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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 interferenceFlorie Borel, Mark A Kay, Christian MuellerMolecular 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 KayTranslational Research : the Journal of Laboratory and Clinical Medicine|May 21, 2022
Intranasal application of adeno-associated viruses: a systematic reviewAnselm J Gadenstaetter, Lukas Schmutzler, Dirk Grimm, et al.Proceedings of the National Academy of Sciences of the United States of America|July 15, 2015
Alleviation of off-target effects from vector-encoded shRNAs via codelivered RNA decoysStefan Mockenhaupt, Stefanie Grosse, Daniel Rupp, et al.FEBS Letters|April 28, 2016
Plasmodium meets AAV-the (un)likely marriage of parasitology and virology, and how to make the matchFranziska Hentzschel, Anne-Kathrin Herrmann, Ann-Kristin Mueller, et al.Methods 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 ContagPageof 30