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Journal Articles

The neutrophil antigen 3a/b polymorphism in SLC44A2 unexpectedly encodes the Cs a /Cs b red cell antigens

Blood (2025) 146 (2): 247–253.

https://doi.org/10.1182/blood.2024026285

Published: 2025

Includes: Supplemental data

Journal Articles

Oxygen Gradient Ektacytometry Is Associated with Markers of Hemolysis and Inflammation in a Large Sickle Cell Disease Cohort within the GenoMed4ALL Project

Blood (2024) 144 (Supplement 1): 290.

https://doi.org/10.1182/blood-2024-200639

Published: 2024

Journal Articles

Defining Mechanistic Responses to Different Vaso-Occlusive Triggers in Sickle Cell Disease: A Step Towards Personalized VOC Reversal Strategies

Lucas F.S. Gushiken, Sarah Liane Linguet, Erica M.F. Gotardo, Pamela L Brito, Flavia C. Leonardo, Laetitia Claer, Slim Azouzi, Caroline Le Van Kim, Fernando Ferreira Costa, Sandrine Laurance, Berengere Khoel, Nicola Conran

Blood (2024) 144 (Supplement 1): 2489.

https://doi.org/10.1182/blood-2024-193820

Published: 2024

Journal Articles

The Cs a and Cs b Red Cell Antigens of the Cost Blood Group Collection Correspond to the HNA-3a and HNA-3b Neutrophil Antigens: Unexpected Twins with Implications for Sickle Cell Anemia

Jonathan De Oliveira Rios, Alisa Soudry, Romain Duval, Alexandre Raneri, Thomas Poyot, Jérome Babinet, Mariane De Montalembert, Claudia Regina Bonini Domingos, Caroline Le Van Kim, Marc Romana, Thierry Peyrard, Slim Azouzi

Blood (2023) 142 (Supplement 1): 698.

https://doi.org/10.1182/blood-2023-178250

Published: 2023

Journal Articles

Hydroxyurea's Impact on Erythropoiesis, Cell Death and HbF Expression in the Hudep-2 Model

Lea Kuznicki, Sandrine Laurance, Laetitia Claer, Caroline Le Van Kim

Blood (2023) 142 (Supplement 1): 2493.

https://doi.org/10.1182/blood-2023-177625

Published: 2023

Journal Articles

Single Cell Analysis and Functional Features of Circulating CD34 + Cells from Patients with Sickle Cell Anaemia Unveil a Defect in the Myeloid Lineage

Marion Serra, Patricia Hermand, Romain Duval, Carine Lefevre, Jade Merrer, Fallou Leye, Mohammad Salma, Marine Aglave, William Vainchenker, Caroline Le Van Kim, Slim Azouzi, Berengere Koehl

Blood (2023) 142 (Supplement 1): 1111.

https://doi.org/10.1182/blood-2023-180900

Published: 2023

Journal Articles

Genetic Evidence That Dimerization of Glycophorin a Is Critical for Red Cell Invasion By Plasmodium Falciparum but Not for the Binding of EBA-175

Slim Azouzi, Mahmoud Mikdar, Patricia Hermand-Tournamille, Kunal More, Sébastien Dechavanne, Romain Duval, Vincent Thonier, Caroline Le Van Kim, Isabelle Mouro-Chanteloup, Olivier Bertrand, Chetan Chitnis, Thierry Peyrard, Yves Colin Aronovicz

Blood (2022) 140 (Supplement 1): 2431.

https://doi.org/10.1182/blood-2022-165253

Published: 2022

Journal Articles

Adenosine Signaling Perturbs Erythropoiesis and Promotes Myeloid Differentiation

Mahmoud Mikdar, Marion Serra, Elia Colin, Yves Colin Aronovicz, Caroline Le Van Kim, Thierry Peyrard, Bérengère Koehl, Slim Azouzi

Blood (2021) 138 (Supplement 1): 1992.

https://doi.org/10.1182/blood-2021-146144

Published: 2021

Journal Articles

Persistence of Chronic Inflammation Despite Years of Transfusion Program in SCD Patients: Changing Red Blood Cells Is Not Sufficient to Treat Sickle Cell Disease

