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Developing a guideline for predictive genetic testing in motor neuron disease (MND) School of Medicine and Population Health PhD Research Project Self Funded Dr A McNeill Application Deadline
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Deep phenotyping of genetic syndromes associated with autism School of Psychology PhD Research Project Self Funded Dr M Freeth Application Deadline: Applications accepted all year round Details
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conditions such as COPD. The complexity of the human innate immune system, difficulties of working in vivo with higher organisms and genetic redundancy in vertebrates, has meant that simpler model organisms
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will need to fund the overseas fee difference of around £24,000 per year. References 1. K. J. De Vos, M. Hafezparast, Neurobiol Dis 105, 283 (2017). 2. A. Moller, et al., Hum Mol Genet 26
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to silence gene expression, gene replacement approaches based on viral and non-viral vectors, moreover genome editing (BE, PE) to target single nucleotide mutations. COL4A1-related disorders are rare, genetic
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will have wide-ranging therapeutic application across the lifecourse. Given the complexity of the human innate immune system, and the difficulties of working in vivo and genetic redundancy in vertebrates
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Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL). CADASIL is a devastating genetic disorder characterised by recurrent strokes, cognitive decline, and other neurological symptoms, with
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studied to-date but have no treatment. Importantly, a large proportion (80%) of these diseases are caused by specific alterations (mistakes) in the genetic building blocks or DNA of affected patients. New
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Developing a clinical pathway to support nurse led whole genome sequencing for neurological diseases
), the majority of adult neurological conditions have a genetic component to their aetiology. Identifying a genetic cause can prove crucial to management. For example, selection of anti-epileptic drugs in
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A McNeill Application Deadline: Applications accepted all year round Details In the UK, a rare condition is one that affects fewer than 1/2000 people. Around 70% of rare conditions have a genetic