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Sickle-cell disease

Lancet, 2004-10, Vol.364 (9442), p.1343-1360

2004

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

Blood, 1994-04, Vol.83 (8), p.2171-2179

1994

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

Blood, 1994-04, Vol.83 (8), p.2171-2179

1994

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Correction of Sickle Cell Disease in Transgenic Mouse Models by Gene Therapy

Science (American Association for the Advancement of Science), 2001-12, Vol.294 (5550), p.2368-2371

2001

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Liquid-Liquid Separation in Solutions of Normal and Sickle Cell Hemoglobin

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (13), p.8479-8483

2002

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Malaria and Red Cell Genetic Defects

Blood, 1989-09, Vol.74 (4), p.1213-1221

1989

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Epistasis and the genetics of human diseases

Comptes rendus. Biologies, 2005-07, Vol.328 (7), p.606-615

Nagel, Ronald L.

2005

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The paradox of hemoglobin SC disease

Blood reviews, 2003-09, Vol.17 (3), p.167-178

2003

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High-level beta-globin expression and preferred intragenic integration after lentiviral transduction of human cord blood stem cells

The Journal of clinical investigation, 2004-10, Vol.114 (7), p.953-962

2004

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Effect of fetal hemoglobin on microvascular regulation in sickle transgenic-knockout mice

The Journal of clinical investigation, 2004-10, Vol.114 (8), p.1136-1145

2004

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Sickle cell anemia day hospital: an approach for the management of uncomplicated painful crises

Blood, 2000-02, Vol.95 (4), p.1130-1137

2000

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Plasma lipids in Iranians with sickle cell disease: Hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait

Clinica chimica acta, 2006-03, Vol.365 (1), p.217-220

2006

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Human genetic polymorphisms and asymptomatic Plasmodium falciparum malaria in Gabonese schoolchildren

The American journal of tropical medicine and hygiene, 2003-02, Vol.68 (2), p.186-190

2003

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Arginine supplementation of sickle transgenic mice reduces red cell density and Gardos channel activity

Blood, 2002-02, Vol.99 (4), p.1103-1108

2002

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Impaired nitric oxide-mediated vasodilation in transgenic sickle mouse

American journal of physiology. Heart and circulatory physiology, 2000-06, Vol.278 (6), p.H1799-H1806

2000

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Liganded Hemoglobin Structural Perturbations by the Allosteric Effector L35

Biophysical journal, 2005-03, Vol.88 (3), p.2057-2067

2005

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Decreased cerebral perfusion correlates with increased BOLD hyperoxia response in transgenic mouse models of sickle cell disease

Magnetic resonance in medicine, 2004-03, Vol.51 (3), p.525-532

2004

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Intermolecular Interactions, Nucleation, and Thermodynamics of Crystallization of Hemoglobin C

Biophysical journal, 2002-08, Vol.83 (2), p.1147-1156

2002

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The panoply of animal models for sickle cell anaemia

British journal of haematology, 2001-01, Vol.112 (1), p.19-25

2001

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Accuracy of pulse oximetry in sickle cell disease

American journal of respiratory and critical care medicine, 1999-02, Vol.159 (2), p.447-451

1999

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Moyamoya and stroke in sickle cell anemia: bad news and good news

Blood, 2002-05, Vol.99 (9), p.3081-3081

Nagel, Ronald L.

2002

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Crystallization Mechanisms of Hemoglobin C in the R State

Biophysical journal, 2004-10, Vol.87 (4), p.2621-2629

2004

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Expression of HbC and HbS, but not HbA, results in activation of K-Cl cotransport activity in transgenic mouse red cells

Blood, 2004-03, Vol.103 (6), p.2384-2390

2004

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Beta-globin-gene haplotypes, mitochondrial DNA, the Y-chromosome: their impact on the genetic epidemiology of the major structural hemoglobinopathies

Cellular and molecular biology (Noisy-le-Grand, France), 2004-02, Vol.50 (1), p.5

Nagel, R L

2004

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Circulating cytokines response and the level of erythropoiesis in sickle cell anemia

American journal of hematology, 1999-02, Vol.60 (2), p.105-115

1999

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Sickle-cell disease

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

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

Correction of Sickle Cell Disease in Transgenic Mouse Models by Gene Therapy

Liquid-Liquid Separation in Solutions of Normal and Sickle Cell Hemoglobin

Malaria and Red Cell Genetic Defects

Epistasis and the genetics of human diseases

The paradox of hemoglobin SC disease

High-level beta-globin expression and preferred intragenic integration after lentiviral transduction of human cord blood stem cells

Effect of fetal hemoglobin on microvascular regulation in sickle transgenic-knockout mice

Sickle cell anemia day hospital: an approach for the management of uncomplicated painful crises

Plasma lipids in Iranians with sickle cell disease: Hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait

Human genetic polymorphisms and asymptomatic Plasmodium falciparum malaria in Gabonese schoolchildren

Arginine supplementation of sickle transgenic mice reduces red cell density and Gardos channel activity

Impaired nitric oxide-mediated vasodilation in transgenic sickle mouse

Liganded Hemoglobin Structural Perturbations by the Allosteric Effector L35

Decreased cerebral perfusion correlates with increased BOLD hyperoxia response in transgenic mouse models of sickle cell disease

Intermolecular Interactions, Nucleation, and Thermodynamics of Crystallization of Hemoglobin C

The panoply of animal models for sickle cell anaemia

Accuracy of pulse oximetry in sickle cell disease

Moyamoya and stroke in sickle cell anemia: bad news and good news

Crystallization Mechanisms of Hemoglobin C in the R State

Expression of HbC and HbS, but not HbA, results in activation of K-Cl cotransport activity in transgenic mouse red cells

Beta-globin-gene haplotypes, mitochondrial DNA, the Y-chromosome: their impact on the genetic epidemiology of the major structural hemoglobinopathies

Circulating cytokines response and the level of erythropoiesis in sickle cell anemia

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