Human tRNA-derived small RNAs in the global regulation of RNA silencingDirk Haussecker, Mark A. Kay|RNA|2010Cited by 749
Genome engineering with Cas9 and AAV repair templates generates frequent concatemeric insertions of viral vectorsFabian P. Suchy, Hiromitsu Nakauchi, Yusuke Nakauchi et al.|Nature Biotechnology|2024Cited by 56
Selection of rAAV Vectors that Cross the Human Blood-Brain Barrier and Target the Central Nervous System Using a Transwell ModelMark A. Kay|bioRxiv (Cold Spring Harbor Laboratory)|2022Cited by 1
Using a barcoded AAV capsid library to select for novel clinically relevant gene therapy vectorsKatja Pekrun, Mark A. Kay|bioRxiv (Cold Spring Harbor Laboratory)|2019Cited by 0
Improving the efficiency of liver targeting rAAV-mediated homologous recombination using ribonucleotide reductase inhibitorsShinnosuke Tsuji, Mark A. Kay|Research Square|2020Cited by 0