J. Carver

Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations

Matthew J. Daniels, N. Ashley, M. Zeviani, 2017, Neurology.

Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children

Iain G. Johnston, I. Johnston, D. Wells, 2016, Biochemical Society transactions.

Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation

Matthew J. Daniels, T. Enver, F. Iborra, 2018, Front. Cell Dev. Biol..

Clinical/scientific Notes Supplemental Data at Neurology.org the M.13051g.a Mitochondrial Dna Mutation Results in Variable Neurology and Activated Mitophagy We Also Have Additional Data Supporting the Same Effect in Fibroblasts from Other Classical Mitochondrial

Robert W. Taylor, S. Hickman, P. Yu-Wai-Man, 2022 .

A novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNA.

Iain G. Johnston, I. Johnston, C. Sue, 2015, Pharmacological research.

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

Robert W. Taylor, N. Ashley, A. Seller, 2013, European Journal of Human Genetics.

De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity

M. Simpson, S. Jayawant, J. Poulton, 2018, Neurology: Genetics.