Mutations in the connexin 26 (Cx26) gene (GJB2) are associated with autosomal nonsyndromic sensorineural hearing loss. This study describes mutations in the Cx26 gene in cases of familial and sporadic ...
Fabio Anselmi, Victor H. Hernandez, Giulia Crispino, Anke Seydel, Saida Ortolano, Stephen D. Roper, Nicoletta Kessaris, William Richardson, Gesa Rickheit, Mikhail A. Filippov, Hannah Monyer, Fabio ...
The protein Connexin 26 has been previously identified as being directly sensitive to Carbon dioxide and linked to conditions such as KIDS syndrome and deafness. Thanks to a £686,956 grant from the ...
In a study of 530 individuals with non-syndromic, sensorineural hearing loss, we identified 18 mutations at connexin 26 (Cx26), four of which are novel (−23G>T, I33T, 377_383dupTCCGCAT, W172R) and the ...
People love to talk, and such chattiness may have catalyzed a divergence from chimpanzees. A clue to how that may have happened lies in deaf populations where sign language has facilitated marriage ...
monoclonal reacts strongly with Connexin-26, which has a predicted molecular weight of 26.5 kDa; anti-Cx26 appears to exhibit minimal cross reaction with Cx30 by western blotting ...
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