7 results for author:"Komulainen J." in Literature citations
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| Heavy resistance exercise training and skeletal muscle androgen receptor expression in younger and older men. Ahtiainen J.P., Hulmi J.J., Kraemer W.J., Lehti M., Nyman K., Selanne H., Alen M., Pakarinen A., Komulainen J., Kovanen V. et al. Steroids 76:183-192(2011) · Mapped (11) |
| Repeated bout effect on the cytoskeletal proteins titin, desmin, and dystrophin in rat skeletal muscle. Lehti T.M., Kalliokoski R., Komulainen J. J. Muscle Res. Cell. Motil. 28:39-47(2007) · Mapped (10) |
| Acute insulin response tests for the differential diagnosis of congenital hyperinsulinism. Huopio H., Jaeaeskelaeinen J., Komulainen J., Miettinen R., Kaerkkaeinen P., Laakso M., Tapanainen P., Voutilainen R., Otonkoski T. J. Clin. Endocrinol. Metab. 87:4502-4507(2002) · UniProtKB (2) |
| Lack of cytosolic and transmembrane domains of type XIII collagen results in progressive myopathy. Kvist A.-P., Latvanlehto A., Sund M., Eklund L., Vaisanen T., Hagg P., Sormunen R., Komulainen J., Fassler R., Pihlajaniemi T. Am. J. Pathol. 159:1581-1592(2001) · UniProtKB (1) · Mapped (5) |
| Lack of type XV collagen causes a skeletal myopathy and cardiovascular defects in mice. Eklund L., Piuhola J., Komulainen J., Sormunen R., Ongvarrasopone C., Faessler R., Muona A., Ilves M., Ruskoaho H., Takala T.E.S. et al. Proc. Natl. Acad. Sci. U.S.A. 98:1194-1199(2001) · UniProtKB (1) · Mapped (5) |
| Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1. Huopio H., Reimann F., Ashfield R., Komulainen J., Lenko H.-L., Rahier J., Vauhkonen I., Kere J., Laakso M., Ashcroft F. et al. J. Clin. Invest. 106:897-906(2000) · UniProtKB (1) |
| A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland. Otonkoski T., Aemmaelae C., Huopio H., Cote G.J., Chapman J., Cosgrove K., Ashfield R., Huang E., Komulainen J., Ashcroft F.M. et al. Diabetes 48:408-415(1999) · UniProtKB (1) |