Lehrstuhl für Humangenetik

PERIPHERAL PULSE MEASUREMENTS FOR THE DETECTION OF SILENT ATRIAL FIBRILLATION: RESULTS FROM THE PROSPECTIVE, CONTROLLED TRIAL "KNOW YOUR PULSE POST STROKE" (2020) Kallmünzer B, Macha K, Wang R, Siedler G, Stoll S, Marsch A, Gerner S, et al. Conference contribution MANAGEMENT OF INSUFFICIENT FUNCTIONAL ANTITHROMBOTIC ACTIVITY DURING TREATMENT WITH DIRECT ORAL ANTICOAGULANTS FOR STROKE PREVENTION (2020) Macha K, Stoll S, Siedler G, Volbers B, Strasser E, Schwab S, Kallmünzer B Conference contribution Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND) (2020) Vera G, Sorlin A, Delplancq G, Lecoquierre F, Brasseur-Daudruy M, Petit F, Smol T, et al. Journal article Mycobacterial Cord Factor Reprograms the Macrophage Response to IFN-γ towards Enhanced Inflammation yet Impaired Antigen Presentation and Expression of GBP1 (2020) Huber A, Killy B, Grummel N, Bodendorfer B, Paul S, Wiesmann V, Naschberger E, et al. Journal article, Original article Macrophage migration inhibitory factor is regulated by HIF-1α and cAMP and promotes renal cyst cell proliferation in a macrophage-independent manner (2020) Safi W, Kraus A, Grampp S, Schödel J, Buchholz B Journal article Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases (2020) Haskamp S, Bruns H, Hahn M, Hoffmann M, Gregor A, Löhr S, Hahn J, et al. Journal article Genome-wide cooperation ofEMTtranscription factorZEB1 withYAPandAP-1 in breast cancer (2020) Feldker N, Ferrazzi F, Schuhwerk H, Widholz SA, Guenther K, Frisch I, Jakob K, et al. Journal article A case of severe autosomal recessive spinocerebellar ataxia type 18 with a novel nonsense variant in GRID2 (2020) Hetzelt K, Kraus C, Kusnik S, Thiel C, Uebe S, Ekici AB, Trollmann R, et al. Journal article Human sensory neurons derived from pluripotent stem cells for disease modelling and personalized medicine (2020) Lampert A, Bennett DL, McDermott LA, Neureiter A, Eberhardt E, Winner B, Zenke M Journal article CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome (2020) Börstler T, Wend H, Krumbiegel M, Kavyanifar A, Wiesmann da Silva Reis A, Lie DC, Winner B, Turan S Journal article, Original article