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Serge Carillo

Centre national de la recherche scientifique

33

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MPL Mutations in Essential Thrombocythemia Uncover A Common Path of Activation with Eltrombopag Dependent on W491

2020 Blood
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Gene editing rescue of a novel MPL mutant associated with congenital amegakaryocytic thrombocytopenia

2017 Blood Advances
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In Vitro Functional Rescue of a Double MPL K39N/W272R Mutant Associated with Congenital Amegakaryocytic Thrombocytopenia (CAMT) Using Crispr/Cas9

2015 Blood
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Clinical and molecular response to interferon-α therapy in essential thrombocythemia patients with CALR mutations

2015 Blood
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Presence of calreticulin mutations in JAK2-negative polycythemia vera

2014 Blood
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JAK2Exon 12 Mutant Allele Burden Study (JETMABS): A European Multicenter Study

2013 Blood
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Interlaboratory Quality Control Round of MPL Mutation Detection in Fourteen European Laboratories: A MPN&MPNr-EuroNet Study,

2011 Blood
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Significant increase in the apparent incidence of essential thrombocythemia related to new WHO diagnostic criteria: a population-based study

2009 Haematologica
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Concordance of assays designed for the quantification of JAK2V617F: a multicenter study.

2009 Haematologica
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Association of essential thrombocythemia and chronic lymphocytic leukemia: Absence of the V617F JAK2 mutation in the lymphoid compartment

2007 American Journal of Hematology
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Citations (21)