Multicolor CRISPR labeling of chromosomal loci in human cells von Ma, Hanhui, Naseri, Ardalan, Reyes-Gutierrez, Pablo, Wolfe, Scot A., Zhang, Shaojie, Pederson, Thoru

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Creating and evaluating accurate CRISPR-Cas9 scalpels for genomic surgery von Bolukbasi, Mehmet Fatih, Gupta, Ankit, Wolfe, Scot A

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Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing von Yin, Hao, Song, Chun-Qing, Suresh, Sneha, Wu, Qiongqiong, Walsh, Stephen, Rhym, Luke Hyunsik, Mintzer, Esther, Bolukbasi, Mehmet Fatih, Zhu, Lihua Julie, Kauffman, Kevin, Mou, Haiwei, Oberholzer, Alicia, Ding, Junmei, Kwan, Suet-Yan, Bogorad, Roman L, Zatsepin, Timofei, Koteliansky, Victor, Wolfe, Scot A, Xue, Wen, Langer, Robert, Anderson, Daniel G

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Forward and Reverse Genetic Approaches for the Analysis of Vertebrate Development in the Zebrafish von Lawson, Nathan D., Wolfe, Scot A.

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Therapeutic base editing of human hematopoietic stem cells von Zeng, Jing, Wu, Yuxuan, Ren, Chunyan, Bonanno, Jasmine, Shen, Anne H., Shea, Devlin, Gehrke, Jason M., Clement, Kendell, Luk, Kevin, Yao, Qiuming, Kim, Rachel, Wolfe, Scot A., Manis, John P., Pinello, Luca, Joung, J. Keith, Bauer, Daniel E.

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Improved prime editors enable pathogenic allele correction and cancer modelling in adult mice von Liu, Pengpeng, Liang, Shun-Qing, Zheng, Chunwei, Mintzer, Esther, Zhao, Yan G., Ponnienselvan, Karthikeyan, Mir, Aamir, Sontheimer, Erik J., Gao, Guangping, Flotte, Terence R., Wolfe, Scot A., Xue, Wen

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Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo von Yin, Hao, Song, Chun-Qing, Dorkin, Joseph R, Zhu, Lihua J, Li, Yingxiang, Wu, Qiongqiong, Park, Angela, Yang, Junghoon, Suresh, Sneha, Bizhanova, Aizhan, Gupta, Ankit, Bolukbasi, Mehmet F, Walsh, Stephen, Bogorad, Roman L, Gao, Guangping, Weng, Zhiping, Dong, Yizhou, Koteliansky, Victor, Wolfe, Scot A, Langer, Robert, Xue, Wen, Anderson, Daniel G

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Highly efficient therapeutic gene editing of human hematopoietic stem cells von Wu, Yuxuan, Zeng, Jing, Roscoe, Benjamin P., Liu, Pengpeng, Yao, Qiuming, Lazzarotto, Cicera R., Clement, Kendell, Cole, Mitchel A., Luk, Kevin, Baricordi, Cristina, Shen, Anne H., Ren, Chunyan, Esrick, Erica B., Manis, John P., Dorfman, David M., Williams, David A., Biffi, Alessandra, Brugnara, Carlo, Biasco, Luca, Brendel, Christian, Pinello, Luca, Tsai, Shengdar Q., Wolfe, Scot A., Bauer, Daniel E.

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Reducing the inherent auto-inhibitory interaction within the pegRNA enhances prime editing efficiency von Ponnienselvan, Karthikeyan, Liu, Pengpeng, Nyalile, Thomas, Oikemus, Sarah, Maitland, Stacy A, Lawson, Nathan D, Luban, Jeremy, Wolfe, Scot A

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Cas9 effector-mediated regulation of transcription and differentiation in human pluripotent stem cells von Kearns, Nicola A, Genga, Ryan M J, Enuameh, Metewo S, Garber, Manuel, Wolfe, Scot A, Maehr, René

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Arterial-venous network formation during brain vascularization involves hemodynamic regulation of chemokine signaling von Bussmann, Jeroen, Wolfe, Scot A, Siekmann, Arndt F

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A Novel miRNA Processing Pathway Independent of Dicer Requires Argonaute2 Catalytic Activity von Cifuentes, Daniel, Xue, Huiling, Taylor, David W., Patnode, Heather, Mishima, Yuichiro, Cheloufi, Sihem, Ma, Enbo, Mane, Shrikant, Hannon, Gregory J., Lawson, Nathan D., Wolfe, Scot A., Giraldez, Antonio J.

