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Seng H Cheng

Showing results (11-20 of 157) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|January 23, 2017
CRISPR/Cas9-Mediated Genome Editing as a Therapeutic Approach for Leber Congenital Amaurosis 10Guo-Xiang Ruan, Elizabeth Barry, Dan Yu, et al.
Neuro-Degenerative Diseases|February 14, 2012
Mutant GBA1 expression and synucleinopathy risk: first insights from cellular and mouse modelsS Pablo Sardi, Priyanka Singh, Seng H Cheng, et al.
Human Molecular Genetics|September 24, 2013
Reversibility of neuropathology in Tay-Sachs-related diseasesMaría-Begoña Cachón-González, Susan Z Wang, Robin Ziegler, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 5, 2004
Contribution of Toll-like receptor 9 signaling to the acute inflammatory response to nonviral vectorsHongmei Zhao, Hiraoki Hemmi, Shizuo Akira, et al.
Plos One|April 20, 2012
Proteasome inhibition is partially effective in attenuating pre-existing immunity against recombinant adeno-associated viral vectorsJozsef Karman, Nathan K Gumlaw, Jinhua Zhang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2009
AAV8-mediated gene therapy prevents induced biochemical attacks of acute intermittent porphyria and improves neuromotor functionMakiko Yasuda, David F Bishop, Mary Fowkes, et al.
The Journal of Gene Medicine|March 14, 2007
Identification of transfected cell types following non-viral gene transfer to the murine lungLee A Davies, Claire Seguela, Anusha Varathalingam, et al.
The Journal of Gene Medicine|July 27, 2007
Acute intermittent porphyria: vector optimization for gene therapyMakiko Yasuda, Maciej E Domaradzki, Donna Armentano, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2006
Effective gene therapy in an authentic model of Tay-Sachs-related diseasesM Begoña Cachón-González, Susan Z Wang, Andrew Lynch, et al.
Human Gene Therapy|March 18, 2003
DNA sequences in cationic lipid:pDNA-mediated systemic toxicitiesJennifer D Tousignant, Hongmei Zhao, Nelson S Yew, et al.
Pageof 16

Showing results (11-20 of 157) with videos related to

Sort By:
Pageof 16
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 23, 2017
CRISPR/Cas9-Mediated Genome Editing as a Therapeutic Approach for Leber Congenital Amaurosis 10Guo-Xiang Ruan, Elizabeth Barry, Dan Yu, et al.
Neuro-Degenerative Diseases|February 14, 2012
Mutant GBA1 expression and synucleinopathy risk: first insights from cellular and mouse modelsS Pablo Sardi, Priyanka Singh, Seng H Cheng, et al.
Human Molecular Genetics|September 24, 2013
Reversibility of neuropathology in Tay-Sachs-related diseasesMaría-Begoña Cachón-González, Susan Z Wang, Robin Ziegler, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 5, 2004
Contribution of Toll-like receptor 9 signaling to the acute inflammatory response to nonviral vectorsHongmei Zhao, Hiraoki Hemmi, Shizuo Akira, et al.
Plos One|April 20, 2012
Proteasome inhibition is partially effective in attenuating pre-existing immunity against recombinant adeno-associated viral vectorsJozsef Karman, Nathan K Gumlaw, Jinhua Zhang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2009
AAV8-mediated gene therapy prevents induced biochemical attacks of acute intermittent porphyria and improves neuromotor functionMakiko Yasuda, David F Bishop, Mary Fowkes, et al.
The Journal of Gene Medicine|March 14, 2007
Identification of transfected cell types following non-viral gene transfer to the murine lungLee A Davies, Claire Seguela, Anusha Varathalingam, et al.
The Journal of Gene Medicine|July 27, 2007
Acute intermittent porphyria: vector optimization for gene therapyMakiko Yasuda, Maciej E Domaradzki, Donna Armentano, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2006
Effective gene therapy in an authentic model of Tay-Sachs-related diseasesM Begoña Cachón-González, Susan Z Wang, Andrew Lynch, et al.
Human Gene Therapy|March 18, 2003
DNA sequences in cationic lipid:pDNA-mediated systemic toxicitiesJennifer D Tousignant, Hongmei Zhao, Nelson S Yew, et al.
Pageof 16