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Author Report for: Kuivenhoven JA

No contact information in database for Kuivenhoven JA

    Title: Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia
    Surendran RP, Visser ME, Heemelaar S, Wang J, Peter J, Defesche JC, Kuivenhoven JA, Hosseini M, Peterfy M and Dallinga-Thie GM <4 more author(s)>
    Ref: J Intern Med, 272:185, 2012 : PubMed


    Title: Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase
    Holleboom AG, Kuivenhoven JA, van Olden CC, Peter J, Schimmel AW, Levels JH, Valentijn RM, Vos P, Defesche JC and Hollak CE <3 more author(s)>
    Ref: Atherosclerosis, 216:161, 2011 : PubMed


    Title: Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase
    Beigneux AP, Franssen R, Bensadoun A, Gin P, Melford K, Peter J, Walzem RL, Weinstein MM, Davies BS and Young SG <4 more author(s)>
    Ref: Arterioscler Thromb Vasc Biol, 29:956, 2009 : PubMed


    Title: Effects of six APOA5 variants, identified in patients with severe hypertriglyceridemia, on in vitro lipoprotein lipase activity and receptor binding
    Dorfmeister B, Zeng WW, Dichlberger A, Nilsson SK, Schaap FG, Hubacek JA, Merkel M, Cooper JA, Lookene A and Talmud PJ <13 more author(s)>
    Ref: Arterioscler Thromb Vasc Biol, 28:1866, 2008 : PubMed


    Title: High HDL cholesterol does not protect against coronary artery disease when associated with combined cholesteryl ester transfer protein and hepatic lipase gene variants
    van Acker BA, Botma GJ, Zwinderman AH, Kuivenhoven JA, Dallinga-Thie GM, Sijbrands EJ, Boer JM, Seidell JC, Jukema JW and Verhoeven AJ <2 more author(s)>
    Ref: Atherosclerosis, 200:161, 2008 : PubMed


    Title: Adeno-associated virus LPL(S447X) gene therapy in LDL receptor knockout mice
    Rip J, Sierts JA, Vaessen SF, Kastelein JJ, Twisk J, Kuivenhoven JA
    Ref: Atherosclerosis, 194:55, 2007 : PubMed


    Title: Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels
    Boekholdt SM, Souverein OW, Tanck MW, Hovingh GK, Kuivenhoven JA, Peters RI, Jansen H, Schiffers PM, van der Wall EE and Jukema JW <4 more author(s)>
    Ref: Clin Genet, 69:263, 2006 : PubMed


    Title: Serum lipoprotein lipase concentration and risk for future coronary artery disease: the EPIC-Norfolk prospective population study
    Rip J, Nierman MC, Wareham NJ, Luben R, Bingham SA, Day NE, van Miert JN, Hutten BA, Kastelein JJ and Boekholdt SM <2 more author(s)>
    Ref: Arterioscler Thromb Vasc Biol, 26:637, 2006 : PubMed


    Title: Lipoprotein lipase S447X: a naturally occurring gain-of-function mutation
    Rip J, Nierman MC, Ross CJ, Jukema JW, Hayden MR, Kastelein JJ, Stroes ES, Kuivenhoven JA
    Ref: Arterioscler Thromb Vasc Biol, 26:1236, 2006 : PubMed


    Title: Correction of feline lipoprotein lipase deficiency with adeno-associated virus serotype 1-mediated gene transfer of the lipoprotein lipase S447X beneficial mutation
    Ross CJ, Twisk J, Bakker AC, Miao F, Verbart D, Rip J, Godbey T, Dijkhuizen P, Hermens WT and Hayden MR <3 more author(s)>
    Ref: Hum Gene Therapy, 17:487, 2006 : PubMed


    Title: Gene therapy for genetic lipoprotein lipase deficiency: from promise to practice
    Nierman MC, Rip J, Twisk J, Meulenberg JJ, Kastelein JJ, Stroes ES, Kuivenhoven JA
    Ref: Neth J Med, 63:14, 2005 : PubMed


    Title: Enhanced conversion of triglyceride-rich lipoproteins and increased low-density lipoprotein removal in LPLS447X carriers
    Nierman MC, Prinsen BH, Rip J, Veldman RJ, Kuivenhoven JA, Kastelein JJ, de Sain-van der Velden MG, Stroes ES
    Ref: Arterioscler Thromb Vasc Biol, 25:2410, 2005 : PubMed


    Title: Carriers of the frequent lipoprotein lipase S447X variant exhibit enhanced postprandial apoprotein B-48 clearance
    Nierman MC, Rip J, Kuivenhoven JA, van Raalte DH, Hutten BA, Sakai N, Kastelein JJ, Stroes ES
    Ref: Metabolism, 54:1499, 2005 : PubMed


    Title: Gene therapy for lipoprotein lipase deficiency: working toward clinical application
    Rip J, Nierman MC, Sierts JA, Petersen W, Van den Oever K, Van Raalte D, Ross CJ, Hayden MR, Bakker AC and Meulenberg JM <6 more author(s)>
    Ref: Hum Gene Therapy, 16:1276, 2005 : PubMed


    Title: Complete rescue of lipoprotein lipase-deficient mice by somatic gene transfer of the naturally occurring LPLS447X beneficial mutation
    Ross CJ, Liu G, Kuivenhoven JA, Twisk J, Rip J, van Dop W, Excoffon KJ, Lewis SM, Kastelein JJ, Hayden MR
    Ref: Arterioscler Thromb Vasc Biol, 25:2143, 2005 : PubMed


    Title: Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins
    Boer JM, Kuivenhoven JA, Feskens EJ, Schouten EG, Havekes LM, Seidell JC, Kastelein JJ, Kromhout D
    Ref: Clin Genet, 56:158, 1999 : PubMed


    Title: Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the lipoprotein lipase gene. REGRESS Study Group
    Groenemeijer BE, Hallman MD, Reymer PW, Gagne E, Kuivenhoven JA, Bruin T, Jansen H, Lie KI, Bruschke AV and Kastelein JJ <2 more author(s)>
    Ref: Circulation, 95:2628, 1997 : PubMed


    Title: An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)
    Kuivenhoven JA, Weibusch H, Pritchard PH, Funke H, Benne R, Assmann G, Kastelein JJ
    Ref: J Clinical Investigation, 98:358, 1996 : 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 unique genetic and biochemical presentation of fish-eye disease
    Kuivenhoven JA, van Voorst tot Voorst EJ, Wiebusch H, Marcovina SM, Funke H, Assmann G, Pritchard PH, Kastelein JJ
    Ref: J Clinical Investigation, 96:2783, 1995 : PubMed


    Title: Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent
    Kastelein JJ, Pritchard PH, Erkelens DW, Kuivenhoven JA, Albers JJ, Frohlich JJ
    Ref: J Intern Med, 231:413, 1992 : PubMed


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