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  1. Fabry:Mapping point mutations/HGMD
  2. Fabry:Mapping point mutations/Journal
  3. Fabry:Mapping point mutations/OMIM data
  4. Fabry:Mapping point mutations/SNPdbe data
  5. Fabry:Mapping point mutations/SNPedia data
  6. Fabry:Molecular Dynamics Simulations
  7. Fabry:Molecular Dynamics Simulations/Journal
  8. Fabry:Molecular Dynamics Simulations Analysis
  9. Fabry:Normal mode analysis
  10. Fabry:Normal mode analysis/Deformation Energies
  11. Fabry:Normal mode analysis/Journal
  12. Fabry:Sequence-based analyses
  13. Fabry:Sequence-based analyses/Journal
  14. Fabry:Sequence-based mutation analysis
  15. Fabry:Sequence-based mutation analysis/Journal
  16. Fabry:Sequence-based mutation analysis/SNAP2
  17. Fabry:Sequence alignments (sequence searches and multiple alignments)
  18. Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal
  19. Fabry:Sequence alignments (sequence searches and multiple alignments)/Scripts
  20. Fabry:Sequence alignments (sequence searches and multiple alignments):Results
  21. Fabry:Structure-based mutation analysis
  22. Fabry:Structure-based mutation analysis/FoldXtables
  23. Fabry:Structure-based mutation analysis/Journal
  24. Fabry:Structure-based mutation analysis/MinimiseTables
  25. Fabry Disease 2011
  26. Fabry Disease 2012
  27. Fabry Disease Mutation Analysis Sequence PSSM
  28. Fabry Disease Selected Mutations
  29. Fabry Disease mutation analysis sequence msa sequences
  30. Fabry Disease sequence-based prediction of tm-helices and signal peptides A4 HUMAN
  31. Fabry Disease sequence-based prediction of tm-helices and signal peptides BARC HALSA
  32. Fabry Disease sequence-based prediction of tm-helices and signal peptides GLA
  33. Fabry Disease sequence-based prediction of tm-helices and signal peptides INSL5 HUMAN
  34. Fabry Disease sequence-based prediction of tm-helices and signal peptides LAMP1 HUMAN
  35. Fabry Disease sequence-based prediction of tm-helices and signal peptides RET4 HUMAN
  36. Fabry Disease sequence prediction GO terms venn
  37. Fabry Disease swiss 1KTB graphics
  38. Fabry Disease swiss 3CC1 graphics
  39. Fabry Disease swiss 3HG3 graphics
  40. FoldX Difference Mutant/Wildtype
  41. Foldx hexa
  42. Format to wiki table.r
  43. G249S
  44. GO Terms A4 HUMAN
  45. GO Terms BACR HALSA
  46. GO Terms HEXA HUMAN
  47. GO Terms INSL5 HUMAN
  48. GO Terms LAMP1 HUMAN
  49. GO Terms RET4 HUMAN
  50. GO annotation of the proteins
  51. GO terms general
  52. Gaucher Disease
  53. Gaucher Disease: Task 02 - Alignments
  54. Gaucher Disease: Task 02 - Lab Journal
  55. Gaucher Disease: Task 03 - Lab Journal
  56. Gaucher Disease: Task 03 - Sequence-based predictions
  57. Gaucher Disease: Task 04 - Lab Journal
  58. Gaucher Disease: Task 04 - Structural Alignment
  59. Gaucher Disease: Task 05 - Homology Modelling
  60. Gaucher Disease: Task 05 - Lab Journal
  61. Gaucher Disease: Task 06 - Lab Journal
  62. Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation
  63. Gaucher Disease: Task 07 - Research SNPs
  64. Gaucher Disease: Task 08 - LabJournal
  65. Gaucher Disease: Task 08 - Sequence-based mutation analysis
