Mark A. Kay, MD PhD

Affiliations: 
Stanford University, Palo Alto, CA 
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"Mark Kay"
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Publications

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Suchy FP, Karigane D, Nakauchi Y, et al. (2024) Genome engineering with Cas9 and AAV repair templates generates frequent concatemeric insertions of viral vectors. Nature Biotechnology
Gonzalez-Sandoval A, Pekrun K, Tsuji S, et al. (2023) The AAV capsid can influence the epigenetic marking of rAAV delivered episomal genomes in a species dependent manner. Nature Communications. 14: 2448
Puzzo F, Zhang C, Powell Gray B, et al. (2023) Aptamer-programmable adeno-associated viral vectors as a novel platform for cell-specific gene transfer. Molecular Therapy. Nucleic Acids. 31: 383-397
Sabatino DE, Bushman CFD, Chandler RJ, et al. (2022) Evaluating the State of the Science for Adeno-Associated Virus (AAV) Integration:An Integrated Perspective. Molecular Therapy : the Journal of the American Society of Gene Therapy
Tsuji S, Stephens CJ, Bortolussi G, et al. (2022) Fludarabine increases nuclease-free AAV- and CRISPR/Cas9-mediated homologous recombination in mice. Nature Biotechnology
Lisjak M, De Caneva A, Marais T, et al. (2022) Promoterless Gene Targeting Approach Combined to CRISPR/Cas9 Efficiently Corrects Hemophilia B Phenotype in Neonatal Mice. Frontiers in Genome Editing. 4: 785698
Chandler RJ, Venturoni LE, Liao J, et al. (2020) Promoterless, nuclease-free genome editing confers a growth advantage for corrected hepatocytes in mice with methylmalonic acidemia. Hepatology (Baltimore, Md.)
Kim HK, Yeom JH, Kay MA. (2020) Transfer RNA-Derived Small RNAs: Another Layer of Gene Regulation and Novel Targets for Disease Therapeutics. Molecular Therapy : the Journal of the American Society of Gene Therapy
Course MM, Gudsnuk K, Smukowski SN, et al. (2020) Evolution of a Human-Specific Tandem Repeat Associated with ALS. American Journal of Human Genetics
Su Y, Walker JR, Park Y, et al. (2020) Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals. Nature Methods
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