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Journal Articles

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

Hao Xu, Nancy J. Wandersee, YiHe Guo, Deron W. Jones, Sandra L. Holzhauer, Madelyn S. Hanson, Evans Machogu, David C. Brousseau, Neil Hogg, John C. Densmore, Sushma Kaul, Cheryl A. Hillery, Kirkwood A. Pritchard, Jr

Blood (2014) 124 (26): 3978–3981.

https://doi.org/10.1182/blood-2014-04-560813

Published: 2014

Includes: Supplemental data

Journal Articles

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

Carmen C Wallace, MD, Hilda Mata, Nancy J Wandersee, PhD, J. Paul Scott, MD, Amanda M Brandow, DO, MS, Joshua J. Field, MD MS, Matthew Karafin, MD, Cheryl A. Hillery, MD

Blood (2014) 124 (21): 4282.

https://doi.org/10.1182/blood.V124.21.4282.4282

Published: 2014

Journal Articles

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

Nancy J. Wandersee, PhD, Sandra L. Holzhauer, Dawn M. Retherford, Thomas D. Foster, Cheryl A. Hillery, MD

Blood (2014) 124 (21): 1373.

https://doi.org/10.1182/blood.V124.21.1373.1373

Published: 2014

Journal Articles

HMGB1 Release and TLR4-Mediated Inflammation In Sickle Cell Disease At Baseline and During Acute Vaso-Occlusive Crisis

Hao Xu, PhD, Nancy J. Wandersee, PhD, YiHe H. Guo, PhD, Deron W. Jones, Sandra L. Holzhauer, Madelyn S. Hanson, PhD, Neil Hogg, PhD, John C. Densmore, MD, Sushma Kaul, MS, Cheryl A. Hillery, MD, Kirkwood A. Pritchard, Jr., PhD

Blood (2013) 122 (21): 181.

https://doi.org/10.1182/blood.V122.21.181.181

Published: 2013

Journal Articles

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

Madelyn S. Hanson, PhD, Nancy J. Wandersee, PhD, Martin Hessner, PhD, Kirkwood A. Pritchard, Jr., PhD, Neil Hogg, PhD, Cheryl A. Hillery, MD

Blood (2013) 122 (21): 992.

https://doi.org/10.1182/blood.V122.21.992.992

Published: 2013

Journal Articles

Dietary Supplementation with Docosahexanoic Acid (DHA) Improves RBC Flexibility and Reduces Cold Hypersensitivity in Mice with Sickle Cell Disease.

Nancy J. Wandersee, PhD, Madelyn S. Hanson, PhD, Jamie L. Maciaszek, Michael C. Larson, Katie M. Giger, PhD, Suilan Zheng, Dawn M. Retherford, Barbara Mickelson, PhD, Cheryl L. Stucky, PhD, Philip S. Low, PhD, George Lykotrafitis, PhD, Neil Hogg, PhD, Cheryl A. Hillery, MD

Blood (2012) 120 (21): 2116.

https://doi.org/10.1182/blood.V120.21.2116.2116

Published: 2012

Journal Articles

A Novel Hemoglobin Binding Peptide Increases Intracellular Heme and Potentiates Hemoglobin-Induced HO-1 Levels in Endothelial Cells

Madelyn S. Hanson, PhD, Timothy C. Flewelen, Hao Xu, PhD, Kirkwood A Pritchard, Jr., PhD, Nancy J Wandersee, PhD, Neil Hogg, PhD, Cheryl A. Hillery, MD

Blood (2011) 118 (21): 1065.

https://doi.org/10.1182/blood.V118.21.1065.1065

Published: 2011

Journal Articles

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

Cheryl A. Hillery, Patrick C. Kerstein, Daniel Vilceanu, Marie E. Barabas, Dawn Retherford, Amanda M. Brandow, Nancy J. Wandersee, Cheryl L. Stucky

Blood (2011) 118 (12): 3376–3383.

