Pages with the most revisions

From Bioinformatikpedia

Showing below up to 500 results in range #1 to #500.

View (previous 500 | next 500) (20 | 50 | 100 | 250 | 500)

  1. Molecular Dynamics Analysis BCKDHA‏‎ (584 revisions)
  2. Sequence-based predictions (Phenylketonuria)‏‎ (500 revisions)
  3. Gaucher Disease: Task 03 - Sequence-based predictions‏‎ (471 revisions)
  4. Homology based structure predictions BCKDHA‏‎ (413 revisions)
  5. Secondary Structure Prediction BCKDHA‏‎ (408 revisions)
  6. Canavan Task 6 - Sequence-based mutation analysis‏‎ (377 revisions)
  7. Werner Syndrome‏‎ (363 revisions)
  8. Sequence-based predictions‏‎ (353 revisions)
  9. Canavan Task 4 - Homology based structure predictions‏‎ (350 revisions)
  10. Sequence-based predictions HEXA‏‎ (343 revisions)
  11. Canavan Task 3 - Sequence-based predictions‏‎ (336 revisions)
  12. Sequence searches and multiple sequence alignments (Phenylketonuria)‏‎ (304 revisions)
  13. Gaucher Disease: Task 02 - Alignments‏‎ (275 revisions)
  14. Canavan Disease: Task 02 - Alignments‏‎ (268 revisions)
  15. Canavan Disease 2012‏‎ (268 revisions)
  16. Molecular Dynamcis analysis‏‎ (262 revisions)
  17. Homology based structure predictions‏‎ (255 revisions)
  18. Glucocerebrosidase sequence based prediction‏‎ (251 revisions)
  19. Homology-modelling HEXA‏‎ (241 revisions)
  20. Canavan Task 2 - Sequence alignments‏‎ (241 revisions)
  21. Sequence-based mutation analysis BCKDHA‏‎ (237 revisions)
  22. Gaucher Disease: Task 05 - Homology Modelling‏‎ (236 revisions)
  23. Task 4: Structural Alignments‏‎ (223 revisions)
  24. Task 3: Sequence-based predictions‏‎ (209 revisions)
  25. Homology based structure prediction (Phenylketonuria)‏‎ (205 revisions)
  26. Hemochromatosis: Sequence based predictions‏‎ (200 revisions)
  27. Gaucher Disease: Task 04 - Structural Alignment‏‎ (196 revisions)
  28. Structure-based mutation analysis‏‎ (196 revisions)
  29. Sequence-based mutation analysis (Phenylketonuria)‏‎ (195 revisions)
  30. Mapping SNPs HEXA‏‎ (192 revisions)
  31. Sequence-based predictions GLA‏‎ (190 revisions)
  32. Homology modelling TSD‏‎ (189 revisions)
  33. Sequence-based analyses of ARS A‏‎ (188 revisions)
  34. Task 4: Homology based structure predictions‏‎ (182 revisions)
  35. Sequence-based predictions TSD‏‎ (181 revisions)
  36. Sequence-Based Mutation Analysis Hemochromatosis‏‎ (177 revisions)
  37. Molecular Dynamics Simulations HEXA‏‎ (177 revisions)
  38. Sequence-based analyses Gaucher Disease‏‎ (176 revisions)
  39. Gaucher Disease‏‎ (174 revisions)
  40. Molecular Dynamics Simulations Analysis (PKU)‏‎ (174 revisions)
  41. Gaucher Disease: Task 07 - Research SNPs‏‎ (173 revisions)
  42. Homology Modeling of ARS A‏‎ (170 revisions)
  43. Sequence based mutation analysis of GBA‏‎ (169 revisions)
  44. Hemochromatosis 2011‏‎ (168 revisions)
  45. Sequence-based mutation analysis‏‎ (168 revisions)
  46. Hemochromatosis‏‎ (167 revisions)
  47. Task 6: Sequence-based mutation analysis‏‎ (166 revisions)
  48. Normal mode analysis HEXA‏‎ (165 revisions)
  49. Sequence Alignments TSD‏‎ (164 revisions)
  50. Canavan Task 10 - Molecular Dynamics Simulations‏‎ (164 revisions)
  51. Task 2: Alignments‏‎ (163 revisions)
  52. Homology Based Structure Predictions Hemochromatosis‏‎ (162 revisions)
  53. Canavan Task 9 - Normal Mode Analysis‏‎ (162 revisions)
  54. Sequence-based mutation analysis Gaucher Disease‏‎ (161 revisions)
