Medicine & Life Sciences

1. Polynucleotide 5'-Hydroxyl-Kinase 100%
2. Microcephaly 97%
3. Mutation 96%
4. Genomic Instability 90%
5. Early-onset ataxia with oculomotor apraxia and hypoalbuminemia 75%
6. DNA Repair 65%
7. Phosphoric Monoester Hydrolases 65%
8. DNA Replication 59%
9. DNA Breaks 57%
10. DNA 52%
11. DNA Damage 45%
12. Seizures 37%
13. Homologous Recombination 35%
14. DNA Ligases 32%
15. Autosomal recessive 1 Spinocerebellar ataxia 31%
16. Methylation 30%
17. Phenotype 29%
18. Single-Stranded DNA Breaks 27%
19. Ataxia Telangiectasia 27%
20. Missense Mutation 25%
21. Neuropathology 24%
22. Genome 23%
23. DNA Helicases 23%
24. Dwarfism 23%
25. Poly (ADP-Ribose) Polymerase-1 23%
26. Ligation 20%
27. Nucleosomes 20%
28. RNA Polymerase II 19%
29. Double-Stranded DNA Breaks 19%
30. Histones 19%
31. Fanconi Anemia 19%
32. RecQ Helicases 17%
33. Genes 17%
34. Chromosomal Instability 17%
35. Zebrafish 17%
36. S Phase 16%
37. Strudwick syndrome 16%
38. Chromosomes 16%
39. Chromosome Breakage 16%
40. Chromatin 15%
41. Proteins 14%
42. Coxa Vara 14%
43. Inborn Genetic Diseases 12%
44. G-Quadruplexes 12%
45. Enzymes 12%
46. methylphosphate 11%
47. Agammaglobulinemia 11%
48. Nose 11%
49. Neoplasms 11%
50. Camptothecin 11%