Pages with the most revisions

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Showing below up to 100 results in range #121 to #220.

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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. Normal Mode Analysis of Glucocerebrosidase‏‎ (91 revisions)
  5. Researching SNPs (Phenylketonuria)‏‎ (91 revisions)
  6. Sequence Alignment GLA‏‎ (89 revisions)
  7. Sequence Alignments HEXA‏‎ (89 revisions)
  8. Structure-Based Mutation Analysis Hemochromatosis‏‎ (87 revisions)
  9. Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal‏‎ (86 revisions)
  10. Resource software‏‎ (84 revisions)
  11. Canavan Disease: Task 05 - Homology Modelling‏‎ (84 revisions)
  12. Maple Syrup Urine Disease 2012‏‎ (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. Gaucher Disease: Task 09 - Lab Journal‏‎ (79 revisions)
  18. Researching And Mapping Point Mutations Hemochromatosis‏‎ (79 revisions)
  19. Researching SNPs (PKU)‏‎ (79 revisions)
  20. Rs61731240‏‎ (78 revisions)
  21. Hemochromatosis 2012‏‎ (78 revisions)
  22. Fabry:Mapping point mutations‏‎ (77 revisions)
  23. Task 3 - Sequence-based predictions 2011‏‎ (77 revisions)
  24. Metachromatic leukodystrophy reference aminoacids‏‎ (77 revisions)
  25. Normal Mode Analysis Hemochromatosis‏‎ (76 revisions)
  26. Researching SNPs Gaucher Disease‏‎ (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)
  51. Task 7 (MSUD)‏‎ (58 revisions)
  52. ASPA Sequence Based Predictions‏‎ (58 revisions)
  53. AllBio Forum‏‎ (57 revisions)
  54. Task 6 (MSUD)‏‎ (56 revisions)
  55. Rs4777505‏‎ (53 revisions)
  56. Mapping mutations of ARS A‏‎ (53 revisions)
  57. Fabry:Structure-based mutation analysis‏‎ (53 revisions)
  58. Phenylketonuria 2012‏‎ (53 revisions)
  59. Sequence Alignments‏‎ (52 revisions)
  60. Task 9 - Normal Mode Analysis‏‎ (51 revisions)
  61. Molecular Dynamics Simulations‏‎ (50 revisions)
  62. Gaucher Disease: Task 08 - LabJournal‏‎ (50 revisions)
  63. Lab Journal - Task 8 (PAH)‏‎ (48 revisions)
  64. Rs1800430‏‎ (48 revisions)
  65. Rs61747114‏‎ (47 revisions)
  66. Lab journal task 4‏‎ (46 revisions)
  67. Task 6 - Protein structure prediction from evolutionary sequence variation‏‎ (46 revisions)
  68. Task 5: Researching SNPs‏‎ (46 revisions)
  69. Researching SNPs TSD Journal‏‎ (45 revisions)
  70. Molecular Dynamics Simulations (PKU)‏‎ (44 revisions)
  71. Homology modelling Gaucher Disease‏‎ (44 revisions)
  72. Molecular Dynamics Analysis GLA‏‎ (44 revisions)
  73. Reference Sequence BCKDHA‏‎ (44 revisions)
  74. Normal mode analysis GLA‏‎ (42 revisions)
  75. Gaucher Disease: Task 02 - Lab Journal‏‎ (42 revisions)
  76. Canavan Disease: Task 06 - Protein Structure Prediction‏‎ (42 revisions)
  77. Lab Journal - Task 6 (PAH)‏‎ (41 revisions)
  78. Rs121907982‏‎ (41 revisions)
  79. Fabry:Sequence-based analyses‏‎ (41 revisions)
  80. Fabry:Homology based structure predictions/Journal‏‎ (41 revisions)
  81. Task 5 - Researching SNPs‏‎ (40 revisions)
  82. Rs1054374‏‎ (39 revisions)
  83. Task 9: MSUD - Normal Mode Analysis‏‎ (39 revisions)
  84. Task 4 (MSUD)‏‎ (39 revisions)
  85. Task 9 (MSUD)‏‎ (39 revisions)
  86. Task 5 - Mapping SNPs 2011‏‎ (39 revisions)
  87. Fabry:Sequence-based mutation analysis/Journal‏‎ (38 revisions)
  88. Molecular Dynamics Simulations Analysis Gaucher Disease‏‎ (36 revisions)
  89. Task 5: Mapping point mutations‏‎ (36 revisions)
  90. Task 5 (MSUD)‏‎ (36 revisions)
  91. Lab Journal of Task 3 (MSUD)‏‎ (36 revisions)
  92. Canavan Task 8 - Molecular Dynamics Simulations‏‎ (36 revisions)
  93. Metachromatic leukodystrophy‏‎ (35 revisions)
  94. Gaucher Disease: Task 03 - Lab Journal‏‎ (34 revisions)
  95. Task 10 - Journal (PKU)‏‎ (34 revisions)
  96. Metachromatic leukodystrophy 2011‏‎ (33 revisions)
  97. Rs121907979‏‎ (33 revisions)
  98. Molecular Dynamics Simulations TSD‏‎ (33 revisions)
  99. Task alignments‏‎ (32 revisions)
  100. Rs121907968‏‎ (32 revisions)

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