  55. Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation‏‎ (160 revisions)
  56. Homology-based structure prediction (PKU)‏‎ (158 revisions)
  57. Sequence-based mutation analysis of ARSA‏‎ (156 revisions)
  58. Gaucher Disease: Task 08 - Sequence-based mutation analysis‏‎ (156 revisions)
  59. Structure-based mutation analysis (Phenylketonuria)‏‎ (155 revisions)
  60. Structure-based mutation analysis (PKU)‏‎ (153 revisions)
  61. Protein structure prediction from evolutionary sequence variation (Phenylketonuria)‏‎ (153 revisions)
  62. Sequence-based predictions (PKU)‏‎ (152 revisions)
  63. Gaucher Disease: Task 09 - Structure-based mutation analysis‏‎ (147 revisions)
  64. Sequence Alignments Hemochromatosis‏‎ (143 revisions)
  65. Structure-based mutation analysis BCKDHA‏‎ (142 revisions)
  66. Canavan Disease: Task 07 - Researching SNPs‏‎ (142 revisions)
  67. Sequence-based mutation analysis HEXA‏‎ (141 revisions)
  68. Normal mode analysis (Phenylketonuria)‏‎ (140 revisions)
  69. MD Mutation436‏‎ (140 revisions)
  70. Normal Mode Analysis BCKDHA‏‎ (139 revisions)
  71. Glucocerebrosidase homology modelling‏‎ (132 revisions)
  72. Task 3: odba human Sequence-based predictions‏‎ (132 revisions)
  73. Gaucher Disease 2012‏‎ (130 revisions)
  74. Canavan Disease: Task 08 - Sequence-based Mutation Analysis‏‎ (130 revisions)
  75. Task 10: Molecular Dynamics Analysis‏‎ (129 revisions)
  76. Mapping SNPs‏‎ (129 revisions)
  77. Task 3 - Sequence-based predictions‏‎ (129 revisions)
  78. Task 7: MSUD - Structure-based mutation analysis‏‎ (129 revisions)
  79. Tay-Sachs Disease 2012‏‎ (127 revisions)
  80. Structural Alignments (Phenylketonuria)‏‎ (127 revisions)
  81. Sequence Search and Multiple Sequence Alignment (PKU)‏‎ (126 revisions)
  82. Structure based mutation analysis of GBA‏‎ (126 revisions)
  83. Task 5 - Mapping SNPs Canavan‏‎ (126 revisions)
  84. Task 5: Homology Modeling‏‎ (125 revisions)
  85. Sequence and multiple alignments‏‎ (123 revisions)
  86. Molecular Dynamics Simulations Analysis Hemochromatosis‏‎ (122 revisions)
  87. Task 8: Sequence-based mutation analysis‏‎ (122 revisions)
  88. Homology Modelling GLA‏‎ (122 revisions)
  89. Canavan Disease: Task 09 - Structure-based Mutation Analysis‏‎ (120 revisions)
  90. Task 6: MSUD - Sequence-based mutation analysis‏‎ (120 revisions)
  91. Normal mode analysis TSD‏‎ (119 revisions)
  92. Task 7: Structure-based mutation analysis‏‎ (119 revisions)
  93. MD WildType‏‎ (117 revisions)
  94. Molecular Dynamics Simulations Analysis of Glucocerebrosidase‏‎ (116 revisions)
  95. Canavan Disease: Task 03 - Sequence-based Predictions‏‎ (116 revisions)
  96. Researching SNPs TSD‏‎ (116 revisions)
  97. Gaucher Disease 2011‏‎ (114 revisions)
  98. Sequence-Based Predictions Hemochromatosis‏‎ (114 revisions)
  99. Canavan Disease: Task 10 - Normal Mode Analysis‏‎ (112 revisions)
  100. Glucocerebrosidase sequence alignments‏‎ (112 revisions)
  101. Sequence-based mutation analysis TSD‏‎ (109 revisions)
  102. Fabry Disease 2012‏‎ (108 revisions)
  103. Canavan Disease‏‎ (108 revisions)
  104. Normal mode analysis‏‎ (107 revisions)
  105. MD simulation analysis TSD‏‎ (107 revisions)
  106. Structure-based mutation analysis TSD‏‎ (106 revisions)
  107. Task 3 (MSUD)‏‎ (106 revisions)
  108. Phenylketonuria 2011‏‎ (105 revisions)
  109. Task 2: Sequence alignments (sequence searches and multiple alignments)‏‎ (104 revisions)
