Works matching IS 09462716 AND DT 2008 AND VI 86 AND IP 10


Results: 10
    1

    Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.

    Published in:
    Journal of Molecular Medicine, 2008, v. 86, n. 10, p. 1163, doi. 10.1007/s00109-008-0376-5
    By:
    • Wolfgang Lieb;
    • Zeller, Tanja;
    • Mangino, Massimo;
    • Götz, Anika;
    • Braund, Peter;
    • Wenzel, Juergen;
    • Horn, Christian;
    • Proust, Carole;
    • Linsel-Nitschke, Patrick;
    • Amouyel, Philippe;
    • Bruse, Petra;
    • Arveiler, Dominique;
    • König, Inke;
    • Ferrières, Jean;
    • Ziegler, Andreas;
    • Balmforth, Anthony;
    • Evans, Alun;
    • Ducimetière, Pierre;
    • Cambien, Francois;
    • Hengstenberg, Christian
    Publication type:
    Article
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    Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas.

    Published in:
    Journal of Molecular Medicine, 2008, v. 86, n. 10, p. 1171, doi. 10.1007/s00109-008-0377-4
    By:
    • Yamazawa, Kazuki;
    • Kagami, Masayo;
    • Nagai, Toshiro;
    • Kondoh, Tatsuro;
    • Onigata, Kazumichi;
    • Maeyama, Katsuhiro;
    • Hasegawa, Tomonobu;
    • Hasegawa, Yukihiro;
    • Yamazaki, Toshio;
    • Mizuno, Seiji;
    • Miyoshi, Yoko;
    • Miyagawa, Shinichiro;
    • Horikawa, Reiko;
    • Matsuoka, Kentaro;
    • Ogata, Tsutomu
    Publication type:
    Article
    10