Prof. Dr. Heinrich Sticht

Professur für Bioinformatik

Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly (2022) Kloeckner C, Murray JPF, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, et al. Journal article De novo missense variants in FBXO11 alter its protein expression and subcellular localization (2022) Gregor A, Meerbrei T, Gerstner T, Toutain A, Lynch SA, Stals K, Maxton C, et al. Journal article, Original article Effect of Ions and Sequence Variants on the Antagonist Binding Properties of the Histamine H1 Receptor (2022) Conrad M, Söldner C, Sticht H Journal article, Original article A novel D-amino acid peptide with therapeutic potential (ISAD1) inhibits aggregation of neurotoxic disease-relevant mutant Tau and prevents Tau toxicity in vitro (2022) Aillaud I, Kaniyappan S, Chandupatla RR, Ramirez LM, Alkhashrom S, Eichler J, Horn A, et al. Journal article Characterizing the interaction between the htlv-1 transactivator tax-1 with transcription elongation factor ell2 and its impact on viral transactivation (2021) Kohrt S, Strobel S, Mann M, Sticht H, Fleckenstein B, Thoma-Kreß A Journal article, Original article N-Terminus to Arginine Side-Chain Cyclization of Linear Peptidic Neuropeptide y Y4Receptor Ligands Results in Picomolar Binding Constants (2021) Konieczny A, Conrad M, Ertl FJ, Gleixner J, Gattor AO, Grätz L, Schmidt MF, et al. Journal article, Original article Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss (2021) Richard EM, Bakhtiari S, Marsh AP, Kaiyrzhanov R, Wagner M, Shetty S, Pagnozzi A, et al. Journal article Homodimerization of a proximal region within the C-terminus of the orphan G-protein coupled receptor GPR179 (2021) Bachert W, Klotz L, Sticht H, Enz R Journal article The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype (2021) Averdunk L, Sticht H, Surowy H, Luedecke HJ, Koch-Hogrebe M, Alsaif HS, Kahrizi K, et al. Journal article Computational decomposition reveals reshaping of the SARS‐CoV‐2–ACE2 interface among viral variants expressing the N501Y mutation (2021) Socher E, Conrad M, Heger L, Paulsen F, Sticht H, Zunke F, Arnold P Journal article, Original article