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Neurobiology of Disease
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October 9, 2016
N-acetylaspartate supports the energetic demands of developmental myelination via oligodendroglial aspartoacylase
Jeremy S Francis, Ireneusz Wojtas, Vladimir Markov, et al.
Molecular Therapy. Methods & Clinical Development
|
August 25, 2018
An Observational Study from Long-Term AAV Re-administration in Two Hemophilia Dogs
Junjiang Sun, Wenwei Shao, Xiaojing Chen, et al.
Nature Biotechnology
|
December 29, 2009
Reengineering a receptor footprint of adeno-associated virus enables selective and systemic gene transfer to muscle
Aravind Asokan, Julia C Conway, Jana L Phillips, et al.
Circulation. Heart Failure
|
December 29, 2012
AAV9.I-1c delivered via direct coronary infusion in a porcine model of heart failure improves contractility and mitigates adverse remodeling
Kenneth M Fish, Dennis Ladage, Yoshiaki Kawase, et al.
Human Gene Therapy
|
February 21, 2012
X-linked inhibitor of apoptosis protein-mediated attenuation of apoptosis, using a novel cardiac-enhanced adeno-associated viral vector
Valentino Piacentino, Carmelo A Milano, Michael Bolanos, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 6, 2011
Self-complementary AAV2.5-BMP2-coated femoral allografts mediated superior bone healing versus live autografts in mice with equivalent biomechanics to unfractured femur
Cemal Yazici, Masahiko Takahata, David G Reynolds, et al.
Journal of Molecular and Genetic Medicine : an International Journal of Biomedical Research
|
March 8, 2016
The Adeno-Associated Virus Genome Packaging Puzzle
Chen Ling, Yuan Wang, Yuan Lu, et al.
Journal of Virology
|
October 31, 2014
Enhanced transgene expression from recombinant single-stranded D-sequence-substituted adeno-associated virus vectors in human cell lines in vitro and in murine hepatocytes in vivo
Chen Ling, Yuan Wang, Yuan Lu, et al.
Molecular Therapy. Methods & Clinical Development
|
September 25, 2023
Evaluation of an AAV9-mini-dystrophin gene therapy candidate in a rat model of Duchenne muscular dystrophy
Caroline Le Guiner, Xiao Xiao, Thibaut Larcher, et al.
Nature Medicine
|
February 16, 2005
Remodeling of cortical bone allografts mediated by adherent rAAV-RANKL and VEGF gene therapy
Hiromu Ito, Mette Koefoed, Prarop Tiyapatanaputi, et al.
Page
of 23
Search research articles
Search
Showing results (201-210 of 221) with videos related to
Sort By:
Page
of 23
Neurobiology of Disease
|
October 9, 2016
N-acetylaspartate supports the energetic demands of developmental myelination via oligodendroglial aspartoacylase
Jeremy S Francis, Ireneusz Wojtas, Vladimir Markov, et al.
Molecular Therapy. Methods & Clinical Development
|
August 25, 2018
An Observational Study from Long-Term AAV Re-administration in Two Hemophilia Dogs
Junjiang Sun, Wenwei Shao, Xiaojing Chen, et al.
Nature Biotechnology
|
December 29, 2009
Reengineering a receptor footprint of adeno-associated virus enables selective and systemic gene transfer to muscle
Aravind Asokan, Julia C Conway, Jana L Phillips, et al.
Circulation. Heart Failure
|
December 29, 2012
AAV9.I-1c delivered via direct coronary infusion in a porcine model of heart failure improves contractility and mitigates adverse remodeling
Kenneth M Fish, Dennis Ladage, Yoshiaki Kawase, et al.
Human Gene Therapy
|
February 21, 2012
X-linked inhibitor of apoptosis protein-mediated attenuation of apoptosis, using a novel cardiac-enhanced adeno-associated viral vector
Valentino Piacentino, Carmelo A Milano, Michael Bolanos, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 6, 2011
Self-complementary AAV2.5-BMP2-coated femoral allografts mediated superior bone healing versus live autografts in mice with equivalent biomechanics to unfractured femur
Cemal Yazici, Masahiko Takahata, David G Reynolds, et al.
Journal of Molecular and Genetic Medicine : an International Journal of Biomedical Research
|
March 8, 2016
The Adeno-Associated Virus Genome Packaging Puzzle
Chen Ling, Yuan Wang, Yuan Lu, et al.
Journal of Virology
|
October 31, 2014
Enhanced transgene expression from recombinant single-stranded D-sequence-substituted adeno-associated virus vectors in human cell lines in vitro and in murine hepatocytes in vivo
Chen Ling, Yuan Wang, Yuan Lu, et al.
Molecular Therapy. Methods & Clinical Development
|
September 25, 2023
Evaluation of an AAV9-mini-dystrophin gene therapy candidate in a rat model of Duchenne muscular dystrophy
Caroline Le Guiner, Xiao Xiao, Thibaut Larcher, et al.
Nature Medicine
|
February 16, 2005
Remodeling of cortical bone allografts mediated by adherent rAAV-RANKL and VEGF gene therapy
Hiromu Ito, Mette Koefoed, Prarop Tiyapatanaputi, et al.
Page
of 23