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Loss of polycystin-1 causes centrosome amplification and genomic instability
Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenetic disease predominantly caused by alteration or dysregulation of the PKD1 gene, which encodes polycystin-1 (PC1). The disease is characterized by the progressive expansion of bilateral fluid-filled renal cysts that ult...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2722891/ https://ncbi.nlm.nih.gov/pubmed/18566106 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn180 |
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