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Small (Weinheim an Der Bergstrasse, Germany)|November 3, 2023
Propelling Multi-Modal Therapeutics of PEEK Implants through the Power of NO evolving Covalent Organic Frameworks (COFs)Leizhen Huang, Meixuan Du, Dan Sun, et al.Nano Letters|June 9, 2026
Selenium Doping and Vacancy Engineering to Regulate the P-Band Center of Sulfur in Zinc Sulfide for High-Performance Sodium-Ion StorageWenbo Zhao, Yuhang Li, Yulin Jiang, et al.Journal of Experimental & Clinical Cancer Research : CR|October 23, 2016
Leptin promotes epithelial-mesenchymal transition of breast cancer via the upregulation of pyruvate kinase M2Lan Wei, Kuangfa Li, Xueli Pang, et al.Journal of Translational Medicine|January 20, 2026
Evaluation of the efficacy of optical genome mapping in prenatal diagnosis: a retrospective cohort studyKaili Yin, Yan Lü, Hanzhe Zhang, et al.Acta Biomaterialia|August 19, 2023
A hydrogel reservoir as a self-contained nucleus pulposus cell delivery vehicle for immunoregulation and repair of degenerated intervertebral discYulin Jiang, Juehan Wang, Dan Sun, et al.Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|June 29, 2017
Pyruvate kinase M2 interacts with mammalian sterile 20-like kinase 1 and inhibits tamoxifen-induced apoptosis in human breast cancer cellsFeihu Ji, Bianqin Guo, Nian Wang, et al.Small (Weinheim an Der Bergstrasse, Germany)|May 17, 2023
FeN Coordination Induced Ultralong Lifetime of Sodium-Ion Battery with the Cycle Number Exceeding 65 000Wang Feng, Xia Wen, Yanan Peng, et al.Nano Letters|February 8, 2024
Coexistence of Ferroelectricity and Ferromagnetism in Atomically Thin Two-Dimensional Cr2S3/WS2 Vertical HeterostructuresLuying Song, Ying Zhao, Ruofan Du, et al.Plos One|March 11, 2024
Feasibility of a family-oriented mHealth intervention for Chinese Americans with type 2 diabetes: A pilot randomized control trialLu Hu, Yun Shi, Judith Wylie-Rosett, et al.BMC Musculoskeletal Disorders|January 15, 2025
Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese familiesBin Mao, Xiaoling Cai, Na Lin, et al.Pageof 13