Discoidin Domain Receptor 1 Contributes to the Survival of Lung Fibroblast in Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF), characterized by fibroblast proliferation and accumulation of extracellular matrix, including collagen, is a chronic progressive disorder that results in lung remodeling and fibrosis. However, the cellular mechanisms that may make fibroblasts resistant to apoptos...

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Detalhes bibliográficos
Main Authors: Matsuyama, Wataru, Watanabe, Masaki, Shirahama, Yuko, Mitsuyama, Hideo, Higashimoto, Ikkou, Osame, Mitsuhiro, Arimura, Kimiyoshi
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2006
Assuntos:
Original Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1606536/
https://ncbi.nlm.nih.gov/pubmed/16507902
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2006.050801
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