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Matrix Metalloproteinase 3 Is a Mediator of Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) may be triggered by epithelial injury that results in aberrant production of growth factors, cytokines, and proteinases, leading to proliferation of myofibroblasts, excess deposition of collagen, and destruction of the lung architecture. The precise mechanisms and...

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Detalhes bibliográficos
Main Authors: Yamashita, Cory M., Dolgonos, Lior, Zemans, Rachel L., Young, Scott K., Robertson, Jennifer, Briones, Natalie, Suzuki, Tomoko, Campbell, Megan N., Gauldie, Jack, Radisky, Derek C., Riches, David W.H., Yu, Guoying, Kaminski, Naftali, McCulloch, Christopher A.G., Downey, Gregory P.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3181358/
https://ncbi.nlm.nih.gov/pubmed/21871427
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2011.06.041
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