Ohcanbohtosat - Claude Preudhomme

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  1. 1
    THE CLINICAL SIGNIFICANCE OF MUTATIONS OF THE P52 TUMOUR SUPPRESSOR GENE IN HAEMATOLOGICAL MALIGNANCIES

    THE CLINICAL SIGNIFICANCE OF MUTATIONS OF THE P52 TUMOUR SUPPRESSOR GENE IN HAEMATOLOGICAL MALIGNANCIES Dahkki Claude Preudhomme, Pierre Fenaux

    Almmustuhtton 1997
    Viečča ollesdeavstta Viečča ollesdeavstta
    Revisão
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  2. 2
    A Mutation Conferring Resistance to Imatinib at the Time of Diagnosis of Chronic Myelogenous Leukemia

    A Mutation Conferring Resistance to Imatinib at the Time of Diagnosis of Chronic Myelogenous Leukemia Dahkki Catherine Roche‐Lestienne, Jean‐Luc Laï, Stéphane Darré, Thierry Façon, Claude Preudhomme

    Almmustuhtton 2003
    Viečča ollesdeavstta Viečča ollesdeavstta
    Carta
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  3. 3
    17p Deletion in Acute Myeloid Leukemia and Myelodysplastic Syndrome. Analysis of Breakpoints and Deleted Segments by Fluorescence In Situ

    17p Deletion in Acute Myeloid Leukemia and Myelodysplastic Syndrome. Analysis of Breakpoints and Deleted Segments by Fluorescence In Situ Dahkki Valérie Soenen, Claude Preudhomme, Christophe Roumier, Agnès Daudignon, Jean Luc Laı̈, Pierre Fenaux

    Almmustuhtton 1998
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    Artigo
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  4. 4
    p53 mutations are associated with resistance to chemotherapy and short survival in hematologic malignancies

    p53 mutations are associated with resistance to chemotherapy and short survival in hematologic malignancies Dahkki Eric Wattel, Claude Preudhomme, B Hecquet, M Vanrumbeke, Bruno Quesnel, I Dervite, Pierre Morel, Pierre Fenaux

    Almmustuhtton 1994
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  5. 5
    Methylation of the p15INK4b Gene in Myelodysplastic Syndromes Is Frequent and Acquired During Disease Progression

    Methylation of the p15INK4b Gene in Myelodysplastic Syndromes Is Frequent and Acquired During Disease Progression Dahkki Bruno Quesnel, Gaëlle Guillerm, Rodolphe Vereecque, Eric Wattel, Claude Preudhomme, F Bauters, Michaël Vanrumbeke, Pierre Fenaux

    Almmustuhtton 1998
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  6. 6
    p16 gene homozygous deletions in acute lymphoblastic leukemia

    p16 gene homozygous deletions in acute lymphoblastic leukemia Dahkki Bruno Quesnel, Claude Preudhomme, N Philippe, M Vanrumbeke, Isabelle Dervite, JL Laï, F Bauters, Eric Wattel, Pierre Fenaux

    Almmustuhtton 1995
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  7. 7
    Occupational and environmental risk factors of the myelodysplastic syndromes in the North of France

    Occupational and environmental risk factors of the myelodysplastic syndromes in the North of France Dahkki Catherine Nisse, J. M. Haguenoer, Bruno Grandbastien, Claude Preudhomme, B. Fontaine, Jeanne Marie Brillet, Regis Lejeune, Pierre Fenaux

    Almmustuhtton 2001
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  8. 8
    Several types of mutations of the Abl gene can be found in chronic myeloid leukemia patients resistant to STI571, and they can pre-exist to the onset of treatment

    Several types of mutations of the Abl gene can be found in chronic myeloid leukemia patients resistant to STI571, and they can pre-exist to the onset of treatment Dahkki Catherine Roche‐Lestienne, Valérie Soenen, Nathalie Grardel, Jean-Luc Laı̈, N Philippe, Thierry Façon, Pierre Fenaux, Claude Preudhomme

    Almmustuhtton 2002
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  9. 9
    Fast multiclonal clusterization of V(D)J recombinations from high-throughput sequencing

    Fast multiclonal clusterization of V(D)J recombinations from high-throughput sequencing Dahkki Mathieu Giraud, Mikaël Salson, Marc Duez, Céline Villenet, Sabine Quief, Aurélie Caillault, Nathalie Grardel, Christophe Roumier, Claude Preudhomme, Martin Figeac

    Almmustuhtton 2014
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  10. 10
    Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia

    Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia Dahkki Aline Renneville, Nicolas Boissel, Virginie Zurawski, Laura Llopis, Valéria Biggio, Olivier Nibourel, N Philippe, Xavier Thomas, Hervé Dombret, Claude Preudhomme

    Almmustuhtton 2009
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  11. 11
    Acute Myeloid Leukemia and Myelodysplastic Syndromes Following Essential Thrombocythemia Treated With Hydroxyurea: High Proportion of Cases With 17p Deletion

    Acute Myeloid Leukemia and Myelodysplastic Syndromes Following Essential Thrombocythemia Treated With Hydroxyurea: High Proportion of Cases With 17p Deletion Dahkki Yvon Sterkers, Claude Preudhomme, Jean-Luc Laı̈, Jean‐Loup Demory, Marie‐Thérèse Caulier, Eric Wattel, Dominique Bordessoule, F Bauters, Pierre Fenaux

