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- Fabry:Mapping point mutations/HGMD
- Fabry:Mapping point mutations/Journal
- Fabry:Mapping point mutations/OMIM data
- Fabry:Mapping point mutations/SNPdbe data
- Fabry:Mapping point mutations/SNPedia data
- Fabry:Molecular Dynamics Simulations
- Fabry:Molecular Dynamics Simulations/Journal
- Fabry:Molecular Dynamics Simulations Analysis
- Fabry:Normal mode analysis
- Fabry:Normal mode analysis/Deformation Energies
- Fabry:Normal mode analysis/Journal
- Fabry:Sequence-based analyses
- Fabry:Sequence-based analyses/Journal
- Fabry:Sequence-based mutation analysis
- Fabry:Sequence-based mutation analysis/Journal
- Fabry:Sequence-based mutation analysis/SNAP2
- Fabry:Sequence alignments (sequence searches and multiple alignments)
- Fabry:Sequence alignments (sequence searches and multiple alignments)/Journal
- Fabry:Sequence alignments (sequence searches and multiple alignments)/Scripts
- Fabry:Sequence alignments (sequence searches and multiple alignments):Results
- Fabry:Structure-based mutation analysis
- Fabry:Structure-based mutation analysis/FoldXtables
- Fabry:Structure-based mutation analysis/Journal
- Fabry:Structure-based mutation analysis/MinimiseTables
- Fabry Disease 2011
- Fabry Disease 2012
- Fabry Disease Mutation Analysis Sequence PSSM
- Fabry Disease Selected Mutations
- Fabry Disease mutation analysis sequence msa sequences
- Fabry Disease sequence-based prediction of tm-helices and signal peptides A4 HUMAN
- Fabry Disease sequence-based prediction of tm-helices and signal peptides BARC HALSA
- Fabry Disease sequence-based prediction of tm-helices and signal peptides GLA
- Fabry Disease sequence-based prediction of tm-helices and signal peptides INSL5 HUMAN
- Fabry Disease sequence-based prediction of tm-helices and signal peptides LAMP1 HUMAN
- Fabry Disease sequence-based prediction of tm-helices and signal peptides RET4 HUMAN
- Fabry Disease sequence prediction GO terms venn
- Fabry Disease swiss 1KTB graphics
- Fabry Disease swiss 3CC1 graphics
- Fabry Disease swiss 3HG3 graphics
- FoldX Difference Mutant/Wildtype
- Foldx hexa
- Format to wiki table.r
- G249S
- GO Terms A4 HUMAN
- GO Terms BACR HALSA
- GO Terms HEXA HUMAN
- GO Terms INSL5 HUMAN
- GO Terms LAMP1 HUMAN
- GO Terms RET4 HUMAN
- GO annotation of the proteins
- GO terms general
- Gaucher Disease
- Gaucher Disease: Task 02 - Alignments
- Gaucher Disease: Task 02 - Lab Journal
- Gaucher Disease: Task 03 - Lab Journal
- Gaucher Disease: Task 03 - Sequence-based predictions
- Gaucher Disease: Task 04 - Lab Journal
- Gaucher Disease: Task 04 - Structural Alignment
- Gaucher Disease: Task 05 - Homology Modelling
- Gaucher Disease: Task 05 - Lab Journal
- Gaucher Disease: Task 06 - Lab Journal
- Gaucher Disease: Task 06 - Protein structure prediction from evolutionary sequence variation
- Gaucher Disease: Task 07 - Research SNPs
- Gaucher Disease: Task 08 - LabJournal
- Gaucher Disease: Task 08 - Sequence-based mutation analysis
- Gaucher Disease: Task 09 - Lab Journal
- Gaucher Disease: Task 09 - Lab Journal: run minimise.sh
- Gaucher Disease: Task 09 - Structure-based mutation analysis
- Gaucher Disease: Task 10 - Lab Journal
- Gaucher Disease: Task 10 - Normal mode analysis
- Gaucher Disease - Task 06 - Lab Journal
- Gaucher Disease 2011
- Gaucher Disease 2012
- Gaucher Task05 Protocol
- Gaucher Task06 Protocol
- Gaucher Task07 Protocol
- Gaucher Task09 Protocol
- Gaucher Task10 Protocol
- Gaucher dbSNP Deletions
- Gaucher dbSNP Missense
- Gaucher dbSNP Synonymous
- Gaucher hgmd mutations
- Glu285ala
- Glucocerebrosidase Molecular Dynamics Simulation
- Glucocerebrosidase disease causing mutations
- Glucocerebrosidase homology modelling
- Glucocerebrosidase mapping snps
- Glucocerebrosidase neutral mutations
- Glucocerebrosidase sequence alignments
- Glucocerebrosidase sequence based prediction
- Go annotations here
- HEXA Reference sequence
- HFE HUMAN NM
- HHSearch
- Hemo Task7 Minimise Table
- Hemo Task7 SCWRL FoldX Table
- Hemo seq based pred
- Hemochromatosis
- Hemochromatosis: Sequence based predictions
- Hemochromatosis 2011
- Hemochromatosis 2012
- Hemochromatosis ALL SNP TABLE
- Hemochromatosis DBSNP SNP TABLE
- Hemochromatosis HGMD SNP TABLE
- Hemochromatosis Normal modes
- Hemochromatosis PSSM Matrix
- Hemochromatosis SNP Mapping MSA
- Hemochromatosis SNPdbe SNP TABLE
- Hemochromatosis SS Alignments
- Hemochromatosis gromacs energy table pictures
