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Desmosterol in human nonalcoholic steatohepatitis.
Simonen M, Männistö V, Leppänen J, Kaminska D, Kärjä V, Venesmaa S, Käkelä P, Kuusisto J, Gylling H, Laakso M, Pihlajamäki J. Simonen M, et al. Among authors: laakso m. Hepatology. 2013 Sep;58(3):976-82. doi: 10.1002/hep.26342. Epub 2013 Jul 29. Hepatology. 2013. PMID: 23447451
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: laakso m. 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
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: laakso m. Diabetes Care. 2003 Jan;26(1):179-82. doi: 10.2337/diacare.26.1.179. Diabetes Care. 2003. PMID: 12502677
First-pass MR imaging in the assessment of perfusion impairment in patients with hypertrophic cardiomyopathy and the Asp175Asn mutation of the alpha-tropomyosin gene.
Sipola P, Lauerma K, Husso-Saastamoinen M, Kuikka JT, Vanninen E, Laitinen T, Manninen H, Niemi P, Peuhkurinen K, Jääskeläinen P, Laakso M, Kuusisto J, Aronen HJ. Sipola P, et al. Among authors: laakso m. Radiology. 2003 Jan;226(1):129-37. doi: 10.1148/radiol.2261011874. Radiology. 2003. PMID: 12511681
1,375 results