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High-throughput phosphotyrosine profiling using SH2 domains.
Machida K, Thompson CM, Dierck K, Jablonowski K, Kärkkäinen S, Liu B, Zhang H, Nash PD, Newman DK, Nollau P, Pawson T, Renkema GH, Saksela K, Schiller MR, Shin DG, Mayer BJ. Machida K, et al. Among authors: karkkainen s. Mol Cell. 2007 Jun 22;26(6):899-915. doi: 10.1016/j.molcel.2007.05.031. Mol Cell. 2007. PMID: 17588523 Free article.
Pregnancy and childbirth in carriers of the lamin A/C-gene mutation.
Palojoki E, Kaartinen M, Kaaja R, Reissell E, Kärkkäinen S, Kuusisto J, Heliö T. Palojoki E, et al. Among authors: karkkainen s. Eur J Heart Fail. 2010 Jun;12(6):630-3. doi: 10.1093/eurjhf/hfq059. Epub 2010 Apr 22. Eur J Heart Fail. 2010. PMID: 20413395 Free article.
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: karkkainen p, karkkainen s. 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
79 results