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Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo von Ibraheim, Raed, Tai, Phillip W. L., Mir, Aamir, Javeed, Nida, Wang, Jiaming, Rodríguez, Tomás C., Namkung, Suk, Nelson, Samantha, Khokhar, Eraj Shafiq, Mintzer, Esther, Maitland, Stacy, Chen, Zexiang, Cao, Yueying, Tsagkaraki, Emmanouela, Wolfe, Scot A., Wang, Dan, Pai, Athma A., Xue, Wen, Gao, Guangping, Sontheimer, Erik J.

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Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases von Meng, Xiangdong, Noyes, Marcus B, Lawson, Nathan D, Wolfe, Scot A, Zhu, Lihua J

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Precise therapeutic gene correction by a simple nuclease-induced double-stranded break von Iyer, Sukanya, Suresh, Sneha, Guo, Dongsheng, Daman, Katelyn, Chen, Jennifer C. J., Liu, Pengpeng, Zieger, Marina, Luk, Kevin, Roscoe, Benjamin P., Mueller, Christian, King, Oliver D., Emerson, Charles P., Wolfe, Scot A.

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Rational targeting of a NuRD subcomplex guided by comprehensive in situ mutagenesis von Sher, Falak, Hossain, Mir, Seruggia, Davide, Schoonenberg, Vivien A. C., Yao, Qiuming, Cifani, Paolo, Dassama, Laura M. K., Cole, Mitchel A., Ren, Chunyan, Vinjamur, Divya S., Macias-Trevino, Claudio, Luk, Kevin, McGuckin, Connor, Schupp, Patrick G., Canver, Matthew C., Kurita, Ryo, Nakamura, Yukio, Fujiwara, Yuko, Wolfe, Scot A., Pinello, Luca, Maeda, Takahiro, Kentsis, Alex, Orkin, Stuart H., Bauer, Daniel E.

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Analysis of Homeodomain Specificities Allows the Family-wide Prediction of Preferred Recognition Sites von Noyes, Marcus B., Christensen, Ryan G., Wakabayashi, Atsuya, Stormo, Gary D., Brodsky, Michael H., Wolfe, Scot A.

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CRISPR-enhanced human adipocyte browning as cell therapy for metabolic disease von Tsagkaraki, Emmanouela, Nicoloro, Sarah M., DeSouza, Tiffany, Solivan-Rivera, Javier, Desai, Anand, Lifshitz, Lawrence M., Shen, Yuefei, Kelly, Mark, Guilherme, Adilson, Henriques, Felipe, Amrani, Nadia, Ibraheim, Raed, Rodriguez, Tomas C., Luk, Kevin, Maitland, Stacy, Friedline, Randall H., Tauer, Lauren, Hu, Xiaodi, Kim, Jason K., Wolfe, Scot A., Sontheimer, Erik J., Corvera, Silvia, Czech, Michael P.

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Genomic Access to Monarch Migration Using TALEN and CRISPR/Cas9-Mediated Targeted Mutagenesis von Markert, Matthew J, Zhang, Ying, Enuameh, Metewo S, Reppert, Steven M, Wolfe, Scot A, Merlin, Christine

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NmeCas9 is an intrinsically high-fidelity genome-editing platform von Amrani, Nadia, Gao, Xin D, Liu, Pengpeng, Edraki, Alireza, Mir, Aamir, Ibraheim, Raed, Gupta, Ankit, Sasaki, Kanae E, Wu, Tong, Donohoue, Paul D, Settle, Alexander H, Lied, Alexandra M, McGovern, Kyle, Fuller, Chris K, Cameron, Peter, Fazzio, Thomas G, Zhu, Lihua Julie, Wolfe, Scot A, Sontheimer, Erik J

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