Lehrstuhl für Humangenetik

ALS is imprinted in the chromatin accessibility of blood cells (2023) Kühlwein JK, Ruf WP, Kandler K, Witzel S, Lang C, Mulaw MA, Ekici AB, et al. Journal article Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons (2023) Asadollahi R, Delvendahl , Muff R, Tan G, Rodrieguez DG, Turan S, Russo M, et al. Journal article Nanomaterial-based ophthalmic therapies (2023) Unterweger H, Janko C, Civelek M, Cicha I, Spielvogel H, Tietze R, Friedrich B, Alexiou C Journal article Expanding the phenotype of 12q21 deletions: A role of BTG1 in speech development? (2023) Blum K, Krumbiegel M, Kraus C, Reis A, Hüffmeier U Journal article CRISPR/Cas9-mediated generation of hESC lines with homozygote and heterozygote p.R331W mutation in CTBP1 to model HADDTS syndrome. (2023) Winner B, Akdas EY, Turan S, Guhathakurta D, Ekici AB, Salar S, Lie DC, Fejtová A Journal article Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice (2023) Sheppard SE, Bryant L, Wickramasekara RN, Vaccaro C, Robertson B, Hallgren J, Hulen J, et al. Journal article Orally administered nanoparticles for gastrointestinal applications (2023) Tietze R, Unterweger H, Janko C, Civelek M, Cicha I, Spielvogel H, Alexiou C Journal article, Editorial CRISPR/Cas9-mediated generation of hESC lines with homozygote and heterozygote p.R331W mutation in CTBP1 to model HADDTS syndrome (2023) Akdas EY, Turan S, Guhathakurta D, Ekici AB, Salar S, Lie DC, Winner B, Fejtová A Journal article Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells (2023) Enders M, Weier A, Chunder R, An Y, Bremm F, Feigenspan A, Büttner C, et al. Journal article Cardiovascular changes in the NZB/W F1 mouse model of lupus nephritis (2023) Böhme R, Daniel C, Ferrazzi F, Angeloni M, Ekici AB, Winkler T, Hilgers KF, et al. Journal article