Search research articles
Contact Us
Filters
Showing results (1-10 of 20) with videos related to
Page
of 2
Sort By:
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 Activity
Peipei Wang, Li Xu, Yandi Gao, et al.
Skeletal Muscle
|
October 20, 2018
Automated muscle histopathology analysis using CellProfiler
Yeh 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 Mice
Li 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 tRNA
Li 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 Mice
Li 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 peptide
Jing Xu, Li Xu, Yeh S Lau, et al.
Cell & Bioscience
|
December 29, 2021
BVES is a novel interactor of ANO5 and regulates myoblast differentiation
Haiwen 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 mutations
Tingting 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 mutations
Tingting 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/Cas9
Tingting Sui, Yeh Siang Lau, Di Liu, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 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 Activity
Peipei Wang, Li Xu, Yandi Gao, et al.
Skeletal Muscle
|
October 20, 2018
Automated muscle histopathology analysis using CellProfiler
Yeh 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 Mice
Li 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 tRNA
Li 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 Mice
Li 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 peptide
Jing Xu, Li Xu, Yeh S Lau, et al.
Cell & Bioscience
|
December 29, 2021
BVES is a novel interactor of ANO5 and regulates myoblast differentiation
Haiwen 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 mutations
Tingting 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 mutations
Tingting 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/Cas9
Tingting Sui, Yeh Siang Lau, Di Liu, et al.
Page
of 2