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Clinical Chemistry and Laboratory Medicine|May 21, 2020
A novel mitochondrial m.14430A>G (MT-ND6, p.W82R) variant causes complex I deficiency and mitochondrial Leigh syndromeMiaomiao Du, Xiujuan Wei, Pu Xu, et al.
ACS Applied Materials & Interfaces|September 23, 2025
Mitigating Voltage Decay and Enhancing Structural Stability of Li-Rich Cathodes via a Robust Polysaccharide Binding NetworkHao Chen, Xirong Mai, Xuqi Lin, et al.
ACS Applied Materials & Interfaces|December 14, 2022
Three-Dimensional Crosslinked PAA-TA Hybrid Binders for Long-Cycle-Life SiO<sub></sub> Anodes in Lithium-Ion BatteriesWeiting Tang, Li Feng, Xiujuan Wei, et al.
ACS Applied Materials & Interfaces|April 13, 2022
Cross-Linked γ-Polyglutamic Acid as an Aqueous SiO<sub></sub> Anode Binder for Long-Term Lithium-Ion BatteriesHuayan Xiao, Juncheng Qiu, Shuxing Wu, et al.
ACS Applied Materials & Interfaces|September 12, 2025
Self-Healing Ion-Conductive Binder for High-Performance SiO<sub><i>x</i></sub> Anodes in Lithium-Ion BatteriesXianhao Long, Liangxin Xie, Chuxiong Huang, et al.
Small (Weinheim an Der Bergstrasse, Germany)|January 30, 2015
Three-Dimensional Interconnected Vanadium Pentoxide Nanonetwork Cathode for High-Rate Long-Life Lithium BatteriesQinyou An, Qiulong Wei, Pengfei Zhang, et al.
Gene|June 23, 2018
SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequencesYuanyuan Li, Shumeng Wen, Dongxiao Li, et al.
The Journal of Biological Chemistry|August 30, 2025
β-hydroxybutyrate dehydrogenase promotes pancreatic cancer cell proliferation through regulation of the NAD<sup>+</sup>/NADH balance and mitochondrial acetylationXiujuan Wei, Chengkai Zhang, Xiaoguang Zheng, et al.
ACS Applied Materials & Interfaces|November 26, 2015
Copper Silicate Hydrate Hollow Spheres Constructed by Nanotubes Encapsulated in Reduced Graphene Oxide as Long-Life Lithium-Ion Battery AnodeXiujuan Wei, Chunjuan Tang, Xuanpeng Wang, et al.
Journal of Human Genetics|September 30, 2018
Correction: A novel NDUFS3 mutation in a Chinese patient with severe Leigh syndromeXiaoting Lou, Hao Shi, Shumeng Wen, et al.
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