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Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland.
Jääskeläinen P, Kuusisto J, Miettinen R, Kärkkäinen P, Kärkkäinen S, Heikkinen S, Peltola P, Pihlajamäki J, Vauhkonen I, Laakso M. Jääskeläinen P, et al. Among authors: miettinen r. J Mol Med (Berl). 2002 Jul;80(7):412-22. doi: 10.1007/s00109-002-0323-9. Epub 2002 Apr 11. J Mol Med (Berl). 2002. PMID: 12110947
Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
Kärkkäinen S, Heliö T, Jääskeläinen P, Miettinen R, Tuomainen P, Ylitalo K, Kaartinen M, Reissell E, Toivonen L, Nieminen MS, Kuusisto J, Laakso M, Peuhkurinen K. Kärkkäinen S, et al. Among authors: miettinen r. Eur J Heart Fail. 2004 Dec;6(7):861-8. doi: 10.1016/j.ejheart.2004.04.017. Eur J Heart Fail. 2004. PMID: 15556047 Free article.
Promoter polymorphisms -359T/C and -303A/G of the catalytic subunit p110beta gene of human phosphatidylinositol 3-kinase are not associated with insulin secretion or insulin sensitivity in finnish subjects.
Kossila M, Pihlajamäki J, Kärkkäinen P, Miettinen R, Kekäläinen P, Vauhkonen I, Ylä-Herttuala S, Laakso M. Kossila M, et al. Among authors: miettinen r. Diabetes Care. 2003 Jan;26(1):179-82. doi: 10.2337/diacare.26.1.179. Diabetes Care. 2003. PMID: 12502677
118 results