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	1.	Hyperghrelinemia is a common feature of Prader-Willi syndrome and pituitary stalk interruption: a pathophysiological hypothesis. [electronic resource] by Tauber, Maithé Conte Auriol, Françoise Moulin, Pierre Molinas, Catherine Delagnes, Véronique Salles, Jean Pierre Producer: 20041221 In: Hormone research vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Bone defects in LPA receptor genetically modified mice. [electronic resource] by Salles, Jean Pierre Laurencin-Dalicieux, Sara Conte-Auriol, Françoise Briand-Mésange, Fabienne Gennero, Isabelle Producer: 20130612 In: Biochimica et biophysica acta vol. 1831 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Hyperghrelinemia precedes obesity in Prader-Willi syndrome. [electronic resource] by Feigerlová, Eva Diene, Gwenaëlle Conte-Auriol, Françoise Molinas, Catherine Gennero, Isabelle Salles, Jean-Pierre Arnaud, Catherine Tauber, Maïthé Producer: 20080821 In: The Journal of clinical endocrinology and metabolism vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice. [electronic resource] by Touvier, Thierry Conte-Auriol, Françoise Briand, Olivier Cudejko, Céline Paumelle, Réjane Caron, Sandrine Baugé, Eric Rouillé, Yves Salles, Jean-Pierre Staels, Bart Bailleul, Bernard Producer: 20100111 In: The Journal of clinical investigation vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype. [electronic resource] by Haine, Elsa Salles, Jean-Pierre Khau Van Kien, Philippe Conte-Auriol, Françoise Gennero, Isabelle Plancke, Aurélie Julia, Sophie Dulac, Yves Tauber, Maithé Edouard, Thomas Producer: 20160516 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome. [electronic resource] by Bieth, Eric Eddiry, Sanaa Gaston, Véronique Lorenzini, Françoise Buffet, Alexandre Conte Auriol, Françoise Molinas, Catherine Cailley, Dorothée Rooryck, Caroline Arveiler, Benoit Cavaillé, Jérome Salles, Jean Pierre Tauber, Maïthé Producer: 20150929 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Human dental follicle cells acquire cementoblast features under stimulation by BMP-2/-7 and enamel matrix derivatives (EMD) in vitro. [electronic resource] by Kémoun, Philippe Laurencin-Dalicieux, Sara Rue, Jacqueline Farges, Jean-Christophe Gennero, Isabelle Conte-Auriol, Françoise Briand-Mesange, Fabienne Gadelorge, Mélanie Arzate, Higinio Narayanan, A Sampath Brunel, Gérard Salles, Jean-Pierre Producer: 20071213 In: Cell and tissue research vol. 329 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Functional effects of PTPN11 (SHP2) mutations causing LEOPARD syndrome on epidermal growth factor-induced phosphoinositide 3-kinase/AKT/glycogen synthase kinase 3beta signaling. [electronic resource] by Edouard, Thomas Combier, Jean-Philippe Nédélec, Audrey Bel-Vialar, Sophie Métrich, Mélanie Conte-Auriol, Francoise Lyonnet, Stanislas Parfait, Béatrice Tauber, Maithé Salles, Jean-Pierre Lezoualc'h, Frank Yart, Armelle Raynal, Patrick Producer: 20100602 In: Molecular and cellular biology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass. [electronic resource] by Gennero, Isabelle Laurencin-Dalicieux, Sara Conte-Auriol, Françoise Briand-Mésange, Fabienne Laurencin, Danielle Rue, Jackie Beton, Nicolas Malet, Nicole Mus, Marianne Tokumura, Akira Bourin, Philippe Vico, Laurence Brunel, Gérard Oreffo, Richard O C Chun, Jerold Salles, Jean Pierre Producer: 20120213 In: Bone vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)