This is a Validated Antibody Database (VAD) review about human GJB1, based on 51 published articles (read how Labome selects the articles), using GJB1 antibody in all methods. It is aimed to help Labome visitors find the most suited GJB1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
GJB1 synonym: CMTX; CMTX1; CX32; gap junction beta-1 protein; GAP junction 28 kDa liver protein; connexin-32; gap junction protein, beta 1, 32kDa

Knockout validation
Invitrogen
mouse monoclonal (CX-2C2)
  • immunocytochemistry knockout validation; mouse; 1.0 ug/ml; fig 4
  • western blot knockout validation; mouse; 1:250; fig 2, 3
In order to discuss the limitations of using antibodies to study connexin 32 expression in the central nervous system, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in immunocytochemistry knockout validation on mouse samples at 1.0 ug/ml (fig 4) and in western blot knockout validation on mouse samples at 1:250 (fig 2, 3). Cell Commun Adhes (2009) ncbi
Invitrogen
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; loading ...; fig 7
In order to examine the effect of different substrates on the self-assembly of liver organoids, Invitrogen GJB1 antibody (Invitrogen, 13-8200) was used in immunocytochemistry on human samples (fig 7). PLoS ONE (2017) ncbi
rabbit polyclonal
  • western blot; mouse; 1:1000; fig 4c
In order to assess the contributions of Sig-1Rs and connexin 43 to the induction of central neuropathic pain during spinal cord injury, Invitrogen GJB1 antibody (Invitrogen, 71-0600) was used in western blot on mouse samples at 1:1000 (fig 4c). Neuropharmacology (2016) ncbi
rabbit polyclonal
  • immunohistochemistry; mouse; loading ...; fig 6c
In order to investigate how prostaglandin E2 regulates breathing in young mice, Invitrogen GJB1 antibody (Invitrogen, 71-0600) was used in immunohistochemistry on mouse samples (fig 6c). elife (2016) ncbi
mouse monoclonal (CX-2C2)
  • western blot; mouse; 1:500; fig 2
In order to study differential expression of astrocytic connexins by a prenatal alcohol exposure mouse model, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in western blot on mouse samples at 1:500 (fig 2). Neurobiol Dis (2016) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; fig 4
  • western blot; human; fig 4
In order to characterize the differential modulation of connexin expression and function in human capillary endothelial cells in regards to primary tumor- and metastasis-derived colon cancer cells, Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in immunocytochemistry on human samples (fig 4) and in western blot on human samples (fig 4). Oncotarget (2015) ncbi
mouse monoclonal (CX-2C2)
  • western blot; human; 0.5 ug/ml
In order to determine the role of growth media composition on classic EMT responses using HK-2 cells, Invitrogen GJB1 antibody (Life Technologies, CX-2C2) was used in western blot on human samples at 0.5 ug/ml. PLoS ONE (2015) ncbi
mouse monoclonal (CX-2C2)
  • blocking or activating experiments; human
Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in blocking or activating experiments on human samples . Atherosclerosis (2014) ncbi
mouse monoclonal (CX-2C2)
  • western blot; sheep
In order to study the effect of maternal glucocorticoid treatment on gap junction protein expression in the ovine fetal brain, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in western blot on sheep samples . Neuroscience (2014) ncbi
rabbit polyclonal
  • immunocytochemistry; mouse
  • immunocytochemistry; rat
In order to characterize connexins associated with motoneurons in rodent spinal cord, sexually dimorphic motor nuclei and trigeminal motor nucleus, Invitrogen GJB1 antibody (Life Technologies, 34-5700) was used in immunocytochemistry on mouse samples and in immunocytochemistry on rat samples . Eur J Neurosci (2014) ncbi
mouse monoclonal (CX-2C2)
  • western blot; human; 1:500
