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Nature Communications
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July 15, 2024
Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
Jiajia Lin, Ming Jin, Dong Yang, et al.
Cell Reports
|
November 14, 2024
Engineered IscB-ωRNA system with improved base editing efficiency for disease correction via single AAV delivery in mice
Ruochen Guo, Xiaozhi Sun, Feizuo Wang, et al.
Nature Communications
|
January 27, 2024
Engineering a transposon-associated TnpB-ωRNA system for efficient gene editing and phenotypic correction of a tyrosinaemia mouse model
Zhifang Li, Ruochen Guo, Xiaozhi Sun, et al.
Protein & Cell
|
June 7, 2023
Human 8-cell embryos enable efficient induction of disease-preventive mutations without off-target effect by cytosine base editor
Yinghui Wei, Meiling Zhang, Jing Hu, et al.
Nature Structural & Molecular Biology
|
March 26, 2026
Structural insight into IscB's RNA-lid-based inactivation mechanism
Feizuo Wang, Ruochen Guo, Senfeng Zhang, et al.
Nature Biotechnology
|
August 11, 2022
High-fidelity Cas13 variants for targeted RNA degradation with minimal collateral effects
Huawei Tong, Jia Huang, Qingquan Xiao, et al.
Nature Genetics
|
May 22, 2019
Genome-scale screens identify JNK-JUN signaling as a barrier for pluripotency exit and endoderm differentiation
Qing V Li, Gary Dixon, Nipun Verma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 2, 2018
Silencing of retrotransposon-derived imprinted gene RTL1 is the main cause for postimplantational failures in mammalian cloning
Dawei Yu, Jing Wang, Huiying Zou, et al.
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Search research articles
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Showing results (31-40 of 38) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 38 results.
Nature Communications
|
July 15, 2024
Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
Jiajia Lin, Ming Jin, Dong Yang, et al.
Cell Reports
|
November 14, 2024
Engineered IscB-ωRNA system with improved base editing efficiency for disease correction via single AAV delivery in mice
Ruochen Guo, Xiaozhi Sun, Feizuo Wang, et al.
Nature Communications
|
January 27, 2024
Engineering a transposon-associated TnpB-ωRNA system for efficient gene editing and phenotypic correction of a tyrosinaemia mouse model
Zhifang Li, Ruochen Guo, Xiaozhi Sun, et al.
Protein & Cell
|
June 7, 2023
Human 8-cell embryos enable efficient induction of disease-preventive mutations without off-target effect by cytosine base editor
Yinghui Wei, Meiling Zhang, Jing Hu, et al.
Nature Structural & Molecular Biology
|
March 26, 2026
Structural insight into IscB's RNA-lid-based inactivation mechanism
Feizuo Wang, Ruochen Guo, Senfeng Zhang, et al.
Nature Biotechnology
|
August 11, 2022
High-fidelity Cas13 variants for targeted RNA degradation with minimal collateral effects
Huawei Tong, Jia Huang, Qingquan Xiao, et al.
Nature Genetics
|
May 22, 2019
Genome-scale screens identify JNK-JUN signaling as a barrier for pluripotency exit and endoderm differentiation
Qing V Li, Gary Dixon, Nipun Verma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 2, 2018
Silencing of retrotransposon-derived imprinted gene RTL1 is the main cause for postimplantational failures in mammalian cloning
Dawei Yu, Jing Wang, Huiying Zou, et al.
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of 4