  66. Gaucher Disease: Task 09 - Lab Journal
  67. Gaucher Disease: Task 09 - Lab Journal: run minimise.sh
  68. Gaucher Disease: Task 09 - Structure-based mutation analysis
  69. Gaucher Disease: Task 10 - Lab Journal
  70. Gaucher Disease: Task 10 - Normal mode analysis
  71. Gaucher Disease - Task 06 - Lab Journal
  72. Gaucher Disease 2011
  73. Gaucher Disease 2012
  74. Gaucher Task05 Protocol
  75. Gaucher Task06 Protocol
  76. Gaucher Task07 Protocol
  77. Gaucher Task09 Protocol
  78. Gaucher Task10 Protocol
  79. Gaucher dbSNP Deletions
  80. Gaucher dbSNP Missense
  81. Gaucher dbSNP Synonymous
  82. Gaucher hgmd mutations
  83. Glu285ala
  84. Glucocerebrosidase Molecular Dynamics Simulation
  85. Glucocerebrosidase disease causing mutations
  86. Glucocerebrosidase homology modelling
  87. Glucocerebrosidase mapping snps
  88. Glucocerebrosidase neutral mutations
  89. Glucocerebrosidase sequence alignments
  90. Glucocerebrosidase sequence based prediction
  91. Go annotations here
  92. HEXA Reference sequence
  93. HFE HUMAN NM
  94. HHSearch
  95. Hemo Task7 Minimise Table
  96. Hemo Task7 SCWRL FoldX Table
  97. Hemo seq based pred
  98. Hemochromatosis
  99. Hemochromatosis: Sequence based predictions
  100. Hemochromatosis 2011
  101. Hemochromatosis 2012
  102. Hemochromatosis ALL SNP TABLE
  103. Hemochromatosis DBSNP SNP TABLE
  104. Hemochromatosis HGMD SNP TABLE
  105. Hemochromatosis Normal modes
  106. Hemochromatosis PSSM Matrix
  107. Hemochromatosis SNP Mapping MSA
  108. Hemochromatosis SNPdbe SNP TABLE
  109. Hemochromatosis SS Alignments
  110. Hemochromatosis gromacs energy table pictures
  111. Hemochromatosis gromacs mdp
  112. Hereditary hemochromatosis
  113. Hex A Reference sequence
  114. Hhr2tsv
  115. Homology-based structure prediction (PKU)
  116. Homology-modelling HEXA
  117. Homology-modelling HEXA/3bc9.pir
  118. Homology-modelling HEXA/3cui.pir
  119. Homology-modelling HEXA/3lut.pir,
  120. Homology-modelling HEXA/hh search output
  121. Homology-modelling HEXA/swissmodel 3CUI
  122. Homology-modelling HEXA/swissmodel 3LUT
  123. Homology-modelling HEXA/swissmodel ali
  124. Homology Based Structure Predictions Hemochromatosis
  125. Homology Based Structure Predictions Hemochromatosis Alignments
  126. Homology Modeling of ARS A
  127. Homology Modelling GLA
  128. Homology based Structure prediction protocol BCKDHA
  129. Homology based structure prediction (Phenylketonuria)
  130. Homology based structure predictions
  131. Homology based structure predictions BCKDHA
  132. Homology modelling Gaucher Disease
  133. Homology modelling TSD
  134. How to search dbSNP
  135. I326T
  136. Imm ev hotspots
  137. Isoform CRA a
  138. Isoform CRA b
  139. Iupred
  140. Journal Task4 PKU
  141. Journal structure based mutation analysis (PKU)
  142. Jpred
  143. Lab Journal -Task 4 (PAH)
  144. Lab Journal - Task 10 (PAH)
  145. Lab Journal - Task 2 (PAH)
  146. Lab Journal - Task 3 (PAH)
  147. Lab Journal - Task 4 (PAH)
  148. Lab Journal - Task 5 (PAH)
  149. Lab Journal - Task 6 (PAH)
  150. Lab Journal - Task 7 (PAH)
  151. Lab Journal - Task 8 (PAH)
  152. Lab Journal - Task 9 (PAH)
  153. Lab Journal Hemochromatosis Task9
