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The Mitochondrial Epigenome: An Unexplored Avenue to Explain Unexplained Myopathies?
Mposhi A, Liang L, Mennega KP, Yildiz D, Kampert C, Hof IH, Jellema PG, de Koning TJ, Faber KN, Ruiters MHJ, Niezen-Koning KE, Rots MG. Mposhi A, et al. Among authors: niezen koning ke. Int J Mol Sci. 2022 Feb 16;23(4):2197. doi: 10.3390/ijms23042197. Int J Mol Sci. 2022. PMID: 35216315 Free PMC article.
A fatal, systemic mitochondrial disease with decreased mitochondrial enzyme activities, abnormal ultrastructure of the mitochondria and deficiency of heat shock protein 60.
Agsteribbe E, Huckriede A, Veenhuis M, Ruiters MH, Niezen-Koning KE, Skjeldal OH, Skullerud K, Gupta RS, Hallberg R, van Diggelen OP, et al. Agsteribbe E, et al. Biochem Biophys Res Commun. 1993 May 28;193(1):146-54. doi: 10.1006/bbrc.1993.1602. Biochem Biophys Res Commun. 1993. PMID: 8503901 Free article.
The past and presence of gene targeting: from chemicals and DNA via proteins to RNA.
Geel TM, Ruiters MHJ, Cool RH, Halby L, Voshart DC, Andrade Ruiz L, Niezen-Koning KE, Arimondo PB, Rots MG. Geel TM, et al. Among authors: niezen koning ke. Philos Trans R Soc Lond B Biol Sci. 2018 Jun 5;373(1748):20170077. doi: 10.1098/rstb.2017.0077. Philos Trans R Soc Lond B Biol Sci. 2018. PMID: 29685979 Free PMC article. Review.
Dopaminergic and serotonergic alterations in plasma in three groups of dystonia patients.
Timmers ER, van Faassen M, Smit M, Kuiper A, Hof IH, Kema IP, Tijssen MAJ, Niezen-Koning KE, de Koning TJ. Timmers ER, et al. Among authors: niezen koning ke. Parkinsonism Relat Disord. 2021 Oct;91:48-54. doi: 10.1016/j.parkreldis.2021.08.019. Epub 2021 Sep 2. Parkinsonism Relat Disord. 2021. PMID: 34482194 Free article.
Gut Microbiome Composition in Dystonia Patients.
Timmers ER, Swarte JC, Gacesa R, Björk JR, Weersma RK, Tijssen MAJ, de Koning TJ, Harmsen HJM, Niezen-Koning KE. Timmers ER, et al. Among authors: niezen koning ke. Int J Mol Sci. 2023 Jan 25;24(3):2383. doi: 10.3390/ijms24032383. Int J Mol Sci. 2023. PMID: 36768705 Free PMC article.
Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy.
Almomani R, Herkert JC, Posafalvi A, Post JG, Boven LG, van der Zwaag PA, Willems PHGM, van Veen-Hof IH, Verhagen JMA, Wessels MW, Nikkels PGJ, Wintjes LT, van den Berg MP, Sinke RJ, Rodenburg RJ, Niezen-Koning KE, van Tintelen JP, Jongbloed JDH. Almomani R, et al. Among authors: niezen koning ke. J Med Genet. 2020 Jan;57(1):23-30. doi: 10.1136/jmedgenet-2019-106330. Epub 2019 Sep 7. J Med Genet. 2020. PMID: 31494578
59 results