Yuxian Wang

Role of agonistic autoantibodies against type-1 angiotensin II receptor in the pathogenesis of retinopathy in preeclampsia

J. Zhi, Zhu Jin, Fang Liu, 2016, Scientific Reports.

Functional evaluation of a novel GLA causative mutation in Fabry disease

Changxing Wu, X. Cui, Lijuan Zhang, 2019, Molecular genetics & genomic medicine.

A novel pathogenic splice site variation in STK11 gene results in Peutz–Jeghers syndrome

Changxing Wu, Li Dong, Ping Li, 2021, Molecular genetics & genomic medicine.

miR-183-5p suppressed the invasion and migration of HTR-8/SVneo trophoblast cells partly via targeting MMP-9 in preeclampsia

Hailan Yang, M. Hao, Liyuan Dong, 2020, Bioscience reports.

Identification of a novel compound heterozygous IDUA mutation underlies Mucopolysaccharidoses type I in a Chinese pedigree

Chao Li, Zhonghua Zhao, Ping Li, 2019, Molecular genetics & genomic medicine.

Role and mechanism of AT1-AA in the pathogenesis of HELLP syndrome

J. Zhi, S. Bu, Zhu Jin, 2018, Scientific Reports.