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Summary Expression Phenotypes Gene Literature (89) GO Terms (6) Nucleotides (391) Proteins (60) Interactants (350) Wiki

Papers associated with gjb2

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2 paper(s) referencing morpholinos

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Understanding the Role of ATP Release through Connexins Hemichannels during Neurulation., Tovar LM, Burgos CF, Yévenes GE, Moraga-Cid G, Fuentealba J, Coddou C, Bascunan-Godoy L, Catrupay C, Torres A, Castro PA., Int J Mol Sci. January 21, 2023; 24 (3):                     

Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevis., Pizzo L, Lasser M, Yusuff T, Jensen M, Ingraham P, Huber E, Singh MD, Monahan C, Iyer J, Desai I, Karthikeyan S, Gould DJ, Yennawar S, Weiner AT, Pounraja VK, Krishnan A, Rolls MM, Lowery LA, Girirajan S., PLoS Genet. April 5, 2021; 17 (4): e1009112.                    

A novel voltage-clamp/dye uptake assay reveals saturable transport of molecules through CALHM1 and connexin channels., Gaete PS, Lillo MA, López W, Liu Y, Jiang W, Luo Y, Harris AL, Contreras JE., J Gen Physiol. November 2, 2020; 152 (11):                   

Structural determinants underlying permeant discrimination of the Cx43 hemichannel., Nielsen BS, Zonta F, Farkas T, Litman T, Nielsen MS, MacAulay N., J Biol Chem. November 8, 2019; 294 (45): 16789-16803.              

Microarray-based screening system identifies temperature-controlled activity of Connexin 26 that is distorted by mutations., Wang H, Stahl F, Scheper T, Steffens M, Warnecke A, Zeilinger C., Sci Rep. September 19, 2019; 9 (1): 13543.

The connexin26 human mutation N14K disrupts cytosolic intersubunit interactions and promotes channel opening., Valdez Capuccino JM, Chatterjee P, García IE, Botello-Smith WM, Zhang H, Harris AL, Luo Y, Contreras JE., J Gen Physiol. March 4, 2019; 151 (3): 328-341.                  

A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma., Youssefian L, Vahidnezhad H, Saeidian AH, Mahmoudi H, Karamzadeh R, Kariminejad A, Huang J, Li L, Jannace TF, Fortina P, Zeinali S, White TW, Uitto J., Hum Mutat. February 1, 2019; 40 (2): 217-229.

Pathogenic FAM83G palmoplantar keratoderma mutations inhibit the PAWS1:CK1α association and attenuate Wnt signalling., Wu KZL, Jones RA, Tachie-Menson T, Macartney TJ, Wood NT, Varghese J, Gourlay R, Soares RF, Smith JC, Sapkota GP., Wellcome Open Res. January 1, 2019; 4 133.          

Concatenation of Human Connexin26 (hCx26) and Human Connexin46 (hCx46) for the Analysis of Heteromeric Gap Junction Hemichannels and Heterotypic Gap Junction Channels., Schadzek P, Hermes D, Stahl Y, Dilger N, Ngezahayo A., Int J Mol Sci. September 13, 2018; 19 (9):             

The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels., García IE, Villanelo F, Contreras GF, Pupo A, Pinto BI, Contreras JE, Pérez-Acle T, Alvarez O, Latorre R, Martínez AD, González C., J Gen Physiol. May 7, 2018; 150 (5): 697-711.                          

Charged Residues at the First Transmembrane Region Contribute to the Voltage Dependence of the Slow Gate of Connexins., Pinto BI, García IE, Pupo A, Retamal MA, Martínez AD, Latorre R, González C., J Biol Chem. July 22, 2016; 291 (30): 15740-52.

Syndromic deafness mutations at Asn 14 differentially alter the open stability of Cx26 hemichannels., Sanchez HA, Slavi N, Srinivas M, Verselis VK., J Gen Physiol. July 1, 2016; 148 (1): 25-42.                      

Gap-junctional channel and hemichannel activity of two recently identified connexin 26 mutants associated with deafness., Dalamon V, Fiori MC, Figueroa VA, Oliva CA, Del Rio R, Gonzalez W, Canan J, Elgoyhen AB, Altenberg GA, Retamal MA., Pflugers Arch. May 1, 2016; 468 (5): 909-18.

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D, Powers TR, van Velkinburgh JC, Trujillo-Provencio C, Schilkey F, Serrano EE., BMC Res Notes. November 18, 2015; 8 691.      

