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International Journal of Molecular Sciences, ISSN 1661-6596, 09/2018, Volume 19, Issue 9, p. 2535
GJB2 mutations are the leading cause of non-syndromic inherited hearing loss. GJB2 encodes connexin-26 (CX26), which is a connexin (CX) family protein... 
Connexin 26 | GJB2 gene | TJP1 | Connexin | Deafness | DAAM1 | Protein-protein interaction | Organ of corti | FLNB | CGN | MOUSE-BRAIN | PDZ DOMAIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | connexin 26 | CARDIAC MYOCYTES | CHEMISTRY, MULTIDISCIPLINARY | DIRECTLY BINDS | GAP-JUNCTIONS | ZO-1 | INTERACTS | TIGHT-JUNCTION | protein-protein interaction | deafness | connexin | F-BOX PROTEIN | organ of Corti | ZONULA OCCLUDENS-1 | Zonula Occludens-1 Protein - genetics | Amino Acid Sequence | Mice, Inbred C57BL | Intercellular Junctions - metabolism | Connexins - genetics | Argininosuccinate Synthase - metabolism | Connexins - metabolism | Protein Interaction Maps | Sequence Homology, Amino Acid | Animals | Argininosuccinate Synthase - genetics | Connexin 26 - genetics | Cytoskeleton - metabolism | Protein Binding | Mice, Inbred BALB C | Connexin 26 - metabolism | Zonula Occludens-1 Protein - metabolism | Organ of Corti - metabolism | Brain | Immunoprecipitation | Organ of Corti | Membrane junctions | Liver | Cell junctions | Mass spectroscopy | Connexin 43 | C-Terminus | Precipitates | Membrane proteins | Hearing loss | Proteins | Cochlea | Glyceraldehyde-3-phosphate dehydrogenase | Cytoskeleton | Skin | Mutation | Mass spectrometry | Candidates | Peptides | Amino acids | Biology | Genomes | Data bases | Genetics | Bioinformatics | Informatics | Hearing impairment | Gene expression | Scientific imaging
Journal Article
01/2010
Background : The common GJB2 gene mutation (35delG) has been previously reported from Iranian patients that were affected with nonsyndromic autosomal recessive... 
Connexin 26 | GJB2 | Iranian Arabs | nonsyndromic autosomal recessive deafness
Web Resource
Journal Article
International Journal of Audiology, ISSN 1499-2027, 06/2012, Volume 51, Issue 6, pp. 433 - 436
Journal Article
FASEB Journal, ISSN 0892-6638, 11/2006, Volume 20, Issue 13, pp. 2329 - 2338
Mutations of connexin-26 (Cx26) cause nonsyndromic hearing loss and other syndromes affecting ectoderm-derived tissues. While the exact mechanisms underlying... 
Deafness | Genodermatosis | GJB2 | Hearing | Skin | INNER-EAR | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | skin | GAP-JUNCTION HEMICHANNELS | PLASMA-MEMBRANE | CELL BIOLOGY | HELA-CELLS | BIOLOGY | hearing | XENOPUS-OOCYTES | genodermatosis | ATP RELEASE | deafness | SUPPORTING CELLS | EXPRESSION | Connexin 26 | Xenopus | Animals | Flow Cytometry | Oocytes - physiology | Species Specificity | Connexins - physiology | Humans | Rats | Female | Sheep | Ion Channels - physiology
Journal Article
Genetics in Medicine, ISSN 1098-3600, 2010, Volume 12, Issue 3, pp. 174 - 181
Journal Article
Journal of Molecular Liquids, ISSN 0167-7322, 02/2017, Volume 227, pp. 168 - 177
Approximately, two third cases of non-syndromic deafness are caused by mutation in ; which encodes a β-class gap-junction protein, connexin-26 (Cx26). Cx26 is... 
Nonsyndromic deafness | Deafness | Gap-junction | In-silico | Molecular dynamics simulation | Connexion | GAP-JUNCTION CHANNELS | MOLECULAR-DYNAMICS | PROTEIN | DOCKING | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | AUTOSOMAL RECESSIVE DEAFNESS | GJB2 | HEMICHANNELS | SELECTIVE PERMEABILITY | SYSTEMS | COMMUNICATION | Membrane lipids | Inositol | Genetic aspects | Hearing loss
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 04/2003, Volume 148, Issue 4, pp. 649 - 653
Journal Article
NEW ENGLAND JOURNAL OF MEDICINE, ISSN 0028-4793, 05/2006, Volume 354, Issue 20, pp. 2151 - 2164
Journal Article
Indian Journal of Human Genetics, ISSN 0971-6866, 01/2009, Volume 15, Issue 1, pp. 9 - 12
The common GJB2 gene mutation (35delG) has been previously reported from Iranian patients that were affected with nonsyndromic autosomal recessive deafness.... 
Connexin 26 | GJB2 | Iranian Arabs | Nonsyndromic autosomal recessive deafness | Deafness | Demographic aspects | Gene mutations | Physiological aspects | Genetic aspects | Research | Health aspects | Risk factors | Membrane proteins | Genetic research | Minority & ethnic groups | Mutation | nonsyndromic autosomal recessive deafness | Original
Journal Article