Doug M. Turnbull

Framlington Place
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 155 publications

Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA Variant.

Identification of Nuclear Genetic Loci Linked to Clinical Features of the m.3243A>G Mitochondrial DNA Variant.

Journal: Neurology. Genetics

Published: November 10, 2025

Quantifying variability of mitochondrial markers in m3243A > G myopathy.

Quantifying variability of mitochondrial markers in m3243A > G myopathy.

Journal: Scientific reports

Published: September 04, 2025

Variant load of mitochondrial DNA in single human mesenchymal stem cells.

Variant load of mitochondrial DNA in single human mesenchymal stem cells.

Journal: Scientific reports

Published: July 23, 2024

Mapping mitochondrial morphology and function: COX-SBFSEM reveals patterns in mitochondrial disease.

Mapping mitochondrial morphology and function: COX-SBFSEM reveals patterns in mitochondrial disease.

Journal: Communications biology

Published: February 27, 2024

A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disorders.

A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disorders.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: November 21, 2023

Uncoupling of energy production.

Uncoupling of energy production.

Journal: Cell metabolism

Published: December 08, 2022

A novel mouse model of mitochondrial disease exhibits juvenile-onset severe neurological impairment due to parvalbumin cell mitochondrial dysfunction.

A novel mouse model of mitochondrial disease exhibits juvenile-onset severe neurological impairment due to parvalbumin cell mitochondrial dysfunction.

Journal: Communications biology

Published: October 14, 2022

Dynamics of the most common pathogenic mtDNA variant m.3243A > G demonstrate frequency-dependency in blood and positive selection in the germline.

Dynamics of the most common pathogenic mtDNA variant m.3243A > G demonstrate frequency-dependency in blood and positive selection in the germline.

Journal: Human molecular genetics

Published: May 17, 2022

Mitochondrial complex I subunit deficiency promotes pancreatic α-cell proliferation.

Mitochondrial complex I subunit deficiency promotes pancreatic α-cell proliferation.

Journal: Molecular metabolism

Published: March 01, 2022

Author Correction: Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis.

Author Correction: Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis.

Journal: Nature cancer

Published: February 05, 2022

A subcellular cookie cutter for spatial genomics in human tissue.

A subcellular cookie cutter for spatial genomics in human tissue.

Journal: Analytical and bioanalytical chemistry

Published: November 26, 2021

100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.

100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.

Journal: The New England journal of medicine

Published: November 10, 2021

Showing 1-12 of 155

Last Updated: 09/26/2026