Search Results - "Lee, Simon P"

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    Glutathione S-Transferase M1 and P1 Genotype, Passive Smoking, and Peak Expiratory Flow in Asthma by Palmer, Colin N.A, Doney, Alex S.F, Lee, Simon P, Murrie, Inez, Ismail, Tahmina, Macgregor, Donald F, Mukhopadhyay, Somnath

    Published in Pediatrics (Evanston) (01-08-2006)
    “…Our purpose with this work was to assess the contribution of glutathione S-transferase gene variants to asthma susceptibility and pulmonary function in…”
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    Journal Article
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    Loss-of-function Variants of the Filaggrin Gene are Associated with Atopic Eczema and Associated Phenotypes in Swedish Families by EKELUND, Elisabeth, LIEDEN, Agne, LINK, Jenny, LEE, Simon P, D'AMATO, Mauro, PALMER, Colin N. A, KOCKUM, Ingrid, BRADLEY, Maria

    Published in Acta dermato-venereologica (2008)
    “…Recent studies have identified 2 loss-of-function variants, R501X and 2282del4, in the filaggrin gene as predisposing factors in the development of eczema. In…”
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    Journal Article
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    A Discussion on the Impact of CFC12 Emission Rate from XPS Insulation on Atmospheric Banks by Paquet, Andrew N., Mutton, John, Lee, Simon P.

    Published in Journal of cellular plastics (01-01-2010)
    “…This report presents new information regarding emissions of CFC12 used to make extruded polystyrene foam products. Earlier reports identified a significant…”
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    Global Atmospheric Emissions Model of HCFC142b with Respect to Extruded Polystyrene Foam Applications by Paquet, Andrew N., Mutton, John, Lee, Simon P.

    Published in Journal of cellular plastics (01-05-2009)
    “…This paper will address significant issues related to discrepancies between the atmospheric measurements of HCFC142b and estimated emissions from production…”
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    Journal Article
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    Association of common variation in the PPARA gene with incident myocardial infarction in individuals with type 2 diabetes: a Go-DARTS study by Doney, Alex S F, Fischer, Bettina, Lee, Simon P, Morris, Andrew D, Leese, Graham, Palmer, Colin N A

    Published in Nuclear receptor (25-11-2005)
    “…Common variants of the PPARA gene have been found to associate with ischaemic heart disease in non diabetic men. The L162V variant was found to be protective…”
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