Endothelial Depletion of Acvrl1 in Mice Leads to Arteriovenous Malformations Associated with Reduced Endoglin Expression

Rare inherited cardiovascular diseases are frequently caused by mutations in genes that are essential for the formation and/or function of the cardiovasculature. Hereditary Haemorrhagic Telangiectasia is a familial disease of this type. The majority of patients carry mutations in either Endoglin (EN...

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Hauptverfasser: Tual-Chalot, Simon, Mahmoud, Marwa, Allinson, Kathleen R., Redgrave, Rachael E., Zhai, Zhenhua, Oh, S. Paul, Fruttiger, Marcus, Arthur, Helen M.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Public Library of Science 2014
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4045906/
https://ncbi.nlm.nih.gov/pubmed/24896812
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0098646
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