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Items: 1 to 20 of 151

2.

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.

J Neurochem. 2011 Nov;119(3):447-59. doi: 10.1111/j.1471-4159.2011.07423.x. Epub 2011 Sep 28.

3.

Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.

Poirier R, Jacquot S, Vaillend C, Soutthiphong AA, Libbey M, Davis S, Laroche S, Hanauer A, Welzl H, Lipp HP, Wolfer DP.

Behav Genet. 2007 Jan;37(1):31-50. Epub 2006 Oct 11.

PMID:
17033934
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.

Hum Genet. 2011 Mar;129(3):255-69. doi: 10.1007/s00439-010-0918-0. Epub 2010 Nov 30. Erratum in: Hum Genet. 2011 Mar;129(3):271. Sibillec, Jérémie [corrected to Sibille, Jérémie].

PMID:
21116650
5.

Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.

Delaunoy JP, Dubos A, Marques Pereira P, Hanauer A.

Clin Genet. 2006 Aug;70(2):161-6.

PMID:
16879200
6.

Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome.

Morice E, Farley S, Poirier R, Dallerac G, Chagneau C, Pannetier S, Hanauer A, Davis S, Vaillend C, Laroche S.

Neurobiol Dis. 2013 Oct;58:156-68. doi: 10.1016/j.nbd.2013.05.016. Epub 2013 Jun 3.

PMID:
23742761
7.

Coffin-Lowry syndrome: a role for RSK2 in mammalian neurogenesis.

Dugani CB, Paquin A, Kaplan DR, Miller FD.

Dev Biol. 2010 Nov 15;347(2):348-59. doi: 10.1016/j.ydbio.2010.08.035. Epub 2010 Sep 8.

8.

The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient.

Marques Pereira P, Heron D, Hanauer A.

Hum Genet. 2007 Dec;122(5):541-3. Epub 2007 Aug 24.

PMID:
17717706
9.

The Coffin-Lowry syndrome-associated protein RSK2 and neurosecretion.

Zeniou-Meyer M, Gambino F, Ammar MR, Humeau Y, Vitale N.

Cell Mol Neurobiol. 2010 Nov;30(8):1401-6. doi: 10.1007/s10571-010-9578-9. Review.

PMID:
21061166
10.

The RSK factors of activating the Ras/MAPK signaling cascade.

Carriere A, Ray H, Blenis J, Roux PP.

Front Biosci. 2008 May 1;13:4258-75. Review.

PMID:
18508509
11.

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.

Am J Hum Genet. 2002 Jun;70(6):1421-33. Epub 2002 Apr 25.

12.

RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes.

Nakamura M, Yamagata T, Mori M, Momoi MY.

Brain Dev. 2005 Mar;27(2):114-7.

PMID:
15668050
13.

Expression of the RSK2 gene during early human development.

Guimiot F, Delezoide AL, Hanauer A, Simonneau M.

Gene Expr Patterns. 2004 Jan;4(1):111-4.

PMID:
14678837
14.

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.

Hum Mutat. 2001 Feb;17(2):103-16.

PMID:
11180593
15.

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.

Am J Hum Genet. 1998 Dec;63(6):1631-40.

16.

Regulation and interaction of pp90(rsk) isoforms with mitogen-activated protein kinases.

Zhao Y, Bjorbaek C, Moller DE.

J Biol Chem. 1996 Nov 22;271(47):29773-9.

17.

Loss of the Coffin-Lowry syndrome-associated gene RSK2 alters ERK activity, synaptic function and axonal transport in Drosophila motoneurons.

Beck K, Ehmann N, Andlauer TF, Ljaschenko D, Strecker K, Fischer M, Kittel RJ, Raabe T.

Dis Model Mech. 2015 Nov;8(11):1389-400. doi: 10.1242/dmm.021246. Epub 2015 Sep 3.

18.

Activation of p90 Rsk1 is sufficient for differentiation of PC12 cells.

Silverman E, Frödin M, Gammeltoft S, Maller JL.

Mol Cell Biol. 2004 Dec;24(24):10573-83.

19.

P90 Ribosomal s6 kinase 2 negatively regulates axon growth in motoneurons.

Fischer M, Pereira PM, Holtmann B, Simon CM, Hanauer A, Heisenberg M, Sendtner M.

Mol Cell Neurosci. 2009 Oct;42(2):134-41. doi: 10.1016/j.mcn.2009.06.006. Epub 2009 Jun 22.

PMID:
19555761
20.

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.

PLoS One. 2014 Jan 8;9(1):e84343. doi: 10.1371/journal.pone.0084343. eCollection 2014.

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