Institut für Biochemie


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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

A New Printable Alginate/Hyaluronic Acid/Gelatin Hydrogel Suitable for Biofabrication of In Vitro and In Vivo Metastatic Melanoma Models (2021) Schmid R, Schmidt S, Detsch R, Horder H, Blunk T, Schrüfer S, Schubert DW, et al. Journal article Matrix stiffness mechanosensing modulates the expression and distribution of transcription factors in Schwann cells (2021) Rosso G, Wehner D, Schweitzer C, Sock E, Guck J, Shahin V, Möllmert S Journal article Using the lineage determinants Olig2 and Sox10 to explore transcriptional regulation of oligodendrocyte development (2021) Sock E, Wegner M Journal article, Review article Potent Tau Aggregation Inhibitor D-Peptides Selected against Tau-Repeat 2 Using Mirror Image Phage Display (2021) Malhis M, Kaniyappan S, Aillaud I, Chandupatla RR, Ramirez LM, Zweckstetter M, Horn A, et al. Journal article A glutaminyl cyclase-catalyzed α-synuclein modification identified in human synucleinopathies (2021) Hartlage-Rübsamen M, Bluhm A, Moceri S, Machner L, Köppen J, Schenk M, Hilbrich I, et al. Journal article Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype (2021) Zanoni P, Steindl K, Sengupta D, Joset P, Bahr A, Sticht H, Lang-Muritano M, et al. Journal article Modulation of recombinant human alpha 1 glycine receptor by flavonoids and gingerols (2021) Breitinger U, Sticht H, Breitinger HG Journal article Role of fibroblast growth factor signalling in hepatic fibrosis (2021) Seitz T, Hellerbrand C Journal article, Review article Clinical and molecular delineation of spondylocostal dysostosis type 3 (2021) Schuhmann S, Koller H, Sticht H, Kraus C, Krumbiegel M, Uebe S, Ekici AB, et al. Journal article Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy (Genetics in Medicine, (2020), 10.1038/s41436-020-01020-w) (2021) Klöckner C, Sticht H, Zacher P, Popp B, Babcock HE, Bakker DP, Barwick K, et al. Journal article, Erratum