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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | 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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