Mingbing Zeng
State Key Laboratory Of Ophthalmology, Guangdong Provincial Key Laboratory Of Ophthalmology And Visual Science
Guangzhou, China
Guangzhou, China
Last Updated: 09/26/2026
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Found 16 publications
TGFBI p.H626R Mutation in a Chinese Family with Lattice Corneal Dystrophy: A Short Report and Literature Review.
Journal: Genetic testing and molecular biomarkers
Published: August 11, 2026
Seminuclear Flip Phacoemulsification for Soft Nuclear Cataract Surgery: A New Soft Nucleus Cataract Chopping Technique.
Journal: Journal of ophthalmology
Published: January 16, 2026
Modified Intrascleral Suture Technique for Repairing Iridodialysis Combined with Phacoemulsification Cataract Surgery.
Journal: Journal of investigative surgery : the official journal of the Academy of Surgical Research
Published: October 27, 2025
Intraocular Lens Power Calculation for Combined Cataract and Pterygium Surgeries.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: October 26, 2025
Suprachoroidal hemorrhage associated with cataract surgery: A case series analysis.
Journal: The Journal of international medical research
Published: April 29, 2025
Shootin1 Regulates Retinal Ganglion Cell Neurite Development: Insights From an RGC Direct Somatic Cell Reprogramming Model.
Journal: Investigative ophthalmology & visual science
Published: June 27, 2024
Retinal Ganglion Cell Fate Induction by Ngn-Family Transcription Factors.
Journal: Investigative ophthalmology & visual science
Published: December 22, 2023
Subnuclear Phacoemulsification to Reduce Corneal Injury in Nuclear Cataract Surgery: Evidence From a Randomized Controlled Trial.
Journal: Journal of ophthalmology
Published: October 26, 2023
The impact of preloaded intraocular lens implantation system (TECNIS iTec®) in routine cataract surgery in China: a time-motion analysis.
Journal: BMC ophthalmology
Published: August 01, 2022
Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract.
Identification of a New Mutation p.P88L in Connexin 50 Associated with Dominant Congenital Cataract.
Journal: Frontiers in cell and developmental biology
Published: October 14, 2021
A Novel Mutation p.S93R in CRYBB1 Associated with Dominant Congenital Cataract and Microphthalmia.
Journal: Current eye research
Published: October 01, 2019
Last Updated: 09/26/2026