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Wenqin Ying
Researcher at Chinese Academy of Sciences
Publications - 21
Citations - 1711
Wenqin Ying is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: CRISPR & Genome editing. The author has an hindex of 11, co-authored 19 publications receiving 1123 citations.
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Journal ArticleDOI
Cytosine base editor generates substantial off-target single-nucleotide variants in mouse embryos.
Erwei Zuo,Yidi Sun,Wu Wei,Wu Wei,Wu Wei,Tanglong Yuan,Wenqin Ying,Hao Sun,Liyun Yuan,Lars M. Steinmetz,Lars M. Steinmetz,Yixue Li,Yixue Li,Hui Yang +13 more
TL;DR: A method named GOTI (genome-wide off-target analysis by two-cell embryo injection) is developed to detect off- target mutations by editing one blastomere of two- cell mouse embryos using either CRISPR-Cas9 or base editors.
Journal ArticleDOI
Homology-mediated end joining-based targeted integration using CRISPR/Cas9
Xuan Yao,Xing Wang,Xinde Hu,Zhen Liu,Junlai Liu,Haibo Zhou,Xiaowen Shen,Yu Wei,Yu Wei,Zijian Huang,Wenqin Ying,Yan Wang,Yanhong Nie,Chen-Chen Zhang,Sanlan Li,Leping Cheng,Qifang Wang,Yan Wu,Pengyu Huang,Qiang Sun,Linyu Shi,Hui Yang +21 more
TL;DR: A homology-mediated end joining (HMEJ)-based strategy is devised, using CRISPR/Cas9-mediated cleavage of both transgene donor vector that contains guide RNA target sites and ∼800 bp of homology arms, and the targeted genome, with an efficiency much greater than HR-, NHEJ- and MMEJ-based strategies.
Journal ArticleDOI
In vivo simultaneous transcriptional activation of multiple genes in the brain using CRISPR-dCas9-activator transgenic mice
Haibo Zhou,Junlai Liu,Junlai Liu,Changyang Zhou,Ni Gao,Zhiping Rao,He Li,Xinde Hu,Changlin Li,Xuan Yao,Xiaowen Shen,Yidi Sun,Yu Wei,Fei Liu,Wenqin Ying,Junming Zhang,Cheng Tang,Xu Zhang,Hua-Tai Xu,Linyu Shi,Leping Cheng,Pengyu Huang,Hui Yang +22 more
TL;DR: A transgenic mouse is generated using an improved dCas9 system that enables simultaneous and precise in vivo transcriptional activation of multiple genes and long noncoding RNAs in the nervous system and is able to use targeted activation of endogenous neurogenic genes in these transgenic mice to directly and efficiently convert astrocytes into functional neurons in vivo.
Journal ArticleDOI
One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs
Erwei Zuo,Yijun Cai,Kui Li,Yu Wei,Yu Wei,Bang-An Wang,Yidi Sun,Zhen Liu,Ji-Wei Liu,Xinde Hu,Wei Wei,Wei Wei,Xiaona Huo,Linyu Shi,Cheng Tang,Dan Liang,Yan Wang,Yanhong Nie,Chen-Chen Zhang,Xuan Yao,Xing Wang,Changyang Zhou,Wenqin Ying,Qifang Wang,Renchao Chen,Qi Shen,Guoliang Xu,Jinsong Li,Qiang Sun,Zhi-Qi Xiong,Hui Yang +30 more
TL;DR: It is shown that single gene or multiple genes can be completely knocked out in mouse and monkey embryos by zygotic injection of Cas9 mRNA and multiple adjacent single-guide RNAs that target only a single key exon of each gene.
Journal ArticleDOI
CRISPR/Cas9-mediated targeted chromosome elimination
Erwei Zuo,Xiaona Huo,Xuan Yao,Xinde Hu,Yidi Sun,Jianhang Yin,Bingbing He,Xing Wang,Linyu Shi,Jie Ping,Yu Wei,Yu Wei,Wenqin Ying,Wei Wei,Wei Wei,Wenjia Liu,Cheng Tang,Yixue Li,Jiazhi Hu,Hui Yang +19 more
TL;DR: CRISPR/Cas9-mediated targeted chromosome elimination offers a new approach to develop animal models with chromosome deletions, and a potential therapeutic strategy for human aneuploidy diseases involving additional chromosomes.