Increased tissue perfusion promotes capillary dysplasia in the ALK1-deficient mouse brain following VEGF stimulation

Loss-of-function activin receptor-like kinase 1 gene mutation (ALK1(+/−)) is associated with brain arteriovenous malformations (AVM) in hereditary hemorrhagic telangiectasia type 2. Other determinants of the lesional phenotype are unknown. In the present study, we investigated the influence of high...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Hao, Qi, Su, Hua, Marchuk, Douglas A., Rola, Radoslaw, Wang, Yongqiang, Liu, Weizhong, Young, William L., Yang, Guo-Yuan
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Physiological Society 2008
Gaiak:
Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2614529/
https://ncbi.nlm.nih.gov/pubmed/18835925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpheart.00083.2008
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