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Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 1, 2010
Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpression
Samantha L Ginn, Sophia H Y Liao, Allison P Dane, et al.
The Journal of Gene Medicine
|
April 6, 2007
Lentivirus vector-mediated gene transfer to the developing bronchiolar airway epithelium in the fetal lamb
Ze-Yan Yu, Karen McKay, Peter van Asperen, et al.
Molecular Therapy. Methods & Clinical Development
|
April 1, 2024
Novel AAV variants with improved tropism for human Schwann cells
Matthieu Drouyer, Tak-Ho Chu, Elodie Labit, et al.
JHEP Reports : Innovation in Hepatology
|
February 11, 2020
Efficient <i>in vivo</i> editing of OTC-deficient patient-derived primary human hepatocytes
Samantha L Ginn, Anais K Amaya, Sophia H Y Liao, et al.
Molecular Cancer
|
November 13, 2024
The PI3K-AKT-mTOR axis persists as a therapeutic dependency in KRAS<sup>G12D</sup>-driven non-small cell lung cancer
W J McDaid, L Wilson, H Adderley, et al.
Molecular Therapy. Nucleic Acids
|
March 23, 2017
Limiting Thymic Precursor Supply Increases the Risk of Lymphoid Malignancy in Murine X-Linked Severe Combined Immunodeficiency
Samantha L Ginn, Claus V Hallwirth, Sophia H Y Liao, et al.
Molecular Therapy. Methods & Clinical Development
|
December 12, 2018
Codon-Optimization of Wild-Type Adeno-Associated Virus Capsid Sequences Enhances DNA Family Shuffling while Conserving Functionality
Marti Cabanes-Creus, Samantha L Ginn, Anais K Amaya, et al.
Molecular Therapy. Methods & Clinical Development
|
June 2, 2015
Coherence analysis discriminates between retroviral integration patterns in CD34(+) cells transduced under differing clinical trial conditions
Claus V Hallwirth, Gagan Garg, Timothy J Peters, et al.
The Medical Journal of Australia
|
May 4, 2005
Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in Australia
Samantha L Ginn, Julie A Curtin, Belinda Kramer, et al.
Science Translational Medicine
|
September 10, 2020
Restoring the natural tropism of AAV2 vectors for human liver
Marti Cabanes-Creus, Claus V Hallwirth, Adrian Westhaus, et al.
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Search research articles
Search
Showing results (41-50 of 52) with videos related to
Sort By:
Page
of 6
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 1, 2010
Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpression
Samantha L Ginn, Sophia H Y Liao, Allison P Dane, et al.
The Journal of Gene Medicine
|
April 6, 2007
Lentivirus vector-mediated gene transfer to the developing bronchiolar airway epithelium in the fetal lamb
Ze-Yan Yu, Karen McKay, Peter van Asperen, et al.
Molecular Therapy. Methods & Clinical Development
|
April 1, 2024
Novel AAV variants with improved tropism for human Schwann cells
Matthieu Drouyer, Tak-Ho Chu, Elodie Labit, et al.
JHEP Reports : Innovation in Hepatology
|
February 11, 2020
Efficient <i>in vivo</i> editing of OTC-deficient patient-derived primary human hepatocytes
Samantha L Ginn, Anais K Amaya, Sophia H Y Liao, et al.
Molecular Cancer
|
November 13, 2024
The PI3K-AKT-mTOR axis persists as a therapeutic dependency in KRAS<sup>G12D</sup>-driven non-small cell lung cancer
W J McDaid, L Wilson, H Adderley, et al.
Molecular Therapy. Nucleic Acids
|
March 23, 2017
Limiting Thymic Precursor Supply Increases the Risk of Lymphoid Malignancy in Murine X-Linked Severe Combined Immunodeficiency
Samantha L Ginn, Claus V Hallwirth, Sophia H Y Liao, et al.
Molecular Therapy. Methods & Clinical Development
|
December 12, 2018
Codon-Optimization of Wild-Type Adeno-Associated Virus Capsid Sequences Enhances DNA Family Shuffling while Conserving Functionality
Marti Cabanes-Creus, Samantha L Ginn, Anais K Amaya, et al.
Molecular Therapy. Methods & Clinical Development
|
June 2, 2015
Coherence analysis discriminates between retroviral integration patterns in CD34(+) cells transduced under differing clinical trial conditions
Claus V Hallwirth, Gagan Garg, Timothy J Peters, et al.
The Medical Journal of Australia
|
May 4, 2005
Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in Australia
Samantha L Ginn, Julie A Curtin, Belinda Kramer, et al.
Science Translational Medicine
|
September 10, 2020
Restoring the natural tropism of AAV2 vectors for human liver
Marti Cabanes-Creus, Claus V Hallwirth, Adrian Westhaus, et al.
Page
of 6