This is a Validated Antibody Database (VAD) review about rat TH, based on 243 published articles (read how Labome selects the articles), using TH antibody in all methods. It is aimed to help Labome visitors find the most suited TH antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
TH synonym: The

Abcam
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; rat; 0.3 ug/ml; loading ...; fig 4b
Abcam TH antibody (Abcam, ab112) was used in immunohistochemistry - frozen section on rat samples at 0.3 ug/ml (fig 4b). elife (2020) ncbi
domestic rabbit monoclonal (EP1532Y)
  • western blot; mouse; 1:5000; loading ...; fig 5a
Abcam TH antibody (Abcam, ab137869) was used in western blot on mouse samples at 1:5000 (fig 5a). Am J Physiol Endocrinol Metab (2019) ncbi
chicken polyclonal
Abcam TH antibody (Abcam, AB76442) was used . J Comp Neurol (2019) ncbi
chicken polyclonal
  • immunocytochemistry; human; 1:1000; fig 7b
Abcam TH antibody (Abcam, ab76442) was used in immunocytochemistry on human samples at 1:1000 (fig 7b). Hum Mol Genet (2017) ncbi
chicken polyclonal
  • immunohistochemistry - free floating section; mouse; 1:1000
In order to characterize oxytocin receptor-expressing neurons originating within the ventral tegmental area, Abcam TH antibody (Abcam, AB76442) was used in immunohistochemistry - free floating section on mouse samples at 1:1000. J Comp Neurol (2017) ncbi
domestic rabbit polyclonal
  • western blot; mouse; 1:1000; loading ...; fig 4e
In order to test if miR-133a is involved in the crosstalk between tyrosine hydroxylase and tyrosine aminotransferase in the diabetic heart, Abcam TH antibody (Abcam, ab112) was used in western blot on mouse samples at 1:1000 (fig 4e). Diabetes (2016) ncbi
chicken polyclonal
  • immunocytochemistry; mouse; 1:500; fig 4
Abcam TH antibody (Abcam, ab76442) was used in immunocytochemistry on mouse samples at 1:500 (fig 4). Histochem Cell Biol (2016) ncbi
chicken polyclonal
  • immunohistochemistry; mouse; 1:1000; fig 4
Abcam TH antibody (abcam, ab76442) was used in immunohistochemistry on mouse samples at 1:1000 (fig 4). Sci Rep (2016) ncbi
chicken polyclonal
  • immunohistochemistry - free floating section; rat; 1:400; fig 1
In order to characterize how astrocytes respond to dopaminergic denervation of the striatum, Abcam TH antibody (Abcam, ab76442) was used in immunohistochemistry - free floating section on rat samples at 1:400 (fig 1). J Neurochem (2016) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; mouse; loading ...; fig s5C-1
Abcam TH antibody (Abcam, ab6211) was used in immunocytochemistry on mouse samples (fig s5C-1). Proc Natl Acad Sci U S A (2016) ncbi
domestic rabbit monoclonal (EP1532Y)
  • western blot; human; fig 3
In order to study cooperation in cancer cell invadopodia and filopodia by fascin rigidity and L-plastin flexibility, Abcam TH antibody (Abcam, ab137869) was used in western blot on human samples (fig 3). J Biol Chem (2016) ncbi
chicken polyclonal
  • immunohistochemistry - free floating section; mouse; fig s16
Abcam TH antibody (Abcam, ab76442) was used in immunohistochemistry - free floating section on mouse samples (fig s16). Nat Commun (2016) ncbi
chicken polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:100
Abcam TH antibody (Abcam, ab76442) was used in immunohistochemistry - paraffin section on mouse samples at 1:100. Neuropharmacology (2016) ncbi
Santa Cruz Biotechnology
mouse monoclonal (F-11)
  • immunohistochemistry; mouse; fig 2b
  • western blot; mouse; fig 2c
Santa Cruz Biotechnology TH antibody (Santa Cruz, F-11) was used in immunohistochemistry on mouse samples (fig 2b) and in western blot on mouse samples (fig 2c). Br J Pharmacol (2018) ncbi
mouse monoclonal
  • immunohistochemistry; mouse; fig 2b
  • western blot; mouse; fig 2c
Santa Cruz Biotechnology TH antibody (Santa Cruz, F-11) was used in immunohistochemistry on mouse samples (fig 2b) and in western blot on mouse samples (fig 2c). Br J Pharmacol (2018) ncbi
mouse monoclonal (F-11)
  • immunohistochemistry - paraffin section; human; 1:10,000; fig s9d
Santa Cruz Biotechnology TH antibody (Santa Cruz, sc-25269) was used in immunohistochemistry - paraffin section on human samples at 1:10,000 (fig s9d). Nat Genet (2017) ncbi
mouse monoclonal (F-11)
  • immunohistochemistry; mouse; loading ...; fig 5
  • western blot; mouse; loading ...; fig 7a
In order to examine the dopaminergic abnormalities in Histone deacetylase 6 knockout mice, Santa Cruz Biotechnology TH antibody (Santa Cruz, F11) was used in immunohistochemistry on mouse samples (fig 5) and in western blot on mouse samples (fig 7a). Neuropharmacology (2016) ncbi
mouse monoclonal
  • immunohistochemistry; mouse; loading ...; fig 5
  • western blot; mouse; loading ...; fig 7a
In order to examine the dopaminergic abnormalities in Histone deacetylase 6 knockout mice, Santa Cruz Biotechnology TH antibody (Santa Cruz, F11) was used in immunohistochemistry on mouse samples (fig 5) and in western blot on mouse samples (fig 7a). Neuropharmacology (2016) ncbi
mouse monoclonal (A-6)
  • immunohistochemistry - frozen section; human; fig 2
Santa Cruz Biotechnology TH antibody (Santa Cruz, sc-374048) was used in immunohistochemistry - frozen section on human samples (fig 2). PLoS ONE (2016) ncbi
mouse monoclonal (F-11)
  • immunocytochemistry; human; 1:500; fig 7
Santa Cruz Biotechnology TH antibody (Santa Cruz Biotechnology, sc-25269) was used in immunocytochemistry on human samples at 1:500 (fig 7). PLoS ONE (2015) ncbi
mouse monoclonal (F-11)
  • western blot; mouse; loading ...; fig 1
Santa Cruz Biotechnology TH antibody (Santa Cruz, SC25269) was used in western blot on mouse samples (fig 1). Oxid Med Cell Longev (2015) ncbi
mouse monoclonal (TOH A1.1)
  • immunohistochemistry - paraffin section; rat; 1:500; loading ...; fig 5a
  • western blot; rat; 1:2000; loading ...; fig 5c
Santa Cruz Biotechnology TH antibody (Santa Cruz Biotechnology, sc-47708) was used in immunohistochemistry - paraffin section on rat samples at 1:500 (fig 5a) and in western blot on rat samples at 1:2000 (fig 5c). Neural Regen Res (2012) ncbi
Novus Biologicals
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; loading ...; fig s3
Novus Biologicals TH antibody (Novus Biologicals, NB300-109) was used in immunohistochemistry - frozen section on mouse samples (fig s3). Proc Natl Acad Sci U S A (2018) ncbi
domestic sheep polyclonal
  • immunohistochemistry; mouse; 1:2000; loading ...; fig 6b
Novus Biologicals TH antibody (Novus Biologicals, NB300-110) was used in immunohistochemistry on mouse samples at 1:2000 (fig 6b). Science (2017) ncbi
domestic sheep polyclonal
  • immunohistochemistry; human; fig 5
  • immunohistochemistry; mouse; fig 5
Novus Biologicals TH antibody (Novus, NB300-110) was used in immunohistochemistry on human samples (fig 5) and in immunohistochemistry on mouse samples (fig 5). Cell (2016) ncbi
domestic sheep polyclonal
  • immunohistochemistry; rat; 1:2000; loading ...; fig 1a
In order to examine intrarenal perivascular afferent and sympathetic efferent nerves after unilateral surgical renal denervation, Novus Biologicals TH antibody (Novus Biologicals, NB 300-110) was used in immunohistochemistry on rat samples at 1:2000 (fig 1a). Am J Physiol Regul Integr Comp Physiol (2016) ncbi
domestic sheep polyclonal
  • immunohistochemistry - frozen section; mouse; 1:1000; loading ...; fig 1a
In order to find catecholaminergic neuronal elements and determine their relationship to other innervation components in the esophagus, Novus Biologicals TH antibody (Novus Biologicals, NB300-110) was used in immunohistochemistry - frozen section on mouse samples at 1:1000 (fig 1a). Histochem Cell Biol (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:500-1:1000; loading ...; fig 1a
In order to find catecholaminergic neuronal elements and determine their relationship to other innervation components in the esophagus, Novus Biologicals TH antibody (Novus Biologicals, NB300-109) was used in immunohistochemistry - frozen section on mouse samples at 1:500-1:1000 (fig 1a). Histochem Cell Biol (2016) ncbi
Invitrogen
domestic sheep polyclonal
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 5d
  • western blot; mouse; 1:1000; loading ...; fig 5c
In order to assess the effect of increased Parkin deletion mutagenesis in the absence of mitochondrial quality control, Invitrogen TH antibody (ThermoFisher, PA1-4679) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 5d) and in western blot on mouse samples at 1:1000 (fig 5c). Neurobiol Dis (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 3
In order to elucidate role of the IL-1 pathway on dopaminergic neurodegeneration and motor skills during aging, Invitrogen TH antibody (Life Technology, P21962) was used in immunohistochemistry on mouse samples at 1:1000 (fig 3). Mol Neurobiol (2017) ncbi
domestic sheep polyclonal
  • immunohistochemistry - frozen section; mouse; 1:2000; fig 2
In order to determine how the loss of a transcription factor, Meis1, prevents innervation of sympathetic neurons and increases the likelihood of sudden cardiac death, Invitrogen TH antibody (Thermo Scientific, PA1-4679) was used in immunohistochemistry - frozen section on mouse samples at 1:2000 (fig 2). elife (2016) ncbi
domestic rabbit polyclonal
  • western blot; rat; 1:400; fig 4
In order to characterize the differential effects of angiotensin II and mineralocorticoid on incentive and mesolimbic activity, Invitrogen TH antibody (Life Technologies, 36-9900) was used in western blot on rat samples at 1:400 (fig 4). Horm Behav (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; rat; 1:25,000; fig 7
In order to study prolactin secretion in female rats and oestrogen regulation of luteinising hormone by the hypothalamic effects of tamoxifen, Invitrogen TH antibody (Zymed Laboratories, 36-8600) was used in immunohistochemistry - free floating section on rat samples at 1:25,000 (fig 7). J Neuroendocrinol (2016) ncbi
Synaptic Systems
guinea-pigs polyclonal (/)
  • immunohistochemistry; mouse; fig 5a
Synaptic Systems TH antibody (Synaptic Systems, 213104) was used in immunohistochemistry on mouse samples (fig 5a). Cell (2018) ncbi
guinea-pigs polyclonal (/)
  • immunohistochemistry; mouse; 1:1000; loading ...; tbl 1
Synaptic Systems TH antibody (SySy, 213104) was used in immunohistochemistry on mouse samples at 1:1000 (tbl 1). J Comp Neurol (2017) ncbi
guinea-pigs polyclonal (/)
  • immunocytochemistry; rat; 1:1000; fig 3b
Synaptic Systems TH antibody (Synaptic Systems, 213004) was used in immunocytochemistry on rat samples at 1:1000 (fig 3b). Int J Neuropsychopharmacol (2017) ncbi
BioLegend
mouse monoclonal (2/40/15)
  • immunohistochemistry; mouse; loading ...; fig st1
In order to develop a method for super-resolution imaging of the multiscale organization of intact tissues and use it to image the mouse brain, BioLegend TH antibody (BioLegend, 818001) was used in immunohistochemistry on mouse samples (fig st1). Nat Biotechnol (2016) ncbi
MilliporeSigma
mouse monoclonal (TH-2)
  • immunohistochemistry - paraffin section; mouse; 1:1000; loading ...; fig 2d
MilliporeSigma TH antibody (Sigma-Aldrich, TH-2) was used in immunohistochemistry - paraffin section on mouse samples at 1:1000 (fig 2d). Peerj (2018) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; mouse; 1:2000; loading ...; fig 6b
MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry on mouse samples at 1:2000 (fig 6b). Science (2017) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry; rat; 1:4000; loading ...; fig 1
In order to research the effect of hypotension on the neurons in the ventrolateral medulla, MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry on rat samples at 1:4000 (fig 1). J Comp Neurol (2017) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; mouse; loading ...; fig 1b
  • western blot; mouse; 1:1000; loading ...; fig 3a
In order to test if activin A has anti-inflammatory and neuroprotective effects in in vivo mouse models of Parkinson's disease, MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry on mouse samples (fig 1b) and in western blot on mouse samples at 1:1000 (fig 3a). PLoS ONE (2017) ncbi
mouse monoclonal (TH-16)
  • western blot; rat; loading ...; fig 6a
In order to report the effects of dietary calcium supplementation on brown adipose tissue, autonomic nerve activity, sympathoadrenal function, and cardiovascular parameters in adult obese rats that were raised in small litters, MilliporeSigma TH antibody (Sigma Aldrich, T2928) was used in western blot on rat samples (fig 6a). J Nutr Biochem (2017) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; mouse; fig 5
  • immunohistochemistry; human; fig 5
MilliporeSigma TH antibody (Sigma-Aldrich, T2928) was used in immunohistochemistry on mouse samples (fig 5) and in immunohistochemistry on human samples (fig 5). Cell (2016) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry; rat; loading ...; fig 1b
MilliporeSigma TH antibody (Sigma-Aldrich, T1299) was used in immunohistochemistry on rat samples (fig 1b). Brain Res (2016) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry - frozen section; rat; fig 2a
In order to develop and characterize a new rat model of Parkinson's disease using the endoplasmic reticulum stressor tunicamycin, MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry - frozen section on rat samples (fig 2a). Mol Neurobiol (2017) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - paraffin section; human; 1:2000; fig 4
MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry - paraffin section on human samples at 1:2000 (fig 4). Reprod Biol Endocrinol (2016) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry - paraffin section; mouse; 1:1000; fig 8
MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry - paraffin section on mouse samples at 1:1000 (fig 8). EMBO J (2016) ncbi
mouse monoclonal (TH-2)
  • western blot; human; 1:500; loading ...; fig 3d
In order to test if glucocerebrosidase activation reduces alpha-synuclein levels, MilliporeSigma TH antibody (Sigma-Aldrich, TH-2) was used in western blot on human samples at 1:500 (fig 3d). J Neurosci (2016) ncbi
mouse monoclonal (TH-16)
  • immunocytochemistry; mouse; 1:8000; loading ...; fig 5a
  • western blot; mouse; 1:8000; loading ...; fig 6a
