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Nature, ISSN 0028-0836, 04/2009, Volume 458, Issue 7238, pp. 597 - 602
Journal Article
The Journal of Physiology, ISSN 0022-3751, 10/2010, Volume 588, Issue 20, pp. 3921 - 3931
Journal Article
Connexin 26 and autosomal recessive non-syndromic hearing loss, 07/2003
Prelingual deafness occurs with a frequency of 1 in 1000 live births and is divided into syndromic and non-syndromic forms contributing 40 and 60%... 
hg03010 Non-syndromic, Hearing loss, Autosomal recessive, Connexin 26, DFNB1, mutation detection, Gap junction proteins, GJB2 | Genetics
Journal
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 13975 - 11
Connexins are a family of membrane-spanning proteins named according to their molecular weight. They are known to form membrane channels mediating cell-cell... 
HEART | CELLS | H9C2 | CX26 | MULTIDISCIPLINARY SCIENCES | DISEASE | GENES | Heart | Deafness | Intercellular signalling | Phenotypes | Cardiomyocytes | Cell interactions | Membrane channels | Molecular weight | Connexin 26 | Skin diseases | Connexins | Localization | Cytoplasm
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2012, Volume 287, Issue 48, pp. 40826 - 40834
Journal Article
International journal of oncology, ISSN 1019-6439, 09/2019, Volume 55, Issue 4, pp. 845 - 859
Reports have highlighted an association between connexins (CXs) or gap junction proteins and non‑small cell lung cancer (NSCLC). In the present study, it was... 
non-small cell lung cancer | pulmonary epithelial cells | PROTEIN | proliferation | CX26 | connexin 26 | SENSITIVITY | TIME | CX43 | P53 | ONCOLOGY | murine double minute-2 signaling pathway | migration | GENE-EXPRESSION | DEGRADATION | epithelial-mesenchymal transition | connexin 43
Journal Article
Human Genetics, ISSN 0340-6717, 10/2002, Volume 111, Issue 4, pp. 394 - 397
Mutations in GJB2, encoding gap junction beta 2 protein (connexin 26), are responsible for the commonest form of non-syndromic recessive deafness in many... 
NONSYNDROMIC HEARING-LOSS | CHILDHOOD DEAFNESS | FREQUENCY | GENETICS & HEREDITY | JAPANESE | GENE GJB2 | RECESSIVE DEAFNESS | IMPAIRMENT | Connexin 26 | Deafness - genetics | China | Humans | Alleles | Connexins - genetics | Deafness - ethnology | Female | Genotype | Male | Mutation
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 05/2014, Volume 448, Issue 1, pp. 28 - 32
Journal Article
Nature, ISSN 0028-0836, 05/1998, Volume 393, Issue 6683, pp. 319 - 320
A high proportion of all cases of congenital deafness is causedby mutations in a gene coding for a gap-junction protein,connexin 26. The deafness associated... 
MULTIDISCIPLINARY SCIENCES | Connexin 26 | Deafness - genetics | Genes, Dominant | DNA Mutational Analysis | Humans | Chromosomes, Human, Pair 13 | Connexins - genetics | Cysteine - chemistry | Mutation | Connexins - chemistry | Polymorphism, Genetic | Hearing | Genetic aspects | Research | Human genetics
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 01/2000, Volume 37, Issue 1, pp. 41 - 43
Journal Article