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Fibrillin-1 genetic deficiency leads to pathological aging of arteries in mice

Fibrillin-1, the major component of extracellular microfibrils that associate with insoluble elastin in elastic fibers, is mainly synthesized during development and postnatal growth and is believed to guide elastogenesis. Mutations in the fibrillin-1 gene cause Marfan syndrome, a multisystem disorde...

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Detaylı Bibliyografya
Asıl Yazarlar: Mariko, B, Pezet, M, Escoubet, B, Bouillot, S, Andrieu, JP, Starcher, B, Quaglino, D, Jacob, MP, Huber, P, Ramirez, F, Faury, G
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3075583/
https://ncbi.nlm.nih.gov/pubmed/21432852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/path.2840
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