14 algorithm-development-"Multiple"-"Prof"-"Prof"-"St" PhD positions at University of Cambridge
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therapy (Simpson et al. in preparation*). When these local metabolic / immunologic changes happen during pancreatic cancer evolution remains unknown. More importantly, whether these spatial changes can be
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target, since all known treatment resistance mechanisms are downstream of, and dependent on FOXA1. However, FOXA1 has been a difficult protein to study for technical reasons. We have developed a novel tool
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Ascl1 are important. We have undertaken a comprehensive discovery experiment to identify all the proteins that can physically interact with Ascl1, using a method we developed called RIME (Rapid
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studies, and misinformation and information deception-will also be considered. In the first half year, the candidate will work closely with Dr. Seaborn and senior researchers to train and gain experience