TRAIL-Dependent Resolution of Pulmonary Fibrosis

• Glavni autori: David M. Habiel (Autor), Ana Paula Moreira (Autor), Ugur B. Ismailoglu (Autor), Michael P. Dunleavy (Autor), Karen A. Cavassani (Autor), Nico van Rooijen (Autor), Ana Lucia Coelho (Autor), Cory M. Hogaboam (Autor)
• Format: Knjiga
• Izdano: Hindawi Limited, 2018-01-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

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...