The cytoplasmic accumulations of the cataract-associated mutant, Connexin50P88S, are long-lived and form in the endoplasmic reticulum

Mutant connexins have been linked to hereditary congenital cataracts. One such mutant causes a proline-to-serine substitution at position 88 in human connexin 50 (CX50P88S). In transfected cells, CX50P88S does not form gap junctions, but localizes in cytoplasmic multilamellar structures. We studied...

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Detaylı Bibliyografya
Asıl Yazarlar: Lichtenstein, Alexandra, Gaietta, Guido M., Deerinck, Thomas J., Crum, John, Sosinsky, Gina E., Beyer, Eric C., Berthoud, Viviana M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2695785/
https://ncbi.nlm.nih.gov/pubmed/19073179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2008.11.024
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