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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Detalles Bibliográficos
Autores principales: Kim, So-Young, Park, Samel, Lee, Seong-Woo, Lee, Ji-Hye, Lee, Eun Soo, Kim, Miri, Kim, Youngjo, Kang, Jeong Suk, Chung, Choon Hee, Moon, Jong-Seok, Lee, Eun Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911493/
https://www.ncbi.nlm.nih.gov/pubmed/33513913
http://dx.doi.org/10.3390/cells10020245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911493/
https://www.ncbi.nlm.nih.gov/pubmed/33513913
http://dx.doi.org/10.3390/cells10020245

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