Dr Edwin Wong
Thomas Hallam
Dr Vicky Brocklebank
Dr Patrick Walsh
Dr Kate Smith-Jackson
et al. | Functional characterisation of rare genetic variants in the N-terminus of complement factor H in aHUS, C3G and AMD | 2021 |
|
Nina Jordan
Dr Sam Tingle
Victoria Shuttleworth
Katie Cooke
Dr Rachael Redgrave
et al. | MiR-126-3p Is Dynamically Regulated in Endothelial-to-Mesenchymal Transition during Fibrosis | 2021 |
|
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 Cascade | 2021 |
|
Victoria Shuttleworth
| Defining the susceptibility of colorectal cancers to BH3-mimetic compounds | 2020 |
|
Dr Sam Tingle
Dr Avinash Sewpaul
Lucy Bates
Dr Emily Thompson
Victoria Shuttleworth
et al. | Dual microRNA blockade increases expression of antioxidant protective proteins; implications for ischaemia reperfusion injury | 2020 |
|
Tom Hallam
Professor Kevin Marchbank
Professor Claire Harris
Victoria Shuttleworth
Professor David Kavanagh
et al. | Rare Genetic Variants in Complement Factor I Lead to Low FI Plasma Levels Resulting in Increased Risk of Age-Related Macular Degeneration | 2020 |
|
Dr Christopher Duncan
Dr Benjamin Thompson
Dr Rui Chen
Dr Florian Gothe
Victoria Shuttleworth
et al. | Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2 | 2019 |
|
