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Journal Abstract Search

146 related items for PubMed ID: 2574033

  • 1. Two distinct truncated apolipoprotein B species in a kindred with hypobetalipoproteinemia.
    Krul ES, Kinoshita M, Talmud P, Humphries SE, Turner S, Goldberg AC, Cook K, Boerwinkle E, Schonfeld G.
    Arteriosclerosis; 1989; 9(6):856-68. PubMed ID: 2574033
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  • 5. A novel truncated apolipoprotein B (apo B55) in a patient with familial hypobetalipoproteinemia and atypical retinitis pigmentosa.
    Talmud PJ, Converse C, Krul E, Huq L, McIlwaine GG, Series JJ, Boyd P, Schonfeld G, Dunning A, Humphries S.
    Clin Genet; 1992 Aug; 42(2):62-70. PubMed ID: 1424233
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  • 8. Homozygous hypobetalipoproteinemia with spared chylomicron formation.
    Harano Y, Kojima H, Nakano T, Harada M, Kashiwagi A, Nakajima Y, Hidaka TH, Ohtsuki T, Suzuki T, Tamura A.
    Metabolism; 1989 Jan; 38(1):1-7. PubMed ID: 2909827
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  • 9. The molecular basis of truncated forms of apolipoprotein B in a kindred with compound heterozygous hypobetalipoproteinemia.
    Talmud P, King-Underwood L, Krul E, Schonfeld G, Humphries S.
    J Lipid Res; 1989 Nov; 30(11):1773-9. PubMed ID: 2614276
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  • 10. Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred.
    Leppert M, Breslow JL, Wu L, Hasstedt S, O'Connell P, Lathrop M, Williams RR, White R, Lalouel JM.
    J Clin Invest; 1988 Sep; 82(3):847-51. PubMed ID: 2901434
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  • 11. 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
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  • 13. Dual mechanisms for the low plasma levels of truncated apolipoprotein B proteins in familial hypobetalipoproteinemia. Analysis of a new mouse model with a nonsense mutation in the Apob gene.
    Kim E, Cham CM, Véniant MM, Ambroziak P, Young SG.
    J Clin Invest; 1998 Mar 15; 101(6):1468-77. PubMed ID: 9502790
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  • 14. 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 15; 33(3):361-70. PubMed ID: 11019990
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  • 16. 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 15; 33(5):699-710. PubMed ID: 1619363
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