Abstract
Gene-modified monkey models would be particularly valuable in biomedical and neuroscience research. Virus-based transgenic and programmable nucleases-based site-specific gene editing methods (TALEN, CRISPR-cas9) enable the generation of gene-modified monkeys with gain or loss of function of specific genes. Here, we describe the generation of transgenic and knock-out (KO) monkeys with high efficiency by lentivirus and programmable nucleases.
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Acknowledgment
This work was supported by grant “National Key Technology R&D Program of China 2014BAI03B00629(Q.S.)” and “Shanghai City Committee of science and technology project 14140900100 630 (Q.S.).”
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Liu, Z., Cai, Y., Sun, Q. (2017). Genome Editing of Monkey. In: Hatada, I. (eds) Genome Editing in Animals. Methods in Molecular Biology, vol 1630. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7128-2_12
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DOI: https://doi.org/10.1007/978-1-4939-7128-2_12
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Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4939-7127-5
Online ISBN: 978-1-4939-7128-2
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