Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.
about
Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variationRAId_DbS: mass-spectrometry based peptide identification web server with knowledge integrationClinical assessment incorporating a personal genomeStructural and physico-chemical effects of disease and non-disease nsSNPs on proteinsMolecular mechanisms of disease-causing missense mutationsA method and server for predicting damaging missense mutationsAnalysis of genetic variation and potential applications in genome-scale metabolic modelingDeleterious GRM1 mutations in schizophreniaIdentification and glycerol-induced correction of misfolding mutations in the X-linked mental retardation gene CASKBioinformatics for personal genome interpretationConnecting protein interaction data, mutations, and disease using bioinformaticsNext generation tools for the annotation of human SNPsIn silico investigation of the ATP7B gene: insights from functional prediction of non-synonymous substitution to protein structure.Status quo of annotation of human disease variants.Structural and functional analysis of human SOD1 in amyotrophic lateral sclerosis.Evolution- and structure-based computational strategy reveals the impact of deleterious missense mutations on MODY 2 (maturity-onset diabetes of the young, type 2)Mutational analysis of FUS gene and its structural and functional role in amyotrophic lateral sclerosis 6.Computational identification of pathogenic associated nsSNPs and its structural impact in UROD gene: a molecular dynamics approach.Bioinformatic Analysis of GJB2 Gene Missense Mutations.Computational Analysis Reveals the Association of Threonine 118 Methionine Mutation in PMP22 Resulting in CMT-1ACharacterization of all possible single-nucleotide change caused amino acid substitutions in the kinase domain of Bruton tyrosine kinase.Atomic Insight into the Altered O6-Methylguanine-DNA Methyltransferase Protein Architecture in Gastric CancerCoagVDb: a comprehensive database for coagulation factors and their associated SAPsComputational approaches to study the effects of small genomic variations.Protein Destabilization as a Common Factor in Diverse Inherited Disorders.Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing.Human allelic variation: perspective from protein function, structure, and evolution.Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation.Structural and functional impacts of amino acid substitutions that create blood group antigens: implications for immunogenicity.Computational Modeling of complete HOXB13 protein for predicting the functional effect of SNPs and the associated role in hereditary prostate cancer.Meet me halfway: when genomics meets structural bioinformatics.Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.Simulation based investigation of deleterious nsSNP's in ATXN2 gene and its structural consequence towards Spinocerebellar Ataxia.Improving the prediction of disease-related variants using protein three-dimensional structureEvidence of colorectal cancer-associated mutation in MCAK: a computational report.Knowledge discovery in variant databases using inductive logic programming.Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy.Impact of genetic variation on three dimensional structure and function of proteins.In silico comparative characterization of pharmacogenomic missense variants.The role of balanced training and testing data sets for binary classifiers in bioinformatics.
P2860
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P2860
Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Predicting the insurgence of h ...... and evolutionary information.
@ast
Predicting the insurgence of h ...... and evolutionary information.
@en
Predicting the insurgence of h ...... and evolutionary information.
@nl
type
label
Predicting the insurgence of h ...... and evolutionary information.
@ast
Predicting the insurgence of h ...... and evolutionary information.
@en
Predicting the insurgence of h ...... and evolutionary information.
@nl
prefLabel
Predicting the insurgence of h ...... and evolutionary information.
@ast
Predicting the insurgence of h ...... and evolutionary information.
@en
Predicting the insurgence of h ...... and evolutionary information.
@nl
P2093
P2860
P356
P1433
P1476
Predicting the insurgence of h ...... and evolutionary information.
@en
P2093
Calabrese R
Capriotti E
P2860
P304
P356
10.1093/BIOINFORMATICS/BTL423
P407
P577
2006-08-07T00:00:00Z