Scott Zeitlin
Affiliations: | University of Virginia, Charlottesville, VA |
Area:
Neuroscience BiologyGoogle:
"Scott Zeitlin"Mean distance: 53433
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Publications
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| Marchionini DM, Liu JP, Ambesi-Impiombato A, et al. (2022) Benefits of global mutant huntingtin lowering diminish over time in a Huntington's disease mouse model. Jci Insight. 7 |
| Greco TM, Secker C, Ramos ES, et al. (2022) Dynamics of huntingtin protein interactions in the striatum identifies candidate modifiers of Huntington disease. Cell Systems |
| Braatz EM, André EA, Liu JP, et al. (2021) Characterization of a Knock-In Mouse Model with a Huntingtin Exon 1 Deletion. Journal of Huntington's Disease |
| Barnat M, Capizzi M, Aparicio E, et al. (2020) Huntington's disease alters human neurodevelopment. Science (New York, N.Y.) |
| Burrus CJ, McKinstry SU, Kim N, et al. (2020) Striatal Projection Neurons Require Huntingtin for Synaptic Connectivity and Survival. Cell Reports. 30: 642-657.e6 |
| Franich NR, Hickey MA, Zhu C, et al. (2019) Phenotype onset in Huntington's disease knock-in mice is correlated with the incomplete splicing of the mutant huntingtin gene. Journal of Neuroscience Research |
| Franich NR, Basso M, André EA, et al. (2018) Striatal Mutant Huntingtin Protein Levels Decline with Age in Homozygous Huntington's Disease Knock-In Mouse Models. Journal of Huntington's Disease |
| Liu JP, Zeitlin SO. (2017) Is Huntingtin Dispensable in the Adult Brain? Journal of Huntington's Disease |
| André EA, Braatz EM, Liu JP, et al. (2017) Generation and Characterization of Knock-in Mouse Models Expressing Versions of Huntingtin with Either an N17 or a Combined PolyQ and Proline-Rich Region Deletion. Journal of Huntington's Disease |
| Ochaba J, Lukacsovich T, Csikos G, et al. (2014) Potential function for the Huntingtin protein as a scaffold for selective autophagy. Proceedings of the National Academy of Sciences of the United States of America. 111: 16889-94 |