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Evidence of Aortopathy in Mice with Haploinsufficiency of Notch1 in Nos3-Null Background
Thoracic aortic aneurysms (TAA) are a significant cause of morbidity and mortality in humans. While the exact etiology is unknown, genetic factors play an important role. Mutations in NOTCH1 have been linked to bicuspid aortic valve (BAV) and aortopathy in humans. The aim of this study was to determ...
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| Publicado no: | J Cardiovasc Dev Dis |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4407710/ https://ncbi.nlm.nih.gov/pubmed/25914885 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcdd2010017 |
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