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Dissociation of globotriaosylceramide and impaired endothelial function in α-galactosidase-A deficient EA.hy926 cells
Fabry disease, a rare, X-linked lysosomal storage disease, arises from deficiency of the lysosomal hydrolase, α-galactosidase A (GLA) which disrupts the catabolism of globo-series glycosphingolipids (GSLs). One potential link between GLA deficiency and vascular dysfunction may be changes in endothel...
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| Yayımlandı: | Mol Genet Metab |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6554739/ https://ncbi.nlm.nih.gov/pubmed/30413389 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2018.10.007 |
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