Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Patrick Duthilleul"'
Autor:
Stéphanie Poulain, Isabelle Dervite, Xavier Leleu, Valérie Coiteux, Patrick Duthilleul, Pierre Morel
Publikováno v:
Haematologica, Vol 93, Iss 7 (2008)
Externí odkaz:
https://doaj.org/article/5ba8503d8597450a80e65b0bbcbce2ae
Autor:
Xavier Leleu, Claude Preudhomme, Patrick Duthilleul, Bruno Quesnel, Agnès Daudignon, Sabine Tricot, Aline Renneville, Eileen Mary Boyle, Audrey Decambron, Olivier Nibourel, Frédéric Lepretre, Sandrine Geffroy, Elisabeth Bertrand, Emmanuelle Doye, Guillemette Marot, Charles Herbaux, Martin Figeac, Aurélie Venet-Caillault, Christophe Roumier, Stéphanie Poulain
List of pathways analyzed for GSEA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8ba9801c9d58f5c04e61a01b495eda
https://doi.org/10.1158/1078-0432.22459223
https://doi.org/10.1158/1078-0432.22459223
Autor:
Xavier Leleu, Claude Preudhomme, Patrick Duthilleul, Bruno Quesnel, Agnès Daudignon, Sabine Tricot, Aline Renneville, Eileen Mary Boyle, Audrey Decambron, Olivier Nibourel, Frédéric Lepretre, Sandrine Geffroy, Elisabeth Bertrand, Emmanuelle Doye, Guillemette Marot, Charles Herbaux, Martin Figeac, Aurélie Venet-Caillault, Christophe Roumier, Stéphanie Poulain
Purpose: Whole-genome sequencing has revealed MYD88 L265P and CXCR4 mutations (CXCR4mut) as the most prevalent somatic mutations in Waldenström macroglobulinemia. CXCR4 mutation has proved to be of critical importance in Waldenström macroglobulinem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07a72998027ec0942d37a4069a503b3e
https://doi.org/10.1158/1078-0432.c.6524165
https://doi.org/10.1158/1078-0432.c.6524165
Autor:
Catherine Roche-Lestienne, Sylvie Galiègue-Zouitina, Patrick Duthilleul, Agnès Daudignon, Xavier Leleu, Valérie Soenen, Christophe Roumier, Stéphanie Poulain, Olivier Theisen, Aline Renneville, Sabine Tricot, Bruno Quesnel, Nathalie Grardel, Elisabeth Bertrand, Charles Herbaux, Claude Preudhomme, Audrey Decambron, Olivier Nibourel
Publikováno v:
Blood. 121:4504-4511
Mutation of the MYD88 gene has recently been identified in activated B-cell-like diffuse cell lymphoma and enhanced Janus kinase/signal transducer and activator of transcription (JAK-STAT) and nuclear factor κB (NF-κB) signaling pathways. A whole e
Autor:
Patrick Duthilleul, Sabine Tricot, Aline Renneville, Agnès Daudignon, Stéphanie Poulain, Olivier Theisen, Rolf Marschalek, Charles Herbaux, Marc Simon, Jose Fernandes, Claus Meyer
Publikováno v:
British Journal of Haematology. 157:128-131
Autor:
Pierre Morel, Stéphanie Poulain, José Fernandes, Françoise Parmentier, Dominique Penther, Agnès Daudignon, Christian Bastard, Patrick Duthilleul, Brigitte Bouchindhomme
Publikováno v:
Leukemia Research. 34:580-584
Small lymphocytic lymphoma (SLL) and chronic lymphocytic leukemia (CLL) are considered as similar entity by the WHO classification. We assessed the distribution of the four prognostic cytogenetic markers (deletion 11q23, 13q14, 17p13 and trisomy 12)
Autor:
Laure Stalnikiewicz, José Fernandes, Stéphanie Poulain, Pierre Morel, Patrick Duthilleul, Valérie Coiteux, Xavier Leleu, Marjan Ertault
Publikováno v:
Leukemia Research. 33:1204-1207
The interaction of the chemokine CXCL12 with CXCR4 regulates homing of tumoral cells in bone marrow in Waldenstrom macroglobulinemia (WM). We assessed the distribution and the clinical influence of the CXCL12 (−801GA) polymorphism using PCR RFLP in
Autor:
Guillemette Marot, Eileen M Boyle, Sabine Tricot, Stéphanie Poulain, Frédéric Leprêtre, Xavier Leleu, Agnès Daudignon, Martin Figeac, Audrey Decambron, Emmanuelle Doye, Bruno Quesnel, Olivier Nibourel, Aline Renneville, Claude Preudhomme, Aurélie Venet-Caillault, Christophe Roumier, Patrick Duthilleul, Sandrine Geffroy, Elisabeth Bertrand, Charles Herbaux
Publikováno v:
Clinical Cancer Research
Clinical Cancer Research, 2015, 21 (22), ⟨10.1158/1078-0432.CCR-15-0646⟩
Clinical Cancer Research, American Association for Cancer Research, 2015, 21 (22), ⟨10.1158/1078-0432.CCR-15-0646⟩
Clinical Cancer Research, 2015, 21 (22), ⟨10.1158/1078-0432.CCR-15-0646⟩
Clinical Cancer Research, American Association for Cancer Research, 2015, 21 (22), ⟨10.1158/1078-0432.CCR-15-0646⟩
Purpose: Whole-genome sequencing has revealed MYD88 L265P and CXCR4 mutations (CXCR4mut) as the most prevalent somatic mutations in Waldenström macroglobulinemia. CXCR4 mutation has proved to be of critical importance in Waldenström macroglobulinem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de66288aac27ce3f4cc4a1a94fa5076
https://inria.hal.science/hal-01230058
https://inria.hal.science/hal-01230058
Autor:
Audrey Decambron, Stéphanie Poulain, Xavier Leleu, Christophe Roumier, Guillemette Fouquet, Eileen M Boyle, Patrick Duthilleul, Elisabeth Bertrand, Charles Herbaux, Salomon Manier
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 13:202-204
The pathophysiology of Waldenström macroglobulinemia (WM), a lymphoproliferative disorder characterized by lymphoplasmacytic bone marrow infiltration associated with serum IgM paraprotein, is rather unclear; however, progress has been made in recent
Autor:
Rafael Fonseca, Stéphanie Poulain, Xavier Leleu, Sylvie Galiègue-Zouitina, Salomon Manier, Rachid Aijjou, Natacha Broucqsault, Olivier Nibourel, Valérie Soenen, Patrick Duthilleul, Esteban Braggio, Christophe Roumier
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 11:106-108
Single-nucleotide polymorphism array (SNPa) and array-based comparative genomic hybridization (aCGH) are among the most sensitive genomic high-throughput screening techniques used in the exploration of genetic abnormalities in Waldenström's macroglo