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精神疾病小鼠模型验证标准。

Criteria for validating mouse models of psychiatric diseases.

作者信息

Chadman Kathryn K, Yang Mu, Crawley Jacqueline N

机构信息

Laboratory of Behavioral Neuroscience, Intramural Research Program, National Institute of Mental Health, Bethesda 20892-3730, Maryland, USA.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):1-11. doi: 10.1002/ajmg.b.30777.

Abstract

Animal models of human diseases are in widespread use for biomedical research. Mouse models with a mutation in a single gene or multiple genes are excellent research tools for understanding the role of a specific gene in the etiology of a human genetic disease. Ideally, the mouse phenotypes will recapitulate the human phenotypes exactly. However, exact matches are rare, particularly in mouse models of neuropsychiatric disorders. This article summarizes the current strategies for optimizing the validity of a mouse model of a human brain dysfunction. We address the common question raised by molecular geneticists and clinical researchers in psychiatry, "what is a 'good enough' mouse model"?

摘要

人类疾病的动物模型在生物医学研究中被广泛使用。单基因或多基因发生突变的小鼠模型是理解特定基因在人类遗传疾病病因中作用的优秀研究工具。理想情况下,小鼠表型将精确重现人类表型。然而,完全匹配的情况很少见,尤其是在神经精神疾病的小鼠模型中。本文总结了当前优化人类脑功能障碍小鼠模型有效性的策略。我们探讨了分子遗传学家和精神病学临床研究人员提出的常见问题:“什么是‘足够好’的小鼠模型?”

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1dd/2914616/0a43c7a86bfc/nihms222129f1.jpg

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