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Investigative Ophthalmology & Visual Science|January 10, 2016
Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet GenesWenmin Sun, Li Huang, Yan Xu, et al.
Molecular Vision|March 9, 2010
Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopiaQin Wang, Panfeng Wang, Shiqiang Li, et al.
Genes|August 26, 2023
Clinical and Genetic Features of <i>NR2E3</i>-Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature ReviewSainan Xiao, Zhen Yi, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Replication study supports CTNND2 as a susceptibility gene for high myopiaBoyu Lu, Dan Jiang, Panfeng Wang, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 4, 2021
Lipid Receptor G2A-Mediated Signal Pathway Plays a Critical Role in Inflammatory Response by Promoting Classical Macrophage ActivationQing Li, Chunlei Feng, Lingyun Li, et al.
Investigative Ophthalmology & Visual Science|May 19, 2021
Characterization of PROM1 p.Arg373Cys Variant in a Cohort of Chinese Patients: Macular Dystrophy Plus Peripheral Bone-Spicule DegenerationYingwei Wang, Panfeng Wang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|May 17, 2022
Autosomal Dominant Retinitis Pigmentosa-Associated TOPORS Protein Truncating Variants Are Exclusively Located in the Region of Amino Acid Residues 807 to 867Junwen Wang, Yingwei Wang, Yi Jiang, et al.
Molecular Medicine Reports|November 8, 2014
Mutation analysis of Leber congenital amaurosis‑associated genes in patients with retinitis pigmentosaTao Shen, Liping Guan, Shiqiang Li, et al.
Oncotarget|November 29, 2017
GSK-3β phosphorylation-dependent degradation of ZNF281 by β-TrCP2 suppresses colorectal cancer progressionYuekun Zhu, Qingxin Zhou, Guiling Zhu, et al.
Molecular Vision|September 6, 2018
Phenotypic characterization of patients with early-onset high myopia due to mutations in <i>COL2A1</i> or <i>COL11A1</i>: Why not Stickler syndrome?Lin Zhou, Xueshan Xiao, Shiqiang Li, et al.
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