Washington University in St. Louis

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (2020) Kloeckner C, Sticht H, Zacher P, Popp B, Babcock HE, Bakker DP, Barwick K, et al. Journal article Guidelines and definitions for research on epithelial–mesenchymal transition (2020) Yang J, Antin P, Berx G, Blanpain C, Brabletz T, Bronner M, Campbell K, et al. Journal article, Review article Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects (2020) Körber I, Klein OD, Morhart P, Faschingbauer F, Grange DK, Clarke A, Bodemer C, et al. Journal article Chandra Spectral and Timing Analysis of Sgr A∗'s Brightest X-Ray Flares (2019) Haggard D, Nynka M, Mon B, Hernandez NDLC, Nowak M, Heinke C, Neilsen J, et al. Journal article CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019) Konrad E, Nardini N, Caliebe A, Nagel I, Young D, Horvath G, Santoro SL, et al. Journal article Clinical utilization of Chimeric Antigen Receptor T-cells (CAR-T) in B-cell acute lymphoblastic leukemia (ALL)–an expert opinion from the European Society for Blood and Marrow Transplantation (EBMT) and the American Society for Blood and Marrow Transplantation (ASBMT) (2019) Kansagra AJ, Frey NV, Bar M, Laetsch TW, Carpenter PA, Savani BN, Heslop HE, et al. Journal article CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019) Konrad E, Nardini N, Blyth M, Prescott K, Bouman AM, Brilstra EH, Caliebe A, et al. Conference contribution Mitochondria Permeability Transition versus Necroptosis in Oxalate-Induced AKI (2019) Mulay SR, Honarpisheh MM, Foresto-Neto O, Shi C, Desai J, Zhao ZB, Marschner JA, et al. Journal article Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria (2019) Teumer A, Li Y, Ghasemi S, Prins BP, Wuttke M, Hermle T, Giri A, et al. Journal article Cryptic activation of an Irf8 enhancer governs cDC1 fate specification (2019) Durai V, Bagadia P, Granja JM, Satpathy AT, Kulkarni DH, Davidson JT, Wu R, et al. Journal article