Conrad Weihl

Medicine & Life Sciences

1. Muscular Diseases 100%
2. Valosin Containing Protein 80%
3. Mutation 59%
4. Autophagy 55%
5. Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia 48%
6. Inclusion Bodies 46%
7. Limb-Girdle Muscular Dystrophies 44%
8. Muscles 43%
9. Inclusion Body Myositis 42%
10. Osteitis Deformans 38%
11. Proteins 30%
12. Skeletal Muscle 28%
13. Protein Aggregates 26%
14. Pathology 23%
15. Frontotemporal Dementia 22%
16. Autophagosomes 20%
17. Distal Myopathies 19%
18. Ubiquitin 18%
19. Nonaka type Distal myopathy 18%
20. Myositis 16%
21. Vacuoles 15%
22. Amyotrophic Lateral Sclerosis 14%
23. Frontotemporal Dementia With Motor Neuron Disease 14%
24. Muscular Dystrophies 14%
25. Muscular Dystrophy, Limb-Girdle, Type 1D 14%
26. Genes 13%
27. Ubiquitinated Proteins 13%
28. Presenilin-1 12%
29. Sirolimus 12%
30. Vacuolar myopathy 11%
31. Dementia 11%
32. Prions 11%
33. polyglutamine 10%
34. Ubiquitination 10%
35. Phenotype 9%
36. Mitophagy 9%
37. Proteolysis 9%
38. ATPases Associated with Diverse Cellular Activities 9%
39. Lysosomes 9%
40. Macroautophagy 8%
41. High-Protein Diet 8%
42. Crystallins 8%
43. Muscular Atrophy 8%
44. DNA-Binding Proteins 8%
45. Adenosine Triphosphatases 8%
46. Exome 8%
47. Colchicine 8%
48. Missense Mutation 7%
49. Motor Neurons 7%
50. Proteostasis 7%