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Kidney International|February 17, 2016
Eculizumab in children with hemolytic uremic syndromeDavid Kavanagh, Kate Smith-JacksonImmunological Reviews|November 15, 2022
Alternative pathway activation in pregnancy, a measured amount "complements" a successful pregnancy, too much results in adverse eventsKate Smith-Jackson, Richard Alexander HarrisonJournal of the American Society of Nephrology : JASN|March 29, 2018
An Engineered Complement Factor H Construct for Treatment of C3 GlomerulopathyYi Yang, Harriet Denton, Owen R Davies, et al.Pregnancy Hypertension|June 25, 2015
PP011. Placental expression of the major protein components of caveolae, eNOS and iNOS in pre-eclampsiaMarta Hentschke, Kate Smith-Jackson, Carlos E Poli-de-Figueiredo, et al.Immunobiology|June 9, 2016
Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndromePatrick J Gleeson, Valerie Wilson, Thomas E Cox, et al.Frontiers in Immunology|May 14, 2026
Properdin deficiency or anti-properdin treatment ameliorates disease in the C3 gain-of-function mouse model of atypical haemolytic uraemic syndromeGrace Mallett, Ola Kamala, Isabel Y Pappworth, et al.Transplantation|November 22, 2022
Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic SyndromeEmily K Glover, Kate Smith-Jackson, Vicky Brocklebank, et al.Kidney International|January 23, 2025
The membrane attack complex drives thrombotic microangiopathy in complement mediated atypical hemolytic uremic syndromeKate Smith-Jackson, Patrick Walsh, Wioleta M Zelek, et al.Haematologica|September 29, 2022
Plasminogen activator-coated nanobubbles targeting cellbound β2-glycoprotein I as a novel thrombus-specific thrombolytic strategyPaolo Macor, Paolo Durigutto, Monica Argenziano, et al.The Journal of Clinical Investigation|February 5, 2019
Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in miceKate Smith-Jackson, Yi Yang, Harriet Denton, et al.Pageof 2