Zhaolan (Joe) Zhou, Ph.D.
Affiliations: | Genetics | University of Pennsylvania, Philadelphia, PA, United States |
Website:
http://www.med.upenn.edu/zhoulab/#/Google:
"Zhaolan (Joe) Zhou"Mean distance: 14.26 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Robin Reed | grad student | Harvard Medical School | |
| Michael E. Greenberg | post-doc | Harvard Medical School |
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Publications
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| Mulcahey PJ, Tang S, Takano H, et al. (2020) Aged heterozygous Cdkl5 mutant mice exhibit spontaneous epileptic spasms. Experimental Neurology. 113388 |
| Connolly DR, Zhou Z. (2019) Genomic insights into MeCP2 function: A role for the maintenance of chromatin architecture. Current Opinion in Neurobiology. 59: 174-179 |
| Tang S, Terzic B, Wang IJ, et al. (2019) Altered NMDAR signaling underlies autistic-like features in mouse models of CDKL5 deficiency disorder. Nature Communications. 10: 2655 |
| Zhao YT, Kwon DY, Johnson BS, et al. (2018) Long genes linked to autism spectrum disorders harbor broad enhancer-like chromatin domains. Genome Research |
| Hu P, Fabyanic E, Kwon DY, et al. (2017) Dissecting Cell-Type Composition and Activity-Dependent Transcriptional State in Mammalian Brains by Massively Parallel Single-Nucleus RNA-Seq. Molecular Cell. 68: 1006-1015.e7 |
| Iwase S, Bérubé NG, Zhou Z, et al. (2017) Epigenetic Etiology of Intellectual Disability. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 37: 10773-10782 |
| Johnson BS, Zhao YT, Fasolino M, et al. (2017) Biotin tagging of MeCP2 in mice reveals contextual insights into the Rett syndrome transcriptome. Nature Medicine |
| Tang S, Wang IJ, Yue C, et al. (2017) Loss of CDKL5 in glutamatergic neurons disrupts hippocampal microcircuitry and leads to memory impairment in mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Fasolino M, Zhou Z. (2017) The Crucial Role of DNA Methylation and MeCP2 in Neuronal Function. Genes. 8 |
| Lamonica JM, Kwon DY, Goffin D, et al. (2017) Elevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome-like phenotypes. The Journal of Clinical Investigation |