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Mice expressing BMPR2(R899X) transgene in smooth muscle develop pulmonary vascular lesions

Familial pulmonary arterial hypertension (PAH) is associated with mutations in bone morphogenetic protein type II receptor (BMPR2). Many of these mutations occur in the BMPR2 tail domain, leaving the SMAD functions intact. To determine the in vivo consequences of BMPR2 tail domain mutation, we creat...

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Detalhes bibliográficos
Main Authors: West, James, Harral, Julie, Lane, Kirk, Deng, Yupu, Ickes, Brian, Crona, Daniel, Albu, Sebastian, Stewart, Duncan, Fagan, Karen
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2584890/
https://ncbi.nlm.nih.gov/pubmed/18723761
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.90255.2008
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