Mitochondrial dysfunction in the pathophysiology of renal diseases. - Test2 - elhamkhani - TriplyDB

Mitochondrial dysfunction in the pathophysiology of renal diseases.

Mitochondrial dysfunction in the pathophysiology of renal diseases.

http://www.wikidata.org/entity/Q38168664

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RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement New Pathogenic Concepts and Therapeutic Approaches to Oxidative Stress in Chronic Kidney Disease Transcriptomics: A Step behind the Comprehension of the Polygenic Influence on Oxidative Stress, Immune Deregulation, and Mitochondrial Dysfunction in Chronic Kidney Disease Autophagy, Innate Immunity and Tissue Repair in Acute Kidney Injury Mitochondria: a new therapeutic target in chronic kidney disease Recent advances in renal hemodynamics: insights from bench experiments and computer simulations Pathogenesis of target organ damage in hypertension: role of mitochondrial oxidative stress Loss of Renal Tubular PGC-1α Exacerbates Diet-Induced Renal Steatosis and Age-Related Urinary Sodium Excretion in Mice Mitophagy: Basic Mechanism and Potential Role in Kidney Diseases Serendipity and the discovery of novel compounds that restore mitochondrial plasticity Evaluation of molecular profiles in calcineurin inhibitor toxicity post-kidney transplant: input to chronic allograft dysfunction.The metabolic profile of a rat model of chronic kidney disease.Mitochondrial dysfunction in inherited renal disease and acute kidney injury Dietary supplementation with essential amino acids boosts the beneficial effects of rosuvastatin on mouse kidney Suppression of mitochondrial biogenesis through toll-like receptor 4-dependent mitogen-activated protein kinase kinase/extracellular signal-regulated kinase signaling in endotoxin-induced acute kidney injury.Circulatory mitochondrial DNA is a pro-inflammatory agent in maintenance hemodialysis patients.Urinary ATP Synthase Subunit β Is a Novel Biomarker of Renal Mitochondrial Dysfunction in Acute Kidney Injury.Disruption of renal tubular mitochondrial quality control by Myo-inositol oxygenase in diabetic kidney disease.Inhibition of Aerobic Glycolysis Attenuates Disease Progression in Polycystic Kidney Disease.Mitochondrial and cytoskeletal alterations are involved in the pathogenesis of hydronephrosis in ICR/Mlac-hydro mice Rotenone Attenuates Renal Injury in Aldosterone-Infused Rats by Inhibiting Oxidative Stress, Mitochondrial Dysfunction, and Inflammasome Activation.Mass Spectrometry Imaging of Kidney Tissue Sections of Rat Subjected to Unilateral Ureteral Obstruction.Farnesoid X Receptor Protects against Kidney Injury in Uninephrectomized Obese Mice.Mitochonic Acid 5 Binds Mitochondria and Ameliorates Renal Tubular and Cardiac Myocyte Damage.Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation.The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease.Mitochondrial Dysregulation Secondary to Endoplasmic Reticulum Stress in Autosomal Dominant Tubulointerstitial Kidney Disease - UMOD (ADTKD-UMOD)Development and Application of Human Renal Proximal Tubule Epithelial Cells for Assessment of Compound Toxicity.Chronic kidney disease in lithium-treated older adults: a review of epidemiology, mechanisms, and implications for the treatment of late-life mood disorders.Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations.Mitochondrial dysfunction confers albumin-induced NLRP3 inflammasome activation and renal tubular injury.The Emerging Role of Mitochondrial Targeting in Kidney Disease.Effects of antipsychotic drug administration on antioxidative defense enzymes in male rat kidney.Urinary Mitochondrial DNA Copy Number Identifies Chronic Renal Injury in Hypertensive Patients.Ameliorative effect of berberine against gentamicin-induced nephrotoxicity in rats via attenuation of oxidative stress, inflammation, apoptosis and mitochondrial dysfunction.Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study.Astragaloside IV ameliorates diabetic nephropathy by modulating the mitochondrial quality control network.Caffeic Acid Phenethyl Ester Reduces Ischemia-Induced Kidney Mitochondrial Injury in Rats.Dahuang Fuzi Decoction Attenuates Renal Fibrosis and Ameliorates Mitochondrial Dysfunction in Chronic Aristolochic Acid Nephropathy.Mitochondria in Kidney Injury: When the Power Plant Fails.

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Mitochondrial dysfunction in the pathophysiology of renal diseases.

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Mitochondrial dysfunction in the pathophysiology of renal diseases.

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Mitochondrial dysfunction in the pathophysiology of renal diseases.

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Mitochondrial dysfunction in the pathophysiology of renal diseases.

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Ruochen Che

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Songming Huang

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Yanggang Yuan

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P2860

Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells

PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

Mitochondrial outer-membrane protein FUNDC1 mediates hypoxia-induced mitophagy in mammalian cells

Parkin interacts with Ambra1 to induce mitophagy

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

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

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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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