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Possible role of transforming growth factor-β1 and vascular endothelial growth factor in Fabry disease nephropathy

Fabry disease is a lysosomal storage disorder (LSD) caused by deficiency of α-galactosidase A (α-gal A), resulting in deposition of globotriaosylceramide (Gb3; also known as ceramide trihexoside) in the vascular endothelium of many organs. A gradual accumulation of Gb3 leads to cardiovascular, cereb...

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Detalhes bibliográficos
Main Authors: LEE, MI HEE, CHOI, EUN NAM, JEON, YEO JIN, JUNG, SUNG-CHUL
Formato: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4042857/
https://ncbi.nlm.nih.gov/pubmed/23007467
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ijmm.2012.1139
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