Coenzyme Q Cytochrome C Reductase Deficiency Latest Advances

Find the Latest Research About Coenzyme Q Cytochrome C Reductase Deficiency

Last Updated: 04/28/2026

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Found 137 publications

Activation of the protective arm of renin-angiotensin system enhances mitochondrial turnover improving respiration and decreasing integrated stress response in a human Complex III deficiency model.

Activation of the protective arm of renin-angiotensin system enhances mitochondrial turnover improving respiration and decreasing integrated stress response in a human Complex III deficiency model.

Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026

Reversible Metabolic and Liver Disease in Complex III Deficiency: Novel Variants Expand the Reported UQCRC2-Associated Phenotype.

Reversible Metabolic and Liver Disease in Complex III Deficiency: Novel Variants Expand the Reported UQCRC2-Associated Phenotype.

Journal: Cells
Published: December 23, 2025

Restoration of Interaction Between Fatty Acid Oxidation and Electron Transport Chain Proteins In Vitro by Addition of Recombinant VLCAD.

Restoration of Interaction Between Fatty Acid Oxidation and Electron Transport Chain Proteins In Vitro by Addition of Recombinant VLCAD.

Journal: Biomedicines
Published: November 28, 2025

TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.

TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.

Journal: Molecular genetics and metabolism
Published: October 07, 2025

UQCRC1 deficiency impairs mitophagy via PINK1-dependent mechanisms in Parkinson's disease.

UQCRC1 deficiency impairs mitophagy via PINK1-dependent mechanisms in Parkinson's disease.

Journal: NPJ Parkinson's disease
Published: April 28, 2025

Leber's hereditary optic neuropathy - current status of idebenone and gene replacement therapies.

Leber's hereditary optic neuropathy - current status of idebenone and gene replacement therapies.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
Published: February 18, 2025

A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III Deficiency.

A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III Deficiency.

Journal: American journal of medical genetics. Part A
Published: October 29, 2024

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts.

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts.

Journal: Rare (Amsterdam, Netherlands)
Published: October 18, 2024

Spermidine toxicity in Saccharomyces cerevisiae due to mitochondrial complex III deficiency.

Spermidine toxicity in Saccharomyces cerevisiae due to mitochondrial complex III deficiency.

Journal: Biogerontology
Published: September 25, 2024

Pathological variants in nuclear genes causing mitochondrial complex III deficiency: An update.

Pathological variants in nuclear genes causing mitochondrial complex III deficiency: An update.

Journal: Journal of inherited metabolic disease
Published: January 17, 2024

Cavitating leukodystrophy in a case of mitochondrial complex III deficiency due to LYRM7 mutation.

Cavitating leukodystrophy in a case of mitochondrial complex III deficiency due to LYRM7 mutation.

Journal: Acta neurologica Belgica
Published: November 10, 2023

MYC-an emerging player in mitochondrial diseases.

MYC-an emerging player in mitochondrial diseases.

Journal: Frontiers in cell and developmental biology
Published: July 12, 2023
Showing 1-12 of 137

Last Updated: 04/28/2026