Glutathione release through connexin hemichannels: Implications for chemical modification of pores permeable to large molecules., Tong X, Lopez W, Ramachandran J, Ayad WA, Liu Y, Lopez-Rodriguez A, Harris AL, Contreras JE., J Gen Physiol. September 1, 2015; 146 (3): 245-54.            

Monitoring channel activities of proteoliposomes with SecA and Cx26 gap junction in single oocytes., Hsieh YH, Zou J, Jin JS, Yang H, Chen Y, Chen Y, Jiang C, Yang J, Tai PC., Anal Biochem. July 1, 2015; 480 58-66.

Cell communication across gap junctions: a historical perspective and current developments., Evans WH., Biochem Soc Trans. June 1, 2015; 43 (3): 450-9.

Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine., Levit NA, Sellitto C, Wang HZ, Li L, Srinivas M, Brink PR, White TW., J Invest Dermatol. April 1, 2015; 135 (4): 1033-1042.        

Long-range gap junctional signaling controls oncogene-mediated tumorigenesis in Xenopus laevis embryos., Chernet BT, Fields C, Levin M., Front Physiol. January 19, 2015; 5 519.                

The comprehensive analysis of DEG/ENaC subunits in Hydra reveals a large variety of peptide-gated channels, potentially involved in neuromuscular transmission., Assmann M, Kuhn A, Dürrnagel S, Holstein TW, Gründer S., BMC Biol. October 14, 2014; 12 84.                      

Activation, permeability, and inhibition of astrocytic and neuronal large pore (hemi)channels., Hansen DB, Ye ZC, Calloe K, Braunstein TH, Hofgaard JP, Ransom BR, Nielsen MS, MacAulay N., J Biol Chem. September 19, 2014; 289 (38): 26058-26073.

Altered inhibition of Cx26 hemichannels by pH and Zn2+ in the A40V mutation associated with keratitis-ichthyosis-deafness syndrome., Sanchez HA, Bienkowski R, Slavi N, Srinivas M, Verselis VK., J Biol Chem. August 1, 2014; 289 (31): 21519-32.

Extracellular gentamicin reduces the activity of connexin hemichannels and interferes with purinergic Ca(2+) signaling in HeLa cells., Figueroa VA, Retamal MA, Cea LA, Salas JD, Vargas AA, Verdugo CA, Jara O, Martínez AD, Sáez JC., Front Cell Neurosci. May 27, 2014; 8 265.                  

The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions., Sanchez HA, Villone K, Srinivas M, Verselis VK., J Gen Physiol. July 1, 2013; 142 (1): 3-22.                      

The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity., Mhaske PV, Levit NA, Li L, Wang HZ, Lee JR, Shuja Z, Brink PR, White TW., Am J Physiol Cell Physiol. June 15, 2013; 304 (12): C1150-8.

Linoleic acid induces opening of connexin26 hemichannels through a PI3K/Akt/Ca(2+)-dependent pathway., Figueroa V, Sáez PJ, Salas JD, Salas D, Jara O, Martínez AD, Sáez JC, Retamal MA., Biochim Biophys Acta. March 1, 2013; 1828 (3): 1169-79.

Voltage-dependent gating of the Cx32*43E1 hemichannel: conformational changes at the channel entrances., Kwon T, Tang Q, Bargiello TA., J Gen Physiol. February 1, 2013; 141 (2): 243-59.                  

Analysis of trafficking, stability and function of human connexin 26 gap junction channels with deafness-causing mutations in the fourth transmembrane helix., Ambrosi C, Walker AE, Depriest AD, Cone AC, Lu C, Badger J, Skerrett IM, Sosinsky GE., PLoS One. January 1, 2013; 8 (8): e70916.                        

Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss., Hashemi SB, Ashraf MJ, Saboori M, Azarpira N, Darai M., Mol Biol Rep. December 1, 2012; 39 (12): 10481-7.

Resting potential, oncogene-induced tumorigenesis, and metastasis: the bioelectric basis of cancer in vivo., Lobikin M, Chernet B, Lobo D, Levin M., Phys Biol. December 1, 2012; 9 (6): 065002.

Voltage-dependent conformational changes in connexin channels., Bargiello TA, Tang Q, Oh S, Kwon T., Biochim Biophys Acta. August 1, 2012; 1818 (8): 1807-22.

Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome., Levit NA, Mese G, Basaly MG, White TW., Biochim Biophys Acta. August 1, 2012; 1818 (8): 2014-9.

