Pannetier S - Search Results

1

Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation.

Dubos A, Pannetier S, Hanauer A. Dubos A, et al. Among authors: pannetier s. Am J Med Genet A. 2008 May 15;146A(10):1267-79. doi: 10.1002/ajmg.a.32274. Am J Med Genet A. 2008. PMID: 18412109

2

Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome.

Zeniou M, Pannetier S, Fryns JP, Hanauer A. Zeniou M, et al. Among authors: pannetier s. Am J Hum Genet. 2002 Jun;70(6):1421-33. doi: 10.1086/340607. Epub 2002 Apr 25. Am J Hum Genet. 2002. PMID: 11992250 Free PMC article.

3

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome.

Mehmood T, Schneider A, Sibille J, Marques Pereira P, Pannetier S, Ammar MR, Dembele D, Thibault-Carpentier C, Rouach N, Hanauer A. Mehmood T, et al. Among authors: pannetier s. Hum Genet. 2011 Mar;129(3):255-69. doi: 10.1007/s00439-010-0918-0. Epub 2010 Nov 30. Hum Genet. 2011. PMID: 21116650

4

Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin-Lowry syndrome.

Schneider A, Mehmood T, Pannetier S, Hanauer A. Schneider A, et al. Among authors: pannetier s. J Neurochem. 2011 Nov;119(3):447-59. doi: 10.1111/j.1471-4159.2011.07423.x. Epub 2011 Sep 28. J Neurochem. 2011. PMID: 21838783 Free article.

5

Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome.

Trivier E, De Cesare D, Jacquot S, Pannetier S, Zackai E, Young I, Mandel JL, Sassone-Corsi P, Hanauer A. Trivier E, et al. Among authors: pannetier s. Nature. 1996 Dec 12;384(6609):567-70. doi: 10.1038/384567a0. Nature. 1996. PMID: 8955270

6

Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome.

Merienne K, Jacquot S, Trivier E, Pannetier S, Rossi A, Scott C, Schinzel A, Castellan C, Kress W, Hanauer A. Merienne K, et al. Among authors: pannetier s. J Med Genet. 1998 Nov;35(11):890-4. doi: 10.1136/jmg.35.11.890. J Med Genet. 1998. PMID: 9832033 Free PMC article.

7

Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations.

Jacquot S, Merienne K, De Cesare D, Pannetier S, Mandel JL, Sassone-Corsi P, Hanauer A. Jacquot S, et al. Among authors: pannetier s. Am J Hum Genet. 1998 Dec;63(6):1631-40. doi: 10.1086/302153. Am J Hum Genet. 1998. PMID: 9837815 Free PMC article.

8

Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome.

Marques Pereira P, Gruss M, Braun K, Foos N, Pannetier S, Hanauer A. Marques Pereira P, et al. Among authors: pannetier s. J Neurochem. 2008 Dec;107(5):1325-34. doi: 10.1111/j.1471-4159.2008.05703.x. Epub 2008 Sep 24. J Neurochem. 2008. PMID: 18823370 Free article.

9

Coffin-Lowry syndrome.

Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A. Pereira PM, et al. Among authors: pannetier s. Eur J Hum Genet. 2010 Jun;18(6):627-33. doi: 10.1038/ejhg.2009.189. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888300 Free PMC article. Review.

10

RSK2 signaling in medial habenula contributes to acute morphine analgesia.

Darcq E, Befort K, Koebel P, Pannetier S, Mahoney MK, Gaveriaux-Ruff C, Hanauer A, Kieffer BL. Darcq E, et al. Among authors: pannetier s. Neuropsychopharmacology. 2012 Apr;37(5):1288-96. doi: 10.1038/npp.2011.316. Epub 2012 Jan 4. Neuropsychopharmacology. 2012. PMID: 22218090 Free PMC article.

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