Canlyniadau Chwilio

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

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Generation of α1,3-galactosyltransferase and cytidine monophospho-<i>N</i>-acetylneuraminic acid hydroxylase gene double-knockout pigs gan Shuji Miyagawa, Hitomi Matsunari, Masahito Watanabe, Kazuaki Nakano, Kazuhiro Umeyama, Rieko Sakai, Shuko Takayanagi, Toki TAKEISHI, T. Fukuda, Sayaka Yashima, Akira Maeda, Hiroshi Eguchi, Hiroomi Okuyama, Masaki Nagaya, Hiroshi Nagashima

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CRISPR/Cas9-based generation of knockdown mice by intronic insertion of artificial microRNA using longer single-stranded DNA gan 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 gan 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 gan Nadège Véron, Zhengdong Qu, Phoebe A S Kipen, Claire E. Hirst, Christophe Marcelle

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Asymmetrical recognition of the palindromic AP1 binding site (TRE) by Fos protein complexes. gan G Risse, Karin Jooss, Manfred Neuberg, Hans-Joachim Brüller, Rolf Müller

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Cas9-Assisted Targeting of CHromosome segments CATCH enables one-step targeted cloning of large gene clusters gan 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 gan 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 gan Junjun Wu, Guocheng Du, Jian Chen, Jingwen Zhou

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

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

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In vivo genome editing of the albumin locus as a platform for protein replacement therapy gan Rajiv P. Sharma, Xavier M. Anguela, Yannick Doyon, Thomas Wechsler, Russell C. DeKelver, Scott Sproul, David E. Paschon, Jeffrey C. Miller, Robert J. Davidson, David A. Shivak, Shangzhen Zhou, Julianne Rieders, Philip D. Gregory, Michael C. Holmes, Edward J. Rebar, Katherine A. High

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Choosing the Right Tool for the Job: RNAi, TALEN, or CRISPR gan Michael Boettcher, Michael T. McManus

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

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Biallelic genome modification in F₀<i>Xenopus tropicalis</i> embryos using the CRISPR/Cas system gan Ira L. Blitz, Jacob Biesinger, Xiaohui Xie, Ken W.Y. Cho

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

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Nucleotide sequence of the enterotoxin B gene from Staphylococcus aureus gan Christopher L. Jones, S A Khan

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Multiplexable, locus-specific targeting of long RNAs with CRISPR-Display gan 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 gan Timothy R. Sampson, David S. Weiss

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

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