Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia

Tiklamalar: 226
ID: 270287
2018
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Ozet
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular disorder that leads to abnormal connections between arteries and veins termed arteriovenous malformations (AVM). Mutations in TGFβ pathway members ALK1, ENG and SMAD4 ...
Referans Anahtari
meadows2018angiogenesisvascular Kullanarak makale yazarken otomatik alinti icin bu anahtari kullanin SciMatic Makale Yoneticisi veya Tez Yoneticisi
Yazarlar Angela M. Crist, Amanda R. Lee, Nehal R. Patel, Dawn E. Westhoff, Stryder M. Meadows;Angela M. Crist;Amanda R. Lee;Nehal R. Patel;Dawn E. Westhoff;Stryder M. Meadows;
Dergi angiogenesis
Yil 2018
DOI
10.1007/s10456-018-9602-0
URL
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5878194
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