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Page 1
Adult neurogenesis in Parkinson's disease.
Marxreiter F, Regensburger M, Winkler J. Marxreiter F, et al. Among authors: regensburger m. Cell Mol Life Sci. 2013 Feb;70(3):459-73. doi: 10.1007/s00018-012-1062-x. Epub 2012 Jul 6. Cell Mol Life Sci. 2013. PMID: 22766974 Review.
Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia.
Pérez-Brangulí F, Mishra HK, Prots I, Havlicek S, Kohl Z, Saul D, Rummel C, Dorca-Arevalo J, Regensburger M, Graef D, Sock E, Blasi J, Groemer TW, Schlötzer-Schrehardt U, Winkler J, Winner B. Pérez-Brangulí F, et al. Among authors: regensburger m. Hum Mol Genet. 2014 Sep 15;23(18):4859-74. doi: 10.1093/hmg/ddu200. Epub 2014 May 2. Hum Mol Genet. 2014. PMID: 24794856 Free PMC article.
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: regensburger m. Sci Rep. 2018 Nov 21;8(1):17201. doi: 10.1038/s41598-018-35506-0. Sci Rep. 2018. PMID: 30464253 Free PMC article.
Human SPG11 cerebral organoids reveal cortical neurogenesis impairment.
Pérez-Brangulí F, Buchsbaum IY, Pozner T, Regensburger M, Fan W, Schray A, Börstler T, Mishra H, Gräf D, Kohl Z, Winkler J, Berninger B, Cappello S, Winner B. Pérez-Brangulí F, et al. Among authors: regensburger m. Hum Mol Genet. 2019 Mar 15;28(6):961-971. doi: 10.1093/hmg/ddy397. Hum Mol Genet. 2019. PMID: 30476097 Free PMC article.
76 results