In order to investigate the expression of connexin 43 in eutopic endometrium and cultured endometrial stromal cells, Invitrogen GJB1 antibody (Life Technologies, 13-8200) was used in western blot on human samples at 1:500. Mol Hum Reprod (2014) ncbi
mouse monoclonal (CX-2C2)
  • western blot; mouse; 1:500; fig 1
In order to investigate the effects of antioxidants on Nf1 loss or HRas hyper activation in mouse oligodendrocytes, Invitrogen GJB1 antibody (Invitrogen, 138200) was used in western blot on mouse samples at 1:500 (fig 1). Cell Rep (2013) ncbi
mouse monoclonal (CX-2C2)
  • western blot; mouse; fig s1
In order to isolate and characterize connexin32-enriched membrane microdomains from murine liver, Invitrogen GJB1 antibody (Zymed, Invitrogen, 13-8200) was used in western blot on mouse samples (fig s1). J Proteome Res (2013) ncbi
rabbit polyclonal
  • immunohistochemistry - frozen section; mouse
In order to investigate the role of Cx37 during vasculogenesis in mice, Invitrogen GJB1 antibody (Invitrogen, 71-0600) was used in immunohistochemistry - frozen section on mouse samples . Dev Biol (2013) ncbi
rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 3 ug/ml
In order to study localization of connexins in the brain, Invitrogen GJB1 antibody (Invitrogen, 34-5700) was used in immunohistochemistry - frozen section on mouse samples at 3 ug/ml. Eur J Neurosci (2011) ncbi
mouse monoclonal (CX-2C2)
  • western blot; mouse; 1:500; fig 4
In order to study connexin 26 and connexin 32 isoforms in the cochlea, Invitrogen GJB1 antibody (Zymed, CX-2C2) was used in western blot on mouse samples at 1:500 (fig 4). Eur J Cell Biol (2011) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; rat; 1:100; fig 3
In order to study connexin-32 localization in fetal rat hepatocytes, Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in immunocytochemistry on rat samples at 1:100 (fig 3). Acta Histochem (2012) ncbi
rabbit polyclonal
  • immunohistochemistry; rat; fig 2
In order to compare the growth patterns of normal and nodular hepatocytes in a transplantation system, Invitrogen GJB1 antibody (Zymed Labs, 34-5700) was used in immunohistochemistry on rat samples (fig 2). Histochem Cell Biol (2011) ncbi
rabbit polyclonal
  • western blot; human; fig 6
In order to discuss the use and limitations of a mesothelin-specific antibody fused to a bacterial toxin to treat mesothelioma, Invitrogen GJB1 antibody (Invitrogen, 71-0600) was used in western blot on human samples (fig 6). PLoS ONE (2011) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; 1:100; fig 3
In order to determine the connexin composition of intracellular channels present in astrocytes and oligodendrocytes, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in immunocytochemistry on human samples at 1:100 (fig 3). Glia (2011) ncbi
rabbit polyclonal
  • immunocytochemistry; human; 1:100; fig 3
In order to determine the connexin composition of intracellular channels present in astrocytes and oligodendrocytes, Invitrogen GJB1 antibody (Zymed, 34-5700) was used in immunocytochemistry on human samples at 1:100 (fig 3). Glia (2011) ncbi
rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:250; fig 4
In order to report that beta-cateninregulates the zone-specificity of a hepatocyte's gene expression profile, Invitrogen GJB1 antibody (Invitrogen, 34-5700) was used in immunohistochemistry - paraffin section on mouse samples at 1:250 (fig 4). Histochem Cell Biol (2010) ncbi
mouse monoclonal (CX-2C2)
  • immunohistochemistry - frozen section; human; 1:200; fig 1
In order to test if Cx32-induced metastasis involves cancer stem cells, Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in immunohistochemistry - frozen section on human samples at 1:200 (fig 1). Int J Cancer (2011) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry knockout validation; mouse; 1.0 ug/ml; fig 4
  • western blot knockout validation; mouse; 1:250; fig 2, 3
