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Jane A Little

Showing results (51-60 of 64) with videos related to

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Blood Advances|January 18, 2023
Membrane bending and sphingomyelinase-associated, sulfatide-dependent hypoxic adhesion of sickle mature erythrocytesUtku Goreke, Erdem Kucukal, Fang Wang, et al.
Lab on a Chip|September 29, 2021
Point-of-care microchip electrophoresis for integrated anemia and hemoglobin variant testingRan An, Yuncheng Man, Shamreen Iram, et al.
British Journal of Haematology|July 13, 2022
Antithrombin-III mitigates thrombin-mediated endothelial cell contraction and sickle red blood cell adhesion in microscale flowWilliam J Wulftange, Erdem Kucukal, Yuncheng Man, et al.
British Journal of Haematology|January 6, 2023
Sickle red blood cell-derived extracellular vesicles activate endothelial cells and enhance sickle red cell adhesion mediated by von Willebrand factorRan An, Yuncheng Man, Kevin Cheng, et al.
British Journal of Haematology|December 17, 2013
Haemoglobinuria is associated with chronic kidney disease and its progression in patients with sickle cell anaemiaSantosh L Saraf, Xu Zhang, Tamir Kanias, et al.
British Journal of Haematology|August 23, 2021
Gaps in the diagnosis and management of iron overload in sickle cell disease: a 'real-world' report from the GRNDaD registrySamuel R Wilson, Matthew Sears, Elizabeth Williams, et al.
Blood. Red Cells & Iron|November 28, 2025
Red cell physiologic stress results in lower quality transfusions: a randomized trial in adults with sickle cell diseaseMatthew S Karafin, Ross M Fasano, Anton Ilich, et al.
The Journal of Clinical Investigation|July 3, 2025
Blood-storage duration affects hematological and metabolic profiles in patients with sickle cell disease receiving transfusionsMatthew S Karafin, Abby L Grier, Ross M Fasano, et al.
Circulation|September 9, 2011
Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United KingdomVandana Sachdev, Gregory J Kato, J Simon R Gibbs, et al.
Plos One|July 3, 2014
Risk factors for death in 632 patients with sickle cell disease in the United States and United KingdomMark T Gladwin, Robyn J Barst, J Simon R Gibbs, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Blood Advances|January 18, 2023
Membrane bending and sphingomyelinase-associated, sulfatide-dependent hypoxic adhesion of sickle mature erythrocytesUtku Goreke, Erdem Kucukal, Fang Wang, et al.
Lab on a Chip|September 29, 2021
Point-of-care microchip electrophoresis for integrated anemia and hemoglobin variant testingRan An, Yuncheng Man, Shamreen Iram, et al.
British Journal of Haematology|July 13, 2022
Antithrombin-III mitigates thrombin-mediated endothelial cell contraction and sickle red blood cell adhesion in microscale flowWilliam J Wulftange, Erdem Kucukal, Yuncheng Man, et al.
British Journal of Haematology|January 6, 2023
Sickle red blood cell-derived extracellular vesicles activate endothelial cells and enhance sickle red cell adhesion mediated by von Willebrand factorRan An, Yuncheng Man, Kevin Cheng, et al.
British Journal of Haematology|December 17, 2013
Haemoglobinuria is associated with chronic kidney disease and its progression in patients with sickle cell anaemiaSantosh L Saraf, Xu Zhang, Tamir Kanias, et al.
British Journal of Haematology|August 23, 2021
Gaps in the diagnosis and management of iron overload in sickle cell disease: a 'real-world' report from the GRNDaD registrySamuel R Wilson, Matthew Sears, Elizabeth Williams, et al.
Blood. Red Cells & Iron|November 28, 2025
Red cell physiologic stress results in lower quality transfusions: a randomized trial in adults with sickle cell diseaseMatthew S Karafin, Ross M Fasano, Anton Ilich, et al.
The Journal of Clinical Investigation|July 3, 2025
Blood-storage duration affects hematological and metabolic profiles in patients with sickle cell disease receiving transfusionsMatthew S Karafin, Abby L Grier, Ross M Fasano, et al.
Circulation|September 9, 2011
Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United KingdomVandana Sachdev, Gregory J Kato, J Simon R Gibbs, et al.
Plos One|July 3, 2014
Risk factors for death in 632 patients with sickle cell disease in the United States and United KingdomMark T Gladwin, Robyn J Barst, J Simon R Gibbs, et al.
Pageof 7