    Almmustuhtton 1998
    Viečča ollesdeavstta
    Artigo
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  12. 12
    RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistance

    RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and im... Dahkki Catherine Roche‐Lestienne, Lauréline Deluche, Sélim Corm, Isabelle Tigaud, Sami Joha, N Philippe, Sandrine Geffroy, Jean‐Luc Laï, Franck‐Emmanuel Nicolini, Claude Preudhomme

    Almmustuhtton 2008
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  13. 13
    Prospective long-term minimal residual disease monitoring using RQ-PCR in RUNX1-RUNX1T1-positive acute myeloid leukemia: results of the French CBF-2006 trial

    Prospective long-term minimal residual disease monitoring using RQ-PCR in RUNX1-RUNX1T1-positive acute myeloid leukemia: results of the French CBF-2006 trial Dahkki Christophe Willekens, Odile Blanchet, Aline Renneville, Pascale Cornillet‐Lefèbvre, Cécile Pautas, Romain Guièze, Norbert Ifrah, Hervé Dombret, Éric Jourdan, Claude Preudhomme, Nicolas Boissel

    Almmustuhtton 2015
    Viečča ollesdeavstta
    Artigo
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  14. 14
    Genetic typing of <i>CBL</i>, <i>ASXL1</i>, <i>RUNX1</i>, <i>TET2</i> and <i>JAK2</i> in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

    Genetic typing of <i>CBL</i>, <i>ASXL1</i>, <i>RUNX1</i>, <i>TET2</i> and <i>JAK2</i> in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomono... Dahkki B. Perez, Olivier Kosmider, Bruno Cassinat, Aline Renneville, Julie Lachenaud, Sophie Kaltenbach, Yves Bertrand, André Baruchel, Christine Chomienne, Michaëla Fontenay, Claude Preudhomme, Hélène Cavé

    Almmustuhtton 2010
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  15. 15
    Genetic polymorphisms associated with increased risk of developing chronic myelogenous leukemia

    Genetic polymorphisms associated with increased risk of developing chronic myelogenous leukemia Dahkki Heriberto Bruzzoni‐Giovanelli, Juan R. González, François Sigaux, Bruno O. Villoutreix, Jean Michel Cayuela, Joëlle Guilhot, Claude Preudhomme, François Guilhot, Jean‐Luc Poyet, Philippe Rousselot

    Almmustuhtton 2015
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  16. 16
    AML engraftment in the NOD/SCID assay reflects the outcome of AML: implications for our understanding of the heterogeneity of AML

    AML engraftment in the NOD/SCID assay reflects the outcome of AML: implications for our understanding of the heterogeneity of AML Dahkki Daniel J. Pearce, David Taussig, Kazem Zibara, Lan‐Lan Smith, Christopher M. Ridler, Claude Preudhomme, Bryan D. Young, A. Z. S. Rohatiner, T. Andrew Lister, Dominique Bonnet

    Almmustuhtton 2005
    Viečča ollesdeavstta
    Artigo
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  17. 17
    Favorable prognostic significance of CEBPA mutations in patients with de novo acute myeloid leukemia: a study from the Acute Leukemia French Association (ALFA)

    Favorable prognostic significance of CEBPA mutations in patients with de novo acute myeloid leukemia: a study from the Acute Leukemia French Association (ALFA) Dahkki Claude Preudhomme, C. Sagot, Nicolas Boissel, Jean‐Michel Cayuela, Isabelle Tigaud, Stéphane de Botton, Xavier Thomas, Emmanuel Raffoux, Charlotte Lamandin, Sylvie Castaigné, Pierre Fenaux, Hervé Dombret

    Almmustuhtton 2002
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  18. 18
    Cost of cancer diagnosis using next-generation sequencing targeted gene panels in routine practice: a nationwide French study

    Cost of cancer diagnosis using next-generation sequencing targeted gene panels in routine practice: a nationwide French study Dahkki Patricia Marino, Rajae Touzani, Lionel Perrier, Étienne Rouleau, Dede Sika Kossi, Zhaomin Zou, Nathanaël Charrier, Nicolas Goardon, Claude Preudhomme, Isabelle Durand‐Zaleski, Isabelle Borget, Sandrine Baffert

    Almmustuhtton 2018
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    Artigo
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  19. 19
    Next-generation sequencing of FLT3 internal tandem duplications for minimal residual disease monitoring in acute myeloid leukemia

    Next-generation sequencing of FLT3 internal tandem duplications for minimal residual disease monitoring in acute myeloid leukemia Dahkki Jean‐Emmanuel Bibault, Martin Figeac, Nathalie Hélevaut, Céline Rodriguez, Sabine Quief, Shéhérazade Sebda, Aline Renneville, Olivier Nibourel, Philippe Rousselot, Bérengère Gruson, Hervé Dombret, Sylvie Castaigné, Claude Preudhomme

    Almmustuhtton 2015
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  20. 20
    High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder

    High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder Dahkki Claude Preudhomme, Aline Renneville, Violaine Bourdon, N Philippe, Catherine Roche‐Lestienne, Nicolas Boissel, Nathalie Dhédin, Jean‐Marie André, Pascale Cornillet‐Lefèbvre, André Baruchel, Julien Mozziconacci, Hagay Sobol

    Almmustuhtton 2009
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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