Shiyi Zhou

发表

The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy

Xu Ma, Liwen Wu, Q. Lu, 2011, Epilepsy Research.

Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)

Binbin Wang, Xu Ma, Shanshan Hu, 2010, Molecular vision.

A novel mutation impairing the tertiary structure and stability of γC‐crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens

P. Li, Juhua Yang, Yong-Bin Yan, 2012, Human mutation.

A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family

Binbin Wang, Jing Wang, Sirui Zhou, 2011, Human mutation.

A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family

Binbin Wang, Jing Wang, Xu Ma, 2009, Molecular vision.

The study of copy number variations in the regions of NOTCH1 among Chinese VSD and TOF patients.

Binbin Wang, Jing Wang, Xu Ma, 2011, International journal of cardiology.

Knockdown of p66Shc by siRNA injection rescues arsenite-induced developmental retardation in mouse preimplantation embryos.

Xu Ma, Baiqing Yang, Cailing Lu, 2014, Reproductive toxicology.

Hairy-related transcription factor 2 is not potentially related to congenital heart disease in Chinese patients.

Binbin Wang, Jing Wang, Xu Ma, 2011, International journal of cardiology.

Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Binbin Wang, Jing Wang, Xu Ma, 2010, International journal of cardiology.

Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population

Dongmei Meng, Shiguo Liu, Binbin Wang, 2010, Human Genetics.