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Podocyte p53 Limits the Severity of Experimental Alport Syndrome
Alport syndrome (AS) is one of the most common types of inherited nephritis caused by mutation in one of the glomerular basement membrane components. AS is characterized by proteinuria at early stage of the disease and glomerular hyperplastic phenotype and renal fibrosis at late stage. Here, we show...
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| Publicado no: | J Am Soc Nephrol |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4696573/ https://ncbi.nlm.nih.gov/pubmed/25967122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2014111109 |
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