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relevant training and development as part of the apprenticeship programme As a member of our Professional staff you will be expected to demonstrate a commitment to the professional behaviours set out in
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Developing a Developmentally Appropriate AI Chatbot to Support Young People with Inflammatory Bowel Disease Transitioning to Adult Healthcare
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this, they can no longer function properly. The aim of this PhD project is to apply cutting-edge microscopy, genetics and biochemistry to understand the fundamental mechanisms of how cells process phagosomes and
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to join our Programme and Development team as an Administrative Assistant. This role is ideal for someone who is passionate about sports and excels in a setting that promotes initiative and collaboration
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Developing a clinical pathway to support nurse led whole genome sequencing for neurological diseases
), the majority of adult neurological conditions have a genetic component to their aetiology. Identifying a genetic cause can prove crucial to management. For example, selection of anti-epileptic drugs in
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to the advancement of digital imaging technique and computing power. In this project, high speed stereo imaging for flame studies developed in Prof. Zhang’s research lab will be further developed for more quantitative
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facilities. The CDT-GIF has an exciting and challenging programme specifically designed for top performing junior researchers. Alongside the four-year research project, students will receive expert training
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Photosynthesis/water loss measurement Stress response assays Molecular biology and genetics 3D printing Microcontroller usage Lab Culture A culture of respect, dignity and safety and are at the heart of the Rowe
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to explore include mono-chromatic and multi-chromatic illumination, structured illumination, and telecentric illumination distortions. Computer based image analysis approaches will be developed, including
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Christopher Webster, Prof Mimoun Azzouz Application Deadline: 17 August 2025 Details A repeat expansion in the first intron of C9orf72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS