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    Results: 1 to 20 of 102

    1.

    Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.

    Van Ness B, Ramos C, Haznadar M, Hoering A, Haessler J, Crowley J, Jacobus S, Oken M, Rajkumar V, Greipp P, Barlogie B, Durie B, Katz M, Atluri G, Fang G, Gupta R, Steinbach M, Kumar V, Mushlin R, Johnson D, Morgan G.

    BMC Med. 2008 Sep 8;6:26.PMID: 18778477 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Rationale and study design of the CardioGene Study: genomics of in-stent restenosis.

    Ganesh SK, Skelding KA, Mehta L, O'Neill K, Joo J, Zheng G, Goldstein J, Simari R, Billings E, Geller NL, Holmes D, O'Neill WW, Nabel EG.

    Pharmacogenomics. 2004 Oct;5(7):952-1004.PMID: 15469413 [PubMed - indexed for MEDLINE]Related articles

    3.

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

    Kim BC, Kim WY, Park D, Chung WH, Shin KS, Bhak J.

    BMC Bioinformatics. 2008;9 Suppl 1:S2.PMID: 18315851 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Insulin-like growth factor-1- and interleukin-6-related gene variation and risk of multiple myeloma.

    Birmann BM, Tamimi RM, Giovannucci E, Rosner B, Hunter DJ, Kraft P, Mitsiades C, Anderson KC, Colditz GA.

    Cancer Epidemiol Biomarkers Prev. 2009 Jan;18(1):282-8.PMID: 19124510 [PubMed - indexed for MEDLINE]Related articles

    5.

    Disease phenocode analysis identifies SNP-guided microRNA maps (MirMaps) associated with human "master" disease genes.

    Glinsky GV.

    Cell Cycle. 2008 Dec;7(23):3680-94. Epub 2008 Dec 6.PMID: 19029827 [PubMed - indexed for MEDLINE]Related articles

    6.

    A comprehensive analysis of common genetic variation in prolactin (PRL) and PRL receptor (PRLR) genes in relation to plasma prolactin levels and breast cancer risk: the multiethnic cohort.

    Lee SA, Haiman CA, Burtt NP, Pooler LC, Cheng I, Kolonel LN, Pike MC, Altshuler D, Hirschhorn JN, Henderson BE, Stram DO.

    BMC Med Genet. 2007 Dec 1;8:72.PMID: 18053149 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Genetic associations with thalidomide mediated venous thrombotic events in myeloma identified using targeted genotyping.

    Johnson DC, Corthals S, Ramos C, Hoering A, Cocks K, Dickens NJ, Haessler J, Goldschmidt H, Child JA, Bell SE, Jackson G, Baris D, Rajkumar SV, Davies FE, Durie BG, Crowley J, Sonneveld P, Van Ness B, Morgan GJ.

    Blood. 2008 Dec 15;112(13):4924-34. Epub 2008 Sep 19.PMID: 18805967 [PubMed - indexed for MEDLINE]Related articles

    8.

    Common genetic variation in six lipid-related and statin-related genes, statin use and risk of incident nonfatal myocardial infarction and stroke.

    Hindorff LA, Lemaitre RN, Smith NL, Bis JC, Marciante KD, Rice KM, Lumley T, Enquobahrie DA, Li G, Heckbert SR, Psaty BM.

    Pharmacogenet Genomics. 2008 Aug;18(8):677-82.PMID: 18622260 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Integration of HapMap-based SNP pattern analysis and gene expression profiling reveals common SNP profiles for cancer therapy outcome predictor genes.

    Glinsky GV.

    Cell Cycle. 2006 Nov;5(22):2613-25. Epub 2006 Nov 15.PMID: 17172834 [PubMed - indexed for MEDLINE]Related articles

    10.

    Potential regulatory SNPs in promoters of human genes: a systematic approach.

    Stepanova M, Tiazhelova T, Skoblov M, Baranova A.

    Mol Cell Probes. 2006 Dec;20(6):348-58. Epub 2006 May 6.PMID: 16806810 [PubMed - indexed for MEDLINE]Related articles

    11.

    Large-scale evaluation of genetic variants in candidate genes for colorectal cancer risk in the Nurses' Health Study and the Health Professionals' Follow-up Study.

    Hazra A, Chanock S, Giovannucci E, Cox DG, Niu T, Fuchs C, Willett WC, Hunter DJ.

    Cancer Epidemiol Biomarkers Prev. 2008 Feb;17(2):311-9.PMID: 18268114 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes.

    Wang X, Tomso DJ, Liu X, Bell DA.

    Toxicol Appl Pharmacol. 2005 Sep 1;207(2 Suppl):84-90. Review.PMID: 16002116 [PubMed - indexed for MEDLINE]Related articles

    13.

    [DNA diagnosis in the age of individual made-to-order medications]

    Mashima Y.

    Nippon Ganka Gakkai Zasshi. 2004 Dec;108(12):863-85; discussion 886. Review. Japanese. PMID: 15656090 [PubMed - indexed for MEDLINE]Related articles

    14.

    Multi-SNP pharmacogenomic classifier is superior to single-SNP models for predicting drug outcome in complex diseases.

    Petrovski S, Szoeke CE, Sheffield LJ, D'souza W, Huggins RM, O'brien TJ.

    Pharmacogenet Genomics. 2009 Feb;19(2):147-52.PMID: 19077679 [PubMed - indexed for MEDLINE]Related articles

    15.

    F-SNP: computationally predicted functional SNPs for disease association studies.

    Lee PH, Shatkay H.

    Nucleic Acids Res. 2008 Jan;36(Database issue):D820-4. Epub 2007 Nov 5.PMID: 17986460 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases.

    Yang JO, Hwang S, Oh J, Bhak J, Sohn TK.

    BMC Bioinformatics. 2008 Dec 12;9 Suppl 12:S19.PMID: 19091018 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Genetic polymorphisms of EPHX1, Gsk3beta, TNFSF8 and myeloma cell DKK-1 expression linked to bone disease in myeloma.

    Durie BG, Van Ness B, Ramos C, Stephens O, Haznadar M, Hoering A, Haessler J, Katz MS, Mundy GR, Kyle RA, Morgan GJ, Crowley J, Barlogie B, Shaughnessy J Jr.

    Leukemia. 2009 Oct;23(10):1913-9. Epub 2009 Aug 6.PMID: 19657367 [PubMed - indexed for MEDLINE]Related articles

    18.

    Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma.

    Hayden PJ, Tewari P, Morris DW, Staines A, Crowley D, Nieters A, Becker N, de Sanjosé S, Foretova L, Maynadié M, Cocco PL, Boffetta P, Brennan P, Chanock SJ, Browne PV, Lawler M.

    Hum Mol Genet. 2007 Dec 15;16(24):3117-27. Epub 2007 Sep 26.PMID: 17901044 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Missingness in the T1DGC MHC fine-mapping SNP data: association with HLA genotype and potential influence on genetic association studies.

    James I, McKinnon E, Gaudieri S, Morahan G; Diabetes Genetics Consortium.

    Diabetes Obes Metab. 2009 Feb;11 Suppl 1:101-7.PMID: 19143822 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    SNP-SNP interactions in breast cancer susceptibility.

    Onay VU, Briollais L, Knight JA, Shi E, Wang Y, Wells S, Li H, Rajendram I, Andrulis IL, Ozcelik H.

    BMC Cancer. 2006 May 3;6:114.PMID: 16672066 [PubMed - indexed for MEDLINE]Related articlesFree article

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