apl. Prof. Dr. Ursula Schlötzer-Schrehardt

Medizinische Fakultät

Laminin-511 and -521-based matrices for efficient ex vivo-expansion of human limbal epithelial progenitor cells (2017) Polisetti N, Sorokin L, Okumura N, Koizumi N, Kinoshita S, Kruse F, Schlötzer-Schrehardt U Journal article The emerging technology of tissue engineering : Focus on stem cell niche (2017) Schlötzer-Schrehardt U, Freudenberg U, Kruse F Journal article A dual role for UCMA in osteoarthritis-Inhibition of aggrecanases and promotion of bone turnover (2017) Stock M, Menges S, Eitzinger N, Gesslein M, Botschner R, Wormser L, Distler A, et al. Journal article Sustained Activation of the Unfolded Protein Response Induces Cell Death in Fuchs' Endothelial Corneal Dystrophy (2017) Okumura N, Kitahara M, Okuda H, Hashimoto K, Ueda E, Nakahara M, Kinoshita S, et al. Journal article Posttranscriptional Regulation of LOXL1 Expression Via Alternative Splicing and Nonsense-Mediated mRNA Decay as an Adaptive Stress Response (2017) Berner D, Zenkel M, Pasutto F, Hoja U, Liravi P, Gusek-Schneider GC, Kruse F, et al. Journal article Autophagy inhibition promotes SNCA/alpha-synuclein release and transfer via extracellular vesicles with a hybrid autophagosome-exosome-like phenotype (2017) Minakaki G, Menges S, Kittel A, Emmanouilidou E, Schäffner I, Barkovits K, Bergmann A, et al. Journal article Activation of TGF-β signaling induces cell death via the unfolded protein response in Fuchs endothelial corneal dystrophy (2017) Okumura N, Hashimoto K, Kitahara M, Okuda H, Ueda E, Watanabe K, Nakahara M, et al. Journal article Mitochondrial and Morphologic Alterations in Native Human Corneal Endothelial Cells Associated With Diabetes Mellitus (2017) Aldrich BT, Schlötzer-Schrehardt U, Skeie JM, Burckart KA, Schmidt GA, Reed CR, Zimmerman MB, et al. Journal article Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1 (2017) Pasutto F, Zenkel M, Hoja U, Berner D, Uebe S, Ferrazzi F, Schödel J, et al. Journal article Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci (2017) Aung T, Ozaki M, Lee MC, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP, et al. Journal article