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Experimental Hematology|September 1, 2015
Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scramblingElena B Kostova, Boukje M Beuger, Martijn Veldthuis, et al.Hemoglobin|June 14, 2019
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic AnemiaThomas R L Klei, Sima Kheradmand Kia, Martijn Veldthuis, et al.Blood Advances|December 22, 2020
The Gardos effect drives erythrocyte senescence and leads to Lu/BCAM and CD44 adhesion molecule activationThomas R L Klei, Jill J Dalimot, Boukje M Beuger, et al.Human Genomics|October 17, 2020
Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1BPetros Papadopoulos, Athanassia Kafasi, Iris M De Cuyper, et al.Pageof 3