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Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|December 8, 2024
Low-concentration atropine for controlling myopia onset and progression in East AsiaEbenezer Zaabaar, Yuzhou Zhang, Ka Wai Kam, et al.
Experimental Eye Research|January 4, 2020
COL2A1 protective variant reduces sporadic rhegmatogenous retinal detachment severityTsz Kin Ng, Wanghao Chen, Qianwen Chen, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 31, 2020
Pharmacotherapeutic candidates for myopia: A reviewWen-Yi Wang, Camille Chen, Justine Chang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 12, 2020
Splice variant of growth hormone-releasing hormone receptor drives esophageal squamous cell carcinoma conferring a therapeutic targetXiao Xiong, Xiurong Ke, Lu Wang, et al.
Molecular Vision|December 15, 2007
A novel deletion variant of gammaD-crystallin responsible for congenital nuclear cataractLi-Yun Zhang, Gary Hin-Fai Yam, Dorothy Shu-Ping Fan, et al.
Ophthalmology|October 6, 2007
Comparative study of central corneal thickness measurement with slit-lamp optical coherence tomography and visante optical coherence tomographyHaitao Li, Christopher Kai Shun Leung, Lee Wong, et al.
The British Journal of Ophthalmology|July 31, 2014
CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patientsYuqin Wang, Xiu-Feng Huang, Ming-Ming Yang, et al.
Cancer & Metabolism|October 27, 2024
GCN2-SLC7A11 axis coordinates autophagy, cell cycle and apoptosis and regulates cell growth in retinoblastoma upon arginine deprivationDan Wang, Wai Kit Chu, Jason Cheuk Sing Yam, et al.
Scientific Reports|November 10, 2015
Transdifferentiation of periodontal ligament-derived stem cells into retinal ganglion-like cells and its microRNA signatureTsz Kin Ng, Jasmine S Y Yung, Kwong Wai Choy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencingXiu-Feng Huang, Fang Huang, Kun-Chao Wu, et al.
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