716 results on '"Turnbull, D M"'
Search Results
2. Review: Central nervous system involvement in mitochondrial disease
3. Supplement to: Mitochondrial donation — how many women could benefit?
4. Potential compounds for the treatment of mitochondrial disease
5. Selective Impairments of Mitochondrial Respiratory Chain Activity During Aging and Ischemic Brain Damage
6. Loss of respiratory chain complex I in substantia nigra neurons from Parkinsonʼs disease patients coincides with reduced abundance of complex IV: 33
7. Mitochondrial diabetes
8. Age-related decline in mitochondrial DNA copy number in isolated human pancreatic islets
9. Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletions
10. Prevalence and progression of diabetes in mitochondrial disease
11. Somatic mitochondrial DNA mutations in adult-onset leukaemia
12. The use of PNAs and their derivatives in mitochondrial gene therapy
13. Mitochondrial DNA deletions and depletion within paraspinal muscles
14. Mitochondrial encephalomyopathies
15. A novel mitochondrial tRNAGlu (MT-TE) gene mutation associated with early-onset cataracts, retinopathy, progressive spastic paraparesis, and ataxia: a clinical, molecular and neuropathological study: O21
16. Understanding the mechanisms underpinning ischaemic-like lesion formation in mitochondrial DNA disease.: O20
17. Peptide nucleic acid delivery to human mitochondria
18. Mitochondrial DNA Mutations in Disease and Ageing
19. Mitochondrial cytopathies: clinical and experimental studies
20. Sodium Valproate : clinical and biochemical studies
21. Annotation: Mitochondrial genotype and clinical phenotype
22. Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiation
23. Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children
24. Batteries not included: diagnosis and management of mitochondrial disease
25. Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions
26. A diagnostic tattoo
27. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation
28. Disorders of the electron transport chain
29. Variant sequences of the Hexokinase II gene in familial NIDDM
30. Modelling of the expansion of normal human colonic crypts
31. Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement
32. The role of mitochondrial haplogroups in primary open angle glaucoma
33. MONOCLONAL CONVERSION IN HUMAN GASTRIC GLANDS: INSIGHTS INTO STEM CELL AND CLONAL ARCHITECTURE
34. Sequence variation in mitochondrial complex I genes: mutation or polymorphism?
35. Mitochondrial diabetes
36. Anthralin interacts with the Q pool and induces cytochrome c release, caspase 3 activation and apoptosis in human keratinocytes: 252
37. Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
38. Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets
39. No evidence of an association between the mtDNA 16184-93 polyC tract and late onset dementia
40. African Haplogroup L mtDNA Sequences Show Violations of Clock-like Evolution
41. Mutations of the mitochondrial ND1 gene as a cause of MELAS
42. Mitochondrial DNA diseases: MT6-1
43. No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation
44. Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees
45. Mitochondrial DNA deletion in “identical” twin brothers
46. The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head
47. No evidence of an association between the T16189C mtDNA variant and late onset dementia
48. Mitochondrial DNA mutations in the haematopoietic system
49. Neuronal loss in multiple sclerosis: Role of mitochondria in the axonal response to demyelination
50. Frequency of rare mitochondrial DNA mutations in patients with suspected Leberʼs hereditary optic neuropathy
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