These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

160 related items for PubMed ID: 21061166

  • 1. 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. PubMed ID: 21061166
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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. PubMed ID: 26398944
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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. PubMed ID: 24336713
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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 01; 11(23):2929-40. PubMed ID: 12393804
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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 01; 10(1):2-5. PubMed ID: 11896450
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 70(6):509-15. PubMed ID: 17100996
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.