V
Véronique Fauveau
Researcher at French Institute of Health and Medical Research
Publications - 16
Citations - 1639
Véronique Fauveau is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Insulin resistance & Insulin receptor. The author has an hindex of 13, co-authored 15 publications receiving 1476 citations. Previous affiliations of Véronique Fauveau include Paris Descartes University & Centre national de la recherche scientifique.
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Journal ArticleDOI
Hepatic glucokinase is required for the synergistic action of ChREBP and SREBP-1c on glycolytic and lipogenic gene expression.
Renaud Dentin,Jean-Paul Pégorier,Fadila Benhamed,Fabienne Foufelle,Pascal Ferré,Véronique Fauveau,Mark A. Magnuson,Jean Girard,Catherine Postic +8 more
TL;DR: It is demonstrated that in hGK-KO hepatocytes overexpressing SREBP-1c, the effect of glucose on glycolytic and lipogenic genes is lost because of the impaired ability of these hepatocytes to efficiently metabolize glucose, despite a marked increase in low Km hexokinase activity.
Journal ArticleDOI
Liver-Specific Inhibition of ChREBP Improves Hepatic Steatosis and Insulin Resistance in ob/ob Mice
Renaud Dentin,Fadila Benhamed,Isabelle Hainault,Véronique Fauveau,Fabienne Foufelle,Jason R.B. Dyck,Jean Girard,Catherine Postic +7 more
TL;DR: It is demonstrated that ChREBP is central for the regulation of lipogenesis in vivo and plays a determinant role in the development of the hepatic steatosis and of insulin resistance in ob/ob mice.
Journal ArticleDOI
Intestinal Gluconeogenesis Is a Key Factor for Early Metabolic Changes after Gastric Bypass but Not after Gastric Lap-Band in Mice
Stéphanie Troy,Maud Soty,Maud Soty,Lara Ribeiro,Laure Laval,Laure Laval,Stéphanie Migrenne,Xavier Fioramonti,Bruno Pillot,Bruno Pillot,Véronique Fauveau,Roberte Aubert,Benoit Viollet,Benoit Viollet,Marc Foretz,Marc Foretz,Jocelyne Leclerc,Jocelyne Leclerc,A. Duchampt,A. Duchampt,Carine Zitoun,Carine Zitoun,Bernard Thorens,Christophe Magnan,Gilles Mithieux,Gilles Mithieux,Fabrizio Andreelli +26 more
TL;DR: Mechanistic evidence is provided that the beneficial effects of the EGA procedure on food intake and glucose homeostasis involve intestinal gluconeogenesis and its detection via a GLUT-2 and hepatoportal sensor pathway.
Journal ArticleDOI
Diet and Gastrointestinal Bypass-Induced Weight Loss The Roles of Ghrelin and Peptide YY
Keval Chandarana,Cigdem Gelegen,Efthimia Karra,Agharul I. Choudhury,Megan E. Drew,Véronique Fauveau,Benoit Viollet,Fabrizio Andreelli,Dominic J. Withers,Rachel L. Batterham +9 more
TL;DR: PYY plays a key role in mediating the early weight loss observed post-GIBP, whereas relative PYY deficiency during dieting may compromise weight-loss attempts.
Journal ArticleDOI
A Specific ChREBP and PPARα Cross-Talk Is Required for the Glucose-Mediated FGF21 Response
Alison Iroz,Alison Iroz,Alison Iroz,Alexandra Montagner,Fadila Benhamed,Fadila Benhamed,Fadila Benhamed,Françoise Levavasseur,Françoise Levavasseur,Françoise Levavasseur,Arnaud Polizzi,Elodie Anthony,Elodie Anthony,Elodie Anthony,Marion Régnier,Edwin Fouché,Céline Lukowicz,Michele Cauzac,Michele Cauzac,Michele Cauzac,Emilie Tournier,Emilie Tournier,Emilie Tournier,Marcio Do-Cruzeiro,Marcio Do-Cruzeiro,Marcio Do-Cruzeiro,Martine Daujat-Chavanieu,Martine Daujat-Chavanieu,Sabine Gerbal-Chalouin,Sabine Gerbal-Chalouin,Véronique Fauveau,Véronique Fauveau,Véronique Fauveau,Solenne Marmier,Solenne Marmier,Solenne Marmier,Anne-Françoise Burnol,Anne-Françoise Burnol,Anne-Françoise Burnol,Sandra Guilmeau,Sandra Guilmeau,Sandra Guilmeau,Yannick Lippi,Jean Girard,Jean Girard,Jean Girard,Walter Wahli,Walter Wahli,Walter Wahli,Renaud Dentin,Renaud Dentin,Renaud Dentin,Hervé Guillou,Catherine Postic,Catherine Postic,Catherine Postic +55 more
TL;DR: It is reported that peroxisome-proliferator-activated receptor α (PPARα), a nuclear receptor of the fasting response, is required with the carbohydrate-sensitive transcription factor carbohydrate-responsive element-binding protein (ChREBP) to balance FGF21 glucose response.