of adult rat myenteric neurons in culture. J Neurosci Res. 2003;72:595-602 pubmed
  286. Hu H, Liu S, Gao N, Xia Y, Mostafa R, Ren J, et al. Actions of bradykinin on electrical and synaptic behavior of neurones in the myenteric plexus of guinea-pig small intestine. Br J Pharmacol. 2003;138:1221-32 pubmed
  287. Chiocchetti R, Poole D, Kimura H, Aimi Y, Robbins H, Castelucci P, et al. Evidence that two forms of choline acetyltransferase are differentially expressed in subclasses of enteric neurons. Cell Tissue Res. 2003;311:11-22 pubmed
  288. Wierup N, Svensson H, Mulder H, Sundler F. The ghrelin cell: a novel developmentally regulated islet cell in the human pancreas. Regul Pept. 2002;107:63-9 pubmed
  289. Hu H, Gao N, Lin Z, Gao C, Liu S, Ren J, et al. P2X(7) receptors in the enteric nervous system of guinea-pig small intestine. J Comp Neurol. 2001;440:299-310 pubmed
  290. Fornaro M, Geuna S, Fasolo A, Giacobini Robecchi M. Evidence of very early neuronal migration from the olfactory placode of the chick embryo. Neuroscience. 2001;107:191-7 pubmed
  291. Fornaro M, Geuna S. Confocal imaging of HuC/D RNA-binding proteins in adult rat primary sensory neurons. Ann Anat. 2001;183:471-3 pubmed
  292. Miyata T, Kawaguchi A, Okano H, Ogawa M. Asymmetric inheritance of radial glial fibers by cortical neurons. Neuron. 2001;31:727-41 pubmed
  293. Kay J, Finger Baier K, Roeser T, Staub W, Baier H. Retinal ganglion cell genesis requires lakritz, a Zebrafish atonal Homolog. Neuron. 2001;30:725-36 pubmed
  294. Fischer A, Reh T. Müller glia are a potential source of neural regeneration in the postnatal chicken retina. Nat Neurosci. 2001;4:247-52 pubmed
  295. King P, Redden D, Palmgren J, Nabors L, Lennon V. Hu antigen specificities of ANNA-I autoantibodies in paraneoplastic neurological disease. J Autoimmun. 1999;13:435-43 pubmed
  296. Barami K, Iversen K, Furneaux H, Goldman S. Hu protein as an early marker of neuronal phenotypic differentiation by subependymal zone cells of the adult songbird forebrain. J Neurobiol. 1995;28:82-101 pubmed
  297. Szabo A, Dalmau J, Manley G, Rosenfeld M, Wong E, Henson J, et al. HuD, a paraneoplastic encephalomyelitis antigen, contains RNA-binding domains and is homologous to Elav and Sex-lethal. Cell. 1991;67:325-33 pubmed