Zhi-Qi Xiong
Affiliations: | Institute of Neuroscience | Chinese Academy of Sciences, Beijing, China |
Google:
"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 |
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. |
| Liu JW, Zhang ZQ, Zhu ZC, et al. (2024) Loss of TET Activity in the Postnatal Mouse Brain Perturbs Synaptic Gene Expression and Impairs Cognitive Function. Neuroscience Bulletin |
| Zhao M, Cheng X, Chen L, et al. (2024) Antisense oligonucleotides enhance SLC20A2 expression and suppress brain calcification in a humanized mouse model. Neuron |
| Cheng X, Zhao M, Chen L, et al. (2024) Astrocytes modulate brain phosphate homeostasis via polarized distribution of phosphate uptake transporter PiT2 and exporter XPR1. Neuron |
| Li YL, Lin J, Huang X, et al. (2024) Heterozygous Variants in KCNJ10 Cause Paroxysmal Kinesigenic Dyskinesia Via Haploinsufficiency. Annals of Neurology |
| 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 |