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World Journal of Pediatrics : WJP|August 10, 2013
The HHEX gene is not related to congenital heart disease in 296 Chinese patientsXiao-Peng Deng, Li-Xi Zhao, Bin-Bin Wang, et al.The Journal of Headache and Pain|February 21, 2026
SP1 recruits TET1 to mediate Kif1a demethylation and synaptic remodeling in a mouse model of chronic migraineWei Jiang, Peng Yu, Guo-Hua Liang, et al.Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|February 24, 2021
Oxymatrine improves blood-brain barrier integrity after cerebral ischemia-reperfusion injury by downregulating CAV1 and MMP9 expressionYu Jiao-Yan, Liu Qing-Qing, Li Xi, et al.Scientific Reports|October 2, 2015
Natural small molecule FMHM inhibits lipopolysaccharide-induced inflammatory response by promoting TRAF6 degradation via K48-linked polyubiquitinationKe-Wu Zeng, Li-Xi Liao, Hai-Ning Lv, et al.Current Vascular Pharmacology|July 24, 2015
MiR-135a Suppresses Calcification in Senescent VSMCs by Regulating KLF4/STAT3 PathwayLin Lin, Yue He, Bei-Li Xi, et al.Journal of Molecular Neuroscience : MN|April 1, 2021
Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and OphthalmoparesisLi-Xi Li, Li-Ting Jiang, You-Gui Pan, et al.Pacing and Clinical Electrophysiology : PACE|October 20, 2012
Long-term follow-up impact of dual-chamber pacing on patients with hypertrophic obstructive cardiomyopathyHu Yue-Cheng, Li Zuo-Cheng, Li Xi-Ming, et al.Nanoscale Research Letters|August 17, 2018
Current-Induced Domain Wall Motion and Tilting in Perpendicularly Magnetized RacetracksDong Li, Baoshan Cui, Jijun Yun, et al.BMC Plant Biology|May 22, 2026
Chromium tolerance mechanisms in Cosmos sulphureus: antioxidant defense and potential role of pectin chelation-based detoxificationYu Xiaofang, Xu Fan, Yang Xuan, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 19, 2022
Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defectsLin Yang, Bo Liu, Xinran Dong, et al.Pageof 35