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Journal Abstract Search

181 related items for PubMed ID: 7947592

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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; 32(6):1001-11. PubMed ID: 1940616
    [Abstract] [Full Text] [Related]

  • 4. Apolipoprotein B-38.9 does not associate with apo[a] and forms two distinct HDL density particle populations that are larger than HDL.
    Groenewegen WA, Averna MR, Pulai J, Krul ES, Schonfeld G.
    J Lipid Res; 1994 Jun; 35(6):1012-25. PubMed ID: 8077841
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. A truncated species of apolipoprotein B, B-83, associated with hypobetalipoproteinemia.
    Farese RV, Garg A, Pierotti VR, Vega GL, Young SG.
    J Lipid Res; 1992 Apr; 33(4):569-77. PubMed ID: 1527480
    [Abstract] [Full Text] [Related]

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  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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; 19(11):2714-21. PubMed ID: 10559016
    [Abstract] [Full Text] [Related]

  • 11. Two apolipoprotein B gene defects in a kindred with hypobetalipoproteinemia, one of which results in a truncated variant, apoB-61, in VLDL and LDL.
    Pullinger CR, Hillas E, Hardman DA, Chen GC, Naya-Vigne JM, Iwasa JA, Hamilton RL, Lalouel JM, Williams RR, Kane JP.
    J Lipid Res; 1992 May; 33(5):699-710. PubMed ID: 1619363
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. Apolipoprotein B-52 mutation associated with hypobetalipoproteinemia is compatible with a misaligned pairing deletion mechanism.
    Groenewegen WA, Krul ES, Schonfeld G.
    J Lipid Res; 1993 Jun; 34(6):971-81. PubMed ID: 8354962
    [Abstract] [Full Text] [Related]

  • 14. The hypobetalipoproteinemias.
    Schonfeld G.
    Annu Rev Nutr; 1995 Jun; 15():23-34. PubMed ID: 8527219
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Diabetes mellitus in a new kindred with familial hypobetalipoproteinemia and an apolipoprotein B truncation (apoB-55).
    Pulai JI, Latour MA, Kwok PY, Schonfeld G.
    Atherosclerosis; 1998 Feb; 136(2):289-95. PubMed ID: 9543100
    [Abstract] [Full Text] [Related]

  • 17. Genetic factors precipitating type III hyperlipoproteinemia in hypolipidemic transgenic mice expressing human apolipoprotein E2.
    Huang Y, Rall SC, Mahley RW.
    Arterioscler Thromb Vasc Biol; 1997 Nov; 17(11):2817-24. PubMed ID: 9409260
    [Abstract] [Full Text] [Related]

  • 18. Frequency of ApoB and ApoE gene mutations as causes of hypobetalipoproteinemia in the framingham offspring population.
    Welty FK, Lahoz C, Tucker KL, Ordovas JM, Wilson PW, Schaefer EJ.
    Arterioscler Thromb Vasc Biol; 1998 Nov; 18(11):1745-51. PubMed ID: 9812913
    [Abstract] [Full Text] [Related]

  • 19. 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; 137(1):125-31. PubMed ID: 9568744
    [Abstract] [Full Text] [Related]

  • 20. Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.
    Young SG, Hubl ST, Smith RS, Snyder SM, Terdiman JF.
    J Clin Invest; 1990 Mar; 85(3):933-42. PubMed ID: 2312735
    [Abstract] [Full Text] [Related]

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