apl. Prof. Dr. Ursula Schlötzer-Schrehardt

Medizinische Fakultät

Levels of aqueous humor trace elements in patients with open-angle glaucoma (2018) Hohberger B, Chaudhri A, Michalke B, Lucio M, Nowomiejska K, Schlötzer-Schrehardt U, Grieb P, et al. Journal article Feasibility of cell-based therapy combined with descemetorhexis for treating Fuchs endothelial corneal dystrophy in rabbit model (2018) Okumura N, Matsumoto D, Fukui Y, Teramoto M, Imai H, Kurosawa T, Shimada T, et al. Journal article Establishment of a drug screening system for Fuchs endothelial corneal dystrophy (2018) Oshima T, Okumura N, Onishi T, Ueda E, Watanabe K, Tourtas T, Schlötzer-Schrehardt U, et al. Conference contribution FoxO Function Is Essential for Maintenance of Autophagic Flux and Neuronal Morphogenesis in Adult Neurogenesis (2018) Schäffner I, Minakaki G, Khan MA, Balta EA, Schlötzer-Schrehardt U, Schwarz TJ, Beckervordersandforth R, et al. Journal article Aqueous humor selenium level and open-angle glaucoma (2018) Juenemann AGM, Michalke B, Lucio M, Chaudhri A, Schlötzer-Schrehardt U, Rejdak R, Rekas M, Hohberger B Journal article Association of rs613872 and trinucleotide repeat expansion in the TCF4 gene in Fuchs endothelial corneal dystrophy in Germany (2018) Komori Y, Okumura N, Hayashi R, Nakano M, Tashiro K, Yoshii K, Aleff R, et al. Conference contribution RNA-seq and pathway analysis of ocular tissues in PEX patients and healthy subjects (2018) Pasutto F, Zenkel M, Berner D, Uebe S, Ekici AB, Kruse F, Reis A, Schlötzer-Schrehardt U Conference contribution Melanocytes as an emerging key player in niche regulation of limbal stem cells (2018) Schlötzer-Schrehardt U, Polisetti N, Zenkel M, Naschberger E, Heger L, Dudziak D, Stürzl M, Kruse F Conference contribution Nutritional and hormonal regulation of lysyl oxidase-like 1 and elastic proteins involved in pseudoexfoliation syndrome/glaucoma (2018) Zenkel M, Berner D, Hoja U, Pasutto F, Kruse F, Schlötzer-Schrehardt U Conference contribution Pseudoexfoliation associated protective variant, rs7173049, reveals a novel regulatory region downstream of LOXL1 (2018) Berner D, Pasutto F, Hoja U, Zenkel M, Ozaki M, Williams S, Ramsay M, et al. Conference contribution