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A Polycystin-1 Multiprotein Complex Is Disrupted in Polycystic Kidney Disease Cells
Autosomal dominant polycystic kidney disease (ADPKD) is typified by the accumulation of fluid-filled cysts and abnormalities in renal epithelial cell function. The disease is principally caused by mutations in the gene encoding polycystin-1, a large basolateral plasma membrane protein expressed in k...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The American Society for Cell Biology
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC363138/ https://ncbi.nlm.nih.gov/pubmed/14718571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E03-05-0296 |
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