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Molecular Therapy. Oncology
|
December 24, 2025
Reprogramming AAV tropism with tumor-associated targeting ligands
Stephen L Trisno, Mark A Kay
Journal of Virology
|
June 14, 2003
Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivo
Anja Ehrhardt, Hui Xu, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 20, 2013
Recombinant AAV as a platform for translating the therapeutic potential of RNA interference
Florie Borel, Mark A Kay, Christian Mueller
Methods in Enzymology
|
January 13, 2005
Adeno-associated virus vectors for short hairpin RNA expression
Dirk Grimm, Kusum Pandey, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 30, 2007
Characterization of the relationship of AAV capsid domain swapping to liver transduction efficiency
Xuan Shen, Terry Storm, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 6, 2013
A mini-intronic plasmid (MIP): a novel robust transgene expression vector in vivo and in vitro
Jiamiao Lu, Feijie Zhang, Mark A Kay
Nature Medicine
|
June 7, 2008
Wandering eye for RNAi
John Rossi, Phil Zamore, Mark A Kay
Human Gene Therapy
|
March 28, 2002
Role of hepatocyte direct hyperplasia in lentivirus-mediated liver transduction in vivo
Kazuo Ohashi, Frank Park, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 9, 2003
The effect of age on hepatic gene transfer with self-inactivating lentiviral vectors in vivo
Frank Park, Kazuo Ohashi, Mark A Kay
Nucleic Acid Therapeutics
|
August 9, 2016
Dieter C. Gruenert, PhD (1949-2016)
Petra Disterer, Mark A Kay, Graham C Parker
Page
of 20
Search research articles
Search
Showing results (21-30 of 197) with videos related to
Sort By:
Page
of 20
Molecular Therapy. Oncology
|
December 24, 2025
Reprogramming AAV tropism with tumor-associated targeting ligands
Stephen L Trisno, Mark A Kay
Journal of Virology
|
June 14, 2003
Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivo
Anja Ehrhardt, Hui Xu, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 20, 2013
Recombinant AAV as a platform for translating the therapeutic potential of RNA interference
Florie Borel, Mark A Kay, Christian Mueller
Methods in Enzymology
|
January 13, 2005
Adeno-associated virus vectors for short hairpin RNA expression
Dirk Grimm, Kusum Pandey, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 30, 2007
Characterization of the relationship of AAV capsid domain swapping to liver transduction efficiency
Xuan Shen, Terry Storm, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 6, 2013
A mini-intronic plasmid (MIP): a novel robust transgene expression vector in vivo and in vitro
Jiamiao Lu, Feijie Zhang, Mark A Kay
Nature Medicine
|
June 7, 2008
Wandering eye for RNAi
John Rossi, Phil Zamore, Mark A Kay
Human Gene Therapy
|
March 28, 2002
Role of hepatocyte direct hyperplasia in lentivirus-mediated liver transduction in vivo
Kazuo Ohashi, Frank Park, Mark A Kay
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 9, 2003
The effect of age on hepatic gene transfer with self-inactivating lentiviral vectors in vivo
Frank Park, Kazuo Ohashi, Mark A Kay
Nucleic Acid Therapeutics
|
August 9, 2016
Dieter C. Gruenert, PhD (1949-2016)
Petra Disterer, Mark A Kay, Graham C Parker
Page
of 20