Generation of a tyrosine hydroxylase-2A-Cre knockin non-human primate model by homology-directed-repair-biased CRISPR genome editing-Reference-Cited by-同舟云学术

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Generation of a tyrosine hydroxylase-2A-Cre knockin non-human primate model by homology-directed-repair-biased CRISPR genome editing

Published:2023-09 Issue:9 Volume:3 Page:100590
ISSN:2667-2375
Container-title:Cell Reports Methods
language:en
Short-container-title:Cell Reports Methods

Author:

Yoshimatsu Sho,Okahara Junko,Yoshie Junko,Igarashi Yoko,Nakajima Ryusuke,Sanosaka Tsukasa,Qian Emi,Sato Tsukika,Kobayashi Hiroya,Morimoto Satoru,Kishi Noriyuki,Pillis Devin M.,Malik Punam,Noce Toshiaki,Okano Hideyuki^ORCID

Publisher

Elsevier BV

Subject

Computer Science Applications,Radiology, Nuclear Medicine and imaging,Genetics,Biochemistry, Genetics and Molecular Biology (miscellaneous),Biochemistry,Biotechnology

Reference47 articles.

1. The common marmoset as a novel animal model system for biomedical and neuroscience research applications;Okano;Semin. Fetal Neonatal Med.,2012

2. Common marmoset as a new model animal for neuroscience research and genome editing technology;Kishi;Dev. Growth Differ.,2014

3. Generation of transgenic non-human primates with germline transmission;Sasaki;Nature,2009

4. Generation of a Nonhuman Primate Model of Severe Combined Immunodeficiency Using Highly Efficient Genome Editing;Sato;Cell Stem Cell,2016

5. Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset;Heide;Science,2020

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