Kuronen M - Search Results

1

Galactolipid deficiency in the early pathogenesis of neuronal ceroid lipofuscinosis model Cln8mnd : implications to delayed myelination and oligodendrocyte maturation.

Kuronen M, Hermansson M, Manninen O, Zech I, Talvitie M, Laitinen T, Gröhn O, Somerharju P, Eckhardt M, Cooper JD, Lehesjoki AE, Lahtinen U, Kopra O. Kuronen M, et al. Neuropathol Appl Neurobiol. 2012 Aug;38(5):471-86. doi: 10.1111/j.1365-2990.2011.01233.x. Neuropathol Appl Neurobiol. 2012. PMID: 22044361

2

Genetic modifiers of degeneration in the cathepsin D deficient Drosophila model for neuronal ceroid lipofuscinosis.

Kuronen M, Talvitie M, Lehesjoki AE, Myllykangas L. Kuronen M, et al. Neurobiol Dis. 2009 Dec;36(3):488-93. doi: 10.1016/j.nbd.2009.09.001. Epub 2009 Sep 15. Neurobiol Dis. 2009. PMID: 19761846

3

Selective spatiotemporal patterns of glial activation and neuron loss in the sensory thalamocortical pathways of neuronal ceroid lipofuscinosis 8 mice.

Kuronen M, Lehesjoki AE, Jalanko A, Cooper JD, Kopra O. Kuronen M, et al. Neurobiol Dis. 2012 Sep;47(3):444-57. doi: 10.1016/j.nbd.2012.04.018. Epub 2012 May 5. Neurobiol Dis. 2012. PMID: 22569358

4

The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy.

Lonka L, Aalto A, Kopra O, Kuronen M, Kokaia Z, Saarma M, Lehesjoki AE. Lonka L, et al. Among authors: kuronen m. BMC Neurosci. 2005 Apr 13;6:27. doi: 10.1186/1471-2202-6-27. BMC Neurosci. 2005. PMID: 15826318 Free PMC article.

5

Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism.

Schmiedt ML, Blom T, Blom T, Kopra O, Wong A, von Schantz-Fant C, Ikonen E, Kuronen M, Jauhiainen M, Cooper JD, Jalanko A. Schmiedt ML, et al. Among authors: kuronen m. Neurobiol Dis. 2012 Apr;46(1):19-29. doi: 10.1016/j.nbd.2011.12.009. Epub 2011 Dec 13. Neurobiol Dis. 2012. PMID: 22182690

6

Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patients.

Joensuu T, Kuronen M, Alakurtti K, Tegelberg S, Hakala P, Aalto A, Huopaniemi L, Aula N, Michellucci R, Eriksson K, Lehesjoki AE. Joensuu T, et al. Among authors: kuronen m. Eur J Hum Genet. 2007 Feb;15(2):185-93. doi: 10.1038/sj.ejhg.5201723. Epub 2006 Sep 27. Eur J Hum Genet. 2007. PMID: 17003839

7

Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions.

Forsström S, Jackson CB, Carroll CJ, Kuronen M, Pirinen E, Pradhan S, Marmyleva A, Auranen M, Kleine IM, Khan NA, Roivainen A, Marjamäki P, Liljenbäck H, Wang L, Battersby BJ, Richter U, Velagapudi V, Nikkanen J, Euro L, Suomalainen A. Forsström S, et al. Among authors: kuronen m. Cell Metab. 2019 Dec 3;30(6):1040-1054.e7. doi: 10.1016/j.cmet.2019.08.019. Epub 2019 Sep 12. Cell Metab. 2019. PMID: 31523008 Free article.

8

Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia.

Tanner SM, Aminoff M, Wright FA, Liyanarachchi S, Kuronen M, Saarinen A, Massika O, Mandel H, Broch H, de la Chapelle A. Tanner SM, et al. Among authors: kuronen m. Nat Genet. 2003 Mar;33(3):426-9. doi: 10.1038/ng1098. Epub 2003 Feb 18. Nat Genet. 2003. PMID: 12590260

9

efdm-An R package offering a scenario tool beyond forestry.

Räty M, Kuronen M. Räty M, et al. Among authors: kuronen m. PLoS One. 2022 Aug 15;17(8):e0264380. doi: 10.1371/journal.pone.0264380. eCollection 2022. PLoS One. 2022. PMID: 35969582 Free PMC article.

10

New methods for multiple testing in permutation inference for the general linear model.

Mrkvička T, Myllymäki M, Kuronen M, Narisetty NN. Mrkvička T, et al. Among authors: kuronen m. Stat Med. 2022 Jan 30;41(2):276-297. doi: 10.1002/sim.9236. Epub 2021 Oct 23. Stat Med. 2022. PMID: 34687243

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