Ursula Schlötzer-Schrehardt

Prof. Dr. Ursula Schlötzer-Schrehardt

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Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 August 2002 in Graefe's Archive for Clinical and Experimental Ophthalmology
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Journal Article
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Ursula Schlötzer-SchrehardtUrsula Schlötzer-Schrehardt
Ursula Schlötzer-Schrehardt
AVArne Viestenz
Arne Viestenz
GNGottfried O. Naumann
Gottfried O. Naumann
HLHorst Laqua
Horst Laqua
SMS. Michels
S. Michels
USUrsula Schmidt-Erfurth
Ursula Schmidt-Erfurth

1 December 2007 in Experimental Eye Research
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Journal Article
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Ursula Schlötzer-SchrehardtUrsula Schlötzer-Schrehardt
Ursula Schlötzer-Schrehardt
TDT. Dietrich
T. Dietrich
KSK. Saito
K. Saito
LSL. Sorokin
L. Sorokin
TST. Sasaki
T. Sasaki
FKF.E. Kruse
F.E. Kruse

1 March 2003 in Investigative Ophthalmology & Visual Science
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Journal Article
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Ursula Schlötzer-SchrehardtUrsula Schlötzer-Schrehardt
Ursula Schlötzer-Schrehardt
JLJu¨rgen Lommatzsch
Ju¨rgen Lommatzsch
MKMichael Ku¨chle
Michael Ku¨chle
AKAnastasios G. P. Konstas
Anastasios G. P. Konstas
GNGottfried O. H. Naumann
Gottfried O. H. Naumann
Purpose. To determine the presence, activity, and quantitative differences of matrix metalloproteinases (MMPs) and their endogenous inhibitors (TIMPs) in aqueous humor and serum samples of patients with pseudoexfoliation (PEX) syndrome, PEX glaucoma (PEXG), primary open-angle glaucoma (POAG), and cataract. methods. Aqueous humor and serum samples were collected from 100 patients with PEX syndrome, PEX glaucoma (PEXG), POAG, and cataract, respectively. Levels of MMP-1, -2, -3, -7, -9, and -12 and TIMP-1 and -2 were determined by zymography, Western blot analysis, and specific immunoassays. Activity assay kits were used to quantitate levels of endogenously activated MMP-2 and -9. results. MMP-2, -3, -7, -9, and -12 and TIMP-1 and -2 were identified in human aqueous humor samples from all groups of patients with a six to sevenfold molar excess of TIMPs over MMPs. Whereas serum samples showed no significant differences, total MMP-2 and -3 and TIMP-1 and -2 were detected at significantly higher concentrations in aqueous samples from PEX eyes with and without glaucoma compared with cataractous eyes. MMP-2 and -3 and TIMP-1 were also detected in higher, but not significantly different, amounts in aqueous samples of POAG eyes. However, levels of endogenously activated MMP-2 were significantly decreased in both PEX and POAG samples. The ratio of MMP-2 to its principal inhibitor TIMP-2 was balanced in cataract samples, but was decreased in samples from patients with PEXG, resulting in an excess of TIMP-2 over MMP-2. conclusions. The findings suggest that complex changes in the local MMP-TIMP balance and reduced MMP activity in aqueous humor may promote the abnormal matrix accumulation characteristic of PEX syndrome and may be causally involved in the pathogenesis of both PEX glaucoma and POAG.

1 April 2005 in Ophthalmology
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Journal Article
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Ursula Schlötzer-SchrehardtUrsula Schlötzer-Schrehardt
Ursula Schlötzer-Schrehardt
MSM Stojkovic
M Stojkovic
CHC Hofmannrummelt
C Hofmannrummelt
CCC Cursiefen
C Cursiefen
FKF Kruse
F Kruse
LHL Holbach
L Holbach


1 December 2008 in The American Journal of Pathology
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Journal Article
Closed access
Ursula Schlötzer-SchrehardtUrsula Schlötzer-Schrehardt
Ursula Schlötzer-Schrehardt
FPFrancesca Pasutto
Francesca Pasutto
PSPascal Sommer
Pascal Sommer
IHIan Hornstra
Ian Hornstra
FKFriedrich E. Kruse
Friedrich E. Kruse
MZMatthias Zenkel
Matthias Zenkel