赵春杰教授承担着国家重点研发计划、国家自然科学基金重点项目等科研任务,曾作为首席科学家主持国家973和863项目,在智力障碍、自闭症、FOXG1综合征、癫痫等疾病研究领域取得系列研究成果,成果发表于Cell、Development、J. Neurosci.、Cerebral Cortex等神经科学领域国际著名学术刊物,引起领域内同行广泛关注。
代表性成果:
1.Han X#, Wei Y#, WuX, Gao J, Yang Z, Zhao C*.PDK1 Regulates Transition Period of Apical Progenitors to Basal Progenitors byControlling Asymmetric Cell Division. Cereb Cortex. 2020,Jan 10; 30 (1):406-420, doi: 10.1093/cercor/bhz146.
2.Du A#, Wu X#, ChenH, Bai QR, Han X, Liu B, Zhang X, Ding Z, Shen Q, Zhao C*. Foxg1 DirectlyRepresses Dbx1 to Maintain the POAand Subsequently Regulates the Ventral Telencephalic Patterning. Cereb Cortex. 2019, Dec17; 29 (12): 4968-4981.doi: 10.1093/cercor/bhz037.
3.Chen D, Wang C, Li M, Yuan Y, Chen H*,Zhang W*, Zhao C*. Loss of Foxg1 Impairs the Development ofCortical SST-interneurons Leading to Abnormal Emotional and Social Behaviors. Cereb Cortex. 2019Aug 29 (8), 3666-3682, doi: 10.1093/cercor/bhz114.
4.Shen W#, Ba R#, SuY, Ni Y, Chen D, Xie W, Pleasure SJ, ZhaoC*. Foxg1 regulates the postnatal development of cortical interneurons. Cereb Cortex. 2019 Apr.29 (4), 1547–1560, doi: 10.1093/cercor/bhy051.
5.Xu M#, Han X#,Liu R, Qi C, Yang Z, Zhao C*, Gao J*. PDK1 DeficitImpairs the Development of the Dentate Gyrus in Mice.Cereb Cortex.2019 Mar 29 (3) 1185-1198. doi: 10.1093/cercor/bhy024.
6.Yang Y#, Shen W#, Ni Y, Su Y, YangZ, ZhaoC*. Impaired interneuron development after Foxg1disruption. Cerebral Cortex.doi:10.1093/cercor/bhv297. 2017,Jan 27(1)793-808.
7.Wu X, Gu X, Han X, Du A, Jiang Y, ZhangX, Wang Y, Cao G, ZhaoC*. A Novel Function for FoxM1 in Interkinetic Nuclear Migration in the DevelopingTelencephalon And Anxiety-related Behavior.The Journal of Neuroscience. 2014Jan; 34(4):1510-1522.
8.Tian C, Gong Y, Yang Y, Shen W, Wang K,Liu J, Xu B, Zhao J, Zhao C*. Foxg1 Has An essential Role in Postnatal Development of The Dentategyrus. The Journal of Neuroscience.2012. Feb., 32(9):2931-2949.
9.Zhao C*, Avilés C, AbelRA, Almli CR, McQuillen P, Pleasure SJ*. Hippocampal and Visuospatial Learning Defectsin Mice with Deletion of Frizzled9, a Gene in the Williams Syndrome DeletionInterval.Development.2005 Jun; 132(12):2917-2927.
10.Zhao C,Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T,Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N*. Charcot-Marie-Tooth DiseaseType 2A Caused byMutation in a Microtubule Motor KIF1B. Cell. 2001 Jun 1;105(5):587-597.(cover story)