Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Publications

Prolidase Deficiency Causes Spontaneous T Cell Activation and Lupus-Like Autoimmunity.

Hodgson R. et al, (2023), J Immunol

Determining the Relationship Between Blood Pressure, Kidney Function, and Chronic Kidney Disease: Insights From Genetic Epidemiology

Staplin N. et al, (2022), Hypertension, 79, 2671 - 2681

Exploring the relevance of NUP93 variants in steroid-resistant nephrotic syndrome using next generation sequencing and a fly kidney model.

Bierzynska A. et al, (2022), Pediatric nephrology (Berlin, Germany), 37, 2643 - 2656

NDRG1 is induced by antigen-receptor signaling but dispensable for B and T cell self-tolerance.

Hodgson R. et al, (2022), Communications biology, 5

SARS-CoV-2-Specific T Cell Responses Are Not Associated with Protection against Reinfection in Hemodialysis Patients

Shankar S. et al, (2022), Journal of the American Society of Nephrology, 33, 883 - 887

Neutralising antibodies after COVID-19 vaccination in UK haemodialysis patients

Carr EJ. et al, (2021), The Lancet, 398, 1038 - 1041

Regular RNA screening detects asymptomatic SARS-CoV-2 infection in haemodialysis patients

Storey B. et al, (2021), Nephrology Dialysis Transplantation, 36, 1130 - 1132

An ontogenetic switch drives the positive and negative selection of B cells

Xu X. et al, (2020), Proceedings of the National Academy of Sciences, 117, 3718 - 3727

High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation.

Abeler-Dörner L. et al, (2020), Nature immunology, 21, 86 - 100

Systemic silencing of Phd2 causes reversible immune regulatory dysfunction

Yamamoto A. et al, (2019), Journal of Clinical Investigation, 129, 3640 - 3656

High-throughput phenotyping reveals expansive genetic and structural underpinnings of immune variation

Abeler-Dörner L. et al, (2019)

An essential role for the Zn2+ transporter ZIP7 in B cell development

Anzilotti C. et al, (2019), Nature Immunology, 20, 350 - 361

Interventions for chronic kidney disease in people with sickle cell disease

Roy NBA. et al, (2017), Cochrane Database of Systematic Reviews, 2017

Themis2 lowers the threshold for B cell activation during positive selection

Cheng D. et al, (2017), Nature Immunology, 18, 205 - 213

VEGF regulates local inhibitory complement proteins in the eye and kidney

Keir LS. et al, (2016), Journal of Clinical Investigation, 127, 199 - 214

Interventions for chronic kidney disease in people with sickle cell disease

Roy NBA. et al, (2016)

Mutation of Fnip1 is associated with B-cell deficiency, cardiomyopathy, and elevated AMPK activity

Siggs OM. et al, (2016), Proceedings of the National Academy of Sciences, 113, E3706 - E3715

Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing

Simon MM. et al, (2015), Mammalian Genome, 26, 486 - 500

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Taylor JC. et al, (2015), Nature Genetics, 47, 717 - 726

Next‐generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome

Bull KR. et al, (2014), The Journal of Pathology, 233, 18 - 26

Load More

Include forthcoming?