Type V collagen induced tolerance suppresses collagen deposition, TGF-β and associated transcripts in pulmonary fibrosis
about
Human genome-wide expression analysis reorients the study of inflammatory mediators and biomechanics in osteoarthritisRegulation of Collagen V Expression and Epithelial-Mesenchymal Transition by miR-185 and miR-186 during Idiopathic Pulmonary Fibrosis.Precision Medicine: The New Frontier in Idiopathic Pulmonary FibrosisC-X-C motif chemokine 13 (CXCL13) is a prognostic biomarker of idiopathic pulmonary fibrosis.Crosstalk between TGF-β1 and complement activation augments epithelial injury in pulmonary fibrosis.Autoantibody-Targeted Treatments for Acute Exacerbations of Idiopathic Pulmonary FibrosisThe future of the development of medicines in idiopathic pulmonary fibrosis.Contribution of the anaphylatoxin receptors, C3aR and C5aR, to the pathogenesis of pulmonary fibrosis.SMAD3 expression and regulation of fibroplasia in vocal fold injury.Novel Drug Targets For Idiopathic Pulmonary Fibrosis.Idiopathic pulmonary fibrosis and a role for autoimmunity.Type V Collagen in Health, Disease, and Fibrosis.Basement membranes and autoimmune diseases.New treatment directions for IPF: current status of ongoing and upcoming clinical trials.Lrp5/β-Catenin Signaling Controls Lung Macrophage Differentiation and Inhibits Resolution of Fibrosis.Pulmonary fibrosis, part I: epidemiology, pathogenesis, and diagnosis.Permanent alveolar collapse is the predominant mechanism in idiopathic pulmonary fibrosis.MUC5B promoter polymorphisms and risk of coal workers' pneumoconiosis in a Chinese population.Autoimmune Reactivity in Graft Injury: Player or Bystander?Investigational drugs for idiopathic pulmonary fibrosis.Mesenchymal stem cells in idiopathic pulmonary fibrosis.Idiopathic Pulmonary Fibrosis: Molecular Endotypes of Fibrosis Stratifying Existing and Emerging Therapies.IL-17A deficiency mitigates bleomycin-induced complement activation during lung fibrosis.Are newly launched pharmacotherapies efficacious in treating idiopathic pulmonary fibrosis? Or is there still more work to be done?A Novel Antifibrotic Mechanism of Nintedanib and Pirfenidone. Inhibition of Collagen Fibril Assembly.Idiopathic Pulmonary Fibrosis (IPF): An Overview
P2860
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P2860
Type V collagen induced tolerance suppresses collagen deposition, TGF-β and associated transcripts in pulmonary fibrosis
description
2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@ast
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@en
type
label
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@ast
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@en
prefLabel
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@ast
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@en
P2093
P2860
P1433
P1476
Type V collagen induced tolera ...... nscripts in pulmonary fibrosis
@en
P2093
Amanda J Fisher
Amir Emtiazdjoo
Chen Zhang
David S Wilkes
Elizabeth A Mickler
George E Sandusky
Gerald N Smith
Hongmei Gu
Jeremy M Lott
Katia Rothhaar
P2860
P304
P356
10.1371/JOURNAL.PONE.0076451
P407
P577
2013-10-21T00:00:00Z