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Expert Opinion on Therapeutic Targets|February 21, 2023
Emerging drug targets for sickle cell disease: shedding light on new knowledge and advances at the molecular levelJohn S Gibson, David C ReesBritish Journal of Haematology|November 30, 2011
Biomarkers in sickle cell diseaseDavid C Rees, John S GibsonBritish Journal of Haematology|September 7, 2023
The cation-leaky hereditary stomatocytosis syndromes: A tale of six proteinsGordon W Stewart, John S Gibson, David C ReesThe Journal of Physiology|July 13, 2014
Effects of 5-hydroxymethyl-2-furfural on the volume and membrane permeability of red blood cells from patients with sickle cell diseaseAnke Hannemann, Urszula M Cytlak, David C Rees, et al.Cell Calcium|December 27, 2011
Deoxygenation-induced and Ca(2+) dependent phosphatidylserine externalisation in red blood cells from normal individuals and sickle cell patientsErwin Weiss, Urszula M Cytlak, David C Rees, et al.British Journal of Haematology|June 26, 2018
Oxidative stress and phosphatidylserine exposure in red cells from patients with sickle cell anaemiaAnke Hannemann, David C Rees, John N Brewin, et al.Physiological Reports|March 6, 2018
The effect of xanthine oxidase and hypoxanthine on the permeability of red cells from patients with sickle cell anemiaHalima W M Al Balushi, David C Rees, John N Brewin, et al.British Journal of Haematology|January 5, 2026
Across species: A comparative perspective on red cell homeostasis and its influence on our understanding of human physiology and diseaseKathleen M Connolly, Pengyi Ding, Rasiqh Wadud, et al.Hemasphere|November 15, 2019
Early Markers of Sickle Nephropathy in Children With Sickle Cell Anemia Are Associated With Red Cell Cation Transport ActivityJohn Brewin, Sanjay Tewari, Anke Hannemann, et al.Haematologica|March 10, 2015
The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC diseaseDavid C Rees, Swee Lay Thein, Anna Osei, et al.Pageof 16