(Q38433524)

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SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases.

scientific article published on February 2010

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19921752%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases (English)

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12 February 2020

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12 February 2020

Gilbert Deleage

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12 February 2020

Jean-Louis Mandel

12

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12 February 2020

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Odile Lecompte

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12 February 2020

Valérie Biancalana

6

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Valérie Biancalana

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12 February 2020

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Anne Friedrich

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12 February 2020

Nicolas Garnier

2

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12 February 2020

Nicolas Gagnière

3

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12 February 2020

Hoan Nguyen

4

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12 February 2020

Laurent-Philippe Albou

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12 February 2020

Emmanuel Bettler

7

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12 February 2020

Dino Moras

11

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12 February 2020

Thierry Toursel

13

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12 February 2020

Luc Moulinier

14

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12 February 2020

Olivier Poch

15

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12 February 2020

publication date

1 February 2010

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12 February 2020

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12 February 2020

31

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12 February 2020

2

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12 February 2020

127-135

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12 February 2020

Defining and characterizing protein surface using alpha shapes.

1 reference

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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McKusick's Online Mendelian Inheritance in Man (OMIM)

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Mendelian disorders deserve more attention

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Disease-causing mutations in the human genome

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7 January 2021

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The Protein Data Bank

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UMD (Universal Mutation Database): 2005 update

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7 January 2021

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I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure

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Protein structure modeling with MODELLER

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MAGOS: multiple alignment and modelling server.

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The Gene Ontology (GO) database and informatics resource

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6th International HUGO Mutation Database Meeting, March 27, 1999, Brisbane, Australia.

1 reference

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A database of locus-specific databases

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The SAAPdb web resource: a large-scale structural analysis of mutant proteins.

1 reference

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STRING 8--a global view on proteins and their functional interactions in 630 organisms

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Environmental epigenomics and disease susceptibility

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LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.

1 reference

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IntAct--open source resource for molecular interaction data

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SNP@Promoter: a database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions

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coliSNP database server mapping nsSNPs on protein structures.

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Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing

1 reference

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Evolutionarily conserved pathways of energetic connectivity in protein families

1 reference

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7 January 2021

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Mendelian Inheritance in Man and its online version, OMIM

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SIFT: Predicting amino acid changes that affect protein function

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PipeAlign: A new toolkit for protein family analysis

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MUTbase: maintenance and analysis of distributed mutation databases.

1 reference

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Human Variome Project: an international collaboration to catalogue human genetic variation

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Human Gene-Centric Databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDE

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Evaluation of structural and evolutionary contributions to deleterious mutation prediction.

1 reference

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MutDB: update on development of tools for the biochemical analysis of genetic variation

1 reference

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Automated analysis of interatomic contacts in proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21155

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inferred from DOI database lookup

Human Gene Mutation Database: towards a comprehensive central mutation database

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topoSNP: a topographic database of non-synonymous single nucleotide polymorphisms with and without known disease association

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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In silico analysis of missense substitutions using sequence-alignment based methods

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1 reference

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1 reference

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The International HapMap Project

1 reference

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inferred from DOI database lookup

MAO: a Multiple Alignment Ontology for nucleic acid and protein sequences

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

MACSIMS: multiple alignment of complete sequences information management system

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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1 reference

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inferred from DOI database lookup

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1 reference

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1 reference

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10.1002/HUMU.21155

1 reference

Europe PubMed Central

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12 February 2020

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12 February 2020

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