SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs - Wikidata - wikimedia - TriplyDB

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs

http://www.wikidata.org/entity/Q24795858

about

The FoldX web server: an online force field Prediction of water and metal binding sites and their affinities by using the Fold-X force field.Modeling effects of human single nucleotide polymorphisms on protein-protein interactions SNPs3D: candidate gene and SNP selection for association studies.SNP@Domain: a web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences.The SH2B gene is associated with serum leptin and body fat in normal female twins.coliSNP database server mapping nsSNPs on protein structures.F-SNP: computationally predicted functional SNPs for disease association studies Structure-PPi: a module for the annotation of cancer-related single-nucleotide variants at protein-protein interfaces Meet me halfway: when genomics meets structural bioinformatics.MSV3d: database of human MisSense Variants mapped to 3D protein structure.The SAAP pipeline and database: tools to analyze the impact and predict the pathogenicity of mutations Genomic signatures of near-extinction and rebirth of the crested ibis and other endangered bird species.Fold designability, distribution, and disease SNP@Promoter: a database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions.Distribution and effects of nonsense polymorphisms in human genes.PhosSNP for systematic analysis of genetic polymorphisms that influence protein phosphorylation.High frequency of rare variants with a moderate-to-high predicted biological effect in protocadherin genes of extremely obese CanProVar: a human cancer proteome variation database.Domain altering SNPs in the human proteome and their impact on signaling pathways.Improved detection of rare genetic variants for diseases.Genetic defects in the human glycome.Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.Single nucleotide variations: biological impact and theoretical interpretation.Genome and proteome annotation: organization, interpretation and integration.Chapter 15: disease gene prioritization.PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes Prediction and experimental characterization of nsSNPs altering human PDZ-binding motifs.Functional marker detection and analysis on a comprehensive transcriptome of large yellow croaker by next generation sequencing Distinctive Genome Reduction Rates Revealed by Genomic Analyses of Two Coxiella-Like Endosymbionts in Ticks The Characteristics of Heterozygous Protein Truncating Variants in the Human Genome.The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants.Gene-expression changes caused by inbreeding protect against inbreeding depression in Drosophila.Functional nsSNPs from carcinogenesis-related genes expressed in breast tissue: potential breast cancer risk alleles and their distribution across human populations.MutDB: update on development of tools for the biochemical analysis of genetic variation Prediction of Genes Related to Positive Selection Using Whole-Genome Resequencing in Three Commercial Pig Breeds Association between Genetic Variants in DNA Double-Strand Break Repair Pathways and Risk of Radiation Therapy-Induced Pneumonitis and Esophagitis in Non-Small Cell Lung Cancer Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach SysPIMP: the web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometry A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity.

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P2860

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs

http://www.wikidata.org/entity/Q24795858

description

2005 nî lūn-bûn

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2005 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2005 թվականի հունվարին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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Nucleic Acids Research

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SNPeffect: a database mapping ...... man non-synonymous coding SNPs

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Francois Stricher

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Frederic Rousseau

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Jesper Ferkinghoff-Borg

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Luis Serrano

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P2860

The Pfam protein families database

BRENDA, the enzyme database: updates and major new developments

PDBsum: summaries and analyses of PDB structures

The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003

The Gene Ontology (GO) database and informatics resource

PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization

Predicting subcellular localization of proteins using machine-learned classifiers

Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteins

In vivo half-life of a protein is a function of its amino-terminal residue

Prediction of protein secondary structure at better than 70% accuracy

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D527-32

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scholarly article

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10.1093/NAR/GKI086

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Database issue

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33

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Joost Schymkowitz

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8122318

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15608254

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540040

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