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150 related items for PubMed ID: 7749818

  • 1. Apoprotein B-100 production is decreased in subjects heterozygous for truncations of apoprotein B.
    Aguilar-Salinas CA, Barrett PH, Parhofer KG, Young SG, Tessereau D, Bateman J, Quinn C, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 1995 Jan; 15(1):71-80. PubMed ID: 7749818
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  • 4. 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; 100(11):E1484-90. PubMed ID: 26323024
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  • 5. 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; 49(9):720-722. PubMed ID: 26916057
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  • 6. In vivo metabolism of ApoB, ApoA-I, and VLDL triglycerides in a form of hypobetalipoproteinemia not linked to the ApoB gene.
    Elias N, Patterson BW, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 2000 May; 20(5):1309-15. PubMed ID: 10807747
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  • 7. Familial hypobetalipoproteinemia: genetics and metabolism.
    Schonfeld G, Lin X, Yue P.
    Cell Mol Life Sci; 2005 Jun; 62(12):1372-8. PubMed ID: 15818469
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  • 8. Production of apolipoprotein B-67 in apolipoprotein B-67/B-100 heterozygotes: technical problems associated with leucine contamination in stable isotope studies.
    Welty FK, Lichtenstein AH, Barrett PH, Dolnikowski GG, Ordovas JM, Schaefer EJ.
    J Lipid Res; 1997 Aug; 38(8):1535-43. PubMed ID: 9300775
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  • 9. 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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  • 12. 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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  • 13. Homozygous familial hypobetalipoproteinemia. Increased LDL catabolism in hypobetalipoproteinemia due to a truncated apolipoprotein B species, apo B-87Padova.
    Gabelli C, Bilato C, Martini S, Tennyson GE, Zech LA, Corsini A, Albanese M, Brewer HB, Crepaldi G, Baggio G.
    Arterioscler Thromb Vasc Biol; 1996 Sep; 16(9):1189-96. PubMed ID: 8792774
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  • 14. 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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  • 15. Lipoproteins containing the truncated apolipoprotein, Apo B-89, are cleared from human plasma more rapidly than Apo B-100-containing lipoproteins in vivo.
    Parhofer KG, Barrett PH, Bier DM, Schonfeld G.
    J Clin Invest; 1992 Jun; 89(6):1931-7. PubMed ID: 1602000
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  • 16. Normal intestinal dietary fat and cholesterol absorption, intestinal apolipoprotein B (ApoB) mRNA levels, and ApoB-48 synthesis in a hypobetalipoproteinemic kindred without any ApoB truncation.
    Pulai JI, Averna M, Srivastava RA, Latour MA, Clouse RE, Ostlund RE, Schonfeld G.
    Metabolism; 1997 Sep; 46(9):1095-100. PubMed ID: 9284903
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  • 17. Familial hypobetalipoproteinemia is not associated with low levels of lipoprotein(a).
    Averna M, Marcovina SM, Noto D, Cole TG, Krul ES, Schonfeld G.
    Arterioscler Thromb Vasc Biol; 1995 Dec; 15(12):2165-75. PubMed ID: 7489238
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  • 18. Hepatic secretion of apoB-100 is impaired in hypobetalipoproteinemic mice with an apoB-38.9-specifying allele.
    Chen Z, Fitzgerald RL, Li G, Davidson NO, Schonfeld G.
    J Lipid Res; 2004 Jan; 45(1):155-63. PubMed ID: 13130124
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  • 19. 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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  • 20. Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease.
    Gutiérrez-Cirlos C, Ordóñez-Sánchez ML, Tusié-Luna MT, Patterson BW, Schonfeld G, Aguilar-Salinas CA.
    Ann Hepatol; 2011 Nov; 10(2):155-64. PubMed ID: 21502677
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