Menghan Wu

发表

A novel splice site mutation of CRYBA3/A1 gene associated with congenital cataract in a Chinese family.

K. Yao, X. Gong, Menghan Wu, 2017, International journal of ophthalmology.

Identification and functional analysis of two novel connexin 50 mutations associated with autosome dominant congenital cataracts

X. Gong, Xinyi Chen, K. Yao, 2016, Scientific Reports.

Comparative outcomes of femtosecond laser‐assisted cataract surgery and manual phacoemusification: a six‐month follow‐up

Xinyi Chen, K. Yao, Menghan Wu, 2016, Clinical & experimental ophthalmology.

Evaluation of dry eye after femtosecond laser–assisted cataract surgery

Yibo Yu, K. Yao, Menghan Wu, 2015, Journal of cataract and refractive surgery.

A novel phenotype-genotype correlation with an Arg555Trp mutation of TGFBI gene in Thiel-Behnke corneal dystrophy in a Chinese pedigree

Buyi Zhang, K. Yao, Jinyu Li, 2015, BMC Ophthalmology.

Targeted Exome Sequencing of Congenital Cataracts Related Genes: Broadening the Mutation Spectrum and Genotype–Phenotype Correlations in 27 Chinese Han Families

Guizhen Sun, X. Gong, K. Yao, 2017, Scientific Reports.

Identification of a novel small-molecule inhibitor targeting TIM-3 for cancer immunotherapy.

Yang Li, X. Niu, Yanfeng Gao, 2023, Biochemical pharmacology.

Identification and preliminary functional analysis of two novel congenital cataract associated mutations of Cx46 and Cx50

Tingting Xie, K. Yao, Menghan Wu, 2019, Ophthalmic genetics.

Comparative outcomes of femtosecond laser‐assisted cataract surgery and manual phacoemusification: a six‐month follow‐up

Xinyi Chen, K. Yao, Menghan Wu, 2016, Clinical & experimental ophthalmology.