Sickle Cell Trait Increases Red Blood Cell Storage Hemolysis and Post-Transfusion Clearance in Mice

Author:

Osei-Hwedieh David O.,Kanias Tamir,Croix Claudette St.,Jessup Morgan,Xiong Zeyu,Sinchar Derek,Franks Jonathan,Xu Qinzi,M. Novelli Enrico,Sertorio Jonas T.,Potoka Karin,Binder Robert J.,Basu Swati,Belanger Andrea M.,Kim-Shapiro Daniel B.,Triulzi Darrell,Lee Janet S.,Gladwin Mark T.

Funder

NIH

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference36 articles.

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3. Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes;Brittenham;Blood,1985

4. Sickle cell disease; studied by measuring the survival of transfused red blood cells;Callender;J. Lab. Clin. Med.,1949

5. Exposure of phosphatidylserine in the outer leaflet of human red blood cells. Relationship to cell density, cell age, and clearance by mononuclear cells;Connor;J. Biol. Chem.,1994

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