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Frontiers in Cardiovascular Medicine|September 23, 2024
Case Report: A Chinese child with Barth syndrome caused by a novel TAFAZZIN mutationMingxuan Che, Fuhai Li, Yaning Jia, et al.Optics Express|December 25, 2012
Pyroelectric effect in green light-assisted domain reversal of Mg-doped LiNbO3 crystalsShoujun Zheng, Yongfa Kong, Hongde Liu, et al.BMC Endocrine Disorders|September 22, 2025
Relationship between TYG mediated pregnancy diabetes history and SII in American women: a retrospective cohort study of NHANES 2011-2018Yanan Duan, Ru Zhang, Yan Zhang, et al.Brain and Behavior|February 3, 2022
Role of histidine decarboxylase gene in the pathogenesis of Tourette syndromeLulu Xu, Cheng Zhang, Meixiang Zhong, et al.Molecular Medicine Reports|November 21, 2019
A novel ATRX mutation causes Smith‑Fineman‑Myers syndrome in a Chinese familyLiangshan Li, Jing Yu, Xiao Zhang, et al.Journal of Nutritional Science and Vitaminology|October 30, 2022
Impact of SLC23A1 and SLC23A2 Polymorphisms on the Risk for Preeclampsia in a Chinese Han PopulationHuabin Hou, Yongjie Zhang, Hongjing Wu, et al.The Journal of Pharmacy and Pharmacology|January 11, 2005
Inhibition of Nox-4 activity by plumbagin, a plant-derived bioactive naphthoquinoneYaxian Ding, Zi-Jiang Chen, Shiguo Liu, et al.International Journal of Cardiology|October 27, 2009
Teratocarcinoma-derived growth factor 1 (TDGF1) sequence variants in patients with congenital heart defectBinbin Wang, Jinting Yan, Zuoqi Peng, et al.Optics Express|May 15, 2013
Fast UV-Vis photorefractive response of Zr and Mg codoped LiNbO3:MoTian Tian, Yongfa Kong, Shiguo Liu, et al.Pregnancy Hypertension|July 3, 2024
Association of NLRP3 and IL-4 VNTR polymorphisms and genetic susceptibility to preeclampsia: A case-control studyMingxuan Che, Yinglei Xu, Yucui Zang, et al.Pageof 22