  154. Lab Journal Task 3 Hemo
  155. Lab Journal of Task 3 (MSUD)
  156. Lab Journal of Task 4 (MSUD)
  157. Lab Journal of Task 5 (MSUD)
  158. Lab journal
  159. Lab journal Task 7
  160. Lab journal task 2
  161. Lab journal task 4
  162. Lab journal task 5
  163. Lab journal task 8
  164. Labjournal NMA-Hemochromatosis
  165. List of known Hex A mutations
  166. M82L
  167. MAFFT 30
  168. MAFFT 360
  169. MAFFT 60
  170. MAFFT whole
  171. MDP condiguration (PKU)
  172. MD Mutation436
  173. MD Mutation485
  174. MD WildType
  175. MD WildeType
  176. MD simulation analysis TSD
  177. MD simulation analysis TSD Journal
  178. MSUD Q80E
  179. MSUD Task 9 Protocoll
  180. MSUP-task7-journal
  181. Main Page
  182. MapleSyrupDisease disease causing mutations
  183. Maple Syrup Urine Disease
  184. Maple Syrup Urine Disease 2012
  185. Maple syrup urine disease 2011
  186. Mapping SNPs
  187. Mapping SNPs BCKDHA
  188. Mapping SNPs GLA
  189. Mapping SNPs HEXA
  190. Mapping SNPs HEXA/DETAIL
  191. Mapping mutations of ARS A
  192. Metachromatic leukodistrophy
  193. Metachromatic leukodystrophy
  194. Metachromatic leukodystrophy 2011
  195. Metachromatic leukodystrophy reference aminoacids
  196. Metachromatic leukodystrophy reference nucleotide
  197. Missense nonsense CFTR
  198. Missense nonsense HFE
  199. Modeller.py
  200. Modeller protocol BCKDHA
  201. Modeller protokoll BCKDHA
  202. Molecular Dynamcis analysis
  203. Molecular Dynamics Analysis BCKDHA
  204. Molecular Dynamics Analysis GLA
  205. Molecular Dynamics Simulation of ARSA
  206. Molecular Dynamics Simulations
  207. Molecular Dynamics Simulations (PKU)
  208. Molecular Dynamics Simulations Analysis (PKU)
  209. Molecular Dynamics Simulations Analysis Gaucher Disease
  210. Molecular Dynamics Simulations Analysis Hemochromatosis
  211. Molecular Dynamics Simulations Analysis of Glucocerebrosidase
  212. Molecular Dynamics Simulations BCKDHA
  213. Molecular Dynamics Simulations GLA
  214. Molecular Dynamics Simulations Gaucher Disease
  215. Molecular Dynamics Simulations Gaucher Disease Scripts
  216. Molecular Dynamics Simulations HEXA
  217. Molecular Dynamics Simulations Hemochromatosis
  218. Molecular Dynamics Simulations TSD
  219. Molecular Dynamics Simulations TSD Journal
  220. Msa-conservation.py
  221. Multiple Alignment Mammalian PheOH
  222. Multiple Sequence Alignment: ClustalW - set 1
  223. Multiple Sequence Alignment: ClustalW - set 2
  224. Multiple Sequence Alignment: ClustalW - set 3
  225. Multiple Sequence Alignment: Espresso - set 1
  226. Multiple Sequence Alignment: Muscle - set 1
  227. Multiple Sequence Alignment: Muscle - set 2
  228. Multiple Sequence Alignment: Muscle - set 3
  229. Multiple Sequence Alignment: T-Coffee - set 1
  230. Multiple Sequence Alignment: T-Coffee - set 2
  231. Multiple Sequence Alignment: T-Coffee - set 3
  232. MutEn.pl
  233. Mutation Minimization Plots (PKU)
  234. Normal Mode Analysis (PKU)
  235. Normal Mode Analysis BCKDHA
  236. Normal Mode Analysis Hemochromatosis
  237. Normal Mode Analysis of ARSA
  238. Normal Mode Analysis of Glucocerebrosidase
  239. Normal mode analysis
  240. Normal mode analysis (Phenylketonuria)
