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Claudia Lennicke
Researcher at Martin Luther University of Halle-Wittenberg
Publications - 9
Citations - 516
Claudia Lennicke is an academic researcher from Martin Luther University of Halle-Wittenberg. The author has contributed to research in topics: Signal transduction & LGR5. The author has an hindex of 5, co-authored 8 publications receiving 358 citations.
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Journal ArticleDOI
Hydrogen peroxide – production, fate and role in redox signaling of tumor cells
TL;DR: This article reviews the current knowledge about the intracellular production of H2O2 along with redox signaling pathways mediating either the growth or apoptosis of tumor cells and how the targeting of H 2O2-linked sources and/or signaling components involved in tumor progression and survival might lead to novel therapeutic targets.
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Redox proteomics: Methods for the identification and enrichment of redox-modified proteins and their applications
Claudia Lennicke,Jette Rahn,Nadine Heimer,Rudolf Lichtenfels,Ludger A. Wessjohann,Barbara Seliger +5 more
TL;DR: This review will focus on the methods and technologies, which are currently applied for the detection, identification, and quantification of oxPTMs including the design of high throughput approaches and the analyses ofOxPTMs related to physiological and pathological conditions.
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Individual effects of different selenocompounds on the hepatic proteome and energy metabolism of mice.
Claudia Lennicke,Jette Rahn,Anna P. Kipp,Biljana Dojčinović,Andreas Müller,Ludger A. Wessjohann,Rudolf Lichtenfels,Barbara Seliger +7 more
TL;DR: Comparisons of effects of feeding distinct Se compounds and concentrations on hepatic metabolism and expression profiles of mice indicate that compound-specific effects of high doses appear to be independent of selenoproteins.
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Modulation of MHC class I surface expression in B16F10 melanoma cells by methylseleninic acid.
Claudia Lennicke,Jette Rahn,Jürgen Bukur,Falko Hochgräfe,Ludger A. Wessjohann,Rudolf Lichtenfels,Barbara Seliger +6 more
TL;DR: MSA might affect the malignant phenotype of various tumor cells by restoring MHC class I APM component expression due to an altered redox status and by partially mimicking IFN-gamma signaling thereby providing a novel mechanism for the chemotherapeutic potential of methylselenol generating Se compounds.
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Loss of epithelium-specific GPx2 results in aberrant cell fate decisions during intestinal differentiation
Claudia Lennicke,Jette Rahn,Claudia Wickenhauser,Rudolf Lichtenfels,Andreas Müller,Ludger A. Wessjohann,Anna P. Kipp,Barbara Seliger +7 more
TL;DR: The observed expression pattern suggests that GPx2 KO goblet cells might be limited in synthesizing CLCA1, which seems to be important for the modulation of cell fate decisions in the murine intestinal epithelium.