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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

256 related items for PubMed ID: 7574457

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  • 3. PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus-Merzbacher disease.
    Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Kirkham D, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M.
    Glia; 2007 Mar; 55(4):341-51. PubMed ID: 17133418
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  • 5. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus.
    Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le Merrer M, Gil R, Boespflug-Tanguy O.
    Nat Genet; 1994 Mar; 6(3):257-62. PubMed ID: 8012387
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  • 7. A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease.
    Pratt VM, Trofatter JA, Schinzel A, Dlouhy SR, Conneally PM, Hodes ME.
    Am J Med Genet; 1991 Jan; 38(1):136-9. PubMed ID: 1707231
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  • 13. Pelizaeus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus.
    Pratt VM, Boyadjiev S, Green K, Hodes ME, Dlouhy SR.
    Am J Med Genet; 1995 Jul 31; 58(1):70-3. PubMed ID: 7573159
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  • 14. PLP/DM20 expression and turnover in a transgenic mouse model of Pelizaeus-Merzbacher disease.
    Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Iden DL, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M.
    Glia; 2010 Nov 01; 58(14):1727-38. PubMed ID: 20629189
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  • 17. DM20 mRNA splice product of the myelin proteolipid protein gene is expressed in the murine heart.
    Campagnoni CW, Garbay B, Micevych P, Pribyl T, Kampf K, Handley VW, Campagnoni AT.
    J Neurosci Res; 1992 Sep 01; 33(1):148-55. PubMed ID: 1280689
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