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Journal Abstract Search

126 related items for PubMed ID: 9279208

  • 1. Compound heterozygote for both rare apolipoprotein E1 (Gly127-->Asp, Arg158-->Cys) and E3(Cys112-->Arg, Arg251-->Gly) alleles in a multigeneration pedigree with hyperlipoproteinaemia.
    Richard P, Beucler I, Pascual De Zulueta M, Biteau N, De Gennes JL, Iron A.
    Clin Sci (Lond); 1997 Jul; 93(1):89-95. PubMed ID: 9279208
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  • 2. Severe type III hyperlipoproteinemia associated with unusual apolipoprotein E1 phenotype and epsilon 1/'null' genotype.
    Feussner G, Funke H, Weng W, Assmann G, Lackner KJ, Ziegler R.
    Eur J Clin Invest; 1992 Sep; 22(9):599-608. PubMed ID: 1360898
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  • 9. The functional characteristics of a human apolipoprotein E variant (cysteine at residue 142) may explain its association with dominant expression of type III hyperlipoproteinemia.
    Horie Y, Fazio S, Westerlund JR, Weisgraber KH, Rall SC.
    J Biol Chem; 1992 Jan 25; 267(3):1962-8. PubMed ID: 1730728
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  • 12. Apolipoprotein E2 (Arg-136-->Cys), a variant of apolipoprotein E associated with late-onset dominance of type III hyperlipoproteinaemia.
    Feussner G, Albanese M, Mann WA, Valencia A, Schuster H.
    Eur J Clin Invest; 1996 Jan 25; 26(1):13-23. PubMed ID: 8682150
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  • 14. Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia.
    Lohse P, Mann WA, Stein EA, Brewer HB.
    J Biol Chem; 1991 Jun 05; 266(16):10479-84. PubMed ID: 1674745
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  • 17. Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemia.
    Feussner G, Dobmeyer J, Nissen H, Hansen TS.
    Am J Med Genet; 1996 Oct 16; 65(2):149-54. PubMed ID: 8911609
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  • 20. Apolipoprotein E polymorphism in health and disease.
    Utermann G.
    Am Heart J; 1987 Feb 16; 113(2 Pt 2):433-40. PubMed ID: 3544759
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