Regulation of Transforming Growth Factor-β1-driven Lung Fibrosis by Galectin-3
Regulation of Transforming Growth Factor-β1-driven Lung Fibrosis by Galectin-3
About this item
Full title
Author / Creator
Publisher
New York, NY: American Thoracic Society
Journal title
Language
English
Formats
Publication information
Publisher
New York, NY: American Thoracic Society
Subjects
More information
Scope and Contents
Contents
Idiopathic pulmonary fibrosis (IPF) is a chronic dysregulated response to alveolar epithelial injury with differentiation of epithelial cells and fibroblasts into matrix-secreting myofibroblasts resulting in lung scaring. The prognosis is poor and there are no effective therapies or reliable biomarkers. Galectin-3 is a β-galactoside binding lectin...
Alternative Titles
Full title
Regulation of Transforming Growth Factor-β1-driven Lung Fibrosis by Galectin-3
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3410728
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3410728
Other Identifiers
ISSN
1073-449X
E-ISSN
1535-4970
DOI
10.1164/rccm.201106-0965oc
