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Podocyte Depletion in Thin GBM and Alport Syndrome
The proximate genetic cause of both Thin GBM and Alport Syndrome (AS) is abnormal α3, 4 and 5 collagen IV chains resulting in abnormal glomerular basement membrane (GBM) structure/function. We previously reported that podocyte detachment rate measured in urine is increased in AS, suggesting that pod...
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| Publié dans: | PLoS One |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Public Library of Science
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4871445/ https://ncbi.nlm.nih.gov/pubmed/27192434 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0155255 |
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