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Huan Jing Ke Xue= Huanjing Kexue|July 2, 2020
[Use of Iron-modified Calcite as an Active Capping Material to Control Phosphorus Release from Sediments in Surface Water Bodies]Xiao-Yun Bai, Jian-Wei Lin, Yan-Hui Zhan, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|January 20, 2012
Effects of cumulus cells on vitreous cryopreservation of human mature oocytes and clinical pregnancy outcomesHai-Xia Jin, Wen-Yang Song, Zhi-Min Xin, et al.
Biochemical and Biophysical Research Communications|March 4, 2006
Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutationsQingfeng Yan, Yelena Bykhovskaya, Ronghua Li, et al.
Frontiers in Pharmacology|July 3, 2025
Intracerebroventricular calycosin attenuates cerebral ischemia-reperfusion injury in rats via HMGB1-dependent pyroptosis inhibitionYuhui Zhang, Qiguang Wu, Yanjin Pan, et al.
Frontiers in Public Health|May 16, 2025
The association between multimorbidity patterns and physical frailty among middle-aged and older community-dwelling adults: the mediating role of depressive symptomsYuhan Geng, Ming Zhou, Yangxiaoxue Liu, et al.
Thrombosis Research|December 30, 2023
A novel GATA1 variant p.G229D causing the defect of procoagulant platelet formationBiying Ding, Yinqi Mao, Yang Li, et al.
BMC Psychiatry|April 11, 2026
Neurocognitive function profiles in Chinese patients with melancholic vs. non-melancholic major depressive disorderLi-Min Xin, Jing-Yu Lin, Hong-Zhen Fan, et al.
Frontiers in Medicine|May 8, 2026
The post-pandemic transformation in Pathophysiology teaching strategiesHuiling Lu, Xin Li, Lingli Zhang, et al.
Acta Biochimica Et Biophysica Sinica|January 4, 2026
Calycosin alleviates blood-brain barrier disruption after cerebral ischemia-reperfusion injury by inhibiting NLRP3-mediated pyroptosisQiguang Wu, Zeyu Bai, Min Xin, et al.
JCI Insight|March 4, 2025
Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutationCheng Ai, Huiying Li, Chunyan Wang, et al.
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