Lehrstuhl für Humangenetik

Dopaminergic lesioning impairs adult hippocampal neurogenesis by distinct modification of α-synuclein (2016) Schlachetzki J, Grimm T, Schlachetzki Z, Ben Abdallah NMB, Ettle B, Voehringer P, Ferger B, et al. Journal article Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency (2016) Saunier C, Stove SI, Popp B, Gerard B, Blenski M, Ahmew N, De Bie C, et al. Journal article Infiltrating T lymphocytes reduce myeloid phagocytosis activity in synucleinopathy model (2016) Sommer A, Fadler T, Dorfmeister E, Hoffmann AC, Xiang W, Winner B, Prots I Journal article Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition (2016) Kuechler A, Czeschik JC, Graf E, Grasshoff U, Hüffmeier U, Busa T, Beck-Woedl S, et al. Journal article Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly (2016) Breuss MW, Sultan T, James KN, Rosti RO, Scott E, Musaev D, Furia B, et al. Journal article, Erratum Model Testing of PluriTest with Next-Generation Sequencing Data (2016) Schulze M, Hoja S, Winner B, Winkler J, Edenhofer F, Riemenschneider MJ Journal article Zeb2 recruits HDAC-NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination (2016) Wu LMN, Wang J, Conidi A, Zhao C, Wang H, Ford Z, Zhang L, et al. Journal article Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1 (2016) Popp B, Trollmann R, Büttner C, Caliebe A, Thiel C, Hüffmeier U, Reis A, Zweier C Journal article SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss (2016) Buchert R, Nesbitt AI, Tawamie H, Krantz ID, Medne L, Helbig I, Matalon DR, et al. Journal article Kdm6b and Pmepa1 as Targets of Bioelectrically and Behaviorally Induced Activin A Signaling (2016) Link A, Kurinna S, Havlicek S, Lehnert S, Reichel M, Kornhuber J, Winner B, et al. Journal article