32 results on '"Tarnopolsky, Mark"'
Search Results
2. Mitochondrial neuropathy and neurogenic features in mitochondrial myopathy
3. A mitochondrial disorder with ptosis and exercise intolerance without ophthalmoparesis secondary to m.5865 T > C variant
4. Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort
5. Myasthenia graves-like symptoms associated with rare mitochondrial mutation (m.5728T>C)
6. CPEO – Like mitochondrial myopathy associated with m.8340G>A mutation
7. Complete elimination of a pathogenic homoplasmic mtDNA mutation in one generation
8. Clinical and demographic features of chronic progressive external ophthalmoplegia in a large adult-onset cohort
9. Two novel mitochondrial tRNA mutations, A7495G (tRNASer(UCN)) and C5577T (tRNATrp), are associated with seizures and cardiac dysfunction
10. Meteorin-like and irisin — Effective therapies to treat diet-induced obesity and glucose intolerance?
11. Rotenone-elevated mitochondrial respiration with inflammatory myopathies indicates a secondary impairment to NADH: Ubiquinone oxidoreductase that attenuates succinate dehydrogenase activity
12. EXERsomes induce systemic mitochondrial rejuvenation and ameliorate diet-induced obesity: Thinking inside the box for a change!
13. Mitochondrial genome sequencing: A valuable addition to whole exome sequencing for the molecular diagnosis of mitochondrial disorders
14. Whole exome sequencing and whole mitochondrial genome sequencing for molecular diagnosis of mitochondrial disorders: Lessons from 865 Cases
15. Dysfunctional mitochondria? Let's make more… exercise in a bottle
16. Polymerase gamma mutator mice rely on increased glycolytic flux for energy production
17. Practice patterns of mitochondrial disease physicians in North America. Part 1: Diagnostic and clinical challenges
18. Whole mitochondrial genome amplification and next generation sequencing for the diagnosis of mitochondrial disorders: Yield of 613 cases
19. Resveratrol improves mitochondrial functions in respiratory chain-deficient cells
20. Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and management
21. The effects of BDNF supplementation on polymerase gamma (POLG) 1 mutator mice
22. Comprehensive analysis of entire mitochondrial genome by long-range PCR and next generation sequencing for the diagnosis of mitochondrial disorders: Yield of 216 cases
23. The psychiatric manifestations of mitochondrial cytopathies: A clinical and MR spectroscopy investigation
24. Endurance exercise reduces mitochondrial DNA random point mutations and reverses the premature aging transcriptome in PolG mutator mouse: I believe in miracle!
25. Insights in the pathogenesis of impaired glucose tolerance in patients with mitochondrial cytopathy
26. 121 Mitochondrial aging countermeasure—Endurance exercise confers complete phenotypic protection in PolG mutator mouse
27. 22. Akt/mTOR/PGC-1αswitch – energizing mitochondrial rejuvenescence for two billion years
28. 81 Differential gene expression response to point mutations, A3243G and A3260G, in mitochondrial DNA of human skeletal muscle
29. 83 Increased risk of type 2 diabetes in patients with mitochondrial cytopathy and the relationship with obesity
30. 84 Mitochondrial gene shifting and aging: Resistance is not futile
31. Exercise testing as a diagnostic entity in mitochondrial myopathies
32. Two novel mitochondrial tRNA mutations, A7495G (tRNA Ser(UCN) ) and C5577T (tRNA Trp ), are associated with seizures and cardiac dysfunction.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.