检索结果 - Claudine Junien

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  1. 1
    Nutritional Epigenomics of Metabolic Syndrome

    Nutritional Epigenomics of Metabolic Syndrome 由 Catherine Gallou‐Kabani, Claudine Junien

    出版 2005
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  2. 2
    Sexual dimorphism in environmental epigenetic programming

    Sexual dimorphism in environmental epigenetic programming 由 Anne Gabory, Linda Attig, Claudine Junien

    出版 2009
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  3. 3
    Developmental programming and epigenetics

    Developmental programming and epigenetics 由 Anne Gabory, Linda Attig, Claudine Junien

    出版 2011
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  4. 4
    Genetics of neonatal hyperinsulinism

    Genetics of neonatal hyperinsulinism 由 Benjamin Gläser, Paul Thornton, Timo Otonkoski, Claudine Junien

    出版 2000
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  5. 5
    Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism

    Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism 由 Anne Couturier‐Tarrade, Polina Panchenko, Claudine Junien, Anne Gabory

    出版 2015
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  6. 6
    Placental contribution to the origins of sexual dimorphism in health and diseases: sex chromosomes and epigenetics

    Placental contribution to the origins of sexual dimorphism in health and diseases: sex chromosomes and epigenetics 由 Anne Gabory, Tessa J. Roseboom, Tom Moore, Lorna G. Moore, Claudine Junien

    出版 2013
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  7. 7
    MSH2-Dependent Germinal CTG Repeat Expansions Are Produced Continuously in Spermatogonia from DM1 Transgenic Mice

    MSH2-Dependent Germinal CTG Repeat Expansions Are Produced Continuously in Spermatogonia from DM1 Transgenic Mice 由 Cédric Savouret, Corinne Cordier, Jérôme Mégret, Hein te Riele, Claudine Junien, Geneviève Gourdon

    出版 2003
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  8. 8
    CTG Trinucleotide Repeat “Big Jumps”: Large Expansions, Small Mice

    CTG Trinucleotide Repeat “Big Jumps”: Large Expansions, Small Mice 由 Mário Gomes-Pereira, Laurent Foiry, Annie Nicole, Aline Huguet, Claudine Junien, Arnold Münnich, Geneviève Gourdon

    出版 2007
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  9. 9
    Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (<i>PCSK9</i>) gene in cholesterol metabolism and disease

    Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (<i>PCSK9</i>) gene in cholesterol metabolism and disease 由 Marianne Abifadel, Jean‐Pierre Rabès, Martine Devillers, Arnold Münnich, D. Erlich, Claudine Junien, Mathilde Varret, Cathérine Boileau

    出版 2009
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  10. 10
    CTG repeat instability and size variation timing in DNA repair-deficient mice

    CTG repeat instability and size variation timing in DNA repair-deficient mice 由 Cédric Savouret, E Brisson, Jeroen Essers, Roland Kanaar, Albert Pastink, Hein te Riele, Claudine Junien, Geneviève Gourdon

    出版 2003
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  11. 11
    Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

    Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. 由 Isabelle Henry, S Grandjouan, P. Couillin, F. Barichard, Marc Jeanpierre, Thomas Gläser, Thierry Philip, Gilbert Lenoir, J. L. Chaussain, Claudine Junien

    出版 1989
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  12. 12
    Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice

    Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice 由 Polina Panchenko, Sarah Voisin, Mélanie Jouin, Luc Jouneau, Audrey Prézelin, Simon Lecoutre, Christophe Breton, Hélène Jammes, Claudine Junien, Anne Gabory

    出版 2016
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  13. 13
    The UMD-LDLR database: additions to the software and 490 new entries to the database

    The UMD-LDLR database: additions to the software and 490 new entries to the database 由 Ludovic Villéger, Marianne Abifadel, Delphine Allard, Jean‐Pierre Rabès, Rochelle Thiart, Maritha J. Kotze, Christophe Béroud, Claudine Junien, Cathérine Boileau, Mathilde Varret

    出版 2002
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  14. 14
    Depot- and sex-specific effects of maternal obesity in offspring’s adipose tissue

    Depot- and sex-specific effects of maternal obesity in offspring’s adipose tissue 由 Simon Lecoutre, Barbara Deracinois, Christine Laborie, Delphine Eberlé, Céline Guinez, Polina Panchenko, Jean Lésage, Didier Vieau, Claudine Junien, Anne Gabory, Christophe Breton

    出版 2016
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  15. 15
    Relationships Among Electrophysiological Findings and Clinical Status, Heart Function, and Extent of DNA Mutation in Myotonic Dystrophy

    Relationships Among Electrophysiological Findings and Clinical Status, Heart Function, and Extent of DNA Mutation in Myotonic Dystrophy 由 Arnaud Lazarus, J. Varin, Z. Ounnoughene, H. Radvanyi, Claudine Junien, Jöel Coste, P. Laforêt, B. Eymard, Henri Marc Bécane, Simon Weber, Denis Duboc

    出版 1999
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  16. 16
    Role for the Wilms tumor gene in genital development?

    Role for the Wilms tumor gene in genital development? 由 Veronica van Heyningen, Wendy A. Bickmore, Anne Seawright, Judy Fletcher, John Maule, G. Fekete, Manfred Gessler, G.A.P. Bruns, Marc Jeanpierre, Claudine Junien

    出版 1990
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  17. 17
    A second locus for Marfan syndrome maps to chromosome 3p24.2–p25

    A second locus for Marfan syndrome maps to chromosome 3p24.2–p25 由 Gwenaëlle Collod‐Béroud, Marie‐Claude Babron, Guillaume Jondeau, M Coulon, Jean Weissenbach, Olivier Dubourg, Jean‐Pierre Bourdarias, Catherine Bonaïti‐Pellié, Claudine Junien, Cathérine Boileau

    出版 1994
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  18. 18
    Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database

    Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Muta... 由 Marc Jeanpierre, Érick Denamur, Isabelle Henry, M.-O. Cabanis, Sandrine Luce, A Cécille, Jacques Élion, M. Peuchmaur, Chantal Loirat, Patrick Niaudet, Marie‐Claire Gubler, Claudine Junien

    出版 1998
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  19. 19
    Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.

    Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. 由 Virginie Verkarre, Jean‐Christophe Fournet, Pascale de Lonlay, M S Gross-Morand, Martine Devillers, Jacques Rahier, Françis Brunelle, J.J. Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien

    出版 1998
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  20. 20
    Dietary Alleviation of Maternal Obesity and Diabetes: Increased Resistance to Diet-Induced Obesity Transcriptional and Epigenetic Signatures

    Dietary Alleviation of Maternal Obesity and Diabetes: Increased Resistance to Diet-Induced Obesity Transcriptional and Epigenetic Signatures 由 Linda Attig, Alexandre Vigé, Anne Gabory, Moshen Karimi, Aurore A. Beauger, Marie‐Sylvie Gross, Anne Athias, Catherine Gallou‐Kabani, Philippe Gambert, Tomas J. Ekström, Jean-Philippe Jaı̈s, Claudine Junien

    出版 2013
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