Abdoul Karim Dembele, Patricia Hermand-Tournamille, Florence Missud, Emmanuelle Lesprit, Malika Benkerrou, Caroline Le Van Kim, Berengere Koehl

Blood (2021) 138 (Supplement 1): 764.

https://doi.org/10.1182/blood-2021-147787

Published: 2021

Journal Articles

Revisiting Spleen Function and Pneumococcal Risk in Children with Hemoglobin SC Disease

Charlotte Pourdieu, Sara El Hoss, Enora Le Roux, Justine Pages, Berengere Koehl, Florence Missud, Laurent Holvoet, Ghislaine Ithier, Malika Benkerrou, Zine-Eddine Haouari, Lydie M. Da Costa, Wassim El Nemer, Yves Colin Aronovicz, Caroline Le Van Kim, Elodie Lainey, Valentine Brousse

Blood (2021) 138 (Supplement 1): 768.

https://doi.org/10.1182/blood-2021-150629

Published: 2021

Journal Articles

Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders

Blood (2021) 137 (26): 3660–3669.

https://doi.org/10.1182/blood.2020009810

Published: 2021

Includes: Supplemental data

Journal Articles

The equilibrative nucleoside transporter ENT1 is critical for nucleotide homeostasis and optimal erythropoiesis

Blood (2021) 137 (25): 3548–3562.

https://doi.org/10.1182/blood.2020007281

Published: 2021

Includes: Supplemental data

Journal Articles

Rapid clearance of storage-induced microerythrocytes alters transfusion recovery

Blood (2021) 137 (17): 2285–2298.

https://doi.org/10.1182/blood.2020008563

Published: 2021

Includes: Supplemental data

Journal Articles

Persistance of Inflammatory Phenotype of Neutrophils in Sickle Cell Disease Children Despite Chronic Exchange Transfusion Program: A Cause of the Progression of Cerebral Vasculopathy?

Abdoul Karim Dembele, MD, Patricia Hermand-Tournamille, PhD, Florence Missud, MD, Emmanuelle Lesprit, MD, Malika Benkerrou, MD, Yves Colin Aronovicz, PhD, Caroline Le Van Kim, PhD, Bérengère Koehl, MDPhD

Blood (2020) 136 (Supplement 1): 2–3.

https://doi.org/10.1182/blood-2020-136098

Published: 2020

Journal Articles

Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation

Blood (2020) 135 (6): 441–448.

https://doi.org/10.1182/blood.2019002320

Published: 2020

Includes: Supplemental data

Journal Articles

Studying the Determinant of Sickle Cell Disease Vasculopathy in Sub-Saharan Africa : The Biocadre Study

Brigitte Ranque, Abdoul Karim Dembele, MD, Mor Diaw, PhD, Claudine Lapoumeroulie, PhD, Lucile Offredo, MS, Dapa Aly Diallo, MD, Diop Saliou, MD, Yves Colin Aronovicz, PhD, Olivier Blanc Brude, PhD, Philippe Connes, PhD, Pierre-Louis Tharaux, MD PhD, Marc Romana, PhD, Xavier Jouven, MD PhD, Caroline Le Van Kim, PhD

Blood (2019) 134 (Supplement_1): 2310.

https://doi.org/10.1182/blood-2019-126713

Published: 2019

Journal Articles

The Multidrug Transporter MRP4/ABCC4 Involved in the Leukemia Clinical Course Specifies the Novel PEL Human Blood Group System

Blood (2019) 134 (Supplement_1): 715.

https://doi.org/10.1182/blood-2019-124082

Published: 2019

Journal Articles

Storage-Induced Micro-Erythrocytes Are Rapidly Cleared from Recipient Circulation and Predict Transfusion Recovery

Blood (2019) 134 (Supplement_1): 717.

https://doi.org/10.1182/blood-2019-128161

Published: 2019

Journal Articles

CELL-Derived Microparticles and Sickle CELL Disease Chronic Vasculopathy in Sub-Saharan Africa

