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Chronic pain in adults with sickle cell disease is associated with alterations in functional connectivity of the brain

PloS one, 2019-05, Vol.14 (5), p.e0216994-e0216994

2019

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Contrast-enhanced ultrasound detects changes in microvascular blood flow in adults with sickle cell disease

PloS one, 2019-07, Vol.14 (7), p.e0218783-e0218783

2019

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A novel hemoglobin-binding peptide reduces cell-free hemoglobin in murine hemolytic anemia

American journal of physiology. Heart and circulatory physiology, 2013-01, Vol.304 (2), p.H328-H336

2013

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Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease

Blood, 2011-09, Vol.118 (12), p.3376-3383

2011

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Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use

British journal of haematology, 2016-10, Vol.175 (2), p.237-245

2016

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Characterization of a mouse model of sickle cell trait: parallels to human trait and a novel finding of cutaneous sensitization

British journal of haematology, 2017-11, Vol.179 (4), p.657-666

2017

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Sickle cell disease increases high mobility group box 1: a novel mechanism of inflammation

Blood, 2014-12, Vol.124 (26), p.3978-3981

2014

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The spectrin-based membrane skeleton stabilizes mouse megakaryocyte membrane systems and is essential for proplatelet and platelet formation

Blood, 2011-08, Vol.118 (6), p.1641-1652

2011

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Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice

Blood, 2008-11, Vol.112 (9), p.3900-3906

2008

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Dietary supplementation with docosahexanoic acid (DHA) increases red blood cell membrane flexibility in mice with sickle cell disease

Blood cells, molecules, & diseases, 2015-02, Vol.54 (2), p.183-188

2015

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Circulating fibrocytes as biomarkers of impaired lung function in adults with sickle cell disease

Blood advances, 2017-11, Vol.1 (24), p.2217-2224

2017

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Ca2+‐CaM activation of AMP deaminase contributes to adenine nucleotide dysregulation and phosphatidylserine externalization in human sickle erythrocytes

British journal of haematology, 2009-02, Vol.144 (3), p.434-445

2009

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Vascular dysfunction in a murine model of severe hemolysis

Blood, 2008-07, Vol.112 (2), p.398-405

2008

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Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

Blood, 2001-01, Vol.97 (2), p.543-550

2001

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Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosis

Blood, 2004-01, Vol.103 (2), p.710-716

2004

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Erythrocyte adhesion is modified by alterations in cellular tonicity and volume

British journal of haematology, 2005-11, Vol.131 (3), p.366-377

2005

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Mutations in the murine erythroid α-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton

Blood, 2003-01, Vol.101 (1), p.325-330

2003

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Thrombosis and secondary hemochromatosis play major roles in the pathogenesis of jaundiced and spherocytic mice, murine models for hereditary spherocytosis

Blood, 1997-12, Vol.90 (11), p.4610-4619

1997

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Thrombosis in heritable hemolytic disorders

Current opinion in hematology, 1999-03, Vol.6 (2), p.71-71

1999

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Evidence for Transient Acute Liver Injury in Mouse Models of Sickle Cell Disease during Steady State Health

Blood, 2014-12, Vol.124 (21), p.1373-1373

2014

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Reduced incidence of thrombosis in mice with hereditary spherocytosis following neonatal treatment with normal hematopoietic cells

Blood, 2001-06, Vol.97 (12), p.3972-3975

2001

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Neutrophil Activation In Sickle Cell Disease: Biochemical and Functional Changes At Baseline and During Acute Vaso-Occlusive Crises

Blood, 2013-11, Vol.122 (21), p.992-992

2013

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Children with Sickle Cell Disease on Chronic Red Cell Transfusion Experience Fewer Hospitalizations for Acute Vaso-Occlusive Episodes Irrespective of the Indication for Transfusion

Blood, 2014-12, Vol.124 (21), p.4282-4282

2014

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PSS140 - Neutrophil Activation in Sickle Cell Disease: Biochemical and Functional Changes at Baseline and during Acute Vaso-Occlusive Crises

Free radical biology & medicine, 2013-11, Vol.65, p.S71-S71

2013

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Neutrophil Activation in Sickle Cell Disease: Biochemical and Functional Changes at Baseline and during Acute Vaso-Occlusive Crises

Free radical biology & medicine, 2013-11, Vol.65, p.S71

2013

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Chronic pain in adults with sickle cell disease is associated with alterations in functional connectivity of the brain

Contrast-enhanced ultrasound detects changes in microvascular blood flow in adults with sickle cell disease

A novel hemoglobin-binding peptide reduces cell-free hemoglobin in murine hemolytic anemia

Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease

Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use

Characterization of a mouse model of sickle cell trait: parallels to human trait and a novel finding of cutaneous sensitization

Sickle cell disease increases high mobility group box 1: a novel mechanism of inflammation

The spectrin-based membrane skeleton stabilizes mouse megakaryocyte membrane systems and is essential for proplatelet and platelet formation

Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice

Dietary supplementation with docosahexanoic acid (DHA) increases red blood cell membrane flexibility in mice with sickle cell disease

Circulating fibrocytes as biomarkers of impaired lung function in adults with sickle cell disease

Ca2+‐CaM activation of AMP deaminase contributes to adenine nucleotide dysregulation and phosphatidylserine externalization in human sickle erythrocytes

Vascular dysfunction in a murine model of severe hemolysis

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosis

Erythrocyte adhesion is modified by alterations in cellular tonicity and volume

Mutations in the murine erythroid α-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton

Thrombosis and secondary hemochromatosis play major roles in the pathogenesis of jaundiced and spherocytic mice, murine models for hereditary spherocytosis

Thrombosis in heritable hemolytic disorders

Evidence for Transient Acute Liver Injury in Mouse Models of Sickle Cell Disease during Steady State Health

Reduced incidence of thrombosis in mice with hereditary spherocytosis following neonatal treatment with normal hematopoietic cells

Neutrophil Activation In Sickle Cell Disease: Biochemical and Functional Changes At Baseline and During Acute Vaso-Occlusive Crises

Children with Sickle Cell Disease on Chronic Red Cell Transfusion Experience Fewer Hospitalizations for Acute Vaso-Occlusive Episodes Irrespective of the Indication for Transfusion

PSS140 - Neutrophil Activation in Sickle Cell Disease: Biochemical and Functional Changes at Baseline and during Acute Vaso-Occlusive Crises

Neutrophil Activation in Sickle Cell Disease: Biochemical and Functional Changes at Baseline and during Acute Vaso-Occlusive Crises

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