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Journal Abstract Search

132 related items for PubMed ID: 7585299

  • 1. Genetic variation of apolipoprotein B can produce both low and high levels of apoB-containing lipoproteins in plasma.
    Schonfeld G.
    Can J Cardiol; 1995 Oct; 11 Suppl G():86G-92G. PubMed ID: 7585299
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  • 2. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK.
    Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
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  • 3. Novel mutations of APOB cause ApoB truncations undetectable in plasma and familial hypobetalipoproteinemia.
    Yue P, Yuan B, Gerhard DS, Neuman RJ, Isley WL, Harris WS, Schonfeld G.
    Hum Mutat; 2002 Aug; 20(2):110-6. PubMed ID: 12124991
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  • 4. Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia.
    Whitfield AJ, Marais AD, Robertson K, Barrett PH, van Bockxmeer FM, Burnett JR.
    Hum Mutat; 2003 Aug; 22(2):178. PubMed ID: 12872264
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  • 9. Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.
    van der Hoek YY, Lingenhel A, Kraft HG, Defesche JC, Kastelein JJ, Utermann G.
    J Clin Invest; 1997 May 01; 99(9):2269-73. PubMed ID: 9151801
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  • 10. Pediatric gallstone disease in familial hypobetalipoproteinemia.
    Lancellotti S, Zaffanello M, Di Leo E, Costa L, Lonardo A, Tarugi P.
    J Hepatol; 2005 Jul 01; 43(1):188-91. PubMed ID: 15894400
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  • 11. Influence of LDL receptor gene mutations and the R3500Q mutation of the apoB gene on lipoprotein phenotype of familial hypercholesterolemic patients from a South European population.
    Real JT, Chaves FJ, Ejarque I, García-García AB, Valldecabres C, Ascaso JF, Armengod ME, Carmena R.
    Eur J Hum Genet; 2003 Dec 01; 11(12):959-65. PubMed ID: 14508510
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  • 13. Major locus inheritance of apolipoprotein B in Utah pedigrees.
    Hasstedt SJ, Wu L, Williams RR.
    Genet Epidemiol; 1987 Dec 01; 4(2):67-76. PubMed ID: 3108070
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  • 14. Metabolism of apolipoprotein B-100 in a kindred with familial hypobetalipoproteinemia without a truncated form of apoB.
    Latour MA, Patterson BW, Pulai J, Chen Z, Schonfeld G.
    J Lipid Res; 1997 Mar 01; 38(3):592-9. PubMed ID: 9101440
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  • 15. ApoB-54.8, a truncated apolipoprotein found primarily in VLDL, is associated with a nonsense mutation in the apoB gene and hypobetalipoproteinemia.
    Wagner RD, Krul ES, Tang J, Parhofer KG, Garlock K, Talmud P, Schonfeld G.
    J Lipid Res; 1991 Jun 01; 32(6):1001-11. PubMed ID: 1940616
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  • 16. Postprandial lipemia in subjects with hypobetalipoproteinemia and a single intestinal allele for apoB-48.
    Averna M, Seip RL, Mankowitz K, Schonfeld G.
    J Lipid Res; 1993 Nov 01; 34(11):1957-67. PubMed ID: 8263419
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  • 17. Genetic heterogeneity in familial hypobetalipoproteinemia: linkage and non-linkage to the apoB gene in Caucasian families.
    Pulai JI, Neuman RJ, Groenewegen AW, Wu J, Schonfeld G.
    Am J Med Genet; 1998 Feb 26; 76(1):79-86. PubMed ID: 9508071
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  • 18. Known mutations of apoB account for only a small minority of hypobetalipoproteinemia.
    Wu J, Kim J, Li Q, Kwok PY, Cole TG, Cefalu B, Averna M, Schonfeld G.
    J Lipid Res; 1999 May 26; 40(5):955-9. PubMed ID: 10224165
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  • 19. Hypobetalipoproteinemia: genetics, biochemistry, and clinical spectrum.
    Tarugi P, Averna M.
    Adv Clin Chem; 2011 May 26; 54():81-107. PubMed ID: 21874758
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  • 20. Apolipoprotein B levels, APOB alleles, and risk of ischemic cardiovascular disease in the general population, a review.
    Benn M.
    Atherosclerosis; 2009 Sep 26; 206(1):17-30. PubMed ID: 19200547
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