In order to discuss the limitations of using antibodies to study connexin 32 expression in the central nervous system, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in immunocytochemistry knockout validation on mouse samples at 1.0 ug/ml (fig 4) and in western blot knockout validation on mouse samples at 1:250 (fig 2, 3). Cell Commun Adhes (2009) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; 1:500
In order to investigate connexin32 in endothelial cells, Invitrogen GJB1 antibody (Zymed, CX-2C2) was used in immunocytochemistry on human samples at 1:500. Biochem Biophys Res Commun (2009) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; fig 4
  • western blot; human; fig 3a
In order to examine calcium wave propagation and connexin 26, 32 and 43 expression in normal and malignant urothelial cells, Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in immunocytochemistry on human samples (fig 4) and in western blot on human samples (fig 3a). Cell Commun Adhes (2007) ncbi
rabbit polyclonal
In order to determine the abundance and connexin composition of neuronal and glial gap junctions in developing and adult rat and mouse locus coeruleus, Invitrogen GJB1 antibody (Invitrogen/Zymed, 34-5700) was used . Neuroscience (2007) ncbi
rabbit polyclonal
In order to determine the abundance and connexin composition of neuronal and glial gap junctions in developing and adult rat and mouse locus coeruleus, Invitrogen GJB1 antibody (Invitrogen/Zymed, 71-0600) was used . Neuroscience (2007) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; 1:500
  • immunohistochemistry; human; 1:200
In order to study the impact of connexin32 on hepatocellular carcinoma, Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in immunocytochemistry on human samples at 1:500 and in immunohistochemistry on human samples at 1:200. Int J Cancer (2007) ncbi
mouse monoclonal (CX-2C2)
  • western blot; human; 1:500; fig 6
In order to examine the biological responses imparted by Matrigel overlays on primary human hepatocyte cultures, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in western blot on human samples at 1:500 (fig 6). Toxicol Sci (2007) ncbi
mouse monoclonal (CX-2C2)
  • western blot; human; 1:500
In order to examine the contribution of connexin43 to gap junctional intercellular communication in various cell types, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in western blot on human samples at 1:500. Biotechnol J (2007) ncbi
rabbit polyclonal
In order to examine connexin expression in chromaffin cells of normal human adrenal glands and benign and malignant pheochromocytomas, Invitrogen GJB1 antibody (ZYMED, 71-0600) was used . Ann N Y Acad Sci (2006) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; dog
  • western blot; dog
In order to study ouabain-sensitive and -resistant MDCK cells, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in immunocytochemistry on dog samples and in western blot on dog samples . Proc Natl Acad Sci U S A (2006) ncbi
rabbit polyclonal
In order to examine Paneth and enterochromaffin cells in Min-mice, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . Anticancer Res (2006) ncbi
rabbit polyclonal
In order to identify residues that are critical for connexin functions, Invitrogen GJB1 antibody (Invitrogen/Zymed, 71-0600) was used . J Cell Sci (2006) ncbi
mouse monoclonal (CX-2C2)
  • immunohistochemistry - paraffin section; human; 1:500
In order to present the clinicopathological findings of patient with astroblastoma, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in immunohistochemistry - paraffin section on human samples at 1:500. Neuropathology (2006) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; 1:50; fig 2
In order to evaluate gap junction protein connexin 43 as a negative marker of the pluripotency of human limbal epithelial cells, Invitrogen GJB1 antibody (Invitrogen, CX-2C2) was used in immunocytochemistry on human samples at 1:50 (fig 2). Stem Cells (2006) ncbi
rabbit polyclonal
In order to study connexin-specific cell-to-cell transfer of short interfering RNA by gap junctions, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . J Physiol (2005) ncbi
