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Molecular Vision|July 21, 2012
Evaluation of NTF4 as a causative gene for primary open-angle glaucomaLi Jia Chen, Tsz Kin Ng, Alex H Fan, et al.Experimental Eye Research|October 2, 2025
Plasma N-glycan signature as biomarker for primary open angle glaucomaTsz Kin Ng, Chunxian Zhang, Qingping Liu, et al.Ophthalmology|February 9, 2016
Genetic Associations of Primary Angle-Closure Disease: A Systematic Review and Meta-analysisShi Song Rong, Fang Yao Tang, Wai Kit Chu, et al.Experimental Eye Research|August 5, 2019
Identification and characterization of a novel promoter variant in placental growth factor for neovascular age-related macular degenerationLi Ma, Tsz Kin Ng, Haoyu Chen, et al.Plos One|June 25, 2011
MicroRNA-145 regulates human corneal epithelial differentiationSharon Ka-Wai Lee, Yufei Teng, Hoi-Kin Wong, et al.American Journal of Human Genetics|November 3, 2009
Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAsChen Zhao, Deepti L Bellur, Shasha Lu, et al.BMC Ophthalmology|August 7, 2023
Magnetic resonance imaging parameters on lacrimal gland in thyroid eye disease: a systematic review and meta-analysisNicole Tsz Yan Wong, Ka Fai Kevin Yuen, Fatema Mohamed Ali Abdulla Aljufairi, et al.Human Molecular Genetics|January 15, 2014
PRPF4 mutations cause autosomal dominant retinitis pigmentosaXue Chen, Yuan Liu, Xunlun Sheng, et al.Journal of Clinical Medicine|May 13, 2023
Ocular Surface Changes in Treatment-Naive Thyroid Eye DiseaseXulin Liao, Kenneth Ka Hei Lai, Fatema Mohamed Ali Abdulla Aljufairi, et al.Acta Ophthalmologica|November 13, 2025
Advances in the genetics of refractive errors: Contributions from the CREAM consortiumSze Wai Rosa Li, Xi He, Louise Terry, et al.Pageof 51