  110. Hemochromatosis Normal modes‏‎ (104 revisions)
  111. Gaucher Disease: Task 10 - Normal mode analysis‏‎ (102 revisions)
  112. Structure-based mutation analysis GLA‏‎ (102 revisions)
  113. Canavan Task 7 - Structure-based mutation analysis‏‎ (102 revisions)
  114. Fabry:Homology based structure predictions‏‎ (102 revisions)
  115. Sequence-based mutation analysis GLA‏‎ (102 revisions)
  116. MD Mutation485‏‎ (101 revisions)
  117. Task 9: Normal Mode Analysis‏‎ (100 revisions)
  118. Task 7: Research SNPs‏‎ (100 revisions)
  119. Sequence Alignments Gaucher Disease‏‎ (100 revisions)
  120. Mapping SNPs BCKDHA‏‎ (97 revisions)
  121. Predicting the Effect of SNPs (PKU)‏‎ (95 revisions)
  122. Task 9: Structure-based mutation analysis‏‎ (92 revisions)
  123. Maple syrup urine disease 2011‏‎ (92 revisions)
  124. Researching SNPs (Phenylketonuria)‏‎ (91 revisions)
  125. Normal Mode Analysis of Glucocerebrosidase‏‎ (91 revisions)
  126. Sequence Alignments HEXA‏‎ (89 revisions)
  127. Sequence Alignment GLA‏‎ (89 revisions)
  128. Structure-Based Mutation Analysis Hemochromatosis‏‎ (87 revisions)
  129. Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal‏‎ (86 revisions)
  130. Maple Syrup Urine Disease 2012‏‎ (84 revisions)
  131. Canavan Disease: Task 05 - Homology Modelling‏‎ (84 revisions)
  132. Resource software‏‎ (84 revisions)
  133. Task 6: Protein structure prediction from evolutionary sequence variation‏‎ (83 revisions)
  134. Normal Mode Analysis of ARSA‏‎ (82 revisions)
  135. Fabry:Normal mode analysis‏‎ (81 revisions)
  136. Fabry Disease 2011‏‎ (81 revisions)
  137. Researching And Mapping Point Mutations Hemochromatosis‏‎ (79 revisions)
  138. Researching SNPs (PKU)‏‎ (79 revisions)
  139. Gaucher Disease: Task 09 - Lab Journal‏‎ (79 revisions)
  140. Hemochromatosis 2012‏‎ (78 revisions)
  141. Rs61731240‏‎ (78 revisions)
  142. Metachromatic leukodystrophy reference aminoacids‏‎ (77 revisions)
  143. Fabry:Mapping point mutations‏‎ (77 revisions)
  144. Task 3 - Sequence-based predictions 2011‏‎ (77 revisions)
  145. Researching SNPs Gaucher Disease‏‎ (76 revisions)
  146. Normal Mode Analysis Hemochromatosis‏‎ (76 revisions)
  147. Task 4: Homology-based structure prediction‏‎ (75 revisions)
  148. Phenylketonuria‏‎ (73 revisions)
  149. Task 2 (MSUD)‏‎ (73 revisions)
  150. Structure-based mutation analysis ARSA‏‎ (72 revisions)
  151. Protein Structure and Function Analysis (SS 2013)‏‎ (72 revisions)
  152. ARS A Sequence alignments‏‎ (72 revisions)
  153. Maple Syrup Urine Disease‏‎ (71 revisions)
  154. Fabry:Sequence-based mutation analysis‏‎ (70 revisions)
  155. Fabry:Sequence alignments (sequence searches and multiple alignments)‏‎ (70 revisions)
  156. Sequence Alignments BCKDHA‏‎ (70 revisions)
  157. Normal Mode Analysis (PKU)‏‎ (69 revisions)
  158. Task 2: Multiple Sequence Alignment‏‎ (68 revisions)
  159. Fabry:Sequence alignments (sequence searches and multiple alignments):Results‏‎ (68 revisions)
  160. Structure-based mutation analysis HEXA‏‎ (68 revisions)
  161. Normal mode analysis Gaucher Disease‏‎ (67 revisions)
  162. Protein Structure and Function Analysis (version: SS 2011)‏‎ (66 revisions)
  163. Gaucher Disease - Task 06 - Lab Journal‏‎ (65 revisions)
  164. Lab journal task 8‏‎ (64 revisions)
  165. Gaucher Disease: Task 04 - Lab Journal‏‎ (64 revisions)
  166. Structure-based mutation analysis Gaucher Disease‏‎ (64 revisions)
