BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 17375650)

  • 21. A systematic method for mapping multiple loci: an application to construct a genetic network for rheumatoid arthritis.
    Li C; Zhang G; Li X; Rao S; Gong B; Jiang W; Hao D; Wu P; Wu C; Du L; Xiao Y; Wang Y
    Gene; 2008 Jan; 408(1-2):104-11. PubMed ID: 18082339
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Copy-number variation and association studies of human disease.
    McCarroll SA; Altshuler DM
    Nat Genet; 2007 Jul; 39(7 Suppl):S37-42. PubMed ID: 17597780
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Innate immunity genes as candidate genes: searching for relevant natural polymorphisms in databases and assessing family-based association of polymorphisms with human diseases.
    Rihet P
    Methods Mol Biol; 2008; 415():17-48. PubMed ID: 18370146
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Introduction to SNPs: discovery of markers for disease.
    Weiner MP; Hudson TJ
    Biotechniques; 2002 Jun; Suppl():4-7, 10, 12-3. PubMed ID: 12083396
    [No Abstract]   [Full Text] [Related]  

  • 25. The genetics of multiple sclerosis: SNPs to pathways to pathogenesis.
    Oksenberg JR; Baranzini SE; Sawcer S; Hauser SL
    Nat Rev Genet; 2008 Jul; 9(7):516-26. PubMed ID: 18542080
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Common polymorphic transcript variation in human disease.
    Fraser HB; Xie X
    Genome Res; 2009 Apr; 19(4):567-75. PubMed ID: 19189928
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [The Human Genome Project, genetic viability and genetic epidemiology].
    Hagymási K; Tulassay Z
    Orv Hetil; 2005 Dec; 146(51):2575-80. PubMed ID: 16468611
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [The single nucleotide polymorphisms and its application to forensic medicine].
    Hu R; Wu XY
    Fa Yi Xue Za Zhi; 2001 Nov; 17(4):249-51, 254. PubMed ID: 12533878
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.
    Beckmann JS; Estivill X; Antonarakis SE
    Nat Rev Genet; 2007 Aug; 8(8):639-46. PubMed ID: 17637735
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Microarray-based DNA profiling to study genomic aberrations.
    Waddell N
    IUBMB Life; 2008 Jul; 60(7):437-40. PubMed ID: 18553550
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The challenge of using SNPs in the understanding and treatment of disease.
    Schifreen RS; Storts DR; Buller AM
    Biotechniques; 2002 Jun; Suppl():14-6, 18, 20-1. PubMed ID: 12083392
    [No Abstract]   [Full Text] [Related]  

  • 32. Structural variation in the human genome.
    Feuk L; Carson AR; Scherer SW
    Nat Rev Genet; 2006 Feb; 7(2):85-97. PubMed ID: 16418744
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 'Other' applications of single nucleotide polymorphisms.
    Ding C
    Trends Biotechnol; 2007 Jul; 25(7):279-83. PubMed ID: 17493698
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Single nucleotide polymorphism discovery in barley using autoSNPdb.
    Duran C; Appleby N; Vardy M; Imelfort M; Edwards D; Batley J
    Plant Biotechnol J; 2009 May; 7(4):326-33. PubMed ID: 19386041
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes.
    Sinnett D; Beaulieu P; Bélanger H; Lefebvre JF; Langlois S; Théberge MC; Drouin S; Zotti C; Hudson TJ; Labuda D
    Genomics; 2006 Jun; 87(6):704-10. PubMed ID: 16500075
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Joe Doupe Young Investigators Award. The Human Genome Project: tools for the identification of disease genes.
    Hudson TJ
    Clin Invest Med; 1998 Dec; 21(6):267-76. PubMed ID: 9885761
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Application of the duplex-specific nuclease preference method to the analysis of point mutations in human genes].
    Al'tshuler IM; Zhulidov PA; Bogdanova EA; Mudrik NN; Shagin DA
    Bioorg Khim; 2005; 31(6):627-36. PubMed ID: 16363136
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The future of genetic research on appetitive behavior.
    Kowalski TJ
    Appetite; 2004 Feb; 42(1):11-4. PubMed ID: 15036778
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies.
    Tan EC; Loh M; Chuon D; Lim YP
    Hum Mutat; 2006 Mar; 27(3):232-5. PubMed ID: 16429432
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Singleton SNPs in the human genome and implications for genome-wide association studies.
    Ke X; Taylor MS; Cardon LR
    Eur J Hum Genet; 2008 Apr; 16(4):506-15. PubMed ID: 18197193
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.