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Quercetin-3-rutinoside Inhibits Protein Disulfide Isomerase by Binding to Its b′x Domain

The Journal of biological chemistry, 2015-09, Vol.290 (39), p.23543-23552

2015

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Apohemoglobin-haptoglobin complex alleviates iron toxicity in mice with β-thalassemia via scavenging of cell-free hemoglobin and heme

Biomedicine & pharmacotherapy, 2022-12, Vol.156, p.113911-113911, Article 113911

2022

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Prevalence, Mortality, and Access to Care for Chronic Kidney Disease in Medicaid-Enrolled Adults With Sickle Cell Disease in California: Retrospective Cohort Study

JMIR public health and surveillance, 2024-07, Vol.10, p.e57290

2024

Volltextzugriff (PDF)

Molecular mechanisms for vascular complications of targeted cancer therapies

Clinical science (1979), 2016-10, Vol.130 (20), p.1763

2016

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A Nurse-Led Education Intervention to Improve Infusion Center Management of Sickle Cell Pain

Blood, 2022-11, Vol.140 (Supplement 1), p.13045-13045

2022

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The Impact of Same Day Infusion Treatment Protocols for Uncomplicated Vaso-Occlusive Crises within an Embedded Sickle Cell Care Model

Blood, 2021-11, Vol.138 (Supplement 1), p.2976-2976

2021

Volltextzugriff (PDF)

Apohemoglobin‐haptoglobin (Apohb‐Hp) Complex as a Vasculo‐protective Agent in Hypoxia Induced Vaso‐occlusion in Sickle Cell Disease

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

Volltextzugriff (PDF)

A phosphoproteomic signature in endothelial cells predicts vascular toxicity of tyrosine kinase inhibitors used in CML

Blood advances, 2018-07, Vol.2 (14), p.1680-1684

2018

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PEGylation of Apohemoglobin Haptoglobin Complex reduces Associated Free Stroma Hemoglobin Toxicities

Physiology (Bethesda, Md.), 2023-05, Vol.38 (S1)

2023

Volltextzugriff (PDF)

Apohemoglobin-Haptoglobin Complex Prevents Microvascular Dysfunction in Sickle Cell Mice: Potential Therapeutic Approach for Vaso-Occlusive Crisis

Blood, 2022-11, Vol.140 (Supplement 1), p.5405-5406

2022

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Defective PDI release from platelets and endothelial cells impairs thrombus formation in Hermansky-Pudlak syndrome

Blood, 2015-03, Vol.125 (10), p.1633-1642

2015

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Patient‐derived assessment tool using musculoskeletal ultrasound for validation of haemarthrosis

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-09, Vol.28 (5), p.842-848

2022

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Both platelet- and endothelial cell–derived ERp5 support thrombus formation in a laser-induced mouse model of thrombosis

Blood, 2015-04, Vol.125 (14), p.2276-2285

2015

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Real-World Data of Crizanlizumab in Sickle Cell Disease: A Single-Center Analysis

Journal of hematology, 2023-06, Vol.12 (3), p.105-108

2023

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Systemic Vascular Basement Membrane Markers Linked to Synovial Vascular Remodeling Are Bio-Markers of Hemarthrosis in Patients with Hemophilia

Blood, 2018-11, Vol.132 (Supplement 1), p.380-380

2018

Volltextzugriff (PDF)

Systemic Transcriptional Responses to Hemarthrosis and FVIII Replacement in FVIII-Deficient Mice

Blood, 2018-11, Vol.132 (Supplement 1), p.381-381

2018

Volltextzugriff (PDF)

Protein disulfide isomerase regulation by nitric oxide maintains vascular quiescence and controls thrombus formation

Journal of thrombosis and haemostasis, 2018-11, Vol.16 (11), p.2322-2335

2018

Volltextzugriff (PDF)

The Impact of Chemotherapeutic Agents on Signaling and Epigenetics in Vascular Endothelial Cells

Blood, 2016-12, Vol.128 (22), p.1353-1353

2016

Volltextzugriff (PDF)

Effects of Hemostasis Correction on Vascular Remodeling and Synovial Gene Expression Changes in Mice after Induced Hemarthrosis

Blood, 2018-11, Vol.132 (Supplement 1), p.1188-1188

2018

Volltextzugriff (PDF)

