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Phosphatidylserine in the outer leaflet of red blood cells from β‐thalassemia patients may explain the chronic hypercoagulable state and thrombotic episodes
Author(s) -
Yashar Vered BorenstainBen,
Barenholz Yechezkel,
HyAm Esther,
Rachmilewitz Eliezer A.,
Eldor Amiram
Publication year - 1993
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.2830440114
Subject(s) - phosphatidylserine , prothrombinase , phagocytosis , thalassemia , medicine , platelet , coagulopathy , red blood cell , cardiology , immunology , thrombin , biology , membrane , genetics , phospholipid
Investigation of red blood cells from β‐thalassemia patients by means of prothrombinase assay reveals phosphatidylserine in the outer leaflet of the plasma membrane. This might explain their elevated susceptibility to phagocytosis by macrophages and the chronic hypercoagulable state, frequent thrombotic events, and life‐long platelet activation that are found in thalassemic patients. © 1993 Wiley‐Liss, Inc.
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