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Institut für Biochemie
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören
Overview
Publications
(1,024)
Research Grants
(2)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Distinct forebrain regions define a dichotomous astrocytic profile in multiple system atrophy (2024)
Schneider Y, Gauer C, Andert M, Hoffmann A, Riemenschneider MJ, Krebs W, Chalmers N, et al.
Journal article
Loss of miR-101-3p in melanoma stabilizes genomic integrity, leading to cell death prevention (2024)
Lämmerhirt L, Kappelmann-Fenzl M, Fischer S, Meier P, Stäbler S, Kuphal S, Boßerhoff AK
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
NRN1 interacts with Notch to increase oncogenic STAT3 signaling in melanoma (2024)
Devitt L, Westphal D, Pieger K, Schneider N, Boßerhoff AK, Kuphal S
Journal article
Temporal patterning of the vertebrate developing neural tube (2024)
Sagner A
Journal article, Review 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
A vascularized in vivo melanoma model suitable for metastasis research of different tumor stages using fundamentally different bioinks (2024)
Schmid R, Schmidt S, Schrüfer S, Schubert DW, Heltmann-Meyer S, Schicht M, Paulsen F, et al.
Journal article
Absence of the RING domain in MID1 results in patterning defects in the developing human brain (2024)
Frank S, Gabassi E, Käseberg S, Bertin M, Zografidou L, Pfeiffer D, Brennenstuhl H, et al.
Journal article
Comparison of Extracellular Vesicles from Induced Pluripotent Stem Cell-Derived Brain Cells (2024)
Xavier G, Navarrete Santos A, Hartmann C, Santoro ML, Flegel N, Reinsch J, Majer A, 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
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