The genetics of neurodegenerative diseases

被引:58
作者
Hardy, John
Orr, Harry
机构
[1] NIA, Neurogenet Lab, Bethesda, MD 20892 USA
[2] UCL Natl Hosp Neurol & Neurosurg, Reta Lila Weston Inst Neurol Studies, London, England
[3] Univ Minnesota, Dept Biochem, Dept Lab Med & Pathol, Minneapolis, MN USA
[4] Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA
基金
英国医学研究理事会;
关键词
ataxia; dementia; parkinsonism; polyglutamine; alpha-synuclein; tau;
D O I
10.1111/j.1471-4159.2006.03979.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the last 50 years, an enormous amount of progress has been made in dissecting the etiology of hereditary neurodegenerative diseases, including the dementias, the parkinsonisms, the ataxias and the motor-neuron diseases. In addition, these genetic findings are beginning to provide insights into the pathogeneses of the sporadic forms of the diseases. Through animal and cellular modeling studies we are beginning to gain insights into the pathogenic pathways to disease. This mechanistic understanding is now leading to therapeutic strategies based on this new understanding. As yet, however, no mechanistic therapies are in use in the clinic.
引用
收藏
页码:1690 / 1699
页数:10
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