Essential role for TMEM100 in vascular integrity but limited contributions to the pathogenesis of hereditary haemorrhagic telangiectasia

AIMS: TMEM100 was previously identified as a downstream target of activin receptor-like kinase 1 (ALK1; ACVRL1) signalling. Mutations on ALK1 cause hereditary haemorrhagic telangiectasia (HHT), a vascular disorder characterized by mucocutaneous telangiectases and visceral arteriovenous malformations...

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Publicado en:Cardiovasc Res
Autores principales: Moon, Eun-Hye, Kim, Yoo Sung, Seo, Jiyoung, Lee, Sabin, Lee, Young Jae, Oh, Suk Paul
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2015
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6279201/
https://ncbi.nlm.nih.gov/pubmed/25538155
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cvr/cvu260
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