In order to assess the differentiation potential of hippocampal neural stem cells, MilliporeSigma TH antibody (Sigma, T2928) was used in immunocytochemistry on mouse samples at 1:8000 (fig 5a) and in western blot on mouse samples at 1:8000 (fig 6a). Mol Med Rep (2016) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry - free floating section; rat; 1:12,000; fig 1
In order to characterize how astrocytes respond to dopaminergic denervation of the striatum, MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry - free floating section on rat samples at 1:12,000 (fig 1). J Neurochem (2016) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - frozen section; mouse; 1:1000; loading ...; fig 1a
In order to propose that SLC35D3 regulates tissue-specific autophagy which could influence Parkinson disease, MilliporeSigma TH antibody (Sigma-Aldrich, T1299) was used in immunohistochemistry - frozen section on mouse samples at 1:1000 (fig 1a). Autophagy (2016) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; rat; fig 9
  • western blot; rat; fig 5
MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry on rat samples (fig 9) and in western blot on rat samples (fig 5). Cell Death Dis (2016) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; rat; 1:500; loading ...; fig 5b
In order to study the role of neuromedin U in drugs of abuse and visualize its receptor, MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry on rat samples at 1:500 (fig 5b). Biol Psychiatry (2016) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; rat; 1:2000; fig s1
MilliporeSigma TH antibody (Sigma, T-2928) was used in immunohistochemistry on rat samples at 1:2000 (fig s1). Front Neural Circuits (2016) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - free floating section; mouse; 1:200; fig s6
MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry - free floating section on mouse samples at 1:200 (fig s6). Nat Neurosci (2016) ncbi
mouse monoclonal (TH-16)
  • western blot; rat; 1:8000; fig 4
In order to characterize the differential effects of angiotensin II and mineralocorticoid on incentive and mesolimbic activity, MilliporeSigma TH antibody (Sigma, T2928) was used in western blot on rat samples at 1:8000 (fig 4). Horm Behav (2016) ncbi
mouse monoclonal (TH-16)
  • western blot; rat; 1:1000; fig 4
MilliporeSigma TH antibody (Sigma, T2928) was used in western blot on rat samples at 1:1000 (fig 4). Mar Drugs (2015) ncbi
mouse monoclonal (TH-16)
  • immunocytochemistry; human; 1:1000; fig s1
In order to research the role of increased alpha-synuclein due to SNCA gene triplication and its role in Parkinson stem cells, MilliporeSigma TH antibody (Sigma, T2928) was used in immunocytochemistry on human samples at 1:1000 (fig s1). Cell Death Dis (2015) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - free floating section; rat; 1:70,000; fig 8
In order to study prolactin secretion in female rats and oestrogen regulation of luteinising hormone by the hypothalamic effects of tamoxifen, MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry - free floating section on rat samples at 1:70,000 (fig 8). J Neuroendocrinol (2016) ncbi
mouse monoclonal (TH-2)
  • immunocytochemistry; rat; fig 2
MilliporeSigma TH antibody (Sigma, T1299) was used in immunocytochemistry on rat samples (fig 2). Sci Rep (2015) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; mouse; 1:2000; loading ...; fig 6b
  • western blot; mouse; 1:4000; loading ...; fig 1e
MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry on mouse samples at 1:2000 (fig 6b) and in western blot on mouse samples at 1:4000 (fig 1e). Sci Rep (2015) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry; mouse; 1:100; fig s1
MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry on mouse samples at 1:100 (fig s1). Science (2015) ncbi
mouse monoclonal (TH-2)
  • immunocytochemistry; mouse; 1:500; fig 3
MilliporeSigma TH antibody (Sigma, T1299) was used in immunocytochemistry on mouse samples at 1:500 (fig 3). J Neurosci (2015) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry - frozen section; mouse; 1:1000; loading ...; fig 1a
MilliporeSigma TH antibody (Sigma Aldrich, T2928) was used in immunohistochemistry - frozen section on mouse samples at 1:1000 (fig 1a). PLoS ONE (2015) ncbi
mouse monoclonal (TH-2)
  • immunocytochemistry; human; 1:200; fig 3
In order to discuss methods to generate and study neural crest cells, MilliporeSigma TH antibody (Sigma, T1299) was used in immunocytochemistry on human samples at 1:200 (fig 3). Cell J (2015) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry - frozen section; rat; 1:5000
In order to study the Pavlovian-instrumental transfer effect of the rostral medial ventral pallidum region innervated by the nucleus accumbens shell, MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry - frozen section on rat samples at 1:5000. J Neurosci (2015) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - frozen section; mouse; 1:200
MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry - frozen section on mouse samples at 1:200. Neuroscience (2015) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - frozen section; rat; 1:5000
  • western blot; rat; 1:10000; fig 8
MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry - frozen section on rat samples at 1:5000 and in western blot on rat samples at 1:10000 (fig 8). Transl Res (2015) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry; rat; 1:4000; fig 3
MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry on rat samples at 1:4000 (fig 3). Nat Neurosci (2015) ncbi
mouse monoclonal (TH-16)
  • western blot; rat; 1:5000
MilliporeSigma TH antibody (Sigma-Aldrich, T2928) was used in western blot on rat samples at 1:5000. Int J Dev Neurosci (2015) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - paraffin section; human; 1:2000
MilliporeSigma TH antibody (Sigma-Aldrich, T 1299) was used in immunohistochemistry - paraffin section on human samples at 1:2000. Dev Neurobiol (2015) ncbi
mouse monoclonal (TH-16)
  • western blot; rat; 1:8000
In order to investigate the effect of early postnatal overfeeding on insulin signaling in the ventral tegmental area, MilliporeSigma TH antibody (Sigma, T2928) was used in western blot on rat samples at 1:8000. Behav Brain Res (2015) ncbi
mouse monoclonal (TH-16)
  • immunohistochemistry - frozen section; rat; 1:1000
  • western blot; rat
In order to examine the p.G2019S mutation in the leucine-rich repeat kinase 2 (LRRK2) and it's role in Parkinson's disease, MilliporeSigma TH antibody (Sigma, T2928) was used in immunohistochemistry - frozen section on rat samples at 1:1000 and in western blot on rat samples . J Parkinsons Dis (2014) ncbi
mouse monoclonal (TH-2)
  • immunocytochemistry; rat; 1:2500
MilliporeSigma TH antibody (Sigma, T1299) was used in immunocytochemistry on rat samples at 1:2500. Neurobiol Dis (2014) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry - frozen section; rat
In order to study gastric paresis in a rat model of Parkinson's disease and the the role played by increased levels of beta1-adrenoceptors, MilliporeSigma TH antibody (Sigma, T1299) was used in immunohistochemistry - frozen section on rat samples . Transl Res (2014) ncbi
mouse monoclonal (TH-16)
  • western blot; mouse; 1:1000; fig 5
In order to investigate the contribution of LPA1 receptors to drug abuse, MilliporeSigma TH antibody (SIGMA, T2928) was used in western blot on mouse samples at 1:1000 (fig 5). Psychopharmacology (Berl) (2012) ncbi
mouse monoclonal (TH-2)
  • immunohistochemistry; rat; 1:1000
MilliporeSigma TH antibody (Sigma, 1299) was used in immunohistochemistry on rat samples at 1:1000. J Comp Neurol (2009) ncbi
Cell Signaling Technology
domestic rabbit polyclonal
  • western blot; mouse; loading ...; fig 1a
Cell Signaling Technology TH antibody (Cell Signaling, 2792) was used in western blot on mouse samples (fig 1a). Cell Death Differ (2016) ncbi
EMD Millipore
domestic rabbit polyclonal
  • immunohistochemistry; mouse; loading ...; fig 1a, s10a
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on mouse samples (fig 1a, s10a). Sci Adv (2020) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; mouse; 1:500; loading ...; fig 4b
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - free floating section on mouse samples at 1:500 (fig 4b). Mol Brain (2020) ncbi
mouse monoclonal (LNC1)
EMD Millipore TH antibody (Millipore, MAB318) was used . J Comp Neurol (2020) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; zebrafish ; 1:100; loading ...; fig 1a3
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:100 (fig 1a3). J Comp Neurol (2019) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 2d
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:1000 (fig 2d). elife (2019) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; slender lungfish; 1:1000; loading ...; fig 6a
EMD Millipore TH antibody (Merk-Millipore, MAB318) was used in immunohistochemistry on slender lungfish samples at 1:1000 (fig 6a). J Comp Neurol (2020) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; marine lamprey; 1:400; loading ...; fig 6b
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on marine lamprey samples at 1:400 (fig 6b). J Comp Neurol (2020) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 5
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 5). J Comp Neurol (2019) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:1000; loading ...; fig 1b
EMD Millipore TH antibody (EMD Millipore, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:1000 (fig 1b). J Comp Neurol (2019) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; loading ...; fig ex5c
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on mouse samples (fig ex5c). Nature (2019) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; House crow; 1:200; loading ...; fig 17a
  • immunohistochemistry; House crow; 1:200; loading ...; fig 18a
  • western blot; House crow; 1:5000; loading ...; fig 4
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on House crow samples at 1:200 (fig 17a), in immunohistochemistry on House crow samples at 1:200 (fig 18a) and in western blot on House crow samples at 1:5000 (fig 4). J Comp Neurol (2019) ncbi
mouse monoclonal (LNC1)
EMD Millipore TH antibody (Millipore, MAB318) was used . J Comp Neurol (2019) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 1d
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 1d). elife (2018) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; rat; 1:200; loading ...; fig 1d
EMD Millipore TH antibody (EMD Millipore, AB152) was used in immunohistochemistry on rat samples at 1:200 (fig 1d). J Comp Neurol (2019) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 1b
EMD Millipore TH antibody (Abcam, ab152) was used in immunohistochemistry on mouse samples at 1:1000 (fig 1b). Science (2018) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; loading ...; fig 1c
  • western blot; rat; loading ...; fig 1a
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on rat samples (fig 1c) and in western blot on rat samples (fig 1a). Brain Sci (2018) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; mouse; loading ...; fig 2d
EMD Millipore TH antibody (Calbiochem, 657012) was used in immunohistochemistry - free floating section on mouse samples (fig 2d). Sci Rep (2018) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:200; loading ...; fig s3b
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig s3b). PLoS ONE (2018) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 3
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on mouse samples at 1:1000 (fig 3). Brain Res (2019) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:200; loading ...; fig 2d
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig 2d). J Comp Neurol (2018) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; rat; loading ...; fig 2d
EMD Millipore TH antibody (EMD Millipore, AB152) was used in immunohistochemistry on rat samples (fig 2d). Addict Biol (2018) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:2000; loading ...; fig 6a
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:2000 (fig 6a). J Neurosci (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; marine lamprey; 1:1000; loading ...; fig 7b
In order to research the expression of alpha-transducin in the brain and retina of Sea Lamprey, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on marine lamprey samples at 1:1000 (fig 7b). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:1000; loading ...; tbl 1
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:1000 (tbl 1). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; tbl 1
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (tbl 1). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
EMD Millipore TH antibody (Millipore, AB318) was used . J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:4000; loading ...; fig 1b
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:4000 (fig 1b). J Neurosci (2017) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; Drosophila melanogaster; 1:200; loading ...; fig 2a
  • western blot; human; 1:1000; fig 4
EMD Millipore TH antibody (Millipore, LNC1) was used in immunocytochemistry on Drosophila melanogaster samples at 1:200 (fig 2a) and in western blot on human samples at 1:1000 (fig 4). Hum Mol Genet (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; loading ...; fig 4c
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples (fig 4c). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • 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, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:500 (tbl 2). Dev Biol (2017) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; loading ...; fig 3a
EMD Millipore TH antibody (Cell Signaling, AB152) was used in immunocytochemistry on human samples (fig 3a). Science (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; human; 1:5000
  • immunocytochemistry; human; 1:5000; fig e1b
In order to compare the gene expression in individual cells isolated from human brain organoids, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on human samples at 1:5000 and in immunocytochemistry on human samples at 1:5000 (fig e1b). Nature (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; loading ...; fig 8a
In order to investigate the effect of melatonin in neural stem cell differentiation and engraftment, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - paraffin section on mouse samples (fig 8a). J Pineal Res (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; Xenopus laevis; 1:500; loading ...; fig 1c
