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Journal Abstract Search

112 related items for PubMed ID: 14695526

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  • 2. PicSNP: a browsable catalog of nonsynonymous single nucleotide polymorphisms in the human genome.
    Chang H, Fujita T.
    Biochem Biophys Res Commun; 2001 Sep 14; 287(1):288-91. PubMed ID: 11549289
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  • 3. Go!Poly: A gene-oriented polymorphism database.
    Zhang G, Zhang S, Chen W, Qiu W, Wu H, Wang J, Luo J, Gu X, Cotton RG.
    Hum Mutat; 2001 Nov 14; 18(5):382-7. PubMed ID: 11668631
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  • 6. MedRefSNP: a database of medically investigated SNPs.
    Rhee H, Lee JS.
    Hum Mutat; 2009 Mar 14; 30(3):E460-6. PubMed ID: 19105187
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  • 9. PolyMAPr: programs for polymorphism database mining, annotation, and functional analysis.
    Freimuth RR, Stormo GD, McLeod HL.
    Hum Mutat; 2005 Feb 14; 25(2):110-7. PubMed ID: 15643605
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  • 11. Data mining of public SNP databases for the selection of intragenic SNPs.
    Aerts J, Wetzels Y, Cohen N, Aerssens J.
    Hum Mutat; 2002 Sep 14; 20(3):162-73. PubMed ID: 12203988
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  • 12. Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.
    Capriotti E, Calabrese R, Casadio R.
    Bioinformatics; 2006 Nov 15; 22(22):2729-34. PubMed ID: 16895930
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  • 13. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database.
    Blumenfeld OO, Patnaik SK.
    Hum Mutat; 2004 Jan 15; 23(1):8-16. PubMed ID: 14695527
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  • 18. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
    Wang LL, Li Y, Zhou SF.
    Drug Metab Dispos; 2009 May 15; 37(5):977-91. PubMed ID: 19204079
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