Contact

  • Title: Associate Professor
  • Department: Institute of Biophysics
  • Address: 逸夫生物楼1216室
  • Tel:
  • Fax:
  • Email: zhuli@lzu.edu.cn
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Bio
  • 2015.4至今,6163银河.net163.am,教学、科研。
Academic Appointments
Honors & Awards
Funding

主持国家自然科学基金青年基金1项;

主持教育部中央高校基本科研业务费面上项目1项;

参与国家自然科学基金3项。

Publications

● Zhao J, Zhu L, Fan C, Wu Y, Xiang S, Structure and function of urea amidolyase. Biosci Rep., 2018 Jan 17;38(1). pii: BSR20171617. doi: 10.1042/BSR20171617.

● Xiong J, Liu X, Gong Y, Zhang P, Qiang S, Zhao Q, Guo R, Qian Y, Wang L, Zhu L, Wang R, Hao Z, Wen H, Zhang J, Tang K, Zang WF, Yuchi Z, Chen H, Wayne Chen SR, Zheng W, Wang SQ, Xu YW, Liu Z., Pathogenic mechanism of a catecholaminergic polymorphic ventricular tachycardia causing-mutation in cardiac calcium release channel RyR2, J Mol Cell Cardiol,2018, 117: 26-35 (2016 IF 5.68).

● Yan Ouyang, Li Zhu*, Yifang Li, Miaomiao Guo, Yang Liu, Jin Cheng, Jing Zhao, Yi Wu*, Architectural plasticity of AMPK revealed by electron microscopy and X-ray crystallography, Scientific Reports, 2016, 6:24191, DOI: 10.1038/srep24191 (co-corresponding author) (2016 IF 4.259)

● Zhu Li#, Zhong Xiaowei, Chen S R Wayne, Banavali Nilesh, Liu Zheng*, Modeling a ryanodine receptor N-terminal domain connecting the central vestibule and the corner clamp region, Journal of Biological Chemistry, 2013, 288(2): 903-914 (5-Year IF 4.863)

● Zhong Xiaowei#, Liu Ying#Zhu Li#, Meng Xing, Wang Ruiwu, Van Petegem Filip, Wagenknecht Terence, Chen S R Wayne, Liu Zheng*, Conformational dynamics inside amino-terminal disease hotspot of ryanodine receptor, Structure, 2013, 21(11): 2051-2060 (co-first author) (5-Year IF 6.337)

● Zhu Li#, Chen Lei, Zhou Xiao-Ming, Zhang Yuan-Yuan, Zhang Yi-Jiong, Zhao Jing, Ji Shang-Rong, Wu Jia-Wei*, Wu Yi*, Structural insights into the architecture and allostery of full-length AMP-activated protein kinase, Structure, 2011, 19(4): 515-522 (5-Year IF 6.337)

● Ji S.-R., Wu Y.*Zhu L., Potempa L.A., Sheng F.-L., Lu W., Zhao J. (2007) Cell membranes and liposomes dissociate C-reactive protein (CRP) to form a new, biologically active structural intermediate: mCRPm. FASEB J, 21(1): 284-294. (5-Year IF 6.045)

Latest Time:2022-10-19