Collaborative Research Resources (Laboratory of Gene Medicine)

Medicine & Life Sciences

1. Genes 100%
2. Human Chromosomes 86%
3. Mutation 60%
4. Chromosomes, Human, Pair 21 51%
5. Leber's Hereditary Optic Atrophy 50%
6. Autoimmune Polyendocrinopathies 39%
7. trabecular meshwork-induced glucocorticoid response protein 37%
8. Down Syndrome Critical Region 36%
9. Exons 36%
10. Regulator Genes 34%
11. Complementary DNA 33%
12. Clone Cells 31%
13. Proteins 31%
14. Chromosomes 30%
15. Mitochondrial DNA 28%
16. Down Syndrome 24%
17. Codon 22%
18. Organism Cloning 20%
19. DNA 20%
20. Retinitis Pigmentosa 18%
21. Polymerase Chain Reaction 17%
22. filaggrin 16%
23. Bacillus subtilis 15%
24. Trabecular Meshwork 15%
25. Chromosomes, Human, Pair 11 15%
26. Messenger RNA 15%
27. Type 1 Autoimmune polyendocrinopathy syndrome 15%
28. Cosmids 14%
29. Introns 14%
30. Cell Line 13%
31. Human Artificial Chromosomes 13%
32. Hybrid Cells 13%
33. Autoimmune Diseases 13%
34. Gene Expression 13%
35. Primary Hypertrophic Osteoarthropathy 13%
36. Keratins 12%
37. Retina 12%
38. Bacterial Artificial Chromosomes 12%
39. Amino Acids 11%
40. Fluorescence In Situ Hybridization 11%
41. Open Angle Glaucoma 11%
42. Siblings 11%
43. Multigene Family 10%
44. Drosophila 10%
45. E coli elbB protein 9%
46. Nucleotides 9%
47. Atopic Dermatitis 9%
48. Thymus Gland 9%
49. Human Genome 9%
50. Phenotype 8%
51. Amines 8%
52. Molecular Cloning 8%
53. Phosphoric Diester Hydrolases 8%
54. Photoreceptor Connecting Cilium 8%
55. Firearms 8%
56. Optic Atrophy 8%
57. Optic Disk 8%
58. Brain 8%
59. Ligases 8%
60. betaIG-H3 protein 8%
61. human GLUL protein 7%
62. Leucine 7%
63. Oxidoreductases 7%
64. Mitogen-Activated Protein Kinases 7%
65. Amine Oxidase (Copper-Containing) 7%
66. Oguchi disease 7%
67. Holocarboxylase Synthetase Deficiency 7%
68. RNA 7%
69. Antigens 7%
70. Astrocytes 7%
71. holocarboxylase synthetases 6%
72. Hereditary Corneal Dystrophies 6%
73. Mood Disorders 6%
74. Schmid-Fraccaro syndrome 6%
75. Autosomal Recessive Deafness 6%
76. Immunoglobulin Constant Regions 6%
77. Dyrk kinase 6%
78. Immunoglobulins 6%
79. Islands 6%
80. Recombinant DNA 6%
81. Chromosomes, Human, Pair 22 6%
82. X Chromosome 6%
83. Epithelial Cells 6%
84. Monocytes 6%
85. Pedigree 6%
86. Loss of Function Mutation 6%
87. Candidiasis 6%
88. Cell Lineage 6%
89. Molecular Biology 6%
90. RNA Splice Sites 6%
91. Northern Blotting 6%
92. Genetic Markers 6%
93. Peripherins 6%
94. Glaucoma 5%
95. Retinoschisis 5%
96. Chromosomes, Human, Pair 7 5%
97. Sequence Analysis 5%
98. Thymocytes 5%
99. Mutation Rate 5%