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Kyung Whan Yoo

Showing results (1-10 of 8) with videos related to

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Molecular Therapy. Methods & Clinical Development|October 26, 2022
Lentiviral vector mediated gene therapy for type I Dent disease ameliorates Dent disease-like phenotypes for three months in ClC-5 null miceManish Kumar Yadav, Kyung Whan Yoo, Anthony Atala, et al.
Tissue Engineering. Part C, Methods|October 12, 2018
Large-Scale Preparation of Extracellular Vesicles Enriched with Specific microRNAKyung Whan Yoo, Ning Li, Vishruti Makani, et al.
Gene Therapy|September 25, 2024
Gene therapy of Dent disease type 1 in newborn ClC-5 null mice for sustained transgene expression and gene therapy effectsPin Lyu, Manish Kumar Yadav, Kyung Whan Yoo, et al.
The CRISPR Journal|February 22, 2021
Adenine Base Editor Ribonucleoproteins Delivered by Lentivirus-Like Particles Show High On-Target Base Editing and Undetectable RNA Off-Target ActivitiesPin Lyu, Zuyan Lu, Sung-Ik Cho, et al.
Kidney International Reports|April 20, 2026
Database of <i>CLCN5</i> Pathogenic Variants Causing Dent DiseasePin Lyu, Kyung Whan Yoo, Zhuo Chen, et al.
Plos One|September 24, 2020
Sensitive and reliable evaluation of single-cut sgRNAs to restore dystrophin by a GFP-reporter assayPin Lyu, Kyung Whan Yoo, Manish Kumar Yadav, et al.
Gene Therapy|February 6, 2020
CRISPR/Cas9 increases mitotic gene conversion in human cellsParisa Javidi-Parsijani, Pin Lyu, Vishruti Makani, et al.
Nucleic Acids Research|February 14, 2019
Delivering SaCas9 mRNA by lentivirus-like bionanoparticles for transient expression and efficient genome editingBaisong Lu, Parisa Javidi-Parsijani, Vishruti Makani, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular Therapy. Methods & Clinical Development|October 26, 2022
Lentiviral vector mediated gene therapy for type I Dent disease ameliorates Dent disease-like phenotypes for three months in ClC-5 null miceManish Kumar Yadav, Kyung Whan Yoo, Anthony Atala, et al.
Tissue Engineering. Part C, Methods|October 12, 2018
Large-Scale Preparation of Extracellular Vesicles Enriched with Specific microRNAKyung Whan Yoo, Ning Li, Vishruti Makani, et al.
Gene Therapy|September 25, 2024
Gene therapy of Dent disease type 1 in newborn ClC-5 null mice for sustained transgene expression and gene therapy effectsPin Lyu, Manish Kumar Yadav, Kyung Whan Yoo, et al.
The CRISPR Journal|February 22, 2021
Adenine Base Editor Ribonucleoproteins Delivered by Lentivirus-Like Particles Show High On-Target Base Editing and Undetectable RNA Off-Target ActivitiesPin Lyu, Zuyan Lu, Sung-Ik Cho, et al.
Kidney International Reports|April 20, 2026
Database of <i>CLCN5</i> Pathogenic Variants Causing Dent DiseasePin Lyu, Kyung Whan Yoo, Zhuo Chen, et al.
Plos One|September 24, 2020
Sensitive and reliable evaluation of single-cut sgRNAs to restore dystrophin by a GFP-reporter assayPin Lyu, Kyung Whan Yoo, Manish Kumar Yadav, et al.
Gene Therapy|February 6, 2020
CRISPR/Cas9 increases mitotic gene conversion in human cellsParisa Javidi-Parsijani, Pin Lyu, Vishruti Makani, et al.
Nucleic Acids Research|February 14, 2019
Delivering SaCas9 mRNA by lentivirus-like bionanoparticles for transient expression and efficient genome editingBaisong Lu, Parisa Javidi-Parsijani, Vishruti Makani, et al.
Pageof 1