Lehrstuhl für Biochemie und Pathobiochemie

Th17 Lymphocytes Induce Neuronal Cell Death in a Human iPSC-Based Model of Parkinson's Disease (2018) Sommer A, Maxreiter F, Krach F, Fadler T, Grosch J, Maroni M, Graef D, et al. Journal article The transcription factor prospero homeobox protein 1 is a direct target of SoxC proteins during developmental vertebrate neurogenesis (2018) Jacob A, Wüst H, Thalhammer J, Fröb F, Küspert M, Reiprich S, Balta EA, et al. Journal article, Original article Characterization of Glomerular Sox9+ Cells in Anti-Glomerular Basement Membrane Nephritis in the Rat (2018) Prochnicki A, Amann KU, Wegner M, Sock E, Pfister E, Shankland S, Pippin J, Daniel C Journal article Transcription factor profiling identifies Sox9 as regulator of proliferation and differentiation in corneal epithelial stem/progenitor cells (2018) Menzel-Severing J, Zenkel M, Polisetti N, Sock E, Wegner M, Kruse F, Schlötzer-Schrehardt U Journal article FoxO Function Is Essential for Maintenance of Autophagic Flux and Neuronal Morphogenesis in Adult Neurogenesis (2018) Schäffner I, Minakaki G, Khan MA, Balta EA, Schlötzer-Schrehardt U, Schwarz TJ, Beckervordersandforth R, et al. Journal article Sox8 and Sox10 jointly maintain myelin gene expression in oligodendrocytes. (2018) Turnescu T, Arter J, Reiprich S, Tamm ER, Reiprich S, Waisman A, Wegner M Journal article Nfat/calcineurin signaling promotes oligodendrocyte differentiation and myelination by transcription factor network tuning. (2018) Weider M, Starost LJ, Groll K, Küspert M, Sock E, Wedel M, Fröb F, et al. Journal article, Original article Analysis of the human SOX10 mutation Q377X in mice and its implications for genotype-phenotype correlation in SOX10-related human disease. (2018) Truch K, Arter J, Turnescu T, Weider M, Hartwig A, Tamm ER, Sock E, Wegner M Journal article Analysis of the expression pattern of the schizophrenia-risk and intellectual disability gene TCF4 in the developing and adult brain suggests a role in development and plasticity of cortical and hippocampal neurons (2018) Jung M, Häberle B, Tschaikowsky T, Wittmann MT, Balta EA, Stadler VC, Zweier C, et al. Journal article Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT). (2018) Neirijnck Y, Reginensi A, Renkema KY, Massa F, Kozlov VM, Dhib H, Bongers EMHF, et al. Journal article, Original article