Children
Sign in to add trainee| Julie Park | grad student | 2005 | Stanford |
| Brian S. Garrison | grad student | 2006 | Stanford |
| Alfred Y. Wang | grad student | 2006 | Stanford |
| Jeffery C. Giering | grad student | 2008 | Stanford |
| Dirk Grimm | post-doc | Stanford |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Pekrun K, Stephens CJ, Gonzalez-Sandoval A, et al. (2024) Correlation of antigen expression with epigenetic modifications after rAAV delivery of a hyperactive human Factor IX variant in mice and rhesus macaques. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| 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 |