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to understanding the origins and progression of paediatric brain tumours and developing new therapeutic strategies. The lab combines genetic engineering, molecular biology, and translational research to investigate
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, BRCA2, and PALB2. Through advanced single cell genomics, in vivo modelling, and immune profiling, the team will study early molecular and cellular changes that occur in high-risk breast tissue. The team
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of the lab is the intersection of computational psychiatry and brain-body interactions. The post holder will assist with neuroimaging studies exploring body-brain interactions, working closely with postdocs
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and recent publications of staff and postdocs can be found on the Department's website: http://www.sociology.cam.ac.uk The post is fixed term from 1st October 2025 for 24 months (please note that the
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hundreds of samples from multiple independent marine transmissible cancer clones. The role provides an exciting opportunity to combine single-cell cancer genomics with molecular cytogenetics and statistical
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the lab. This work will explore the molecular mechanisms of DNA damage responses and mutagenesis, and how sensitivity and resistance arise in different cancer cells and genetic backgrounds in response
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modelling of the C. elegans neural network. The lab also uses Two Electrode Voltage Clamp (TEVC) electrophysiology and molecular biology techniques to characterise receptors. There are a broad range of
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will be expected to work on estimating dynamic models of medical spending and savings and is expected to publish in high-impact academic journals, and to contribute to the collegial and intellectual life
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. The role will be based at Douglas House, Department of Psychiatry, Cambridge, and in Oxford, at Akrivia Health (where the postdoc will be seconded to), with the option of working flexibly for one/two
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P. Grey in the Yusuf Hamied Department of Chemistry, working on a project focused on understanding solid-state ion dynamics and phase transformations in lithium- and sodium-ion battery electrode