In order to compare the organization of cerebrospinal fluid-contacting cells in chicken, Xenopus, and zebrafish, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on Xenopus laevis samples at 1:500 (fig 1c). J Comp Neurol (2017) ncbi
domestic rabbit polyclonal
  • western blot; mouse; 1:1000; loading ...; fig 2c
In order to elucidate the effects of mutations in leucine-rich repeat kinase 2 on nigro0striatal dopamine neurons, EMD Millipore TH antibody (Millipore, AB152) was used in western blot on mouse samples at 1:1000 (fig 2c). Acta Neuropathol Commun (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:2000; loading ...; fig 2a
  • western blot; mouse; 1:2000; loading ...; fig 9a
In order to analyze the effects of dopamine related metabolite concentrations in M1 and M2 microglia phenotypes, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:2000 (fig 2a) and in western blot on mouse samples at 1:2000 (fig 9a). Front Cell Neurosci (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 6c
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 6c). Mol Ther (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; mouse; loading ...; fig 7a
In order to research the protective effect of Mfn2 on dopaminergic neurons, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - paraffin section on mouse samples (fig 7a). Biochim Biophys Acta Mol Basis Dis (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; mouse; 1:2000; loading ...; fig st15
In order to outline the protocols for antibodies used for immunohistochemical studies, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - paraffin section on mouse samples at 1:2000 (fig st15). J Toxicol Pathol (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; rat; 1:1000; loading ...; fig s6c
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on rat samples at 1:1000 (fig s6c). PLoS ONE (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; zebrafish ; 1:1000; loading ...; tbl 1
In order to establish a novel transgenic animal model to visualize Nr4a2 expression during zebrafish retinogenesis, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:1000 (tbl 1). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; human; 1:1000; loading ...; tbl 1
In order to characterize melanopsin-positive human retinal ganglion cells, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on human samples at 1:1000 (tbl 1). J Comp Neurol (2017) ncbi
domestic rabbit polyclonal
  • western blot; human; 1:1000; loading ...; fig 1a
EMD Millipore TH antibody (Millipore, AB 152) was used in western blot on human samples at 1:1000 (fig 1a). Proc Natl Acad Sci U S A (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; Chondrichthyes; 1:1000; loading ...; fig 2a
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on Chondrichthyes samples at 1:1000 (fig 2a). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; mouse; 1:500; loading ...; fig 5a
  • western blot; mouse; 1:2000
In order to study the effects of genetic background, natural aging, and prolonged oral administration of rotenone to mutant knock in LRRK2 mice, EMD Millipore TH antibody (Millipore, AB318) was used in immunohistochemistry - paraffin section on mouse samples at 1:500 (fig 5a) and in western blot on mouse samples at 1:2000. Sci Rep (2017) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; zebrafish ; loading ...; fig 2-s2a
In order to investigate the effects of the developmental transcription factor orthopedia on hypothalamic development and function, EMD Millipore TH antibody (Milipore, MAB318) was used in immunocytochemistry on zebrafish samples (fig 2-s2a). elife (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:1000; loading ...; fig 1a
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry on rat samples at 1:1000 (fig 1a). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:2000; loading ...; fig 5
In order to perform morphological and electrophysiological investigations of axons from parvalbumin-Cre rat neurons in globus pallidus, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:2000 (fig 5). Brain Struct Funct (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; rat; 1:1000; loading ...; fig 4a
In order to characterize Kiss1r-positive neurons in the arcuate nucleus of the rat hypothalamus, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - free floating section on rat samples at 1:1000 (fig 4a). J Neuroendocrinol (2017) ncbi
domestic rabbit polyclonal
  • western blot; mouse; 1:1000; loading ...; fig st1
EMD Millipore TH antibody (Millipore, AB152) was used in western blot on mouse samples at 1:1000 (fig st1). Mov Disord (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; African green monkey; 1:5000; loading ...; fig 2A
In order to develop a non-human primate model of synucleinopathy using cynomolgus macaque, EMD Millipore TH antibody (Chemicon, AB152) was used in immunohistochemistry - free floating section on African green monkey samples at 1:5000 (fig 2A). PLoS ONE (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:10,000; loading ...; fig 1c
  • immunohistochemistry; mouse; 1:10,000
In order to examine the synaptic inputs to tyrosine hydroxylase-immunoreactive neurons, EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:10,000 (fig 1c) and in immunohistochemistry on mouse samples at 1:10,000. J Comp Neurol (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:100; loading ...; fig 4b
In order to demonstrate the protective effects of an oligomer-specific single-chain variable fragment antibody in Parkinson's disease and Huntington's disease mouse models, EMD Millipore TH antibody (Abcam, ab152) was used in immunohistochemistry - paraffin section on mouse samples at 1:100 (fig 4b). Sci Rep (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; African green monkey; 1:400; fig 5
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on African green monkey samples at 1:400 (fig 5). Sci Rep (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:500-1:1000; loading ...; fig 1b
In order to test if tyrosine hydroxylase-driven Cre recombinase can be used to identify type II afferents, EMD Millipore TH antibody (Millipore, 657012) was used in immunohistochemistry on mouse samples at 1:500-1:1000 (fig 1b). J Assoc Res Otolaryngol (2017) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; mouse; 1:1000; fig s1a
  • western blot; mouse; 1:1000; fig 7b
EMD Millipore TH antibody (Milipore, AB152) was used in immunohistochemistry - free floating section on mouse samples at 1:1000 (fig s1a) and in western blot on mouse samples at 1:1000 (fig 7b). Nat Commun (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 7t
In order to elucidate the function of Hoxa5 in the brain, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 7t). J Comp Neurol (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:500; loading ...; fig 4b
In order to test if chronic stress enhances the progression of Parkinson's disease, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:500 (fig 4b). Exp Neurol (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:100; loading ...; fig 1b
In order to develop a method for cell-type-specific channelrhodopsin expression in Rhesus monkeys and use this approach modulate dopamine activity and monkey choice behavior, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:100 (fig 1b). Cell (2016) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; 1:1000; loading ...; tbl s4
EMD Millipore TH antibody (Millipore, AB152) was used in immunocytochemistry on human samples at 1:1000 (tbl s4). Stem Cell Res (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:5000; loading ...; fig 2d
In order to test if GABA is involved in feedback regulation of tuberoinfundibular dopamine neurons, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on mouse samples at 1:5000 (fig 2d). J Neurosci (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 2d
In order to test if GABA is involved in feedback regulation of tuberoinfundibular dopamine neurons, EMD Millipore TH antibody (Millipore, MAB 318) was used in immunohistochemistry on mouse samples at 1:1000 (fig 2d). J Neurosci (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 1a
In order to demonstrate that altered cholinergic transmission via M1 and M4 muscarinic acetylcholine receptors of the dorsal striatum are important for the motor symptoms in Parkinson's disease, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:1000 (fig 1a). J Neurosci (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:5000; fig 5c
In order to investigate cholinergic regulation of the olfactory bulb and examine neural morphology, EMD Millipore TH antibody (Millipore, AB318) was used in immunohistochemistry on mouse samples at 1:5000 (fig 5c). J Comp Neurol (2017) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; 1:100; loading ...; fig 3e
In order to test if glucocerebrosidase activation reduces alpha-synuclein levels, EMD Millipore TH antibody (Merck Millipore, 657012) was used in immunocytochemistry on human samples at 1:100 (fig 3e). J Neurosci (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:2000; loading ...; fig 5d
  • western blot; mouse; 1:2000; loading ...; fig 6a
In order to test if arsenic promotes the accumulation of toxic synuclein aggregates and stimulates autophagy, EMD Millipore TH antibody (EMD Millipore, AB 152) was used in immunohistochemistry - paraffin section on mouse samples at 1:2000 (fig 5d) and in western blot on mouse samples at 1:2000 (fig 6a). Toxicol Sci (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:500; fig 4
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 4). Mol Vis (2016) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; mouse; 1:250; fig 1
EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on mouse samples at 1:250 (fig 1). J Neuroinflammation (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; zebrafish ; 1:100; loading ...; fig 5f
In order to describe multifaceted roles of LRRK2 in zebrafish, EMD Millipore TH antibody (Chemicon, AB152) was used in immunohistochemistry on zebrafish samples at 1:100 (fig 5f). J Neurosci Res (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; mouse; 1:500; loading ...; fig 3e
EMD Millipore TH antibody (Abcam, AB152) was used in immunohistochemistry - free floating section on mouse samples at 1:500 (fig 3e). Front Neurosci (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - free floating section; rat; 1:1000; fig 7
EMD Millipore TH antibody (millipore, AB152) was used in immunohistochemistry - free floating section on rat samples at 1:1000 (fig 7). Neuron (2016) ncbi
domestic rabbit polyclonal
  • western blot; human; fig 2
EMD Millipore TH antibody (Millipore, AB152) was used in western blot on human samples (fig 2). Mol Brain (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig s2b
In order to investigate how spinal cord injury above thoracic level 5 causes systemic immune suppression, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig s2b). Nat Neurosci (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:500; loading ...; fig 6c
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:500 (fig 6c). Mol Ther Methods Clin Dev (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:250; fig 2
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on mouse samples at 1:250 (fig 2). Sci Rep (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; loading ...
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples . Nature (2016) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; domestic rabbit; 1:400; loading ...; fig 3
EMD Millipore TH antibody (chemicon, MAB318) was used in immunocytochemistry on domestic rabbit samples at 1:400 (fig 3). Ann Anat (2016) ncbi
domestic rabbit polyclonal
  • western blot; rat; fig 1
  • immunohistochemistry - paraffin section; human; fig 2
  • western blot; human; fig 1
EMD Millipore TH antibody (Millipore, AB 152) was used in western blot on rat samples (fig 1), in immunohistochemistry - paraffin section on human samples (fig 2) and in western blot on human samples (fig 1). J Biol Chem (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:1000; fig 4
EMD Millipore TH antibody (Calbiochem, 657012) was used in immunohistochemistry - frozen section on mouse samples at 1:1000 (fig 4). Nat Neurosci (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; human; loading ...; fig 1
In order to study the role of neuropathy and imbalanced Foxp3/IL-17 in bone marrow microenvironment of acute myeloid leukemia patients, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - paraffin section on human samples (fig 1). Oncotarget (2016) ncbi
domestic rabbit polyclonal
  • western blot; human; 1:1000; fig 4
EMD Millipore TH antibody (Millipore, AB152) was used in western blot on human samples at 1:1000 (fig 4). Stem Cell Res (2016) ncbi
domestic rabbit polyclonal
  • western blot; human; 1:500; fig s3
EMD Millipore TH antibody (EMD, AB152) was used in western blot on human samples at 1:500 (fig s3). Cell Rep (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:250
EMD Millipore TH antibody (Milipore, AB152) was used in immunohistochemistry - frozen section on mouse samples at 1:250. BMC Cell Biol (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rhesus macaque; 1:1000
In order to study AAV9 axonal transport in nonhuman primate brain, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on rhesus macaque samples at 1:1000. Gene Ther (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; fig 1k
EMD Millipore TH antibody (EMD Millipore, AB152) was used in immunohistochemistry - paraffin section on mouse samples (fig 1k). Sci Rep (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; human; loading ...; fig 1c
In order to study nociceptive nerve fibers in affected joint tissue in patients after total knee arthroplasty, EMD Millipore TH antibody (Chemicon, AB152) was used in immunohistochemistry on human samples (fig 1c). J Orthop Surg Res (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; fig 1
EMD Millipore TH antibody (Millipore, LNC1) was used in immunohistochemistry - frozen section on rat samples (fig 1). PLoS ONE (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:100; fig 3
  • western blot; mouse; 1:100; fig 3
EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry - paraffin section on mouse samples at 1:100 (fig 3) and in western blot on mouse samples at 1:100 (fig 3). Transl Psychiatry (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:1000; loading ...
