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个人简介

毕业于南京大学生物学系,获理学学士和硕士学位,1994年赴日本留学,2000年获日本东京大学医学系研究科分子细胞生物学博士学位,同年为日本学术振兴会外国人特别研究员,2001年起,在美国加州大学旧金山分校(UCSF)作博士后,2004年8月起受聘为东南大学教授。主要研究神经系统发育缺陷而致相关神经精神疾病的发生机制。曾获国家杰出青年科学基金资助,作为首席科学家和首席专家主持国家重点基础研究计划(973)以及863项目。研究工作同时受到国家自然科学基金面上及重点项目支持。曾入选首批江苏省“333工程”中青年科技领军人才,江苏省特聘教授;获江苏省有突出贡献中青年专家称号;2009年入选“新世纪百千万人才工程”国家级人选;享受国务院特殊津贴。现任中国神经科学学会理事、江苏省发育生物学会副理事长、江苏省解剖学会副理事长等。

研究领域

端脑发育的调控与相关神经精神疾病的病理机制

近期论文

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

1.Yang Y Shen W, Ni Y,Su Y, Yang Z, ZhaoC*. Impaired interneuron development after Foxg1 disruption. Cerebral cortex. In press. 2.Liu R, Yang Y, Shen J, Chen H, Zhang Q, Ba R, Wei Y, Li KC, Zhang X, ZhaoC*. Fstl1 is involved in the regulation of radial glial scaffold development.Molecular Brain.2015 Sep 17;8(1):53. doi: 10.1186/s13041-015-0144-8. 3.Liu J, Liu B, Zhang X, Yu B, Guan W, Wang K, Yang Y, Gong Y, Wu X, Yanagawa Y, Wu S, Zhao C*. Calretinin-positive L5a pyramidal neurons in the development of the paralemniscal pathway in the barrel cortex. Molecular Brain. 2014, Nov 18, 7 (1) :84 , doi:10.1186/s13041-014-0084-8. 4.Wu X, Gu X, Han X, Du A, Jiang Y, Zhang X, Wang Y, Cao G, Zhao C*. A Novel Function for FoxM1 in Interkinetic Nuclear Migration in the Developing Telencephalon And Anxiety-related Behavior. The Journal of Neuroscience. 2014 Jan; 34(4):1510-1522. 5.Huang Y, Song NN, Lan W, Zhang Q, Zhang L, Zhang L, Hu L, Chen JY, Zhao C, Li L, Xu L, Ding YQ*. Sensory input is required for callosal axon targeting in the somatosensory cortex. Mol Brain. 2013 Dec 5;6(1):53.doi: 10.1186/1756-6606-6-53. 6.Nie B, Chen K, Zhao S, Liu J, Gu X, Yao Q, Hui J, Zhang Z, Teng G, Zhao C, Shan B* . A Rat Brain MRI Template with Digital Stereotaxic Atlas of Fine Anatomical Delineations in Paxinos Space and its Automated Application in Voxel-Wise Analysis. Human Brain Mapping.2013 Jun;34(6):1306-18. 7.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 Dentate gyrus. The Journal of Neuroscience. 2012. Feb., 32(9):2931-2949. 8.Gu X, Liu B, Wu X, Yan Y, Zhang Y, Wei Y,. Pleasure SJ, Zhao C*. Inducible Genetic Lineage Tracing of Cortical Hem Derived Cajal-Retzius Cells Reveals Novel Properties. PLoS ONE. 2011;6(12):e28653. 9.Li Y, Tian C, Yang Y, Yan Y, Ni Y, Wei Y, Pleasure SJ, Zhao C*. An inducible transgenic Cre mouse line for the study of hippocampal development and adult neurogenesis. Genesis. 2011 Dec. 49 (12):919-926. 10.Zhou W, Zhang Y, Li Y, Wei YS, Liu G, Liu DP, Pleasure SJ, Xie W, Zhao C*. A transgenic Cre mouse line for the study of cortical and hippocampal development.Genesis.2010 May; 48(5):343-50. 11.Yang Y, Liu J, Mao H, Hu YA, Yan Y, Zhao C*. The expression pattern of Follistatin-like 1 in mouse central nervous system development.. Gene Expr Patterns. 2009 Oct; 9(7):532-540. 12.Gu X, Yan Y, Li H, He D, Pleasure SJ, Zhao C*.Characterization of the Frizzled10-CreERTM Transgenic Mouse: An Inducible Cre Line for the Study of Cajal–Retzius Cell Development. Genesis. 2009 Mar; 47(3): 210 – 216. 13.Yan Y, Li Y, Hu C, Gu X, Liu J, Hu YA, Yang Y, Wei Y, Zhao C*. Expression of Frizzled10 in mouse nervous system. Gene Expr Patterns. 2009 Mar; 9 (3):173-177. 14.Hu C, Liu J, Zhang Y, Li Y, Xie W, Zhao C*. A useful transgenic mouse line for studying the development of spinal nociceptive circuits.Neuroscience lett. 2009 Jan 30; 450 (2):211-216. 15.Gu X, He D, Li Y, Hu C, Wei YS, Liu G, Liu D, Pleasure SJ, Xie W, Zhao C*. Generation of Frizzled10-Cre Transgenic Mouse Line: A Useful Tool for the Study of Dorsal Telencephalic Development. Genesis. 2008 Oct; 46 (10):523-9. 16.Hu YA, Gu X, Liu J, Yang Y, Yan Y, Zhao C*. Expression pattern of wnt inhibitor factor 1(wif1) during the development in mouse CNS. Gene Expr Patterns. 2008 Sep; 8 (7-8): 515-522. 17.Zhao C, Guan W, Pleasure SJ. A Transgenic Marker Mouse Line Labels Cajal-Retzius Cells from the Cortical Hem and Thalamocortical axons.Brain Res. 2006 Mar 10; 1077 (1):48-53. (cover story) 18.Zhao C*, Avilés C, Abel RA, Almli CR, McQuillen P, Pleasure SJ*. Hippocampal and Visuospatial Learning Defects in Mice with Deletion of Frizzled9, a Gene in the Williams Syndrome Deletion Interval.Development.2005 Jun; 132(12):2917-2927. 19.Zhao C*, Pleasure SJ*.Frizzled9 Protein Is Regionally Expressed in the Developing Medial Wall of the Cortex and the Cells Derived from This Region.Developmental Brain Research. 2005 Jun 9; 157 (1):93-97. 20.Zhao C, Pleasure SJ.The Frizzled9 Promoter Drives Expression of Transgenes in the Medial Wall of the Cortex and Its Chief Derivative the Hippocampus. Genesis.2004 Sep; 40(1):32-9.

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