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Splice variant–specific cellular function of the formin INF2 in maintenance of Golgi architecture
INF2 is a unique formin that can both polymerize and depolymerize actin filaments. Mutations in INF2 cause the kidney disease focal and segmental glomerulosclerosis. INF2 can be expressed as two C-terminal splice variants: CAAX and non-CAAX. The CAAX isoform contains a C-terminal prenyl group and is...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The American Society for Cell Biology
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3237625/ https://ncbi.nlm.nih.gov/pubmed/21998196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E11-05-0457 |
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