Milena Pinto

Medicine & Life Sciences

1. Mitochondrial DNA 100%
2. Parkinson Disease 53%
3. Tumor Necrosis Factor Receptor-Associated Peptides and Proteins 36%
4. RNA, Transfer, Ala 28%
5. Dopaminergic Neurons 28%
6. Mutation 27%
7. Oxidative Phosphorylation 27%
8. Mitochondrial Diseases 26%
9. TNF Receptor-Associated Factor 6 23%
10. DNA Damage 22%
11. Mitochondrial Genome 21%
12. Phenotype 21%
13. Neurons 20%
14. Neurodegenerative Diseases 20%
15. Ubiquitination 17%
16. Brain 17%
17. Mitochondria 15%
18. Alzheimer Disease 14%
19. Substantia Nigra 13%
20. Reactive Oxygen Species 13%
21. CTGCAG-specific type II deoxyribonucleases 12%
22. Huntington Disease 12%
23. Lewy Bodies 12%
24. Oligodendroglia 11%
25. Huntingtin Protein 11%
26. Transcription Activator-Like Effector Nucleases 11%
27. Friedreich Ataxia 11%
28. Missense Mutation 11%
29. Endonucleases 10%
30. Prosencephalon 10%
31. Glycolysis 10%
32. Corpus Striatum 10%
33. Pioglitazone 10%
34. Globins 10%
35. alpha-Synuclein 9%
36. Inflammation 9%
37. Amyloid Plaques 8%
38. Genes 8%
39. Cytochromes c 8%
40. Metformin 8%
41. Demyelinating Diseases 8%
42. 3' Untranslated Regions 8%
43. Mesenchymal Stem Cells 8%
44. Mitophagy 8%
45. Gold 8%
46. Neuroglia 8%
47. Apoptosis 7%
48. Mitochondrial encephalopathy 7%
49. Intravenous Administration 7%