rabbit polyclonal
In order to study rhesus monkey embryonic stem cells, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . Stem Cells (2005) ncbi
mouse monoclonal (CX-2C2)
  • immunohistochemistry - frozen section; rat; 1:100
In order to determine the spatio-temporal expression of gap junction connexins and correlate their expression with the progression of cell cycle control in regenerating soleus muscle of Wistar rats, Invitrogen GJB1 antibody (Zymed, CX-2C2) was used in immunohistochemistry - frozen section on rat samples at 1:100. Histochem Cell Biol (2005) ncbi
rabbit polyclonal
In order to investigate the role of connexin 43 in intestinal cancer, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . Eur J Cancer (2004) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; 1:500
  • western blot; human; 1:500; fig 5
In order to investigate the influence of estrogen and its receptor in connexin expression and gap junctional intercellular communication in endometrial carcinoma cells, Invitrogen GJB1 antibody (Zymed, CX-2C2) was used in immunocytochemistry on human samples at 1:500 and in western blot on human samples at 1:500 (fig 5). Oncogene (2004) ncbi
rabbit polyclonal
In order to examine the connexin associations at oligodendrocyte/astrocyte gap junctions on oligodendrocytes in normal and Cx32 knockout mice, Invitrogen GJB1 antibody (Zymed, 34?C5700) was used . Glia (2003) ncbi
mouse monoclonal (CX-2C2)
  • immunohistochemistry - frozen section; mouse; 1:500
  • immunohistochemistry; mouse
  • western blot; mouse
In order to examine the connexin associations at oligodendrocyte/astrocyte gap junctions on oligodendrocytes in normal and Cx32 knockout mice, Invitrogen GJB1 antibody (Zymed, 13?C8200) was used in immunohistochemistry - frozen section on mouse samples at 1:500, in immunohistochemistry on mouse samples and in western blot on mouse samples . Glia (2003) ncbi
rabbit polyclonal
In order to examine the connexin associations at oligodendrocyte/astrocyte gap junctions on oligodendrocytes in normal and Cx32 knockout mice, Invitrogen GJB1 antibody (Zymed, 71?C0600) was used . Glia (2003) ncbi
mouse monoclonal (CX-2C2)
  • immunocytochemistry; human; fig 4
In order to study connexins and gap junction proteins in endometrial carcinoma cells, Invitrogen GJB1 antibody (Zymed, CX-2C2) was used in immunocytochemistry on human samples (fig 4). Carcinogenesis (2003) ncbi
rabbit polyclonal
In order to elucidate the relationship between gap junctional intercellular communication and mammary cell differentiation, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . J Cell Sci (2003) ncbi
mouse monoclonal (CX-2C2)
  • immunohistochemistry; rat; 10 ug/ml
In order to study connexins in retinal glial cells, Invitrogen GJB1 antibody (Zymed, 13-8200) was used in immunohistochemistry on rat samples at 10 ug/ml. J Comp Neurol (2003) ncbi
rabbit polyclonal
In order to study connexins in retinal glial cells, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . J Comp Neurol (2003) ncbi
mouse monoclonal (CX-2C2)
  • immunohistochemistry - paraffin section; human; 1:250; fig 2
In order to determine the expression of connexin-43 and 32 in patients of epilepsy, Invitrogen GJB1 antibody (Zymed Laboratories, clone CX-2C2) was used in immunohistochemistry - paraffin section on human samples at 1:250 (fig 2). Acta Neuropathol (2001) ncbi
mouse monoclonal (CX-2C2)
  • western blot; human; fig 3
In order to study intercellular adherens junctions and gap junctions in human gingival fibroblasts, Invitrogen GJB1 antibody (Zymed, CX-2C2) was used in western blot on human samples (fig 3). Am J Physiol Cell Physiol (2000) ncbi
rabbit polyclonal
In order to investigate the intracellular transport, assembly, and degradation of three Charcot-Marie-Tooth disease-linked connexin32 mutants stably expressed in PC12 cells, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . Mol Biol Cell (2000) ncbi
rabbit polyclonal
