Chwilio rhaglenni ymchwil
1-26 o 26 canlyniadau chwilio
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BiomeddygaethMae Biofeddygaeth yn faes ymchwil lle galwch ganolbwyntio eich astudiaethau fel rhan o’n cyfres o raglenni ymchwil Biowyddorau. |
PhD, MPhil, MD | Amser llawn, rhan-amser | Maes |
NiwrowyddoniaethMae’r adran Niwrowyddoniaeth yn mynd ar drywydd amrywiaeth eang o ymchwil niwrofiolegol, yn cwmpasu lefelau moleciwlaidd i ymddygiadol. |
PhD, MPhil, MD | Amser llawn, rhan-amser | Maes |
MeddygaethThe School of Medicine offers research degrees in the medical disciplines such as cancer, immunology, infection, immunity, neurosciences, mental health and population medicine. |
PhD, MPhil, MD | Amser llawn, rhan-amser | Rhaglen |
Biowyddorau MoleciwlaiddMae Biowyddorau Moleciwl yn canolbwyntio ar fecanweithiau moleciwlaidd sy’n sail i swyddogaeth biolegol. |
PhD, MPhil, MD | Amser llawn, rhan-amser | Maes |
Bioffiseg AdeileddolMae Bioffiseg Adeileddol yn faes ymchwil y gallwch chi ganolbwyntio eich astudiaethau yn ein rhaglen PhD Gwyddorau’r Golwg ynddo. |
PhD | Amser llawn, rhan-amser | Maes |
Canser a GenetegBydd y rhaglen hon yn arwain at radd ymchwil mewn canser a/neu geneteg y gellid eu defnyddio mewn amrywiaeth o leoliadau academaidd, clinigol a diwydiannol. |
PhD, MPhil, MD | Amser llawn, rhan-amser | Maes |
Haint ac ImiwneddI gynnig gwybodaeth eang ac arbenigedd ym mhob agwedd ar brosesau clefyd imiwnolegol yn seiliedig ar y lefel cellog a moleciwlaidd, gyda chryfderau mewn imiwnedd cynhenid, imiwnoleg canser, bioleg celloedd-T a heintiau bacteriol a firaol. |
PhD, MPhil, MD | Amser llawn, rhan-amser | Maes |
Gwyddorau Biofeddygol a'r GegMae ein Gwyddorau Biofeddygol a’r Geg yn faes ymchwil lle galwch ganolbwyntio eich astudiaethau fel rhan o’n cyfres o raglenni ymchwil Deintyddiaeth (MPhil, PhD). |
PhD, MPhil | Amser llawn, rhan-amser | Maes |
Ymchwilio Clinigol a Gwyddorau'r GolwgMae Ymchwilio Clinigol a Gwyddorau’r Golwg yn faes ymchwil y gallwch chi ganolbwyntio eich astudiaethau yn ein rhaglen PhD Gwyddorau’r Golwg ynddo. |
PhD | Amser llawn, rhan-amser | Maes |
Astudio clefyd niwroseiciatrig dynol mewn niwronau dynol diffygiol DLG2Mae'r prosiect PhD hwn mewn Meddygaeth yn ceisio deall rôl y DLG2 yn ystod datblygiad niwral a niwronau aeddfed gan ddefnyddio amrywiaeth o dechnegau. |
Prosiect | ||
Integration of genetic and functional data to identify drug targets and enhance risk predictionIntegrating brain expression and protein-protein interaction data with genomic data identified a network of immune-related genes implicated in Alzheimer’s disease (AD) susceptibility. |
Prosiect | ||
Characterising DNA damage repair in Huntington’s diseaseParkinson’s disease (PD) is the second most common neurodegenerative disorder and results from the selective loss of dopaminergic neurons within the Substantia nigra pars compacta. |
Prosiect | ||
Detecting dysfunction in the single-cell gene networks underlying Parkinson’s diseaseParkinson’s disease (PD) is the second most common neurodegenerative disorder and results from the selective loss of dopaminergic neurons within the Substantia nigra pars compacta. |
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Microglial NFAT signalling and Alzheimer’s disease genetic risk networksIn this project, you will develop skills in molecular biological, cell culture, genome biology and bioinformatics. |
Prosiect | ||
The molecular basis of cognitive flexibilityThis project examines transcriptomes in key brain regions at critical periods to determine the molecular bases of flexible behaviour. |
Prosiect | ||
Investigating peroxisome dysregulation in Alzheimer’s diseaseIn this project you will first determine how peroxisomes respond to the specific pathogenic proteins associated with AD in vivo. |
Prosiect | ||
Machine Learning for Prediction in Alzheimer's Disease: Identifying Novel Biologically Valid Diagnostic Categories to Inform Precision MedicineThe project will involve investigating the ability of machine learning. |
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Targeting LAG3+ T cells for Cancer ImmunotherapyThis study will look at the control of adaptive immunity in health and inflammation by human blood and mucosal gamma/delta T cells. |
Prosiect | ||
Alzheimer’s disease: Understanding the interaction of microglia risk genesThe aim of this project is to understand the interdependence of specific risk alleles and highlight the possibility of adjunctive therapies targeting different ‘arms’ of the immune cells to treat the disease. |
Prosiect | ||
Investigating the childhood neurodevelopmental origins of adult mental illnessThis PhD utilises new data generated by a Wellcome Trust Collaborative Award between Cardiff and Bristol Universities to test hypotheses on why child NDDs show links with later adult mental illness. |
Prosiect | ||
Flexible vectors for immunotherapy against cancer and pathogensThis project aims to determine pathways that can drive the growth of particular types of NK and T cells that are optimised to provide better protection from disease. We will use cytomegalovirus and leukaemic cells as systems of analysis. |
Prosiect | ||
Role of a mouse ortholog of CR1 (crry) in the 3xTG model of Alzheimer’s Disease (AD)In order to explore further roles of Crry, we have generated and established a 3xTG/Crry-/- colony, but have not yet had resources to explore further the impact of Crry deficiency in this model. |
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Enhancing immune stimulation for novel anti-cancer viral vaccine vectorsWe will combine cutting-edge proteomics with molecular virology and immunology to determine how HCMV induces such strong responses, enabling us to generate optimised vaccine vectors. |
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Optimizing adult mental health outcomes in children with neurodevelopmental problems: interplay of social and genetic factorsThis PhD project provides a unique opportunity to develop advanced methodological and analytic skills in the field of developmental psychopathology. |
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School experiences in children at high genetic risk of mental health problemsThis project will provide important insights into why children with a genomic disorder struggle in school. |
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Molecular mechanisms of CRISPR Cas9 nickase-induced CAG/CTG repeat contraction: Implications for gene editing in expanded repeat disordersThe aim of this project is to understand how contractions occur at the molecular level such that we can make a potential gene editing-based treatment safer and more efficient. |
Prosiect |
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