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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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| Foilsithe in: | J Am Soc Nephrol |
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| Main Authors: | , , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
American Society of Nephrology
2016
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| Ábhair: | |
| Rochtain Ar Líne: | 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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