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Journal Abstract Search

498 related items for PubMed ID: 17055652

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  • 2. 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; 37(5):977-91. PubMed ID: 19204079
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  • 7. Prediction of deleterious non-synonymous single nucleotide polymorphisms of genes related to ethanol-induced toxicity.
    Wang LL, Li Y, Zhou SF.
    Toxicol Lett; 2009 Jun 01; 187(2):99-114. PubMed ID: 19429251
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  • 8. LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.
    Karchin R, Diekhans M, Kelly L, Thomas DJ, Pieper U, Eswar N, Haussler D, Sali A.
    Bioinformatics; 2005 Jun 15; 21(12):2814-20. PubMed ID: 15827081
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  • 9. Applications of computational algorithm tools to identify functional SNPs in cytokine genes.
    Shen J, Deininger PL, Zhao H.
    Cytokine; 2006 Jul 15; 35(1-2):62-6. PubMed ID: 16919468
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  • 10. Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins.
    Savas S, Ahmad MF, Shariff M, Kim DY, Ozcelik H.
    Proteins; 2005 Feb 15; 58(3):697-705. PubMed ID: 15617026
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  • 14. [Computational analysis of human genome polymorphism].
    Ramenskiĭ VE, Siuniaev ShR.
    Mol Biol (Mosk); 2009 Feb 15; 43(2):286-94. PubMed ID: 19425497
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  • 15. Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function.
    Xi T, Jones IM, Mohrenweiser HW.
    Genomics; 2004 Jun 15; 83(6):970-9. PubMed ID: 15177551
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  • 16. Identification and structural comparison of deleterious mutations in nsSNPs of ABL1 gene in chronic myeloid leukemia: a bio-informatics study.
    George Priya Doss C, Sudandiradoss C, Rajasekaran R, Purohit R, Ramanathan K, Sethumadhavan R.
    J Biomed Inform; 2008 Aug 15; 41(4):607-12. PubMed ID: 18243808
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  • 17. Phenotype prediction of nonsynonymous single nucleotide polymorphisms in human phase II drug/xenobiotic metabolizing enzymes: perspectives on molecular evolution.
    Hao D, Xiao P, Chen S.
    Sci China Life Sci; 2010 Oct 15; 53(10):1252-62. PubMed ID: 20953949
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  • 18. 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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  • 19. Bayesian approach to discovering pathogenic SNPs in conserved protein domains.
    Cai Z, Tsung EF, Marinescu VD, Ramoni MF, Riva A, Kohane IS.
    Hum Mutat; 2004 Aug 15; 24(2):178-84. PubMed ID: 15241800
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  • 20. DR-GAS: a database of functional genetic variants and their phosphorylation states in human DNA repair systems.
    Sehgal M, Singh TR.
    DNA Repair (Amst); 2014 Apr 15; 16():97-103. PubMed ID: 24548788
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