Endoglin is a conserved regulator of vasculogenesis in zebrafish – implications for hereditary haemorrhagic telangiectasia

Hereditary haemorrhagic telangiectasia (HHT) is a progressive vascular disease with high mortality and prevalence. There is no effective treatment of HHT due to the lack of comprehensive knowledge of its underlying pathological mechanisms. The majority of HHT1 patients carry endoglin (ENG) mutations...

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Detalles Bibliográficos
Autores principales: Zhang, Ding, Zhou, Fang, Zhao, Xiuli, Liu, Bao, Chen, Jingyu, Yang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527926/
https://www.ncbi.nlm.nih.gov/pubmed/31064821
http://dx.doi.org/10.1042/BSR20182320

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527926/
https://www.ncbi.nlm.nih.gov/pubmed/31064821
http://dx.doi.org/10.1042/BSR20182320

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