Molecular and Cellular Basis of Human Disease
Department of Biomedical Science,
Faculty of Science
Whole genome sequencing has opened up a new era of studies into the molecular and cellular basis of human disease. This unique research-led masters course provides training to future scientists in the production and use of animal models for basic research into disease mechanisms and for therapeutic studies.
The new molecular genetic and cellular approaches to understand human disease and disease processes in model systems are well established in our department, with some of the world’s foremost research in these areas being conducted in Sheffield. As the research base broadens and industry begins to adopt new technologies, the demand for this type of specialist training is strong across the healthcare industry and academia.
- Practical Research Project
- Literature Review
- Analysis of Current Science
- Ethics and Public Understanding
Choose from a range of optional modules. These might include:
- Practical Cell Biology
- Practical Developmental Genetics
- Cancer Biology
- Modelling Human Diseases
- Epithelia in Health and Disease
Throughout your degree, you’ll be taught through lectures, practical sessions, lab placements, tutorials and seminars. In small group teaching classes you’ll discuss, debate and present on scientific and ethical topics. The biggest part of the course will be your individual research project, working alongside professional scientists.
Our teaching covers ethics, practical scientific skills and an overview of the current literature. You’ll also develop useful career skills such as presentation, communication and time management.
Assessment is by formal examinations, coursework assignments, debates, poster presentations and a dissertation.
1 year full-time
You’ll need a 2:1 honours degree in a biomedical-related subject.
English language requirements
Overall IELTS grade of 6.5 with a minimum of 6.0 in each component, or equivalent.
Fees and funding
Dr Louise Robson
I work on the disease cystic fibrosis (CF), which is one of the most common inherited diseases in caucasians, with an incidence of 1 in 2,500 live births. In CF a faulty gene means that the protein CFTR does not work properly. My research is looking at how CFTR is regulated normally, and what happens with faulty CFTR. In addition I am in the process of setting up a new diagnostic tool, with the aim of helping our CF clinic in the early diagnosis of children suffering from CF.
You can apply for postgraduate study using our Postgraduate Online Application Form. It's a quick and easy process.
+44 114 222 2319
The course information set out here may change before you begin, particularly if you are applying significantly in advance of the start date.