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    Article

    Genetic Background Influences UPR but not PLP Processing in the rumpshaker Model of PMD/SPG2

    Mutations of the proteolipid protein gene (PLP1) cause Pelizaeus-Merzbacher disease (PMD) and Spastic paraplegia type 2 (SPG2). The rumpshaker mutation is associated with mild forms of PMD or SPG2 in man and the ...

    M. McLaughlin, S. A. Karim, P. Montague, J. A. Barrie, D. Kirkham… in Neurochemical Research (2007)

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    Article

    Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene

    The PLP1/Plp gene encodes proteolipid protein (PLP) and DM20, the major central nervous system myelin proteins. Mutations in the PLP1/Plp gene cause dysmyelinating disorders in man and animals. The rumpshaker mut...

    J. M. Edgar, M. McLaughlin, J. A. Barrie, M. C. McCulloch… in Acta Neuropathologica (2004)

  3. Article

    Erratum: Association between variants at the GABAAβ2, GABAAα6 and GABAAγ2 gene cluster and alcohol dependence in a Scottish population

    The sentence on page 540 of this article ‘A silent exonic gCt → gTt substitution (Ala → Ala) at nucleotide 1412 was found by SSCP analysis’ is incorrect. The correct sentence should read ‘A silent exonic GCT →...

    E-W Loh, I Smith, R Murray, M McLaughlin, S McNulty, D Ball in Molecular Psychiatry (2000)

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    Article

    Association between variants at the GABAAβ2, GABAAα6 and GABAAγ2 gene cluster and alcohol dependence in a Scottish population

    A role for the GABA/benzodiazepine receptor complex in alcohol dependence syndrome has been suggested by several lines of evidence. To elucidate the role of GABAA subunits in human alcohol dependence syndrome, we...

    E-W Loh, I Smith, R Murray, M McLaughlin, S McNulty, D Ball in Molecular Psychiatry (1999)