Pages with the fewest revisions
From Bioinformatikpedia
Showing below up to 191 results in range #501 to #691.
View (previous 500 | next 500) (20 | 50 | 100 | 250 | 500)
- Molecular Dynamics Simulations (PKU) (44 revisions)
- Homology modelling Gaucher Disease (44 revisions)
- Researching SNPs TSD Journal (45 revisions)
- Task 6 - Protein structure prediction from evolutionary sequence variation (46 revisions)
- Task 5: Researching SNPs (46 revisions)
- Lab journal task 4 (46 revisions)
- Rs61747114 (47 revisions)
- Lab Journal - Task 8 (PAH) (48 revisions)
- Rs1800430 (48 revisions)
- Molecular Dynamics Simulations (50 revisions)
- Gaucher Disease: Task 08 - LabJournal (50 revisions)
- Task 9 - Normal Mode Analysis (51 revisions)
- Sequence Alignments (52 revisions)
- Rs4777505 (53 revisions)
- Mapping mutations of ARS A (53 revisions)
- Fabry:Structure-based mutation analysis (53 revisions)
- Phenylketonuria 2012 (53 revisions)
- Task 6 (MSUD) (56 revisions)
- AllBio Forum (57 revisions)
- ASPA Sequence Based Predictions (58 revisions)
- Task 7 (MSUD) (58 revisions)
- Glucocerebrosidase mapping snps (59 revisions)
- Rs121907974 (61 revisions)
- Tay-Sachs Disease 2011 (62 revisions)
- Structure-based mutation analysis Gaucher Disease (64 revisions)
- Lab journal task 8 (64 revisions)
- Gaucher Disease: Task 04 - Lab Journal (64 revisions)
- Canavan Disease: Task 04 - Structural Alignments (64 revisions)
- Gaucher Disease - Task 06 - Lab Journal (65 revisions)
- Protein Structure and Function Analysis (version: SS 2011) (66 revisions)
- Normal mode analysis Gaucher Disease (67 revisions)
- Structure-based mutation analysis HEXA (68 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments):Results (68 revisions)
- Task 2: Multiple Sequence Alignment (68 revisions)
- Normal Mode Analysis (PKU) (69 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments) (70 revisions)
- Sequence Alignments BCKDHA (70 revisions)
- Fabry:Sequence-based mutation analysis (70 revisions)
- Maple Syrup Urine Disease (71 revisions)
- Protein Structure and Function Analysis (SS 2013) (72 revisions)
- ARS A Sequence alignments (72 revisions)
- Structure-based mutation analysis ARSA (72 revisions)
- Phenylketonuria (73 revisions)
- Task 2 (MSUD) (73 revisions)
- Task 4: Homology-based structure prediction (75 revisions)
- Normal Mode Analysis Hemochromatosis (76 revisions)
- Researching SNPs Gaucher Disease (76 revisions)
- Fabry:Mapping point mutations (77 revisions)
- Metachromatic leukodystrophy reference aminoacids (77 revisions)
- Task 3 - Sequence-based predictions 2011 (77 revisions)
- Rs61731240 (78 revisions)
- Hemochromatosis 2012 (78 revisions)
- Gaucher Disease: Task 09 - Lab Journal (79 revisions)
- Researching And Mapping Point Mutations Hemochromatosis (79 revisions)
- Researching SNPs (PKU) (79 revisions)
- Fabry:Normal mode analysis (81 revisions)
- Fabry Disease 2011 (81 revisions)
- Normal Mode Analysis of ARSA (82 revisions)
- Task 6: Protein structure prediction from evolutionary sequence variation (83 revisions)
- Resource software (84 revisions)
- Maple Syrup Urine Disease 2012 (84 revisions)
- Canavan Disease: Task 05 - Homology Modelling (84 revisions)
- Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal (86 revisions)
- Structure-Based Mutation Analysis Hemochromatosis (87 revisions)
- Sequence Alignment GLA (89 revisions)
- Sequence Alignments HEXA (89 revisions)
