Zhi-Qi Xiong
Affiliations: | Institute of Neuroscience | Chinese Academy of Sciences, Beijing, China |
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"Zhi-Qi Xiong"Mean distance: 17.83 (cluster 17)
Children
Sign in to add trainee| Shanshan Zhu | research assistant | 2003-2004 | ION, CAS |
| Xuewen Cheng | grad student | CAS | |
| Xiaoling Hu | grad student | 2004-2010 | CAS |
| Ming-Yue Wu | grad student | 2011-2015 | ION, CAS |
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Publications
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| Zhu ZA, Li YY, Xu J, et al. (2023) CDKL5 deficiency in adult glutamatergic neurons alters synaptic activity and causes spontaneous seizures via TrkB signaling. Cell Reports. 42: 113202 |
| Xu X, Sun H, Luo J, et al. (2022) The Pathology of Primary Familial Brain Calcification: Implications for Treatment. Neuroscience Bulletin |
| Zhao M, Su HZ, Zeng YH, et al. (2022) Loss of function of CMPK2 causes mitochondria deficiency and brain calcification. Cell Discovery. 8: 128 |
| Wang HT, Zhu ZA, Li YY, et al. (2021) CDKL5 deficiency in forebrain glutamatergic neurons results in recurrent spontaneous seizures. Epilepsia |
| Wang T, Wang J, Wang J, et al. (2019) HAP1 is an in vivo UBE3A target that augments autophagy in a mouse model of Angelman syndrome. Neurobiology of Disease. 104585 |
| Lin X, Su HZ, Dong EL, et al. (2019) Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia. Brain : a Journal of Neurology |
| Wang J, Lou SS, Wang T, et al. (2019) UBE3A-mediated PTPA ubiquitination and degradation regulate PP2A activity and dendritic spine morphology. Proceedings of the National Academy of Sciences of the United States of America |
| Xu Q, Liu YY, Wang X, et al. (2018) Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons. Molecular Autism. 9: 65 |
| Zhu YC, Xiong ZQ. (2018) Molecular and Synaptic Bases of CDKL5 Disorder. Developmental Neurobiology |
| Yao XP, Cheng X, Wang C, et al. (2018) Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification. Neuron |