LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice

Por Touvier, Thierry, Conte-Auriol, Françoise, Briand, Olivier, Cudejko, Céline, Paumelle, Réjane, Caron, Sandrine, Baugé, Eric, Rouillé, Yves, Salles, Jean-Pierre, Staels, Bart, Bailleul, Bernard
Publicado em 2009

Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Por 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
Publicado no Eur J Hum Genet (2015)

Functional Effects of PTPN11 (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling

Por 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
Publicado em 2010

Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass(,)

Por 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
Publicado em 2011