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Items: 1 to 20 of 111

1.

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
2.

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
3.

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.

4.

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
6.

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
7.

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.

J Neurochem. 2008 Dec;107(5):1325-34. doi: 10.1111/j.1471-4159.2008.05703.x. Epub 2008 Sep 24.

8.

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
9.

p90 ribosomal S6 kinase 2 exerts a tonic brake on G protein-coupled receptor signaling.

Sheffler DJ, Kroeze WK, Garcia BG, Deutch AY, Hufeisen SJ, Leahy P, Brüning JC, Roth BL.

Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4717-22. Epub 2006 Mar 10.

10.

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.

11.

Coffin-Lowry syndrome.

Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A.

Eur J Hum Genet. 2010 Jun;18(6):627-33. doi: 10.1038/ejhg.2009.189. Epub 2009 Nov 4. Review.

12.

A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome.

Wang Y, Martinez JE, Wilson GL, He XY, Tuck-Muller CM, Maertens P, Wertelecki W, Chen TJ.

Am J Med Genet A. 2006 Jun 15;140(12):1274-9.

PMID:
16691578
13.

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.

Int J Mol Sci. 2013 Feb 6;14(2):3358-75. doi: 10.3390/ijms14023358.

14.

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
15.

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
16.
17.

Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation.

Field M, Tarpey P, Boyle J, Edkins S, Goodship J, Luo Y, Moon J, Teague J, Stratton MR, Futreal PA, Wooster R, Raymond FL, Turner G.

Clin Genet. 2006 Dec;70(6):509-15.

18.

The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid.

Ammar MR, Humeau Y, Hanauer A, Nieswandt B, Bader MF, Vitale N.

J Neurosci. 2013 Dec 11;33(50):19470-9. doi: 10.1523/JNEUROSCI.2283-13.2013.

19.

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
20.

Essential role of RSK2 in c-Fos-dependent osteosarcoma development.

David JP, Mehic D, Bakiri L, Schilling AF, Mandic V, Priemel M, Idarraga MH, Reschke MO, Hoffmann O, Amling M, Wagner EF.

J Clin Invest. 2005 Mar;115(3):664-72.

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