  241. Normal mode analysis GLA
  242. Normal mode analysis GLA supplementary
  243. Normal mode analysis Gaucher Disease
  244. Normal mode analysis HEXA
  245. Normal mode analysis TSD
  246. Normal mode analysis TSD Journal
  247. Overlap between all databases (HGMD free)
  248. P01112 EVcouplings Configuration DI
  249. P01112 EVcouplings Configuration PLM
  250. P01112 EVfold Configuration DI
  251. P01112 EVfold Configuration PLM
  252. PAH G312D
  253. PAH I65T
  254. PAH P275S
  255. PAH P281L
  256. PAH R158Q
  257. PAH R261Q
  258. PAH R408W
  259. PAH R71H
  260. PAH Structure
  261. PAH T266A
  262. PAH T278N
  263. PKU journal Task5
  264. PSI-BLAST
  265. PSIBlasttrainer.pl
  266. PSSM
  267. PSSM of close homologous sequences
  268. Parse output.pl
  269. Pearson cc.r (Gaucher Disease)
  270. Phenylalanine hydroxylase reference
  271. Phenylalanine hydroxylase reference mRNA
  272. Phenylketonuria
  273. Phenylketonuria/Task2/Scripts
  274. Phenylketonuria/Task2 Scripts
  275. Phenylketonuria/Task3/Scripts
  276. Phenylketonuria/Task6 Scripts
  277. Phenylketonuria 2011
  278. Phenylketonuria 2012
  279. Polyphobius.pl
  280. Poodle
  281. Predicting the Effect of SNPs (PKU)
  282. Prediction of Disordered Regions
  283. Prediction of transmembrane alpha-helices and signal peptides A4 HUMAN
  284. Prediction of transmembrane alpha-helices and signal peptides BACR HALSA
  285. Prediction of transmembrane alpha-helices and signal peptides HEXA HUMAN
  286. Prediction of transmembrane alpha-helices and signal peptides INSL5 HUMAN
  287. Prediction of transmembrane alpha-helices and signal peptides LAMP1 HUMAN
  288. Prediction of transmembrane alpha-helices and signal peptides RET4 HUMAN
  289. ProtFun2.2 output
  290. Protein Structure and Function Analysis (SS 2011)
  291. Protein Structure and Function Analysis (SS 2013)
  292. Protein Structure and Function Analysis (version: SS 2011)
  293. Protein Structure and Function Analysis (version: SS 2012)
  294. Protein structure prediction from evolutionary sequence variation (Phenylketonuria)
  295. Protocol
  296. Protocol-msud-task5 protocol
  297. Protocol BCKDHA MD
  298. Protocol search
  299. PsiBlast in Big80 (PKU)
  300. PsiPred of Mutated PAH
  301. Psipred
  302. Q125E
  303. QMEAN score information BCKDHA
  304. R265W
  305. Ras DI Score Configuration
  306. Ras PLM Score Configuration
  307. Rebecca Kaßner
  308. Reference Alignment BCKDHA
  309. Reference Sequence
  310. Reference Sequence (pdb)
  311. Reference Sequence Aspartoacyclase
  312. Reference Sequence BCKDHA
  313. Reference amino acid sequence of Glucocerebrosidase
  314. Reference mRNA of Glucocerebrosidase
  315. Reference nucleotide sequence of Glucocerebrosidase
  316. Reference sequence
  317. Reference sequence (uniprot)
  318. Researching And Mapping Point Mutations Hemochromatosis
  319. Researching SNPs (PKU)
  320. Researching SNPs (Phenylketonuria)
  321. Researching SNPs Gaucher Disease
  322. Researching SNPs TSD
  323. Researching SNPs TSD Journal
  324. Researching and mapping point mutations TSD Journal
  325. Resource data
  326. Resource discussion
  327. Resource language
  328. Resource literature
  329. Resource software
