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Specificity for human hemoglobin enhances Staphylococcus aureus infection

Cell host & microbe, 2010-12, Vol.8 (6), p.544-550

2010

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Transferrin therapy ameliorates disease in β-thalassemic mice

Nature medicine, 2010-02, Vol.16 (2), p.177-182

2010

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Arginine therapy of transgenic-knockout sickle mice improves microvascular function by reducing non-nitric oxide vasodilators, hemolysis, and oxidative stress

American journal of physiology. Heart and circulatory physiology, 2008-07, Vol.295 (1), p.H39-H47

2008

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Heme degradation and oxidative stress in murine models for hemoglobinopathies: Thalassemia, sickle cell disease and hemoglobin C disease

Blood cells, molecules, & diseases, 2008-07, Vol.41 (1), p.60-66

2008

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Antisickling property of fetal hemoglobin enhances nitric oxide bioavailability and ameliorates organ oxidative stress in transgenic-knockout sickle mice

American journal of physiology. Regulatory, integrative and comparative physiology, 2010-02, Vol.298 (2), p.R394-R402

2010

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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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Antisickling fetal hemoglobin reduces hypoxia-inducible factor-1α expression in normoxic sickle mice: microvascular implications

American journal of physiology. Heart and circulatory physiology, 2013-01, Vol.304 (1), p.H42-H50

2013

Volltextzugriff (PDF)

The scientific legacy of Ronald L. Nagel (1936–2016), a true renaissance man

American journal of hematology, 2016-09, Vol.91 (9), p.865-866

2016

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Permanent and Panerythroid Correction of Murine β Thalassemia by Multiple Lentiviral Integration in Hematopoietic Stem Cells

Proceedings of the National Academy of Sciences - PNAS, 2002-10, Vol.99 (22), p.14380-14385

2002

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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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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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In Vivo Studies of Sickle Red Blood Cells

Microcirculation (New York, N.Y. 1994), 2004-03, Vol.11 (2), p.153-165

2004

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Exogenous iron increases hemoglobin in β–thalassemic mice

Experimental hematology, 2009-02, Vol.37 (2), p.172-183

2009

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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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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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Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B

American journal of hematology, 2007-03, Vol.82 (3), p.179-184

2007

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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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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

Volltextzugriff (PDF)

Preselection of Retrovirally Transduced Bone Marrow Avoids Subsequent Stem Cell Gene Silencing and Age-Dependent Extinction of Expression of Human β -Globin in Engrafted Mice

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (10), p.5411-5415

2000

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Second generation knockout sickle mice: the effect of HbF

Blood, 2001-01, Vol.97 (2), p.410-418

2001

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Hemoglobinopathies

Hematology, 2003, Vol.2003 (1), p.14-39

2003

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Expression of an anti-sickling β-globin in human erythroblasts derived from retrovirally transduced primitive normal and sickle cell disease hematopoietic cells

Experimental hematology, 2004-05, Vol.32 (5), p.461-469

2004

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Murine glutathione S‐transferase A1‐1 in sickle transgenic mice

American journal of hematology, 2007-10, Vol.82 (10), p.911-915

2007

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Arterial access for sickle stroke predictors

Blood, 2008-04, Vol.111 (7), p.3310-3311

Fabry, Mary E.

2008

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Anemia, Sickle Cell - Blood
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Specificity for human hemoglobin enhances Staphylococcus aureus infection

Transferrin therapy ameliorates disease in β-thalassemic mice

Arginine therapy of transgenic-knockout sickle mice improves microvascular function by reducing non-nitric oxide vasodilators, hemolysis, and oxidative stress

Heme degradation and oxidative stress in murine models for hemoglobinopathies: Thalassemia, sickle cell disease and hemoglobin C disease

Antisickling property of fetal hemoglobin enhances nitric oxide bioavailability and ameliorates organ oxidative stress in transgenic-knockout sickle mice

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

Antisickling fetal hemoglobin reduces hypoxia-inducible factor-1α expression in normoxic sickle mice: microvascular implications

The scientific legacy of Ronald L. Nagel (1936–2016), a true renaissance man

Permanent and Panerythroid Correction of Murine β Thalassemia by Multiple Lentiviral Integration in Hematopoietic Stem Cells

The paradox of hemoglobin SC disease

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

In Vivo Studies of Sickle Red Blood Cells

Exogenous iron increases hemoglobin in β–thalassemic mice

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

Impaired nitric oxide-mediated vasodilation in transgenic sickle mouse

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

Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B

The panoply of animal models for sickle cell anaemia

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

Preselection of Retrovirally Transduced Bone Marrow Avoids Subsequent Stem Cell Gene Silencing and Age-Dependent Extinction of Expression of Human β -Globin in Engrafted Mice

Second generation knockout sickle mice: the effect of HbF

Hemoglobinopathies

Expression of an anti-sickling β-globin in human erythroblasts derived from retrovirally transduced primitive normal and sickle cell disease hematopoietic cells

Murine glutathione S‐transferase A1‐1 in sickle transgenic mice

Arterial access for sickle stroke predictors

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