Einrichtungen, die nicht zum Universitätsklinikum Erlangen gehören

Assessment of the different skin sensitization potentials of irritants and allergens as single substances and in combination using the KeratinoSens assay. (2020) De Rentis A, Pink M, Verma N, Schmitz-Spanke S Journal article, Original article Inducible mouse models of colon cancer for the analysis of sporadic and inflammation-driven tumor progression and lymph node metastasis (2020) Neufert C, Heichler C, Brabletz T, Scheibe K, Boonsanay V, Greten FR, Neurath M Journal article Campylobacter jejuni Serine Protease HtrA Cleaves the Tight Junction Component Claudin-8 (2020) Sharafutdinov I, Soltan Esmaeili D, Harrer A, Tegtmeyer N, Sticht H, Backert S Journal article Retrospective 3D analysis of bone regeneration after cystectomy of odontogenic cysts. (2020) Buchbender M, Koch B, Kesting MR, Matta R, Adler W, Seidel A, Schmitt CM Journal article Investigation of magnetically driven passage of magnetic nanoparticles through eye tissues for magnetic drug targeting (2020) Zahn D, Klein K, Radon P, Berkov D, Erokhin S, Nagel E, Eichhorn M, et al. Journal article A new method for quantitative assessment of hand muscle volume and fat in magnetic resonance images (2020) Friedberger A, Figueiredo C, Bäuerle T, Schett G, Engelke K Journal article Changes in R 3.6-4.0 (2020) Kalibera T, Meyer S, Hornik K Journal article, Editorial Expanding the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and functional proof of aberrant WRC-mediated actin dynamics (2020) Begemann A, Sticht H, Mcwalter K, Vitobello A, Faivre L, Alhaddad B, Banka S, et al. Conference contribution Common RUNX3 missense variant contributes to psoriatic arthritis by affecting splicing and modifying signaling, activation and differentiation of T-cells (2020) Hüffmeier U, Löhr S, Uebe S, Popp B, Bowes J, Kirchner P, Giardina E, et al. Conference contribution Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype (2020) Zanoni P, Steindl K, Sengupta D, Sticht H, Joset P, Baar A, Van Ravenswaaij-Arts CMA, et al. Conference contribution