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谭拥军教授个人简介

谭拥军  Yongjun Tan  
教授,博士生导师 教育部新世纪优秀人才
Tel: 86-731-88823211
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研究方向:细胞与组织工程学
Reserch Interest: Cell and Tissue Engineering

中文简介
1967年出生。1989年获南开大学生物化学学士学位。1992年获南开大学分子生物学硕士学位。1999年获美国芝加哥医学院药理和分子生物学博士学位。1999年至2005年,在美国伊利诺斯大学芝加哥分校生物化学和分子遗传系完成博士后研究,先后任该系讲师和研究助理教授。2006年任湖南大学“985”工程细胞与组织工程学方向首席科学家。2007年获湖南省“芙蓉学者”特聘教授、教育部“新世纪优秀人才”支持计划。2008年任科技部“生物医学与生命分析化学国际科技合作基地”主任。获国家自然科学基金、湖南省杰出青年基金等基金多项。现任湖南大学生物学院院长。

Introduction
2015 – present, Professor, Dean, College of Biology, Hunan University
2010 – 2015, Professor, Director, Dept. of Biomedical Engineering, Vice Dean, College of Biology, Hunan University
2006 – 2010, Professor and Chief Scientist of Cell and Tissue Engineering, Hunan University; “Fu-Rong” Scholar
2002 – 2005 Research Assistant Professor, Dept. of Biochemistry and Molecular Genetics, University of Illinois at Chicago, USA
1999 – 2002 Postdoctoral Research Associate, Dept. of Biochemistry and Molecular Genetics, University of Illinois at Chicago, USA
1994 – 1999 Ph.D. in Pharmacology and Molecular Biology, Finch University of Health Sciences/Chicago Medical School, USA
1989 – 1992 M.S. in Molecular Biology, Nankai University
1985 – 1989 B.S. in Biochemistry, Nankai University

Recent Publications:
1.Qin Xiang, Guixiang Tan*, Xia Jiang, Kuangpei Wu, Weihong Tan, and Yongjun Tan*. (2017) Suppression of FOXM1 Transcriptional Activities via a Single-Stranded DNA Aptamer Generated by SELEX. Scientific Reports. In press.
2.Zhen Zhang, Chao Yang, Wei Gao, Tuanhui Chen, Tingting Qian, Jun Hu, and Yongjun Tan*. (2015) FOXA2 Attenuates the Epithelial to Mesenchymal Transition by Regulating the Transcription of E-cadherin and ZEB2 in Human Breast Cancer. Cancer Letters 361: 240-250.
3.Yan Chen, Lei Meng, Qiqi Yu, Difei Dong, Guixiang Tan, Xiaoqin, Huang*, and Yongjun Tan*. (2015) The miR-134 attenuates the expression of transcription factor FOXM1 during pluripotent NT2/D1 embryonal carcinoma cell differentiation. Exp Cell Res 330: 442-450.
4.Guixiang Tan, Liang Cheng, Tuanhui Chen, Li Yu*, and Yongjun Tan*. (2014) Foxm1 Mediates LIF/Stat3-Dependent Self-Renewal in Mouse Embryonic Stem Cells and Is Essential for the Generation of Induced Pluripotent Stem Cells. PLoS One 9: e92304.
5.Tuanhui Chen, Sijia He, Zhen Zhang, Wei Gao, Li Yu*, and Yongjun Tan*. (2014) Foxa1 Contributes to the Repression of Nanog Expression by Recruiting Grg3 during the Differentiation of Pluripotent P19 Embryonal Carcinoma Cells. Exp Cell Res 326: 326-335.
6.Tuanhui Chen, Jiawan Xiong, Chao Yang, Lianhua Shan, Guixiang Tan, Li Yu*, and Yongjun Tan*. (2014) Silencing of FOXM1 transcription factor expression by adenovirus-mediated RNA interference inhibits human hepatocellular carcinoma growth. Cancer Gene Ther 21: 133-138.\7.Chao Yang, Hui Chen, Guixiang Tan, Wei Gao, Liang Cheng, Xia Jiang, Li Yu, and Yongjun Tan*. (2013) FOXM1 Promotes the Epithelial to Mesenchymal Transition by Stimulating the Transcription of Slug in Human Breast Cancer. Cancer Letters 340: 104-112.
8.Chao Yang, Hui Chen, Li Yu, Lianhua Shan, Li Xie, Jun Hu, Tuanhui Chen, and Yongjun Tan*. (2013) Inhibition of FOXM1 Transcription Factor Suppresses Cell Proliferation and Tumor Growth of Breast Cancer. Cancer Gene Ther 20: 117-124.
9.Hui Chen, Chao Yang, Li Yu, Li Xie, Jun Hu, Liang Zeng, and Yongjun Tan*. (2012) Adenovirus-Mediated RNA Interference Targeting FOXM1 Transcription Factor Suppresses Cell Proliferation and Tumor Growth of Nasopharyngeal Carcinoma. J Gene Med 14: 231-240.
10.Difei Dong, Lei Meng, Qiqi Yu, Guixiang Tan, Miao Ding, and Yongjun Tan*. (2012) Stable expression of FoxA1 promotes pluripotent P19 embryonal carcinoma cells to be neural stem-like cells. Gene Expression 15: 153-162.