TGF-β1 → SMAD/p53/USF2 → PAI-1 transcriptional axis in ureteral obstruction-induced renal fibrosis.
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Key fibrogenic mediators: old players. Renin–angiotensin systemTGF-β/Smad signaling in renal fibrosisTGF-β signaling in tissue fibrosis: redox controls, target genes and therapeutic opportunitiesThe role of the p53 tumor suppressor in metabolism and diabetesOxidative stress in obesity: a critical component in human diseasesRedox control of p53 in the transcriptional regulation of TGF-β1 target genes through SMAD cooperativity.Antifibrotic effects of KS370G, a caffeamide derivative, in renal ischemia-reperfusion injured mice and renal tubular epithelial cells.Role of microRNA 1207-5P and its host gene, the long non-coding RNA Pvt1, as mediators of extracellular matrix accumulation in the kidney: implications for diabetic nephropathyTumor suppressor ataxia telangiectasia mutated functions downstream of TGF-β1 in orchestrating profibrotic responses.Impact of AMP-Activated Protein Kinase α1 Deficiency on Tissue Injury following Unilateral Ureteral Obstruction.Loss of tumour suppressor PTEN expression in renal injury initiates SMAD3- and p53-dependent fibrotic responsesGlycogen synthase kinase-3 inhibition attenuates fibroblast activation and development of fibrosis following renal ischemia-reperfusion in mice.Activation of AMP-activated protein kinase prevents TGF-β1-induced epithelial-mesenchymal transition and myofibroblast activation.Differentially expressed microRNAs in bone marrow mesenchymal stem cell-derived microvesicles in young and older rats and their effect on tumor growth factor-β1-mediated epithelial-mesenchymal transition in HK2 cells.Comprehensive genomic profiling in diabetic nephropathy reveals the predominance of proinflammatory pathways.Transforming growth factor-β-induced cross talk between p53 and a microRNA in the pathogenesis of diabetic nephropathyCentral Nodes in Protein Interaction Networks Drive Critical Functions in Transforming Growth Factor Beta-1 Stimulated Kidney Cells.Grape seed extract attenuates arsenic-induced nephrotoxicity in rats.Genome-wide transcriptional analysis of differentially expressed genes in diabetic, healing corneal epithelial cells: hyperglycemia-suppressed TGFβ3 expression contributes to the delay of epithelial wound healing in diabetic corneas.PHF14: an innate inhibitor against the progression of renal fibrosis following folic acid-induced kidney injury.Klotho as a potential biomarker and therapy for acute kidney injury.Klotho and renal fibrosisKnockdown of elF3a inhibits collagen synthesis in renal fibroblasts via Inhibition of transforming growth factor-β1/Smad signaling pathwayTime-resolved dissection of early phosphoproteome and ensuing proteome changes in response to TGF-β.Gender-specific role of HDAC11 in kidney ischemia- and reperfusion-induced PAI-1 expression and injury.The molecular biology of pelvi-ureteric junction obstruction.Age-dependent shifts in renal response to injury relate to altered BMP6/CTGF expression and signaling.Effect of testosterone therapy on the urinary bladder in experimental hypogonadism of rats.Protective effect of rosuvastatin treatment by regulating oxidized low-density lipoprotein expression in a rat model of liver fibrosisTransforming growth factor-β1/Smad3-independent epithelial-mesenchymal transition in type I collagen glomerulopathy.Loss of expression of protein phosphatase magnesium-dependent 1A during kidney injury promotes fibrotic maladaptive repair.Complex Regulation of the Pericellular Proteolytic Microenvironment during Tumor Progression and Wound Repair: Functional Interactions between the Serine Protease and Matrix Metalloproteinase Cascades.Ureteral Obstruction-Induced Renal Fibrosis: An In Vivo Platform for Mechanistic Discovery and Therapeutic Intervention.Cell-Based Therapies for Tissue Fibrosis.A nonclassical vitamin D receptor pathway suppresses renal fibrosis.Bcl-3 is a novel biomarker of renal fibrosis in chronic kidney disease.Deregulation of Hippo-TAZ pathway during renal injury confers a fibrotic maladaptive phenotype.Roles of p21, p53, cyclin D1, CDK-4, estrogen receptor α in aflatoxin B1-induced cytotoxicity in testicular tissue of mice.Thermodynamic Aspects and Reprogramming Cellular Energy Metabolism during the Fibrosis Process.TGF-β1/p53 signaling in renal fibrogenesis.
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TGF-β1 → SMAD/p53/USF2 → PAI-1 transcriptional axis in ureteral obstruction-induced renal fibrosis.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 04 June 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@en
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@nl
type
label
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@en
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@nl
prefLabel
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@en
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@nl
P2093
P2860
P1476
TGF-β1 → SMAD/p53/USF2 → PAI-1 ...... uction-induced renal fibrosis.
@en
P2093
Jessica M Overstreet
Paul J Higgins
Rohan Samarakoon
Stephen P Higgins
P2860
P2888
P304
P356
10.1007/S00441-011-1181-Y
P577
2011-06-04T00:00:00Z