Robert W Taylor
Robert W Taylor
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Cited by
Cited by
Mitochondrial DNA mutations in human disease
RW Taylor, DM Turnbull
Nature Reviews Genetics 6 (5), 389-402, 2005
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
A Bender, KJ Krishnan, CM Morris, GA Taylor, AK Reeve, RH Perry, ...
Nature genetics 38 (5), 515-517, 2006
Periodontitis and diabetes: a two-way relationship
PM Preshaw, AL Alba, D Herrera, S Jepsen, A Konstantinidis, ...
Diabetologia 55 (1), 21-31, 2012
Prevalence of mitochondrial DNA disease in adults
AM Schaefer, R McFarland, EL Blakely, L He, RG Whittaker, RW Taylor, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
Mitochondrial DNA mutations and human disease
HAL Tuppen, EL Blakely, DM Turnbull, RW Taylor
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1797 (2), 113-128, 2010
Mitochondrial DNA mutations in human colonic crypt stem cells
RW Taylor, MJ Barron, GM Borthwick, A Gospel, PF Chinnery, ...
The Journal of clinical investigation 112 (9), 1351-1360, 2003
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease
GS Gorman, AM Schaefer, Y Ng, N Gomez, EL Blakely, CL Alston, ...
Annals of neurology 77 (5), 753-759, 2015
The epidemiology of pathogenic mitochondrial DNA mutations
PF Chinnery, MA Johnson, TM Wardell, R Singh‐Kler, C Hayes, ...
Annals of Neurology: Official Journal of the American Neurological …, 2000
Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease
L Craven, HA Tuppen, GD Greggains, SJ Harbottle, JL Murphy, LM Cree, ...
Nature 465 (7294), 82-85, 2010
The epidemiology of mitochondrial disorders—past, present and future
AM Schaefer, RW Taylor, DM Turnbull, PF Chinnery
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1659 (2-3), 115-120, 2004
What causes mitochondrial DNA deletions in human cells?
KJ Krishnan, AK Reeve, DC Samuels, PF Chinnery, JK Blackwood, ...
Nature genetics 40 (3), 275, 2008
Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene
R Horvath, G Hudson, G Ferrari, N Fütterer, S Ahola, E Lamantea, ...
Brain 129 (7), 1674-1684, 2006
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of …
G Hudson, P Amati-Bonneau, EL Blakely, JD Stewart, L He, AM Schaefer, ...
Brain 131 (2), 329-337, 2008
Biochemical assays of respiratory chain complex activity
DM Kirby, DR Thorburn, DM Turnbull, RW Taylor
Methods in cell biology 80, 93-119, 2007
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, PG Griffiths, GS Gorman, CM Lourenco, AF Wright, ...
Brain 133 (3), 771-786, 2010
Detection and quantification of mitochondrial DNA deletions in individual cells by real‐time PCR
L He, PF Chinnery, SE Durham, EL Blakely, TM Wardell, GM Borthwick, ...
Nucleic acids research 30 (14), e68-e68, 2002
Universal heteroplasmy of human mitochondrial DNA
BAI Payne, IJ Wilson, P Yu-Wai-Man, J Coxhead, D Deehan, R Horvath, ...
Human molecular genetics 22 (2), 384-390, 2013
Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis
FM Menzies, MR Cookson, RW Taylor, DM Turnbull, ...
Brain 125 (7), 1522-1533, 2002
Mitochondrial DNA and disease
LC Greaves, AK Reeve, RW Taylor, DM Turnbull
The Journal of pathology 226 (2), 274-286, 2012
Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids
RW Taylor, PF Chinnery, DM Turnbull, RN Lightowlers
Nature genetics 15 (2), 212-215, 1997
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