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Journal of Virology|June 14, 2003
Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivoAnja Ehrhardt, Hui Xu, Mark A KayMolecular 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 interferenceFlorie Borel, Mark A Kay, Christian MuellerMethods in Enzymology|January 13, 2005
Adeno-associated virus vectors for short hairpin RNA expressionDirk Grimm, Kusum Pandey, Mark A KayMolecular 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 efficiencyXuan Shen, Terry Storm, Mark A KayMolecular 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 vitroJiamiao Lu, Feijie Zhang, Mark A KayHuman Gene Therapy|March 28, 2002
Role of hepatocyte direct hyperplasia in lentivirus-mediated liver transduction in vivoKazuo Ohashi, Frank Park, Mark A KayMolecular 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 vivoFrank Park, Kazuo Ohashi, Mark A KayMethods in Enzymology|February 14, 2025
Functional analysis of tRNA-derived small translational regulationDongjin Kim, Hak Kyun Kim, Mark A KayMolecular Imaging|September 11, 2003
Advancing molecular therapies through in vivo bioluminescent imagingAnton McCaffrey, Mark A Kay, Christopher H ContagNature Reviews. Genetics|May 3, 2003
Progress and problems with the use of viral vectors for gene therapyClare E Thomas, Anja Ehrhardt, Mark A KayPageof 19