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Mitochondrial dysfunction in inherited renal disease and acute kidney injuryLoss of Krüppel-like factor 6 cripples podocyte mitochondrial function.Spectrum of combined respiratory chain defects.Mitochondrial and cytoskeletal alterations are involved in the pathogenesis of hydronephrosis in ICR/Mlac-hydro miceCompound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case reportMutations in mitochondrial DNA causing tubulointerstitial kidney disease.Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations.Metabolism and homeostasis in the kidney: metabolic regulation through insulin signaling in the kidney.COXPD9 an Evolving Multisystem Disease; Congenital Lactic Acidosis, Sensorineural Hearing Loss, Hypertrophic Cardiomyopathy, Cirrhosis and Interstitial Nephritis.Increasing the level of peroxisome proliferator-activated receptor γ coactivator-1α in podocytes results in collapsing glomerulopathy.Pharmacologic Approaches to Improve Mitochondrial Function in AKI and CKD.Relatives in silent kidney disease screening (RISKS) study: A Chinese cohort study.Prohibitin Signaling at the Kidney Filtration Barrier.Mitochondrial Disease in Children: The Nephrologist's Perspective.Mitochondria Damage and Kidney Disease.7501 T > A mitochondrial DNA variant in a patient with glomerulosclerosis.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Renal manifestations of genetic mitochondrial disease.
@en
type
label
Renal manifestations of genetic mitochondrial disease.
@en
prefLabel
Renal manifestations of genetic mitochondrial disease.
@en
P2860
P356
P1476
Renal manifestations of genetic mitochondrial disease.
@en
P2093
John F O'Toole
P2860
P356
10.2147/IJNRD.S37887
P407
P577
2014-01-31T00:00:00Z