221 results on '"Turnbull, Douglass M."'
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2. RRM2B-Related Mitochondrial Disease
3. Detection of Mitochondrial DNA Variation in Human Cells
4. Interventions for promoting physical activity in people with neuromuscular disease
5. METABOLIC MYOPATHIES (INCLUDING MITOCHONDRIAL DISEASES)
6. Biochemical Assays of Respiratory Chain Complex Activity
7. Chapter 7 Current and Future Prospects for the Treatment of Mitochondrial Disorders
8. Chapter 5 Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues
9. Mitochondrial involvement in the ageing process. Facts and controversies
10. Assessing mitochondrial heteroplasmy using next generation sequencing: A note of caution
11. Identification of Mitochondrial Dysfunction at Coupling Site II
12. Study of Skeletal Muscle Mitochondrial Dysfunction
13. Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia
14. Impact of Age-Related Mitochondrial Dysfunction and Exercise on Intestinal Microbiota Composition
15. Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy
16. Naked mole-rats maintain healthy skeletal muscle and Complex IV mitochondrial enzyme function into old age
17. Mitochondrial diseases
18. Genetic and biochemical intricacy shapes mitochondrial cytopathies
19. Erratum: Corrigendum: Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease
20. Reply
21. Analysis of primary visual cortex in dementia with Lewy bodies indicates GABAergic involvement associated with recurrent complex visual hallucinations
22. Fatty acid oxidation is required for the respiration and proliferation of malignant glioma cells
23. Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease
24. Neuronal oscillations: A physiological correlate for targeting mitochondrial dysfunction in neurodegenerative diseases?
25. Epilepsy in adults with mitochondrial disease: A cohort study
26. The prevalence of mitochondrial disease in the adult population
27. Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults
28. Perceived fatigue is highly prevalent and debilitating in patients with mitochondrial disease
29. Neural Stem Cells in the Adult Subventricular Zone Oxidize Fatty Acids to Produce Energy and Support Neurogenic Activity
30. Preliminary Evaluation of Clinician Rated Outcome Measures in Mitochondrial Disease
31. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease
32. Concise Reviews: Assisted Reproductive Technologies to Prevent Transmission of Mitochondrial DNA Disease
33. Clonal Expansion of Secondary Mitochondrial DNA Deletions Associated With Spinocerebellar Ataxia Type 28
34. Analysis of Mitochondrial DNA Mutations: Point Mutations
35. Clinical Diagnosis of Oxidative Phosphorylation Disorders
36. The Use of PNAs and Their Derivatives in Mitochondrial Gene Therapy
37. Analysis of Mitochondrial DNA Mutations: Deletions
38. Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing
39. Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies
40. Similar patterns of clonally expanded somatic mtDNA mutations in the colon of heterozygous mtDNA mutator mice and ageing humans
41. Distal weakness with respiratory insufficiency caused by the m.8344A>G “MERRF” mutation
42. The Challenges of Mitochondrial Replacement
43. Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
44. Human stem cell aging: do mitochondrial DNA mutations have a causal role?
45. Therapeutic potential of somatic cell nuclear transfer for degenerative disease caused by mitochondrial DNA mutations
46. Mitochondrial Abnormality Associates with Type-Specific Neuronal Loss and Cell Morphology Changes in the Pedunculopontine Nucleus in Parkinson Disease
47. Acute exercise remodels mitochondrial membrane interactions in mouse skeletal muscle
48. Chronic progressive external ophthalmoplegia — Disease mechanisms and clinical outcome measures
49. Discrete gait characteristics are associated with m.3243A>G and m.8344A>G variants of mitochondrial disease and its pathological consequences
50. Endocrine disorders in mitochondrial disease
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