Search Results - "Gerdes, L.U."

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    Phenotypic Variation in Patients Heterozygous for Familial Defective Apolipoprotein B (FDB) in Three European Countries by Hansen, P.S, Defesche, J.C, Kastelein, J.J.P, Gerdes, L.U, Fraza, L, Gerdes, C, Tato, F, Jensen, H.K, Jensen, L.G, Klausen, I.C, Faergeman, O, Schuster, H

    “…A glutamine-for-arginine substitution at amino acid position 3500 of apolipoprotein B (apo B) causes synthesis of LDL with reduced binding affinity to the LDL…”
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    Genotyping compared with protein phenotyping of the common apolipoprotein E polymorphism by Hansen, P S, Gerdes, L U, Klausen, I C, Gregersen, N, Faergeman, O

    Published in Clinica chimica acta (31-01-1994)
    “…Apolipoprotein E (apo E) genotypes have been determined in 460 Danish men, with the use of the polymerase chain reaction (PCR) to amplify a 244 base pair…”
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    Incidence of the apolipoprotein B-3500 mutation in Denmark by Hansen, P S, Nørgaard-Petersen, B, Meinertz, H, Jensen, H K, Hansen, A B, Klausen, I C, Gerdes, L U, Faergeman, O

    Published in Clinica chimica acta (14-10-1994)
    “…A total of 5000 consecutively samples newborn screening cards were anonymously selected for screening for the apolipoprotein B-3500 (apo B-3500) mutation,…”
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