Pages with the most revisions
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Showing below up to 50 results in range #51 to #100.
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- Task 2: Alignments (163 revisions)
- Homology Based Structure Predictions Hemochromatosis (162 revisions)
- Canavan Task 9 - Normal Mode Analysis (162 revisions)
- Sequence-based mutation analysis Gaucher Disease (161 revisions)
- Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation (160 revisions)
- Homology-based structure prediction (PKU) (158 revisions)
- Gaucher Disease: Task 08 - Sequence-based mutation analysis (156 revisions)
- Sequence-based mutation analysis of ARSA (156 revisions)
- Structure-based mutation analysis (Phenylketonuria) (155 revisions)
- Structure-based mutation analysis (PKU) (153 revisions)
- Protein structure prediction from evolutionary sequence variation (Phenylketonuria) (153 revisions)
- Sequence-based predictions (PKU) (152 revisions)
- Gaucher Disease: Task 09 - Structure-based mutation analysis (147 revisions)
- Sequence Alignments Hemochromatosis (143 revisions)
- Structure-based mutation analysis BCKDHA (142 revisions)
- Canavan Disease: Task 07 - Researching SNPs (142 revisions)
- Sequence-based mutation analysis HEXA (141 revisions)
- Normal mode analysis (Phenylketonuria) (140 revisions)
- MD Mutation436 (140 revisions)
- Normal Mode Analysis BCKDHA (139 revisions)
- Glucocerebrosidase homology modelling (132 revisions)
- Task 3: odba human Sequence-based predictions (132 revisions)
- Gaucher Disease 2012 (130 revisions)
- Canavan Disease: Task 08 - Sequence-based Mutation Analysis (130 revisions)
- Task 7: MSUD - Structure-based mutation analysis (129 revisions)
- Task 3 - Sequence-based predictions (129 revisions)
- Mapping SNPs (129 revisions)
- Task 10: Molecular Dynamics Analysis (129 revisions)
- Structural Alignments (Phenylketonuria) (127 revisions)
- Tay-Sachs Disease 2012 (127 revisions)
- Task 5 - Mapping SNPs Canavan (126 revisions)
- Sequence Search and Multiple Sequence Alignment (PKU) (126 revisions)
- Structure based mutation analysis of GBA (126 revisions)
- Task 5: Homology Modeling (125 revisions)
- Sequence and multiple alignments (123 revisions)
- Homology Modelling GLA (122 revisions)
- Molecular Dynamics Simulations Analysis Hemochromatosis (122 revisions)
- Task 8: Sequence-based mutation analysis (122 revisions)
- Canavan Disease: Task 09 - Structure-based Mutation Analysis (120 revisions)
- Task 6: MSUD - Sequence-based mutation analysis (120 revisions)
- Task 7: Structure-based mutation analysis (119 revisions)
- Normal mode analysis TSD (119 revisions)
- MD WildType (117 revisions)
- Canavan Disease: Task 03 - Sequence-based Predictions (116 revisions)
- Researching SNPs TSD (116 revisions)
- Molecular Dynamics Simulations Analysis of Glucocerebrosidase (116 revisions)
- Sequence-Based Predictions Hemochromatosis (114 revisions)
- Gaucher Disease 2011 (114 revisions)
- Glucocerebrosidase sequence alignments (112 revisions)
- Canavan Disease: Task 10 - Normal Mode Analysis (112 revisions)