  167. Canavan Disease: Task 04 - Structural Alignments‏‎ (64 revisions)
  168. Tay-Sachs Disease 2011‏‎ (62 revisions)
  169. Rs121907974‏‎ (61 revisions)
  170. Glucocerebrosidase mapping snps‏‎ (59 revisions)
  171. ASPA Sequence Based Predictions‏‎ (58 revisions)
  172. Task 7 (MSUD)‏‎ (58 revisions)
  173. AllBio Forum‏‎ (57 revisions)
  174. Task 6 (MSUD)‏‎ (56 revisions)
  175. Fabry:Structure-based mutation analysis‏‎ (53 revisions)
  176. Phenylketonuria 2012‏‎ (53 revisions)
  177. Rs4777505‏‎ (53 revisions)
  178. Mapping mutations of ARS A‏‎ (53 revisions)
  179. Sequence Alignments‏‎ (52 revisions)
  180. Task 9 - Normal Mode Analysis‏‎ (51 revisions)
  181. Gaucher Disease: Task 08 - LabJournal‏‎ (50 revisions)
  182. Molecular Dynamics Simulations‏‎ (50 revisions)
  183. Lab Journal - Task 8 (PAH)‏‎ (48 revisions)
  184. Rs1800430‏‎ (48 revisions)
  185. Rs61747114‏‎ (47 revisions)
  186. Lab journal task 4‏‎ (46 revisions)
  187. Task 6 - Protein structure prediction from evolutionary sequence variation‏‎ (46 revisions)
  188. Task 5: Researching SNPs‏‎ (46 revisions)
  189. Researching SNPs TSD Journal‏‎ (45 revisions)
  190. Homology modelling Gaucher Disease‏‎ (44 revisions)
  191. Molecular Dynamics Analysis GLA‏‎ (44 revisions)
  192. Reference Sequence BCKDHA‏‎ (44 revisions)
  193. Molecular Dynamics Simulations (PKU)‏‎ (44 revisions)
  194. Normal mode analysis GLA‏‎ (42 revisions)
  195. Gaucher Disease: Task 02 - Lab Journal‏‎ (42 revisions)
  196. Canavan Disease: Task 06 - Protein Structure Prediction‏‎ (42 revisions)
  197. Lab Journal - Task 6 (PAH)‏‎ (41 revisions)
  198. Rs121907982‏‎ (41 revisions)
  199. Fabry:Sequence-based analyses‏‎ (41 revisions)
  200. Fabry:Homology based structure predictions/Journal‏‎ (41 revisions)
  201. Task 5 - Researching SNPs‏‎ (40 revisions)
  202. Task 9: MSUD - Normal Mode Analysis‏‎ (39 revisions)
  203. Task 4 (MSUD)‏‎ (39 revisions)
  204. Task 9 (MSUD)‏‎ (39 revisions)
  205. Task 5 - Mapping SNPs 2011‏‎ (39 revisions)
  206. Rs1054374‏‎ (39 revisions)
  207. Fabry:Sequence-based mutation analysis/Journal‏‎ (38 revisions)
  208. Molecular Dynamics Simulations Analysis Gaucher Disease‏‎ (36 revisions)
  209. Task 5: Mapping point mutations‏‎ (36 revisions)
  210. Lab Journal of Task 3 (MSUD)‏‎ (36 revisions)
  211. Task 5 (MSUD)‏‎ (36 revisions)
  212. Canavan Task 8 - Molecular Dynamics Simulations‏‎ (36 revisions)
  213. Metachromatic leukodystrophy‏‎ (35 revisions)
  214. Gaucher Disease: Task 03 - Lab Journal‏‎ (34 revisions)
  215. Task 10 - Journal (PKU)‏‎ (34 revisions)
  216. Metachromatic leukodystrophy 2011‏‎ (33 revisions)
  217. Rs121907979‏‎ (33 revisions)
  218. Molecular Dynamics Simulations TSD‏‎ (33 revisions)
  219. Sequence Alignments Protocol TSD‏‎ (32 revisions)
  220. Rs121907968‏‎ (32 revisions)
  221. Lab Journal - Task 5 (PAH)‏‎ (32 revisions)
  222. Gaucher Disease: Task 05 - Lab Journal‏‎ (32 revisions)
  223. Task 3 - Normal Mode Analysis‏‎ (32 revisions)
  224. Task alignments‏‎ (32 revisions)
  225. Rs121907967‏‎ (31 revisions)
  226. ARSA search protocol‏‎ (31 revisions)
  227. Protein Structure and Function Analysis (version: SS 2012)‏‎ (31 revisions)
  228. Lab Journal - Task 4 (PAH)‏‎ (30 revisions)
  229. Task 10 (MSUD)‏‎ (30 revisions)
  230. Workflow homology modelling glucocerebrosidase‏‎ (28 revisions)
  231. Lab journal Task 7‏‎ (28 revisions)
