Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells

by Zhenwei Shang, Wenjing Sun, Mingming Zhang, Lidan Xu, Xueyuan Jia, Ruijie Zhang, Songbin Fu
Published 2020-02-01

The distribution of three candidate cold-resistant SNPs in six minorities in North China

by Qiuyan Li, Kexian Dong, Lidan Xu, Xueyuan Jia, Jie Wu, Wenjing Sun, Xuelong Zhang, Songbin Fu
Published 2018-02-01

Evaluation of a Novel Missense Mutation in ABCB4 Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3

by Komal Saleem, Qingbo Cui, Tahir Zaib, Siqi Zhu, Qian Qin, Yusi Wang, Jinxi Dam, Wei Ji, Peng Liu, Xueyuan Jia, Jie Wu, Jing Bai, Songbin Fu, Wenjing Sun
Published 2020-01-01

Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease

by Kexian Dong, Xiaogang Liu, Xueyuan Jia, Huanhuan Miao, Wei Ji, Jie Wu, Yun Huang, Lidan Xu, Xuelong Zhang, Hui Su, Guohua Ji, Peng Liu, Rongwei Guan, Jing Bai, Songbin Fu, Xianli Zhou, Wenjing Sun
Published 2020-11-01

Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree

by Tahir Zaib, Chunhui Zhang, Komal Saleem, Lidan Xu, Qian Qin, Yusi Wang, Wei Ji, Hanif Khan, Hanfei Yu, Siqi Zhu, Wei Gao, Yun Huang, Xueyuan Jia, Jie Wu, Hongtao Song, Yanqiao Zhang, Wenjing Sun, Songbin Fu
Published 2020-01-01

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family

by Tahir Zaib, Wei Ji, Komal Saleem, Guangchen Nie, Chao Li, Lin Cao, Baijun Xu, Kexian Dong, Hanfei Yu, Xuguang Hao, Yan Xue, Shuhan Si, Xueyuan Jia, Jie Wu, Xuelong Zhang, Rongwei Guan, Guohua Ji, Jing Bai, Feng Chen, Yong Liu, Wenjing Sun, Songbin Fu
Published 2019-12-01