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Author Report for: Stalenhoef AF

No contact information in database for Stalenhoef AF




    Title: The expression of type III hyperlipoproteinemia: involvement of lipolysis genes
    Henneman P, van der Sman-de Beer F, Moghaddam PH, Huijts P, Stalenhoef AF, Kastelein JJ, van Duijn CM, Havekes LM, Frants RR and Smelt AH <1 more author(s)>
    Ref: Eur J Hum Genet, 17:620, 2009 : PubMed

            

    Title: Paraoxonase (PON1) and the risk for coronary heart disease and myocardial infarction in a general population of Dutch women
    van Himbergen TM, van der Schouw YT, Voorbij HA, van Tits LJ, Stalenhoef AF, Peeters PH, Roest M
    Ref: Atherosclerosis, 199:408, 2008 : PubMed

            

    Title: Paraoxonase (PON1) is associated with familial combined hyperlipidemia
    van Himbergen TM, van Tits LJ, Ter Avest E, Roest M, Voorbij HA, de Graaf J, Stalenhoef AF
    Ref: Atherosclerosis, 199:87, 2008 : PubMed

            

    Title: The story of PON1: how an organophosphate-hydrolysing enzyme is becoming a player in cardiovascular medicine
    van Himbergen TM, van Tits LJ, Roest M, Stalenhoef AF
    Ref: Neth J Med, 64:34, 2006 : PubMed

            

    Title: Proportion of oxidized LDL relative to plasma apolipoprotein B does not change during statin therapy in patients with heterozygous familial hypercholesterolemia
    van Tits LJ, van Himbergen TM, Lemmers HL, de Graaf J, Stalenhoef AF
    Ref: Atherosclerosis, 185:307, 2006 : PubMed

            

    Title: Indications that paraoxonase-1 contributes to plasma high density lipoprotein levels in familial hypercholesterolemia
    van Himbergen TM, Roest M, de Graaf J, Jansen EH, Hattori H, Kastelein JJ, Voorbij HA, Stalenhoef AF, van Tits LJ
    Ref: J Lipid Res, 46:445, 2005 : PubMed

            

    Title: Paraoxonase-1 and linoleic acid oxidation in familial hypercholesterolemia
    van Himbergen TM, van Tits LJ, Hectors MP, de Graaf J, Roest M, Stalenhoef AF
    Ref: Biochemical & Biophysical Research Communications, 333:787, 2005 : PubMed

            

    Title: The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia
    Hoffer MJ, Snieder H, Bredie SJ, Demacker PN, Kastelein JJ, Frants RR, Stalenhoef AF
    Ref: Atherosclerosis, 151:443, 2000 : PubMed

            

    Title: Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia
    Hoffer MJ, Bredie SJ, Snieder H, Reymer PW, Demacker PN, Havekes LM, Boomsma DI, Stalenhoef AF, Frants RR, Kastelein JJ
    Ref: Atherosclerosis, 138:91, 1998 : PubMed

            

    Title: Two novel molecular defects in the LCAT gene are associated with fish eye disease
    Kuivenhoven JA, Stalenhoef AF, Hill JS, Demacker PN, Errami A, Kastelein JJ, Pritchard PH
    Ref: Arterioscler Thromb Vasc Biol, 16:294, 1996 : PubMed

            

    Title: A missense mutation Pro157 Arg in lipoprotein lipase (LPLNijmegen) resulting in loss of catalytic activity
    Bruin T, Kastelein JJ, Van Diermen DE, Ma Y, Henderson HE, Stuyt PM, Stalenhoef AF, Sturk A, Brunzell JD, Hayden MR
    Ref: European Journal of Biochemistry, 208:267, 1992 : PubMed

            


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