712 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. Systematic review of cognitive deficits in adult mitochondrial disease
20. Mitochondrial cytopathies: clinical and experimental studies
21. Sodium Valproate : clinical and biochemical studies
22. Annotation: Mitochondrial genotype and clinical phenotype
23. Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiation
24. Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children
25. Batteries not included: diagnosis and management of mitochondrial disease
26. Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions
27. A diagnostic tattoo
28. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation
29. Disorders of the electron transport chain
30. Variant sequences of the Hexokinase II gene in familial NIDDM
31. Modelling of the expansion of normal human colonic crypts
32. Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement
33. The role of mitochondrial haplogroups in primary open angle glaucoma
34. MONOCLONAL CONVERSION IN HUMAN GASTRIC GLANDS: INSIGHTS INTO STEM CELL AND CLONAL ARCHITECTURE
35. Sequence variation in mitochondrial complex I genes: mutation or polymorphism?
36. Mitochondrial diabetes
37. Anthralin interacts with the Q pool and induces cytochrome c release, caspase 3 activation and apoptosis in human keratinocytes: 252
38. Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
39. Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets
40. No evidence of an association between the mtDNA 16184-93 polyC tract and late onset dementia
41. African Haplogroup L mtDNA Sequences Show Violations of Clock-like Evolution
42. Mutations of the mitochondrial ND1 gene as a cause of MELAS
43. Mitochondrial DNA diseases: MT6-1
44. No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation
45. Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees
46. Mitochondrial DNA deletion in “identical” twin brothers
47. The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head
48. No evidence of an association between the T16189C mtDNA variant and late onset dementia
49. Mitochondrial DNA mutations in the haematopoietic system
50. Neuronal loss in multiple sclerosis: Role of mitochondria in the axonal response to demyelination
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.