BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 20832397)

  • 1. Coffin-Lowry syndrome: a role for RSK2 in mammalian neurogenesis.
    Dugani CB; Paquin A; Kaplan DR; Miller FD
    Dev Biol; 2010 Nov; 347(2):348-59. PubMed ID: 20832397
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 21838783
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 16879200
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 17033934
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 23742761
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 15668050
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome.
    Castillon C; Lunion S; Desvignes N; Hanauer A; Laroche S; Poirier R
    Neurobiol Dis; 2018 Jul; 115():69-81. PubMed ID: 29627578
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contrasting roles of neuronal Msk1 and Rsk2 in Bad phosphorylation and feedback regulation of Erk signalling.
    Clark CJ; McDade DM; O'Shaughnessy CT; Morris BJ
    J Neurochem; 2007 Aug; 102(4):1024-34. PubMed ID: 17663748
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 19555761
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.
    Zeniou M; Gattoni R; Hanauer A; Stévenin J
    Nucleic Acids Res; 2004; 32(3):1214-23. PubMed ID: 14973203
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-linked Coffin-Lowry syndrome (CLS, MIM 303600, RPS6KA3 gene, protein product known under various names: pp90(rsk2), RSK2, ISPK, MAPKAP1).
    Jacquot S; Zeniou M; Touraine R; Hanauer A
    Eur J Hum Genet; 2002 Jan; 10(1):2-5. PubMed ID: 11896450
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rsk2, the Kinase Mutated in Coffin-Lowry Syndrome, Controls Cementum Formation.
    Koehne T; Jeschke A; Petermann F; Seitz S; Neven M; Peters S; Luther J; Schweizer M; Schinke T; Kahl-Nieke B; Amling M; David JP
    J Dent Res; 2016 Jul; 95(7):752-60. PubMed ID: 26927527
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stimulus-induced drop episodes in Coffin-Lowry syndrome.
    Hahn JS; Hanauer A
    Eur J Med Genet; 2012 May; 55(5):335-7. PubMed ID: 22490425
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The historical Coffin-Lowry syndrome family revisited: identification of two novel mutations of RPS6KA3 in three male patients.
    Nishimoto HK; Ha K; Jones JR; Dwivedi A; Cho HM; Layman LC; Kim HG
    Am J Med Genet A; 2014 Sep; 164A(9):2172-9. PubMed ID: 25044551
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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. PubMed ID: 17717706
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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. PubMed ID: 11180593
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning.
    Zeniou M; Ding T; Trivier E; Hanauer A
    Hum Mol Genet; 2002 Nov; 11(23):2929-40. PubMed ID: 12393804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 21116650
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Coffin-Lowry syndrome-associated protein RSK2 controls neuroendocrine secretion through the regulation of phospholipase D1 at the exocytotic sites.
    Zeniou-Meyer M; Béglé A; Bader MF; Vitale N
    Ann N Y Acad Sci; 2009 Jan; 1152():201-8. PubMed ID: 19161391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-application of NMDA and dopamine-induced rapid translation of RSK2 in the mature hippocampus.
    Kaphzan H; Doron G; Rosenblum K
    J Neurochem; 2007 Oct; 103(1):388-99. PubMed ID: 17645456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.