Sort by
Refine Your Search
-
Listed
-
Category
-
Employer
- University of Cambridge
- University of East Anglia
- The University of Manchester
- University of Warwick;
- King's College London
- University of Birmingham;
- University of East Anglia;
- ;
- Bangor University
- Cranfield University
- The University of Manchester;
- University of Birmingham
- University of Cambridge;
- University of Newcastle
- ; Swansea University
- ; University of Birmingham
- ; University of Plymouth
- ; University of Surrey
- ; University of Sussex
- Brunel University
- Manchester Metropolitan University
- NORTHUMBRIA UNIVERSITY
- Nature Careers
- Newcastle University
- Oxford Brookes University
- Swansea University
- The Institute of Cancer Research
- The University of Edinburgh;
- University of Exeter
- University of Hertfordshire
- University of Plymouth
- University of Reading
- University of Sheffield
- University of Sussex;
- 24 more »
- « less
-
Field
-
their anticancer and neuroprotective activities in human cell-based assays. Generate SAR data linking specific enzymatic modifications to pharmacological properties. This PhD project offers extensive research
-
contributors to obesity and liver steatosis, where lipid accumulation becomes toxic for hepatocytes leading to cell death and consequent inflammation. Autophagy, which removes intracellular components, is key
-
. The aim of this project is to determine how ppRHOs underpin this ecosystem service. Thus, the PhD candidate will physiologically characterise ppRHO knock-in diatom cell lines and investigate how those
-
biochemistry, cellular biology, and plant biology, using facilities across the School of Chemistry, Pharmacy and Pharmacology and The Sainsbury Laboratory. The student will be based in a highly collaborative
-
, Melbourne, Kuala Lumpur and Florence. We are interested in the challenges that electrification (electrical and fuel cell propulsion) brings to energy provision at an airport ecosystem, and novel solutions
-
survival by sustaining essential cellular functions. Together, these pathways may offer a powerful strategy to protect neurons from secondary degeneration and promote long-range axon regeneration after
-
, with exciting implications for future crop improvement and environmental sustainability. By combining state-of-the-art technics in cell biology, genetics, molecular biology, and proteomic, this project
-
be placed into the context of human physiology looking at the impact on glycaemic responses and gut hormone signalling, e.g. GLP-1 and PYY, using advanced cell culture models. The partnership with ADM
-
measure how variants alter force generation, myofibroblast transition and extracellular matrix deposition to contract the fingers. These quantitative, single cell readouts promise to reveal the
-
the mechanisms associated with loss of virulence, as well as identifying novel genetic determinants of pathogenicity. The project will provide broad training in molecular genetics, genomics, cell biology, and