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Nina Ebel

Researcher at University of Erlangen-Nuremberg

Publications -  12
Citations -  168

Nina Ebel is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: Hydrostatic pressure & Antigen. The author has an hindex of 5, co-authored 12 publications receiving 150 citations.

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Cells under pressure - treatment of eukaryotic cells with high hydrostatic pressure, from physiologic aspects to pressure induced cell death.

TL;DR: High hydrostatic pressure offers both, an economic, easy to apply, clean, and fast technique for the generation of vaccines, and a promising tool to study physiological aspects of pressure on eukaryotic cells.
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High hydrostatic pressure treatment generates inactivated mammalian tumor cells with immunogeneic features.

TL;DR: The complete tumor cell inactivation, the degradation of the cell’s nuclei, and the retention of the immunogeneic potential of these dead tumor cells induced by HHP favor the use of this technique as a powerful and low-cost technique for the inactivation of tumor cells to be used as a vaccine.
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Characterization of Escherichia coli suspensions using UV/Vis/NIR absorption spectroscopy

TL;DR: It is demonstrated that conventional absorption spectroscopy in the ultraviolet, visible and near-infrared spectral range facilitates characterization of Escherichia coli (E. coli) suspensions and provides a tool for the investigation of the inactivation mechanisms.
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Selected anti-tumor vaccines merit a place in multimodal tumor therapies

TL;DR: High hydrostatic pressure (HHP) is introduced as an innovative inactivation technology for tumor cell-based vaccines and studies are presented proving that anti-tumor immune responses can be triggered by combining RT with selected immune therapies.
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Tumor Cell-Based Vaccine Generated With High Hydrostatic Pressure Synergizes With Radiotherapy by Generating a Favorable Anti-tumor Immune Microenvironment.

TL;DR: It is shown for the first time that tumor cell-based vaccine acts synergistically with RTx to significantly retard tumor growth by generating a favorable anti-tumor immune microenvironment.