Oestrogen receptor alpha in pulmonary hypertension

AIMS: Pulmonary arterial hypertension (PAH) occurs more frequently in women with mutations in bone morphogenetic protein receptor type 2 (BMPR2) and dysfunctional BMPR2 signalling underpinning heritable PAH. We have previously shown that serotonin can uncover a pulmonary hypertensive phenotype in BM...

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Detalhes bibliográficos
Publicado no:Cardiovasc Res
Main Authors: Wright, Audrey F., Ewart, Marie-Ann, Mair, Kirsty, Nilsen, Margaret, Dempsie, Yvonne, Loughlin, Lynn, Maclean, Margaret R.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4615797/
https://ncbi.nlm.nih.gov/pubmed/25765937
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cvr/cvv106
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