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Journal of Molecular Neuroscience : MN|October 7, 2020
Functional Analysis of a Compound Heterozygous Mutation in the VPS13B Gene in a Chinese Pedigree with Cohen SyndromeGuiyu Lou, Yang Ke, Yuwei Zhang, et al.European Journal of Medical Genetics|July 27, 2016
A novel MIP mutation in familial congenital nuclear cataractsLitao Qin, Liangjie Guo, Hongdan Wang, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 2017
Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndromeLitao Qin, Xiaobo Li, Qiaofang Hou, et al.Scientific Reports|August 26, 2018
Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese populationLitao Qin, Guiyu Lou, Liangjie Guo, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 15, 2019
[Genetic analysis of a pedigree affected with Bartter's syndrome]Ke Yang, Xiaodong Huo, Yuwei Zhang, et al.Gene|March 23, 2019
Novel compound heterozygous mutations of the DOCK6 gene in a familial case of Adams-Oliver syndrome 2Zhaokun Wang, Xin Wang, Guiyu Lou, et al.Hepatology (Baltimore, Md.)|June 20, 2012
Promotion of liver regeneration/repair by farnesoid X receptor in both liver and intestine in miceLisheng Zhang, Yan-Dong Wang, Wei-Dong Chen, et al.Journal of Applied Genetics|February 19, 2025
Identification of novel biallelic mutations in CFAP53 associated with fetal situs inversus totalis and literature reviewZhenglong Guo, Mengyao Tan, Hongjie Zhu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome]Yan Chu, Qiaofang Hou, Dong Wu, et al.Plos One|April 24, 2014
GPBAR1/TGR5 mediates bile acid-induced cytokine expression in murine Kupffer cellsGuiyu Lou, Xiaoxiao Ma, Xianghui Fu, et al.Pageof 5