Institut für Biochemie

Common RUNX3 missense variant contributes to psoriatic arthritis by affecting splicing and modifying signaling, activation and differentiation of T-cells (2020) Hüffmeier U, Löhr S, Uebe S, Popp B, Bowes J, Kirchner P, Giardina E, et al. Conference contribution Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype (2020) Zanoni P, Steindl K, Sengupta D, Sticht H, Joset P, Baar A, Van Ravenswaaij-Arts CMA, et al. Conference contribution Further clinical and molecular delineation of spondylocostal dysostosis type 3 (2020) Schuhmann S, Koller H, Sticht H, Kraus C, Krumbiegel M, Uebe S, Ekici AB, et al. Conference contribution Mono-allelic deleterious variants in autosomal recessive skeletal dysplasia genes are strongly associated with idiopathic short stature (2020) Thiel CT, Hauer N, Vogl C, Uebe S, Sticht H, Ekici AB, Kraus C, et al. Conference contribution Enriched environment ameliorates adult hippocampal neurogenesis deficits in Tcf4 haploinsufficient mice (2020) Braun K, Häberle B, Wittmann MT, Lie DC Journal article Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons (2020) Hauberg ME, Creus-Muncunill J, Bendl J, Kozlenkov A, Zeng B, Corwin C, Chowdhury S, et al. Journal article Loss of PHF6 leads to aberrant development of human neuron-like cells (2020) Fliedner A, Gregor A, Ferrazzi F, Ekici AB, Sticht H, Zweier C Journal article The transcription factor Sox10 is an essential determinant of branching morphogenesis and involution in the mouse mammary gland (2020) Mertelmeyer S, Weider M, Baroti T, Reiprich S, Fröb F, Stolt C, Wagner KU, Wegner M Journal article Compensatory neuritogenesis of serotonergic afferents within the striatum of a transgenic rat model of Parkinson's disease (2020) Stemick J, Gauer C, Wihan J, Moceri S, Xiang W, von Hörsten S, Kohl Z, Winkler J Journal article CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair (2020) Wang J, Wang J, Yang L, Zhao C, Wu LN, Xu L, Zhang F, et al. Journal article