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Journal Articles

Immunohistochemical localization of hepatic nitric oxide synthase in normal and transgenic sickle cell mice: the effect of hypoxia

SY Osei, RS Ahima, ME Fabry, RL Nagel, N Bank

Blood (1996) 88 (9): 3583–3588.

https://doi.org/10.1182/blood.V88.9.3583.bloodjournal8893583

Published: 1996

Journal Articles

Age dependence of the gene frequency of alpha-thalassemia in sickle cell anemia in Cuba [letter]

G Martinez, A Muniz, E Svarch, E Espinosa, RL Nagel

Blood (1996) 88 (5): 1898–1899.

https://doi.org/10.1182/blood.V88.5.1898.1898

Published: 1996

Journal Articles

Protection from lethal malaria in transgenic mice expressing sickle hemoglobin

AT Hood, ME Fabry, F Costantini, RL Nagel, HL Shear

Blood (1996) 87 (4): 1600–1603.

https://doi.org/10.1182/blood.V87.4.1600.bloodjournal8741600

Published: 1996

Journal Articles

Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia [letter; comment]

HH Billett, RL Nagel, ME Fabry

Blood (1995) 86 (11): 4382.

https://doi.org/10.1182/blood.V86.11.4382a.bloodjournal86114382a

Published: 1995

Journal Articles

Shear stress enhances the proteolysis of von Willebrand factor in normal plasma

HM Tsai, II Sussman, RL Nagel

Blood (1994) 83 (8): 2171–2179.

https://doi.org/10.1182/blood.V83.8.2171.2171

Published: 1994

Journal Articles

Compound heterozygosity for hemoglobin C and Korle-Bu: moderate microcytic hemolytic anemia and acceleration of crystal formation [corrected] [published erratum appears in Blood 1994 May 15;83(10):3105]

RL Nagel, MJ Lin, HE Witkowska, ME Fabry, M Bestak, RE Hirsch

Blood (1993) 82 (6): 1907–1912.

https://doi.org/10.1182/blood.V82.6.1907.1907

Published: 1993

Journal Articles

Sickle erythrocyte-endothelial interactions in microcirculation: the role of von Willebrand factor and implications for vasoocclusion

DK Kaul, RL Nagel, D Chen, HM Tsai

Blood (1993) 81 (9): 2429–2438.

https://doi.org/10.1182/blood.V81.9.2429.2429

Published: 1993

Journal Articles

Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid-->lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore)

AC Rybicki, JJ Qiu, S Musto, NL Rosen, RL Nagel, RS Schwartz

Blood (1993) 81 (8): 2155–2165.

https://doi.org/10.1182/blood.V81.8.2155.2155

Published: 1993

Journal Articles

Transgenic mice expressing human sickle hemoglobin are partially resistant to rodent malaria

HL Shear, EF Jr Roth, ME Fabry, FD Costantini, A Pachnis, A Hood, RL Nagel

Blood (1993) 81 (1): 222–226.

https://doi.org/10.1182/blood.V81.1.222.222

Published: 1993

Journal Articles

F reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: a double-blind study

RL Nagel, E Vichinsky, M Shah, R Johnson, E Spadacino, ME Fabry, L Mangahas, R Abel, G Stamatoyannopoulos

Blood (1993) 81 (1): 9–14.

https://doi.org/10.1182/blood.V81.1.9.9

Published: 1993

Journal Articles

Trial of recombinant human erythropoietin: three patients with thalassemia intermedia [letter]

NF Olivieri, MH Freedman, SP Perrine, GJ Dover, B Sheridan, DL Essentine, RL Nagel

Blood (1992) 80 (12): 3258–3260.

https://doi.org/10.1182/blood.V80.12.3258.3258

Published: 1992

Journal Articles

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)

EE Bouhassira, RS Schwartz, Y Yawata, K Ata, A Kanzaki, JJ Qiu, RL Nagel, AC Rybicki

Blood (1992) 79 (7): 1846–1854.

https://doi.org/10.1182/blood.V79.7.1846.1846

Published: 1992

Journal Articles

Demonstration of endothelial adhesion of sickle cells in vivo: a distinct role for deformable sickle cell discocytes

ME Fabry, E Fine, V Rajanayagam, SM Factor, J Gore, M Sylla, RL Nagel

Blood (1992) 79 (6): 1602–1611.

