Rezultati - Yves Le Bouc

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  1. 1
    Increased Levels of Insulin-Like Growth Factor II (IGF-II) and IGF-Binding Protein-2 Are Associated with Malignancy in Sporadic Adrenocortical Tumors<sup>1</sup>

    Increased Levels of Insulin-Like Growth Factor II (IGF-II) and IGF-Binding Protein-2 Are Associated with Malignancy in Sporadic Adrenocortical Tumors<sup>1</sup> od Nathalie Boulle, Armelle Logié, Christine Gicquel, Laurence Périn, Yves Le Bouc

    Izdano 1998
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  2. 2
    Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.

    Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome. od H Schneid, Danielle Seurin, M.-P. Vazquez, M Gourmelen, S Cabrol, Yves Le Bouc

    Izdano 1993
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  3. 3
    In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

    In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene od Christine Gicquel, Véronique Gaston, Jacqueline Mandelbaum, Jean‐Pierre Siffroi, Antoine Flahault, Yves Le Bouc

    Izdano 2003
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  4. 4
    A Targeted Partial Invalidation of the Insulin-Like Growth Factor I Receptor Gene in Mice Causes a Postnatal Growth Deficit*

    A Targeted Partial Invalidation of the Insulin-Like Growth Factor I Receptor Gene in Mice Causes a Postnatal Growth Deficit* od Martin Holzenberger, Patricia Leneuve, Ghislaine Hamard, Bertrand Ducos, Laurence Périn, M Binoux, Yves Le Bouc

    Izdano 2000
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  5. 5
    Autocrine role of IGF-II in proliferation of human adrenocortical carcinoma NCI H295R cell line

    Autocrine role of IGF-II in proliferation of human adrenocortical carcinoma NCI H295R cell line od Armelle Logié, Nathalie Boulle, Véronique Gaston, Laurence Périn, Philippe Boudou, Yves Le Bouc, Christine Gicquel

    Izdano 1999
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  6. 6
    A Liquid Chromatography/Tandem Mass Spectometry Profile of 16 Serum Steroids, Including 21-Deoxycortisol and 21-Deoxycorticosterone, for Management of Congenital Adrenal Hyperplasia

    A Liquid Chromatography/Tandem Mass Spectometry Profile of 16 Serum Steroids, Including 21-Deoxycortisol and 21-Deoxycorticosterone, for Management of Congenital Adrenal Hyperplasi... od Jean Fiet, Yves Le Bouc, Jérôme Guechot, Nicolas Hélin, Marie-Anne Maubert, Dominique Farabos, Antonin Lamazière

    Izdano 2017
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  7. 7
    Chick oviduct glucocorticosteroid receptor

    Chick oviduct glucocorticosteroid receptor od André Groyer, Yves Le Bouc, Irène Joab, Christine Radanyi, Jack‐Michel Renoir, P Röbel, Étienne-Émile Baulieu

    Izdano 1985
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  8. 8
    Experimental IGF-I Receptor Deficiency Generates a Sexually Dimorphic Pattern of Organ-Specific Growth Deficits in Mice, Affecting Fat Tissue in Particular

    Experimental IGF-I Receptor Deficiency Generates a Sexually Dimorphic Pattern of Organ-Specific Growth Deficits in Mice, Affecting Fat Tissue in Particular od Martin Holzenberger, Ghislaine Hamard, Randa Zaoui, Patricia Leneuve, Bertrand Ducos, C Beccavin, Laurence Périn, Yves Le Bouc

    Izdano 2001
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  9. 9
    IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice

    IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice od Martin Holzenberger, Joëlle Dupont, Bertrand Ducos, Patricia Leneuve, Alain Géloën, Patrick C. Even, Pascale Cervera, Yves Le Bouc

    Izdano 2002
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  10. 10
    Recessive Isolated Growth Hormone Deficiency and Mutations in the Ghrelin Receptor

    Recessive Isolated Growth Hormone Deficiency and Mutations in the Ghrelin Receptor od Jacques Pantel, Marie Legendre, Sylvie Nivot, Séverine Morisset‐Lopez, Marie Vie-Luton, Yves Le Bouc, Jacques Epelbaum, Serge Amselem

    Izdano 2009
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  11. 11
    The epigenetic imprinting defect of patients with Beckwith--Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