  330. Resource wiki
  331. Rs1054374
  332. Rs1054374 SNAP
  333. Rs121907967
  334. Rs121907967 SNAP
  335. Rs121907968
  336. Rs121907968 SNAP
  337. Rs121907974
  338. Rs121907974 SNAP
  339. Rs121907979
  340. Rs121907979 SNAP
  341. Rs121907982
  342. Rs121907982 SNAP
  343. Rs1800430
  344. Rs1800430 SNAP
  345. Rs1800431
  346. Rs4777505
  347. Rs4777505 SNAP
  348. Rs61731240
  349. Rs61731240 SNAP
  350. Rs61747114
  351. Rs61747114 SNAP
  352. Run-blast.pl
  353. Run.pl
  354. Run MD HEXA
  355. Runscript BCKDHA
  356. Runscript for foldx
  357. SNP effect predictions (PKU)
  358. SNPdbe conservation score (PKU)
  359. SNPs for Hema
  360. Scrip pdb distance check.py
  361. Script calc hotspot.py
  362. Script distance check.py
  363. Script rank contacts.py
  364. Secondary Structure Prediction
  365. Secondary Structure Prediction BCKDHA
  366. Secstr general
  367. Seq.-based mut. analysis HEXA
  368. Sequence-Based Mutation Analysis Hemochromatosis
  369. Sequence-Based Predictions Hemochromatosis
  370. Sequence-based analyses Gaucher Disease
  371. Sequence-based analyses of ARS A
  372. Sequence-based mutation analysis
  373. Sequence-based mutation analysis (Phenylketonuria)
  374. Sequence-based mutation analysis BCKDHA
  375. Sequence-based mutation analysis BCKDHA protocol
  376. Sequence-based mutation analysis GLA
  377. Sequence-based mutation analysis Gaucher Disease
  378. Sequence-based mutation analysis HEXA
  379. Sequence-based mutation analysis HEXA/Mutation Summary
  380. Sequence-based mutation analysis HEXA/rs4777505 SNAP
  381. Sequence-based mutation analysis TSD
  382. Sequence-based mutation analysis TSD Journal
  383. Sequence-based mutation analysis of ARSA
  384. Sequence-based predictions
  385. Sequence-based predictions (PKU)
  386. Sequence-based predictions (Phenylketonuria)
  387. Sequence-based predictions GLA
  388. Sequence-based predictions GLA diagrams
  389. Sequence-based predictions HEXA
  390. Sequence-based predictions Protocol TSD
  391. Sequence-based predictions TSD
  392. Sequence Alignment GLA
  393. Sequence Alignments
  394. Sequence Alignments BCKDHA
  395. Sequence Alignments Gaucher Disease
  396. Sequence Alignments HEXA
  397. Sequence Alignments Hemochromatosis
  398. Sequence Alignments Protocol TSD
  399. Sequence Alignments TSD
  400. Sequence Search and Multiple Sequence Alignment (PKU)
  401. Sequence and multiple alignments
  402. Sequence and structure based mutation analysis of GBA
  403. Sequence based mutation analysis of GBA
  404. Sequence searches and multiple sequence alignments (Phenylketonuria)
  405. Sift probability HFE
  406. SignalP scores TSD
  407. Solution HFE SNPs
  408. Structural Alignments (Phenylketonuria)
  409. Structure-Based Mutation Analysis Hemochromatosis
  410. Structure-based mutation analysis
  411. Structure-based mutation analysis (PKU)
  412. Structure-based mutation analysis (Phenylketonuria)
  413. Structure-based mutation analysis ARSA
  414. Structure-based mutation analysis BCKDHA
  415. Structure-based mutation analysis GLA
  416. Structure-based mutation analysis Gaucher Disease
  417. Structure-based mutation analysis HEXA
