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Yandi Gao

Showing results (1-10 of 20) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|May 1, 2020
BEON: A Functional Fluorescence Reporter for Quantification and Enrichment of Adenine Base-Editing ActivityPeipei Wang, Li Xu, Yandi Gao, et al.
Skeletal Muscle|October 20, 2018
Automated muscle histopathology analysis using CellProfilerYeh Siang Lau, Li Xu, Yandi Gao, et al.
Journal of Visualized Experiments : Jove|August 21, 2018
Adeno-Associated Virus-Mediated Delivery of CRISPR for Cardiac Gene Editing in MiceLi Xu, Yandi Gao, Yeh Siang Lau, et al.
Nucleic Acids Research|November 2, 2016
Empower multiplex cell and tissue-specific CRISPR-mediated gene manipulation with self-cleaving ribozymes and tRNALi Xu, Lixia Zhao, Yandi Gao, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 27, 2019
Life-Long AAV-Mediated CRISPR Genome Editing in Dystrophic Heart Improves Cardiomyopathy without Causing Serious Lesions in mdx MiceLi Xu, Yeh Siang Lau, Yandi Gao, et al.
The Journal of Pathology. Clinical Research|April 18, 2018
A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptideJing Xu, Li Xu, Yeh S Lau, et al.
Cell & Bioscience|December 29, 2021
BVES is a novel interactor of ANO5 and regulates myoblast differentiationHaiwen Li, Li Xu, Yandi Gao, et al.
Cell Death & Disease|June 20, 2020
Correction: Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutationsTingting Sui, Li Xu, Yeh Siang Lau, et al.
Cell Death & Disease|May 24, 2018
Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutationsTingting Sui, Li Xu, Yeh Siang Lau, et al.
Disease Models & Mechanisms|June 7, 2018
A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9Tingting Sui, Yeh Siang Lau, Di Liu, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 1, 2020
BEON: A Functional Fluorescence Reporter for Quantification and Enrichment of Adenine Base-Editing ActivityPeipei Wang, Li Xu, Yandi Gao, et al.
Skeletal Muscle|October 20, 2018
Automated muscle histopathology analysis using CellProfilerYeh Siang Lau, Li Xu, Yandi Gao, et al.
Journal of Visualized Experiments : Jove|August 21, 2018
Adeno-Associated Virus-Mediated Delivery of CRISPR for Cardiac Gene Editing in MiceLi Xu, Yandi Gao, Yeh Siang Lau, et al.
Nucleic Acids Research|November 2, 2016
Empower multiplex cell and tissue-specific CRISPR-mediated gene manipulation with self-cleaving ribozymes and tRNALi Xu, Lixia Zhao, Yandi Gao, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 27, 2019
Life-Long AAV-Mediated CRISPR Genome Editing in Dystrophic Heart Improves Cardiomyopathy without Causing Serious Lesions in mdx MiceLi Xu, Yeh Siang Lau, Yandi Gao, et al.
The Journal of Pathology. Clinical Research|April 18, 2018
A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptideJing Xu, Li Xu, Yeh S Lau, et al.
Cell & Bioscience|December 29, 2021
BVES is a novel interactor of ANO5 and regulates myoblast differentiationHaiwen Li, Li Xu, Yandi Gao, et al.
Cell Death & Disease|June 20, 2020
Correction: Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutationsTingting Sui, Li Xu, Yeh Siang Lau, et al.
Cell Death & Disease|May 24, 2018
Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutationsTingting Sui, Li Xu, Yeh Siang Lau, et al.
Disease Models & Mechanisms|June 7, 2018
A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9Tingting Sui, Yeh Siang Lau, Di Liu, et al.
Pageof 2