Connexins in epidermal homeostasis and skin disease., Scott CA, Tattersall D, O'Toole EA, Kelsell DP., Biochim Biophys Acta. August 1, 2012; 1818 (8): 1952-61.        

Connexin26-mediated transfer of laterality cues in Xenopus., Beyer T, Thumberger T, Schweickert A, Blum M., Biol Open. May 15, 2012; 1 (5): 473-81.            

Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium., Rubinos C, Sánchez HA, Verselis VK, Srinivas M., J Gen Physiol. January 1, 2012; 139 (1): 69-82.                    

Molecular dynamics simulations of the Cx26 hemichannel: evaluation of structural models with Brownian dynamics., Kwon T, Harris AL, Rossi A, Bargiello TA., J Gen Physiol. November 1, 2011; 138 (5): 475-93.            

Inhibition of connexin 26 by the AMP-activated protein kinase., Alesutan I, Sopjani M, Munoz C, Fraser S, Kemp BE, Föller M, Lang F., J Membr Biol. April 1, 2011; 240 (3): 151-8.

Asymmetric configurations and N-terminal rearrangements in connexin26 gap junction channels., Oshima A, Tani K, Toloue MM, Hiroaki Y, Smock A, Inukai S, Cone A, Nicholson BJ, Sosinsky GE, Fujiyoshi Y., J Mol Biol. January 21, 2011; 405 (3): 724-35.

Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin., Tao L, DeRosa AM, White TW, Valdimarsson G., Dev Dyn. October 1, 2010; 239 (10): 2627-36.

Pannexin1 and Pannexin2 channels show quaternary similarities to connexons and different oligomerization numbers from each other., Ambrosi C, Gassmann O, Pranskevich JN, Boassa D, Smock A, Wang J, Dahl G, Steinem C, Sosinsky GE., J Biol Chem. August 6, 2010; 285 (32): 24420-31.                    

Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome., Sánchez HA, Mese G, Srinivas M, White TW, Verselis VK., J Gen Physiol. July 1, 2010; 136 (1): 47-62.                  

Analysis of four connexin26 mutant gap junctions and hemichannels reveals variations in hexamer stability., Ambrosi C, Boassa D, Pranskevich J, Smock A, Oshima A, Xu J, Nicholson BJ, Sosinsky GE., Biophys J. May 19, 2010; 98 (9): 1809-19.

GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf., Tekin M, Xia XJ, Erdenetungalag R, Cengiz FB, White TW, Radnaabazar J, Dangaasuren B, Tastan H, Nance WE, Pandya A., Ann Hum Genet. March 1, 2010; 74 (2): 155-64.

Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss., Mohamed MR, Alesutan I, Föller M, Sopjani M, Bress A, Baur M, Salama RH, Bakr MS, Mohamed MA, Blin N, Lang F, Pfister M., Cell Physiol Biochem. January 1, 2010; 26 (6): 959-66.

Connexin mutations causing skin disease and deafness increase hemichannel activity and cell death when expressed in Xenopus oocytes., Lee JR, Lee JR, Derosa AM, White TW., J Invest Dermatol. April 1, 2009; 129 (4): 870-8.

Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness., Gerido DA, DeRosa AM, Richard G, White TW., Am J Physiol Cell Physiol. July 1, 2007; 293 (1): C337-45.

Deficient membrane integration of the novel p.N14D-GJB2 mutant associated with non-syndromic hearing impairment., Haack B, Schmalisch K, Palmada M, Böhmer C, Kohlschmidt N, Keilmann A, Zechner U, Limberger A, Beckert S, Zenner HP, Lang F, Kupka S., Hum Mutat. November 1, 2006; 27 (11): 1158-9.

Species specificity of mammalian connexin-26 to form open voltage-gated hemichannels., González D, Gómez-Hernández JM, Barrio LC., FASEB J. November 1, 2006; 20 (13): 2329-38.

Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis., de Boer TP, Kok B, Roël G, van Veen TA, Destrée OH, Rook MB, Vos MA, de Bakker JM, van der Heyden MA., Biochem Biophys Res Commun. October 20, 2006; 349 (2): 855-62.                  

Mutations of connexin 26 at position 75 and dominant deafness: essential role of arginine for the generation of functional gap-junctional channels., Deng Y, Chen Y, Reuss L, Altenberg GA., Hear Res. October 1, 2006; 220 (1-2): 87-94.

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