In order to examine the involvement of MC3R in the modulation of food intake, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:1000. Neuropsychopharmacology (2016) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; 1:1000; tbl 1
In order to study of normal human retina and macromolecular markers and applications to human retinal disease, EMD Millipore TH antibody (Chemicon, AB152) was used in immunocytochemistry on human samples at 1:1000 (tbl 1). Exp Eye Res (2016) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; loading ...; fig 3a
In order to present the trophic and modulatory potential of statins in a dopaminergic cell line, EMD Millipore TH antibody (Millipore, AB152) was used in immunocytochemistry on human samples (fig 3a). Synapse (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; zebrafish ; 1:500; loading ...; fig 1f
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on zebrafish samples at 1:500 (fig 1f). Pharmacol Res (2016) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; mouse; 1:500; fig 5
In order to characterize sonic hedgehog-mediated dopaminergic neurogenesis in the embryonic midbrain by primary cilia, EMD Millipore TH antibody (Millipore, AB152) was used in immunohistochemistry on mouse samples at 1:500 (fig 5). Dev Biol (2016) ncbi
domestic rabbit polyclonal
  • western blot; rat; 1:2000; loading ...; fig 2
EMD Millipore TH antibody (Calbiochem, AB152) was used in western blot on rat samples at 1:2000 (fig 2). Dev Neurobiol (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:1000; fig 4
EMD Millipore TH antibody (Millipore Corporation, MAB318) was used in immunohistochemistry on rat samples at 1:1000 (fig 4). Prog Neuropsychopharmacol Biol Psychiatry (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:500
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry on rat samples at 1:500. Nat Commun (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; zebrafish ; 1:1000; fig 4
In order to study galaninergic innervation, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on zebrafish samples at 1:1000 (fig 4). Histochem Cell Biol (2016) ncbi
mouse monoclonal (LNC1)
  • western blot; rat; 1:1000
In order to report that Orai-mediated store operated calcium entry is required in dopaminergic interneurons of the flight circuit during pupal development, EMD Millipore TH antibody (Merck, MAB318) was used in western blot on rat samples at 1:1000. J Neurosci (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:10,000; loading ...; fig 3a
EMD Millipore TH antibody (Chemicon, MAB 318) was used in immunohistochemistry - frozen section on rat samples at 1:10,000 (fig 3a). PLoS ONE (2015) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; mouse; 1:1000; tbl 1
  • immunohistochemistry; mouse; 1:1000; tbl 1
  • western blot; mouse; 1:2000; tbl 1
EMD Millipore TH antibody (Millipore, AB152) was used in immunocytochemistry on mouse samples at 1:1000 (tbl 1), in immunohistochemistry on mouse samples at 1:1000 (tbl 1) and in western blot on mouse samples at 1:2000 (tbl 1). J Neurosci Res (2016) ncbi
mouse monoclonal (LNC1)
  • western blot; mouse; loading ...; fig 8b
EMD Millipore TH antibody (Millipore, MAB318) was used in western blot on mouse samples (fig 8b). Sci Rep (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; human; 1:250; fig 6
In order to test if testosterone can have a direct effect on dopamine neurons, EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on human samples at 1:250 (fig 6). Schizophr Res (2015) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; rat; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on rat samples at 1:1000. PLoS ONE (2015) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; human; fig 3
In order to investigate the contribution of the Trib3 signaling pathway to neuron death, EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on human samples (fig 3). J Neurosci (2015) ncbi
domestic rabbit polyclonal
  • immunocytochemistry; human; 1:500; fig 3
In order to evaluate the efficacy of a neural induction method for human induced pluripotent stem cells and transplant these cells into guinea-pig cochleae for replacement of spiral ganglion neurons, EMD Millipore TH antibody (Millipore, AB152) was used in immunocytochemistry on human samples at 1:500 (fig 3). J Tissue Eng Regen Med (2017) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:5000; fig 3
  • immunohistochemistry; rat; 1:5000; fig 1
In order to study alpha-synuclein overexpression by lack of an additive role of aging in nigrostriatal neurodegeneration, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:5000 (fig 3) and in immunohistochemistry on rat samples at 1:5000 (fig 1). Acta Neuropathol Commun (2015) ncbi
mouse monoclonal (LNC1)
  • western blot; rat; 1:40000
EMD Millipore TH antibody (Millipore, MAB318) was used in western blot on rat samples at 1:40000. Neuropsychopharmacology (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:400
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:400. J Biol Chem (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:600
  • immunocytochemistry; mouse; 1:600
In order to identify somatic cell types in vivo that can be reprogrammed, EMD Millipore TH antibody (MerckMillipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:600 and in immunocytochemistry on mouse samples at 1:600. Hum Gene Ther Methods (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:500; loading ...; fig 2
EMD Millipore TH antibody (Merck Millipore, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:500 (fig 2). Mol Neurodegener (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; Hepatitis B virus; 1:500
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on Hepatitis B virus samples at 1:500. Endocrinology (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:400; fig 5
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry on mouse samples at 1:400 (fig 5). PLoS ONE (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; domestic rabbit; 1:1000
  • immunohistochemistry - frozen section; rat; 1:1000
  • immunohistochemistry - frozen section; mouse; 1:1000
In order to study dopamine signaling in the retina and brain, EMD Millipore TH antibody (Merck Millipore Ltd, MAB318) was used in immunohistochemistry - frozen section on domestic rabbit samples at 1:1000, in immunohistochemistry - frozen section on rat samples at 1:1000 and in immunohistochemistry - frozen section on mouse samples at 1:1000. J Neurochem (2015) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; mouse; 1:500; fig S7
EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on mouse samples at 1:500 (fig S7). Nat Neurosci (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:2000
In order to determine if glucose-regulated protein 78 contributes to the development of Parkinson's disease, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:2000. Neurobiol Aging (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; Japanese rice fish; 1:1000; fig 2
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on Japanese rice fish samples at 1:1000 (fig 2). PLoS Genet (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:500
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on rat samples at 1:500. Brain Struct Funct (2016) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:2000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on rat samples at 1:2000. J Neurosci (2015) ncbi
mouse monoclonal (LNC1)
EMD Millipore TH antibody (EMD Millipore, MAB318) was used . Nat Neurosci (2015) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; rat; 1:500; fig 1
  • immunocytochemistry; mouse; 1:500; fig 2
EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on rat samples at 1:500 (fig 1) and in immunocytochemistry on mouse samples at 1:500 (fig 2). J Neurosci (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; mouse; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - paraffin section on mouse samples at 1:1000. PLoS Genet (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:4000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:4000. Neurobiol Aging (2015) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; mouse; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - paraffin section on mouse samples at 1:1000. Cell Tissue Res (2015) ncbi
mouse monoclonal (LNC1)
  • western blot; mouse; fig 7
EMD Millipore TH antibody (Millipore, MAB318) was used in western blot on mouse samples (fig 7). FASEB J (2015) ncbi
domestic rabbit polyclonal
  • immunohistochemistry; rat; 1:2000; loading ...; fig 5a
In order to study the effects of chronic wheel running during withdrawal and protracted abstinence in methamphetamine-dependent rats, EMD Millipore TH antibody (EMD Millipore, AB152) was used in immunohistochemistry on rat samples at 1:2000 (fig 5a). Brain Struct Funct (2016) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; domestic sheep; 1:500
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunocytochemistry on domestic sheep samples at 1:500. Ann Anat (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:5,000
In order to identify the mechanism for serotonergic regulation of neural circuits in the mouse olfactory bulb, EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry on mouse samples at 1:5,000. J Comp Neurol (2015) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; rat; 1:5000
EMD Millipore TH antibody (Merck Millipore, MAB318) was used in immunocytochemistry on rat samples at 1:5000. Acta Histochem Cytochem (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; human
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on human samples . PLoS ONE (2014) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; mouse; 1:2000; fig 8
EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on mouse samples at 1:2000 (fig 8). J Neurosci (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; zebrafish ; 1:400
In order to characterize mpz gene expression during development and axonal injury in zebrafish, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on zebrafish samples at 1:400. J Biol Chem (2014) ncbi
mouse monoclonal (LNC1)
  • western blot; rat; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in western blot on rat samples at 1:1000. PLoS ONE (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:1000. Biochim Biophys Acta (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; Petromyzontiformes; 1:600
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on Petromyzontiformes samples at 1:600. J Comp Neurol (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:500; loading ...; fig 1h
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:500 (fig 1h). Brain Struct Funct (2015) ncbi
mouse monoclonal (LNC1)
EMD Millipore TH antibody (Millipore / Chemicon, MAB318) was used . J Comp Neurol (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; African green monkey; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on African green monkey samples at 1:1000. J Comp Neurol (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:5000
In order to determine the function of the melanocortin-3 receptor in the ventral tegmental area, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:5000. Endocrinology (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:1000. J Comp Neurol (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:2000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:2000. J Virol (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:2000
In order to study the effect of pomegranate juice on oxidative stress and nigrostriatal degeneration in Parkinson disease, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on rat samples at 1:2000. Neurobiol Aging (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:1000
In order to test if Hsp27 or Hsp70 prevents alpha-synuclein-induced early neuronal pathology in a rat model of Parkinson's disease, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on rat samples at 1:1000. CNS Neurosci Ther (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:200
In order to use a SIP1-EGFP reporter mouse to study brain development, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:200. Genesis (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:1000
In order to understand the role of TrkB in the integration of new periglomerular cells in the adult olfactory bulb, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:1000. J Neurosci (2013) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; smaller spotted dogfish; 1:500
In order to study the cerebellar connections in shark embryos and juveniles, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on smaller spotted dogfish samples at 1:500. J Comp Neurol (2014) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; mouse; 1:200
EMD Millipore TH antibody (Chemicon / Millipore, MAB318) was used in immunohistochemistry - paraffin section on mouse samples at 1:200. J Comp Neurol (2013) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; swine; 1:80
EMD Millipore TH antibody (Chemicon, MAB 318) was used in immunohistochemistry - frozen section on swine samples at 1:80. J Mol Neurosci (2013) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:2000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:2000. Brain Behav (2013) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; mouse; 1:200
EMD Millipore TH antibody (Chemicon, Mab318) was used in immunocytochemistry on mouse samples at 1:200. Genesis (2013) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; human; 1:2000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on human samples at 1:2000. Gene Ther (2013) ncbi
mouse monoclonal (LNC1)
  • immunocytochemistry; human
EMD Millipore TH antibody (Millipore, MAB318) was used in immunocytochemistry on human samples . Stem Cell Rev (2012) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; zebrafish ; 1:1000
In order to study the role of MANF during dopaminergic neuron development in larval zebrafish, EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry on zebrafish samples at 1:1000. Dev Biol (2012) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; European river lamprey; 1:600
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on European river lamprey samples at 1:600. J Comp Neurol (2012) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; zebrafish ; 1:400
