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Author Report for: Marcovina SM

No contact information in database for Marcovina SM

    Title: Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband
    Argyropoulos G, Jenkins A, Klein RL, Lyons T, Wagenhorst B, St Armand J, Marcovina SM, Albers JJ, Pritchard PH, Garvey WT
    Ref: J Lipid Res, 39:1870, 1998 : PubMed


    Title: Overexpression of lecithin:cholesterol acyltransferase in transgenic rabbits prevents diet-induced atherosclerosis
    Hoeg JM, Santamarina-Fojo S, Berard AM, Cornhill JF, Herderick EE, Feldman SH, Haudenschild CC, Vaisman BL, Hoyt RF, Jr. and Brewer HB, Jr. <4 more author(s)>
    Ref: Proc Natl Acad Sci U S A, 93:11448, 1996 : PubMed


    Title: A unique genetic and biochemical presentation of fish-eye disease
    Kuivenhoven JA, van Voorst tot Voorst EJ, Wiebusch H, Marcovina SM, Funke H, Assmann G, Pritchard PH, Kastelein JJ
    Ref: J Clinical Investigation, 96:2783, 1995 : PubMed


    Title: Two novel point mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in LCAT deficiency: LCAT (G873 deletion) and LCAT (Gly344-->Ser)
    Moriyama K, Sasaki J, Arakawa F, Takami N, Maeda E, Matsunaga A, Takada Y, Midorikawa K, Yanase T and Arakawa K <3 more author(s)>
    Ref: J Lipid Res, 36:2329, 1995 : PubMed


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