about
Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA diseaseMulti-system neurological disease is common in patients with OPA1 mutationsMitochondrial DNA disease-molecular insights and potential routes to a cureAgeing and Parkinson's disease: why is advancing age the biggest risk factor?Development of passive CLARITY and immunofluorescent labelling of multiple proteins in human cerebellum: understanding mechanisms of neurodegeneration in mitochondrial disease.Analysis of primary visual cortex in dementia with Lewy bodies indicates GABAergic involvement associated with recurrent complex visual hallucinationsAge-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic cryptsPerceived fatigue is highly prevalent and debilitating in patients with mitochondrial diseaseDysferlin mutations and mitochondrial dysfunctionDissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle.Increased mitochondrial content in remyelinated axons: implications for multiple sclerosis.Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease.Habitual physical activity in mitochondrial disease.Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutationMitochondrial DNA deletions and depletion within paraspinal musclesQuantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue.The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO.Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death.Respiratory chain deficiency in aged spinal motor neurons.Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts.In situ lineage tracking of human prostatic epithelial stem cell fate reveals a common clonal origin for basal and luminal cells.Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'.Similar patterns of clonally expanded somatic mtDNA mutations in the colon of heterozygous mtDNA mutator mice and ageing humansClonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing.Mitochondrial abnormality associates with type-specific neuronal loss and cell morphology changes in the pedunculopontine nucleus in Parkinson diseaseA national perspective on prenatal testing for mitochondrial diseaseMitochondrial dysfunction and lipid accumulation in the human diaphragm during mechanical ventilation.Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations.Human stem cell aging: do mitochondrial DNA mutations have a causal role?The challenges of mitochondrial replacement.Concise reviews: Assisted reproductive technologies to prevent transmission of mitochondrial DNA diseaseNeural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic ActivityMitochondrial donation--how many women could benefit?Potential compounds for the treatment of mitochondrial disease.Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.Characterization of mtDNA variation in a cohort of South African paediatric patients with mitochondrial disease.Applying the Airbrakes: Treating Mitochondrial Disease with Hypoxia.Microangiopathy in the cerebellum of patients with mitochondrial DNA diseaseCell-permeable succinate prodrugs bypass mitochondrial complex I deficiencyA novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-8878-9901
@en
name
Doug M Turnbull
@ast
Doug M Turnbull
@en
Doug M Turnbull
@nl
type
label
Doug M Turnbull
@ast
Doug M Turnbull
@en
Doug M Turnbull
@nl
altLabel
Doug Turnbull
@en
prefLabel
Doug M Turnbull
@ast
Doug M Turnbull
@en
Doug M Turnbull
@nl
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P106
P31
P496
0000-0002-8878-9901