Human monogenic disorders -: a source of novel drug targets

被引:62
作者
Brinkman, RR
Dubé, MP
Rouleau, GA
Orr, AC
Samuels, ME [1 ]
机构
[1] Dalhousie Univ, Dept Ophthalmol, Halifax, NS B3H 3J5, Canada
[2] Dalhousie Univ, Dept Visual Sci, Halifax, NS B3H 3J5, Canada
[3] Univ British Columbia, British Columbia Canc Res Ctr, Vancouver, BC V5Z 1C3, Canada
[4] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
[5] Univ Montreal, Dept Med, Montreal, PQ, Canada
[6] Dalhousie Univ, Dept Ophthalmol & Visual Sci, Halifax, NS B3H 2Y9, Canada
关键词
D O I
10.1038/nrg1828
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The decrease in new drug applications and approvals over the past several years results from an underlying crisis in drug target identification and validation. Model organisms are being used to address this problem, in combination with novel approaches such as the International HapMap Project. What has been underappreciated is that discovery of new drug targets can also be revived by traditional Mendelian genetics. A large fraction of the human gene repertoire remains phenotypically uncharacterized, and is likely to encode many unanticipated and novel phenotypes that will be of interest to pharmaceutical and biotechnological drug developers.
引用
收藏
页码:249 / 260
页数:12
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