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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Principais autores:	So-Young Kim, Samel Park, Seong-Woo Lee, Ji-Hye Lee, Eun Soo Lee, Miri Kim, Youngjo Kim, Jeong Suk Kang, Choon Hee Chung, Jong-Seok Moon, Eun Young Lee
格式:	Artigo
語言:	Inglês
出版:	MDPI AG 2021-01-01
叢編:	Cells
主題:	Fabry disease lyso-Gb3 alpha-galactosidase A RIPK3 necroptosis alpha-galactosidase
在線閱讀:	https://www.mdpi.com/2073-4409/10/2/245
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