Mechanosignaling through YAP and TAZ drives fibroblast activation and fibrosis.

Saved in:
Bibliographic Details
Title: Mechanosignaling through YAP and TAZ drives fibroblast activation and fibrosis.
Authors: Liu F; Molecular and Integrative Physiological Sciences, Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts;, Lagares D; Pulmonary and Critical Care Unit and Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Charlestown, Massachusetts;, Choi KM; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota;, Stopfer L; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota;, Marinković A; Molecular and Integrative Physiological Sciences, Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts;, Vrbanac V; Pulmonary and Critical Care Unit and Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Charlestown, Massachusetts;, Probst CK; Pulmonary and Critical Care Unit and Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Charlestown, Massachusetts;, Hiemer SE; Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts;, Sisson TH; Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan;, Horowitz JC; Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Michigan Medical Center, Ann Arbor, Michigan;, Rosas IO; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts;, Fredenburgh LE; Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts;, Feghali-Bostwick C; Division of Rheumatology and Immunology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina., Varelas X; Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts;, Tager AM; Pulmonary and Critical Care Unit and Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Charlestown, Massachusetts;, Tschumperlin DJ; Molecular and Integrative Physiological Sciences, Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota; tschumperlin.daniel@mayo.edu.
Source: American journal of physiology. Lung cellular and molecular physiology [Am J Physiol Lung Cell Mol Physiol] 2015 Feb 15; Vol. 308 (4), pp. L344-57. Date of Electronic Publication: 2014 Dec 12.
Publication Type: Clinical Trial; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: American Physiological Society Country of Publication: United States NLM ID: 100901229 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1522-1504 (Electronic) Linking ISSN: 10400605 NLM ISO Abbreviation: Am J Physiol Lung Cell Mol Physiol Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1522-1504
DOI:10.1152/ajplung.00300.2014