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Therapeutic Advances in Hematology|February 21, 2022
A thrombopoietin receptor agonist to rescue an unusual platelet transfusion-induced reaction in a p.V1316M-associated von Willebrand disease type 2B patientCaterina Casari, Remi Favier, Paulette Legendre, et al.
American Journal of Hematology|March 28, 2019
MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membraneAlyson S Smith, Kasturi Pal, Roberta B Nowak, et al.
American Journal of Hematology|November 2, 2017
Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α-granulesMarie Favier, Jean-Claude Bordet, Remi Favier, et al.
The Journal of Clinical Investigation|January 17, 2014
Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivationDominique Bluteau, Alessandra Balduini, Nathalie Balayn, et al.
Blood|August 18, 2012
Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expressionDominique Bluteau, Ana C Glembotsky, Anna Raimbault, et al.
Blood|May 19, 2021
CALR mutant protein rescues the response of MPL p.R464G variant associated with CAMT to eltrombopagFrancesca Basso-Valentina, Gabriel Levy, Leila N Varghese, et al.
British Journal of Haematology|April 23, 2015
Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disordersElisa Civaschi, Catherine Klersy, Federica Melazzini, et al.
Blood|December 31, 2016
An incomplete trafficking defect to the cell-surface leads to paradoxical thrombocytosis for human and murine MPL P106LFabrizia Favale, Kahia Messaoudi, Leila N Varghese, et al.
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.
Blood|July 26, 2014
A new form of macrothrombocytopenia induced by a germ-line mutation in the PRKACG geneVladimir T Manchev, Morgane Hilpert, Eliane Berrou, et al.
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