Victoria G. Shuttleworth

Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>

C.J. Duncan, Benjamin Thompson, Rui Chen et al. · Science Immunology · 2019 · 108 citations · Full text

Rare Genetic Variants in Complement Factor I Lead to Low FI Plasma Levels Resulting in Increased Risk of Age-Related Macular Degeneration

Thomas M Hallam, Kevin J. Marchbank, Claire L. Harris et al. · Investigative Ophthalmology & Visual Science · 2020 · 53 citations · Full text

MiR-126-3p Is Dynamically Regulated in Endothelial-to-Mesenchymal Transition during Fibrosis

Nina Jordan, Samuel J Tingle, Victoria G. Shuttleworth et al. · International Journal of Molecular Sciences · 2021 · 38 citations · Full text

Endothelial Cell Pathobiology, Undergone Endmt, Fibrosis +14

The methyltransferase SET9 regulates TGFB1 activation of renal fibroblasts via interaction with SMAD3

Victoria G. Shuttleworth, Luke Gaughan, Lotfia Shames Omar Nawafa et al. · Journal of Cell Science · 2017 · 23 citations · Full text

Renal Inflammation, Tgfb1 Activation, Transcriptional Regulation +23

The rare<i>C9</i>P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascade

Orla McMahon, Thomas M Hallam, Shrena Patel et al. · Human Molecular Genetics · 2021 · 18 citations · Full text