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Professur für Bioinformatik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören
Institut für Biochemie
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Publications
(284)
Research Grants
(4)
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Journal article
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De Novo Variants in RAB11B Cause Various Degrees of Global Developmental Delay and Intellectual Disability in Children (2023)
Ahmad N, Fazeli W, Schließke S, Lesca G, Gokce-Samar Z, Mekbib KY, Jin SC, et al.
Journal article
Cytomegalovirus cyclin-dependent kinase ortholog vCDK/pUL97 undergoes regulatory interaction with human cyclin H and CDK7 to codetermine viral replication efficiency (2023)
Schütz M, Wangen C, Sommerer M, Kögler M, Eickhoff J, Degenhart C, Klebl B, et al.
Journal article
A single-nucleotide polymorphism in Helicobacter pylori promotes gastric cancer development (2023)
Sharafutdinov I, Tegtmeyer-Backert N, Linz B, Rohde M, Vieth M, Tay ACY, Lamichhane B, et al.
Journal article
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders (2023)
Langhammer F, Maroofian R, Badar R, Gregor A, Rochman M, Ratliff JB, Koopmans M, et al.
Journal article
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder (2023)
Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, et al.
Journal article
Computational Characterization of the Binding Properties of the HIV1-Neutralizing Antibody PG16 and Design of PG16-Derived CDRH3 Peptides (2023)
Deubler M, Weißenborn L, Leukel S, Horn A, Eichler J, Sticht H
Journal article
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
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