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Journal Abstract Search

248 related items for PubMed ID: 15585207

  • 1. 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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  • 2. 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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  • 3. 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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  • 4. 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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  • 5. Decreased production rates of VLDL triglycerides and ApoB-100 in subjects heterozygous for familial hypobetalipoproteinemia.
    Elias N, Patterson BW, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 1999 Nov 22; 19(11):2714-21. PubMed ID: 10559016
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  • 6. Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation.
    Pulai JI, Zakeri H, Kwok PY, Kim JH, Wu J, Schonfeld G.
    Am J Med Genet; 1998 Nov 16; 80(3):218-20. PubMed ID: 9843041
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  • 7. High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descent.
    Fouchier SW, Sankatsing RR, Peter J, Castillo S, Pocovi M, Alonso R, Kastelein JJ, Defesche JC.
    J Med Genet; 2005 Apr 16; 42(4):e23. PubMed ID: 15805152
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  • 8. 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 16; 40(5):955-9. PubMed ID: 10224165
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  • 9. Lipoprotein Metabolism in APOB L343V Familial Hypobetalipoproteinemia.
    Hooper AJ, Heeks L, Robertson K, Champain D, Hua J, Song S, Parhofer KG, Barrett PH, van Bockxmeer FM, Burnett JR.
    J Clin Endocrinol Metab; 2015 Nov 16; 100(11):E1484-90. PubMed ID: 26323024
    [Abstract] [Full Text] [Related]

  • 10. Lipoprotein(a) Mass Levels Increase Significantly According to APOE Genotype: An Analysis of 431 239 Patients.
    Moriarty PM, Varvel SA, Gordts PL, McConnell JP, Tsimikas S.
    Arterioscler Thromb Vasc Biol; 2017 Mar 16; 37(3):580-588. PubMed ID: 28062489
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  • 12. 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 16; 33(7):1037-50. PubMed ID: 1431583
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  • 14. Lipoprotein metabolism in an apoB-80 familial hypobetalipoproteinemia heterozygote.
    Hooper AJ, Robertson K, Champain D, Hua J, Song S, Parhofer KG, Barrett PHR, van Bockxmeer FM, Burnett JR.
    Clin Biochem; 2016 Jun 16; 49(9):720-722. PubMed ID: 26916057
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  • 15. 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. Postprandial lipoprotein metabolism in familial hypobetalipoproteinemia.
    Hooper AJ, Robertson K, Barrett PH, Parhofer KG, van Bockxmeer FM, Burnett JR.
    J Clin Endocrinol Metab; 2007 Apr 26; 92(4):1474-8. PubMed ID: 17213276
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