https://doi.org/10.1182/blood.V79.6.1602.1602

Published: 1992

Journal Articles

The unique red cell heterogeneity of SC disease: crystal formation, dense reticulocytes, and unusual morphology

C Lawrence, ME Fabry, RL Nagel

Blood (1991) 78 (8): 2104–2112.

https://doi.org/10.1182/blood.V78.8.2104.2104

Published: 1991

Journal Articles

Rosetting of Plasmodium falciparum-infected red blood cells with uninfected red blood cells enhances microvascular obstruction under flow conditions

DK Kaul, EF Jr Roth, RL Nagel, RJ Howard, SM Handunnetti

Blood (1991) 78 (3): 812–819.

https://doi.org/10.1182/blood.V78.3.812.812

Published: 1991

Journal Articles

Rapid increase in red blood cell density driven by K:Cl cotransport in a subset of sickle cell anemia reticulocytes and discocytes

ME Fabry, JR Romero, ID Buchanan, SM Suzuka, G Stamatoyannopoulos, RL Nagel, M Canessa

Blood (1991) 78 (1): 217–225.

https://doi.org/10.1182/blood.V78.1.217.217

Published: 1991

Journal Articles

The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients

RL Nagel, S Erlingsson, ME Fabry, H Croizat, SM Susuka, H Lachman, M Sutton, C Driscoll, E Bouhassira, HH Billett

Blood (1991) 77 (6): 1371–1375.

https://doi.org/10.1182/blood.V77.6.1371.1371

Published: 1991

Journal Articles

Heterogeneity in the properties of burst-forming units of erythroid lineage in sickle cell anemia: DNA synthesis and burst-promoting activity production is related to peripheral hemoglobin F levels

H Croizat, HH Billett, RL Nagel

Blood (1990) 75 (4): 1006–1010.

https://doi.org/10.1182/blood.V75.4.1006.1006

Published: 1990

Journal Articles

Desmopressin induces adhesion of normal human erythrocytes to the endothelial surface of a perfused microvascular preparation

HM Tsai, II Sussman, RL Nagel, DK Kaul

Blood (1990) 75 (1): 261–265.

https://doi.org/10.1182/blood.V75.1.261.261

Published: 1990

Journal Articles

Acceleration of hemoglobin C crystallization by hemoglobin S

MJ Lin, RL Nagel, RE Hirsch

Blood (1989) 74 (5): 1823–1825.

https://doi.org/10.1182/blood.V74.5.1823.1823

Published: 1989

NARROW

Immunohistochemical localization of hepatic nitric oxide synthase in normal and transgenic sickle cell mice: the effect of hypoxia

Age dependence of the gene frequency of alpha-thalassemia in sickle cell anemia in Cuba [letter]

Protection from lethal malaria in transgenic mice expressing sickle hemoglobin

Paradoxical increase of painful crises in sickle cell patients with alpha-thalassemia [letter; comment]

Shear stress enhances the proteolysis of von Willebrand factor in normal plasma

Compound heterozygosity for hemoglobin C and Korle-Bu: moderate microcytic hemolytic anemia and acceleration of crystal formation [corrected] [published erratum appears in Blood 1994 May 15;83(10):3105]

Sickle erythrocyte-endothelial interactions in microcirculation: the role of von Willebrand factor and implications for vasoocclusion

Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid-->lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore)

Transgenic mice expressing human sickle hemoglobin are partially resistant to rodent malaria

F reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: a double-blind study

Trial of recombinant human erythropoietin: three patients with thalassemia intermedia [letter]

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)

Demonstration of endothelial adhesion of sickle cells in vivo: a distinct role for deformable sickle cell discocytes

The unique red cell heterogeneity of SC disease: crystal formation, dense reticulocytes, and unusual morphology

Rosetting of Plasmodium falciparum-infected red blood cells with uninfected red blood cells enhances microvascular obstruction under flow conditions

Rapid increase in red blood cell density driven by K:Cl cotransport in a subset of sickle cell anemia reticulocytes and discocytes

The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients

Heterogeneity in the properties of burst-forming units of erythroid lineage in sickle cell anemia: DNA synthesis and burst-promoting activity production is related to peripheral hemoglobin F levels

Desmopressin induces adhesion of normal human erythrocytes to the endothelial surface of a perfused microvascular preparation

Acceleration of hemoglobin C crystallization by hemoglobin S

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