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RIPK3 Contributes to Lyso-Gb3-Induced Podocyte Death
Fabry disease is a lysosomal storage disease with an X-linked heritage caused by absent or decreased activity of lysosomal enzymes named alpha-galactosidase A (α-gal A). Among the various manifestations of Fabry disease, Fabry nephropathy significantly affects patients’ morbidity and mortality. The...
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| 發表在: | Cells |
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| Main Authors: | , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
MDPI
2021
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7911493/ https://ncbi.nlm.nih.gov/pubmed/33513913 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells10020245 |
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