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Journal Articles

Extremely high avidity association of Fe(III) with the sickle red cell membrane

O Shalev, RP Hebbel

Blood (1996) 88 (1): 349–352.

https://doi.org/10.1182/blood.V88.1.349.349

Published: 1996

Journal Articles

Catalysis of soluble hemoglobin oxidation by free iron on sickle red cell membranes

O Shalev, RP Hebbel

Blood (1996) 87 (9): 3948–3952.

https://doi.org/10.1182/blood.V87.9.3948.bloodjournal8793948

Published: 1996

Journal Articles

Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo

O Shalev, T Repka, A Goldfarb, L Grinberg, A Abrahamov, NF Olivieri, EA Rachmilewitz, RP Hebbel

Blood (1995) 86 (5): 2008–2013.

https://doi.org/10.1182/blood.V86.5.2008.bloodjournal8652008

Published: 1995

Journal Articles

Deformation of swollen erythrocytes provides a model of sickling- induced leak pathways, including a novel bromide-sensitive component

T Sugihara, Y Yawata, RP Hebbel

Blood (1994) 83 (9): 2684–2691.

https://doi.org/10.1182/blood.V83.9.2684.2684

Published: 1994

Journal Articles

Internucleosomal cleavage of DNA is insufficient evidence to conclude that cell death is apoptotic [letter; comment]

H Enright, KA Nath, RP Hebbel

Blood (1994) 83 (7): 2005–2007.

https://doi.org/10.1182/blood.V83.7.2005b.2005b

Published: 1994

Journal Articles

Denaturing interaction between sickle hemoglobin and phosphatidylserine liposomes

E Marva, RP Hebbel

Blood (1994) 83 (1): 242–249.

https://doi.org/10.1182/blood.V83.1.242.242

Published: 1994

Journal Articles

Nonrandom association of free iron with membranes of sickle and beta- thalassemic erythrocytes

T Repka, O Shalev, R Reddy, J Yuan, A Abrahamov, EA Rachmilewitz, PS Low, RP Hebbel

Blood (1993) 82 (10): 3204–3210.

https://doi.org/10.1182/blood.V82.10.3204.3204

Published: 1993

Journal Articles

Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells

K Sugihara, T Sugihara, N Mohandas, RP Hebbel

Blood (1992) 80 (10): 2634–2642.

https://doi.org/10.1182/blood.V80.10.2634.2634

Published: 1992

Journal Articles

Exaggerated cation leak from oxygenated sickle red blood cells during deformation: evidence for a unique leak pathway

T Sugihara, RP Hebbel

Blood (1992) 80 (9): 2374–2378.

https://doi.org/10.1182/blood.V80.9.2374.2374

Published: 1992

Journal Articles

Hydroxyl radical formation by sickle erythrocyte membranes: role of pathologic iron deposits and cytoplasmic reducing agents

T Repka, RP Hebbel

Blood (1991) 78 (10): 2753–2758.

https://doi.org/10.1182/blood.V78.10.2753.2753

Published: 1991

Journal Articles

Lipid hydroperoxides permit deformation-dependent leak of monovalent cation from erythrocytes

T Sugihara, W Rawicz, EA Evans, RP Hebbel

Blood (1991) 77 (12): 2757–2763.

https://doi.org/10.1182/blood.V77.12.2757.2757

Published: 1991

Journal Articles

Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology

RP Hebbel

Blood (1991) 77 (2): 214–237.

https://doi.org/10.1182/blood.V77.2.214.214

Published: 1991

Journal Articles

Oxidation-induced changes in microrheologic properties of the red blood cell membrane

RP Hebbel, A Leung, N Mohandas

Blood (1990) 76 (5): 1015–1020.

https://doi.org/10.1182/blood.V76.5.1015.1015

Published: 1990

Journal Articles

Synergistic effects of oxidation and deformation on erythrocyte monovalent cation leak

PA Ney, MM Christopher, RP Hebbel

Blood (1990) 75 (5): 1192–1198.

https://doi.org/10.1182/blood.V75.5.1192.1192

Published: 1990

Journal Articles

Nonheme iron in sickle erythrocyte membranes: association with phospholipids and potential role in lipid peroxidation

SA Kuross, RP Hebbel

Blood (1988) 72 (4): 1278–1285.

https://doi.org/10.1182/blood.V72.4.1278.1278

Published: 1988

Journal Articles

Vesiculation of sickle erythrocytes during thermal stress

BH Rank, NL Moyer, RP Hebbel

Blood (1988) 72 (3): 1060–1063.

https://doi.org/10.1182/blood.V72.3.1060.1060

Published: 1988

Journal Articles

Excess heme in sickle erythrocyte inside-out membranes: possible role in thiol oxidation

SA Kuross, BH Rank, RP Hebbel

Blood (1988) 71 (4): 876–882.

https://doi.org/10.1182/blood.V71.4.876.876

Published: 1988

Journal Articles

Pluronic F-68 reduces the endothelial adherence and improves the rheology of liganded sickle erythrocytes

CM 2d Smith, RP Hebbel, DP Tukey, CC Clawson, JG White, GM Vercellotti

Blood (1987) 69 (6): 1631–1636.

https://doi.org/10.1182/blood.V69.6.1631.1631

Published: 1987

Journal Articles

Phagocytosis of sickle erythrocytes: immunologic and oxidative determinants of hemolytic anemia

RP Hebbel, WJ Miller

Blood (1984) 64 (3): 733–741.

https://doi.org/10.1182/blood.V64.3.733.733

Published: 1984

Journal Articles

Abnormal erythrocyte calcium homeostasis in oxidant-induced hemolytic disease

O Shalev, MN Leida, RP Hebbel, HS Jacob, JW Eaton

Blood (1981) 58 (6): 1232–1235.

https://doi.org/10.1182/blood.V58.6.1232.1232

Published: 1981

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Extremely high avidity association of Fe(III) with the sickle red cell membrane

Catalysis of soluble hemoglobin oxidation by free iron on sickle red cell membranes

Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo

Deformation of swollen erythrocytes provides a model of sickling- induced leak pathways, including a novel bromide-sensitive component

Internucleosomal cleavage of DNA is insufficient evidence to conclude that cell death is apoptotic [letter; comment]

Denaturing interaction between sickle hemoglobin and phosphatidylserine liposomes

Nonrandom association of free iron with membranes of sickle and beta- thalassemic erythrocytes

Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells

Exaggerated cation leak from oxygenated sickle red blood cells during deformation: evidence for a unique leak pathway

Hydroxyl radical formation by sickle erythrocyte membranes: role of pathologic iron deposits and cytoplasmic reducing agents

Lipid hydroperoxides permit deformation-dependent leak of monovalent cation from erythrocytes

Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology

Oxidation-induced changes in microrheologic properties of the red blood cell membrane

Synergistic effects of oxidation and deformation on erythrocyte monovalent cation leak

Nonheme iron in sickle erythrocyte membranes: association with phospholipids and potential role in lipid peroxidation

Vesiculation of sickle erythrocytes during thermal stress

Excess heme in sickle erythrocyte inside-out membranes: possible role in thiol oxidation

Pluronic F-68 reduces the endothelial adherence and improves the rheology of liganded sickle erythrocytes

Phagocytosis of sickle erythrocytes: immunologic and oxidative determinants of hemolytic anemia

Abnormal erythrocyte calcium homeostasis in oxidant-induced hemolytic disease

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American Society of Hematology

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