- Normal Mode Analysis of Glucocerebrosidase (91 revisions)
- Researching SNPs (Phenylketonuria) (91 revisions)
- Maple syrup urine disease 2011 (92 revisions)
- Task 9: Structure-based mutation analysis (92 revisions)
- Predicting the Effect of SNPs (PKU) (95 revisions)
- Mapping SNPs BCKDHA (97 revisions)
- Task 7: Research SNPs (100 revisions)
- Sequence Alignments Gaucher Disease (100 revisions)
- Task 9: Normal Mode Analysis (100 revisions)
- MD Mutation485 (101 revisions)
- Gaucher Disease: Task 10 - Normal mode analysis (102 revisions)
- Sequence-based mutation analysis GLA (102 revisions)
- Canavan Task 7 - Structure-based mutation analysis (102 revisions)
- Structure-based mutation analysis GLA (102 revisions)
- Fabry:Homology based structure predictions (102 revisions)
- Hemochromatosis Normal modes (104 revisions)
- Task 2: Sequence alignments (sequence searches and multiple alignments) (104 revisions)
- Phenylketonuria 2011 (105 revisions)
- Structure-based mutation analysis TSD (106 revisions)
- Task 3 (MSUD) (106 revisions)
- Normal mode analysis (107 revisions)
- MD simulation analysis TSD (107 revisions)
- Canavan Disease (108 revisions)
- Fabry Disease 2012 (108 revisions)
- Sequence-based mutation analysis TSD (109 revisions)
- Canavan Disease: Task 10 - Normal Mode Analysis (112 revisions)
- Glucocerebrosidase sequence alignments (112 revisions)
- Gaucher Disease 2011 (114 revisions)
- Sequence-Based Predictions Hemochromatosis (114 revisions)
- Molecular Dynamics Simulations Analysis of Glucocerebrosidase (116 revisions)
- Canavan Disease: Task 03 - Sequence-based Predictions (116 revisions)
- Researching SNPs TSD (116 revisions)
- MD WildType (117 revisions)
- Normal mode analysis TSD (119 revisions)
- Task 7: Structure-based mutation analysis (119 revisions)
- Canavan Disease: Task 09 - Structure-based Mutation Analysis (120 revisions)
- Task 6: MSUD - Sequence-based mutation analysis (120 revisions)
- Homology Modelling GLA (122 revisions)
- Task 8: Sequence-based mutation analysis (122 revisions)
- Molecular Dynamics Simulations Analysis Hemochromatosis (122 revisions)
- Sequence and multiple alignments (123 revisions)
- Task 5: Homology Modeling (125 revisions)
- Structure based mutation analysis of GBA (126 revisions)
- Task 5 - Mapping SNPs Canavan (126 revisions)
- Sequence Search and Multiple Sequence Alignment (PKU) (126 revisions)
- Tay-Sachs Disease 2012 (127 revisions)
- Structural Alignments (Phenylketonuria) (127 revisions)
- Task 3 - Sequence-based predictions (129 revisions)
- Task 7: MSUD - Structure-based mutation analysis (129 revisions)
- Mapping SNPs (129 revisions)
- Task 10: Molecular Dynamics Analysis (129 revisions)
- Canavan Disease: Task 08 - Sequence-based Mutation Analysis (130 revisions)
- Gaucher Disease 2012 (130 revisions)
- Task 3: odba human Sequence-based predictions (132 revisions)
- Glucocerebrosidase homology modelling (132 revisions)
- Normal Mode Analysis BCKDHA (139 revisions)
- MD Mutation436 (140 revisions)
- Normal mode analysis (Phenylketonuria) (140 revisions)
- Sequence-based mutation analysis HEXA (141 revisions)
- Structure-based mutation analysis BCKDHA (142 revisions)
- Canavan Disease: Task 07 - Researching SNPs (142 revisions)
- Sequence Alignments Hemochromatosis (143 revisions)
- Gaucher Disease: Task 09 - Structure-based mutation analysis (147 revisions)
- Sequence-based predictions (PKU) (152 revisions)