In order to assess gap junction connectivity, Invitrogen GJB1 antibody (Zymed, 71-0600) was used . Neuroendocrinology (1999) ncbi
Abcam
rabbit polyclonal
  • immunocytochemistry; human; 1:100
In order to test if altering the transcription programming in pancreatic ductal adenocarcinomas can revert these cancerous cells back to quiescent acinar cells, Abcam GJB1 antibody (Abcam, ab66613) was used in immunocytochemistry on human samples at 1:100. Pancreas (2015) ncbi
MilliporeSigma
rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:100; fig 7
In order to investigate breast tumorigenesis due to loss of Panx1 which impairs mammary gland development at lactation, MilliporeSigma GJB1 antibody (Sigma, C3470) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 7). PLoS ONE (2016) ncbi
rabbit polyclonal
  • immunohistochemistry; human; 1:30
In order to correlate connexin expression with tumor progression and prognosis in primary breast cancers, MilliporeSigma GJB1 antibody (Sigma-Aldrich, HPA010663) was used in immunohistochemistry on human samples at 1:30. PLoS ONE (2014) ncbi
rabbit polyclonal
  • western blot; mouse; fig 2
In order to determine if patients with loss-of-function Cx26 mutations have a greater susceptibility to impaired breast development, MilliporeSigma GJB1 antibody (Sigma-Aldrich, C3470) was used in western blot on mouse samples (fig 2). PLoS ONE (2014) ncbi
Articles Reviewed
  1. Mattei G, Magliaro C, Giusti S, Ramachandran S, Heinz S, Braspenning J, et al. On the adhesion-cohesion balance and oxygen consumption characteristics of liver organoids. PLoS ONE. 2017;12:e0173206 pubmed publisher
  2. Choi S, Roh D, Yoon S, Kwon S, Choi H, Han H, et al. Astrocyte sigma-1 receptors modulate connexin 43 expression leading to the induction of below-level mechanical allodynia in spinal cord injured mice. Neuropharmacology. 2016;111:34-46 pubmed publisher
  3. Forsberg D, Horn Z, Tserga E, Smedler E, Silberberg G, Shvarev Y, et al. CO2-evoked release of PGE2 modulates sighs and inspiration as demonstrated in brainstem organotypic culture. elife. 2016;5: pubmed publisher
  4. Stewart M, Plante I, Penuela S, Laird D. Loss of Panx1 Impairs Mammary Gland Development at Lactation: Implications for Breast Tumorigenesis. PLoS ONE. 2016;11:e0154162 pubmed publisher
  5. Ramani M, Mylvaganam S, Krawczyk M, Wang L, Zoidl C, Brien J, et al. Differential expression of astrocytic connexins in a mouse model of prenatal alcohol exposure. Neurobiol Dis. 2016;91:83-93 pubmed publisher
  6. Thuringer D, Berthenet K, Cronier L, Solary E, Garrido C. Primary tumor- and metastasis-derived colon cancer cells differently modulate connexin expression and function in human capillary endothelial cells. Oncotarget. 2015;6:28800-15 pubmed publisher
  7. Kim S, Lahmy R, Riha C, Yang C, Jakubison B, van Niekerk J, et al. The basic helix-loop-helix transcription factor E47 reprograms human pancreatic cancer cells to a quiescent acinar state with reduced tumorigenic potential. Pancreas. 2015;44:718-27 pubmed publisher
  8. Slusser A, Bathula C, Sens D, Somji S, Sens M, Zhou X, et al. Cadherin expression, vectorial active transport, and metallothionein isoform 3 mediated EMT/MET responses in cultured primary and immortalized human proximal tubule cells. PLoS ONE. 2015;10:e0120132 pubmed publisher
  9. Teleki I, Szasz A, Maros M, Gyorffy B, Kulka J, Meggyeshazi N, et al. Correlations of differentially expressed gap junction connexins Cx26, Cx30, Cx32, Cx43 and Cx46 with breast cancer progression and prognosis. PLoS ONE. 2014;9:e112541 pubmed publisher
  10. Okamoto T, Akita N, Hayashi T, Shimaoka M, Suzuki K. Endothelial connexin 32 regulates tissue factor expression induced by inflammatory stimulation and direct cell-cell interaction with activated cells. Atherosclerosis. 2014;236:430-7 pubmed publisher
  11. Stewart M, Plante I, Bechberger J, Naus C, Laird D. Mammary gland specific knockdown of the physiological surge in Cx26 during lactation retains normal mammary gland development and function. PLoS ONE. 2014;9:e101546 pubmed publisher