  418. Structure-based mutation analysis TSD
  419. Structure-based mutation analysis TSD Journal
  420. Structure based mutation analysis of GBA
  421. Structure pdb
  422. Structures for P00439 in PDB
  423. Supplementary data normal mode glucocerebrosidase
  424. Swismsmodel 2gk1 alignment
  425. Swissmodel 1o7a alignment
  426. Swissmodel 2gjx alignment
  427. TSD Homology modelling protocol
  428. TSD Modeller 1o7a 2D
  429. TSD Modeller 1o7a Simple
  430. TSD Modeller 2gk1 2D
  431. TSD Modeller 2gk1 Simple
  432. TSD Modeller 3gh5 2D
  433. TSD Modeller 3gh5 Edited Alignment
  434. TSD Modeller 3gh5 Simple
  435. TSD NM 000520.3 NM 000520.4 NW
  436. TSD PolyPhen2 Full Ouput
  437. TSD SIFT Scaled Probailities
  438. TSD createMap.pl
  439. TSD synonymous SNPs from dbSNP
  440. Table Templates
  441. Task04 protocol
  442. Task10 Hemochromatosis Protocol
  443. Task2 Hemochromatosis Protocol
  444. Task3 Hemochromatosis Protocol
  445. Task3 protocol
  446. Task3 protocoll
  447. Task4 Hemochromatosis Protocol
  448. Task5 Hemochromatosis Protocol
  449. Task6-MSUP-journal
  450. Task6 Hemochromatosis Protocol
  451. Task7 Hemochromatosis Protocol
  452. Task8 Hemochromatosis Protocol
  453. Task9 Hemochromatosis Protocol
  454. Task 10: Molecular Dynamics Analysis
  455. Task 10 (MSUD)
  456. Task 10 - Journal (PKU)
  457. Task 10 - Molecular Dynamics Simulations
  458. Task 10 - Molecular Dynamics Simulations 2011
  459. Task 10 - Normal Mode Analysis
  460. Task 10 Lab Journal (MSUD)
  461. Task 11 - Molecular Dynamics Simulation
  462. Task 1: Collect information on the individual disease
  463. Task 2: Alignments
  464. Task 2: Multiple Sequence Alignment
  465. Task 2: Sequence alignments (sequence searches and multiple alignments)
  466. Task 2 (MSUD)
  467. Task 2 (MUSD) Additional Results
  468. Task 2 - Alignments with PAH Reference
  469. Task 2 lab journal (MSUD)
  470. Task 3: Sequence-based predictions
  471. Task 3: odba human Sequence-based predictions
  472. Task 3 (MSUD)
  473. Task 3 - Normal Mode Analysis
  474. Task 3 - Sequence-based predictions
  475. Task 3 - Sequence-based predictions 2011
  476. Task 3 - Sequence-based predictions 2012
  477. Task 4: Homology-based structure prediction
  478. Task 4: Homology based structure predictions
  479. Task 4: Structural Alignments
  480. Task 4 (MSUD)
  481. Task 4 Protocol
  482. Task 5: Homology Modeling
  483. Task 5: Mapping point mutations
  484. Task 5: Researching SNPs
  485. Task 5 (MSUD)
  486. Task 5 - Mapping SNPs
  487. Task 5 - Mapping SNPs 2011
  488. Task 5 - Mapping SNPs Canavan
  489. Task 5 - Researching SNPs
  490. Task 6: MSUD - Sequence-based mutation analysis
  491. Task 6: Protein structure prediction from evolutionary sequence variation
  492. Task 6: Sequence-based mutation analysis
  493. Task 6 (MSUD)
  494. Task 6 - EVfold
  495. Task 6 - Protein structure prediction from evolutionary sequence variation
  496. Task 6 - Sequence-based mutation analysis
  497. Task 6 - Sequence-based mutation analysis 2011
  498. Task 6 Lab Journal (MSUD)
  499. Task 7: MSUD - Structure-based mutation analysis
  500. Task 7: Research SNPs

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