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Journal Abstract Search

144 related items for PubMed ID: 1936106

  • 1. Familial defective apo B-100, characterization of an Italian family.
    Corsini A, McCarthy BJ, Granata A, Soria LF, Fantappiè S, Bernini, Romano C, Romano L, Fumagalli R, Catapano AL.
    Eur J Clin Invest; 1991 Aug; 21(4):389-97. PubMed ID: 1936106
    [Abstract] [Full Text] [Related]

  • 2. Characterization of a family with moderate hypercholesterolemia and binding defective low density lipoprotein.
    Catapano AL, Corsini A, Mazzotti M, Granata A, Uboldi P, Maggi FM, Romano L, Romano C, Fantappiè S, Fumagalli R.
    Eur J Epidemiol; 1992 May; 8 Suppl 1():26-32. PubMed ID: 1505652
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  • 3. Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function.
    Myant NB, Gallagher JJ, Knight BL, McCarthy SN, Frostegård J, Nilsson J, Hamsten A, Talmud P, Humphries SE.
    Arterioscler Thromb; 1991 May; 11(3):691-703. PubMed ID: 1674216
    [Abstract] [Full Text] [Related]

  • 4. Phenotypic heterogeneity associated with defective apolipoprotein B-100 and occurrence of the familial hypercholesterolemia phenotype in the absence of an LDL-receptor defect within a Canadian kindred.
    Davignon J, Dufour R, Roy M, Bétard C, Ma Y, Ouellette S, Boulet L, Lussier-Cacan S.
    Eur J Epidemiol; 1992 May; 8 Suppl 1():10-7. PubMed ID: 1505645
    [Abstract] [Full Text] [Related]

  • 5. Familial defective apolipoprotein B-100.
    Hansen PS.
    Dan Med Bull; 1998 Sep; 45(4):370-82. PubMed ID: 9777289
    [Abstract] [Full Text] [Related]

  • 6. Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK.
    Wenham PR, Henderson BG, Penney MD, Ashby JP, Rae PW, Walker SW.
    Atherosclerosis; 1997 Mar 21; 129(2):185-92. PubMed ID: 9105560
    [Abstract] [Full Text] [Related]

  • 7. The affinity of low-density lipoproteins and of very-low-density lipoprotein remnants for the low-density lipoprotein receptor in homozygous familial defective apolipoprotein B-100.
    Gallagher JJ, Myant NB.
    Atherosclerosis; 1995 Jun 21; 115(2):263-72. PubMed ID: 7661885
    [Abstract] [Full Text] [Related]

  • 8. Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia.
    Myant NB.
    Atherosclerosis; 1993 Dec 21; 104(1-2):1-18. PubMed ID: 8141833
    [Abstract] [Full Text] [Related]

  • 9. Accumulation of "small dense" low density lipoproteins (LDL) in a homozygous patients with familial defective apolipoprotein B-100 results from heterogenous interaction of LDL subfractions with the LDL receptor.
    März W, Baumstark MW, Scharnagl H, Ruzicka V, Buxbaum S, Herwig J, Pohl T, Russ A, Schaaf L, Berg A.
    J Clin Invest; 1993 Dec 21; 92(6):2922-33. PubMed ID: 8254047
    [Abstract] [Full Text] [Related]

  • 10. Identification of defective binding of low density lipoprotein by the U937 proliferation assay in German patients with familial defective apolipoprotein B-100.
    Schewe CK, Schuster H, Hailer S, Wolfram G, Keller C, Zöllner N.
    Eur J Clin Invest; 1994 Jan 21; 24(1):36-41. PubMed ID: 8187806
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  • 12. Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.
    Weisgraber KH, Innerarity TL, Newhouse YM, Young SG, Arnold KS, Krauss RM, Vega GL, Grundy SM, Mahley RW.
    Proc Natl Acad Sci U S A; 1988 Dec 21; 85(24):9758-62. PubMed ID: 3200853
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  • 13. Occurrence of species of low-density lipoprotein with defective clearance in patients with primary moderate hypercholesterolaemia.
    Vega GL, Grundy SM.
    J Intern Med; 1992 Nov 21; 232(5):405-13. PubMed ID: 1453124
    [Abstract] [Full Text] [Related]

  • 14. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding.
    Innerarity TL, Weisgraber KH, Arnold KS, Mahley RW, Krauss RM, Vega GL, Grundy SM.
    Proc Natl Acad Sci U S A; 1987 Oct 21; 84(19):6919-23. PubMed ID: 3477815
    [Abstract] [Full Text] [Related]

  • 15. Familial defective apolipoprotein B100: clinical characteristics of 54 cases.
    Rauh G, Keller C, Kormann B, Spengel F, Schuster H, Wolfram G, Zöllner N.
    Atherosclerosis; 1992 Feb 21; 92(2-3):233-41. PubMed ID: 1632851
    [Abstract] [Full Text] [Related]

  • 16. Compound heterozygous familial hypercholesterolemia and familial defective apolipoprotein B-100 produce exaggerated hypercholesterolemia.
    Tai ES, Koay ES, Chan E, Seng TJ, Loh LM, Sethi SK, Tan CE.
    Clin Chem; 2001 Mar 21; 47(3):438-43. PubMed ID: 11238294
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  • 18. Identification of the low density lipoprotein receptor-binding site in apolipoprotein B100 and the modulation of its binding activity by the carboxyl terminus in familial defective apo-B100.
    Boren J, Lee I, Zhu W, Arnold K, Taylor S, Innerarity TL.
    J Clin Invest; 1998 Mar 01; 101(5):1084-93. PubMed ID: 9486979
    [Abstract] [Full Text] [Related]

  • 19. Identification of the apo B-3500 mutation in the Norwegian population.
    Leren TP, Rødningen OK, Tonstad S, Røsby O, Urdal P, Ose L.
    Scand J Clin Lab Invest; 1995 May 01; 55(3):217-21. PubMed ID: 7638555
    [Abstract] [Full Text] [Related]

  • 20. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB).
    Azian M, Hapizah MN, Khalid BA, Khalid Y, Rosli A, Jamal R.
    Malays J Pathol; 2006 Jun 01; 28(1):7-15. PubMed ID: 17694954
    [Abstract] [Full Text] [Related]

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