  12. Sadowska G, Stonestreet B. Maternal treatment with glucocorticoids modulates gap junction protein expression in the ovine fetal brain. Neuroscience. 2014;275:248-58 pubmed publisher
  13. Bautista W, Rash J, Vanderpool K, Yasumura T, Nagy J. Re-evaluation of connexins associated with motoneurons in rodent spinal cord, sexually dimorphic motor nuclei and trigeminal motor nucleus. Eur J Neurosci. 2014;39:757-70 pubmed publisher
  14. Yu J, Boicea A, Barrett K, James C, Bagchi I, Bagchi M, et al. Reduced connexin 43 in eutopic endometrium and cultured endometrial stromal cells from subjects with endometriosis. Mol Hum Reprod. 2014;20:260-70 pubmed publisher
  15. Mayes D, Rizvi T, Titus Mitchell H, Oberst R, Ciraolo G, Vorhees C, et al. Nf1 loss and Ras hyperactivation in oligodendrocytes induce NOS-driven defects in myelin and vasculature. Cell Rep. 2013;4:1197-212 pubmed publisher
  16. Fowler S, Akins M, Zhou H, Figeys D, Bennett S. The liver connexin32 interactome is a novel plasma membrane-mitochondrial signaling nexus. J Proteome Res. 2013;12:2597-610 pubmed publisher
  17. Munger S, Kanady J, Simon A. Absence of venous valves in mice lacking Connexin37. Dev Biol. 2013;373:338-48 pubmed publisher
  18. Lynn B, Tress O, May D, Willecke K, Nagy J. Ablation of connexin30 in transgenic mice alters expression patterns of connexin26 and connexin32 in glial cells and leptomeninges. Eur J Neurosci. 2011;34:1783-93 pubmed publisher
  19. Degen J, Schütz M, Dicke N, Strenzke N, Jokwitz M, Moser T, et al. Connexin32 can restore hearing in connexin26 deficient mice. Eur J Cell Biol. 2011;90:817-24 pubmed publisher
  20. Takeuchi A, Fukazawa S, Chida K, Taguchi M, Shirataka M, Ikeda N. Semi-automatic counting of connexin 32s immunolocalized in cultured fetal rat hepatocytes using image processing. Acta Histochem. 2012;114:318-26 pubmed publisher
  21. Doratiotto S, Krause P, Serra M, Marongiu F, Sini M, Koenig S, et al. The growth pattern of transplanted normal and nodular hepatocytes. Histochem Cell Biol. 2011;135:581-91 pubmed publisher
  22. Xiang X, Phung Y, Feng M, Nagashima K, Zhang J, Broaddus V, et al. The development and characterization of a human mesothelioma in vitro 3D model to investigate immunotoxin therapy. PLoS ONE. 2011;6:e14640 pubmed publisher
  23. Magnotti L, Goodenough D, Paul D. Functional heterotypic interactions between astrocyte and oligodendrocyte connexins. Glia. 2011;59:26-34 pubmed publisher
  24. Braeuning A, Singh Y, Rignall B, Buchmann A, Hammad S, Othman A, et al. Phenotype and growth behavior of residual ?-catenin-positive hepatocytes in livers of ?-catenin-deficient mice. Histochem Cell Biol. 2010;134:469-81 pubmed publisher
  25. Kawasaki Y, Omori Y, Li Q, Nishikawa Y, Yoshioka T, Yoshida M, et al. Cytoplasmic accumulation of connexin32 expands cancer stem cell population in human HuH7 hepatoma cells by enhancing its self-renewal. Int J Cancer. 2011;128:51-62 pubmed publisher
  26. Fowler S, McLean A, Bennett S. Tissue-specific cross-reactivity of connexin32 antibodies: problems and solutions unique to the central nervous system. Cell Commun Adhes. 2009;16:117-30 pubmed publisher
  27. Okamoto T, Akiyama M, Takeda M, Gabazza E, Hayashi T, Suzuki K. Connexin32 is expressed in vascular endothelial cells and participates in gap-junction intercellular communication. Biochem Biophys Res Commun. 2009;382:264-8 pubmed publisher
  28. Leinonen P, Aaltonen V, Koskela S, Lehenkari P, Korkiamäki T, Peltonen J. Impaired gap junction formation and intercellular calcium signaling in urinary bladder cancer cells can be improved by Gö6976. Cell Commun Adhes. 2007;14:125-36 pubmed
  29. Rash J, Olson C, Davidson K, Yasumura T, Kamasawa N, Nagy J. Identification of connexin36 in gap junctions between neurons in rodent locus coeruleus. Neuroscience. 2007;147:938-56 pubmed
