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.
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.
We accept medical students who wish to intercalate their studies. Find out more on the Medical School's website.
- Laboratory Research Project
- Literature Review
- Critical Analysis of Current Science
- Ethics and Public Awareness of Science
- Practical Cell Biology
- Practical Developmental Genetics
- Modelling Human Disease and Dysfunction
- Cancer Biology
- Epithelial Physiology 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
A good 2:1 honours degree in a biomedical-related subject.
We also accept medical students who wish to intercalate their studies.
English language requirements
Overall IELTS score 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 content of our courses is reviewed annually to make sure it's up-to-date and relevant. Individual modules are occasionally updated or withdrawn. This is in response to discoveries through our world-leading research; funding changes; professional accreditation requirements; student or employer feedback; outcomes of reviews; and variations in staff or student numbers. In the event of any change we'll consult and inform students in good time and take reasonable steps to minimise disruption. We are no longer offering unrestricted module choice. If your course included unrestricted modules, your department will provide a list of modules from their own and other subject areas that you can choose from.