Ryytty S - Search Results

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Defects in mtDNA replication challenge nuclear genome stability through nucleotide depletion and provide a unifying mechanism for mouse progerias.

Hämäläinen RH, Landoni JC, Ahlqvist KJ, Goffart S, Ryytty S, Rahman MO, Brilhante V, Icay K, Hautaniemi S, Wang L, Laiho M, Suomalainen A. Hämäläinen RH, et al. Among authors: ryytty s. Nat Metab. 2019 Oct;1(10):958-965. doi: 10.1038/s42255-019-0120-1. Epub 2019 Oct 7. Nat Metab. 2019. PMID: 32694840

Reply to: Proofreading deficiency in mitochondrial DNA polymerase does not affect total dNTP pools in mouse embryos.

Hämäläinen RH, Landoni JC, Ahlqvist KJ, Goffart S, Ryytty S, Rahman MO, Brilhante V, Icay K, Hautaniemi S, Wang L, Laiho M, Suomalainen A. Hämäläinen RH, et al. Among authors: ryytty s. Nat Metab. 2020 Aug;2(8):676-677. doi: 10.1038/s42255-020-0265-y. Epub 2020 Aug 10. Nat Metab. 2020. PMID: 32778835 No abstract available.

Author Correction: Defects in mtDNA replication challenge nuclear genome stability through nucleotide depletion and provide a unifying mechanism for mouse progerias.

Hämäläinen RH, Landoni JC, Ahlqvist KJ, Goffart S, Ryytty S, Rahman MO, Brilhante V, Icay K, Hautaniemi S, Wang L, Laiho M, Suomalainen A. Hämäläinen RH, et al. Among authors: ryytty s. Nat Metab. 2020 Aug;2(8):793. doi: 10.1038/s42255-020-0255-0. Nat Metab. 2020. PMID: 32778837

Varied Responses to a High m.3243A>G Mutation Load and Respiratory Chain Dysfunction in Patient-Derived Cardiomyocytes.

Ryytty S, Modi SR, Naumenko N, Shakirzyanova A, Rahman MO, Vaara M, Suomalainen A, Tavi P, Hämäläinen RH. Ryytty S, et al. Cells. 2022 Aug 19;11(16):2593. doi: 10.3390/cells11162593. Cells. 2022. PMID: 36010669 Free PMC article.

The Mitochondrial m.3243A>G Mutation on the Dish, Lessons from In Vitro Models.

Ryytty S, Hämäläinen RH. Ryytty S, et al. Int J Mol Sci. 2023 Aug 30;24(17):13478. doi: 10.3390/ijms241713478. Int J Mol Sci. 2023. PMID: 37686280 Free PMC article. Review.

Generation of a human induced pluripotent stem cell line (UEFi004-A) from a patient with progressive myoclonic epilepsy type 1 (EPM1).

Singh S, Plotnikova L, Karvonen K, Ryytty S, Hyppönen J, Kälviäinen R, Hämäläinen RH. Singh S, et al. Among authors: ryytty s. Stem Cell Res. 2023 Dec;73:103248. doi: 10.1016/j.scr.2023.103248. Epub 2023 Nov 7. Stem Cell Res. 2023. PMID: 37951142 Free article.

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