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Xinde Hu

Showing results (31-40 of 37) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|June 26, 2021
Gene editing in a Myo6 semi-dominant mouse model rescues auditory functionYuanyuan Xue, Xinde Hu, Daqi Wang, et al.
Nature Genetics|June 10, 2026
Linking GWAS risk genes to transcriptional features of major depressive disorder via in vivo Perturb-seqLiansheng Zhang, Xiangrui Kong, Qi Ma, et al.
Nature Neuroscience|January 17, 2018
In vivo simultaneous transcriptional activation of multiple genes in the brain using CRISPR-dCas9-activator transgenic miceHaibo Zhou, Junlai Liu, Changyang Zhou, et al.
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.
Cell Research|May 20, 2017
Homology-mediated end joining-based targeted integration using CRISPR/Cas9Xuan Yao, Xing Wang, Xinde Hu, 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.
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 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 26, 2021
Gene editing in a Myo6 semi-dominant mouse model rescues auditory functionYuanyuan Xue, Xinde Hu, Daqi Wang, et al.
Nature Genetics|June 10, 2026
Linking GWAS risk genes to transcriptional features of major depressive disorder via in vivo Perturb-seqLiansheng Zhang, Xiangrui Kong, Qi Ma, et al.
Nature Neuroscience|January 17, 2018
In vivo simultaneous transcriptional activation of multiple genes in the brain using CRISPR-dCas9-activator transgenic miceHaibo Zhou, Junlai Liu, Changyang Zhou, et al.
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.
Cell Research|May 20, 2017
Homology-mediated end joining-based targeted integration using CRISPR/Cas9Xuan Yao, Xing Wang, Xinde Hu, 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.
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 4