Suchergebnisse

Double strand break repair by capture of retrotransposon sequences and reverse-transcribed spliced mRNA sequences in mouse zygotes von Ryuichi Ono, Masayuki Ishii, Yoshitaka Fujihara, Moe Kitazawa, Takako Usami, Tomoko Kaneko‐Ishino, Jun Kanno, Masahito Ikawa, Fumitoshi Ishino

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CRISPR/Cas9-based generation of knockdown mice by intronic insertion of artificial microRNA using longer single-stranded DNA von Hiromi Miura, Channabasavaiah B. Gurumurthy, Takehito Sato, Masahiro Sato, Masato Ohtsuka

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Efficient CRISPR/Cas9-mediated biallelic gene disruption and site-specific knockin after rapid selection of highly active sgRNAs in pigs von Xianlong Wang, Jinwei Zhou, Chunwei Cao, Jiaojiao Huang, Tang Hai, Yanfang Wang, Qiantao Zheng, Hongyong Zhang, Guosong Qin, Xiangnan Miao, Hongmei Wang, Suizhong Cao, Qi Zhou, Jianguo Zhao

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CRISPR mediated somatic cell genome engineering in the chicken von Nadège Véron, Zhengdong Qu, Phoebe A S Kipen, Claire E. Hirst, Christophe Marcelle

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Transcriptome-wide dynamics of RNA pseudouridylation von John Karijolich, Chengqi Yi, Yi‐Tao Yu

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Cas9-Assisted Targeting of CHromosome segments CATCH enables one-step targeted cloning of large gene clusters von Wenjun Jiang, Xuejin Zhao, Tslil Gabrieli, Chunbo Lou, Yuval Ebenstein, Ting Zhu

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Dual gRNAs guided CRISPR/Cas9 system inhibits hepatitis B virus replication von Jie Wang

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Enhancing flavonoid production by systematically tuning the central metabolic pathways based on a CRISPR interference system in Escherichia coli von Junjun Wu, Guocheng Du, Jian Chen, Jingwen Zhou

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Rapid and efficient one-step generation of paired gRNA CRISPR-Cas9 libraries von Joana A. Vidigal, Andrea Ventura

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Precise Gene Deletion and Replacement Using the CRISPR/Cas9 System in Human Cells von Qiupeng Zheng, Xiaohong Cai, Meng How Tan, Steven Schaffert, Christopher P. Arnold, Xue Gong, Changzheng Chen, Shenglin Huang

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Engineering large viral DNA genomes using the CRISPR‐Cas9 system von Tadahiro Suenaga, Masako Kohyama, Kouyuki Hirayasu, Hisashi Arase

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Engineering Human Stem Cell Lines with Inducible Gene Knockout using CRISPR/Cas9 von Yuejun Chen, Jingyuan Cao, Man Xiong, Andrew J. Petersen, Yi Dong, Yunlong Tao, Cindy Huang, Zhongwei Du, Su‐Chun Zhang

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Multiplexable, locus-specific targeting of long RNAs with CRISPR-Display von David M. Shechner, Ezgi Hacisuleyman, Scott T. Younger, John L. Rinn

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Exploiting <scp>CRISPR</scp>/<scp>C</scp>as systems for biotechnology von Timothy R. Sampson, David S. Weiss

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Targeted mutagenesis in soybean using the CRISPR-Cas9 system von Xianjun Sun, Zheng Hu, Rui Chen, Qiyang Jiang, Guohua Song, Hui Zhang, Yajun Xi

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A Conserved Structural Chassis for Mounting Versatile CRISPR RNA-Guided Immune Responses von Ryan N. Jackson, Blake Wiedenheft

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Mechanism of CRISPR-RNA guided recognition of DNA targets in<i>Escherichia coli</i> von Paul B. G. van Erp, Ryan N. Jackson, Joshua Carter, Sarah Golden, Scott Bailey, Blake Wiedenheft

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Off-target mutations are rare in Cas9-modified mice von Vivek Iyer, Bin Shen, Zhi‐Gang She, Alex Hodgkins, Thomas Keane, Xingxu Huang, William C. Skarnes

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Electroporation enables the efficient mRNA delivery into the mouse zygotes and facilitates CRISPR/Cas9-based genome editing von Masakazu Hashimoto, Tatsuya Takemoto

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Genome Editing in Mouse Spermatogonial Stem Cell Lines Using TALEN and Double-Nicking CRISPR/Cas9 von Takuya Sato, Tetsushi Sakuma, Tetsuhiro Yokonishi, Kumiko Katagiri, Satoshi Kamimura, Narumi Ogonuki, Atsuo Ogura, Takashi Yamamoto, Takehiko Ogawa

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