Hanauer A - Search Results

1

RSK2 is a modulator of craniofacial development.

Laugel-Haushalter V, Paschaki M, Marangoni P, Pilgram C, Langer A, Kuntz T, Demassue J, Morkmued S, Choquet P, Constantinesco A, Bornert F, Schmittbuhl M, Pannetier S, Viriot L, Hanauer A, Dollé P, Bloch-Zupan A. Laugel-Haushalter V, et al. Among authors: hanauer a. PLoS One. 2014 Jan 8;9(1):e84343. doi: 10.1371/journal.pone.0084343. eCollection 2014. PLoS One. 2014. PMID: 24416220 Free PMC article.

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: hanauer a. 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

Coffin-Lowry syndrome.

Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A. Pereira PM, et al. Among authors: hanauer a. 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.

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: hanauer a. 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

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: hanauer a. 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.

6

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: hanauer a. Neuropsychopharmacology. 2012 Apr;37(5):1288-96. doi: 10.1038/npp.2011.316. Epub 2012 Jan 4. Neuropsychopharmacology. 2012. PMID: 22218090 Free PMC article.

7

Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2.

Mehmood T, Schneider A, Pannetier S, Hanauer A. Mehmood T, et al. Among authors: hanauer a. Int J Mol Sci. 2013 Feb 6;14(2):3358-75. doi: 10.3390/ijms14023358. Int J Mol Sci. 2013. PMID: 23389038 Free PMC article.

8

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: hanauer a. Hum Genet. 2011 Mar;129(3):255-69. doi: 10.1007/s00439-010-0918-0. Epub 2010 Nov 30. Hum Genet. 2011. PMID: 21116650

9

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: hanauer a. Am J Hum Genet. 1998 Dec;63(6):1631-40. doi: 10.1086/302153. Am J Hum Genet. 1998. PMID: 9837815 Free PMC article.

10

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: hanauer a. 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

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