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Professur für Bioinformatik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören
Institut für Biochemie
Overview
Publications
(288)
Research Grants
(4)
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Journal article
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Computational Analysis of Histamine Protonation Effects on H1R Binding (2023)
Conrad M, Horn A, Sticht H
Journal article
The large GTPase AtGBPL3 links nuclear envelope formation and morphogenesis to transcriptional repression (2023)
Reimann T, Müdsam C, Schachtler C, Ince S, Sticht H, Herrmann C, Stürzl M, Kost B
Journal article
Assessment of Covalently Binding Warhead Compounds in the Validation of the Cytomegalovirus Nuclear Egress Complex as an Antiviral Target (2023)
Tillmanns J, Häge S, Borst EM, Wardin J, Eickhoff J, Klebl B, Wagner S, et al.
Journal article
De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy. (2023)
von Wintzingerode L, Ben-Zeev B, Cesario C, Chan KM, Depienne C, Elpeleg O, Iascone M, et al.
Journal article
The Interactive Complex between Cytomegalovirus Kinase vCDK/pUL97 and Host Factors CDK7-Cyclin H Determines Individual Patterns of Transcription in Infected Cells. (2023)
Schütz M, Cordsmeier A, Wangen C, Horn A, Wyler E, Enßer A, Sticht H, Marschall M
Journal article
Switchable Signaling Molecules for Media Modulation: Fundamentals, Applications, and Research Directions (2023)
Brand L, Scherer M, Lotter S, tom Dieck T, Schäfer M, Burkovski A, Sticht H, et al.
Journal article
Trimer stability of Helicobacter pylori HtrA is regulated by a natural mutation in the protease domain (2023)
Zarzecka U, Tegtmeyer N, Sticht H, Backert S
Journal article
The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohort (2023)
Zanoni P, Steindl K, Sticht H, Oneda B, Joset P, Ivanovski I, Horn AH, et al.
Journal article
Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies (2022)
Vintschger E, Kraemer D, Joset P, Horn A, Rauch A, Sticht H, Bachmann-Gagescu R
Journal article
Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy (2022)
Luppe J, Sticht H, Lecoquierre F, Goldenberg A, Gorman KM, Molloy B, Agolini E, et al.
Journal article
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