BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 23824852)

  • 1. Pharmacogenetics using Luminex® xMAP® technology: a method for developing a custom multiplex single nucleotide polymorphism mutation assay.
    Spierings G; Dunbar SA
    Methods Mol Biol; 2013; 1015():115-26. PubMed ID: 23824852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical SNP detection by the SmartAmp method.
    Ishikawa T; Hayashizaki Y
    Methods Mol Biol; 2013; 1015():55-69. PubMed ID: 23824848
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies.
    De La Vega FM; Dailey D; Ziegle J; Williams J; Madden D; Gilbert DA
    Biotechniques; 2002 Jun; Suppl():48-50, 52, 54. PubMed ID: 12083398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid and cost-effective SNP detection method: application of SmartAmp2 to pharmacogenomics research.
    Mitani Y; Lezhava A; Sakurai A; Horikawa A; Nagakura M; Hayashizaki Y; Ishikawa T
    Pharmacogenomics; 2009 Jul; 10(7):1187-97. PubMed ID: 19604094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The use of single-nucleotide polymorphism maps in pharmacogenomics.
    McCarthy JJ; Hilfiker R
    Nat Biotechnol; 2000 May; 18(5):505-8. PubMed ID: 10802616
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Biomarkers in the era of personalized medicine - a multiplexed SNP assay using capillary electrophoresis for assessing drug metabolism capacity.
    Rai AJ; Yee J; Fleisher M
    Scand J Clin Lab Invest Suppl; 2010; 242():15-8. PubMed ID: 20515270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification.
    Ye F; Li MS; Taylor JD; Nguyen Q; Colton HM; Casey WM; Wagner M; Weiner MP; Chen J
    Hum Mutat; 2001 Apr; 17(4):305-16. PubMed ID: 11295829
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise.
    Bray MS; Boerwinkle E; Doris PA
    Hum Mutat; 2001 Apr; 17(4):296-304. PubMed ID: 11295828
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DMET microarray technology for pharmacogenomics-based personalized medicine.
    Burmester JK; Sedova M; Shapero MH; Mansfield E
    Methods Mol Biol; 2010; 632():99-124. PubMed ID: 20217574
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of SNPs, or mutations in sequence chromatograms.
    Draper N
    Methods Mol Biol; 2008; 439():35-52. PubMed ID: 18370094
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiplex SNP detection in multiple codons for accurate drug therapy.
    Sayyed DR; Nimse SB; Song KS; Sung N; Kim T
    Chem Commun (Camb); 2014 Dec; 50(93):14585-8. PubMed ID: 25307892
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Random mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods.
    Nickerson ML; Warren MB; Zbar B; Schmidt LS
    Hum Mutat; 2001 Mar; 17(3):210-9. PubMed ID: 11241843
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiplex genotyping for thrombophilia-associated SNPs by universal bead arrays.
    Bortolin S
    Methods Mol Biol; 2009; 496():59-72. PubMed ID: 18839105
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new method for SNP discovery.
    Xu JY; Xu GB; Chen SL
    Biotechniques; 2009 Mar; 46(3):201-8. PubMed ID: 19317663
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dynamic variable selection in SNP genotype autocalling from APEX microarray data.
    Podder M; Welch WJ; Zamar RH; Tebbutt SJ
    BMC Bioinformatics; 2006 Nov; 7():521. PubMed ID: 17137502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SNPs and haplotypes: genetic markers for disease and drug response (review).
    Shastry BS
    Int J Mol Med; 2003 Mar; 11(3):379-82. PubMed ID: 12579344
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exo-proofreading, a versatile SNP scoring technology.
    Cahill P; Bakis M; Hurley J; Kamath V; Nielsen W; Weymouth D; Dupuis J; Doucette-Stamm L; Smith DR
    Genome Res; 2003 May; 13(5):925-31. PubMed ID: 12695330
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A semi-automated system for analysis and storage of SNPs.
    Lehnert V; Holzwarth J; Ott M; Thompson A; Demmak S; Foernzler D
    Hum Mutat; 2001 Apr; 17(4):243-54. PubMed ID: 11295821
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Criteria for the selection of single nucleotide polymorphisms in pathway pharmacogenetics: TNF inhibitors as a case study.
    Kooloos WM; Wessels JA; van der Straaten T; Huizinga TW; Guchelaar HJ
    Drug Discov Today; 2009 Sep; 14(17-18):837-44. PubMed ID: 19524701
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A high-throughput SNP typing system for genome-wide association studies].
    Ohnishi Y
    Gan To Kagaku Ryoho; 2002 Nov; 29(11):2031-6. PubMed ID: 12465410
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.