  232. Gaucher Task07 Protocol‏‎ (27 revisions)
  233. CD task2 protocol‏‎ (27 revisions)
  234. Sequence-based predictions Protocol TSD‏‎ (27 revisions)
  235. M82L‏‎ (26 revisions)
  236. Task2 Hemochromatosis Protocol‏‎ (25 revisions)
  237. Phenylketonuria/Task3/Scripts‏‎ (25 revisions)
  238. Sequence and structure based mutation analysis of GBA‏‎ (25 revisions)
  239. Molecular Dynamics Simulations Hemochromatosis‏‎ (25 revisions)
  240. Task 8 (MSUD)‏‎ (25 revisions)
  241. Task 8 - Molecular Dynamics Simulations 2011‏‎ (25 revisions)
  242. Task alignments 2012‏‎ (25 revisions)
  243. Canavan Disease: Task 02 - Journal‏‎ (24 revisions)
  244. Task 2 lab journal (MSUD)‏‎ (24 revisions)
  245. Lab Journal - Task 9 (PAH)‏‎ (24 revisions)
  246. Modeller protocol BCKDHA‏‎ (24 revisions)
  247. Lab journal‏‎ (24 revisions)
  248. BCKDHA‏‎ (24 revisions)
  249. Lab Journal Hemochromatosis Task9‏‎ (23 revisions)
  250. Mapping SNPs GLA‏‎ (23 revisions)
  251. Fabry:Mapping point mutations/Journal‏‎ (23 revisions)
  252. TSD Homology modelling protocol‏‎ (21 revisions)
  253. Lab Journal - Task 3 (PAH)‏‎ (21 revisions)
  254. Gaucher Task06 Protocol‏‎ (21 revisions)
  255. Table Templates‏‎ (21 revisions)
  256. Task 1: Collect information on the individual disease‏‎ (21 revisions)
  257. Example/Template‏‎ (20 revisions)
  258. Task 7 - Structure-based mutation analysis‏‎ (20 revisions)
  259. Sequence-based mutation analysis TSD Journal‏‎ (20 revisions)
  260. PAH Structure‏‎ (20 revisions)
  261. Structure-based mutation analysis TSD Journal‏‎ (19 revisions)
  262. CD task4 protocol‏‎ (19 revisions)
  263. Canavan Disease: Task 07 - Supplement‏‎ (19 revisions)
  264. ASPA Normal Mode Analysis‏‎ (19 revisions)
  265. CD task10 protocol‏‎ (18 revisions)
  266. Fabry:Sequence-based analyses/Journal‏‎ (18 revisions)
  267. Fabry:Molecular Dynamics Simulations‏‎ (17 revisions)
  268. Canavan Disease 2011‏‎ (17 revisions)
  269. Phenylketonuria/Task2 Scripts‏‎ (17 revisions)
  270. Run MD HEXA‏‎ (17 revisions)
  271. Fabry:Structure-based mutation analysis/Journal‏‎ (17 revisions)
  272. Task 8: Molecular Dynamics Simulations‏‎ (17 revisions)
  273. CD task7 protocol‏‎ (17 revisions)
  274. Protocol BCKDHA MD‏‎ (17 revisions)
  275. Fabry:Sequence alignments (sequence searches and multiple alignments)/Scripts‏‎ (17 revisions)
  276. Task homologyModelling‏‎ (16 revisions)
  277. Q125E‏‎ (16 revisions)
  278. Task homologyModelling 2011‏‎ (16 revisions)
  279. Molecular Dynamics Simulations BCKDHA‏‎ (16 revisions)
  280. Task 10 - Normal Mode Analysis‏‎ (16 revisions)
  281. Lab Journal of Task 5 (MSUD)‏‎ (16 revisions)
  282. Psipred‏‎ (15 revisions)
  283. Collection of scripts‏‎ (15 revisions)
  284. Task 9 Structure-based mutation analysis‏‎ (15 revisions)
  285. Reference amino acid sequence of Glucocerebrosidase‏‎ (15 revisions)
  286. Parse output.pl‏‎ (15 revisions)
  287. Task3 Hemochromatosis Protocol‏‎ (14 revisions)
  288. MSUP-task7-journal‏‎ (14 revisions)
  289. Main Page‏‎ (14 revisions)
  290. Run.pl‏‎ (14 revisions)
  291. Fabian Grandke‏‎ (14 revisions)
  292. Task 6 - Sequence-based mutation analysis‏‎ (14 revisions)
  293. Go annotations here‏‎ (14 revisions)
  294. Task 9 Lab Journal (MSUD)‏‎ (14 revisions)
  295. ASPA Homology Modelling‏‎ (14 revisions)
  296. Disease list 2011‏‎ (14 revisions)
  297. Protocol-msud-task5 protocol‏‎ (14 revisions)
