Identification of cross-species shared transcriptional networks of diabetic nephropathy in human and mouse glomeruli. - Wikidata - awgldk - TriplyDB

Identification of cross-species shared transcriptional networks of diabetic nephropathy in human and mouse glomeruli.

Identification of cross-species shared transcriptional networks of diabetic nephropathy in human and mouse glomeruli.

http://www.wikidata.org/entity/Q36477207

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An Update on the Use of Animal Models in Diabetic Nephropathy Research Pro: 'The usefulness of biomarkers in glomerular diseases'. The problem: moving from syndrome to mechanism--individual patient variability in disease presentation, course and response to therapy Systems biology analysis reveals role of MDM2 in diabetic nephropathy 2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications Role of endothelial nitric oxide synthase in diabetic nephropathy: lessons from diabetic eNOS knockout mice Integrative biology identifies shared transcriptional networks in CKD.Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population New targets for treatment of diabetic nephropathy: what we have learned from animal models.Reduced Krüppel-like factor 2 expression may aggravate the endothelial injury of diabetic nephropathy.Epigenetic mechanisms in diabetic complications and metabolic memory.Glomerular endothelial cell injury and cross talk in diabetic kidney disease Cyclic nucleotide signalling in kidney fibrosis.MicroRNA-21 in glomerular injury.BAMBI elimination enhances alternative TGF-β signaling and glomerular dysfunction in diabetic mice Targeted Lipidomic and Transcriptomic Analysis Identifies Dysregulated Renal Ceramide Metabolism in a Mouse Model of Diabetic Kidney Disease A transcriptional blueprint for human and murine diabetic kidney disease Integrative Biology of Diabetic Kidney Disease Comparison of Glomerular and Podocyte mRNA Profiles in Streptozotocin-Induced Diabetes.Transcriptional networks of murine diabetic peripheral neuropathy and nephropathy: common and distinct gene expression patterns.Bridging translation for acute kidney injury with better preclinical modeling of human disease Transforming growth factor-β-induced cross talk between p53 and a microRNA in the pathogenesis of diabetic nephropathy Local TNF causes NFATc1-dependent cholesterol-mediated podocyte injury.Endothelial-podocyte crosstalk: the missing link between endothelial dysfunction and albuminuria in diabetes.Rhein protects pancreatic β-cells from dynamin-related protein-1-mediated mitochondrial fission and cell apoptosis under hyperglycemia Systems genetics approaches to understand complex traits.JAK inhibition and progressive kidney disease.RNA expression signatures and posttranscriptional regulation in diabetic nephropathy.Key pathways in renal disease progression of experimental diabetes.Renal biopsy-driven molecular target identification in glomerular disease.Developing Treatments for Chronic Kidney Disease in the 21st Century.Defining Glomerular Disease in Mechanistic Terms: Implementing an Integrative Biology Approach in Nephrology.The next generation of therapeutics for chronic kidney disease JAK inhibition in the treatment of diabetic kidney disease.Role of TGF-alpha in the progression of diabetic kidney disease.Increasing the level of peroxisome proliferator-activated receptor γ coactivator-1α in podocytes results in collapsing glomerulopathy.High resolution molecular and histological analysis of renal disease progression in ZSF1 fa/faCP rats, a model of type 2 diabetic nephropathy.Aloe-Emodin Protects RIN-5F (Pancreatic β-cell) Cell from Glucotoxicity via Regulation of Pro-Inflammatory Cytokine and Downregulation of Bax and Caspase 3.Mitochondrial reactive oxygen species in the pathogenesis of early diabetic nephropathy.Murine glomerular transcriptome links endothelial cell-specific molecule-1 deficiency with susceptibility to diabetic nephropathy.From bench to patient: model systems in drug discovery

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P2860

Identification of cross-species shared transcriptional networks of diabetic nephropathy in human and mouse glomeruli.

http://www.wikidata.org/entity/Q36477207

description

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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name

Identification of cross-specie ...... in human and mouse glomeruli.

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Identification of cross-specie ...... in human and mouse glomeruli.

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Identification of cross-specie ...... in human and mouse glomeruli.

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Identification of cross-specie ...... in human and mouse glomeruli.

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Identification of cross-specie ...... in human and mouse glomeruli.

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Identification of cross-specie ...... in human and mouse glomeruli.

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Ann Randolph

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E Jennifer Weil

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Frank C Brosius

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Hongyu Zhang

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James D Cavalcoli

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Jeffrey B Hodgin

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Jignesh M Patel

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Matthias Kretzler

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Raymond C Harris

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Robert G Nelson

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P2860

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Significance analysis of microarrays applied to the ionizing radiation response

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Interleukin-7: from bench to clinic

Dedifferentiation of immortalized human podocytes in response to transforming growth factor-β: a model for diabetic podocytopathy.

Transcript-specific expression profiles derived from sequence-based analysis of standard microarrays.

Mouse models of diabetic nephropathy.

Podocyte-specific overexpression of GLUT1 surprisingly reduces mesangial matrix expansion in diabetic nephropathy in mice

Endothelial nitric oxide synthase deficiency produces accelerated nephropathy in diabetic mice.

Molecular approaches to chronic kidney disease.

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10.2337/DB11-1667

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23139354

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3526018

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