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Transcriptional Alterations in X-Linked Dystonia-Parkinsonism Caused by the SVA Retrotransposon.
Pozojevic J, Algodon SM, Cruz JN, Trinh J, Brüggemann N, Laß J, Grütz K, Schaake S, Tse R, Yumiceba V, Kruse N, Schulz K, Sreenivasan VKA, Rosales RL, Jamora RDG, Diesta CCE, Matschke J, Glatzel M, Seibler P, Händler K, Rakovic A, Kirchner H, Spielmann M, Kaiser FJ, Klein C, Westenberger A. Pozojevic J, et al. Among authors: kirchner h. Int J Mol Sci. 2022 Feb 17;23(4):2231. doi: 10.3390/ijms23042231. Int J Mol Sci. 2022. PMID: 35216353 Free PMC article.
A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members.
Dulovic M, Schäffer E, Leypoldt F, Balck A, Schaake S, Hinrichs F, Kirchner H, Brüggemann N, Berg D, Lohmann K. Dulovic M, et al. Among authors: kirchner h. Parkinsonism Relat Disord. 2018 Sep;54:116-118. doi: 10.1016/j.parkreldis.2018.04.001. Epub 2018 Apr 3. Parkinsonism Relat Disord. 2018. PMID: 29650490 No abstract available.
DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-Parkinsonism.
Krause C, Schaake S, Grütz K, Sievert H, Reyes CJ, König IR, Laabs BH, Jamora RD, Rosales RL, Diesta CCE, Pozojevic J, Gemoll T, Westenberger A, Kaiser FJ, Klein C, Kirchner H. Krause C, et al. Among authors: kirchner h. Mov Disord. 2020 Dec;35(12):2220-2229. doi: 10.1002/mds.28239. Epub 2020 Sep 10. Mov Disord. 2020. PMID: 32914507
The Telomeric Complex and Metabolic Disease.
Kirchner H, Shaheen F, Kalscheuer H, Schmid SM, Oster H, Lehnert H. Kirchner H, et al. Genes (Basel). 2017 Jul 7;8(7):176. doi: 10.3390/genes8070176. Genes (Basel). 2017. PMID: 28686177 Free PMC article. Review.
973 results