Pannetier S - Search Results

1

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.

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

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.

4

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

5

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.

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

Germline mosaicism in Coffin-Lowry syndrome.

Jacquot S, Merienne K, Pannetier S, Blumenfeld S, Schinzel A, Hanauer A. Jacquot S, et al. Among authors: pannetier s. Eur J Hum Genet. 1998 Nov-Dec;6(6):578-82. doi: 10.1038/sj.ejhg.5200230. Eur J Hum Genet. 1998. PMID: 9887375

9

Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.

Delaunoy J, Abidi F, Zeniou M, Jacquot S, Merienne K, Pannetier S, Schmitt M, Schwartz C, Hanauer A. Delaunoy J, et al. Among authors: pannetier s. Hum Mutat. 2001 Feb;17(2):103-16. doi: 10.1002/1098-1004(200102)17:2<103::AID-HUMU2>3.0.CO;2-N. Hum Mutat. 2001. PMID: 11180593

10

RSK2 signaling in brain habenula contributes to place aversion learning.

Darcq E, Koebel P, Del Boca C, Pannetier S, Kirstetter AS, Garnier JM, Hanauer A, Befort K, Kieffer BL. Darcq E, et al. Among authors: pannetier s. Learn Mem. 2011 Aug 18;18(9):574-8. doi: 10.1101/lm.2221011. Print 2011 Sep. Learn Mem. 2011. PMID: 21852432 Free PMC article.

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