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...

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Detalles Bibliográficos
Autores principales: Jerkic, Mirjana, Sotov, Valentin, Letarte, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540964/
https://www.ncbi.nlm.nih.gov/pubmed/23320130
http://dx.doi.org/10.1155/2012/686972

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540964/
https://www.ncbi.nlm.nih.gov/pubmed/23320130
http://dx.doi.org/10.1155/2012/686972

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