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Nature Communications
|
January 10, 2017
Characterization of the interplay between DNA repair and CRISPR/Cas9-induced DNA lesions at an endogenous locus
Anne Bothmer, Tanushree Phadke, Luis A Barrera, et al.
The Journal of Gene Medicine
|
August 20, 2024
Stable transduction of the neonatal mouse liver using a hybrid rAAV/sleeping beauty transposon gene delivery system
Sharon C Cunningham, Philip M Zakas, Natsuki Sasaki, et al.
Nature Methods
|
March 31, 2018
Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo"
Christopher J Wilson, Tim Fennell, Anne Bothmer, et al.
EMBO Molecular Medicine
|
January 21, 2021
Modeling, optimization, and comparable efficacy of T cell and hematopoietic stem cell gene editing for treating hyper-IgM syndrome
Valentina Vavassori, Elisabetta Mercuri, Genni E Marcovecchio, et al.
Cancer & Metabolism
|
January 8, 2020
Tissue of origin dictates GOT1 dependence and confers synthetic lethality to radiotherapy
Barbara S Nelson, Lin Lin, Daniel M Kremer, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 9, 2024
Sleeping Beauty mRNA-LNP enables stable rAAV transgene expression in mouse and NHP hepatocytes and improves vector potency
Philip M Zakas, Sharon C Cunningham, Ann Doherty, et al.
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Search research articles
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Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Nature Communications
|
January 10, 2017
Characterization of the interplay between DNA repair and CRISPR/Cas9-induced DNA lesions at an endogenous locus
Anne Bothmer, Tanushree Phadke, Luis A Barrera, et al.
The Journal of Gene Medicine
|
August 20, 2024
Stable transduction of the neonatal mouse liver using a hybrid rAAV/sleeping beauty transposon gene delivery system
Sharon C Cunningham, Philip M Zakas, Natsuki Sasaki, et al.
Nature Methods
|
March 31, 2018
Response to "Unexpected mutations after CRISPR-Cas9 editing in vivo"
Christopher J Wilson, Tim Fennell, Anne Bothmer, et al.
EMBO Molecular Medicine
|
January 21, 2021
Modeling, optimization, and comparable efficacy of T cell and hematopoietic stem cell gene editing for treating hyper-IgM syndrome
Valentina Vavassori, Elisabetta Mercuri, Genni E Marcovecchio, et al.
Cancer & Metabolism
|
January 8, 2020
Tissue of origin dictates GOT1 dependence and confers synthetic lethality to radiotherapy
Barbara S Nelson, Lin Lin, Daniel M Kremer, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 9, 2024
Sleeping Beauty mRNA-LNP enables stable rAAV transgene expression in mouse and NHP hepatocytes and improves vector potency
Philip M Zakas, Sharon C Cunningham, Ann Doherty, et al.
Page
of 2