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Functional effects of PTPN11 (SHP2) mutations causing LEOPARD syndrome on epidermal growth factor-induced phosphoinositide 3-kinase/AKT/glycogen synthase kinase 3beta signaling.
Edouard T, Combier JP, Nédélec A, Bel-Vialar S, Métrich M, Conte-Auriol F, Lyonnet S, Parfait B, Tauber M, Salles JP, Lezoualc'h F, Yart A, Raynal P. Edouard T, et al. Among authors: conte auriol f. Mol Cell Biol. 2010 May;30(10):2498-507. doi: 10.1128/MCB.00646-09. Epub 2010 Mar 22. Mol Cell Biol. 2010. PMID: 20308328 Free PMC article.
[New molecular mechanisms of growth hormone insensitivity].
Edouard T, Raynal P, Yart A, Conte-Auriol F, Salles JP, Tauber M. Edouard T, et al. Arch Pediatr. 2008 Feb;15(2):179-88. doi: 10.1016/j.arcped.2007.10.023. Epub 2008 Jan 18. Arch Pediatr. 2008. PMID: 18207712 Review. French.
[Osteogenesis factors in childhood].
Salles JP, Gennero I, Moulin P, Conte-Auriol F, Edouard T, Tauber M. Salles JP, et al. Arch Pediatr. 2009 Jun;16(6):611-3. doi: 10.1016/S0929-693X(09)74086-2. Arch Pediatr. 2009. PMID: 19541104 French. No abstract available.
[Translational studies in children].
Salles JP, Edouard T, Gouze JN, Conte-Auriol F, Molinas-Casals C, Raynal P, Yart A, Tauber M, Gouze E. Salles JP, et al. Arch Pediatr. 2009 Jun;16(6):664-6. doi: 10.1016/S0929-693X(09)74104-1. Arch Pediatr. 2009. PMID: 19541122 French. No abstract available.
Hyperghrelinemia precedes obesity in Prader-Willi syndrome.
Feigerlová E, Diene G, Conte-Auriol F, Molinas C, Gennero I, Salles JP, Arnaud C, Tauber M. Feigerlová E, et al. J Clin Endocrinol Metab. 2008 Jul;93(7):2800-5. doi: 10.1210/jc.2007-2138. Epub 2008 May 6. J Clin Endocrinol Metab. 2008. PMID: 18460565
Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Bieth E, Eddiry S, Gaston V, Lorenzini F, Buffet A, Conte Auriol F, Molinas C, Cailley D, Rooryck C, Arveiler B, Cavaillé J, Salles JP, Tauber M. Bieth E, et al. Among authors: conte auriol f. Eur J Hum Genet. 2015 Feb;23(2):252-5. doi: 10.1038/ejhg.2014.103. Epub 2014 Jun 11. Eur J Hum Genet. 2015. PMID: 24916642 Free PMC article.
19 results