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MMPs, inflammation and pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) is characterised by remodelling of small pulmonary arteries leading to a progressive increase in pulmonary vascular resistance and right ventricular failure [1]. PAH can be idiopathic, familial, or associated with a number of conditions or diseases, such as conn...
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| Publicado no: | Matrix Metalloproteinases in Tissue Remodelling and Inflammation |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7122977/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-7643-8585-9_6 |
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