  298. Task Structural Alignments‏‎ (14 revisions)
  299. Phenylalanine hydroxylase reference‏‎ (14 revisions)
  300. Seq.-based mut. analysis HEXA‏‎ (13 revisions)
  301. Phenylketonuria/Task2/Scripts‏‎ (13 revisions)
  302. Y438N‏‎ (13 revisions)
  303. Task3 protocoll‏‎ (13 revisions)
  304. Task 2 - Alignments with PAH Reference‏‎ (13 revisions)
  305. Task4 Hemochromatosis Protocol‏‎ (13 revisions)
  306. Task5 Hemochromatosis Protocol‏‎ (13 revisions)
  307. DLD‏‎ (13 revisions)
  308. CD task6 protocol‏‎ (13 revisions)
  309. Journal structure based mutation analysis (PKU)‏‎ (13 revisions)
  310. Task alignments 2011‏‎ (13 revisions)
  311. Task diseaseInfo‏‎ (13 revisions)
  312. Normal mode analysis GLA supplementary‏‎ (12 revisions)
  313. Lab Journal - Task 7 (PAH)‏‎ (12 revisions)
  314. DBT‏‎ (12 revisions)
  315. ASPA Mapping SNPs‏‎ (12 revisions)
  316. Resource wiki‏‎ (12 revisions)
  317. Mapping SNPs HEXA/DETAIL‏‎ (12 revisions)
  318. Multiple Sequence Alignment: ClustalW - set 1‏‎ (12 revisions)
  319. Fabry:Normal mode analysis/Journal‏‎ (11 revisions)
  320. Phenylketonuria/Task6 Scripts‏‎ (11 revisions)
  321. Reference Sequence‏‎ (11 revisions)
  322. Task 6 Lab Journal (MSUD)‏‎ (11 revisions)
  323. Disease list‏‎ (11 revisions)
  324. Hemochromatosis SS Alignments‏‎ (11 revisions)
  325. Homology Based Structure Predictions Hemochromatosis Alignments‏‎ (11 revisions)
  326. Supplementary data normal mode glucocerebrosidase‏‎ (11 revisions)
  327. Using Modeller for TASK 4‏‎ (11 revisions)
  328. Task 8 Lab Journal (MSUD)‏‎ (11 revisions)
  329. Canavan Disease: Task 09 - Supplement‏‎ (11 revisions)
  330. MD simulation analysis TSD Journal‏‎ (10 revisions)
  331. ASPA Structure Based Mutation Analysis‏‎ (10 revisions)
  332. Task 7 - Structure-based mutation analysis 2011‏‎ (10 revisions)
  333. F409C‏‎ (10 revisions)
  334. Task 4 Protocol‏‎ (10 revisions)
  335. Task 8: MSUD - Molecular Dynamics Simulations‏‎ (10 revisions)
  336. C264W‏‎ (10 revisions)
  337. Task6 Hemochromatosis Protocol‏‎ (10 revisions)
  338. Canavan Disease: Task 07 - Journal‏‎ (10 revisions)
  339. Protocol‏‎ (10 revisions)
  340. Sequence-based mutation analysis BCKDHA protocol‏‎ (10 revisions)
  341. Animated Gifs‏‎ (10 revisions)
  342. MD WildeType‏‎ (10 revisions)
  343. ASPA Sequence Based Mutation Analysis‏‎ (10 revisions)
  344. Secstr general‏‎ (9 revisions)
  345. Workflow structure based mutation analysis GBA‏‎ (9 revisions)
  346. Example sequence‏‎ (9 revisions)
  347. Y166N‏‎ (9 revisions)
  348. G249S‏‎ (9 revisions)
  349. CD task5 protocol‏‎ (9 revisions)
  350. Disopred‏‎ (9 revisions)
  351. Task 8 - Molecular Dynamics Simulations‏‎ (9 revisions)
  352. Task 11 - Molecular Dynamics Simulation‏‎ (9 revisions)
  353. Automated Evaluation of Homoloy Models‏‎ (9 revisions)
  354. CD task8 protocol‏‎ (9 revisions)
  355. Prediction of Disordered Regions‏‎ (9 revisions)
  356. PsiBlast in Big80 (PKU)‏‎ (9 revisions)
  357. Lab journal task 2‏‎ (9 revisions)
  358. PAH R71H‏‎ (8 revisions)
  359. Fabry:Molecular Dynamics Simulations/Journal‏‎ (8 revisions)
  360. Task 6 - EVfold‏‎ (8 revisions)
  361. Molecular Dynamics Simulations Gaucher Disease‏‎ (8 revisions)
  362. Task 6 - Sequence-based mutation analysis 2011‏‎ (8 revisions)
  363. Lab Journal of Task 4 (MSUD)‏‎ (8 revisions)
  364. Hemochromatosis SNPdbe SNP TABLE‏‎ (8 revisions)
  365. Journal Task4 PKU‏‎ (8 revisions)
