蔡 金吾

Medicine & Life Sciences

1. Lissencephaly 100%
2. Neurons 97%
3. Centrosome 80%
4. Neural Stem Cells 73%
5. Microtubules 67%
6. human PRRT2 protein 62%
7. Brain 61%
8. Warburg Sjo Fledelius syndrome 61%
9. Cilia 58%
10. Cytoplasmic Dyneins 54%
11. RNA Interference 51%
12. Mutation 48%
13. Cell Movement 47%
14. Hedgehog Proteins 45%
15. Morphogenesis 44%
16. Electroporation 43%
17. Genes 42%
18. Dyneins 41%
19. Growth Cones 40%
20. Neuroglia 40%
21. Neocortex 40%
22. Human Cep290 protein 38%
23. Familial paroxysmal dystonia 38%
24. Proteins 38%
25. Myosin Type II 38%
26. Stem Cells 37%
27. X-Linked Subcortical Band Heterotopia 36%
28. Amyloidosis 35%
29. Missense Mutation 35%
30. Goldberg-Shprintzen megacolon syndrome 34%
31. Kinesin 33%
32. Classical Lissencephalies and Subcortical Band Heterotopias 33%
33. Microscopy 33%
34. NAD 32%
35. Type 2B Charcot-Marie-Tooth disease 31%
36. Mutagenesis 31%
37. Cell Cycle 31%
38. Autophagy 30%
39. Neurogenesis 30%
40. Contactin 1 29%
41. Dendritic Spines 29%
42. Mutant Proteins 28%
43. Cerebral Cortex 27%
44. EphA1 Receptor 27%
45. Amyloidosis, Hereditary, Transthyretin-Related 27%
46. 1-Methyl-4-phenylpyridinium 26%
47. HSC70 Heat-Shock Proteins 25%
48. Lateral Ventricles 25%
49. Vestibular Hair Cells 24%
50. Prealbumin 24%