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The Finnish genetic heritage in 2022 - from diagnosis to translational research.
Uusimaa J, Kettunen J, Varilo T, Järvelä I, Kallijärvi J, Kääriäinen H, Laine M, Lapatto R, Myllynen P, Niinikoski H, Rahikkala E, Suomalainen A, Tikkanen R, Tyynismaa H, Vieira P, Zarybnicky T, Sipilä P, Kuure S, Hinttala R. Uusimaa J, et al. Among authors: kuure s. Dis Model Mech. 2022 Oct 1;15(10):dmm049490. doi: 10.1242/dmm.049490. Epub 2022 Oct 26. Dis Model Mech. 2022. PMID: 36285626 Free PMC article. Review.
Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage.
Zárybnický T, Heikkinen A, Kangas SM, Karikoski M, Martínez-Nieto GA, Salo MH, Uusimaa J, Vuolteenaho R, Hinttala R, Sipilä P, Kuure S. Zárybnický T, et al. Among authors: kuure s. Cells. 2021 Nov 13;10(11):3158. doi: 10.3390/cells10113158. Cells. 2021. PMID: 34831381 Free PMC article. Review.
Comparative whole-genome transcriptome analysis in renal cell populations reveals high tissue specificity of MAPK/ERK targets in embryonic kidney.
Kurtzeborn K, Kwon HN, Iaroshenko V, Faisal I, Ambrož M, Jin X, Qureshi T, Kupari J, Ihermann-Hella A, Väänänen J, Tyynismaa H, Boušová I, Park S, Kuure S. Kurtzeborn K, et al. Among authors: kuure s. BMC Biol. 2022 May 13;20(1):112. doi: 10.1186/s12915-022-01309-z. BMC Biol. 2022. PMID: 35550069 Free PMC article.
Mouse Models of Congenital Kidney Anomalies.
Kuure S, Sariola H. Kuure S, et al. Adv Exp Med Biol. 2020;1236:109-136. doi: 10.1007/978-981-15-2389-2_5. Adv Exp Med Biol. 2020. PMID: 32304071 Review.
35 results