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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

Mitochondrial dysfunction in inherited renal disease and acute kidney injury

http://www.wikidata.org/entity/Q33793389

about

The COQ2 genotype predicts the severity of coenzyme Q10 deficiency mito-QC illuminates mitophagy and mitochondrial architecture in vivo.Renal manifestations of primary mitochondrial disorders.High glucose repatterns human podocyte energy metabolism during differentiation and diabetic nephropathy.Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway.The Value of Coenzyme Q10 Determination in Mitochondrial Patients.Dynamin-Related Protein 1 Deficiency Promotes Recovery from AKI.Pharmacologic Approaches to Improve Mitochondrial Function in AKI and CKD.Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function.Increased levels of mitochondrial DNA copy number in patients with vitiligo.Hepatocyte Nuclear Factor-1β Controls Mitochondrial Respiration in Renal Tubular Cells.Renal Tubular Mitochondrial Abnormalities in Complex II/III Respiratory Chain Deficiency.PGC1α in the kidney.Mitochondrial energetics in the kidney.Mitochondria Damage and Kidney Disease.Renal scattered tubular-like cells confer protective effects in the stenotic murine kidney mediated by release of extracellular vesicles.Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney.Urinary mitochondrial DNA level is an indicator of intra-renal mitochondrial depletion and renal scarring in diabetic nephropathy.The importance of the thick ascending limb of Henle’s loop in renal physiology and pathophysiology.P53/Drp1-dependent mitochondrial fission mediates aldosterone-induced podocyte injury and mitochondrial dysfunction.PPARγ-Coactivator-1α, Nicotinamide Adenine Dinucleotide and Renal Stress Resistance.Mitochondrial diseases caused by mtDNA mutations: a mini-review

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

http://www.wikidata.org/entity/Q33793389

description

2016 nî lūn-bûn

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2016 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2016 թվականի հունվարին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Nature Reviews Nephrology

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Mitochondrial dysfunction in inherited renal disease and acute kidney injury

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Francesco Emma

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Leonardo Salviati

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Samir M Parikh

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P2860

The genome sequence of Rickettsia prowazekii and the origin of mitochondria

A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression

Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant

Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy

A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease

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nrneph.2015.214

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267-280

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scholarly article

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10.1038/NRNEPH.2015.214

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5

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Giovanni Montini

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1022370035

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26804019

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5469549

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