Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice. - Wikidata - wikimedia - TriplyDB

Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.

Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.

http://www.wikidata.org/entity/Q34145974

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Podocytes Podocyte-Specific Deletion of Murine CXADR Does Not Impair Podocyte Development, Function or Stress Response The minipig as a new model for the evaluation of doxorubicin-induced chronic toxicity.Bone marrow-derived immature myeloid cells are a main source of circulating suPAR contributing to proteinuric kidney disease.Mpv17 in mitochondria protects podocytes against mitochondrial dysfunction and apoptosis in vivo and in vitro.Molecular profiling of a lethal tumor microenvironment, as defined by stromal caveolin-1 status in breast cancers.Modifier genes and the plasticity of genetic networks in mice.Interconnected network motifs control podocyte morphology and kidney function.Pharmacological targeting of GSK3β confers protection against podocytopathy and proteinuria by desensitizing mitochondrial permeability transition.The role of retinoic acid receptors in the signal pathway of all-trans retinoic acid-induced differentiation in adriamycin-induced podocyte injury.Loss of Krüppel-like factor 6 cripples podocyte mitochondrial function.Krüppel-like factor 6 regulates mitochondrial function in the kidney Investigating mechanisms of chronic kidney disease in mouse models APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy Oxidative/Nitrative Stress and Inflammation Drive Progression of Doxorubicin-Induced Renal Fibrosis in Rats as Revealed by Comparing a Normal and a Fibrosis-Resistant Rat Strain.Podocyte injury-driven lipid peroxidation accelerates the infiltration of glomerular foam cells in focal segmental glomerulosclerosis.A monoclonal antibody raised against bacterially expressed MPV17 sequences shows peroxisomal, endosomal and lysosomal localisation in U2OS cells.Impact of a novel homozygous mutation in nicotinamide nucleotide transhydrogenase on mitochondrial DNA integrity in a case of familial glucocorticoid deficiency.Doxycycline down-regulates DNA-PK and radiosensitizes tumor initiating cells: Implications for more effective radiation therapy.Transforming growth factor-β, bioenergetics, and mitochondria in renal disease Physiology and pathophysiology of mitochondrial DNA.Background strain and the differential susceptibility of podocyte-specific deletion of Myh9 on murine models of experimental glomerulosclerosis and HIV nephropathy Initial testing (stage 1) of the topoisomerase II inhibitor pixantrone, by the pediatric preclinical testing program.How many Achilles' heels does a podocyte have? An update on podocyte biology.Causes and pathogenesis of focal segmental glomerulosclerosis.In vivo RNA interference models of inducible and reversible Sirt1 knockdown in kidney cells.Chemical Proteomic Approaches Targeting Cancer Stem Cells: A Review of Current Literature.Tissue regeneration and stem cell distribution in adriamycin induced glomerulopathy Divergent roles of Smad3 and PI3-kinase in murine adriamycin nephropathy indicate distinct mechanisms of proteinuria and fibrogenesis.Doxycycline and therapeutic targeting of the DNA damage response in cancer cells: old drug, new purpose.Protein Kinase A/CREB Signaling Prevents Adriamycin-Induced Podocyte Apoptosis via Upregulation of Mitochondrial Respiratory Chain Complexes.Hyperoside alleviates adriamycin-induced podocyte injury via inhibiting mitochondrial fission.Serum Response Factor Is Essential for Maintenance of Podocyte Structure and Function.Exacerbation of spontaneous autoimmune nephritis following regulatory T cell depletion in B cell lymphoma 2-interacting mediator knock-out mice.Aging and the Krüppel-like factors.Podocyte biology in 2015: New insights into the mechanisms of podocyte health.Protective role of cyclosporine A and minocycline on mitochondrial disequilibrium-related podocyte injury and proteinuria occurrence induced by adriamycin.Molecular and Cellular Mechanisms for Proteinuria in Minimal Change Disease.Plectin protects podocytes from adriamycin-induced apoptosis and F-actin cytoskeletal disruption through the integrin α6β4/FAK/p38 MAPK pathway

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P2860

Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.

http://www.wikidata.org/entity/Q34145974

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

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name

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@ast

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@en

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@nl

type

label

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@ast

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@en

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@nl

prefLabel

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@ast

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@en

Prkdc participates in mitochon ...... n-induced nephropathy in mice.

@nl

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Journal of Clinical Investigation

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Prkdc participates in mitochon ...... in-induced nephropathy in mice

@en

P2093

Ali G Gharavi

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Eric A Schon

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Jochen Reiser

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Natalia Papeta

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Samih H Nasr

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Sonja Brosel

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Vivette D D'Agati

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Zongyu Zheng

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P2860

The role of double-strand break repair — insights from human genetics

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

A role of DNA-PK for the metabolic gene regulation in response to insulin

ATM-mediated serine 72 phosphorylation stabilizes ribonucleotide reductase small subunit p53R2 protein against MDM2 to DNA damage

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

Impaired function of p53R2 in Rrm2b-null mice causes severe renal failure through attenuation of dNTP pools

Identification of DNA-dependent protein kinase as a cofactor for the forkhead transcription factor FoxA2

Transcriptional paradigms in mammalian mitochondrial biogenesis and function

P304

4055-4064

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scholarly article

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10.1172/JCI43721

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P433

11

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120

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Mehmet M. Altintas

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2010-10-18T00:00:00Z

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47556193

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20978358

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2964992

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