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Angiotensin, transforming growth factor β and aortic dilatation in Marfan syndrome: Of mice and humans()
Marfan syndrome is consequent upon mutations in FBN1, which encodes the extracellular matrix microfibrillar protein fibrillin-1. The phenotype is characterised by development of thoracic aortic aneurysm. Current understanding of the pathogenesis of aneurysms in Marfan syndrome focuses upon abnormal...
Gorde:
| Argitaratua izan da: | Int J Cardiol Heart Vasc |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Elsevier
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5988480/ https://ncbi.nlm.nih.gov/pubmed/29876507 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcha.2018.02.009 |
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