7 results for author:"Salonen T." in Literature citations
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| Implications of levels of serum mineral metabolism markers, albumin and C-reactive protein for treatment costs of patients on maintenance dialysis. Salonen T., Piirto J., Reina T., Saha H., Pasternack A. Nephron Clin Pract 106:c17-23(2007) · Mapped (16) |
| Two novel CLN6 mutations in variant late-infantile neuronal ceroid lipofuscinosis patients of Turkish origin. Siintola E., Topcu M., Kohlschutter A., Salonen T., Joensuu T., Anttonen A.K., Lehesjoki A.E. Clin. Genet. 68:167-173(2005) · Mapped (5) |
| Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons. Jalanko A., Vesa J., Manninen T., von Schantz C., Minye H., Fabritius A.L., Salonen T., Rapola J., Gentile M., Kopra O. et al. Neurobiol. Dis. 18:226-241(2005) · Mapped (11) |
| Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells. Lonka L., Salonen T., Siintola E., Kopra O., Lehesjoki A.E., Jalanko A. J. Neurosci. Res. 76:862-871(2004) · Mapped (4) |
| New mutations in the neuronal ceroid lipofuscinosis genes. Mole S.E., Zhong N.A., Sarpong A., Logan W.P., Hofmann S., Yi W., Franken P.F., van Diggelen O.P., Breuning M.H., Moroziewicz D. et al. Eur. J. Paediatr. Neurol. 5:7-10(2001) · UniProtKB (1) |
| CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain. Heinonen O., Salonen T., Jalanko A., Peltonen L., Copp A. J. Comp. Neurol. 426:406-412(2000) |
| Mouse palmitoyl protein thioesterase: gene structure and expression of cDNA. Salonen T., Hellsten E., Horelli-Kuitunen N., Peltonen L., Jalanko A. |