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Walter Berger

Researcher at Medical University of Vienna

Publications -  396
Citations -  16667

Walter Berger is an academic researcher from Medical University of Vienna. The author has contributed to research in topics: Cancer & Cell culture. The author has an hindex of 63, co-authored 359 publications receiving 14045 citations. Previous affiliations of Walter Berger include University of Vienna & Université libre de Bruxelles.

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Temozolomide-induced modification of the CXC chemokine network in experimental gliomas

TL;DR: In conclusion, TMZ affects the expression and secretion of CXCL2 (and, to a lesser extent, C XCL3 and CXcl8) in glioma cells, and CxCL2 directly impacts gliomas cell biology.
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Hellebrin and its aglycone form hellebrigenin display similar in vitro growth inhibitory effects in cancer cells and binding profiles to the alpha subunits of the Na+/K+-ATPase

TL;DR: In this article, the in vitro growth inhibitory effects of seven cardiac glycosides including five cardenolides (ouabain, digoxin, digitoxin, gitoxin, uzarigenin-rhamnoside, and their respective aglycone forms) and two bufadienolides were determined by means of the MTT colorimetric assay and hellebrigenin induced cytotoxic effects were visualized by using quantitative videomicroscopy.
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Overexpression of Hsp27 affects the metastatic phenotype of human melanoma cells in vitro.

TL;DR: Overexpression of the small heat shock protein Hsp27 is shown to inhibit the in vitro proliferation rate and to delay tumor development of a human melanoma cell line (A375) in nude mice and to influence the neoplastic phenotype.
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Self-assembled Pt2L2 boxes strongly bind G-quadruplex DNA and influence gene expression in cancer cells.

TL;DR: Three Pt molecular squares of distinct size show biological activity against cancer cells and heavily influence the expression of genes known to form G-quadruplexes in their promoter regions.
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In vitro studies on cisplatin focusing on kinetic aspects of intracellular chemistry by LC-ICP-MS

TL;DR: The use of liquid chromatography in combination with inductively coupled plasma mass spectrometry (LC-ICP-MS) enabled accurate intact cisplatin quantification in cell model experiments and revealed rapid uptake of the drug into the cytosol and the nucleus, supporting the hypothesis of passive diffusion as an uptake mechanism.