共同利用研究室(遺伝子医学研究室)

Medicine & Life Sciences

1. Genes 100%
2. Human Chromosomes 80%
3. Mutation 60%
4. Leber's Hereditary Optic Atrophy 59%
5. Chromosomes, Human, Pair 21 47%
6. trabecular meshwork-induced glucocorticoid response protein 44%
7. Exons 42%
8. Down Syndrome Critical Region 40%
9. Complementary DNA 38%
10. Autoimmune Polyendocrinopathies 37%
11. Proteins 33%
12. Mitochondrial DNA 33%
13. Clone Cells 32%
14. Regulator Genes 28%
15. Chromosomes 27%
16. Organism Cloning 23%
17. Codon 22%
18. Retinitis Pigmentosa 21%
19. Down Syndrome 21%
20. DNA 20%
21. Polymerase Chain Reaction 19%
22. Trabecular Meshwork 18%
23. Cosmids 17%
24. Messenger RNA 17%
25. Introns 17%
26. Gene Expression 15%
27. Keratins 15%
28. Retina 14%
29. Amino Acids 14%
30. Bacillus subtilis 13%
31. Autoimmune Diseases 13%
32. Cell Line 13%
33. Open Angle Glaucoma 13%
34. Bacterial Artificial Chromosomes 13%
35. Siblings 13%
36. filaggrin 12%
37. Multigene Family 12%
38. Drosophila 12%
39. Chromosomes, Human, Pair 11 11%
40. E coli elbB protein 11%
41. Nucleotides 11%
42. Human Genome 10%
43. Amines 10%
44. Molecular Cloning 10%
45. Phosphoric Diester Hydrolases 10%
46. Type 1 Autoimmune polyendocrinopathy syndrome 10%
47. Photoreceptor Connecting Cilium 10%
48. Firearms 10%
49. Optic Atrophy 10%
50. Optic Disk 9%
51. Brain 9%
52. Ligases 9%
53. Atopic Dermatitis 9%
54. human GLUL protein 9%
55. Hybrid Cells 9%
56. Leucine 9%
57. Fluorescence In Situ Hybridization 9%
58. Oxidoreductases 9%
59. Mitogen-Activated Protein Kinases 8%
60. Phenotype 8%
61. Amine Oxidase (Copper-Containing) 8%
62. Oguchi disease 8%
63. Holocarboxylase Synthetase Deficiency 8%
64. Astrocytes 8%
65. holocarboxylase synthetases 8%
66. Mood Disorders 8%
67. Schmid-Fraccaro syndrome 8%
68. Autosomal Recessive Deafness 8%
69. Immunoglobulin Constant Regions 8%
70. Dyrk kinase 7%
71. Immunoglobulins 7%
72. Islands 7%
73. Human Artificial Chromosomes 7%
74. Recombinant DNA 7%
75. Chromosomes, Human, Pair 22 7%
76. Primary Hypertrophic Osteoarthropathy 7%
77. X Chromosome 7%
78. Monocytes 7%
79. Pedigree 7%
80. Candidiasis 7%
81. Cell Lineage 7%
82. Molecular Biology 7%
83. RNA Splice Sites 7%
84. Northern Blotting 7%
85. Genetic Markers 7%
86. Peripherins 7%
87. Glaucoma 7%
88. Retinoschisis 6%
89. Chromosomes, Human, Pair 7 6%
90. Sequence Analysis 6%
91. Mutation Rate 6%
92. Pituitary Dwarfism 6%
93. Rhodopsin 6%
94. Nuclear Localization Signals 6%
95. CREB-Binding Protein 6%
96. Chromosomes, Human, Pair 17 6%
97. Alternative Splicing 6%
98. Synteny 6%
99. Autosomal Recessive 10 Deafness 6%