Alan J. Robinson

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 39 publications

Water droplet evaporation in varied gravity and electric fields.

Water droplet evaporation in varied gravity and electric fields.

Journal: NPJ microgravity

Published: May 18, 2023

NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms.

NDUFV1 mutations in complex I deficiency: Case reports and review of symptoms.

Journal: Genetics and molecular biology

Published: May 19, 2021

Prognostic implications of troponin T variations in inherited cardiomyopathies using systems biology.

Prognostic implications of troponin T variations in inherited cardiomyopathies using systems biology.

Journal: NPJ genomic medicine

Published: January 18, 2021

Nucleotide-binding sites can enhance N-acylation of nearby protein lysine residues.

Nucleotide-binding sites can enhance N-acylation of nearby protein lysine residues.

Journal: Scientific reports

Published: September 04, 2020

Succinate accumulation drives ischaemia-reperfusion injury during organ transplantation.

Succinate accumulation drives ischaemia-reperfusion injury during organ transplantation.

Journal: Nature metabolism

Published: May 13, 2020

Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by POLR3A mutations.

Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by POLR3A mutations.

Journal: Neurology. Genetics

Published: April 03, 2020

Metabolic effects of bezafibrate in mitochondrial disease.

Metabolic effects of bezafibrate in mitochondrial disease.

Journal: EMBO molecular medicine

Published: October 10, 2019

Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement.

Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement.

Journal: Molecular genetics and metabolism

Published: August 19, 2019

Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease.

Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 28, 2019

MitoMiner v4.0: an updated database of mitochondrial localization evidence, phenotypes and diseases.

MitoMiner v4.0: an updated database of mitochondrial localization evidence, phenotypes and diseases.

Journal: Nucleic acids research

Published: September 13, 2018

Mutations in TIMM50 compromise cell survival in OxPhos-dependent metabolic conditions.

Mutations in TIMM50 compromise cell survival in OxPhos-dependent metabolic conditions.

Journal: EMBO molecular medicine

Published: September 08, 2018

The Causes and Consequences of Nonenzymatic Protein Acylation.

The Causes and Consequences of Nonenzymatic Protein Acylation.

Journal: Trends in biochemical sciences

Published: May 04, 2018

Showing 1-12 of 39

Last Updated: 09/26/2026