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Changyang Zhou

Showing results (21-30 of 25) with videos related to

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Cell|April 10, 2020
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in MiceHaibo Zhou, Jinlin Su, Xinde Hu, et al.
Nature Biotechnology|October 1, 2025
Design of optimized epigenetic regulators for durable gene silencing with application to PCSK9 in nonhuman primatesShaoshuai Mao, Wenbo Peng, Zhengyan Feng, et al.
National Science Review|October 25, 2021
Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and miceJin-Jing Li, Xiang Lin, Cheng Tang, et al.
PNAS Nexus|November 26, 2025
A Del(5<i>Ncf1</i>-<i>Fkbp6</i>) mouse model of Williams syndrome shows coronary, aortic, and cerebral vascular abnormalities with behavioral deficitsLaurens W J Bosman, Hamid El Azzouzi, Lieke Kros, et al.
Cell Research|June 7, 2017
One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAsErwei Zuo, Yi-Jun Cai, Kui Li, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Cell|April 10, 2020
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in MiceHaibo Zhou, Jinlin Su, Xinde Hu, et al.
Nature Biotechnology|October 1, 2025
Design of optimized epigenetic regulators for durable gene silencing with application to PCSK9 in nonhuman primatesShaoshuai Mao, Wenbo Peng, Zhengyan Feng, et al.
National Science Review|October 25, 2021
Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and miceJin-Jing Li, Xiang Lin, Cheng Tang, et al.
PNAS Nexus|November 26, 2025
A Del(5<i>Ncf1</i>-<i>Fkbp6</i>) mouse model of Williams syndrome shows coronary, aortic, and cerebral vascular abnormalities with behavioral deficitsLaurens W J Bosman, Hamid El Azzouzi, Lieke Kros, et al.
Cell Research|June 7, 2017
One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAsErwei Zuo, Yi-Jun Cai, Kui Li, et al.
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