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Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium.
Popp B, Krumbiegel M, Grosch J, Sommer A, Uebe S, Kohl Z, Plötz S, Farrell M, Trautmann U, Kraus C, Ekici AB, Asadollahi R, Regensburger M, Günther K, Rauch A, Edenhofer F, Winkler J, Winner B, Reis A. Popp B, et al. Among authors: gunther k. Sci Rep. 2018 Nov 21;8(1):17201. doi: 10.1038/s41598-018-35506-0. Sci Rep. 2018. PMID: 30464253 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 a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3.
Jansch C, Günther K, Waider J, Ziegler GC, Forero A, Kollert S, Svirin E, Pühringer D, Kwok CK, Ullmann R, Maierhofer A, Flunkert J, Haaf T, Edenhofer F, Lesch KP. Jansch C, et al. Among authors: gunther k. Stem Cell Res. 2018 Apr;28:136-140. doi: 10.1016/j.scr.2018.02.005. Epub 2018 Feb 13. Stem Cell Res. 2018. PMID: 29477591 Free 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.
Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD.
Palladino VS, Chiocchetti AG, Frank L, Haslinger D, McNeill R, Radtke F, Till A, Haupt S, Brüstle O, Günther K, Edenhofer F, Hoffmann P, Reif A, Kittel-Schneider S. Palladino VS, et al. Among authors: gunther k. J Clin Med. 2020 Dec 18;9(12):4092. doi: 10.3390/jcm9124092. J Clin Med. 2020. PMID: 33353000 Free PMC 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.
860 results