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Journal Abstract Search

259 related items for PubMed ID: 8527219

  • 1.
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  • 2. 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; 34(11):1957-67. PubMed ID: 8263419
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  • 3. 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; 40(5):955-9. PubMed ID: 10224165
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  • 4. ApoB-75, a truncation of apolipoprotein B associated with familial hypobetalipoproteinemia: genetic and kinetic studies.
    Krul ES, Parhofer KG, Barrett PH, Wagner RD, Schonfeld G.
    J Lipid Res; 1992 Jul; 33(7):1037-50. PubMed ID: 1431583
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  • 6. Genetic variants of ApoE account for variability of plasma low-density lipoprotein and apolipoprotein B levels in FHBL.
    Yue P, Isley WL, Harris WS, Rosipal S, Akin CD, Schonfeld G.
    Atherosclerosis; 2005 Jan; 178(1):107-13. PubMed ID: 15585207
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  • 7. 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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  • 9. Hypobetalipoproteinemia: genetics, biochemistry, and clinical spectrum.
    Tarugi P, Averna M.
    Adv Clin Chem; 2011 Aug; 54():81-107. PubMed ID: 21874758
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  • 10. Identification and molecular analysis of two apoB gene mutations causing low plasma cholesterol levels.
    Welty FK, Ordovas J, Schaefer EJ, Wilson PW, Young SG.
    Circulation; 1995 Oct 15; 92(8):2036-40. PubMed ID: 7554178
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  • 12. Four new mutations in the apolipoprotein B gene causing hypobetalipoproteinemia, including two different frameshift mutations that yield truncated apolipoprotein B proteins of identical length.
    Young SG, Pullinger CR, Zysow BR, Hofmann-Radvani H, Linton MF, Farese RV, Terdiman JF, Snyder SM, Grundy SM, Vega GL.
    J Lipid Res; 1993 Mar 15; 34(3):501-7. PubMed ID: 8468533
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  • 13. Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene.
    Martín-Morales R, García-Díaz JD, Tarugi P, González-Santos P, Saavedra-Vallejo P, Magnolo L, Mesa-Latorre JM, di Leo E, Valdivielso P.
    Gene; 2013 Nov 15; 531(1):92-6. PubMed ID: 24001780
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  • 14. Identification of a novel mutation in the ANGPTL3 gene in two families diagnosed of familial hypobetalipoproteinemia without APOB mutation.
    Martín-Campos JM, Roig R, Mayoral C, Martinez S, Martí G, Arroyo JA, Julve J, Blanco-Vaca F.
    Clin Chim Acta; 2012 Mar 22; 413(5-6):552-5. PubMed ID: 22155345
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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 22; 32(6):1001-11. PubMed ID: 1940616
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  • 19. Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia.
    Noto D, Cefalù AB, Valenti V, Fayer F, Pinotti E, Ditta M, Spina R, Vigna G, Yue P, Kathiresan S, Tarugi P, Averna MR.
    Arterioscler Thromb Vasc Biol; 2012 Mar 22; 32(3):805-9. PubMed ID: 22247256
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