Making drug discovery a SN(i)P

被引:11
作者
Campbell, DA [1 ]
Valdes, A [1 ]
Spurr, N [1 ]
机构
[1] SmithKline Beecham Pharmaceut, Genet Technol, Harlow CM19 5AW, Essex, England
关键词
D O I
10.1016/S1359-6446(00)01546-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmaceutical world is coming to terms with the fact the fact that genetic variation is the key to identifying the biological basis behind both susceptibility to disease-and the response to drugs. Genetic variation within drug targets is common and we can safely predict that genetic factors influence almost every human disease. Thus, the study of single-nucleotide polymorphisms (SNPs) is crucial for characterizing molecular targets and can also validate the role of these targets in disease. This article reviews the progress to-date and outlines some of the key areas in which SNPs will impact on the drug discovery process.
引用
收藏
页码:388 / 396
页数:9
相关论文
共 70 条
  • [1] Alves S, 2000, HUM MUTAT, V15, P246, DOI 10.1002/(SICI)1098-1004(200003)15:3<246::AID-HUMU5>3.0.CO
  • [2] 2-#
  • [3] [Anonymous], 1999, NAT GENET S, V21
  • [4] BASELGA J, 1997, ONCOLOGY HUNTINGT S2, V3, P43
  • [5] Infrared MALDI mass spectrometry of large nucleic acids
    Berkenkamp, S
    Kirpekar, F
    Hillenkamp, F
    [J]. SCIENCE, 1998, 281 (5374) : 260 - 262
  • [6] BOTSTEIN D, 1980, AM J HUM GENET, V32, P314
  • [7] BOYCEJACINO MT, 1994, AM J HUM GENET, V55, pA2088
  • [8] Brosen K, 1992, Clin Neuropharmacol, V15 Suppl 1 Pt A, p80A
  • [9] Brüss M, 1999, PHARMACOGENETICS, V9, P95
  • [10] Sequence diversity in 36 candidate genes for cardiovascular disorders
    Cambien, F
    Poirier, O
    Nicaud, V
    Herrmann, SM
    Mallet, C
    Ricard, S
    Behague, I
    Hallet, V
    Blanc, H
    Loukaci, V
    Thillet, J
    Evans, A
    Ruidavets, JB
    Arveiler, D
    Luc, G
    Tiret, L
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (01) : 183 - 191