Jinyu Li
No.88 Jiefang Rd
Hangzhou, 310009, China
Hangzhou, 310009, China
Last Updated: 09/26/2026
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Found 23 publications
COL1A2 and APOLD1 Define a Dual-Axis Molecular Framework for Diabetic Nephropathy-Retinopathy Comorbidity: An Integrative Multiomics and Machine Learning Study in Mouse Models.
Journal: International journal of medical sciences
Published: April 22, 2026
Comparison of the efficacy of subthreshold micropulse laser versus intravitreal anti-VEGF therapy for chronic central serous chorioretinopathy.
Journal: Frontiers in medicine
Published: March 16, 2026
Expression and identification of a novel high-activity recombinant humanized type I collagen SynthCol1 in Pichia pastoris GS115.
Journal: Applied microbiology and biotechnology
Published: October 30, 2025
A novel GJA3 mutation causing autosomal dominant congenital perinuclear cataracts.
Journal: BMC ophthalmology
Published: September 12, 2023
Bilateral central retinal artery occlusion as a presenting manifestation of systemic lupus erythematosus: a case-based review.
Journal: Rheumatology international
Published: April 07, 2023
Non-typical persistent hyperplastic primary vitreous: a rare case report and review of the literature.
Journal: BMC ophthalmology
Published: November 03, 2022
Accuracy of Intraocular Lens Power Calculation Formulas in Pediatric Cataract Patients: A Systematic Review and Meta-Analysis.
Journal: Frontiers in medicine
Published: May 16, 2021
Elevated Levels of Endoglin, Endostatin, FGF-α, HGF, and Thrombospondin-2 in Aqueous Humor of nAMD Patients.
Journal: Ocular immunology and inflammation
Published: April 01, 2021
Optical Coherence Tomography Angiography-Based Quantitative Assessment of Morphologic Changes in Active Myopic Choroidal Neovascularization During Anti-vascular Endothelial Growth Factor Therapy.
Journal: Frontiers in medicine
Published: January 24, 2021
A new heterozygous mutation in the stop codon of CRYAB (p.X176Y) is liable for congenital posterior pole cataract in a Chinese family.
Journal: Ophthalmic genetics
Published: December 04, 2020
Identification and characterization of six β-crystallin gene mutations associated with congenital cataract in Chinese families.
Journal: Molecular genetics & genomic medicine
Published: September 07, 2020
A Novel Human Congenital Cataract Mutation in EPHA2 Kinase Domain (p.G668D) Alters Receptor Stability and Function.
Journal: Investigative ophthalmology & visual science
Published: November 15, 2019
Last Updated: 09/26/2026