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The promise of recombinant BMP ligands and other approaches targeting BMPR-II in the treatment of pulmonary arterial hypertension
Human genetic discoveries offer a powerful method to implicate pathways of major importance to disease pathobiology and hence provide targets for pharmacological intervention. The genetics of pulmonary arterial hypertension (PAH) strongly implicates loss-of-function of the bone morphogenetic protein...
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| Publicado no: | Glob Cardiol Sci Pract |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bloomsbury Qatar Foundation Journals
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4710869/ https://ncbi.nlm.nih.gov/pubmed/26779522 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5339/gcsp.2015.47 |
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