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Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease
The congenital polycystic kidney (cpk) mutation is the most extensively characterized mouse model of polycystic kidney disease (PKD). The renal cystic disease is fully expressed in homozygotes and is strikingly similar to human autosomal recessive PKD (ARPKD), whereas genetic background modulates th...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC150876/ https://ncbi.nlm.nih.gov/pubmed/11854326 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI14099 |
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