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We have 11 mibtp PhD Projects, Programmes & Scholarships PhD Projects, Programmes & Scholarships

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mibtp PhD Projects, Programmes & Scholarships PhD Projects, Programmes & Scholarships

We have 11 mibtp PhD Projects, Programmes & Scholarships PhD Projects, Programmes & Scholarships

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Interrogating the cellular and molecular mechanisms of tissue fibrosis

Applications are invited for a four-year Postgraduate studentship, as part of the MIBTP programme, to be undertaken within the Biosciences Research Group at Aston University. Read more

Expression, purification and characterization of membrane proteins which are potential antifungal drug targets

An estimated 1.5 million people die from invasive fungal infections (IFI) each year. As well as the increasing patient population (currently exacerbated by the influence of COVID-associated IFIs), the problem of increasing resistance to current therapies is worrying. Read more

Investigating novel Arabidopsis recombination mutants

Meiosis is a specialised cell division during sexual reproduction that is essential for fertility. It reduces chromosome numbers by half, so that haploid gametes are restored to normal ploidy levels upon fertilisation. Read more

Investigating novel Arabidopsis recombination mutants

Meiosis is a specialised cell division during sexual reproduction that is essential for fertility. It reduces chromosome numbers by half, so that haploid gametes are restored to normal ploidy levels upon fertilisation. Read more

Brain Rhythms and Natural Language Processing (NLP)

The main goal of our research group (Neural Oscillations in Multisensory Communication Group at the Centre for Human Brain Health (CHBH), University of Birmingham) is to understand the brain’s information processing in human communication. Read more

Structure and function of Batten disease proteins

The neuronal ceroid lipofucscinoses are a group of inherited neurodegenerative disorders with primarily childhood onset. The most common form, also known as Batten disease or CLN3 disease, is caused by recessively inherited mutation in the CLN3 gene. Read more
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