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Prof. Dr. Heinrich Sticht
List of publications:
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Professur für Bioinformatik
Award(s)
(1)
Project Leads
(1)
Project Memberships
(3)
Publications
(272)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Authored book
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Translation
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Thesis
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Conference contribution
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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
Cortactin-dependent control of Par1b-regulated epithelial cell polarity in Helicobacter infection (2024)
Sharafutdinov I, Harrer A, Müsken M, Rottner K, Sticht H, Täger C, Naumann M, et al.
Journal article
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly (2024)
Herbst C, Bothe V, Wegler M, Axer-Schaefer S, Audebert-Bellanger S, Gecz J, Cogne B, et al.
Journal article
In Silico Study of Camptothecin-Based Pro-Drugs Binding to Human Carboxylesterase 2 (2024)
Beierlein F, Horn A, Sticht H, Mokhir A, Imhof P
Journal article
Further delineation of the SCAF4-associated neurodevelopmental disorder (2024)
Schmid CM, Gregor A, Ruiz A, Manso Bazús C, Herman I, Ammouri F, Kotzaeridou U, et al.
Journal article
Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling (2024)
Boonsawat P, Asadollahi R, Niedrist D, Steindl K, Begemann A, Joset P, Bhoj EJ, et al.
Journal article
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