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Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy.
Götz A, Tyynismaa H, Euro L, Ellonen P, Hyötyläinen T, Ojala T, Hämäläinen RH, Tommiska J, Raivio T, Oresic M, Karikoski R, Tammela O, Simola KO, Paetau A, Tyni T, Suomalainen A. Götz A, et al. Among authors: karikoski r. Am J Hum Genet. 2011 May 13;88(5):635-42. doi: 10.1016/j.ajhg.2011.04.006. Epub 2011 May 5. Am J Hum Genet. 2011. PMID: 21549344 Free PMC article.
Tissue expression of nephrin in human and pig.
Kuusniemi AM, Kestilä M, Patrakka J, Lahdenkari AT, Ruotsalainen V, Holmberg C, Karikoski R, Salonen R, Tryggvason K, Jalanko H. Kuusniemi AM, et al. Among authors: karikoski r. Pediatr Res. 2004 May;55(5):774-81. doi: 10.1203/01.PDR.0000117842.10241.2C. Epub 2004 Feb 5. Pediatr Res. 2004. PMID: 14764915
Trim37-deficient mice recapitulate several features of the multi-organ disorder Mulibrey nanism.
Kettunen KM, Karikoski R, Hämäläinen RH, Toivonen TT, Antonenkov VD, Kulesskaya N, Voikar V, Hölttä-Vuori M, Ikonen E, Sainio K, Jalanko A, Karlberg S, Karlberg N, Lipsanen-Nyman M, Toppari J, Jauhiainen M, Hiltunen JK, Jalanko H, Lehesjoki AE. Kettunen KM, et al. Among authors: karikoski r. Biol Open. 2016 May 15;5(5):584-95. doi: 10.1242/bio.016246. Biol Open. 2016. PMID: 27044324 Free PMC article.
62 results