- Structure-based mutation analysis (PKU) (153 revisions)
- Protein structure prediction from evolutionary sequence variation (Phenylketonuria) (153 revisions)
- Structure-based mutation analysis (Phenylketonuria) (155 revisions)
- Gaucher Disease: Task 08 - Sequence-based mutation analysis (156 revisions)
- Sequence-based mutation analysis of ARSA (156 revisions)
- Homology-based structure prediction (PKU) (158 revisions)
- Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation (160 revisions)
- Sequence-based mutation analysis Gaucher Disease (161 revisions)
- Canavan Task 9 - Normal Mode Analysis (162 revisions)
- Homology Based Structure Predictions Hemochromatosis (162 revisions)
- Task 2: Alignments (163 revisions)
- Canavan Task 10 - Molecular Dynamics Simulations (164 revisions)
- Sequence Alignments TSD (164 revisions)
- Normal mode analysis HEXA (165 revisions)
- Task 6: Sequence-based mutation analysis (166 revisions)
- Hemochromatosis (167 revisions)
- Sequence-based mutation analysis (168 revisions)
- Hemochromatosis 2011 (168 revisions)
- Sequence based mutation analysis of GBA (169 revisions)
- Homology Modeling of ARS A (170 revisions)
- Gaucher Disease: Task 07 - Research SNPs (173 revisions)
- Molecular Dynamics Simulations Analysis (PKU) (174 revisions)
- Gaucher Disease (174 revisions)
- Sequence-based analyses Gaucher Disease (176 revisions)
- Sequence-Based Mutation Analysis Hemochromatosis (177 revisions)
- Molecular Dynamics Simulations HEXA (177 revisions)
- Sequence-based predictions TSD (181 revisions)
- Task 4: Homology based structure predictions (182 revisions)
- Sequence-based analyses of ARS A (188 revisions)
- Homology modelling TSD (189 revisions)
- Sequence-based predictions GLA (190 revisions)
- Mapping SNPs HEXA (192 revisions)
- Sequence-based mutation analysis (Phenylketonuria) (195 revisions)
- Gaucher Disease: Task 04 - Structural Alignment (196 revisions)
- Structure-based mutation analysis (196 revisions)
- Hemochromatosis: Sequence based predictions (200 revisions)
- Homology based structure prediction (Phenylketonuria) (205 revisions)
- Task 3: Sequence-based predictions (209 revisions)
- Task 4: Structural Alignments (223 revisions)
- Gaucher Disease: Task 05 - Homology Modelling (236 revisions)
- Sequence-based mutation analysis BCKDHA (237 revisions)
- Homology-modelling HEXA (241 revisions)
- Canavan Task 2 - Sequence alignments (241 revisions)
- Glucocerebrosidase sequence based prediction (251 revisions)
- Homology based structure predictions (255 revisions)
- Molecular Dynamcis analysis (262 revisions)
- Canavan Disease: Task 02 - Alignments (268 revisions)
- Canavan Disease 2012 (268 revisions)
- Gaucher Disease: Task 02 - Alignments (275 revisions)
- Sequence searches and multiple sequence alignments (Phenylketonuria) (304 revisions)
- Canavan Task 3 - Sequence-based predictions (336 revisions)
- Sequence-based predictions HEXA (343 revisions)
- Canavan Task 4 - Homology based structure predictions (350 revisions)
- Sequence-based predictions (353 revisions)
- Werner Syndrome (363 revisions)
- Canavan Task 6 - Sequence-based mutation analysis (377 revisions)
- Secondary Structure Prediction BCKDHA (408 revisions)
- Homology based structure predictions BCKDHA (413 revisions)
- Gaucher Disease: Task 03 - Sequence-based predictions (471 revisions)
- Sequence-based predictions (Phenylketonuria) (500 revisions)
- Molecular Dynamics Analysis BCKDHA (584 revisions)