F. Conte-Auriol

Hôpital des Enfants — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index822citations20works0.02yr avg
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Research Topics

Genetic Syndromes and Imprinting(4), Growth Hormone and Insulin-like Growth Factors(3), Prenatal Screening and Diagnostics(3), Bone health and treatments(3), Protein Tyrosine Phosphatases(3)

Publications20 total

The ANTENATAL multicentre study to predict postnatal renal outcome in fetuses with posterior urethral valves: objectives and design
Clinical Kidney Journal·2019· 33 citedOpen Access
Laboratory diagnosis of hypophosphatasia
Archives de Pédiatrie·2017· 14 cited
Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and <i>FBN1</i> Genotype
Journal of Bone and Mineral Research·2015· 36 citedOpen Access
Impairment of adipose tissue in Prader–Willi syndrome rescued by growth hormone treatment
International Journal of Obesity·2014· 34 citedOpen Access
Lysophosphatidic Acid (LPA) Signaling and Bone
2013
Bone defects in LPA receptor genetically modified mice
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids·2012· 15 cited
Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass
Bone·2011· 73 citedOpen Access
R39: Impact des mutations de PTPN11 (SHP2) responsables du syndrome LEOPARD sur la signalisation PI3K/Akt/GSK-3beta induite par l’epidermal growth factor (EGF) : implication dans la tumorogenèse ?
Bulletin du Cancer·2010
Functional Effects of <i>PTPN11</i> (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling
Molecular and Cellular Biology·2010· 102 citedOpen Access
LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice
Journal of Clinical Investigation·2009· 55 citedOpen Access
Facteurs de l’ostéogenèse chez l’enfant
Archives de Pédiatrie·2009
Approches translationnelles chez l’enfant
Archives de Pédiatrie·2009
Hyperghrelinemia Precedes Obesity in Prader-Willi Syndrome
The Journal of Clinical Endocrinology & Metabolism·2008· 137 citedOpen Access
CO57 - OB-RGRP, une protéine qui réduit la sensibilité à l’hormone de croissance en modulant l’expression du récepteur à l’hormone de croissance à la membrane plasmique
Journal of Minimally Invasive Gynecology·2008
Nouveaux mécanismes moléculaires impliqués dans l’insensibilité à l’hormone de croissance
Archives de Pédiatrie·2008· 6 cited
Localization of STRO-1, BMP-2/-3/-7, BMP receptors and phosphorylated Smad-1 during the formation of mouse periodontium
Tissue and Cell·2007· 54 cited
Human dental follicle cells acquire cementoblast features under stimulation by BMP-2/-7 and enamel matrix derivatives (EMD) in vitro
Cell and Tissue Research·2007· 255 cited
Bone mineral density assessment in patients with Pader–Willi syndrome
Bone·2007· 1 cited
FGF 23 et phosphatémie
Immuno-analyse & Biologie Spécialisée·2005· 1 cited
Métabolisme minéral osseux: données récentes et perspectives relatives à l’ostéogenèse
Archives de Pédiatrie·2004· 6 cited

Frequent Co-authors

Jean‐Pierre Salles(18), Isabelle Gennero(10), Thomas Édouard(7), Sara Laurencin‐Dalicieux(5), Fabienne Briand‐Mésange(5), M. Tauber(5), Armelle Yart(4), Patrick Raynal(4), P. Moulin(4), M. Tauber(4), G Brunel(3), Gwénaëlle Diene(3), Philippe Kémoun(2), Jacqueline Rue(2), Jean‐Christophe Farges(2), Higinio Arzate(2), Catherine Molinas(2), Mélanie Metrich(2), Stanislas Lyonnet(2), Thierry Touvier(2)