  366. Reference nucleotide sequence of Glucocerebrosidase‏‎ (8 revisions)
  367. BCKDHB‏‎ (8 revisions)
  368. Secondary Structure Prediction‏‎ (8 revisions)
  369. Lab Journal - Task 2 (PAH)‏‎ (8 revisions)
  370. Lab journal task 5‏‎ (7 revisions)
  371. Canavan Disease: Task 02 - Supplement‏‎ (7 revisions)
  372. CompareCath.py‏‎ (7 revisions)
  373. Homology-modelling HEXA/3bc9.pir‏‎ (7 revisions)
  374. R265W‏‎ (7 revisions)
  375. Missense nonsense CFTR‏‎ (7 revisions)
  376. Multiple Sequence Alignment: T-Coffee - set 1‏‎ (7 revisions)
  377. Normal mode analysis TSD Journal‏‎ (7 revisions)
  378. Lab Journal Task 3 Hemo‏‎ (7 revisions)
  379. Hemochromatosis PSSM Matrix‏‎ (7 revisions)
  380. MutEn.pl‏‎ (7 revisions)
  381. Task8 Hemochromatosis Protocol‏‎ (7 revisions)
  382. Poodle‏‎ (7 revisions)
  383. Molecular Dynamics Simulation of ARSA‏‎ (7 revisions)
  384. Cedric Landerer‏‎ (7 revisions)
  385. Task 2 (MUSD) Additional Results‏‎ (6 revisions)
  386. Molecular Dynamics Simulations GLA‏‎ (6 revisions)
  387. I326T‏‎ (6 revisions)
  388. Tastk 2: Alignments‏‎ (6 revisions)
  389. PKU journal Task5‏‎ (6 revisions)
  390. Foldx hexa‏‎ (6 revisions)
  391. Reference Alignment BCKDHA‏‎ (6 revisions)
  392. Jpred‏‎ (6 revisions)
  393. Glucocerebrosidase Molecular Dynamics Simulation‏‎ (6 revisions)
  394. ASPA Sequence Alignments‏‎ (6 revisions)
  395. Sequence-based mutation analysis HEXA/Mutation Summary‏‎ (6 revisions)
  396. Gaucher Disease: Task 10 - Lab Journal‏‎ (6 revisions)
  397. Reference sequence (uniprot)‏‎ (5 revisions)
  398. BLAST‏‎ (5 revisions)
  399. Fabry:Mapping point mutations/SNPedia data‏‎ (5 revisions)
  400. Ala305glu‏‎ (5 revisions)
  401. Multiple Sequence Alignment: Muscle - set 1‏‎ (5 revisions)
  402. Labjournal NMA-Hemochromatosis‏‎ (5 revisions)
  403. Metachromatic leukodystrophy reference nucleotide‏‎ (5 revisions)
  404. Canavan Disease: Task 03 - Journal‏‎ (5 revisions)
  405. Missense nonsense HFE‏‎ (5 revisions)
  406. Fabry:Alpha-galactosidase‏‎ (5 revisions)
  407. TSD Modeller 3gh5 Edited Alignment‏‎ (5 revisions)
  408. Hemochromatosis HGMD SNP TABLE‏‎ (5 revisions)
  409. Gaucher Task09 Protocol‏‎ (5 revisions)
  410. Task 9 - Normal Mode Analysis 2011‏‎ (5 revisions)
  411. Multiple Sequence Alignment: T-Coffee - set 3‏‎ (5 revisions)
  412. DbSNP Silent Mutations Parser‏‎ (5 revisions)
  413. Resource data‏‎ (5 revisions)
  414. Task7 Hemochromatosis Protocol‏‎ (5 revisions)
  415. Homology-modelling HEXA/swissmodel ali‏‎ (5 revisions)
  416. Fabry Disease Selected Mutations‏‎ (5 revisions)
  417. Task Homology Modelling‏‎ (5 revisions)
  418. Tpr precision.pl‏‎ (5 revisions)
  419. Structures for P00439 in PDB‏‎ (5 revisions)
  420. Task 8 - Jorunal (PKU)‏‎ (5 revisions)
  421. Canavan Disease: Task 08 - Supplement‏‎ (5 revisions)
  422. Pearson cc.r (Gaucher Disease)‏‎ (5 revisions)
  423. Task 8 Sequence-based mutation analysis‏‎ (5 revisions)
  424. Phenylalanine hydroxylase reference mRNA‏‎ (4 revisions)
  425. Prediction of transmembrane alpha-helices and signal peptides HEXA HUMAN‏‎ (4 revisions)
  426. Multiple Sequence Alignment: ClustalW - set 3‏‎ (4 revisions)
  427. Task3 protocol‏‎ (4 revisions)
  428. Task 9 - Journal (PKU)‏‎ (4 revisions)
  429. Homology-modelling HEXA/swissmodel 3CUI‏‎ (4 revisions)
  430. PSI-BLAST‏‎ (4 revisions)
  431. SNPdbe conservation score (PKU)‏‎ (4 revisions)
