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Department of Experimental Therapy
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Clinical and Molecular Virology
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Publications
(382)
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Journal article
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Four-and-a-Half LIM-Domain Protein 2 (FHL2) Induces Neuropeptide Y (NPY) in Macrophages in Visceral Adipose Tissue and Promotes Diet-Induced Obesity (2023)
Sommer J, Ehnis H, Seitz T, Schneider J, Wild A, Moceri S, Buechler C, et al.
Journal article
Gut-to-brain spreading of pathology in synucleinopathies: A focus on molecular signalling mediators (2023)
Schmitt V, Masanetz R, Weidenfeller M, Ebbinghaus LS, Süß P, Rosshart SP, von Hörsten S, 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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