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Unpublished / Preprint

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Abstract

Journal

Activating enhancer binding protein 2 epsilon (AP-2?)-deficient mice exhibit increased matrix metalloproteinase 13 expression and progressive osteoarthritis development (2015) Niebler S, Schubert T, Hunziker EB, Boßerhoff AK Journal article Antagonistic cross-regulation between Sox9 and Sox10 controls an anti-tumorigenic program in melanoma (2015) Shakhova O, Cheng P, Mishra PJ, Zingg D, Schaefer SM, Debbache J, Haeusel J, et al. Journal article Radial glia phagocytose axonal debris from degenerating overextending axons in the developing olfactory bulb (2015) Amaya DA, Wegner M, Stolt C, Chehrehasa F, Ekberg JAK, St John JA Journal article Transcription factors Sox10 and Sox2 functionally interact with positive transcription elongation factor b in Schwann cells (2015) Arter J, Wegner M Journal article Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo (2015) Arndt S, Landthaler M, Zimmermann JL, Unger P, Wacker E, Shimizu T, Li YF, et al. Journal article Brg1-dependent chromatin remodelling is not essentially required during oligodendroglial differentiation (2015) Bischof M, Weider M, Küspert M, Nave KA, Wegner M Journal article CD83 and GRASP55 interact in human dendritic cells (2015) Stein MF, Blume K, Heilingloh C, Kummer M, Biesinger B, Sticht H, Steinkasserer A Journal article Identification of PDGF-BB binding to thymosin ?4 by chemical cross-linking (2015) Knop J, App C, Huff T, Iavarone F, Castagnola M, Hannappel E Journal article Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients (2015) Moessner R, Frambach Y, Wilsmann-Theis D, Loehr S, Jacobi A, Weyergraf A, Mueller M, et al. Journal article De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females (2015) Popp B, Stove SI, Endele S, Myklebust LM, Hoyer J, Sticht H, Azzarello-Burri S, et al. Journal article