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Blood|July 5, 2011
Down-regulation of the RUNX1-target gene NR4A3 contributes to hematopoiesis deregulation in familial platelet disorder/acute myelogenous leukemiaDominique Bluteau, Laure Gilles, Morgane Hilpert, et al.
Ejhaem|December 18, 2025
Development of Machine-Assisted, Human-Centred Bone Marrow Cell Classification: Feasibility Analysis in Patients With Myelodysplastic SyndromesKiyoyuki Ogata, Yuto Mochimaru, Leonie Saft, et al.
Nature Communications|December 22, 2018
A miR-150/TET3 pathway regulates the generation of mouse and human non-classical monocyte subsetDorothée Selimoglu-Buet, Julie Rivière, Hussein Ghamlouch, et al.
Hematological Oncology|December 9, 2017
Prognostic value of multicenter flow cytometry harmonized assessment of minimal residual disease in acute myeloblastic leukemiaFrancis Lacombe, Lydia Campos, Kaoutar Allou, et al.
British Journal of Haematology|March 19, 2016
Morbidity and mortality of sickle cell disease patients starting intermittent haemodialysis: a comparative cohort study with non- Sickle dialysis patientsLouise Nielsen, Florence Canouï-Poitrine, Jean-Philippe Jais, et al.
Communications Biology|February 4, 2022
Macrophage migration inhibitory factor is overproduced through EGR1 in TET2low resting monocytesElodie Pronier, Aygun Imanci, Dorothée Selimoglu-Buet, et al.
Cytometry. Part B, Clinical Cytometry|December 30, 2021
ELN iMDS flow working group validation of the monocyte assay for chronic myelomonocytic leukemia diagnosis by flow cytometryOrianne Wagner-Ballon, Peter Bettelheim, Jeroen Lauf, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 15, 2010
Thrombospondin-1 is a plasmatic marker of peripheral arterial disease that modulates endothelial progenitor cell angiogenic propertiesDavid M Smadja, Clément d'Audigier, Ivan Bièche, et al.
Blood|April 9, 2015
Characteristic repartition of monocyte subsets as a diagnostic signature of chronic myelomonocytic leukemiaDorothée Selimoglu-Buet, Orianne Wagner-Ballon, Véronique Saada, et al.
Orphanet Journal of Rare Diseases|July 10, 2020
Exome sequencing for diagnosis of congenital hemolytic anemiaLamisse Mansour-Hendili, Abdelrazak Aissat, Bouchra Badaoui, et al.
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