Jianqi Xiao

Beijing University of Chemical Technology

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Trends

Author Order

Document Type

Co-Authors

Renzhi Wang

Peking Union Medical College Hospital

Bing Xing

Peking Union Medical College Hospital

Xiaobin Zhao

Beijing Tian Tan Hospital

Yong Yao

AbbVie (United States)

Zhaohui Zhu

Peking Union Medical College Hospital

Lin-hong Yang

First Affiliated Hospital of Jiamusi University

Qiang Hu

Shanghai Mental Health Center

Anqi Xu

Zhujiang Hospital

Xian Zhang

Southern Medical University

Zhenqing Wei

First Affiliated Hospital of Dalian Medical University

Cooperative Institutions

Chinese Academy of Medical Sciences & Peking Union Medical College

Peking Union Medical College Hospital

Southern Medical University

Beijing University of Chemical Technology

Shanghai Jiao Tong University

Nanfang Hospital

Chinese Academy of Sciences

Sun Yat-sen University

Nanjing Medical University

Nanchang University

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Field

WATER TREATMENT AGENT PREPARED BY LEMON RESIDUES FOR REMOVAL OF Cr(6

Wang Yangping Jianqi Xiao Keyu Chen Shen Wangqing

Lemon juice

Source

Cite

Citations (0)

Sex Difference of Egfr Expression and Molecular Pathway in the Liver: Impact on Drug Design and Cancer Treatments?

Journal of Cancer (2016)

Lishi Wang Jianqi Xiao Weikuan Gu Hong Chen

Epidermal growth factor receptor (EGFR) has been used as the target in drug design for cancer treatment including the liver cancer. Men and women have different levels of EGFR expression during the life. The whole genome expression profiles of livers of recombinant inbred (RI) strains derived from C57BL/6J (B6) X DBA/2J (D2) were used to compare three major molecular aspects of Egfr gene: the relative expression levels, gene network and eQTLs that regulate the expression of Egfr between female and male mice. Our data suggest that there is a significant difference in the expression levels in the liver between female and male mice. Several important genes in the gene network of Egfr are differentially expressed between female and male mice. The regulatory elements for the expression levels of Egfr between female and male mice are also different. In summary, our data reveals an important sex difference in the Egfr pathways in the liver of the mice. These data may have substantial impact on drug development and dosage determinant for women and men in the clinical trials.

Liver Cancer

10.7150/jca.13684

Cite

Citations (15)

Fast-Charging Graphite-Based Anode Enabled by Gradient Silicon: From Mechanism Revelation to Electrode Design

Jianqi Xiao Junhui Sun Weihao Song Xushan Zhang Xinyu Li

Fast-charging performance is one of the most important indicators for advanced lithium-ion batteries (LIBs). Herein, the fast-charging performance of routine graphite (Gr) and silicon (Si) anodes has been systematically studied, which shows that the Si anode has better performance than the Gr anode at fast-charging rate due to more reversible lithium (Li) plating/stripping and unique self-dissolve property of Li deposits. It is further revealed that the good fast-charging performance of the Si anode essentially depends on the easy Li+ desolvation in electrolyte and fast Li+ diffusion in solid electrolyte interface and lithiated Si. Based on this finding, a Si/Gr composite anode with gradient Si content (denoted Si/Gr-Grad) is prepared by an industrially feasible spraying method. The tailored design simultaneously improves the capacity and reversibility of Gr-based anode under fast-charging condition. The full cell using the Si/Gr-Grad anode and the LiFePO4 cathode delivers a high capacity retention of 84.3% after 500 cycles at 4C. Even paired with the LiNi0.6Co0.2Mn0.2O2 cathode in Ah-level pouch cell, the Si/Gr-Grad anode enables the full cell to show good safety and cycling performance at 4C. Our work highlights the important roles of Si component and gradient structure in electrode design for fast-charging LIBs.

Revelation

10.2139/ssrn.5087454

Cite

Citations (0)