Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL037462-04
Application #
3098581
Study Section
Heart, Lung, and Blood Research Review Committee B (HLBB)
Project Start
1987-02-01
Project End
1992-01-31
Budget Start
1990-02-01
Budget End
1991-01-31
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
St. Elizabeth's Medical Center of Boston
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02135
Voigt, S; Hanspal, M; LeRoy, P J et al. (2000) The cytoadherence ligand Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) binds to the P. falciparum knob-associated histidine-rich protein (KAHRP) by electrostatic interactions. Mol Biochem Parasitol 110:423-8
Oh, S S; Voigt, S; Fisher, D et al. (2000) Plasmodium falciparum erythrocyte membrane protein 1 is anchored to the actin-spectrin junction and knob-associated histidine-rich protein in the erythrocyte skeleton. Mol Biochem Parasitol 108:237-47
Hanspal, M; Golan, D E; Smockova, Y et al. (1998) Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable species. Blood 92:329-38
Yi, S J; Liu, S C; Derick, L H et al. (1997) Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletons. Biochemistry 36:9596-604
Jarolim, P; Murray, J L; Rubin, H L et al. (1997) Blood group antigens Rb(a), Tr(a), and Wd(a) are located in the third ectoplasmic loop of erythroid band 3. Transfusion 37:607-15
Marfatia, S M; Morais-Cabral, J H; Kim, A C et al. (1997) The PDZ domain of human erythrocyte p55 mediates its binding to the cytoplasmic carboxyl terminus of glycophorin C. Analysis of the binding interface by in vitro mutagenesis. J Biol Chem 272:24191-7
Jarolim, P; Murray, J L; Rubin, H L et al. (1997) A Thr552 -->Ile substitution in erythroid band 3 gives rise to the Warrior blood group antigen. Transfusion 37:398-405
Hassoun, H; Vassiliadis, J N; Murray, J et al. (1997) Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency. Blood 90:398-406
Gwynn, B; Korsgren, C; Cohen, C M et al. (1997) The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics 42:532-5
Hassoun, H; Palek, J (1996) Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease. Blood Rev 10:129-47

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