Fibroblasts isolated from normal lungs and those with idiopathic pulmonary fibrosis differ in interleukin-6/gp130-mediated cell signaling and proliferation
about
Resveratrol inhibits paraquat-induced oxidative stress and fibrogenic response by activating the Nrf2 pathwayEvolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genesInterleukin-6 contributes to inflammation and remodeling in a model of adenosine mediated lung injuryLoss of RAGE in pulmonary fibrosis: molecular relations to functional changes in pulmonary cell typesDynamic probabilistic threshold networks to infer signaling pathways from time-course perturbation data.Red blood cells inhibit proliferation and stimulate apoptosis in human lung fibroblasts in vitro.Fibrotic myofibroblasts manifest genome-wide derangements of translational controlPathogenesis of idiopathic pulmonary fibrosisInterleukin 6 mediates myocardial fibrosis, concentric hypertrophy, and diastolic dysfunction in rats.Inhibition of Wnt/beta-catenin/CREB binding protein (CBP) signaling reverses pulmonary fibrosis.Blockade of IL-6 Trans signaling attenuates pulmonary fibrosisNovel therapeutic approaches for pulmonary fibrosis.Discoidin domain receptor 1 contributes to the survival of lung fibroblast in idiopathic pulmonary fibrosisIL-27 alleviates the bleomycin-induced pulmonary fibrosis by regulating the Th17 cell differentiation.Characterization of Lung Fibroblasts More than Two Decades after Mustard Gas ExposureCytokine-like factor 1 gene expression is enriched in idiopathic pulmonary fibrosis and drives the accumulation of CD4+ T cells in murine lungs: evidence for an antifibrotic role in bleomycin injury.Sputum biomarkers in IPF: Evidence for raised gene expression and protein level of IGFBP-2, IL-8 and MMP-7.Genetic partitioning of interleukin-6 signalling in mice dissociates Stat3 from Smad3-mediated lung fibrosis.STAT-3 contributes to pulmonary fibrosis through epithelial injury and fibroblast-myofibroblast differentiation.Epithelial-mesenchymal interactions in pulmonary fibrosis.Th-17 regulatory cytokines inhibit corticosteroid induced airway structural cells apoptosis.Evolving concepts of apoptosis in idiopathic pulmonary fibrosis.Distinct roles for the A2B adenosine receptor in acute and chronic stages of bleomycin-induced lung injury.Pathological integrin signaling enhances proliferation of primary lung fibroblasts from patients with idiopathic pulmonary fibrosisGenetic ablation of caveolin-2 sensitizes mice to bleomycin-induced injury.Human umbilical cord mesenchymal stem cells reduce fibrosis of bleomycin-induced lung injury.Epigenetic Regulation of Interleukin 6 by Histone Acetylation in Macrophages and Its Role in Paraquat-Induced Pulmonary Fibrosis.Fibrotic extracellular matrix activates a profibrotic positive feedback loop.STAT3: a central mediator of pulmonary fibrosis?Matrix regulation of idiopathic pulmonary fibrosis: the role of enzymes.Heterogeneity in fibroblast proliferation and survival in idiopathic pulmonary fibrosis.Enhanced neointimal fibroblast, myofibroblast content and altered extracellular matrix composition: Implications in the progression of human peripheral artery restenosisBromelain down-regulates myofibroblast differentiation in an in vitro wound healing assay.Absence of Thy-1 results in TGF-β induced MMP-9 expression and confers a profibrotic phenotype to human lung fibroblasts.Deficient repair response of IPF fibroblasts in a co-culture model of epithelial injury and repair.Transcription factor GATA-6 is expressed in quiescent myofibroblasts in idiopathic pulmonary fibrosis.Radiation-induced matrix production of lung fibroblasts is regulated by interleukin-8.Heme oxygenase-1 and interleukin-11 are overexpressed in stress-induced premature senescence of human WI-38 fibroblasts induced by tert-butylhydroperoxide and ethanol.Mesenchymal cell survival in airway and interstitial pulmonary fibrosis.BDNF/TrkB axis activation promotes epithelial-mesenchymal transition in idiopathic pulmonary fibrosis.
P2860
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P2860
Fibroblasts isolated from normal lungs and those with idiopathic pulmonary fibrosis differ in interleukin-6/gp130-mediated cell signaling and proliferation
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Fibroblasts isolated from norm ...... ll signaling and proliferation
@ast
Fibroblasts isolated from norm ...... ll signaling and proliferation
@en
type
label
Fibroblasts isolated from norm ...... ll signaling and proliferation
@ast
Fibroblasts isolated from norm ...... ll signaling and proliferation
@en
prefLabel
Fibroblasts isolated from norm ...... ll signaling and proliferation
@ast
Fibroblasts isolated from norm ...... ll signaling and proliferation
@en
P2093
P2860
P1476
Fibroblasts isolated from norm ...... ll signaling and proliferation
@en
P2093
Amelia K Scaffidi
Carmel Keerthisingam
Darryl A Knight
Geoff J Laurent
Neil L Misso
Philip J Thompson
Robin J McAnulty
Steven E Mutsaers
Yuben P Moodley
P2860
P304
P356
10.1016/S0002-9440(10)63658-9
P407
P577
2003-07-01T00:00:00Z