https://doi.org/10.1182/blood-2010-12-327429

Published: 2011

Includes: Supplemental data

Journal Articles

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

Sunita Patel-Hett, Hongbei Wang, Antonija J. Begonja, Jonathan N. Thon, Eva C. Alden, Nancy J. Wandersee, Xiuli An, Narla Mohandas, John H. Hartwig, Joseph E. Italiano, Jr

Blood (2011) 118 (6): 1641–1652.

https://doi.org/10.1182/blood-2011-01-330688

Published: 2011

Includes: Multimedia, Supplemental data

Journal Articles

A Novel Hemoglobin-Binding Agent Reduces Plasma Free Hemoglobin and Partially Improves Vascular Function In Murine Hemolytic Anemia

Nancy J. Wandersee, PhD, Timothy C. Flewelen, Anne C. Frei, Deron W. Jones, Dawn Retherford, Sandra L. Holzhauer, Soumya Gokuli, Madelyn S. Hanson, PhD, Cheryl A. Hillery, MD, Neil Hogg, PhD, Kirkwood A. Pritchard, Jr., PhD, Hao Xu, Ph.D

Blood (2010) 116 (21): 267.

https://doi.org/10.1182/blood.V116.21.267.267

Published: 2010

Journal Articles

Mechanical Hypersensitivity Occurs in a Mouse Model of Sickle Cell Disease

Nancy J Wandersee, Teresa Uy, Dawn Retherford, Aziz Noon-Abdullah, Anne C Frei, Amanda M Brandow, Cheryl M Stucky, Cheryl A Hillery

Blood (2008) 112 (11): 2473.

https://doi.org/10.1182/blood.V112.11.2473.2473

Published: 2008

Journal Articles

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

M. Estela Campanella, Haiyan Chu, Nancy J. Wandersee, Luanne L. Peters, Narla Mohandas, Diana M. Gilligan, Philip S. Low

Blood (2008) 112 (9): 3900–3906.

https://doi.org/10.1182/blood-2008-03-146159

Published: 2008

Includes: Supplemental data

Journal Articles

Vascular dysfunction in a murine model of severe hemolysis

Anne C. Frei, YiHe Guo, Deron W. Jones, Kirkwood A. Pritchard, Jr, Karen A. Fagan, Neil Hogg, Nancy J. Wandersee

Blood (2008) 112 (2): 398–405.

https://doi.org/10.1182/blood-2007-12-126714

Published: 2008

Journal Articles

Vascular Dysfunction in Murine Models of Hemolytic Anemia.

Nancy J. Wandersee, PhD, Anne C. Frei, Sandra L. Holzhauer, J. Paul Scott, MD, Kirkwood A. Pritchard, PhD, Karen A. Fagan, MD, Neil Hogg, PhD, Cheryl A. Hillery, MD

Blood (2007) 110 (11): 846.

https://doi.org/10.1182/blood.V110.11.846.846

Published: 2007

Journal Articles

Modifications of the Coagulation System Alter Inflammation in Murine Sickle Cell Disease.

Teresa Uy, Nancy J. Wandersee, Cheryl A. Hillery

Blood (2006) 108 (11): 1242.

https://doi.org/10.1182/blood.V108.11.1242.1242

Published: 2006

Journal Articles

Differential Effects of Lovastatin and Allopurinol Therapy in a Murine Model of Sickle Cell Disease.

Kirkwood A. Pritchard, Jr., Terri L. Besch, Jingli Wang, Hao Xu, Deron W. Jones, Thomas D. Foster, Sandra L. Holzhauer, Keith T. Oldham, Nancy J. Wandersee, Cheryl A. Hillery

Blood (2005) 106 (11): 2325.

https://doi.org/10.1182/blood.V106.11.2325.2325

Published: 2005

Journal Articles

Transgenic Targeting of Human FVIII Expression to Endothelial Cells Corrects the Murine Hemophilia A Phenotype and Re-Establishes a Releasable Pool of FVIII Together with VWF.

