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University of Nottingham, School of Pharmacy PhD Projects, Programs & Scholarships

We have 14 University of Nottingham, School of Pharmacy PhD Projects, Programs & Scholarships

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  15 fully-funded 4-year PhD studentships in the EPSRC Centre for Doctoral Training in Transformative Pharmaceutical Technologies

Funding Type

PhD Type

Funded by the Engineering and Physical Sciences Council, Science Foundation Ireland and 19 industry partners, the EPSRC Centre for Doctoral Training (CDT) in Transformative Pharmaceutical Technologies provides world-leading training to prepare strategic-thinking scientists for high achieving careers in the pharmaceutical and healthcare sectors.
  BBSRC iCASE Project: Supercritical Sterilisation for Biological Tissue Transplant Products
  Dr L White
Application Deadline: 31 May 2019

Funding Type

PhD Type

One of the significant challenges for translation of any tissue derived products is to ensure sterility without compromising structural and biochemical integrity and clinical performance.
  Biomolecular Science and Medicinal Chemistry Division PhD project: Proteases in the ubiquitin system – from molecular mechanisms to the development of novel inhibitors
  Dr I Dreveny
Applications accepted all year round

Funding Type

PhD Type

Ubiquitin is a posttranslational modifier that tags substrate proteins for degradation and regulates virtually all known cellular processes.
  CRISPR CAS9 Genome Editing to Study PIP5K1A in Cancer Cells
  Prof D Heery
Applications accepted all year round

Funding Type

PhD Type

Human PIP5K1A is one of a family of kinases that generate the signalling molecule phosphatidylinositol 4,5-bisphosphate (PIP2) in cells.
  CRISPR-Cas9 genome editing and super-resolved live cell imaging to study the extracellular microenvironment at the single molecule level
  Dr A Piccinini, Prof D Heery
Applications accepted all year round

Funding Type

PhD Type

The three-dimensional space around and between mammalian cells is filled with a complex network of extracellular matrix (ECM) molecules, which instruct fundamental processes such as cell survival, differentiation and migration, in addition to providing structural support for cells.
  Cryo electron microscopy to study innate immune complexes on the surface of cancer cells
  Dr J Emsley
Application Deadline: 31 May 2019

Funding Type

PhD Type

Blood vessels of tumors carry specific markers on the cell surface. The innate immune system consisting of complement proteins and white blood cells (macrophages) are involved in the recognition and destruction of cancer cells.
  Discovery and profiling of small-molecule inhibitors of cellular nuclease enzymes
  Dr G S Winkler
Applications accepted all year round

Funding Type

PhD Type

Nuclease enzymes are non-traditional drug targets that attract an increasing amount of interest as potential targets relevant for a variety of therapeutic areas including infection, cancer and bone disease.
  FOXA1 mutations in Lobular Breast Cancer: Reprogramming Responses to Tamoxifen
  Prof D Heery, Dr S Johnston
Applications accepted all year round

Funding Type

PhD Type

Tumours of the breast are often hormone-dependent, meaning their growth is driven by steroid hormones such as estrogen. This hormone acts upon the estrogen receptor (ER), which together with other transcription factors such as FOXA1 drives tumour growth.
  Monitoring bacterial metabolism using advanced metabolomics methods
  Dr D H Kim, Prof D A Barrett
Applications accepted all year round

Funding Type

PhD Type

The University of Nottingham seeks an enthusiastic PhD candidate to work on an exciting multi-disciplinary project that brings together the techniques of synthetic biology, analytical science and systems biology.
  Role of BTG1 and BTG2 in acute lymphocytic leukaemia and diffuse large B-cell lymphoma
  Dr G S Winkler
Applications accepted all year round

Funding Type

PhD Type

Acute lymphocytic leukaemia (ALL) and diffuse large B-cell lymphoma (DLBCL) is often associated with small deletions of or point mutations in the highly related BTG1 or BTG2 genes.
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