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We are seeking an ambitious and intellectually driven post-doctoral researcher to join our dynamic cancer research team at the University of Liverpool. Our research programme investigates how
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Strasbourg on a joint project between CNRS (Team STREINTH, UMR7242, Biotechnology and Cell Signaling, ESBS) and Inserm (Group GP-SMIT, U1260, Nanomedicine, CRBS), starting in 2026. The postdoctoral project
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tumor cell signaling, metabolic reprogramming, immuno-oncology, and therapeutic target identification. The lab focuses on understanding metabolic and molecular vulnerabilities driving cancer progression
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(https://www.precisiononcology.ie ) and is funded jointly by Research Ireland and the National Breast Cancer Research Institute (NBCRI). The post is available from April 2026 to March 2029. The Dwyer Lab
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Description The selected candidate will join the team studying the signaling pathways responsible for the assembly of nuclear pore complexes during the cell cycle in healthy and diseased cells, in
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, 41512056). This position will have the opportunity to gain strong training in cancer metabolism, cell growth signaling, and mouse models. The position is aiming at publishing high-profile papers and pursuing
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. Data Integration: Integrate pan-cancer single-cell atlases with spatial transcriptomics to understand signaling pathways and gene-regulatory dynamics. Explainable AI (XAI): Ensure models
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responsibilities? No Preferred Education/Experience PhD in cancer biology. Experience in cancer metabolism and signaling. Cancer metabolism, cancer biology, epigenetics, and animal experiments preferred Deadline
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reprogramming plays a critical role in the initiation and progression of many human cancers. However, the precise mechanisms underlying metabolic rewiring, as well as its inter-patient and intra-tumoral
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The University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 19 days ago
cellular signaling, and cutting-edge applications in drug discovery of critical targets including G-protein-coupled receptors (GPCRs), membrane-embedded proteases, RNA-binding proteins and RNA. In