Qizhen Shi, Hartmut Weiler, Sandra L. Haberichter, Brian C. Cooley, Scot A. Fahs, Drashti Desai, Nancy J. Wandersee, Mary A. Jozwiak, Robert R. Montgomery

Blood (2005) 106 (11): 3056.

https://doi.org/10.1182/blood.V106.11.3056.3056

Published: 2005

Journal Articles

Nitric Oxide Scavenging, Abnormal Vasoregulation and Oxidative Damage in sph/sph Mice with Severe Hereditary Spherocytosis: Possible Consequences of Red Blood Cell Hemolysis.

Anne C. Schraufnagel, Barb Piknova, PhD, Kirkwood A. Pritchard, Jr., PhD, Neil Hogg, PhD, Nancy J. Wandersee, PhD

Blood (2005) 106 (11): 1660.

https://doi.org/10.1182/blood.V106.11.1660.1660

Published: 2005

Journal Articles

AMP Deaminase Activation Contributes to Accelerated Adenine Nucleotide Pool Depletion during Periods of Energy Imbalance in Sickle Cell Erythrocytes.

Richard L. Sabina, PhD, Nancy J. Wandersee, PhD, Cheryl A. Hillery, MD

Blood (2005) 106 (11): 1671.

https://doi.org/10.1182/blood.V106.11.1671.1671

Published: 2005

Journal Articles

Tissue Factor Deficiency Decreases Sickle Cell-Induced Vascular Stasis in a Hematopoietic Stem Cell Transplant Model of Murine Sickle Cell Disease.

Cheryl A. Hillery, Thomas D. Foster, Sandra L. Holzhauer, J. Paul Scott, Julie A. Panepinto, Narla Mohandas, Nigel Mackman, Nancy J. Wandersee

Blood (2004) 104 (11): 236.

https://doi.org/10.1182/blood.V104.11.236.236

Published: 2004

NARROW

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

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

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

HMGB1 Release and TLR4-Mediated Inflammation In Sickle Cell Disease At Baseline and During Acute Vaso-Occlusive Crisis

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

Dietary Supplementation with Docosahexanoic Acid (DHA) Improves RBC Flexibility and Reduces Cold Hypersensitivity in Mice with Sickle Cell Disease.

A Novel Hemoglobin Binding Peptide Increases Intracellular Heme and Potentiates Hemoglobin-Induced HO-1 Levels in Endothelial Cells

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

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

A Novel Hemoglobin-Binding Agent Reduces Plasma Free Hemoglobin and Partially Improves Vascular Function In Murine Hemolytic Anemia

Mechanical Hypersensitivity Occurs in a Mouse Model of Sickle Cell Disease

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

Vascular dysfunction in a murine model of severe hemolysis

Vascular Dysfunction in Murine Models of Hemolytic Anemia.

Modifications of the Coagulation System Alter Inflammation in Murine Sickle Cell Disease.

Differential Effects of Lovastatin and Allopurinol Therapy in a Murine Model of Sickle Cell Disease.

Transgenic Targeting of Human FVIII Expression to Endothelial Cells Corrects the Murine Hemophilia A Phenotype and Re-Establishes a Releasable Pool of FVIII Together with VWF.

Nitric Oxide Scavenging, Abnormal Vasoregulation and Oxidative Damage in sph/sph Mice with Severe Hereditary Spherocytosis: Possible Consequences of Red Blood Cell Hemolysis.

AMP Deaminase Activation Contributes to Accelerated Adenine Nucleotide Pool Depletion during Periods of Energy Imbalance in Sickle Cell Erythrocytes.

Tissue Factor Deficiency Decreases Sickle Cell-Induced Vascular Stasis in a Hematopoietic Stem Cell Transplant Model of Murine Sickle Cell Disease.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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