Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mitochondrial DNA mutations in renal disease: an overview.

Pediatric nephrology (Berlin, Germany) - 1 Jan 2021

Govers Larissa P, Toka Hakan R, Hariri Ali, Walsh Stephen B, Bockenhauer Detlef

Abstract excerpt

Kidneys have a high energy demand to facilitate the reabsorption of the glomerular filtrate. For this reason, renal cells have a high density of mitochondria. Mitochondrial cytopathies can be the result of a mutation in both mitochondrial and nuclear DNA. Mitochondrial dysfunction can lead to a variety of renal manifestations. Examples of tubular manifestations are renal Fanconi Syndrome, which is often found in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA, Mitochondrial
Share to Kearns-Sayre Syndrome
Share to Metabolism and Genetic Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mitochondria

Share to Mitochondrial Function and Pathology

Share to Mitochondrial Myopathies

Share to Mutation

Share to Nephritis, Interstitial

Source

Open in PubMed Open full text

Identifiers

PMID: 31925537
DOI: 10.1007/s00467-019-04404-6
PMCID: PMC7701126

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial DNA mutations in renal disease: an overview.PMID 31925537Read ↗

Renal function and mitochondrial cytopathy (MC): more questions than answers?Semantic proximity Read ↗

Mitochondrial dysfunction in inherited renal disease and acute kidney injury.Semantic proximity Read ↗

Renal Phenotype in Mitochondrial Diseases: A Multicenter StudySemantic proximity Read ↗

Mitochondrial cytopathies and the kidney.Semantic proximity Read ↗

Renal failure from mitochondrial cytopathies.Semantic proximity Read ↗

The Not So ‘Mighty Chondrion’: Emergence of Renal Diseases due to Mitochondrial DysfunctionSemantic proximity Read ↗

Renal disease and mitochondrial genetics.Semantic proximity Read ↗

Mitochondrial genome mutations and kidney disease.Semantic proximity Read ↗

Roles of Mitochondrial DNA Damage in Kidney Diseases: A New BiomarkerSemantic proximity Read ↗

Importance of urinary mitochondrial DNA in diagnosis and prognosis of kidney diseasesSemantic proximity Read ↗

Mitochondrial dysfunction in the pathophysiology of renal diseasesSemantic proximity Read ↗

Renal mitochondrial injury in the pathogenesis of CKD: mtDNA and mitomiRsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.