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Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome
Germline missense mutations in GJB2 encoding connexin (Cx) 26 have been found in keratitis, ichthyosis and deafness (KID) syndrome. We explored the effects of three mouse Cx26 mutants (Cx26-G12R, -G45E and -D50N) corresponding to KID syndrome-causative human mutants on hemichannel activities leading...
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| Опубликовано в: : | Sci Rep |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Nature Publishing Group UK
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6110719/ https://ncbi.nlm.nih.gov/pubmed/30150638 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-30757-3 |
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