About: TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment?

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About: TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2000 (uk) im September 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 2000 (ast) scientific article published on 01 September 2000 (en)
publication date	wds:Q74219134-EA4C4F6E-51C1-4ECC-827F-74E91DDB40E4
publication date	2000-09-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q74219134-450E097A-4737-4385-B272-D8ABBD338659 wds:Q74219134-47031450-AD29-4AD9-931C-2C8470D2295D wds:Q74219134-53372E98-59FE-4724-9C2B-59E1196159D5 wds:Q74219134-54B58DC4-831A-45B8-99F9-8CC9F9B1BE2D wds:Q74219134-558E7D3C-1654-43D5-AAED-83AA08A2C0EC wds:Q74219134-CCC0A4AA-7BDC-4702-97F0-E5097234D56A wds:Q74219134-E8C96B9F-6C9F-4739-A1F8-C744E7E5EE03
author name string	R Barrios L Segura M Selman A Pardo S Cabrera R Ramírez V Ruiz
rdfs:label	TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (en) TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (nl)
skos:prefLabel	TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (en) TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (nl)
name	TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (en) TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (nl)
title	wds:Q74219134-9ECEEFAF-4D7C-4890-8EA8-1D48E01F3122
title	TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (en)
page(s)	wds:Q74219134-9386B1CF-1F28-428A-BAB8-EBBC6E0C1395
page(s)	L562-74
instance of	wds:Q74219134-0E830ADE-EB52-4425-AF7A-36C255B3B906
instance of	scholarly article
main subject	wds:Q74219134-F33A24BD-E357-4AE0-ADFB-212B7E9B66BB
main subject	pulmonary fibrosis
PubMed ID	wds:Q74219134-F1F32E0D-A827-440B-B10D-CC5A5C30E82B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10956632
PubMed ID	10956632
published in	wds:Q74219134-48627D3F-4752-4907-9147-1E65B20A05B3
published in	American Journal of Physiology - Lung Cellular and Molecular Physiology
issue	wds:Q74219134-D56DA69E-BB1E-4AD0-AC12-301B22C68D53
volume	wds:Q74219134-FEE712ED-54B7-428E-AAD9-E531E33EB80D
issue	3
volume	279
DOI	wds:Q74219134-2BD29050-C5AC-40EA-AEFE-912F185589EB
DOI	http://dx.doi.org/10.1152/AJPLUNG.2000.279.3.L562
DOI	10.1152/AJPLUNG.2000.279.3.L562
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74219134
is cites work of	Bone morphogenetic protein-4 inhibitor gremlin is overexpressed in idiopathic pulmonary fibrosis Inhibition of pulmonary fibrosis in mice by CXCL10 requires glycosaminoglycan binding and syndecan-4 Matrix metalloproteinase (MMP)-19-deficient fibroblasts display a profibrotic phenotype. Multi-walled carbon nanotube instillation impairs pulmonary function in C57BL/6 mice Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF). Accelerated variant of idiopathic pulmonary fibrosis: clinical behavior and gene expression pattern Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study. Idiopathic pulmonary fibrosis Always cleave up your mess: targeting collagen degradation to treat tissue fibrosis Idiopathic pulmonary fibrosis: an epithelial/fibroblastic cross-talk disorder Overlapping and enzyme-specific contributions of matrix metalloproteinases-9 and -12 in IL-13-induced inflammation and remodeling Genetic susceptibility in pneumoconiosis New insights into the pathogenesis and treatment of idiopathic pulmonary fibrosis: a potential role for stem cells in the lung parenchyma and implications for therapy. The absence of reactive oxygen species production protects mice against bleomycin-induced pulmonary fibrosis Macrophage metalloelastase (MMP-12) deficiency does not alter bleomycin-induced pulmonary fibrosis in mice Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans Pulmonary fibrosis: pathogenesis, etiology and regulation The role of osteopontin and osteopontin aptamer (OPN-R3) in fibroblast activity Pathogenetic mechanisms in usual interstitial pneumonia/idiopathic pulmonary fibrosis. Wnt signaling and pulmonary fibrosis Effects of amorphous silica coating on cerium oxide nanoparticles induced pulmonary responses A translational preclinical model of interstitial pulmonary fibrosis and pulmonary hypertension: mechanistic pathways driving disease pathophysiology Induction of pulmonary fibrosis by cerium oxide nanoparticles Inhibition and role of let-7d in idiopathic pulmonary fibrosis The wound healing, chronic fibrosis, and cancer progression triad Relaxin regulates MMP expression and promotes satellite cell mobilization during muscle healing in both young and aged mice. Fibrotic response as a distinguishing feature of resistance and susceptibility to pulmonary infection with Mycobacterium tuberculosis in mice Actin cytoskeleton in myofibroblast differentiation: ultrastructure defining form and driving function Ligand-independent transforming growth factor-β type I receptor signalling mediates type I collagen-induced epithelial-mesenchymal transition Regulation of transforming growth factor-β1-driven lung fibrosis by galectin-3 Absence of Thy-1 results in TGF-β induced MMP-9 expression and confers a profibrotic phenotype to human lung fibroblasts Gene expression profiling of pulmonary fibrosis identifies Twist1 as an antiapoptotic molecular "rectifier" of growth factor signaling Up-regulation and profibrotic role of osteopontin in human idiopathic pulmonary fibrosis Matrix metalloproteinases as therapeutic targets for idiopathic pulmonary fibrosis MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis Matrix metalloproteinase-19 is a key regulator of lung fibrosis in mice and humans Fra-1/AP-1 transcription factor negatively regulates pulmonary fibrosis in vivo Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis Matrix metalloproteinases promote inflammation and fibrosis in asbestos-induced lung injury in mice MMP-1 polymorphisms and the risk of idiopathic pulmonary fibrosis Matrix metalloproteinase (MMP)-1 induces lung alveolar epithelial cell migration and proliferation, protects from apoptosis, and represses mitochondrial oxygen consumption Tissue inhibitor of metalloproteinase-1 deficiency amplifies acute lung injury in bleomycin-exposed mice Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis Matrix metalloproteinases in destructive pulmonary pathology Tissue inhibitor of metalloproteinase-1 modulates allergic lung inflammation in murine asthma Idiopathic pulmonary fibrosis: pathogenesis and therapeutic approaches A review of current and novel therapies for idiopathic pulmonary fibrosis Pivotal role of cathepsin K in lung fibrosis Matrix metalloproteinase-1 polymorphism (-1607G) and disease severity in non-cystic fibrosis bronchiectasis in Taiwan Anti-fibrotic effects of nintedanib in lung fibroblasts derived from patients with idiopathic pulmonary fibrosis. Pharmacotherapy of acute lung injury and acute respiratory distress syndrome

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