Collaborative Research Resources (Laboratory of Gene Medicine)

Medicine & Life Sciences

1. Leber's Hereditary Optic Atrophy 100%
2. Genes 84%
3. Mutation 72%
4. Human Chromosomes 59%
5. Mitochondrial DNA 53%
6. Chromosomes 36%
7. Codon 33%
8. Retinitis Pigmentosa 31%
9. Autoimmune Polyendocrinopathies 29%
10. Down Syndrome Critical Region 29%
11. Clone Cells 29%
12. trabecular meshwork-induced glucocorticoid response protein 28%
13. Regulator Genes 26%
14. Polymerase Chain Reaction 24%
15. Chromosomes, Human, Pair 21 24%
16. DNA 22%
17. Organism Cloning 20%
18. Exons 19%
19. Firearms 19%
20. Ligases 18%
21. Nucleotides 18%
22. Hybrid Cells 17%
23. Optic Atrophy 17%
24. Siblings 17%
25. Complementary DNA 16%
26. Bacillus subtilis 16%
27. Holocarboxylase Synthetase Deficiency 16%
28. Proteins 16%
29. holocarboxylase synthetases 15%
30. Schmid-Fraccaro syndrome 15%
31. Phenotype 15%
32. Immunoglobulin Constant Regions 15%
33. Cell Line 14%
34. Human Genome 14%
35. Primary Hypertrophic Osteoarthropathy 14%
36. X Chromosome 14%
37. Pedigree 13%
38. Messenger RNA 13%
39. Candidiasis 13%
40. Molecular Biology 13%
41. Genetic Markers 13%
42. Peripherins 13%
43. Down Syndrome 13%
44. Cosmids 13%
45. Chromosomes, Human, Pair 7 13%
46. Pituitary Dwarfism 12%
47. filaggrin 12%
48. Amino Acid Sequence Homology 11%
49. Hydatidiform Mole 11%
50. Chromosomes, Human, Pair 4 11%
51. Chromosomes, Human, Pair 22 11%
52. Trabecular Meshwork 11%
53. Introns 11%
54. erbB-1 Genes 11%
55. Drosophila 11%
56. RNA Sequence Analysis 11%
57. Chromosomes, Human, Pair 11 10%
58. human MPO protein 10%
59. Breast Neoplasms 10%
60. Mitochondrial Genes 10%
61. Rhodopsin 10%
62. Immunoglobulin Genes 10%
63. Chromosomes, Human, Pair 17 10%
64. tau Proteins 10%
65. Cellular Microenvironment 10%
66. Adenine Nucleotides 10%
67. Pan troglodytes 10%
68. Retinal Degeneration 10%
69. Chromosome Mapping 10%
70. human ERBB2 protein 10%
71. Papio 10%
72. Libraries 10%
73. Mutation Rate 10%
74. Herpes Simplex 9%
75. Brain 9%
76. Optic Disk 9%
77. Southern Blotting 9%
78. Gene Deletion 9%
79. 3' Flanking Region 9%
80. Multigene Family 9%
81. Cell Lineage 8%
82. Atopic Dermatitis 8%
83. Proteasome Endopeptidase Complex 8%
84. Keratins 8%
85. Fluorescence In Situ Hybridization 8%
86. Genomics 8%
87. Cell Membrane 8%
88. Bacteriophages 8%
89. Epidermal Growth Factor 8%
90. Sequence Analysis 8%
91. Mood Disorders 8%
92. Keratinocytes 8%
93. Peroxidase 8%
94. Corneal dystrophy of Bowman layer, type 1 8%
95. Muscular Dystrophy, Limb-Girdle, Type 2I 8%
96. Growth Hormone 8%
97. Drosophila mnb protein 8%
98. Astrocytes 7%
99. DNA Restriction Enzymes 7%
100. Dendritic Cells 7%