  432. Task 10 - Molecular Dynamics Simulations 2011‏‎ (4 revisions)
  433. Resource language‏‎ (4 revisions)
  434. Structure pdb‏‎ (4 revisions)
  435. HEXA Reference sequence‏‎ (4 revisions)
  436. Polyphobius.pl‏‎ (4 revisions)
  437. Task9 Hemochromatosis Protocol‏‎ (4 revisions)
  438. Molecular Dynamics Simulations TSD Journal‏‎ (4 revisions)
  439. Task 10 Lab Journal (MSUD)‏‎ (4 revisions)
  440. Hemochromatosis gromacs energy table pictures‏‎ (4 revisions)
  441. Reference mRNA of Glucocerebrosidase‏‎ (4 revisions)
  442. Hemo Task7 Minimise Table‏‎ (4 revisions)
  443. Script distance check.py‏‎ (4 revisions)
  444. Multiple Alignment Mammalian PheOH‏‎ (4 revisions)
  445. Lab Journal -Task 4 (PAH)‏‎ (4 revisions)
  446. Canavans Disease‏‎ (4 revisions)
  447. Lab Journal - Task 10 (PAH)‏‎ (4 revisions)
  448. Task04 protocol‏‎ (4 revisions)
  449. PsiPred of Mutated PAH‏‎ (4 revisions)
  450. Multiple Sequence Alignment: ClustalW - set 2‏‎ (4 revisions)
  451. Dssp‏‎ (3 revisions)
  452. Hhr2tsv‏‎ (3 revisions)
  453. PAH R261Q‏‎ (3 revisions)
  454. MSUD Q80E‏‎ (3 revisions)
  455. Prediction of transmembrane alpha-helices and signal peptides INSL5 HUMAN‏‎ (3 revisions)
  456. Fabry Disease sequence prediction GO terms venn‏‎ (3 revisions)
  457. QMEAN score information BCKDHA‏‎ (3 revisions)
  458. Task 7 Research SNPs‏‎ (3 revisions)
  459. Gaucher Task05 Protocol‏‎ (3 revisions)
  460. Compiled list of SNPS‏‎ (3 revisions)
  461. List of known Hex A mutations‏‎ (3 revisions)
  462. FASTA‏‎ (3 revisions)
  463. Hemochromatosis ALL SNP TABLE‏‎ (3 revisions)
  464. Hemochromatosis DBSNP SNP TABLE‏‎ (3 revisions)
  465. Build mutation Script‏‎ (3 revisions)
  466. Canavan Disease: Task 04 - Journal‏‎ (3 revisions)
  467. PAH T278N‏‎ (3 revisions)
  468. Homology-modelling HEXA/hh search output‏‎ (3 revisions)
  469. Runscript for foldx‏‎ (3 revisions)
  470. Task6-MSUP-journal‏‎ (3 revisions)
  471. Gaucher Task10 Protocol‏‎ (3 revisions)
  472. ASPA‏‎ (3 revisions)
  473. SNP effect predictions (PKU)‏‎ (3 revisions)
  474. Task 10 - Molecular Dynamics Simulations‏‎ (3 revisions)
  475. PSIBlasttrainer.pl‏‎ (3 revisions)
  476. Fabry Disease Mutation Analysis Sequence PSSM‏‎ (3 revisions)
  477. Sift probability HFE‏‎ (3 revisions)
  478. Task 5 - Mapping SNPs‏‎ (3 revisions)
  479. MDP condiguration (PKU)‏‎ (3 revisions)
  480. Alpha galactosidase reference amino acid‏‎ (3 revisions)
  481. Resource literature‏‎ (3 revisions)
  482. HFE HUMAN NM‏‎ (3 revisions)
  483. GO Terms BACR HALSA‏‎ (3 revisions)
  484. ASPA Molecular Dynamics Simulation Analysis‏‎ (3 revisions)
  485. Protocol search‏‎ (3 revisions)
  486. PAH P275S‏‎ (3 revisions)
  487. Hemo Task7 SCWRL FoldX Table‏‎ (3 revisions)
  488. Rs4777505 SNAP‏‎ (3 revisions)
  489. Hereditary hemochromatosis‏‎ (3 revisions)
  490. Script rank contacts.py‏‎ (3 revisions)
  491. CD task9 protocol‏‎ (3 revisions)
  492. Metachromatic leukodistrophy‏‎ (3 revisions)
  493. PAH R158Q‏‎ (2 revisions)
  494. Fabry:Mapping point mutations/SNPdbe data‏‎ (2 revisions)
  495. Task10 Hemochromatosis Protocol‏‎ (2 revisions)
  496. GO annotation of the proteins‏‎ (2 revisions)
  497. TSD Modeller 1o7a 2D‏‎ (2 revisions)
  498. BLOSUM62 matrix‏‎ (2 revisions)
  499. Canavan Disease: Task 11 - Molecular Dynamics Simulation‏‎ (2 revisions)
  500. Multiple Sequence Alignment: Espresso - set 1‏‎ (2 revisions)

View (previous 500 | next 500) (20 | 50 | 100 | 250 | 500)