A missense mutation in CRYBA4 associated with congenital cataract and microcornea

por Zhou, Guangkai, Zhou, Nan, Hu, Shanshan, Zhao, Liming, Zhang, Chunmei, Qi, Yanhua
Publicado 2010

A novel mutation in GJA8 causing congenital cataract–microcornea syndrome in a Chinese pedigree

por Hu, Shanshan, Wang, Binbin, Zhou, Zhou, Zhou, Guangkai, Wang, Jing, Ma, Xu, Qi, Yanhua
Publicado 2010

Glucose transporter 3 (GLUT3) promotes lactylation modifications by regulating lactate dehydrogenase A (LDHA) in gastric cancer

por Yang, Hao, Yang, Shifeng, He, Jixing, Li, Wenqiang, Zhang, Ange, Li, Nana, Zhou, Guangkai, Sun, Boshi
Publicado 2023

Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese

por Zhou, Zhou, Wang, Binbin, Luo, Yongfeng, Zhou, Guangkai, Hu, Shanshan, Zhang, Han, Ma, Xu, Qi, Yanhua
Publicado 2011

A Novel MIP Gene Mutation Analysis in a Chinese Family Affected with Congenital Progressive Punctate Cataract

por Ding, Xuchen, Zhou, Nan, Lin, Hui, Chen, Jianjun, Zhao, Chunyuan, Zhou, Guangkai, Hejtmancik, J. Fielding, Qi, Yanhua
Publicado 2014

Genetic analysis of the FOXL2 gene using quantitative real-time PCR in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome

por Hu, Shanshan, Guo, Junjing, Wang, Binbin, Wang, Jing, Zhou, Zhou, Zhou, Guangkai, Ding, Xuchen, Ma, Xu, Qi, Yanhua
Publicado 2011

A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree

por Ding, Xuchen, Wang, Binbin, Luo, Yongfeng, Hu, Shanshan, Zhou, Guangkai, Zhou, Zhou, Wang, Jing, Ma, Xu, Qi, Yanhua
Publicado 2011