In order to investigate neurogenic periventricular zones in the adult zebrafish forebrain, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:400. J Comp Neurol (2012) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rhesus macaque; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on rhesus macaque samples at 1:1000. J Comp Neurol (2011) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:40000
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:40000. J Comp Neurol (2012) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:2000
EMD Millipore TH antibody (Millipore-Chemicon, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:2000. J Comp Neurol (2011) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; mouse; 1:500
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry on mouse samples at 1:500. J Comp Neurol (2012) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; human; 1:100
EMD Millipore TH antibody (Millipore, LNC1) was used in immunohistochemistry on human samples at 1:100. PLoS ONE (2011) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - paraffin section; rhesus macaque; 1:100
  • immunohistochemistry - paraffin section; human; 1:100
In order to study myenteric neurons in the rhesus monkey, EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - paraffin section on rhesus macaque samples at 1:100 and in immunohistochemistry - paraffin section on human samples at 1:100. J Comp Neurol (2011) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:2000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:2000. J Comp Neurol (2011) ncbi
mouse monoclonal (LNC1)
  • western blot; zebrafish ; 1:1000
EMD Millipore TH antibody (Millipore, MAB318) was used in western blot on zebrafish samples at 1:1000. J Comp Neurol (2011) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; zebrafish ; 1:200 - 1:500
In order to investigate the neurochemical coding of enteric neurons in zebrafish, EMD Millipore TH antibody (Chemicon International Inc., MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:200 - 1:500. J Comp Neurol (2010) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:500
EMD Millipore TH antibody (Chemicon International, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:500. J Comp Neurol (2010) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; zebrafish ; 1:1000
In order to localize beta2-adrenoceptors in the adult zebrafish brain, EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:1000. J Comp Neurol (2010) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; mouse; 1:500
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - frozen section on mouse samples at 1:500. J Comp Neurol (2010) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:4000
  • immunocytochemistry; rat; 1:4000
EMD Millipore TH antibody (Millipore-Chemicon, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:4000 and in immunocytochemistry on rat samples at 1:4000. J Comp Neurol (2009) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:5000
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:5000. J Comp Neurol (2009) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; Xenopus laevis; 1:100
  • western blot; Xenopus laevis; 1:200
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on Xenopus laevis samples at 1:100 and in western blot on Xenopus laevis samples at 1:200. J Comp Neurol (2009) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; smaller spotted dogfish; 1:2,500
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on smaller spotted dogfish samples at 1:2,500. J Comp Neurol (2008) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry; rat; 1:2000
EMD Millipore TH antibody (Chemicon / Millipore, MAB318) was used in immunohistochemistry on rat samples at 1:2000. J Comp Neurol (2008) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:400
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:400. J Comp Neurol (2008) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; mouse; 1:2000
EMD Millipore TH antibody (Millipore, MAB318) was used in immunohistochemistry - free floating section on mouse samples at 1:2000. J Comp Neurol (2008) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; zebrafish ; 1:1,000
In order to localize alpha(2A)-adrenoceptors in the adult zebrafish brain, EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on zebrafish samples at 1:1,000. J Comp Neurol (2008) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - frozen section; rat; 1:1,000
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - frozen section on rat samples at 1:1,000. J Comp Neurol (2008) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:500
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:500. J Comp Neurol (2006) ncbi
mouse monoclonal (LNC1)
  • immunohistochemistry - free floating section; rat; 1:5000
EMD Millipore TH antibody (Chemicon, MAB318) was used in immunohistochemistry - free floating section on rat samples at 1:5000. J Comp Neurol (2005) ncbi
Articles Reviewed
  1. You H, Shang W, Min X, Weinreb J, Li Q, Leapman M, et al. Sight and switch off: Nerve density visualization for interventions targeting nerves in prostate cancer. Sci Adv. 2020;6:eaax6040 pubmed publisher
  2. Xie K, Wang N, Lin X, Wang Z, Zhao X, Fang P, et al. Organic electrochemical transistor arrays for real-time mapping of evoked neurotransmitter release in vivo. elife. 2020;9: pubmed publisher
  3. Moriya S, Yamashita A, Masukawa D, Kambe Y, Sakaguchi J, Setoyama H, et al. Involvement of supralemniscal nucleus (B9) 5-HT neuronal system in nociceptive processing: a fiber photometry study. Mol Brain. 2020;13:14 pubmed publisher
  4. Emam A, Yoffe M, Cardona H, Soares D. Retinal morphology in Astyanax mexicanus during eye degeneration. J Comp Neurol. 2020;528:1523-1534 pubmed publisher
  5. Wullimann M, Umeasalugo K. Sonic hedgehog expression in zebrafish forebrain identifies the teleostean pallidal signaling center and shows preglomerular complex and posterior tubercular dopamine cells to arise from shh cells. J Comp Neurol. 2019;: pubmed publisher
  6. Aoki S, Smith J, Li H, Yan X, Igarashi M, Coulon P, et al. An open cortico-basal ganglia loop allows limbic control over motor output via the nigrothalamic pathway. elife. 2019;8: pubmed publisher
  7. L pez J, Morona R, Moreno N, Lozano D, Jim nez S, Gonz lez A. Pax6 expression highlights regional organization in the adult brain of lungfishes, the closest living relatives of land vertebrates. J Comp Neurol. 2020;528:135-159 pubmed publisher
  8. Beaus jour P, Auclair F, Daghfous G, Ngovandan C, Veilleux D, Zielinski B, et al. Dopaminergic modulation of olfactory-evoked motor output in sea lampreys (Petromyzon marinus L.). J Comp Neurol. 2020;528:114-134 pubmed publisher
  9. Wen Y, Zhang Z, Li Z, Liu G, Tao G, Song X, et al. The PROK2/PROKR2 signaling pathway is required for the migration of most olfactory bulb interneurons. J Comp Neurol. 2019;527:2931-2947 pubmed publisher
  10. Gumbs M, Vuuregge A, Eggels L, Unmehopa U, Lamuadni K, Mul J, et al. Afferent neuropeptide Y projections to the ventral tegmental area in normal-weight male Wistar rats. J Comp Neurol. 2019;527:2659-2674 pubmed publisher
  11. McAlpine C, Kiss M, Rattik S, He S, Vassalli A, Valet C, et al. Sleep modulates haematopoiesis and protects against atherosclerosis. Nature. 2019;566:383-387 pubmed publisher
  12. Sen S, Parishar P, Pundir A, Reiner A, Iyengar S. The expression of tyrosine hydroxylase and DARPP-32 in the house crow (Corvus splendens) brain. J Comp Neurol. 2019;527:1801-1836 pubmed publisher
  13. Fischer A, Schlein C, Cannon B, Heeren J, Nedergaard J. Intact innervation is essential for diet-induced recruitment of brown adipose tissue. Am J Physiol Endocrinol Metab. 2019;316:E487-E503 pubmed publisher
  14. 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
  15. Munteanu T, Noronha K, Leung A, Pan S, Lucas J, Schmidt T. Light-dependent pathways for dopaminergic amacrine cell development and function. elife. 2018;7: pubmed publisher
  16. Breton J, Charbit A, Snyder B, Fong P, Dias E, Himmels P, et al. Relative contributions and mapping of ventral tegmental area dopamine and GABA neurons by projection target in the rat. J Comp Neurol. 2019;527:916-941 pubmed publisher
  17. Luo S, Huang J, Li Q, Mohammad H, Lee C, Krishna K, et al. Regulation of feeding by somatostatin neurons in the tuberal nucleus. Science. 2018;361:76-81 pubmed publisher
  18. Tarasova T, Lytkina O, Goloborshcheva V, Skuratovskaya L, Antohin A, Ovchinnikov R, et al. Genetic inactivation of alpha-synuclein affects embryonic development of dopaminergic neurons of the substantia nigra, but not the ventral tegmental area, in mouse brain. Peerj. 2018;6:e4779 pubmed publisher
  19. Balan I, Warnock K, Puche A, GONDRE LEWIS M, JUNE H, Aurelian L. The GABAA Receptor α2 Subunit Activates a Neuronal TLR4 Signal in the Ventral Tegmental Area that Regulates Alcohol and Nicotine Abuse. Brain Sci. 2018;8: pubmed publisher
  20. Sato S, Uchihara T, Fukuda T, Noda S, Kondo H, Saiki S, et al. Loss of autophagy in dopaminergic neurons causes Lewy pathology and motor dysfunction in aged mice. Sci Rep. 2018;8:2813 pubmed publisher
  21. Lin Y, Kuo K, Chen S, Huang H. RBFOX3/NeuN is dispensable for visual function. PLoS ONE. 2018;13:e0192355 pubmed publisher
  22. Liu C, Kershberg L, Wang J, Schneeberger S, Kaeser P. Dopamine Secretion Is Mediated by Sparse Active Zone-like Release Sites. Cell. 2018;172:706-718.e15 pubmed publisher
  23. Xiong Y, Neifert S, Karuppagounder S, Liu Q, Stankowski J, Lee B, et al. Robust kinase- and age-dependent dopaminergic and norepinephrine neurodegeneration in LRRK2 G2019S transgenic mice. Proc Natl Acad Sci U S A. 2018;115:1635-1640 pubmed publisher
  24. Dunn A, Hoffman C, Stout K, Ozawa M, Dhamsania R, Miller G. Immunochemical analysis of the expression of SV2C in mouse, macaque and human brain. Brain Res. 2019;1702:85-95 pubmed publisher
  25. Johnson E, Westbrook T, Shayesteh R, Chen E, Schumacher J, Fitzpatrick D, et al. Distribution and diversity of intrinsically photosensitive retinal ganglion cells in tree shrew. J Comp Neurol. 2019;527:328-344 pubmed publisher
  26. Parmhans N, Sajgo S, Niu J, Luo W, Badea T. Characterization of retinal ganglion cell, horizontal cell, and amacrine cell types expressing the neurotrophic receptor tyrosine kinase Ret. J Comp Neurol. 2018;526:742-766 pubmed publisher
  27. Zhang Z, Chu S, Wang S, Jiang Y, Gao Y, Yang P, et al. RTP801 is a critical factor in the neurodegeneration process of A53T α-synuclein in a mouse model of Parkinson's disease under chronic restraint stress. Br J Pharmacol. 2018;175:590-605 pubmed publisher
  28. Bernstein D, Badve P, Barson J, Bass C, Espana R. Hypocretin receptor 1 knockdown in the ventral tegmental area attenuates mesolimbic dopamine signaling and reduces motivation for cocaine. Addict Biol. 2018;23:1032-1045 pubmed publisher
  29. Salazar S, Gallardo C, Kaufman A, Herber C, Haas L, Robinson S, et al. Conditional Deletion of Prnp Rescues Behavioral and Synaptic Deficits after Disease Onset in Transgenic Alzheimer's Disease. J Neurosci. 2017;37:9207-9221 pubmed publisher
  30. Barreiro Iglesias A, Fernández López B, Sobrido Cameán D, Anadón R. Organization of alpha-transducin immunoreactive system in the brain and retina of larval and young adult Sea Lamprey (Petromyzon marinus), and their relationship with other neural systems. J Comp Neurol. 2017;525:3683-3704 pubmed publisher
  31. González Cabrera C, Meza R, Ulloa L, Merino Sepúlveda P, Luco V, Sanhueza A, et al. Characterization of the axon initial segment of mice substantia nigra dopaminergic neurons. J Comp Neurol. 2017;525:3529-3542 pubmed publisher
  32. Seigneur E, Südhof T. Cerebellins are differentially expressed in selective subsets of neurons throughout the brain. J Comp Neurol. 2017;525:3286-3311 pubmed publisher
  33. Furlan A, Dyachuk V, Kastriti M, Calvo Enrique L, Abdo H, Hadjab S, et al. Multipotent peripheral glial cells generate neuroendocrine cells of the adrenal medulla. Science. 2017;357: pubmed publisher
  34. van Groningen T, Koster J, Valentijn L, Zwijnenburg D, Akogul N, Hasselt N, et al. Neuroblastoma is composed of two super-enhancer-associated differentiation states. Nat Genet. 2017;49:1261-1266 pubmed publisher
  35. López J, González A. Organization of the catecholaminergic systems in the brain of lungfishes, the closest living relatives of terrestrial vertebrates. J Comp Neurol. 2017;525:3083-3109 pubmed publisher
  36. Fischer D, Kemp C, Cole Strauss A, Polinski N, Paumier K, Lipton J, et al. Subthalamic Nucleus Deep Brain Stimulation Employs trkB Signaling for Neuroprotection and Functional Restoration. J Neurosci. 2017;37:6786-6796 pubmed publisher
  37. Shiba Fukushima K, Ishikawa K, Inoshita T, Izawa N, Takanashi M, Sato S, et al. Evidence that phosphorylated ubiquitin signaling is involved in the etiology of Parkinson's disease. Hum Mol Genet. 2017;26:3172-3185 pubmed publisher
  38. Escobar A, González M, Meza R, Noches V, Henny P, Gysling K, et al. Mechanisms of Kappa Opioid Receptor Potentiation of Dopamine D2 Receptor Function in Quinpirole-Induced Locomotor Sensitization in Rats. Int J Neuropsychopharmacol. 2017;20:660-669 pubmed publisher
  39. Watson C, Shimogori T, Puelles L. Mouse Fgf8-Cre-LacZ lineage analysis defines the territory of the postnatal mammalian isthmus. J Comp Neurol. 2017;525:2782-2799 pubmed publisher
  40. 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
  41. Takahashi Y, Wu J, Suzuki K, Martínez Redondo P, Li M, Liao H, et al. Integration of CpG-free DNA induces de novo methylation of CpG islands in pluripotent stem cells. Science. 2017;356:503-508 pubmed publisher
  42. Quadrato G, Nguyen T, Macosko E, Sherwood J, Min Yang S, Berger D, et al. Cell diversity and network dynamics in photosensitive human brain organoids. Nature. 2017;545:48-53 pubmed publisher
  43. Mendivil Perez M, Soto Mercado V, Guerra Librero A, Fernandez Gil B, Florido J, Shen Y, et al. Melatonin enhances neural stem cell differentiation and engraftment by increasing mitochondrial function. J Pineal Res. 2017;63: pubmed publisher
  44. Parker L, Le S, Wearne T, Hardwick K, Kumar N, Robinson K, et al. Neurochemistry of neurons in the ventrolateral medulla activated by hypotension: Are the same neurons activated by glucoprivation?. J Comp Neurol. 2017;525:2249-2264 pubmed publisher
  45. 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
  46. Longo F, Mercatelli D, Novello S, Arcuri L, Brugnoli A, Vincenzi F, et al. Age-dependent dopamine transporter dysfunction and Serine129 phospho-α-synuclein overload in G2019S LRRK2 mice. Acta Neuropathol Commun. 2017;5:22 pubmed publisher
