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PPAR-γ agonists inhibit profibrotic phenotypes in human lung fibroblasts and bleomycin-induced pulmonary fibrosis

Pulmonary fibrosis is characterized by alterations in fibroblast phenotypes resulting in excessive extracellular matrix accumulation and anatomic remodeling. Current therapies for this condition are largely ineffective. Peroxisome proliferator-activated receptor-γ (PPAR-γ) is a member of the nuclear...

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Detalhes bibliográficos
Publicado no:Am J Physiol Lung Cell Mol Physiol
Main Authors: Milam, Jami E., Keshamouni, Venkateshwar G., Phan, Sem H., Hu, Biao, Gangireddy, Srinivasa R., Hogaboam, Cory M., Standiford, Theodore J., Thannickal, Victor J., Reddy, Raju C.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5926773/
https://ncbi.nlm.nih.gov/pubmed/18162602
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00333.2007
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