  30. Li Q, Omori Y, Nishikawa Y, Yoshioka T, Yamamoto Y, Enomoto K. Cytoplasmic accumulation of connexin32 protein enhances motility and metastatic ability of human hepatoma cells in vitro and in vivo. Int J Cancer. 2007;121:536-46 pubmed
  31. Page J, Johnson M, Olsavsky K, Strom S, Zarbl H, Omiecinski C. Gene expression profiling of extracellular matrix as an effector of human hepatocyte phenotype in primary cell culture. Toxicol Sci. 2007;97:384-97 pubmed
  32. Abbaci M, Barberi Heyob M, Stines J, Blondel W, Dumas D, Guillemin F, et al. Gap junctional intercellular communication capacity by gap-FRAP technique: a comparative study. Biotechnol J. 2007;2:50-61 pubmed
  33. Willenberg H, Schott M, Saeger W, Tries A, Scherbaum W, Bornstein S. Expression of connexins in chromaffin cells of normal human adrenals and in benign and malignant pheochromocytomas. Ann N Y Acad Sci. 2006;1073:578-83 pubmed
  34. Larre I, Ponce A, Fiorentino R, Shoshani L, Contreras R, Cereijido M. Contacts and cooperation between cells depend on the hormone ouabain. Proc Natl Acad Sci U S A. 2006;103:10911-6 pubmed
  35. Husøy T, Knutsen H, Løberg E, Alexander J. Intestinal adenomas of Min-mice lack enterochromaffin cells, and have increased lysozyme production in non-Paneth cells. Anticancer Res. 2006;26:1797-802 pubmed
  36. Gemel J, Lin X, Veenstra R, Beyer E. N-terminal residues in Cx43 and Cx40 determine physiological properties of gap junction channels, but do not influence heteromeric assembly with each other or with Cx26. J Cell Sci. 2006;119:2258-68 pubmed
  37. Kubota T, Sato K, Arishima H, Takeuchi H, Kitai R, Nakagawa T. Astroblastoma: immunohistochemical and ultrastructural study of distinctive epithelial and probable tanycytic differentiation. Neuropathology. 2006;26:72-81 pubmed
  38. Chen Z, Evans W, Pflugfelder S, Li D. Gap junction protein connexin 43 serves as a negative marker for a stem cell-containing population of human limbal epithelial cells. Stem Cells. 2006;24:1265-73 pubmed
  39. Valiunas V, Polosina Y, Miller H, Potapova I, Valiuniene L, Doronin S, et al. Connexin-specific cell-to-cell transfer of short interfering RNA by gap junctions. J Physiol. 2005;568:459-68 pubmed
  40. Behr R, Heneweer C, Viebahn C, Denker H, Thie M. Epithelial-mesenchymal transition in colonies of rhesus monkey embryonic stem cells: a model for processes involved in gastrulation. Stem Cells. 2005;23:805-16 pubmed
  41. Gorbe A, Becker D, Dux L, Stelkovics E, Krenacs L, Bagdi E, et al. Transient upregulation of connexin43 gap junctions and synchronized cell cycle control precede myoblast fusion in regenerating skeletal muscle in vivo. Histochem Cell Biol. 2005;123:573-83 pubmed
  42. Husøy T, Ølstørn H, Knutsen H, Løberg E, Cruciani V, Mikalsen S, et al. Truncated mouse adenomatous polyposis coli reduces connexin32 content and increases matrilysin secretion from Paneth cells. Eur J Cancer. 2004;40:1599-603 pubmed
  43. Saito T, Tanaka R, Wataba K, Kudo R, Yamasaki H. Overexpression of estrogen receptor-alpha gene suppresses gap junctional intercellular communication in endometrial carcinoma cells. Oncogene. 2004;23:1109-16 pubmed
  44. Nagy J, Ionescu A, Lynn B, Rash J. Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice. Glia. 2003;44:205-18 pubmed
  45. Nishimura M, Saito T, Yamasaki H, Kudo R. Suppression of gap junctional intercellular communication via 5' CpG island methylation in promoter region of E-cadherin gene in endometrial cancer cells. Carcinogenesis. 2003;24:1615-23 pubmed
  46. El Sabban M, Sfeir A, Daher M, Kalaany N, Bassam R, Talhouk R. ECM-induced gap junctional communication enhances mammary epithelial cell differentiation. J Cell Sci. 2003;116:3531-41 pubmed
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  48. Aronica E, Gorter J, Jansen G, Leenstra S, Yankaya B, Troost D. Expression of connexin 43 and connexin 32 gap-junction proteins in epilepsy-associated brain tumors and in the perilesional epileptic cortex. Acta Neuropathol. 2001;101:449-59 pubmed
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