Prof. Dr. Heinrich Sticht



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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Upregulation versus loss of function of NTRK2 in 44 affected individuals leads to 2 distinct neurodevelopmental disorders (2025) Berger E, Jauss RT, Ranells JD, Zonic E, von Wintzingerode L, Wilson A, Wagner J, et al. Journal article A high proportion of germline variants in pediatric chronic myeloid leukemia (2024) Krumbholz M, Dolnik A, Sträng E, Ghete T, Skambraks S, Hutter S, Simonis A, et al. Journal article Two remarkable serine/leucine polymorphisms in Helicobacter pylori: functional importance for serine protease HtrA and adhesin BabA (2024) Backert S, Tegtmeyer N, Horn A, Sticht H, Linz B Journal article Identification of a Nuclear Localization Signal (NLS) in Human Transcription Elongation Factor ELL2 (2024) Kohrt S, Baheerathan A, Prokscha J, Zwosta A, Sticht H, Thoma-Kreß A Journal article Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy (2024) Bergner CG, Breur M, Soto-Bernardini MC, Schäfer L, Lier J, Le Duc D, Bundalian L, et al. Journal article The Autonomous Fusion Activity of Human Cytomegalovirus Glycoprotein B Is Regulated by Its Carboxy-Terminal Domain (2024) Reuter N, Kropff B, CHEN X, Britt WJ, Sticht H, Mach M, Thomas M Journal article Cancer-associated SNPs in bacteria: lessons from Helicobacter pylori (2024) Linz B, Sticht H, Tegtmeyer N, Backert S Journal article, Review article Closed Loop Molecular Communication Testbed: Setup, Interference Analysis, and Experimental Results (2024) Brand L, Scherer M, tom Dieck T, Lotter S, Schäfer M, Burkovski A, Sticht H, et al. Conference contribution Understanding the Cytomegalovirus Cyclin-Dependent Kinase Ortholog pUL97 as a Multifaceted Regulator and an Antiviral Drug Target (2024) Marschall M, Schütz M, Wild M, Socher E, Wangen C, Dhotre K, Rawlinson WD, Sticht H Journal article Missense variants in ANO4 cause sporadic encephalopathic or familial epilepsy with evidence for a dominant-negative effect (2024) Yang F, Begemann A, Reichhart N, Haeckel A, Steindl K, Schellenberger E, Sturm RF, et al. Journal article