John Kenneth Mich
Affiliations: | 2010-2014 | Children's Research Institute | University of Texas Southwestern Medical Center at Dallas, Dallas, TX, United States |
| 2014- | Allen Institute for Brain Research |
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"John Kenneth Mich"Bio:
http://purl.stanford.edu/mw961nv4891
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Parents
Sign in to add mentor| James K. Chen | grad student | 2010 | Stanford | |
| (Roles for hedgehog signaling in zebrafish development) | ||||
| Sean J. Morrison | post-doc | 2010-2014 | University of Texas Southwestern Medical Center at Dallas | |
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Publications
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| Mich JK, Ryu J, Wei AD, et al. (2025) Interneuron-specific dual-AAV gene replacement corrects epileptic phenotypes in mouse models of Dravet syndrome. Science Translational Medicine. 17: eadn5603 |
| Lalanne JB, Mich JK, Huynh C, et al. (2025) Extensive length and homology dependent chimerism in pool-packaged AAV libraries. Biorxiv : the Preprint Server For Biology |
| Hunker AC, Mich JK, Taskin N, et al. (2025) Technical and biological sources of noise confound multiplexed enhancer AAV screening. Biorxiv : the Preprint Server For Biology |
| Martinez RA, Bishaw YM, Quinlan MA, et al. (2024) A versatile cell line for establishing potency of cell type-specific AAV transgenes. Molecular Therapy. Methods & Clinical Development. 33: 101401 |
| Hunker AC, Wirthlin ME, Gill G, et al. (2024) Enhancer AAV toolbox for accessing and perturbing striatal cell types and circuits. Biorxiv : the Preprint Server For Biology |
| Johansen NJ, Kempynck N, Zemke NR, et al. (2024) Evaluating Methods for the Prediction of Cell Type-Specific Enhancers in the Mammalian Cortex. Biorxiv : the Preprint Server For Biology |
| Ben-Simon Y, Hooper M, Narayan S, et al. (2024) A suite of enhancer AAVs and transgenic mouse lines for genetic access to cortical cell types. Biorxiv : the Preprint Server For Biology |
| Mich JK, Ryu J, Wei AD, et al. (2023) AAV-mediated interneuron-specific gene replacement for Dravet syndrome. Biorxiv : the Preprint Server For Biology |
| Mich JK, Sunil S, Johansen N, et al. (2023) Enhancer-AAVs allow genetic access to oligodendrocytes and diverse populations of astrocytes across species. Biorxiv : the Preprint Server For Biology |
| Chuapoco MR, Flytzanis NC, Goeden N, et al. (2023) Adeno-associated viral vectors for functional intravenous gene transfer throughout the non-human primate brain. Nature Nanotechnology |