CRISPR/Cas9 Mediated Therapeutic Approach in Huntington’s Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Metals and Alloys,Mechanical Engineering,Mechanics of Materials
Link
https://link.springer.com/content/pdf/10.1007/s12035-022-03150-5.pdf
Reference54 articles.
1. Guan L, Han Y, Yang C, Lu S, Du J, Li H, Lin J (2022) CRISPR-Cas9-mediated gene therapy in neurological disorders. Mol Neurobiol 59(2):968–982
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3. Malankhanova TB, Malakhova AA, Medvedev SP et al (2017) Modern genome editing technologies in Huntington’s disease research. J Huntingt Dis 6:19–31
4. Kumar A, Kumar V, Singh K et al (2020) Therapeutic advances for Huntington’s disease. Brain Sci 10:43
5. Liu P-Q, Tan S, Mendel MC et al (2005) Isogenic human cell lines for drug discovery: regulation of target gene expression by engineered zinc-finger protein transcription factors. J Biomol Screen 10:304–313
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