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JCI Insight
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November 15, 2019
Using a barcoded AAV capsid library to select for clinically relevant gene therapy vectors
Katja Pekrun, Gustavo De Alencastro, Qing-Jun Luo, et al.
Molecular Therapy. Methods & Clinical Development
|
September 4, 2023
Selection of viral capsids and promoters affects the efficacy of rescue of <i>Tmprss3</i>-deficient cochlea
Ksenia A Aaron, Katja Pekrun, Patrick J Atkinson, et al.
Frontiers in Immunology
|
May 8, 2023
A strategy for high antibody expression with low anti-drug antibodies using AAV9 vectors
Meredith E Davis-Gardner, Jesse A Weber, Jun Xie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 8, 2021
Improved Genome Editing through Inhibition of FANCM and Members of the BTR Dissolvase Complex
Gustavo de Alencastro, Francesco Puzzo, Mara Pavel-Dinu, et al.
Nature Biotechnology
|
April 8, 2024
Genome engineering with Cas9 and AAV repair templates generates frequent concatemeric insertions of viral vectors
Fabian P Suchy, Daiki Karigane, Yusuke Nakauchi, et al.
Molecular Therapy. Methods & Clinical Development
|
August 14, 2018
Bioengineered Viral Platform for Intramuscular Passive Vaccine Delivery to Human Skeletal Muscle
Nicole K Paulk, Katja Pekrun, Gregory W Charville, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 23, 2017
Bioengineered AAV Capsids with Combined High Human Liver Transduction In Vivo and Unique Humoral Seroreactivity
Nicole K Paulk, Katja Pekrun, Erhua Zhu, et al.
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Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
JCI Insight
|
November 15, 2019
Using a barcoded AAV capsid library to select for clinically relevant gene therapy vectors
Katja Pekrun, Gustavo De Alencastro, Qing-Jun Luo, et al.
Molecular Therapy. Methods & Clinical Development
|
September 4, 2023
Selection of viral capsids and promoters affects the efficacy of rescue of <i>Tmprss3</i>-deficient cochlea
Ksenia A Aaron, Katja Pekrun, Patrick J Atkinson, et al.
Frontiers in Immunology
|
May 8, 2023
A strategy for high antibody expression with low anti-drug antibodies using AAV9 vectors
Meredith E Davis-Gardner, Jesse A Weber, Jun Xie, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 8, 2021
Improved Genome Editing through Inhibition of FANCM and Members of the BTR Dissolvase Complex
Gustavo de Alencastro, Francesco Puzzo, Mara Pavel-Dinu, et al.
Nature Biotechnology
|
April 8, 2024
Genome engineering with Cas9 and AAV repair templates generates frequent concatemeric insertions of viral vectors
Fabian P Suchy, Daiki Karigane, Yusuke Nakauchi, et al.
Molecular Therapy. Methods & Clinical Development
|
August 14, 2018
Bioengineered Viral Platform for Intramuscular Passive Vaccine Delivery to Human Skeletal Muscle
Nicole K Paulk, Katja Pekrun, Gregory W Charville, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 23, 2017
Bioengineered AAV Capsids with Combined High Human Liver Transduction In Vivo and Unique Humoral Seroreactivity
Nicole K Paulk, Katja Pekrun, Erhua Zhu, et al.
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of 2