Mouse models of Huntington’s disease

53Citations
Citations of this article
280Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The identification of the mutation causing Huntington’s disease (HD) has led to the generation of a large number of mouse models. These models are used to further enhance our understanding of the mechanisms underlying the disease, as well as investigating and identifying therapeutic targets for this disorder. Here we review the transgenic, knock-in mice commonly used to model HD, as well those that have been generated to study specific disease mechanisms. We then provide a brief overview of the importance of standardizing the use of HD mice and describe brief protocols used for genotyping the mouse models used within the Bates Laboratory.

Cite

CITATION STYLE

APA

Farshim, P. P., & Bates, G. P. (2018). Mouse models of Huntington’s disease. In Methods in Molecular Biology (Vol. 1780, pp. 97–120). Humana Press Inc. https://doi.org/10.1007/978-1-4939-7825-0_6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free