Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants

Murine oligodendrocytes express the gap junction (GJ) proteins connexin32 (Cx32), Cx47, and Cx29. CNS phenotypes in patients with X-linked Charcot-Marie-Tooth disease may be caused by dominant effects of Cx32 mutations on other connexins. Here we examined the expression of Cx31.3 (the human ortholog...

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Detaylı Bibliyografya
Asıl Yazarlar: Sargiannidou, Irene, Ahn, Meejin, Enriquez, Alan D., Peinado, Alejandro, Reynolds, Richard, Abrams, Charles, Scherer, Steven S., Kleopa, Kleopas A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2704064/
https://ncbi.nlm.nih.gov/pubmed/18353664
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2008.01.009
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