A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family

por Du, Wei, Bu, Juan, Dong, Jiamei, Jia, Yanlei, Li, Jing, Liang, Chen, Si, Shancheng, Wang, Lejin
Publicado 2011

Impaired function of dendritic cells within the tumor microenvironment

por Xiao, Zhihua, Wang, Ruiqi, Wang, Xuyan, Yang, Haikui, Dong, Jiamei, He, Xin, Yang, Yang, Guo, Jiahao, Cui, Jiawen, Zhou, Zhiling
Publicado 2023

A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family

por Dong, Jiamei, Bu, Juan, Du, Wei, Li, Yuan, Jia, Yanlei, Li, Jianchang, Meng, Xiaoli, Yuan, Minghui, Peng, Xiaojuan, Zhou, Aimin, Wang, Lejin
Publicado 2012

GRB10 rs1800504 Polymorphism Is Associated With the Risk of Coronary Heart Disease in Patients With Type 2 Diabetes Mellitus

por Yang, Yang, Qiu, Wentao, Meng, Qian, Liu, Mouze, Lin, Weijie, Yang, Haikui, Wang, Ruiqi, Dong, Jiamei, Yuan, Ningning, Zhou, Zhiling, He, Fazhong
Publicado 2021

TRIB3 promoter 33 bp VNTR is associated with the risk of cerebrovascular disease in type 2 diabetic patients

por Lai, Jiaqi, Ouyang, Jiaying, Lin, Weijie, Liu, Mouze, Yang, Yang, Wang, Ruiqi, Yang, Haikui, Meng, Qian, Dong, Jiamei, Zhang, Jianping, Li, Ling, He, Fazhong
Publicado 2022