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A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes
Dominant mutations in GJA1, the gene encoding the gap junction protein connexin43 (Cx43), cause oculodentodigital dysplasia (ODDD), a syndrome affecting multiple tissues, including the central nervous system (CNS). We investigated the effects of the G60S mutant, which causes a similar, dominant phen...
Bewaard in:
| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3848784/ https://ncbi.nlm.nih.gov/pubmed/21375791 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S1740925X11000019 |
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