Research
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Completed
January 2017 - January 2018
Identifying children with juvenile idiopathic arthritis at risk of uveitis
Aiming to prevent a common cause of childhood blindness
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Active
October 2018 - May 2024
Investigating the role of SIGIRR in geographic atrophy type of age-related macular degeneration
Understanding why the loss of SIGIRR leads to uncontrolled inflammation in AMD.
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Completed
October 2018 - January 2022
Development of a cell therapy treatment for uveitis
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Completed
April 2018 - May 2019
Characterisation of novel neuronal receptors at human corneal limbus
Finding out the nature of nerve terminals using a variety of histological techniques. The results could shed light on the function of these structures and their role in relation to corneal sensation, stem cell mechanism and prevention of blindness.
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Completed
April 2018 - December 2019
Examination of the TrkB receptor signalling pathway throughout the retina of glaucoma patients versus age-matched controls.
This project will improve our understanding of BDNF signalling in human retinal tissue.
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Completed
January 2018 - July 2022
Targeting a receptor pathway for the prevention of retinal fibrosis in neovascular age-related macular degeneration
Researchers aim to understand whether the development of fibrosis in nAMD can be prevented by targeting the C5aR pathway.
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Completed
August 2017 - July 2021
Investigation and treatment of intronic ABCA4 mutations in patients with inherited retinal dystrophy
A proportion of the causative mutations include those that occur within introns of the gene.
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Completed
October 2017 - December 2019
Creation of bio-synthetic corneal endothelial grafts for transplantation
The expansion of corneal endothelial cells in the laboratory onto a suitable material will enable the creation of bio-synthetic endothelial grafts.
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Completed
October 2017 - October 2021
Training in the use of smartphones and tablets to improve quality of life in visual impairment
This study will show whether, and how, mobile electronic devices can best be made accessible to the majority of VI users.