Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Translational Psychiatry|October 25, 2023
Downregulation of mGluR1-mediated signaling underlying autistic-like core symptoms in Shank1 P1812L-knock-in miceYue Qin, Xiao-Yong Zhang, Yanyan Liu, et al.
Molecular Psychiatry|November 6, 2025
Unraveling spatiotemporal dynamics in transdiagnosis subtypes of major depressive disorder and bipolar disorder: insights from co-activation patterns and treatment responseAoling Cai, Jingyu Yang, Huiling Guo, et al.
Vaccine|December 17, 2013
Evaluation of policies and practices to prevent mother to child transmission of hepatitis B virus in China: results from China GAVI project final evaluationFuqiang Cui, Huiming Luo, Fuzhen Wang, et al.
Nature Communications|July 9, 2024
Whole exome sequencing analysis identifies genes for alcohol consumptionJujiao Kang, Yue-Ting Deng, Bang-Sheng Wu, et al.
Psychological Medicine|August 20, 2025
Impact of schizophrenia-associated risk genes on brain functional networks and executive deficits: a study of individuals with schizophrenia and genetic high riskTing Sun, Yue Zhu, Pengfei Zhao, et al.
Molecular Psychiatry|April 7, 2022
A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signalingYue Qin, Yasong Du, Liqiang Chen, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 20, 2022
Associations between hemispheric asymmetry and schizophrenia-related risk genes in people with schizophrenia and people at a genetic high risk of schizophreniaYue Zhu, Shuai Wang, Xiaohong Gong, et al.
Vaccine|July 5, 2011
Surface antibody and cytokine response to recombinant Chinese hamster ovary cell (CHO) hepatitis B vaccineWei Zhang, Lili Han, Changying Lin, et al.
Plos One|April 18, 2012
High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disabilityXiaohong Gong, Yu-Wu Jiang, Xin Zhang, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Pageof 8