Works matching AU Lepretre, Frederic


Results: 32
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    Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia.

    Published in:
    American Journal of Hematology, 2013, v. 88, n. 4, p. 306, doi. 10.1002/ajh.23403
    By:
    • Boudry-Labis, Elise;
    • Roche-Lestienne, Catherine;
    • Nibourel, Olivier;
    • Boissel, Nicolas;
    • Terre, Christine;
    • Perot, Christine;
    • Eclache, Virginie;
    • Gachard, Nathalie;
    • Tigaud, Isabelle;
    • Plessis, Ghislaine;
    • Cuccuini, Wendy;
    • Geffroy, Sandrine;
    • Villenet, Céline;
    • Figeac, Martin;
    • Leprêtre, Frederic;
    • Renneville, Aline;
    • Cheok, Meyling;
    • Soulier, Jean;
    • Dombret, Hervé;
    • Preudhomme, Claude
    Publication type:
    Article
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    The genetics of adiponectin.

    Published in:
    Current Diabetes Reports, 2003, v. 3, n. 2, p. 151, doi. 10.1007/s11892-003-0039-4
    By:
    • Vasseur, Francis;
    • Leprêtre, Frédéric;
    • Lacquemant, Corinne;
    • Froguel, Philippe
    Publication type:
    Article
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    Simple gene signature to assess murine fibroblast polarization.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15640-6
    By:
    • Ledoult, Emmanuel;
    • Jendoubi, Manel;
    • Collet, Aurore;
    • Guerrier, Thomas;
    • Largy, Alexis;
    • Speca, Silvia;
    • Vivier, Solange;
    • Bray, Fabrice;
    • Figeac, Martin;
    • Hachulla, Eric;
    • Labalette, Myriam;
    • Leprêtre, Frédéric;
    • Sebda, Shéhérazade;
    • Sanges, Sébastien;
    • Rolando, Christian;
    • Sobanski, Vincent;
    • Dubucquoi, Sylvain;
    • Launay, David
    Publication type:
    Article
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    Deciphering genetic and nongenetic factors underlying tumour dormancy: insights from multiomics analysis of two syngeneic MRD models of melanoma and leukemia.

    Published in:
    Biological Research, 2024, v. 57, n. 1, p. 1, doi. 10.1186/s40659-024-00540-y
    By:
    • Laguillaumie, Marie-Océane;
    • Titah, Sofia;
    • Guillemette, Aurélie;
    • Neve, Bernadette;
    • Leprêtre, Frederic;
    • Ségard, Pascaline;
    • Shaik, Faruk Azam;
    • Collard, Dominique;
    • Gerbedoen, Jean-Claude;
    • Fléchon, Léa;
    • Hasan Bou Issa, Lama;
    • Vincent, Audrey;
    • Figeac, Martin;
    • Sebda, Shéhérazade;
    • Villenet, Céline;
    • Kluza, Jérôme;
    • Laine, William;
    • Fournier, Isabelle;
    • Gimeno, Jean-Pascal;
    • Wisztorski, Maxence
    Publication type:
    Article
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    Deciphering genetic and nongenetic factors underlying tumour dormancy: insights from multiomics analysis of two syngeneic MRD models of melanoma and leukemia.

    Published in:
    Biological Research, 2024, v. 57, n. 1, p. 1, doi. 10.1186/s40659-024-00540-y
    By:
    • Laguillaumie, Marie-Océane;
    • Titah, Sofia;
    • Guillemette, Aurélie;
    • Neve, Bernadette;
    • Leprêtre, Frederic;
    • Ségard, Pascaline;
    • Shaik, Faruk Azam;
    • Collard, Dominique;
    • Gerbedoen, Jean-Claude;
    • Fléchon, Léa;
    • Hasan Bou Issa, Lama;
    • Vincent, Audrey;
    • Figeac, Martin;
    • Sebda, Shéhérazade;
    • Villenet, Céline;
    • Kluza, Jérôme;
    • Laine, William;
    • Fournier, Isabelle;
    • Gimeno, Jean-Pascal;
    • Wisztorski, Maxence
    Publication type:
    Article
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    Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians.

    Published in:
    Human Molecular Genetics, 2002, v. 11, n. 21, p. 2607, doi. 10.1093/hmg/11.21.2607
    By:
    • Vasseur, Francis;
    • Helbecque, Nicole;
    • Dina, Christian;
    • Lobbens, Stéphane;
    • Delannoy, Valérie;
    • Gaget, Stéphane;
    • Boutin, Philippe;
    • Vaxillaire, Martine;
    • Leprêtre, Frédéric;
    • Dupont, Sophie;
    • Hara, Kazuo;
    • Clément, Karine;
    • Bihain, Bernard;
    • Kadowaki, Takashi;
    • Froguel, Philippe
    Publication type:
    Article
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    A genome-wide scan for coronaryheart disease suggests in Indo-Mauritians a susceptibility locuson chromosome 16p13 and replicates linkage with the metabolic syndromeon 3q27.

    Published in:
    Human Molecular Genetics, 2001, v. 10, n. 24, p. 2751, doi. 10.1093/hmg/10.24.2751
    By:
    • Francke, Stephan;
    • Manraj, Meera;
    • Lacquemant, Corinne;
    • Lecoeur, Cecile;
    • Leprêtre, Frédéric;
    • Passa, Philippe;
    • Hebe, Annick;
    • Corset, Laetitia;
    • Yan, Solange LeeKwai;
    • Lahmidi, Saïda;
    • Jankee, Sarojini;
    • Gunness, Teman K.;
    • Ramjuttun, Uday S.;
    • Balgobin, Vinod;
    • Dina, Christian;
    • Froguel, Philippe
    Publication type:
    Article
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