  47. Shan M, Lin S, Li S, Du Y, Zhao H, Hong H, et al. TIR-Domain-Containing Adapter-Inducing Interferon-? (TRIF) Is Essential for MPTP-Induced Dopaminergic Neuroprotection via Microglial Cell M1/M2 Modulation. Front Cell Neurosci. 2017;11:35 pubmed publisher
  48. Williams C, Uytingco C, Green W, McIntyre J, Ukhanov K, Zimmerman A, et al. Gene Therapeutic Reversal of Peripheral Olfactory Impairment in Bardet-Biedl Syndrome. Mol Ther. 2017;25:904-916 pubmed publisher
  49. Zhao F, Wang W, Wang C, Siedlak S, Fujioka H, Tang B, et al. Mfn2 protects dopaminergic neurons exposed to paraquat both in vitro and in vivo: Implications for idiopathic Parkinson's disease. Biochim Biophys Acta Mol Basis Dis. 2017;1863:1359-1370 pubmed publisher
  50. Furukawa S, Nagaike M, Ozaki K. Databases for technical aspects of immunohistochemistry. J Toxicol Pathol. 2017;30:79-107 pubmed publisher
  51. Roberts H, Schneider B, Brown D. α-Synuclein increases β-amyloid secretion by promoting β-/γ-secretase processing of APP. PLoS ONE. 2017;12:e0171925 pubmed publisher
  52. Goodings L, He J, Wood A, Harris W, Currie P, Jusuf P. In vivo expression of Nurr1/Nr4a2a in developing retinal amacrine subtypes in zebrafish Tg(nr4a2a:eGFP) transgenics. J Comp Neurol. 2017;525:1962-1979 pubmed publisher
  53. Hannibal J, Christiansen A, Heegaard S, Fahrenkrug J, Kiilgaard J. Melanopsin expressing human retinal ganglion cells: Subtypes, distribution, and intraretinal connectivity. J Comp Neurol. 2017;525:1934-1961 pubmed publisher
  54. Green H, Zhang X, Tiklová K, Volakakis N, Brodin L, Berg L, et al. Alterations of p11 in brain tissue and peripheral blood leukocytes in Parkinson's disease. Proc Natl Acad Sci U S A. 2017;114:2735-2740 pubmed publisher
  55. Stayte S, Rentsch P, Tröscher A, Bamberger M, Li K, Vissel B. Activin A Inhibits MPTP and LPS-Induced Increases in Inflammatory Cell Populations and Loss of Dopamine Neurons in the Mouse Midbrain In Vivo. PLoS ONE. 2017;12:e0167211 pubmed publisher
  56. Perelmuter J, Forlano P. Connectivity and ultrastructure of dopaminergic innervation of the inner ear and auditory efferent system of a vocal fish. J Comp Neurol. 2017;525:2090-2108 pubmed publisher
  57. Liu H, Ho P, Leung G, Lam C, Pang S, Li L, et al. Combined LRRK2 mutation, aging and chronic low dose oral rotenone as a model of Parkinson's disease. Sci Rep. 2017;7:40887 pubmed publisher
  58. Wircer E, Blechman J, Borodovsky N, Tsoory M, Nunes A, Oliveira R, et al. Homeodomain protein Otp affects developmental neuropeptide switching in oxytocin neurons associated with a long-term effect on social behavior. elife. 2017;6: pubmed publisher
  59. Song L, McMackin M, Nguyen A, Cortopassi G. Parkin deficiency accelerates consequences of mitochondrial DNA deletions and Parkinsonism. Neurobiol Dis. 2017;100:30-38 pubmed publisher
  60. Fasoli A, Dang J, Johnson J, Gouw A, Fogli Iseppe A, Ishida A. Somatic and neuritic spines on tyrosine hydroxylase-immunopositive cells of rat retina. J Comp Neurol. 2017;525:1707-1730 pubmed publisher
  61. Oh Y, Karube F, Takahashi S, Kobayashi K, Takada M, Uchigashima M, et al. Using a novel PV-Cre rat model to characterize pallidonigral cells and their terminations. Brain Struct Funct. 2017;222:2359-2378 pubmed publisher
  62. Higo S, Iijima N, Ozawa H. Characterisation of Kiss1r (Gpr54)-Expressing Neurones in the Arcuate Nucleus of the Female Rat Hypothalamus. J Neuroendocrinol. 2017;29: pubmed publisher
  63. Dzamko N, Gysbers A, Bandopadhyay R, Bolliger M, Uchino A, Zhao Y, et al. LRRK2 levels and phosphorylation in Parkinson's disease brain and cases with restricted Lewy bodies. Mov Disord. 2017;32:423-432 pubmed publisher
  64. Koprich J, Johnston T, Reyes G, Omana V, Brotchie J. Towards a Non-Human Primate Model of Alpha-Synucleinopathy for Development of Therapeutics for Parkinson's Disease: Optimization of AAV1/2 Delivery Parameters to Drive Sustained Expression of Alpha Synuclein and Dopaminergic Degeneration in Macaque. PLoS ONE. 2016;11:e0167235 pubmed publisher
  65. Kiyokage E, Kobayashi K, Toida K. Spatial distribution of synapses on tyrosine hydroxylase-expressing juxtaglomerular cells in the mouse olfactory glomerulus. J Comp Neurol. 2017;525:1059-1074 pubmed publisher
  66. Conceição E, Moura E, Oliveira E, Guarda D, Figueiredo M, Quitete F, et al. Dietary calcium supplementation in adult rats reverts brown adipose tissue dysfunction programmed by postnatal early overfeeding. J Nutr Biochem. 2017;39:117-125 pubmed publisher
  67. Zha J, Liu X, Zhu J, Liu S, Lu S, Xu P, et al. A scFv antibody targeting common oligomeric epitope has potential for treating several amyloidoses. Sci Rep. 2016;6:36631 pubmed publisher
  68. He J, Xiang Z, Zhu X, Ai Z, Shen J, Huang T, et al. Neuroprotective Effects of 7, 8-dihydroxyflavone on Midbrain Dopaminergic Neurons in MPP+-treated Monkeys. Sci Rep. 2016;6:34339 pubmed publisher
  69. La Manno G, Gyllborg D, Codeluppi S, Nishimura K, Salto C, Zeisel A, et al. Molecular Diversity of Midbrain Development in Mouse, Human, and Stem Cells. Cell. 2016;167:566-580.e19 pubmed publisher
  70. Vyas P, Wu J, Zimmerman A, Fuchs P, Glowatzki E. Tyrosine Hydroxylase Expression in Type II Cochlear Afferents in Mice. J Assoc Res Otolaryngol. 2017;18:139-151 pubmed publisher
  71. Arredondo C, Gonzalez M, Andrés M, Gysling K. Opposite effects of acute and chronic amphetamine on Nurr1 and NF-?B p65 in the rat ventral tegmental area. Brain Res. 2016;1652:14-20 pubmed publisher
  72. Doan K, Kinyua A, Yang D, Ko C, Moh S, Shong K, et al. FoxO1 in dopaminergic neurons regulates energy homeostasis and targets tyrosine hydroxylase. Nat Commun. 2016;7:12733 pubmed publisher
  73. Cóppola Segovia V, Cavarsan C, Maia F, Ferraz A, Nakao L, Lima M, et al. ER Stress Induced by Tunicamycin Triggers ?-Synuclein Oligomerization, Dopaminergic Neurons Death and Locomotor Impairment: a New Model of Parkinson's Disease. Mol Neurobiol. 2017;54:5798-5806 pubmed publisher
  74. Lizen B, Hutlet B, Bissen D, Sauvegarde D, Hermant M, Ahn M, et al. HOXA5 localization in postnatal and adult mouse brain is suggestive of regulatory roles in postmitotic neurons. J Comp Neurol. 2017;525:1155-1175 pubmed publisher
  75. Wu Q, Yang X, Zhang Y, Zhang L, Feng L. Chronic mild stress accelerates the progression of Parkinson's disease in A53T ?-synuclein transgenic mice. Exp Neurol. 2016;285:61-71 pubmed publisher
  76. Peris J, Macfadyen K, Smith J, de Kloet A, Wang L, Krause E. Oxytocin receptors are expressed on dopamine and glutamate neurons in the mouse ventral tegmental area that project to nucleus accumbens and other mesolimbic targets. J Comp Neurol. 2017;525:1094-1108 pubmed publisher
  77. Stauffer W, Lak A, Yang A, Borel M, Paulsen O, Boyden E, et al. Dopamine Neuron-Specific Optogenetic Stimulation in Rhesus Macaques. Cell. 2016;166:1564-1571.e6 pubmed publisher
  78. Hansen S, Stummann T, Borland H, Hasholt L, Tumer Z, Nielsen J, et al. Induced pluripotent stem cell - derived neurons for the study of spinocerebellar ataxia type 3. Stem Cell Res. 2016;17:306-317 pubmed publisher
  79. Brown R, Kokay I, Phillipps H, Yip S, Gustafson P, Wyatt A, et al. Conditional Deletion of the Prolactin Receptor Reveals Functional Subpopulations of Dopamine Neurons in the Arcuate Nucleus of the Hypothalamus. J Neurosci. 2016;36:9173-85 pubmed publisher
  80. Ztaou S, Maurice N, Camon J, Guiraudie Capraz G, Kerkerian Le Goff L, Beurrier C, et al. Involvement of Striatal Cholinergic Interneurons and M1 and M4 Muscarinic Receptors in Motor Symptoms of Parkinson's Disease. J Neurosci. 2016;36:9161-72 pubmed publisher
  81. Fukada M, Nakayama A, Mamiya T, Yao T, Kawaguchi Y. Dopaminergic abnormalities in Hdac6-deficient mice. Neuropharmacology. 2016;110:470-479 pubmed publisher
  82. Dewanto A, Dudas J, Glueckert R, Mechsner S, Schrott Fischer A, Wildt L, et al. Localization of TrkB and p75 receptors in peritoneal and deep infiltrating endometriosis: an immunohistochemical study. Reprod Biol Endocrinol. 2016;14:43 pubmed publisher
  83. Vingill S, Brockelt D, Lancelin C, Tatenhorst L, Dontcheva G, Preisinger C, et al. Loss of FBXO7 (PARK15) results in reduced proteasome activity and models a parkinsonism-like phenotype in mice. EMBO J. 2016;35:2008-25 pubmed publisher
  84. Hamamoto M, Kiyokage E, Sohn J, Hioki H, Harada T, Toida K. Structural basis for cholinergic regulation of neural circuits in the mouse olfactory bulb. J Comp Neurol. 2017;525:574-591 pubmed publisher
  85. Ku T, Swaney J, Park J, Albanese A, Murray E, Cho J, et al. Multiplexed and scalable super-resolution imaging of three-dimensional protein localization in size-adjustable tissues. Nat Biotechnol. 2016;34:973-81 pubmed publisher
  86. Mazzulli J, Zunke F, Tsunemi T, Toker N, Jeon S, Burbulla L, et al. Activation of β-Glucocerebrosidase Reduces Pathological α-Synuclein and Restores Lysosomal Function in Parkinson's Patient Midbrain Neurons. J Neurosci. 2016;36:7693-706 pubmed publisher
  87. Ding Y, Zhang Z, Ma J, Xia H, Wang Y, Liu Y, et al. Directed differentiation of postnatal hippocampal neural stem cells generates nuclear receptor related?1 protein? and tyrosine hydroxylase?expressing cells. Mol Med Rep. 2016;14:1993-9 pubmed publisher
  88. Cholanians A, Phan A, Ditzel E, Camenisch T, Lau S, Monks T. From the Cover: Arsenic Induces Accumulation of α-Synuclein: Implications for Synucleinopathies and Neurodegeneration. Toxicol Sci. 2016;153:271-81 pubmed publisher
  89. Nandi S, Zheng H, Sharma N, Shahshahan H, Patel K, Mishra P. Lack of miR-133a Decreases Contractility of Diabetic Hearts: A Role for Novel Cross Talk Between Tyrosine Aminotransferase and Tyrosine Hydroxylase. Diabetes. 2016;65:3075-90 pubmed publisher
  90. Simmons A, Bloomsburg S, Billingslea S, Merrill M, Li S, Thomas M, et al. Pou4f2 knock-in Cre mouse: A multifaceted genetic tool for vision researchers. Mol Vis. 2016;22:705-17 pubmed
  91. Sommer A, Fadler T, Dorfmeister E, Hoffmann A, Xiang W, Winner B, et al. Infiltrating T lymphocytes reduce myeloid phagocytosis activity in synucleinopathy model. J Neuroinflammation. 2016;13:174 pubmed publisher
  92. Stojakovic A, Paz Filho G, Arcos Burgos M, Licinio J, Wong M, Mastronardi C. Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement. Mol Neurobiol. 2017;54:4486-4495 pubmed publisher
  93. Schmitt D, Funk N, Blum R, Asan E, Andersen L, Rülicke T, et al. Initial characterization of a Syap1 knock-out mouse and distribution of Syap1 in mouse brain and cultured motoneurons. Histochem Cell Biol. 2016;146:489-512 pubmed publisher
  94. Hughes S, Rodgers J, Hickey D, Foster R, Peirson S, Hankins M. Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways. Sci Rep. 2016;6:28086 pubmed publisher
  95. Prabhudesai S, Bensabeur F, Abdullah R, Basak I, Baez S, Alves G, et al. LRRK2 knockdown in zebrafish causes developmental defects, neuronal loss, and synuclein aggregation. J Neurosci Res. 2016;94:717-35 pubmed publisher
  96. Figueres Oñate M, López Mascaraque L. Adult Olfactory Bulb Interneuron Phenotypes Identified by Targeting Embryonic and Postnatal Neural Progenitors. Front Neurosci. 2016;10:194 pubmed publisher
  97. Morales I, Sánchez A, Rodriguez Sabate C, Rodriguez M. The astrocytic response to the dopaminergic denervation of the striatum. J Neurochem. 2016;139:81-95 pubmed publisher
  98. Wei Z, Yuan Y, Jaouen F, Ma M, Hao C, Zhang Z, et al. SLC35D3 increases autophagic activity in midbrain dopaminergic neurons by enhancing BECN1-ATG14-PIK3C3 complex formation. Autophagy. 2016;12:1168-79 pubmed publisher
  99. He J, Zhou R, Wu Z, Carrasco M, Kurshan P, Farley J, et al. Prevalent presence of periodic actin-spectrin-based membrane skeleton in a broad range of neuronal cell types and animal species. Proc Natl Acad Sci U S A. 2016;113:6029-34 pubmed publisher
  100. Aldrin Kirk P, Heuer A, Wang G, Mattsson B, Lundblad M, Parmar M, et al. DREADD Modulation of Transplanted DA Neurons Reveals a Novel Parkinsonian Dyskinesia Mechanism Mediated by the Serotonin 5-HT6 Receptor. Neuron. 2016;90:955-68 pubmed publisher
  101. Gao J, Kang X, Sun S, Li L, Zhang B, Li Y, et al. Transcription factor Six2 mediates the protection of GDNF on 6-OHDA lesioned dopaminergic neurons by regulating Smurf1 expression. Cell Death Dis. 2016;7:e2217 pubmed publisher
  102. Kim H, Oh J, Choi S, Nam Y, Jo A, Kwon A, et al. Down-regulation of p21-activated serine/threonine kinase 1 is involved in loss of mesencephalic dopamine neurons. Mol Brain. 2016;9:45 pubmed publisher
  103. Kasper J, McCue D, Milton A, Szwed A, Sampson C, Huang M, et al. Gamma-Aminobutyric Acidergic Projections From the Dorsal Raphe to the Nucleus Accumbens Are Regulated by Neuromedin U. Biol Psychiatry. 2016;80:878-887 pubmed publisher
  104. Ueno M, Ueno Nakamura Y, Niehaus J, Popovich P, Yoshida Y. Silencing spinal interneurons inhibits immune suppressive autonomic reflexes caused by spinal cord injury. Nat Neurosci. 2016;19:784-7 pubmed publisher
  105. Wang Y, Gratzke C, Tamalunas A, Wiemer N, Ciotkowska A, Rutz B, et al. P21-Activated Kinase Inhibitors FRAX486 and IPA3: Inhibition of Prostate Stromal Cell Growth and Effects on Smooth Muscle Contraction in the Human Prostate. PLoS ONE. 2016;11:e0153312 pubmed publisher
  106. Chtarto A, Humbert Claude M, Bockstael O, Das A, Boutry S, Breger L, et al. A regulatable AAV vector mediating GDNF biological effects at clinically-approved sub-antimicrobial doxycycline doses. Mol Ther Methods Clin Dev. 2016;5:16027 pubmed publisher
  107. Zhang L, Hernandez V, Vázquez Juárez E, Chay F, Barrio R. Thirst Is Associated with Suppression of Habenula Output and Active Stress Coping: Is there a Role for a Non-canonical Vasopressin-Glutamate Pathway?. Front Neural Circuits. 2016;10:13 pubmed publisher
  108. Gómez López S, Martínez Silva A, Montiel T, Osorio Gómez D, Bermudez Rattoni F, Massieu L, et al. Neural ablation of the PARK10 candidate Plpp3 leads to dopaminergic transmission deficits without neurodegeneration. Sci Rep. 2016;6:24028 pubmed publisher
  109. Fourgeaud L, Traves P, Tufail Y, Leal Bailey H, Lew E, Burrola P, et al. TAM receptors regulate multiple features of microglial physiology. Nature. 2016;532:240-244 pubmed publisher
  110. Inokaitis H, Pauziene N, Rysevaite Kyguoliene K, Pauza D. Innervation of sinoatrial nodal cells in the rabbit. Ann Anat. 2016;205:113-21 pubmed publisher
