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Monkeys mutant for PKD1 recapitulate human autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease (ADPKD) caused by PKD1 mutations is one of the most common hereditary disorders. However, the key pathological processes underlying cyst development and exacerbation in pre-symptomatic stages remain unknown, because rodent models do not recapitulate criti...
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| Publicado no: | Nat Commun |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6904451/ https://ncbi.nlm.nih.gov/pubmed/31822676 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-13398-6 |
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