Výsledky vyhledávání - Claudine Junien
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Nutritional Epigenomics of Metabolic Syndrome Autor Catherine Gallou‐Kabani, Claudine Junien
Vydáno 2005Revisão -
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Sexual dimorphism in environmental epigenetic programming Autor Anne Gabory, Linda Attig, Claudine Junien
Vydáno 2009Revisão -
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Developmental programming and epigenetics Autor Anne Gabory, Linda Attig, Claudine Junien
Vydáno 2011Revisão -
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Genetics of neonatal hyperinsulinism Autor Benjamin Gläser, Paul Thornton, Timo Otonkoski, Claudine Junien
Vydáno 2000Revisão -
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Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (<i>PCSK9</i>) gene in cholesterol metabolism and disease Autor Marianne Abifadel, Jean‐Pierre Rabès, Martine Devillers, Arnold Münnich, D. Erlich, Claudine Junien, Mathilde Varret, Cathérine Boileau
Vydáno 2009Revisão -
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Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. Autor Isabelle Henry, S Grandjouan, P. Couillin, F. Barichard, Marc Jeanpierre, Thomas Gläser, Thierry Philip, Gilbert Lenoir, J. L. Chaussain, Claudine Junien
Vydáno 1989Artigo -
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Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice Autor Polina Panchenko, Sarah Voisin, Mélanie Jouin, Luc Jouneau, Audrey Prézelin, Simon Lecoutre, Christophe Breton, Hélène Jammes, Claudine Junien, Anne Gabory
Vydáno 2016Artigo -
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The UMD-LDLR database: additions to the software and 490 new entries to the database Autor Ludovic Villéger, Marianne Abifadel, Delphine Allard, Jean‐Pierre Rabès, Rochelle Thiart, Maritha J. Kotze, Christophe Béroud, Claudine Junien, Cathérine Boileau, Mathilde Varret
Vydáno 2002Revisão -
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Depot- and sex-specific effects of maternal obesity in offspring’s adipose tissue Autor Simon Lecoutre, Barbara Deracinois, Christine Laborie, Delphine Eberlé, Céline Guinez, Polina Panchenko, Jean Lésage, Didier Vieau, Claudine Junien, Anne Gabory, Christophe Breton
Vydáno 2016Artigo -
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Relationships Among Electrophysiological Findings and Clinical Status, Heart Function, and Extent of DNA Mutation in Myotonic Dystrophy Autor Arnaud Lazarus, J. Varin, Z. Ounnoughene, H. Radvanyi, Claudine Junien, Jöel Coste, P. Laforêt, B. Eymard, Henri Marc Bécane, Simon Weber, Denis Duboc
Vydáno 1999Artigo -
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A second locus for Marfan syndrome maps to chromosome 3p24.2–p25 Autor Gwenaëlle Collod‐Béroud, Marie‐Claude Babron, Guillaume Jondeau, M Coulon, Jean Weissenbach, Olivier Dubourg, Jean‐Pierre Bourdarias, Catherine Bonaïti‐Pellié, Claudine Junien, Cathérine Boileau
Vydáno 1994Artigo -
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Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Muta... Autor 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
Vydáno 1998Artigo -
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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. Autor 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
Vydáno 1998Artigo -
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Dietary Alleviation of Maternal Obesity and Diabetes: Increased Resistance to Diet-Induced Obesity Transcriptional and Epigenetic Signatures Autor 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
Vydáno 2013Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Endocrinology
Internal medicine
Mutation
DNA methylation
Gene expression
Epigenetics
Pregnancy
Phenotype
Bioinformatics
Computational biology
Disease
Genomic imprinting
Insulin resistance
Offspring
Cholesterol
Computer science
Hyperinsulinemic hypoglycemia
Hypoglycemia
Insulin
LDL receptor
Lipoprotein
Allele
Fibrillin
Genotype
Missense mutation
Myotonic dystrophy