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Journal Abstract Search

143 related items for PubMed ID: 20832397

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  • 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
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  • 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
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  • 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 Oct; 32(3):1214-23. PubMed ID: 14973203
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  • 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
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  • 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
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