Systemic vascular basement membrane markers linked to synovial vascular remodeling are biomarkers of hemarthrosis in patients with hemophilia

Journal of thrombosis and haemostasis, 2021-05, Vol.19 (5), p.1200-1211

2021

Volltextzugriff (PDF)

Mechanisms of vascular permeability and remodeling associated with hemarthrosis in factor VIII‐deficient mice

Journal of thrombosis and haemostasis, 2019-11, Vol.17 (11), p.1815-1826

2019

Volltextzugriff (PDF)

Comprehensive guide to managing a chronic automated red cell exchange program in sickle cell disease

Journal of clinical apheresis, 2022-10, Vol.37 (5), p.497-506

2022

Volltextzugriff (PDF)

Anemia of Chronic Kidney Disease – Hepcidin Is a Predictor

Blood, 2011-11, Vol.118 (21), p.3182-3182

2011

Volltextzugriff (PDF)

Implementation and Impact of a Multidisciplinary Coagulation Factor Stewardship Program

Blood, 2017-12, Vol.130, p.2083-2083

2017

Volltextzugriff (PDF)

Impact of Tyrosine Kinase Inhibitors Used in Chronic Myeloid Leukemia on Signaling and Epigenetics in Endothelial Cells

Blood, 2017-12, Vol.130, p.2296-2296

2017

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Quercetin-3-rutinoside Inhibits Protein Disulfide Isomerase by Binding to Its b′x Domain

Apohemoglobin-haptoglobin complex alleviates iron toxicity in mice with β-thalassemia via scavenging of cell-free hemoglobin and heme

Prevalence, Mortality, and Access to Care for Chronic Kidney Disease in Medicaid-Enrolled Adults With Sickle Cell Disease in California: Retrospective Cohort Study

Molecular mechanisms for vascular complications of targeted cancer therapies

A Nurse-Led Education Intervention to Improve Infusion Center Management of Sickle Cell Pain

The Impact of Same Day Infusion Treatment Protocols for Uncomplicated Vaso-Occlusive Crises within an Embedded Sickle Cell Care Model

Apohemoglobin‐haptoglobin (Apohb‐Hp) Complex as a Vasculo‐protective Agent in Hypoxia Induced Vaso‐occlusion in Sickle Cell Disease

A phosphoproteomic signature in endothelial cells predicts vascular toxicity of tyrosine kinase inhibitors used in CML

PEGylation of Apohemoglobin Haptoglobin Complex reduces Associated Free Stroma Hemoglobin Toxicities

Apohemoglobin-Haptoglobin Complex Prevents Microvascular Dysfunction in Sickle Cell Mice: Potential Therapeutic Approach for Vaso-Occlusive Crisis

Defective PDI release from platelets and endothelial cells impairs thrombus formation in Hermansky-Pudlak syndrome

Patient‐derived assessment tool using musculoskeletal ultrasound for validation of haemarthrosis

Both platelet- and endothelial cell–derived ERp5 support thrombus formation in a laser-induced mouse model of thrombosis

Real-World Data of Crizanlizumab in Sickle Cell Disease: A Single-Center Analysis

Systemic Vascular Basement Membrane Markers Linked to Synovial Vascular Remodeling Are Bio-Markers of Hemarthrosis in Patients with Hemophilia

Systemic Transcriptional Responses to Hemarthrosis and FVIII Replacement in FVIII-Deficient Mice

Protein disulfide isomerase regulation by nitric oxide maintains vascular quiescence and controls thrombus formation

The Impact of Chemotherapeutic Agents on Signaling and Epigenetics in Vascular Endothelial Cells

Effects of Hemostasis Correction on Vascular Remodeling and Synovial Gene Expression Changes in Mice after Induced Hemarthrosis

Systemic vascular basement membrane markers linked to synovial vascular remodeling are biomarkers of hemarthrosis in patients with hemophilia

Mechanisms of vascular permeability and remodeling associated with hemarthrosis in factor VIII‐deficient mice

Comprehensive guide to managing a chronic automated red cell exchange program in sickle cell disease

Anemia of Chronic Kidney Disease – Hepcidin Is a Predictor

Implementation and Impact of a Multidisciplinary Coagulation Factor Stewardship Program

Impact of Tyrosine Kinase Inhibitors Used in Chronic Myeloid Leukemia on Signaling and Epigenetics in Endothelial Cells

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