Dongjun Xing
Tianjin Key Laboratory Of Retinal Functions And Diseases, Tianjin Branch Of National Clinical Research Center For Ocular Disease, 251 Fukang Road
Tianjin, 300384, China
Tianjin, 300384, China
Last Updated: 09/26/2026
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Found 9 publications
Comprehensive analysis of RS1 gene mutations and clinical manifestations in nine unrelated X-linked retinoschisis (XLRS) Chinese families.
Journal: BMC ophthalmology
Published: September 25, 2025
Gene therapy for Bietti crystalline corneoretinal dystrophy: A phase 1/2 clinical trial.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: May 23, 2025
Optic disc characteristics evaluated with swept source optical coherence tomography angiography (SS-OCTA) in nonarteritic anterior ischemic optic neuropathy (NAION): a cross-sectional study.
Journal: BMC ophthalmology
Published: December 04, 2024
Thrombolytic efficacy and safety of recombinant scu-PA in a rabbit retinal vein occlusion model.
Journal: European journal of pharmacology
Published: August 27, 2024
Responsiveness of anti-VEGF treatment for polypoidal choroidal vasculopathy based on aqueous humour proteomics: A preliminary study.
Journal: Acta ophthalmologica
Published: July 31, 2024
FEATURES OF VASCULATURE IN PATIENTS WITH RETINA ARTERIAL MACROANEURYSM USING OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY.
Journal: Retina (Philadelphia, Pa.)
Published: July 14, 2022
Novel mutations of the USH2A gene cause Usher syndrome in five Chinese families.
Journal: BMC ophthalmology
Published: February 07, 2022
A novel missense mutation locus of cadherin 23 and the interaction of cadherin 23 and protocadherin 15 in a patient with usher syndrome.
Journal: Ophthalmic genetics
Published: August 25, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026