  111. Kumar A, Jagadeeshan S, Subramanian A, Chidambaram S, Surabhi R, Singhal M, et al. Molecular Mechanism of Regulation of MTA1 Expression by Granulocyte Colony-stimulating Factor. J Biol Chem. 2016;291:12310-21 pubmed publisher
  112. Rossi M, Li H, Lu D, Kim I, Bartholomew R, Gaidis E, et al. A GABAergic nigrotectal pathway for coordination of drinking behavior. Nat Neurosci. 2016;19:742-748 pubmed publisher
  113. Chen C, Liu Y, Hua M, Li X, Ji C, Ma D. Neuropathy correlated with imbalanced Foxp3/IL-17 in bone marrow microenvironment of patients with acute myeloid leukemia. Oncotarget. 2016;7:24455-65 pubmed publisher
  114. González Burguera I, Ricobaraza A, Aretxabala X, Barrondo S, Garcia del Caño G, López de Jesús M, et al. Highly efficient generation of glutamatergic/cholinergic NT2-derived postmitotic human neurons by short-term treatment with the nucleoside analogue cytosine ?-D-arabinofuranoside. Stem Cell Res. 2016;16:541-51 pubmed publisher
  115. Wang Y, Jones Tabah J, Chakravarty P, Stewart A, Muotri A, Laposa R, et al. Pharmacological Bypass of Cockayne Syndrome B Function in Neuronal Differentiation. Cell Rep. 2016;14:2554-61 pubmed publisher
  116. Boggild S, Molgaard S, Glerup S, Nyengaard J. Spatiotemporal patterns of sortilin and SorCS2 localization during organ development. BMC Cell Biol. 2016;17:8 pubmed publisher
  117. Green F, Samaranch L, Zhang H, Manning Bog A, Meyer K, Forsayeth J, et al. Axonal transport of AAV9 in nonhuman primate brain. Gene Ther. 2016;23:520-6 pubmed publisher
  118. Van Audenhove I, Denert M, Boucherie C, Pieters L, Cornelissen M, Gettemans J. Fascin Rigidity and L-plastin Flexibility Cooperate in Cancer Cell Invadopodia and Filopodia. J Biol Chem. 2016;291:9148-60 pubmed publisher
  119. Roy A, Rangasamy S, Kundu M, Pahan K. BPOZ-2 Gene Delivery Ameliorates Alpha-Synucleinopathy in A53T Transgenic Mouse Model of Parkinson's Disease. Sci Rep. 2016;6:22067 pubmed publisher
  120. Rodionova K, Fiedler C, Guenther F, Grouzmann E, Neuhuber W, Fischer M, et al. Complex reinnervation pattern after unilateral renal denervation in rats. Am J Physiol Regul Integr Comp Physiol. 2016;310:R806-18 pubmed publisher
  121. Koeck F, Schmitt M, Baier C, Stangl H, Beckmann J, Grifka J, et al. Predominance of synovial sensory nerve fibers in arthrofibrosis following total knee arthroplasty compared to osteoarthritis of the knee. J Orthop Surg Res. 2016;11:25 pubmed publisher
  122. Liu Z, Brown A, Fisher D, Wu Y, Warren J, Cui X. Tissue Specific Expression of Cre in Rat Tyrosine Hydroxylase and Dopamine Active Transporter-Positive Neurons. PLoS ONE. 2016;11:e0149379 pubmed publisher
  123. Lauretti E, Di Meco A, Merali S, Praticò D. Chronic behavioral stress exaggerates motor deficit and neuroinflammation in the MPTP mouse model of Parkinson's disease. Transl Psychiatry. 2016;6:e733 pubmed publisher
  124. Bouilloux F, Thireau J, Ventéo S, Farah C, Karam S, Dauvilliers Y, et al. Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac death. elife. 2016;5: pubmed publisher
  125. Pandit R, Omrani A, Luijendijk M, de Vrind V, van Rozen A, Ophuis R, et al. Melanocortin 3 Receptor Signaling in Midbrain Dopamine Neurons Increases the Motivation for Food Reward. Neuropsychopharmacology. 2016;41:2241-51 pubmed publisher
  126. van der Keylen P, Garreis F, Steigleder R, Sommer D, Neuhuber W, Wörl J. Involvement of catecholaminergic neurons in motor innervation of striated muscle in the mouse esophagus. Histochem Cell Biol. 2016;145:573-85 pubmed publisher
  127. Naudé J, Tolu S, Dongelmans M, Torquet N, Valverde S, Rodriguez G, et al. Nicotinic receptors in the ventral tegmental area promote uncertainty-seeking. Nat Neurosci. 2016;19:471-8 pubmed publisher
  128. de Souza C, Nivison Smith L, Christie D, Polkinghorne P, McGhee C, Kalloniatis M, et al. Macromolecular markers in normal human retina and applications to human retinal disease. Exp Eye Res. 2016;150:135-48 pubmed publisher
  129. Zhou Q, Yen A, Rymarczyk G, Asai H, Trengrove C, Aziz N, et al. Impairment of PARK14-dependent Ca(2+) signalling is a novel determinant of Parkinson's disease. Nat Commun. 2016;7:10332 pubmed publisher
  130. Grafe L, Flanagan Cato L. Differential effects of mineralocorticoid and angiotensin II on incentive and mesolimbic activity. Horm Behav. 2016;79:28-36 pubmed publisher
  131. Schmitt M, Dehay B, Bezard E, Garcia Ladona F. Harnessing the trophic and modulatory potential of statins in a dopaminergic cell line. Synapse. 2016;70:71-86 pubmed publisher
  132. Hjørnevik L, Frøyset A, Grønset T, Rungruangsak Torrissen K, Fladmark K. Algal Toxin Azaspiracid-1 Induces Early Neuronal Differentiation and Alters Peripherin Isoform Stoichiometry. Mar Drugs. 2015;13:7390-402 pubmed publisher
  133. Pinho B, Reis S, Guedes Dias P, Leitão Rocha A, Quintas C, Valentão P, et al. Pharmacological modulation of HDAC1 and HDAC6 in vivo in a zebrafish model: Therapeutic implications for Parkinson's disease. Pharmacol Res. 2016;103:328-39 pubmed publisher
  134. Oliveira L, Falomir Lockhart L, Botelho M, Lin K, Wales P, Koch J, et al. Elevated α-synuclein caused by SNCA gene triplication impairs neuronal differentiation and maturation in Parkinson's patient-derived induced pluripotent stem cells. Cell Death Dis. 2015;6:e1994 pubmed publisher
  135. Aquino N, Araujo Lopes R, Batista I, Henriques P, Poletini M, Franci C, et al. Hypothalamic Effects of Tamoxifen on Oestrogen Regulation of Luteinising Hormone and Prolactin Secretion in Female Rats. J Neuroendocrinol. 2016;28: pubmed publisher
  136. Hajj R, Milet A, Toulorge D, Cholet N, Laffaire J, Foucquier J, et al. Combination of acamprosate and baclofen as a promising therapeutic approach for Parkinson's disease. Sci Rep. 2015;5:16084 pubmed publisher
  137. Gazea M, Tasouri E, Tolve M, Bosch V, Kabanova A, Gojak C, et al. Primary cilia are critical for Sonic hedgehog-mediated dopaminergic neurogenesis in the embryonic midbrain. Dev Biol. 2016;409:55-71 pubmed publisher
  138. Romano López A, Méndez Díaz M, García F, Regalado Santiago C, Ruiz Contreras A, Prospero Garcia O. Maternal separation and early stress cause long-lasting effects on dopaminergic and endocannabinergic systems and alters dendritic morphology in the nucleus accumbens and frontal cortex in rats. Dev Neurobiol. 2016;76:819-31 pubmed publisher
  139. Winiecka Klimek M, Smolarz M, Walczak M, Zieba J, Hulas Bigoszewska K, Kmieciak B, et al. SOX2 and SOX2-MYC Reprogramming Process of Fibroblasts to the Neural Stem Cells Compromised by Senescence. PLoS ONE. 2015;10:e0141688 pubmed publisher
  140. Knowles M, de la Tremblaye P, Azogu I, Plamondon H. Endocannabinoid CB1 receptor activation upon global ischemia adversely impact recovery of reward and stress signaling molecules, neuronal survival and behavioral impulsivity. Prog Neuropsychopharmacol Biol Psychiatry. 2016;66:8-21 pubmed publisher
  141. Wu R, Chen H, Ma J, He Q, Huang Q, Liu Q, et al. c-Abl-p38α signaling plays an important role in MPTP-induced neuronal death. Cell Death Differ. 2016;23:542-52 pubmed publisher
  142. Stouffer M, Woods C, Patel J, Lee C, Witkovsky P, Bao L, et al. Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward. Nat Commun. 2015;6:8543 pubmed publisher
  143. Liu J, Huang D, Xu J, Tong J, Wang Z, Huang L, et al. Tiagabine Protects Dopaminergic Neurons against Neurotoxins by Inhibiting Microglial Activation. Sci Rep. 2015;5:15720 pubmed publisher
  144. 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
  145. Hayashi Y, Kashiwagi M, Yasuda K, Ando R, Kanuka M, Sakai K, et al. Cells of a common developmental origin regulate REM/non-REM sleep and wakefulness in mice. Science. 2015;350:957-61 pubmed publisher
  146. Tuon T, Souza P, Santos M, Pereira F, Pedroso G, Luciano T, et al. Physical Training Regulates Mitochondrial Parameters and Neuroinflammatory Mechanisms in an Experimental Model of Parkinson's Disease. Oxid Med Cell Longev. 2015;2015:261809 pubmed publisher
  147. Pathak T, Agrawal T, Richhariya S, Sadaf S, Hasan G. Store-Operated Calcium Entry through Orai Is Required for Transcriptional Maturation of the Flight Circuit in Drosophila. J Neurosci. 2015;35:13784-99 pubmed publisher
  148. Van Kampen J, Baranowski D, Robertson H, Shaw C, Kay D. The Progressive BSSG Rat Model of Parkinson's: Recapitulating Multiple Key Features of the Human Disease. PLoS ONE. 2015;10:e0139694 pubmed publisher
  149. Hirata H, Umemori J, Yoshioka H, Koide T, Watanabe K, Shimoda Y. Cell adhesion molecule contactin-associated protein 3 is expressed in the mouse basal ganglia during early postnatal stages. J Neurosci Res. 2016;94:74-89 pubmed publisher
  150. Ehrich J, Messinger D, Knakal C, Kuhar J, Schattauer S, Bruchas M, et al. Kappa Opioid Receptor-Induced Aversion Requires p38 MAPK Activation in VTA Dopamine Neurons. J Neurosci. 2015;35:12917-31 pubmed publisher
  151. De Luca R, Suvorava T, Yang D, Baumgärtel W, Kojda G, Haas H, et al. Identification of histaminergic neurons through histamine 3 receptor-mediated autoinhibition. Neuropharmacology. 2016;106:102-15 pubmed publisher
  152. Dearborn J, Harmon S, Fowler S, O Malley K, Taylor G, Sands M, et al. Comprehensive functional characterization of murine infantile Batten disease including Parkinson-like behavior and dopaminergic markers. Sci Rep. 2015;5:12752 pubmed publisher
  153. Morris R, Purves Tyson T, Weickert C, Rothmond D, Lenroot R, Weickert T. Testosterone and reward prediction-errors in healthy men and men with schizophrenia. Schizophr Res. 2015;168:649-60 pubmed publisher
  154. Jiang Y, Jiang P, Yang J, Ma D, Lin H, Su W, et al. Cardiac Dysregulation and Myocardial Injury in a 6-Hydroxydopamine-Induced Rat Model of Sympathetic Denervation. PLoS ONE. 2015;10:e0133971 pubmed publisher
  155. Aimé P, Sun X, Zareen N, Rao A, Berman Z, Volpicelli Daley L, et al. Trib3 Is Elevated in Parkinson's Disease and Mediates Death in Parkinson's Disease Models. J Neurosci. 2015;35:10731-49 pubmed publisher
  156. Ishikawa M, Ohnishi H, Skerleva D, Sakamoto T, Yamamoto N, Hotta A, et al. Transplantation of neurons derived from human iPS cells cultured on collagen matrix into guinea-pig cochleae. J Tissue Eng Regen Med. 2017;11:1766-1778 pubmed publisher
  157. Bourdenx M, Dovero S, Engeln M, Bido S, Bastide M, Dutheil N, et al. Lack of additive role of ageing in nigrostriatal neurodegeneration triggered by α-synuclein overexpression. Acta Neuropathol Commun. 2015;3:46 pubmed publisher
  158. Hryhorczuk C, Florea M, Rodaros D, Poirier I, Daneault C, Des Rosiers C, et al. Dampened Mesolimbic Dopamine Function and Signaling by Saturated but not Monounsaturated Dietary Lipids. Neuropsychopharmacology. 2016;41:811-21 pubmed publisher
  159. Beckman D, Santos L, Americo T, Ledo J, de Mello F, Linden R. Prion Protein Modulates Monoaminergic Systems and Depressive-like Behavior in Mice. J Biol Chem. 2015;290:20488-98 pubmed publisher
  160. Theodorou M, Rauser B, Zhang J, Prakash N, Wurst W, Schick J. Limitations of In Vivo Reprogramming to Dopaminergic Neurons via a Tricistronic Strategy. Hum Gene Ther Methods. 2015;26:107-22 pubmed publisher
  161. Van Rompuy A, Oliveras Salvá M, Van der Perren A, Corti O, Van den Haute C, Baekelandt V. Nigral overexpression of alpha-synuclein in the absence of parkin enhances alpha-synuclein phosphorylation but does not modulate dopaminergic neurodegeneration. Mol Neurodegener. 2015;10:23 pubmed publisher
  162. Fontaine R, Affaticati P, Bureau C, Colin I, Demarque M, Dufour S, et al. Dopaminergic Neurons Controlling Anterior Pituitary Functions: Anatomy and Ontogenesis in Zebrafish. Endocrinology. 2015;156:2934-48 pubmed publisher
  163. Schreglmann S, Regensburger M, Rockenstein E, Masliah E, Xiang W, Winkler J, et al. The temporal expression pattern of alpha-synuclein modulates olfactory neurogenesis in transgenic mice. PLoS ONE. 2015;10:e0126261 pubmed publisher
  164. Debertin G, Kántor O, Kovács Öller T, Balogh L, Szabó Meleg E, Orbán J, et al. Tyrosine hydroxylase positive perisomatic rings are formed around various amacrine cell types in the mammalian retina. J Neurochem. 2015;134:416-28 pubmed publisher
  165. Laguna A, Schintu N, Nobre A, Alvarsson A, Volakakis N, Jacobsen J, et al. Dopaminergic control of autophagic-lysosomal function implicates Lmx1b in Parkinson's disease. Nat Neurosci. 2015;18:826-35 pubmed publisher
  166. Stayte S, Rentsch P, Li K, Vissel B. Activin A protects midbrain neurons in the 6-hydroxydopamine mouse model of Parkinson's disease. PLoS ONE. 2015;10:e0124325 pubmed publisher
  167. Karbalaie K, Tanhaei S, Rabiei F, Kiani Esfahani A, Masoudi N, Nasr Esfahani M, et al. Stem cells from human exfoliated deciduous tooth exhibit stromal-derived inducing activity and lead to generation of neural crest cells from human embryonic stem cells. Cell J. 2015;17:37-48 pubmed
  168. Salganik M, Sergeyev V, Shinde V, Meyers C, Gorbatyuk M, Lin J, et al. The loss of glucose-regulated protein 78 (GRP78) during normal aging or from siRNA knockdown augments human alpha-synuclein (α-syn) toxicity to rat nigral neurons. Neurobiol Aging. 2015;36:2213-23 pubmed publisher
  169. Uemura N, Koike M, Ansai S, Kinoshita M, Ishikawa Fujiwara T, Matsui H, et al. Viable neuronopathic Gaucher disease model in Medaka (Oryzias latipes) displays axonal accumulation of alpha-synuclein. PLoS Genet. 2015;11:e1005065 pubmed publisher
  170. Leung B, Balleine B. Ventral pallidal projections to mediodorsal thalamus and ventral tegmental area play distinct roles in outcome-specific Pavlovian-instrumental transfer. J Neurosci. 2015;35:4953-64 pubmed publisher
  171. Smeyne M, Sladen P, Jiao Y, Dragatsis I, Smeyne R. HIF1α is necessary for exercise-induced neuroprotection while HIF2α is needed for dopaminergic neuron survival in the substantia nigra pars compacta. Neuroscience. 2015;295:23-38 pubmed publisher
  172. Zheng H, Rinaman L. Simplified CLARITY for visualizing immunofluorescence labeling in the developing rat brain. Brain Struct Funct. 2016;221:2375-83 pubmed publisher
  173. Zhang X, Li Y, Liu C, Fan R, Wang P, Zheng L, et al. Alteration of enteric monoamines with monoamine receptors and colonic dysmotility in 6-hydroxydopamine-induced Parkinson's disease rats. Transl Res. 2015;166:152-62 pubmed publisher
  174. Briffaud V, Williams P, Courty J, Broberger C. Excitation of tuberoinfundibular dopamine neurons by oxytocin: crosstalk in the control of lactation. J Neurosci. 2015;35:4229-37 pubmed publisher
