TRAIL-Dependent Resolution of Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is the most common form of interstitial lung disease characterized by the persistence of activated myofibroblasts resulting in excessive deposition of extracellular matrix proteins and profound tissue remodeling. In the present study, the expression of tumor necro...

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Detalles Bibliográficos
Autores principales: Habiel, David M., Moreira, Ana Paula, Ismailoglu, Ugur B., Dunleavy, Michael P., Cavassani, Karen A., van Rooijen, Nico, Coelho, Ana Lucia, Hogaboam, Cory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833466/
https://www.ncbi.nlm.nih.gov/pubmed/29670467
http://dx.doi.org/10.1155/2018/7934362

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833466/
https://www.ncbi.nlm.nih.gov/pubmed/29670467
http://dx.doi.org/10.1155/2018/7934362

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