Abdoul Karim Dembele, MD, Claudine Lapoumeroulie, PhD, Mor Diaw, PhD, Oumar Tessougué, MD, Lucile Offredo, MS, Dapa Aly Diallo, MD, Saliou Diop, MD MSc, Jacques Elion, MD PhD, Yves Colin Aronovicz, Pierre Louis Tharaux, MD PhD, Xavier Jouven, MD PhD, Marc Romana, PhD, Brigitte Ranque, MD PhD, Caroline Le Van Kim, PhD

Blood (2019) 134 (Supplement_1): 3568.

https://doi.org/10.1182/blood-2019-121334

Published: 2019

Journal Articles

New Insights into F-Cells, F-Reticulocytes and the Role of Fetal Hemoglobin in Protecting Sickle Red Cells from Hemolysis upon Mechanical Stress

Sara El Hoss, Maria Alejandra Lizarralde Iragorri, Valentine Brousse, MD, Michaël Dussiot, PhD, Sophie Lefevre, PhD, Alexander Rodrigo Ferreira, Yann Lamarre, PhD, Ana Cristina Silva Pinto, MD PhD, Simone Kashima, PhD, Claudine Lapoumeroulie, PhD, Dimas Tadeu Covas, MD PhD, Caroline Le Van Kim, PhD, Yves Colin Aronovicz, PhD, Jacques Elion, MD PhD, Olivier Français, PhD, Bruno Le Pioufle, PhD, Wassim El Nemer, PhD

Blood (2017) 130 (Supplement 1): 3513.

https://doi.org/10.1182/blood.V130.Suppl_1.3513.3513

Published: 2017

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The neutrophil antigen 3a/b polymorphism in SLC44A2 unexpectedly encodes the Cs a /Cs b red cell antigens

Oxygen Gradient Ektacytometry Is Associated with Markers of Hemolysis and Inflammation in a Large Sickle Cell Disease Cohort within the GenoMed4ALL Project

Defining Mechanistic Responses to Different Vaso-Occlusive Triggers in Sickle Cell Disease: A Step Towards Personalized VOC Reversal Strategies

The Cs a and Cs b Red Cell Antigens of the Cost Blood Group Collection Correspond to the HNA-3a and HNA-3b Neutrophil Antigens: Unexpected Twins with Implications for Sickle Cell Anemia

Hydroxyurea's Impact on Erythropoiesis, Cell Death and HbF Expression in the Hudep-2 Model

Single Cell Analysis and Functional Features of Circulating CD34 + Cells from Patients with Sickle Cell Anaemia Unveil a Defect in the Myeloid Lineage

Genetic Evidence That Dimerization of Glycophorin a Is Critical for Red Cell Invasion By Plasmodium Falciparum but Not for the Binding of EBA-175

Adenosine Signaling Perturbs Erythropoiesis and Promotes Myeloid Differentiation

Persistence of Chronic Inflammation Despite Years of Transfusion Program in SCD Patients: Changing Red Blood Cells Is Not Sufficient to Treat Sickle Cell Disease

Revisiting Spleen Function and Pneumococcal Risk in Children with Hemoglobin SC Disease

Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders

The equilibrative nucleoside transporter ENT1 is critical for nucleotide homeostasis and optimal erythropoiesis

Rapid clearance of storage-induced microerythrocytes alters transfusion recovery

Persistance of Inflammatory Phenotype of Neutrophils in Sickle Cell Disease Children Despite Chronic Exchange Transfusion Program: A Cause of the Progression of Cerebral Vasculopathy?

Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation

Studying the Determinant of Sickle Cell Disease Vasculopathy in Sub-Saharan Africa : The Biocadre Study

The Multidrug Transporter MRP4/ABCC4 Involved in the Leukemia Clinical Course Specifies the Novel PEL Human Blood Group System

Storage-Induced Micro-Erythrocytes Are Rapidly Cleared from Recipient Circulation and Predict Transfusion Recovery

CELL-Derived Microparticles and Sickle CELL Disease Chronic Vasculopathy in Sub-Saharan Africa

New Insights into F-Cells, F-Reticulocytes and the Role of Fetal Hemoglobin in Protecting Sickle Red Cells from Hemolysis upon Mechanical Stress

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