  175. Zhang S, Qi J, Li X, Wang H, Britt J, Hoffman A, et al. Dopaminergic and glutamatergic microdomains in a subset of rodent mesoaccumbens axons. Nat Neurosci. 2015;18:386-92 pubmed publisher
  176. Koo J, Mazei Robison M, LaPlant Q, Egervári G, Braunscheidel K, Adank D, et al. Epigenetic basis of opiate suppression of Bdnf gene expression in the ventral tegmental area. Nat Neurosci. 2015;18:415-22 pubmed publisher
  177. Chand A, Galliano E, Chesters R, Grubb M. A distinct subtype of dopaminergic interneuron displays inverted structural plasticity at the axon initial segment. J Neurosci. 2015;35:1573-90 pubmed publisher
  178. Bifsha P, Yang J, Fisher R, Drouin J. Rgs6 is required for adult maintenance of dopaminergic neurons in the ventral substantia nigra. PLoS Genet. 2014;10:e1004863 pubmed publisher
  179. Polinski N, Gombash S, Manfredsson F, Lipton J, Kemp C, Cole Strauss A, et al. Recombinant adenoassociated virus 2/5-mediated gene transfer is reduced in the aged rat midbrain. Neurobiol Aging. 2015;36:1110-20 pubmed publisher
  180. Colman J, Laureano D, Reis T, Krolow R, Dalmaz C, Benetti C, et al. Variations in the neonatal environment modulate adult behavioral and brain responses to palatable food withdrawal in adult female rats. Int J Dev Neurosci. 2015;40:70-5 pubmed publisher
  181. Sharaf A, Rahhal B, Spittau B, Roussa E. Localization of reelin signaling pathway components in murine midbrain and striatum. Cell Tissue Res. 2015;359:393-407 pubmed publisher
  182. Lee Y, Petkova A, Konkar A, Granneman J. Cellular origins of cold-induced brown adipocytes in adult mice. FASEB J. 2015;29:286-99 pubmed publisher
  183. Pechriggl E, Bitsche M, Glueckert R, Rask Andersen H, Blumer M, Schrott Fischer A, et al. Development of the innervation of the human inner ear. Dev Neurobiol. 2015;75:683-702 pubmed publisher
  184. Huang Y, Chang C, Zhang J, Gao X. Bone marrow-derived mesenchymal stem cells increase dopamine synthesis in the injured striatum. Neural Regen Res. 2012;7:2653-62 pubmed publisher
  185. Sobieraj J, Kim A, Fannon M, Mandyam C. Chronic wheel running-induced reduction of extinction and reinstatement of methamphetamine seeking in methamphetamine dependent rats is associated with reduced number of periaqueductal gray dopamine neurons. Brain Struct Funct. 2016;221:261-76 pubmed publisher
  186. Portella A, Silveira P, Laureano D, Cardoso S, Bittencourt V, Noschang C, et al. Litter size reduction alters insulin signaling in the ventral tegmental area and influences dopamine-related behaviors in adult rats. Behav Brain Res. 2015;278:66-73 pubmed publisher
  187. Pauza D, Rysevaite Kyguoliene K, Vismantaite J, Brack K, Inokaitis H, Pauza A, et al. A combined acetylcholinesterase and immunohistochemical method for precise anatomical analysis of intrinsic cardiac neural structures. Ann Anat. 2014;196:430-40 pubmed publisher
  188. Suzuki Y, Kiyokage E, Sohn J, Hioki H, Toida K. Structural basis for serotonergic regulation of neural circuits in the mouse olfactory bulb. J Comp Neurol. 2015;523:262-80 pubmed publisher
  189. Masuda C, Takeuchi S, J Bisem N, R Vincent S, Tooyama I. Immunohistochemical Localization of an Isoform of TRK-Fused Gene-Like Protein in the Rat Retina. Acta Histochem Cytochem. 2014;47:75-83 pubmed publisher
  190. Sousa J, Vieira Rocha M, Sá C, Ferreirinha F, Correia de Sá P, Fresco P, et al. Lack of endogenous adenosine tonus on sympathetic neurotransmission in spontaneously hypertensive rat mesenteric artery. PLoS ONE. 2014;9:e105540 pubmed publisher
  191. Pinheiro P, Jansen A, de Wit H, Tawfik B, Madsen K, Verhage M, et al. The BAR domain protein PICK1 controls vesicle number and size in adrenal chromaffin cells. J Neurosci. 2014;34:10688-700 pubmed publisher
  192. 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
  193. Walker M, Volta M, Cataldi S, Dinelle K, Beccano Kelly D, Munsie L, et al. Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging. J Parkinsons Dis. 2014;4:483-98 pubmed publisher
  194. Lotan D, Cunningham M, Joel D. Antibiotic treatment attenuates behavioral and neurochemical changes induced by exposure of rats to group a streptococcal antigen. PLoS ONE. 2014;9:e101257 pubmed publisher
  195. Shivers K, Nikolopoulou A, Machlovi S, Vallabhajosula S, Figueiredo Pereira M. PACAP27 prevents Parkinson-like neuronal loss and motor deficits but not microglia activation induced by prostaglandin J2. Biochim Biophys Acta. 2014;1842:1707-19 pubmed publisher
  196. Pérez Fernández J, Stephenson Jones M, Suryanarayana S, Robertson B, Grillner S. Evolutionarily conserved organization of the dopaminergic system in lamprey: SNc/VTA afferent and efferent connectivity and D2 receptor expression. J Comp Neurol. 2014;522:3775-94 pubmed publisher
  197. Nordenankar K, Smith Anttila C, Schweizer N, Viereckel T, Birgner C, Mejía Toiber J, et al. Increased hippocampal excitability and impaired spatial memory function in mice lacking VGLUT2 selectively in neurons defined by tyrosine hydroxylase promoter activity. Brain Struct Funct. 2015;220:2171-90 pubmed publisher
  198. Büchele F, Döbrössy M, Hackl C, Jiang W, Papazoglou A, Nikkhah G. Two-step grafting significantly enhances the survival of foetal dopaminergic transplants and induces graft-derived vascularisation in a 6-OHDA model of Parkinson's disease. Neurobiol Dis. 2014;68:112-25 pubmed publisher
  199. Forlano P, Kim S, Krzyminska Z, Sisneros J. Catecholaminergic connectivity to the inner ear, central auditory, and vocal motor circuitry in the plainfin midshipman fish porichthys notatus. J Comp Neurol. 2014;522:2887-927 pubmed publisher
  200. Bloch J, Brunet J, McEntire C, Redmond D. Primate adult brain cell autotransplantation produces behavioral and biological recovery in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonian St. Kitts monkeys. J Comp Neurol. 2014;522:2729-40 pubmed publisher
  201. Lippert R, Ellacott K, Cone R. Gender-specific roles for the melanocortin-3 receptor in the regulation of the mesolimbic dopamine system in mice. Endocrinology. 2014;155:1718-27 pubmed publisher
  202. O Brien E, Greferath U, Fletcher E. The effect of photoreceptor degeneration on ganglion cell morphology. J Comp Neurol. 2014;522:1155-70 pubmed publisher
  203. Song J, Zheng L, Zhang X, Feng X, Fan R, Sun L, et al. Upregulation of ?1-adrenoceptors is involved in the formation of gastric dysmotility in the 6-hydroxydopamine rat model of Parkinson's disease. Transl Res. 2014;164:22-31 pubmed publisher
  204. Trabalza A, Eleftheriadou I, Sgourou A, Liao T, Patsali P, Lee H, et al. Enhanced central nervous system transduction with lentiviral vectors pseudotyped with RVG/HIV-1gp41 chimeric envelope glycoproteins. J Virol. 2014;88:2877-90 pubmed publisher
  205. Tapias V, Cannon J, Greenamyre J. Pomegranate juice exacerbates oxidative stress and nigrostriatal degeneration in Parkinson's disease. Neurobiol Aging. 2014;35:1162-76 pubmed publisher
  206. Moloney T, Hyland R, O Toole D, Paucard A, Kirik D, O Doherty A, et al. Heat shock protein 70 reduces ?-synuclein-induced predegenerative neuronal dystrophy in the ?-synuclein viral gene transfer rat model of Parkinson's disease. CNS Neurosci Ther. 2014;20:50-8 pubmed publisher
  207. Nishizaki Y, Takagi T, Matsui F, Higashi Y. SIP1 expression patterns in brain investigated by generating a SIP1-EGFP reporter knock-in mouse. Genesis. 2014;52:56-67 pubmed publisher
  208. Bergami M, Vignoli B, Motori E, Pifferi S, Zuccaro E, Menini A, et al. TrkB signaling directs the incorporation of newly generated periglomerular cells in the adult olfactory bulb. J Neurosci. 2013;33:11464-78 pubmed publisher
  209. 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
  210. Milman P, Woulfe J. Novel variant of neuronal intranuclear rodlet immunoreactive for 40 kDa huntingtin associated protein and ubiquitin in the mouse brain. J Comp Neurol. 2013;521:3832-46 pubmed publisher
  211. Wojtkiewicz J, Równiak M, Crayton R, Gonkowski S, Robak A, Zalecki M, et al. Axotomy-induced changes in the chemical coding pattern of colon projecting calbindin-positive neurons in the inferior mesenteric ganglia of the pig. J Mol Neurosci. 2013;51:99-108 pubmed publisher
  212. Bäck S, Peranen J, Galli E, Pulkkila P, Lonka Nevalaita L, Tamminen T, et al. Gene therapy with AAV2-CDNF provides functional benefits in a rat model of Parkinson's disease. Brain Behav. 2013;3:75-88 pubmed publisher
  213. Ohtsuka N, Badurek S, Busslinger M, Benes F, Minichiello L, Rudolph U. GABAergic neurons regulate lateral ventricular development via transcription factor Pax5. Genesis. 2013;51:234-45 pubmed publisher
  214. Trabalza A, Georgiadis C, Eleftheriadou I, Hislop J, Ellison S, Karavassilis M, et al. Venezuelan equine encephalitis virus glycoprotein pseudotyping confers neurotropism to lentiviral vectors. Gene Ther. 2013;20:723-32 pubmed publisher
  215. Liu J, Githinji J, McLaughlin B, Wilczek K, Nolta J. Role of miRNAs in neuronal differentiation from human embryonic stem cell-derived neural stem cells. Stem Cell Rev. 2012;8:1129-37 pubmed publisher
  216. Chen Y, Sundvik M, Rozov S, Priyadarshini M, Panula P. MANF regulates dopaminergic neuron development in larval zebrafish. Dev Biol. 2012;370:237-49 pubmed publisher
  217. Stephenson Jones M, Ericsson J, Robertson B, Grillner S. Evolution of the basal ganglia: dual-output pathways conserved throughout vertebrate phylogeny. J Comp Neurol. 2012;520:2957-73 pubmed publisher
  218. 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
  219. Puthussery T, Gayet Primo J, Taylor W, Haverkamp S. Immunohistochemical identification and synaptic inputs to the diffuse bipolar cell type DB1 in macaque retina. J Comp Neurol. 2011;519:3640-56 pubmed publisher
  220. Sapsford T, Kokay I, Ostberg L, Bridges R, Grattan D. Differential sensitivity of specific neuronal populations of the rat hypothalamus to prolactin action. J Comp Neurol. 2012;520:1062-77 pubmed publisher
  221. Blanco E, Bilbao A, Luque Rojas M, Palomino A, Bermudez Silva F, Suarez J, et al. Attenuation of cocaine-induced conditioned locomotion is associated with altered expression of hippocampal glutamate receptors in mice lacking LPA1 receptors. Psychopharmacology (Berl). 2012;220:27-42 pubmed publisher
  222. Hayes L, Zhang Z, Albert P, Zervas M, Ahn S. Timing of Sonic hedgehog and Gli1 expression segregates midbrain dopamine neurons. J Comp Neurol. 2011;519:3001-18 pubmed publisher
  223. Goemaere J, Knoops B. Peroxiredoxin distribution in the mouse brain with emphasis on neuronal populations affected in neurodegenerative disorders. J Comp Neurol. 2012;520:258-80 pubmed publisher
  224. Rohn T, Catlin L. Immunolocalization of influenza A virus and markers of inflammation in the human Parkinson's disease brain. PLoS ONE. 2011;6:e20495 pubmed publisher
  225. Noorian A, Taylor G, Annerino D, Greene J. Neurochemical phenotypes of myenteric neurons in the rhesus monkey. J Comp Neurol. 2011;519:3387-401 pubmed publisher
  226. Bøttger P, Tracz Z, Heuck A, Nissen P, Romero Ramos M, Lykke Hartmann K. Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain. J Comp Neurol. 2011;519:376-404 pubmed publisher
  227. Gayoso J, Castro A, Anadón R, Manso M. Differential bulbar and extrabulbar projections of diverse olfactory receptor neuron populations in the adult zebrafish (Danio rerio). J Comp Neurol. 2011;519:247-76 pubmed publisher
  228. 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
  229. Phillips M, Otteson D, Sherry D. Progression of neuronal and synaptic remodeling in the rd10 mouse model of retinitis pigmentosa. J Comp Neurol. 2010;518:2071-89 pubmed publisher
  230. 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
  231. Kotani T, Murata Y, Ohnishi H, Mori M, Kusakari S, Saito Y, et al. Expression of PTPRO in the interneurons of adult mouse olfactory bulb. J Comp Neurol. 2010;518:119-36 pubmed publisher
  232. Bérubé Carrière N, Riad M, Dal Bo G, Levesque D, Trudeau L, Descarries L. The dual dopamine-glutamate phenotype of growing mesencephalic neurons regresses in mature rat brain. J Comp Neurol. 2009;517:873-91 pubmed publisher
  233. Madhavan L, Daley B, Paumier K, Collier T. Transplantation of subventricular zone neural precursors induces an endogenous precursor cell response in a rat model of Parkinson's disease. J Comp Neurol. 2009;515:102-15 pubmed publisher
  234. Jhou T, Geisler S, Marinelli M, Degarmo B, Zahm D. The mesopontine rostromedial tegmental nucleus: A structure targeted by the lateral habenula that projects to the ventral tegmental area of Tsai and substantia nigra compacta. J Comp Neurol. 2009;513:566-96 pubmed publisher
  235. Nakano M, Goris R, Atobe Y, Kadota T, Funakoshi K. Mediolateral and rostrocaudal topographic organization of the sympathetic preganglionic cell pool in the spinal cord of Xenopus laevis. J Comp Neurol. 2009;513:292-314 pubmed publisher
  236. Carrera I, Molist P, Anadón R, Rodriguez Moldes I. Development of the serotoninergic system in the central nervous system of a shark, the lesser spotted dogfish Scyliorhinus canicula. J Comp Neurol. 2008;511:804-31 pubmed publisher
  237. Chung E, Chen L, Chan Y, Yung K. Downregulation of glial glutamate transporters after dopamine denervation in the striatum of 6-hydroxydopamine-lesioned rats. J Comp Neurol. 2008;511:421-37 pubmed publisher
  238. Yang Z, You Y, Levison S. Neonatal hypoxic/ischemic brain injury induces production of calretinin-expressing interneurons in the striatum. J Comp Neurol. 2008;511:19-33 pubmed publisher
  239. Luuk H, Koks S, Plaas M, Hannibal J, Rehfeld J, Vasar E. Distribution of Wfs1 protein in the central nervous system of the mouse and its relation to clinical symptoms of the Wolfram syndrome. J Comp Neurol. 2008;509:642-60 pubmed publisher
  240. 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
  241. Tagliaferro P, Morales M. Synapses between corticotropin-releasing factor-containing axon terminals and dopaminergic neurons in the ventral tegmental area are predominantly glutamatergic. J Comp Neurol. 2008;506:616-26 pubmed
  242. Nickerson Poulin A, Guerci A, El Mestikawy S, Semba K. Vesicular glutamate transporter 3 immunoreactivity is present in cholinergic basal forebrain neurons projecting to the basolateral amygdala in rat. J Comp Neurol. 2006;498:690-711 pubmed
  243. Kiyokage E, Toida K, Suzuki Yamamoto T, Ishimura K. Localization of 5alpha-reductase in the rat main olfactory bulb. J Comp Neurol. 2005;493:381-95 pubmed