Oxidative Stress Contributes to Endothelial Dysfunction in Mouse Models of Hereditary Hemorrhagic Telangiectasia

Hereditary hemorrhagic telangiectasia (HHT) is a vascular dysplasia caused by mutations in endoglin (ENG; HHT1) or activin receptor-like kinase (ALK1; HHT2) genes, coding for transforming growth factor-β (TGF-β) superfamily receptors. We demonstrated previously that endoglin and ALK1 interact with e...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Jerkic, Mirjana, Sotov, Valentin, Letarte, Michelle
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Hindawi Publishing Corporation 2012
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3540964/
https://ncbi.nlm.nih.gov/pubmed/23320130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/686972
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