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Françoise Parmentier

French Institute of Health and Medical Research

37

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Transformation of an Unclassified Myeloproliferative Neoplasm with a Rare BCR-JAK2 Fusion Transcript Resulting from the Translocation (9;22)(p24;q11)

2015 Case reports in hematology
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Several mechanisms lead to the inactivation of the CDKN2A (P16), P14ARF, or CDKN2B (P15) genes in the GCB and ABC molecular DLBCL subtypes.

2012 Genes, Chromosomes and Cancer
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TET2 and TP53 mutations are frequently observed in blastic plasmacytoid dendritic cell neoplasm

2011 British Journal of Haematology
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The isotype of the BCR as a surrogate for the GCB and ABC molecular subtypes in diffuse large B-cell lymphoma

2011 Leukemia
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Increased trisomy 12 frequency and a biased IgVH 3–21 gene usage characterize small lymphocytic lymphoma

2010 Leukemia Research
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Development of a multiplex PCR assay for the detection of genomic copy number changes in myelodysplastic syndromes

2009 Leukemia Research
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Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1/S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

2009 Leukemia
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Detection of somatic quantitative genetic alterations by multiplex polymerase chain reaction for the prediction of outcome in diffuse large B-cell lymphomas.

2008 Haematologica
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Le métoclopramide stimule la sécrétion de catécholamines et de peptides dérivés des granines par les phéochromocytomes en activant des récepteurs sérotoninergiques de type 4 (5-HT4).

2008
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Development of a Multiplex PCR Assay for the Detection of Genomic Copy Number Changes in Myelodysplastic Syndromes

2008 Blood
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