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Journal Abstract Search

105 related items for PubMed ID: 8843188

  • 1. A new apolipoprotein B truncation (apo B-43.7) in familial hypobetalipoproteinemia: genetic and metabolic studies.
    Srivastava N, Noto D, Averna M, Pulai J, Srivastava RA, Cole TG, Latour MA, Patterson BW, Schonfeld G.
    Metabolism; 1996 Oct; 45(10):1296-304. PubMed ID: 8843188
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  • 2. 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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  • 3. 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. 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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  • 9. Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100.
    Young SG, Bertics SJ, Curtiss LK, Dubois BW, Witztum JL.
    J Clin Invest; 1987 Jun; 79(6):1842-51. PubMed ID: 3473077
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  • 12. 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; 38(3):592-9. PubMed ID: 9101440
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  • 13. A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia.
    Welty FK, Hubl ST, Pierotti VR, Young SG.
    J Clin Invest; 1991 May; 87(5):1748-54. PubMed ID: 2022744
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  • 14. Dysbetalipoproteinemia in a kindred with hypobetalipoproteinemia due to mutations in the genes for ApoB (ApoB-70.5) and ApoE (ApoE2).
    Groenewegen WA, Krul ES, Averna MR, Pulai J, Schonfeld G.
    Arterioscler Thromb; 1994 Nov; 14(11):1695-704. PubMed ID: 7947592
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  • 15. 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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  • 18. Apolipoprotein B-32: a new truncated mutant of human apolipoprotein B capable of forming particles in the low density lipoprotein range.
    McCormick SP, Fellowes AP, Walmsley TA, George PM.
    Biochim Biophys Acta; 1992 Apr 14; 1138(4):290-6. PubMed ID: 1562615
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  • 19. A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5).
    Tarugi P, Lonardo A, Ballarini G, Erspamer L, Tondelli E, Bertolini S, Calandra S.
    J Hepatol; 2000 Sep 14; 33(3):361-70. PubMed ID: 11019990
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  • 20. Hypobetalipoproteinemia associated with apo B-48.4, a truncated protein only 14 amino acids longer than apo B-48.
    Ruotolo G, Zanelli T, Tettamanti C, Ragogna F, Parlavecchia M, Viganò F, Catapano AL.
    Atherosclerosis; 1998 Mar 14; 137(1):125-31. PubMed ID: 9568744
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