Fibrotic myofibroblasts manifest genome-wide derangements of translational control
about
Recent developments in myofibroblast biology: paradigms for connective tissue remodelingEvolving genomic approaches to idiopathic pulmonary fibrosis: moving beyond genesPulmonary fibrosis: patterns and perpetratorsIdentification of differential translation in genome wide studiesAlveolar epithelium: beyond the barrier.Alveolar epithelial cells express mesenchymal proteins in patients with idiopathic pulmonary fibrosisPathogenesis of idiopathic pulmonary fibrosismiR-210 promotes IPF fibroblast proliferation in response to hypoxia.Profibrotic phenotype of conjunctival fibroblasts from mucous membrane pemphigoid.Severe lung fibrosis requires an invasive fibroblast phenotype regulated by hyaluronan and CD44.IPF fibroblasts are desensitized to type I collagen matrix-induced cell death by suppressing low autophagy via aberrant Akt/mTOR kinasesPlasminogen activator inhibitor-1 suppresses profibrotic responses in fibroblasts from fibrotic lungsMetaQC: objective quality control and inclusion/exclusion criteria for genomic meta-analysis.Pathologic Regulation of Collagen I by an Aberrant Protein Phosphatase 2A/Histone Deacetylase C4/MicroRNA-29 Signal Axis in Idiopathic Pulmonary Fibrosis FibroblastsAlteration of Aging-Dependent MicroRNAs in Idiopathic Pulmonary Fibrosis.Toward a genome-wide landscape of translational controlMechanistic Target of Rapamycin Complex 1 (mTORC1) and mTORC2 as Key Signaling Intermediates in Mesenchymal Cell Activation.Role of microRNAs in gastrointestinal smooth muscle fibrosis and dysfunction: novel molecular perspectives on the pathophysiology and therapeutic targeting.Epithelial cell alpha3beta1 integrin links beta-catenin and Smad signaling to promote myofibroblast formation and pulmonary fibrosis.Transforming Growth Factor-β: Master Regulator of the Respiratory System in Health and DiseaseEmerging concepts in the pathogenesis of lung fibrosisInhibition of protein translation as a novel mechanism for prostaglandin E2 regulation of cell functions.Transcriptome of Cultured Lung Fibroblasts in Idiopathic Pulmonary Fibrosis: Meta-Analysis of Publically Available Microarray Datasets Reveals Repression of Inflammation and Immunity Pathways.Gene profile of fibroblasts identify relation of CCL8 with idiopathic pulmonary fibrosis.Up-regulation of heparan sulfate 6-O-sulfation in idiopathic pulmonary fibrosisFibrotic extracellular matrix activates a profibrotic positive feedback loop.Mouse Lung Fibroblast Resistance to Fas-Mediated Apoptosis Is Dependent on the Baculoviral Inhibitor of Apoptosis Protein 4 and the Cellular FLICE-Inhibitory Protein.Protein tyrosine phosphatase α mediates profibrotic signaling in lung fibroblasts through TGF-β responsiveness.Identification of a cell-of-origin for fibroblasts comprising the fibrotic reticulum in idiopathic pulmonary fibrosis.The molecular mediators of type 2 epithelial to mesenchymal transition (EMT) and their role in renal pathophysiology.Idiopathic pulmonary fibrosis-an epidemiological and pathological review.Systems biology of lung development and regeneration: current knowledge and recommendations for future research.Regulation and Relevance of Myofibroblast Responses in Idiopathic Pulmonary Fibrosis.Translational control of the fibroblast-extracellular matrix association: An application to pulmonary fibrosis.A novel zebrafish embryo xenotransplantation model to study primary human fibroblast motility in health and disease.SPARC suppresses apoptosis of idiopathic pulmonary fibrosis fibroblasts through constitutive activation of beta-cateninCysteine-rich protein 1 is regulated by transforming growth factor-β1 and expressed in lung fibrosis.Absence of Thy-1 results in TGF-β induced MMP-9 expression and confers a profibrotic phenotype to human lung fibroblasts.Exploring the role of sphingolipid machinery during the epithelial to mesenchymal transition program using an integrative approachFibroblast paracrine TNF-α signaling elevates integrin A5 expression in idiopathic pulmonary fibrosis (IPF).
P2860
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P2860
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@ast
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@en
type
label
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@ast
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@en
prefLabel
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@ast
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@en
P2093
P2860
P1433
P1476
Fibrotic myofibroblasts manifest genome-wide derangements of translational control
@en
P2093
Craig A Henke
Danhua Fan
Deanna Diebold
Mark Peterson
Richard Seonghun Nho
P2860
P356
10.1371/JOURNAL.PONE.0003220
P407
P577
2008-09-16T00:00:00Z