Pages with the most revisions

From Bioinformatikpedia

Showing below up to 50 results in range #121 to #170.

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  1. Predicting the Effect of SNPs (PKU)‏‎ (95 revisions)
  2. Task 9: Structure-based mutation analysis‏‎ (92 revisions)
  3. Maple syrup urine disease 2011‏‎ (92 revisions)
  4. Researching SNPs (Phenylketonuria)‏‎ (91 revisions)
  5. Normal Mode Analysis of Glucocerebrosidase‏‎ (91 revisions)
  6. Sequence Alignments HEXA‏‎ (89 revisions)
  7. Sequence Alignment GLA‏‎ (89 revisions)
  8. Structure-Based Mutation Analysis Hemochromatosis‏‎ (87 revisions)
  9. Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal‏‎ (86 revisions)
  10. Maple Syrup Urine Disease 2012‏‎ (84 revisions)
  11. Canavan Disease: Task 05 - Homology Modelling‏‎ (84 revisions)
  12. Resource software‏‎ (84 revisions)
  13. Task 6: Protein structure prediction from evolutionary sequence variation‏‎ (83 revisions)
  14. Normal Mode Analysis of ARSA‏‎ (82 revisions)
  15. Fabry:Normal mode analysis‏‎ (81 revisions)
  16. Fabry Disease 2011‏‎ (81 revisions)
  17. Researching And Mapping Point Mutations Hemochromatosis‏‎ (79 revisions)
  18. Researching SNPs (PKU)‏‎ (79 revisions)
  19. Gaucher Disease: Task 09 - Lab Journal‏‎ (79 revisions)
  20. Rs61731240‏‎ (78 revisions)
  21. Hemochromatosis 2012‏‎ (78 revisions)
  22. Fabry:Mapping point mutations‏‎ (77 revisions)
  23. Metachromatic leukodystrophy reference aminoacids‏‎ (77 revisions)
  24. Task 3 - Sequence-based predictions 2011‏‎ (77 revisions)
  25. Researching SNPs Gaucher Disease‏‎ (76 revisions)
  26. Normal Mode Analysis Hemochromatosis‏‎ (76 revisions)
  27. Task 4: Homology-based structure prediction‏‎ (75 revisions)
  28. Phenylketonuria‏‎ (73 revisions)
  29. Task 2 (MSUD)‏‎ (73 revisions)
  30. Structure-based mutation analysis ARSA‏‎ (72 revisions)
  31. Protein Structure and Function Analysis (SS 2013)‏‎ (72 revisions)
  32. ARS A Sequence alignments‏‎ (72 revisions)
  33. Maple Syrup Urine Disease‏‎ (71 revisions)
  34. Fabry:Sequence alignments (sequence searches and multiple alignments)‏‎ (70 revisions)
  35. Sequence Alignments BCKDHA‏‎ (70 revisions)
  36. Fabry:Sequence-based mutation analysis‏‎ (70 revisions)
  37. Normal Mode Analysis (PKU)‏‎ (69 revisions)
  38. Task 2: Multiple Sequence Alignment‏‎ (68 revisions)
  39. Fabry:Sequence alignments (sequence searches and multiple alignments):Results‏‎ (68 revisions)
  40. Structure-based mutation analysis HEXA‏‎ (68 revisions)
  41. Normal mode analysis Gaucher Disease‏‎ (67 revisions)
  42. Protein Structure and Function Analysis (version: SS 2011)‏‎ (66 revisions)
  43. Gaucher Disease - Task 06 - Lab Journal‏‎ (65 revisions)
  44. Lab journal task 8‏‎ (64 revisions)
  45. Gaucher Disease: Task 04 - Lab Journal‏‎ (64 revisions)
  46. Structure-based mutation analysis Gaucher Disease‏‎ (64 revisions)
  47. Canavan Disease: Task 04 - Structural Alignments‏‎ (64 revisions)
  48. Tay-Sachs Disease 2011‏‎ (62 revisions)
  49. Rs121907974‏‎ (61 revisions)
  50. Glucocerebrosidase mapping snps‏‎ (59 revisions)

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