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Phillip W L Tai

Showing results (1-10 of 58) with videos related to

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Human Gene Therapy|February 20, 2020
ITRs: The Terminal FrontierPhillip W L Tai
Human Gene Therapy|November 6, 2023
Integration of Gene Therapy Vectors: A Risk Factor for Tumorigenesis or Another Commensal Property of Adeno-Associated Viruses That Benefits Long-Term Transgene Expression?Phillip W L Tai
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 25, 2024
AAV-RNAi constructs promote DRG toxicityJun Xie, Phillip W L Tai
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 18, 2023
Learning to lock down genetic diseases without throwing away the keyPhillip W L Tai, Jun Xie
Nature Reviews. Drug Discovery|February 3, 2019
Adeno-associated virus vector as a platform for gene therapy deliveryDan Wang, Phillip W L Tai, Guangping Gao
Frontiers in Immunology|May 28, 2021
Vectored Immunotherapeutics for Infectious Diseases: Can rAAVs Be The Game Changers for Fighting Transmissible Pathogens?Wei Zhan, Manish Muhuri, Phillip W L Tai, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 2, 2011
Analysis of muscle gene transcription in cultured skeletal muscle cellsCharis L Himeda, Phillip W L Tai, Stephen D Hauschka
Human Gene Therapy Methods|May 11, 2017
A Scalable and Accurate Method for Quantifying Vector Genomes of Recombinant Adeno-Associated Viruses in Crude LysateJianzhong Ai, Raed Ibraheim, Phillip W L Tai, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 21, 2019
Intravenous Infusion of AAV for Widespread Gene Delivery to the Nervous SystemDominic J Gessler, Phillip W L Tai, Jia Li, et al.
Signal Transduction and Targeted Therapy|February 9, 2021
Viral vector platforms within the gene therapy landscapeJote T Bulcha, Yi Wang, Hong Ma, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Human Gene Therapy|February 20, 2020
ITRs: The Terminal FrontierPhillip W L Tai
Human Gene Therapy|November 6, 2023
Integration of Gene Therapy Vectors: A Risk Factor for Tumorigenesis or Another Commensal Property of Adeno-Associated Viruses That Benefits Long-Term Transgene Expression?Phillip W L Tai
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 25, 2024
AAV-RNAi constructs promote DRG toxicityJun Xie, Phillip W L Tai
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 18, 2023
Learning to lock down genetic diseases without throwing away the keyPhillip W L Tai, Jun Xie
Nature Reviews. Drug Discovery|February 3, 2019
Adeno-associated virus vector as a platform for gene therapy deliveryDan Wang, Phillip W L Tai, Guangping Gao
Frontiers in Immunology|May 28, 2021
Vectored Immunotherapeutics for Infectious Diseases: Can rAAVs Be The Game Changers for Fighting Transmissible Pathogens?Wei Zhan, Manish Muhuri, Phillip W L Tai, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 2, 2011
Analysis of muscle gene transcription in cultured skeletal muscle cellsCharis L Himeda, Phillip W L Tai, Stephen D Hauschka
Human Gene Therapy Methods|May 11, 2017
A Scalable and Accurate Method for Quantifying Vector Genomes of Recombinant Adeno-Associated Viruses in Crude LysateJianzhong Ai, Raed Ibraheim, Phillip W L Tai, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 21, 2019
Intravenous Infusion of AAV for Widespread Gene Delivery to the Nervous SystemDominic J Gessler, Phillip W L Tai, Jia Li, et al.
Signal Transduction and Targeted Therapy|February 9, 2021
Viral vector platforms within the gene therapy landscapeJote T Bulcha, Yi Wang, Hong Ma, et al.
Pageof 6