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Small fibre neuropathy in Fabry disease: a human-derived neuronal in vitro disease model and pilot data.
Klein T, Grüner J, Breyer M, Schlegel J, Schottmann NM, Hofmann L, Gauss K, Mease R, Erbacher C, Finke L, Klein A, Klug K, Karl-Schöller F, Vignolo B, Reinhard S, Schneider T, Günther K, Fink J, Dudek J, Maack C, Klopocki E, Seibel J, Edenhofer F, Wischmeyer E, Sauer M, Üçeyler N. Klein T, et al. Among authors: gunther k. Brain Commun. 2024 Apr 3;6(2):fcae095. doi: 10.1093/braincomms/fcae095. eCollection 2024. Brain Commun. 2024. PMID: 38638148 Free PMC article.
Establishment of a Human Blood-Brain Barrier Co-culture Model Mimicking the Neurovascular Unit Using Induced Pluri- and Multipotent Stem Cells.
Appelt-Menzel A, Cubukova A, Günther K, Edenhofer F, Piontek J, Krause G, Stüber T, Walles H, Neuhaus W, Metzger M. Appelt-Menzel A, et al. Among authors: gunther k. Stem Cell Reports. 2017 Apr 11;8(4):894-906. doi: 10.1016/j.stemcr.2017.02.021. Epub 2017 Mar 23. Stem Cell Reports. 2017. PMID: 28344002 Free PMC article.
Generation of the human induced pluripotent stem cell line (UKWNLi001-A) from skin fibroblasts of a woman with Fabry disease carrying the X-chromosomal heterozygous c.708 G > C (W236C) missense mutation in exon 5 of the alpha-galactosidase-A gene.
Klein T, Günther K, Kwok CK, Edenhofer F, Üçeyler N. Klein T, et al. Among authors: gunther k. Stem Cell Res. 2018 Aug;31:222-226. doi: 10.1016/j.scr.2018.08.009. Epub 2018 Aug 10. Stem Cell Res. 2018. PMID: 30130681 Free article.
Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation.
Janz A, Chen R, Regensburger M, Ueda Y, Rost S, Klopocki E, Günther K, Edenhofer F, Duff HJ, Ergün S, Gerull B. Janz A, et al. Among authors: gunther k. Stem Cell Res. 2020 Jul;46:101856. doi: 10.1016/j.scr.2020.101856. Epub 2020 Jun 2. Stem Cell Res. 2020. PMID: 32521499 Free article.
Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly.
Jansch C, Ziegler GC, Forero A, Gredy S, Wäldchen S, Vitale MR, Svirin E, Zöller JEM, Waider J, Günther K, Edenhofer F, Sauer M, Wischmeyer E, Lesch KP. Jansch C, et al. Among authors: gunther k. J Neural Transm (Vienna). 2021 Feb;128(2):225-241. doi: 10.1007/s00702-021-02303-5. Epub 2021 Feb 9. J Neural Transm (Vienna). 2021. PMID: 33560471 Free PMC article.
Generation of the human induced pluripotent stem cell line (IBKMOLi002-A) from PBMCs of a patient carrying the heterozygous L271H mutation of the voltage-gated calcium channel subunit Cav1.3-encoding CACNA1D gene.
Tisch M, Carmen De Mingo Alemany M, Suarez-Cubero M, Fauth C, Defrancesco M, Zschocke J, Günther K, Edenhofer F. Tisch M, et al. Among authors: gunther k. Stem Cell Res. 2022 May;61:102784. doi: 10.1016/j.scr.2022.102784. Epub 2022 Apr 9. Stem Cell Res. 2022. PMID: 35453044 Free article.
ADHD-associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient-derived cell lines.
Radtke F, Palladino VS, McNeill RV, Chiocchetti AG, Haslinger D, Leyh M, Gersic D, Frank M, Grünewald L, Klebe S, Brüstle O, Günther K, Edenhofer F, Kranz TM, Reif A, Kittel-Schneider S. Radtke F, et al. Among authors: gunther k. Am J Med Genet B Neuropsychiatr Genet. 2022 Oct;189(7-8):257-270. doi: 10.1002/ajmg.b.32918. Epub 2022 Aug 16. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 35971782
846 results