MC_UU_00007/5 From Microcephaly to Genome Stability, Inflammation and Growth Regulation

Medicine & Life Sciences

1. Dwarfism 100%
2. Mutation 51%
3. Ribonucleotides 41%
4. Lowry Wood syndrome 39%
5. Microcephaly 39%
6. Phenotype 30%
7. lamin B2 30%
8. DNA Replication 30%
9. Variable Immunodeficiency syndrome 30%
10. Aicardi Syndrome 29%
11. lamin B1 28%
12. Gain of Function Mutation 28%
13. DNA Polymerase II 27%
14. Genes 27%
15. Ribonucleases 26%
16. Bloom Syndrome 26%
17. Growth 25%
18. Roifman syndrome 25%
19. Lamins 24%
20. DNA Repair 24%
21. Golgi Apparatus 24%
22. Genome 24%
23. Type 1 Microcephalic osteodysplastic primordial dwarfism 23%
24. Poly(ADP-ribose) Polymerase Inhibitors 22%
25. Severe Acute Respiratory Syndrome 22%
26. Coronavirus 21%
27. Poly(ADP-ribose) Polymerases 20%
28. Interferon Type I 20%
29. RNA Precursors 19%
30. DNA-Directed DNA Polymerase 19%
31. Proteoglycans 18%
32. Glycosylation 17%
33. INDEL Mutation 17%
34. Zebrafish 17%
35. DNA Methylation 16%
36. Mutagenesis 16%
37. Strudwick syndrome 16%
38. Histones 16%
39. Head 15%
40. Fibroblasts 15%
41. Coxa Vara 14%
42. Sister Chromatid Exchange 13%
43. Type I DNA Topoisomerase 13%
44. Proteins 13%
45. Carcinogenesis 13%
46. DNA Primase 13%
47. Catalytic DNA 12%
48. S Phase 12%
49. Decorin 12%
50. Cataract 12%
51. Catalytic Domain 11%
52. Homologous Recombination 11%
53. Agammaglobulinemia 11%
54. Adenosine Diphosphate 11%
55. Cell Proliferation 11%
56. Camptothecin 11%
57. Recombinational DNA Repair 11%
58. Tooth Root 11%
59. Inheritance Patterns 10%
60. Nucleic Acids 10%
61. Neoplasms 10%
62. Human Genome 10%
63. Eukaryota 10%
64. Cell Line 10%
65. Genomic Instability 10%
66. Recycling 9%
67. Nose 9%
68. Amino Acid Substitution 9%
69. Trinitrotoluene 9%
70. Scoliosis 9%
71. DNA 9%
72. Adenosine Triphosphate 8%
73. Osteochondrodysplasias 8%
74. Chromosome Aberrations 8%
75. Weights and Measures 8%
76. Cyclic GMP 7%
77. Mammals 7%
78. Pyle disease 7%
79. ribonuclease HI 7%
80. Extracellular Matrix 7%
81. Lamin Type B 6%
82. Reverse Transcription 6%
83. Cytogenetics 6%
84. Neutrophils 6%
85. Brachydactyly 6%
86. Genetic Variation 6%
87. Body Size 6%
88. Spine 6%
89. Progeria 6%
90. Nuclear Lamina 6%
91. Interferons 6%
92. Ribonuclease H 6%
93. Chromatin 6%
94. Lamin Type A 5%
95. Base Pairing 5%
96. Clubfoot 5%
97. Bilateral Hearing Loss 5%
98. Retroelements 5%
99. Null Lymphocytes 5%
100. Replication Origin 5%
101. Cruciform DNA 5%
102. olaparib 5%
103. Saccharomycetales 5%
104. Exome 5%