Ruvkun and Ambros recognized for miRNAs by Mark A. Kay

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In Vitro Ligation-Based Cloning of Foreign DNAs into the E3 and E1 Deletion Regions for Generation of Recombinant Adenovirus Vectors by Hiroyuki Mizuguchi, Mark A. Kay, Takao Hayakawa

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Advancing Molecular Therapies through In Vivo Bioluminescent Imaging by Anton McCaffrey, Mark A. Kay, Christopher H. Contag

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Method for Multiple Portal Vein Infusions in Mice: Quantitation of Adenovirus-Mediated Hepatic Gene Transfer by Marie-Jeanne T.F.D. Vrancken Peeters, Andre Lieber, James Perkins, Mark A. Kay

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Aptamer-programmable adeno-associated viral vectors as a novel platform for cell-specific gene transfer by Francesco Puzzo, Chuanling Zhang, Bethany Powell Gray, Feijie Zhang, Bruce A. Sullenger, Mark A. Kay

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The AAV capsid can influence the epigenetic marking of rAAV delivered episomal genomes in a species dependent manner by Adriana Gonzalez-Sandoval, Katja Pekrun, Shinnosuke Tsuji, Feijie Zhang, King L. Hung, Howard Y. Chang, Mark A. Kay

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Promoterless gene targeting without nucleases rescues lethality of a Crigler‐Najjar syndrome mouse model by Fabiola Porro, Giulia Bortolussi, Adi Barzel, Alessia De Caneva, Alessandra Iaconcig, Simone Vodret, Lorena Zentilin, Mark A Kay, Andrés F Muro

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Selection of viral capsids and promoters affects the efficacy of rescue of Tmprss3-deficient cochlea by Ksenia A. Aaron, Katja Pekrun, Patrick J. Atkinson, Sara E. Billings, Julia M. Abitbol, Ina A. Lee, Yasmin Eltawil, Yuan-Siao Chen, Wuxing Dong, Rick F. Nelson, Mark A. Kay, Alan G. Cheng

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A strategy for high antibody expression with low anti-drug antibodies using AAV9 vectors by Meredith E. Davis-Gardner, Jesse A. Weber, Jun Xie, Jun Xie, Katja Pekrun, Eric A. Alexander, Kim L. Weisgrau, Jessica R. Furlott, Eva G. Rakasz, Mark A. Kay, Guangping Gao, Guangping Gao, Michael Farzan, Matthew R. Gardner, Matthew R. Gardner

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