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- University of Groningen; Published 28 Nov ’25
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neurological diseases pose major challenges to modern healthcare. Despite their apparent differences, these conditions share striking cellular-level similarities, including altered cell–cell communication
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transcription-coupled and other nucleotide excision repair–related DNA repair mechanisms (https://lanslab.eu/publications/ ). This project builds on our previous findings that persistent DNA repair intermediates
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. These electrical impulses are generated in the muscle cells through the action of ion channels in the cell membrane, allowing entry and exit of charged ions. Variations in the genes encoding ion channels can cause
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cell types and simulate their interactions with joint tissues. You will implement and validate molecular reporter technologies to monitor neuronal activation and pain-related signaling pathways, and
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group. The project aims to characterize ependymoma tumor cells and its tumor microenvironment (TME) on a single cell level. The goal of the project is to use this knowledge of the immune landscape
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stem cells or stem cell-based biomaterials? And eager to explore cutting-edge technologies like genome editing and in vivo imaging? Or are you perhaps fascinated by eye research and do you have an
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like to know more about the different phases within the PhD trajectory? You can read more about this on this page . As part of this project, you will use innovative neuronal cell models and advanced
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on untapped potential of THz and optical wavelengths alongside existing radio technologies. This PhD position focuses on Dynamic Network Architectures and Control for Tropospheric and Cell-Free Networks. You
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contribute directly to this effort by developing patient-specific induced pluripotent stem cell (iPSC)-derived vascular tissues to assess disease severity, drug efficacy and the potential of gene-correction
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modelling approaches (https://www.carlier-insilico-lab.com/who-are-we) . Dr LaPointe’s group (www.lapointelab.com ) is dedicated to developing groundbreaking regenerative cell therapies that can transform the