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Lung fibrotic tenascin-C upregulation is associated with other extracellular matrix proteins and induced by TGFβ1

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a progressive parenchymal lung disease of unknown aetiology and poor prognosis, characterized by altered tissue repair and fibrosis. The extracellular matrix (ECM) is a critical component in regulating cellular homeostasis and appropriate wound heal...

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Detalhes bibliográficos
Main Authors: Estany, Susanna, Vicens-Zygmunt, Vanesa, Llatjós, Roger, Montes, Ana, Penín, Rosa, Escobar, Ignacio, Xaubet, Antoni, Santos, Salud, Manresa, Frederic, Dorca, Jordi, Molina-Molina, Maria
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4123829/
https://ncbi.nlm.nih.gov/pubmed/25064447
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2466-14-120
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