    The epigenetic imprinting defect of patients with Beckwith--Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region od Sylvie Rossignol, Virginie Steunou, Céline Chalas, Antoine Kerjean, Muriel Rigolet, E. Viégas-Pèquignot, Pierre Jouannet, Yves Le Bouc, Christine Gicquel

    Izdano 2006
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  12. 12
    Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

    Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome od Véronique Gaston, Yves Le Bouc, V. Soupre, Lydie Bürglen, Jeam Donadieu, Hubert Oro, G. Audry, Marie‐Paule Vazquez, Christine Gicquel

    Izdano 2001
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  13. 13
    Degree of methylation of<i>ZAC1</i>(<i>PLAGL1</i>) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort

    Degree of methylation of<i>ZAC1</i>(<i>PLAGL1</i>) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort od Salah Azzi, Theo Sas, Yves Akoli Koudou, Yves Le Bouc, Jean‐Claude Souberbielle, Patricia Dargent‐Molina, Irène Netchine, Marie‐Aline Charles

    Izdano 2013
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  14. 14
    Hepatocyte proliferation during liver regeneration is impaired in mice with liver‐specific IGF‐1R knockout

    Hepatocyte proliferation during liver regeneration is impaired in mice with liver‐specific IGF‐1R knockout od Christèle Desbois‐Mouthon, Dominique Wendum, Axelle Cadoret, Colette Rey, Patricia Leneuve, Annick Blaise, Chantal Housset, François Tronche, Yves Le Bouc, Martin Holzenberger

    Izdano 2006
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  15. 15
    Four families with loss of function mutations of the thyrotropin receptor.

    Four families with loss of function mutations of the thyrotropin receptor. od Nicolás de Roux, Micheline Misrahi, Raja Brauner, Muriel Houang, Jean‐Claude Carel, M Granier, Yves Le Bouc, Nicolae Ghinea, A Boumedienne, J E Toublanc, Edwin Milgröm

    Izdano 1996
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  16. 16
    Soluble leptin receptor in serum of subjects with complete resistance to leptin: relation to fat mass.

    Soluble leptin receptor in serum of subjects with complete resistance to leptin: relation to fat mass. od N. Lahlou, Karine Clément, Jean‐Claude Carel, Christian Vaisse, Chantal Lotton, Y Le Bihan, A Basdevant, Yves Le Bouc, Philippe Froguel, M Roger, B Guy-Grand

    Izdano 2000
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  17. 17
    Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with<i>IGF1</i>Mutation Demonstrates Its Critical Role in Growth and Brain Development

    Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with<i>IGF1</i>Mutation Demonstrates Its Critical Role in Growth and Brain Development od Irène Netchine, Salah Azzi, Muriel Houang, Danielle Seurin, Laurence Périn, Jean‐Marc Ricort, Claudine Daubas, Christine Legay, Ján Mešter, R. Herich, François Godeau, Yves Le Bouc

    Izdano 2009
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  18. 18
    Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

    Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylatio... od Salah Azzi, Sylvie Rossignol, Virginie Steunou, Theo Sas, Nathalie Thibaud, Fabienne Danton, Maryline Le Jule, Claudine Heinrichs, Sylvie Cabrol, Christine Gicquel, Yves Le Bouc, Irène Netchine

    Izdano 2009
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  19. 19
    Transcriptional profiling at the <i>DLK1/MEG3</i> domain explains clinical overlap between imprinting disorders

    Transcriptional profiling at the <i>DLK1/MEG3</i> domain explains clinical overlap between imprinting disorders od Walid Abi Habib, Frédéric Brioude, Salah Azzi, Sylvie Rossignol, Agnès Linglart, Marie‐Laure Sobrier, Éloïse Giabicani, Virginie Steunou, Madeleine D. Harbison, Yves Le Bouc, Irène Netchine

    Izdano 2019
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  20. 20
    Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression

    Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression od Fanny Mochel, Perrine Charles, F. Seguin, Julie Barritault, Christiane Coussieu, Laurence Périn, Yves Le Bouc, Christiane Gervais, Guislaine Carcelain, Anne Vassault, Josué Feingold, Daniel Rabier, Alexandra Dürr

    Izdano 2007
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