apl. Prof. Dr. Ursula Schlötzer-Schrehardt

Medizinische Fakultät

Potential functional restoration of corneal endothelial cells in Fuchs corneal dystrophy by ROCK inhibitor (Ripasudil) (2019) Kruse F, Tourtas T, Zenkel M, Kinoshita S, Schlötzer-Schrehardt U Conference contribution Involvement of a disintegrin and metalloproteinase 10 (ADAM10) in excessive extracellular matrix production in Fuchs endothelial corneal dystrophy (2019) Komori Y, Okumura N, Hanada N, Tokunaga A, Tourtas T, Schlötzer-Schrehardt U, Kruse F, Koizumi N Conference contribution Identifying Genes that Underlie Exfoliation Syndrome using Genetically Determined Gene Expression (2019) Hirbo J, Pasutto F, Pawar P, Sealock J, Evans P, Gamazon E, Tao R, et al. Conference contribution Are agonistic beta 2-adrenergic receptor autoantibodies present in normal tension glaucoma and secondary open-angle glaucoma? (2019) Hohberger B, Mardin C, Hosari S, Lämmer R, Kunze R, Juenemann A, Schlötzer-Schrehardt U, et al. Conference contribution Feasibility of mTOR inhibitor for the treatment of Fuchs endothelial corneal dystrophy (2019) Nakayama G, Okumura N, Oshima T, Ueda E, Watanabe K, Tourtas T, Schlötzer-Schrehardt U, et al. Conference contribution Drug discovery for the treatment of Fuchs corneal endothelial dystrophy by cell-based drug screening system (2019) Nakagawa R, Okumura N, Onishi T, Oshima T, Ueda E, Watanabe K, Tourtas T, et al. Conference contribution Generation of Reversible Immortalized Cell Lines to Model Pseudoexfoliation Syndrome (2019) Luna C, Challa P, Schlötzer-Schrehardt U, Gonzalez P Conference contribution A potential role for impaired retinoic acid signaling in the pathophysiology of pseudoexfoliation syndrome/glaucoma (2019) Zenkel M, Berner D, Hoja U, Pasutto F, Kruse F, Schlötzer-Schrehardt U Conference contribution Extracellular matrix regulation of limbal epithelial stem cell function (2019) Schlötzer-Schrehardt U, Kruse F, Kraus K, Zenkel M, Kruse F Conference contribution Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal Dystrophy (2019) Okumura N, Hayashi R, Nakano M, Tashiro K, Yoshii K, Aleff R, Butz M, et al. Journal article