Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Audrey Decambron"'
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:
Hervé Bisiau, José Fernandes, Nicolas Duployez, Benoît Ducourneau, Claire Hemar, Lina Sabor, Audrey Decambron, Malicka Sanfo, Claude Preudhomme
Publikováno v:
Journal of Blood & Lymph.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87c16828e4c382b35d86029eb0bc7cf8
https://doi.org/10.4172/2165-7831.1000206
https://doi.org/10.4172/2165-7831.1000206
Autor:
Audrey Decambron
Publikováno v:
Transfusion Clinique et Biologique. 26:S19
Le diagnostic d’une arthropathie du genou a revele une surcharge en fer post-transfusionnelle. Bien que la fiche technique ANSM de novembre 2015 recommande la recherche d’une surcharge en fer apres la transfusion d’au moins 20 concentres de glo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::295f9ff771bf6f2cf117cb2640132277
https://doi.org/10.1016/j.tracli.2019.06.284
https://doi.org/10.1016/j.tracli.2019.06.284
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::916049e74d2ef26a8a20b2ad8c8e44f8
https://doi.org/10.1182/blood-2012-06-436329
https://doi.org/10.1182/blood-2012-06-436329
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3022628c6a9157dd6a7c93fc3e2d8fe3
https://doi.org/10.1016/j.clml.2013.02.008
https://doi.org/10.1016/j.clml.2013.02.008