Jianyong Zhang——Associate Professor
Nationality:
CANADA
Phone:
022-27401021
Email:
Jianyong.zhang@tju.edu.cn
Office:
Room 506, Building 24, Tianjin University
School:
School of Pharmaceutical Science and Technology
ResearcherID:
L-5934-2015
Group weblink
Education Experience
2007 Postdoctoral McGill University, Canada
2007 Ph. D. University of Tsukuba, Japan
Professional Experience
2014-2015 Assosiate Professor Tianjin University, China
2007-2011 Postdoctoral McGill University, Canada
2001-2007 Teaching Assistant University of Tsukuba, Japan
1992-2000 Physician and Physician-in-charge Tianjin 4th Central Hospital, China
Research Area

The research in the group of ZHANG focuses on two areas: 1) Mechanisms of transcriptional regulation involved in cancer，oxidative stress response and a variety of health disorders by means of molecular biology method, 2) Mechanism study on interaction of host factors with retroelements and HIV-1 such as helicases, interferon-stimulate genes and RNA binding proteins etc.
Honors and Awards
Best Teacher Award, Tianjin 4th central hospital, 1994
Best Teacher Award, Tianjin 4th central hospital, 1995
Patents
Highlighted Publications
Li, Xiaoyu#; Zhang, Jianyong#; Jia, Rui; et al. The MOV10 Helicase Inhibits LINE-1 Mobility.（#Co- first author) Journal of Biological Chemistry Volume: 288 Issue: 29 Pages: 21148-21160 Published: JUL 19 2013
Zhang, Jianyong; Liang, Chen. BST-2 Diminishes HIV-1 Infectivity. Journal of Virology Volume: 84 Issue: 23 Pages: 12336-12343 Published: DEC 2010
Rong, Liwei; Zhang, Jianyong; Lu, Jennifer; et al. The Transmembrane Domain of BST-2 Determines Its Sensitivity to Down-Modulation by Human Immunodeficiency Virus Type 1 Vpu. Journal of Virology Volume: 83 Published: DEC 2009
Zhang, Jianyong; Hosoya, Tomonori; Maruyama, Atsushi; et al. Nrf2 Neh5 domain is differentially utilized in the transactivation of cytoprotective genes. Biochemical Journal 15;404(3):459-66, Jun 2007
Zhang, Jianyong; Ohta, Tsutomu; Maruyama, Atsushi; et al. BRG1 interacts with Nrf2 to selectively mediate HO-1 induction in response to oxidative stress.Molecular and Cellular Biology Volume: 26 Issue: 21 Pages: 7942-7952 Published: NOV 2006