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Browsing publications by David Steel.

Newcastle AuthorsTitleYearFull text
Steven Toh
Professor Boguslaw Obara
David Steel
Expansile gas kinetics for pneumatic retinopexy2023
David Steel
Retinal and Corneal Changes Associated with Intraocular Silicone Oil Tamponade2022
Tom Hallam
Gladys -
Nik Tzoumas
David Steel
Victoria Shuttleworth
et al.
The Rare C9 P167S Risk Variant for Age-related Macular Degeneration Increases Polymerization of the Terminal Component of the Complement Cascade2021
Edvinas Cerniauskas
Dr Marzena Kurzawa-Akanbi
Dr Long Xie
Dr Dean Hallam
Marina Moya Molina
et al.
Complement modulation reverses pathology in Y402H-retinal pigment epithelium cell model of AMD by restoring lysosomal function2020
David Steel
MicroRNA expression profile in the vitreous of proliferative diabetic retinopathy patients and differences from patienttreated with anti-VEGF therapy2020
David Steel
Why ophthalmologists should mask: a perspective from Hong Kong2020
Dr Carla Jackson
Dr Roman Bauer
Dr Joseph Collin
Dr Birthe Hilgen
Dr Darin Zerti
et al.
An integrated transcriptional analysis of the developing human retina2019
David Steel
Diabetic macular oedema and diode subthreshold micropulse laser (DIAMONDS): study protocol for a randomised controlled trial2019
Dr Dean Hallam
David Rawlings
David Steel
Professor Lyle Armstrong
Professor Majlinda Lako
et al.
In Reply to the Letter to the Editor from Hallam et al.: An Induced Pluripotent Stem Cell Patient Specific Model of Complement Factor H (Y402H) Polymorphism Displays Characteristic Features of Age-Related Macular Degeneration and Indicates a Beneficial Role for UV Light Exposure2018
Dr Birthe Hilgen
Majed Felemban
Alex Sharpe
Dr Roman Bauer
Dr Dean Hallam
et al.
Laminin γ3 plays an important role in retinal lamination, photoreceptor organisation and ganglion cell differentiation2018
David Steel
Multimodal imaging in a patient with ocular argyrosis complicated by diabetic retinopathy2018
Dr Simon Ramsbottom
Dr Elisa Molinari
Dr Shalabh Srivastava
Sumaya Alkanderi
Laura Devlin
et al.
Targeted exon skipping of a CEP290 mutation rescues Joubert syndrome phenotypes in vitro and in a murine model2018