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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society for Investigative Pathology 2011
विषय:
Regular Article
ऑनलाइन पहुंच: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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