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Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling.
Kostova EB, Beuger BM, Veldthuis M, van der Werff Ten Bosch J, Kühnle I, van den Akker E, van den Berg TK, van Zwieten R, van Bruggen R. Kostova EB, et al. Among authors: van den akker e, van den berg tk, van zwieten r, van der werff ten bosch j, van bruggen r. Exp Hematol. 2015 Dec;43(12):1072-1076.e2. doi: 10.1016/j.exphem.2015.08.007. Epub 2015 Aug 28. Exp Hematol. 2015. PMID: 26320718 Free article. Clinical Trial.
Hemolysis in the spleen drives erythrocyte turnover.
Klei TRL, Dalimot J, Nota B, Veldthuis M, Mul FPJ, Rademakers T, Hoogenboezem M, Nagelkerke SQ, van IJcken WFJ, Oole E, Svendsen P, Moestrup SK, van Alphen FPJ, Meijer AB, Kuijpers TW, van Zwieten R, van Bruggen R. Klei TRL, et al. Among authors: van zwieten r. Blood. 2020 Oct 1;136(14):1579-1589. doi: 10.1182/blood.2020005351. Blood. 2020. PMID: 32777816 Free article.
Glycophorin-C sialylation regulates Lu/BCAM adhesive capacity during erythrocyte aging.
Klei TRL, de Back DZ, Asif PJ, Verkuijlen PJJH, Veldthuis M, Ligthart PC, Berghuis J, Clifford E, Beuger BM, van den Berg TK, van Zwieten R, El Nemer W, van Bruggen R. Klei TRL, et al. Among authors: van zwieten r. Blood Adv. 2018 Jan 3;2(1):14-24. doi: 10.1182/bloodadvances.2017013094. eCollection 2018 Jan 9. Blood Adv. 2018. PMID: 29344581 Free PMC article.
Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.
Van Zwieten R, François JJ, Van Leeuwen K, Van Wesel AC, Van Bruggen R, Van Solinge WW, Roos D, Verhoeven AJ, Van Wijk R. Van Zwieten R, et al. Among authors: van leeuwen k, van bruggen r, van wesel ac, van wijk r, van solinge ww. Am J Hematol. 2013 Feb;88(2):159-60. doi: 10.1002/ajh.23363. Epub 2012 Dec 17. Am J Hematol. 2013. PMID: 23255290 Free article. No abstract available.
59 results