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of CRC-associated mucin mRNA isoform signatures in predicting the optimal therapy. These research objectives will be approached using established high-throughput next-generation sequencing, molecular
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-metallic clusters that combine plasmonic and catalytic metals These clusters will be deposited with high control over size and composition using cluster beam deposition on morphologically engineered TiO2
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chromatin organisation, chromatin accessibility and gene expression data for all major cell types forming the peripheral nerve environment (as well as controls), generated from the patient-derived iPSCs and
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