- Hemochromatosis gromacs mdp
- Hereditary hemochromatosis
- Hex A Reference sequence
- Hhr2tsv
- Homology-based structure prediction (PKU)
- Homology-modelling HEXA
- Homology-modelling HEXA/3bc9.pir
- Homology-modelling HEXA/3cui.pir
- Homology-modelling HEXA/3lut.pir,
- Homology-modelling HEXA/hh search output
- Homology-modelling HEXA/swissmodel 3CUI
- Homology-modelling HEXA/swissmodel 3LUT
- Homology-modelling HEXA/swissmodel ali
- Homology Based Structure Predictions Hemochromatosis
- Homology Based Structure Predictions Hemochromatosis Alignments
- Homology Modeling of ARS A
- Homology Modelling GLA
- Homology based Structure prediction protocol BCKDHA
- Homology based structure prediction (Phenylketonuria)
- Homology based structure predictions
- Homology based structure predictions BCKDHA
- Homology modelling Gaucher Disease
- Homology modelling TSD
- How to search dbSNP
- I326T
- Imm ev hotspots
- Isoform CRA a
- Isoform CRA b
- Iupred
- Journal Task4 PKU
- Journal structure based mutation analysis (PKU)
- Jpred
- Lab Journal -Task 4 (PAH)
- Lab Journal - Task 10 (PAH)
- Lab Journal - Task 2 (PAH)
- Lab Journal - Task 3 (PAH)
- Lab Journal - Task 4 (PAH)
- Lab Journal - Task 5 (PAH)
- Lab Journal - Task 6 (PAH)
- Lab Journal - Task 7 (PAH)
- Lab Journal - Task 8 (PAH)
- Lab Journal - Task 9 (PAH)
- Lab Journal Hemochromatosis Task9
- Lab Journal Task 3 Hemo
- Lab Journal of Task 3 (MSUD)
- Lab Journal of Task 4 (MSUD)
- Lab Journal of Task 5 (MSUD)
- Lab journal
- Lab journal Task 7
- Lab journal task 2
- Lab journal task 4
- Lab journal task 5
- Lab journal task 8
- Labjournal NMA-Hemochromatosis
- List of known Hex A mutations
- M82L
- MAFFT 30
- MAFFT 360
- MAFFT 60
- MAFFT whole
- MDP condiguration (PKU)
- MD Mutation436
- MD Mutation485
- MD WildType
- MD WildeType
- MD simulation analysis TSD
- MD simulation analysis TSD Journal
- MSUD Q80E
- MSUD Task 9 Protocoll
- MSUP-task7-journal
- Main Page
- MapleSyrupDisease disease causing mutations
- Maple Syrup Urine Disease
- Maple Syrup Urine Disease 2012
- Maple syrup urine disease 2011
- Mapping SNPs
- Mapping SNPs BCKDHA
- Mapping SNPs GLA
- Mapping SNPs HEXA
- Mapping SNPs HEXA/DETAIL
- Mapping mutations of ARS A
- Metachromatic leukodistrophy
- Metachromatic leukodystrophy
- Metachromatic leukodystrophy 2011
- Metachromatic leukodystrophy reference aminoacids
- Metachromatic leukodystrophy reference nucleotide
- Missense nonsense CFTR
- Missense nonsense HFE
- Modeller.py
- Modeller protocol BCKDHA
- Modeller protokoll BCKDHA
- Molecular Dynamcis analysis
- Molecular Dynamics Analysis BCKDHA
- Molecular Dynamics Analysis GLA
- Molecular Dynamics Simulation of ARSA
- Molecular Dynamics Simulations
- Molecular Dynamics Simulations (PKU)
- Molecular Dynamics Simulations Analysis (PKU)
- Molecular Dynamics Simulations Analysis Gaucher Disease
- Molecular Dynamics Simulations Analysis Hemochromatosis
- Molecular Dynamics Simulations Analysis of Glucocerebrosidase
- Molecular Dynamics Simulations BCKDHA
- Molecular Dynamics Simulations GLA
- Molecular Dynamics Simulations Gaucher Disease
- Molecular Dynamics Simulations Gaucher Disease Scripts
- Molecular Dynamics Simulations HEXA
- Molecular Dynamics Simulations Hemochromatosis
- Molecular Dynamics Simulations TSD
- Molecular Dynamics Simulations TSD Journal
- Msa-conservation.py
- Multiple Alignment Mammalian PheOH
- Multiple Sequence Alignment: ClustalW - set 1
- Multiple Sequence Alignment: ClustalW - set 2
- Multiple Sequence Alignment: ClustalW - set 3
- Multiple Sequence Alignment: Espresso - set 1
- Multiple Sequence Alignment: Muscle - set 1
- Multiple Sequence Alignment: Muscle - set 2
- Multiple Sequence Alignment: Muscle - set 3
- Multiple Sequence Alignment: T-Coffee - set 1
- Multiple Sequence Alignment: T-Coffee - set 2
- Multiple Sequence Alignment: T-Coffee - set 3
- MutEn.pl
- Mutation Minimization Plots (PKU)
- Normal Mode Analysis (PKU)
- Normal Mode Analysis BCKDHA
- Normal Mode Analysis Hemochromatosis
- Normal Mode Analysis of ARSA
- Normal Mode Analysis of Glucocerebrosidase
- Normal mode analysis
- Normal mode analysis (Phenylketonuria)
- Normal mode analysis GLA
- Normal mode analysis GLA supplementary
- Normal mode analysis Gaucher Disease
- Normal mode analysis HEXA
- Normal mode analysis TSD
- Normal mode analysis TSD Journal
- Overlap between all databases (HGMD free)
- P01112 EVcouplings Configuration DI
- P01112 EVcouplings Configuration PLM
- P01112 EVfold Configuration DI