James G. Bellingham
11-43 Bath Street
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 20 publications
Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype.
Journal: Investigative ophthalmology & visual science
Published: November 13, 2025
A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants.
Journal: International journal of molecular sciences
Published: February 29, 2024
Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies.
Journal: Human molecular genetics
Published: June 20, 2022
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype.
Journal: NPJ genomic medicine
Published: May 19, 2022
The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision.
Journal: Nature communications
Published: August 06, 2021
New variants and in silico analyses in GRK1 associated Oguchi disease.
Journal: Human mutation
Published: March 26, 2020
AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicity.
Journal: Human molecular genetics
Published: December 04, 2019
The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6.
Journal: Human molecular genetics
Published: January 20, 2018
The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa.
Journal: Human molecular genetics
Published: August 24, 2017
The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.
Journal: Progress in retinal and eye research
Published: July 31, 2017
Last Updated: 09/26/2026