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Neurology|May 27, 2022
Investigating the Genetic Characteristics of Hippocampal Volume and Plasma β-Amyloid in a Chinese Community-Dwelling PopulationXin-Zhuang Yang, Meng-Yao Wan, Ding-Ding Zhang, et al.
Chemistry & Biodiversity|April 15, 2026
New Diketopiperazine Alkaloids From the Tuber of Pinellia Ternata (Thunb.) BreitShu-Jun Zhang, Yi-Qiang Zhang, Lei-Xin Zhuang, et al.
Journal of Cellular Physiology|January 16, 2019
The effects of graphene quantum dots on the maturation of mouse oocytes and development of offspringYan-Hong Lin, Shu-Xin Zhuang, Ya-Long Wang, et al.
Journal of Neurointerventional Surgery|August 12, 2019
Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese familyXinghuan Ding, Sen Zhao, Qianqian Zhang, et al.
Frontiers in Medicine|June 1, 2022
15-Month Health Outcomes and the Related Risk Factors of Hospitalized COVID-19 Patients From Onset: A Cohort StudyLiang-Liang Sun, Jian Wang, Yu-Sheng Wang, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|January 9, 2026
A novel mechanism of Reduning injection in sepsis treatment: Targeting inflammatory kinases TBK1 and IKKβLiang Cao, Zi-Yin Wu, Yan Gao, et al.
Human Genetics|July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to diseaseJiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|December 25, 2024
Clinical features, risk factors, outcomes, and prediction model for intrahepatic and perihepatic abscess following hepatectomy for hepatocellular carcinomaShuo Zhu, Li-Hui Gu, Yang Shen, et al.
Journal of Cellular and Molecular Medicine|April 12, 2020
Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalaciaNan Wu, Zhen Zhang, Xi Zhou, et al.
Molecular Genetics & Genomic Medicine|November 28, 2019
Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1Mao Lin, Zhenlei Liu, Gang Liu, et al.
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