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Journal Abstract Search

128 related items for PubMed ID: 7627691

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  • 4. Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity.
    Pullinger CR, Hennessy LK, Chatterton JE, Liu W, Love JA, Mendel CM, Frost PH, Malloy MJ, Schumaker VN, Kane JP.
    J Clin Invest; 1995 Mar; 95(3):1225-34. PubMed ID: 7883971
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  • 8. 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; 47(3):438-43. PubMed ID: 11238294
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  • 9. Influence of an asparagine to lysine mutation at amino acid 3516 of apolipoprotein B on low-density lipoprotein receptor binding.
    Gaffney D, Pullinger CR, O'Reilly DS, Hoffs MS, Cameron I, Vass JK, Kulkarni MV, Kane JP, Schumaker VN, Watts GF, Packard CJ.
    Clin Chim Acta; 2002 Jul; 321(1-2):113-21. PubMed ID: 12031600
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  • 13. A very conservative region of ApoB-100 in the putative binding region to the LDL receptor in the Toulouse population.
    Avoustin P, Mostachi H, Perret B, Cambou JP, Cambien F, de Préval C.
    Hum Genet; 1992 Dec; 90(4):460-3. PubMed ID: 1483706
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  • 16. Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100.
    Rauh G, Schuster H, Fischer J, Keller C, Wolfram G, Zöllner N.
    Klin Wochenschr; 1991 May 03; 69(7):320-4. PubMed ID: 2067318
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  • 17. Detection of familial defective apoB (FDB) mutations in hypercholesterolemic children and adolescents by denaturing high performance liquid chromatography (DHPLC).
    Nelken J, Meshkani R, Chahal N, McCrindle B, Adeli K.
    Clin Biochem; 2008 Apr 03; 41(6):395-9. PubMed ID: 18222178
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  • 18. Identification and haplotype analysis of apolipoprotein B-100 Arg3500-->Trp mutation in hyperlipidemic Chinese.
    Tai DY, Pan JP, Lee-Chen GJ.
    Clin Chem; 1998 Aug 03; 44(8 Pt 1):1659-65. PubMed ID: 9702952
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