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Institut für Biochemie
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören
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Publications
(1,070)
Research Grants
(43)
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Tumor Cells Develop Defined Cellular Phenotypes After 3D-Bioprinting in Different Bioinks (2019)
Schmidt S, Schmid R, Arkudas A, Kengelbach-Weigand A, Boßerhoff AK
Journal article
Histone deacetylase expressions in hepatocellular carcinoma and functional effects of histone deacetylase inhibitors on liver cancer cells in vitro (2019)
Freese K, Seitz T, Dietrich P, Lee SM, Thasler WE, Boßerhoff AK, Hellerbrand C
Journal article
Ethanol consumption inhibits the development of autoimmunity by blocking IL-21 secretion in T-FH cells (2019)
Azizov V, Dietel K, Kolenbrander A, Seubert S, Steffen F, Meidenbauer J, Steffen U, et al.
Conference contribution
Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures (2019)
Zweier M, Begemann A, Mcwalter K, Cho MT, Abela L, Banka S, Behring B, et al.
Conference contribution
De novo variants in MAPK8IP3 cause intellectual disability with variable brain anomalies (2019)
Platzer K, Sticht H, Edwards SL, Allen W, Angione KM, Bonati MT, Brasington C, et al.
Conference contribution
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size (2019)
Le Duc D, Giulivi C, Hiatt SM, Napoli E, Panoutsopoulos A, De Crescenzo A, Kotzaeridou U, et al.
Conference contribution
Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly (2019)
Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, et al.
Conference contribution
Rare frameshift mutation in SERPINA3 contributes to generalized pustular psoriasis (2019)
Hüffmeier U, Sticht H, Wenzel J, Wilsmann-Theis D, Wolff K, Löhr S, Frey B, et al.
Conference contribution
Phenotype of the first patient harboring a de novo in-frame deletion in the LisH (LIS1 homology) domain of the WDR26 gene (2019)
Steindl K, Kraemer D, Gogoll L, Zanoni P, Sticht H, Rauch A
Conference contribution
Exploring the phenotypical spectrum of BRD4 defects (2019)
Hauer N, Vogl C, Popp B, Buettner C, Uebe S, Sticht H, Ekici AB, et al.
Conference contribution
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