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Commons Zero v1.0 Universal","rightsUri":"https://creativecommons.org/publicdomain/zero/1.0/legalcode","schemeUri":"https://spdx.org/licenses/","rightsIdentifier":"cc0-1.0","rightsIdentifierScheme":"SPDX"}],"descriptions":[{"description":"Gaussian 16 (C01) 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factors on creativity"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-10-04","dateType":"Issued"},{"date":"2026-06-16T13:36:13Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Various cognitive process models have been proposed for creative processes. However, existing models and studies cannot explain why the creative outputs of people who follow the same cognitive process are associated with various creativity-quality levels. The research reported in this thesis explored the influence of cognitive factors in creativity through detecting the performance (sequences, contextual details, and evoked time) of creativity-related cognitive factors (recall, association, combination, and retrieval) and linked the performance (sequences and contextual details) with output creativity quality levels of outputs. The first case study identified which creative outputs assessment methods were suited to the research. Consensual Assessment Technique (CAT) and Cognitive Processes Associated with Creativity (CPSS) were selected, considering their consistency in assessment. A second study identified how sequences and contextual details of cognitive factors in a creative process affected output creativity quality levels using think-aloud and interview research. The results show that the cognitive sequence of recall, common association, remote association, retrieval, and remote combination is associated with the highest creativity quality levels of outputs. A framework has been produced summarising the relations between sequences of cognitive factors and output creativity quality levels. A third study revealed physiological performances of cognitive factors in creative processes through Electroencephalograph (EEG). The study revealed that the evoked time of common association is swifter, than recall, than remote association, than combination, than retrieval. A fourth case study tested the framework. The results indicated that creativity quality levels of outputs, generated by following the specific-creativity-quality-level instruction, are consistent with the followed-creativity-quality level. This also supports the reliability of the proposed framework. The findings and outcomes of this thesis lead to further understanding of creativity in the design context. The performance of cognitive factors detected could be further adapted to develop new creativity stimulation tools and further understand creativity cognition.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130661","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:44Z","registered":"2026-06-17T02:30:23Z","published":null,"updated":"2026-06-17T02:30:23Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130660","type":"dois","attributes":{"doi":"10.25560/130660","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130660","identifierType":"URL"}],"creators":[{"name":"Lewis Marffy, Alexander","nameType":"Personal","givenName":"Alexander","familyName":"Lewis Marffy","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Streptococcal pathogens express surface proteins that target inhibitory LILR and complement regulating factors"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-09-12","dateType":"Issued"},{"date":"2026-06-16T13:27:28Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Background: Streptococcus pyogenes, Streptococcus agalactiae, and Streptococcus pneumonia are major causes of invasive human diseases. Bacteria must evade host immune responses to promote virulence utilising mechanisms such as targeting host inhibitory immune receptors and complement regulators. Whilst inhibitory leukocyte Ig-like receptors (LILR) are known targets of bacteria, the bacterial ligands are unknown. Similarly, streptococcal pathogens are known to target the complement regulator factor H (FH), but the mechanism of immune evasion remains unclear. Thus, the hypothesis proposed was that streptococcal pathogens target inhibitory LILR and FH to enhance bacterial immune evasion. Method: A combination of biochemical and cellular assays using isogenic mutants were used to identify streptococcal ligands that interact with LILR. A panel of recombinant proteins and bacterial mutants were constructed to identify bacterial ligand binding domains in LILR and FH. Finally, ex vivo whole blood and neutrophil assays were performed to assess the functional consequences of the bacterial engagement with LILR and FH. Results: This study identified the first bacterial ligands that bind inhibitory LILR: S. pyogenes M3 protein binds LILRB2 and S. agalactiae β protein binds LILRB3. Data also suggest that S. pneumoniae bind LILRB3 via a subset of PspC proteins. Two LILRB3 binding domains were identified in β protein – B75KN and B6C – and a FH binding domain in a loop in B75KN. The data suggest that β protein inhibits neutrophil phagocytosis through engagement with LILRB3, but not by sequestering FH. In contrast, M3 engagement of LILRB2 does not enhance immune evasion; however, recombinant LILRB2 inhibited M3-mediated S. pyogenes adhesion to host cells...","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130660","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:44Z","registered":"2026-06-17T02:30:22Z","published":null,"updated":"2026-06-17T02:30:22Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130659","type":"dois","attributes":{"doi":"10.25560/130659","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130659","identifierType":"URL"}],"creators":[{"name":"Bi, Yang","nameType":"Personal","givenName":"Yang","familyName":"Bi","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Investigating the metabolic function of the gut microbiota in colorectal carcinogenesis via choline metabolism"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-06-30","dateType":"Issued"},{"date":"2026-06-16T13:20:18Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Colorectal cancer (CRC) stands as the third most frequently diagnosed cancer globally. This thesis delves into the intricate relationship between CRC pathogenesis and the gut microbiota, emphasising the microbiota's role in converting dietary components into oncologic or tumour-suppressive metabolites, thereby influencing CRC development. TMAO, a metabolite derived from both dietary choline and carnitine, emerges as a pivotal intermediate marker connecting dietary choices and gut microbial metabolism to CRC risk. Gut microbiota plays a crucial role in TMA and TMAO metabolism. Using 1H-NMR spectroscopy, the study explores the TMA-producing ability of choline and carnitine on Enterobacteriaceae isolates. Identifying three Klebsiella isolates with robust TMA-producing capability, the subsequent investigation involves assessing their colonisation ability and pro-carcinogenic effects in wild-type and ApcMin/+ mice. Despite successful colonisation in antibiotic-treated mice, the Klebsiella isolates did not significantly impact TMA concentrations or induce global metabolic changes in intestinal tissues, faeces, or urine. This observation prompts further investigation on dietary manipulations to alter TMA concentrations. This thesis then shifts its focus to the role of TMAO in CRC development in FabplCre;Apc15lox/+ mice, employing targeted and non-targeted metabolomics, flow cytometry, and RNA-seq. Contrary to expectations, TMAO exhibits anti-tumour effects in a sex-specific manner, particularly pronounced in male mice. These effects are associated with the downregulation of the pro-inflammatory cytokine TNF-α from immune cells like CD8+, CD4+, and Natural Killer cells in colonic tissues. In summary, this thesis provides valuable insights into the intricate interplay between microbial choline metabolism and CRC risk, unravelling unexpected findings that challenge conventional assumptions regarding the role of TMAO in CRC development.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130659","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:44Z","registered":"2026-06-17T02:30:21Z","published":null,"updated":"2026-06-17T02:30:21Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130658","type":"dois","attributes":{"doi":"10.25560/130658","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130658","identifierType":"URL"}],"creators":[{"name":"Day, Harley","nameType":"Personal","givenName":"Harley","familyName":"Day","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Mathematical modelling of long-term progression of atopic dermatitis"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-09-27","dateType":"Issued"},{"date":"2026-06-16T13:13:49Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"The skin is the largest organ of the human body, and performs a vital defensive and physiological role, protecting the delicate tissues beneath from pathogens and physical damage while preventing water loss and regulating body temperature. Many of these protective functions are performed by the epidermis, a paper-thin layer of cells rich in structural proteins and lipids which produce antimicrobial peptides and plays host to cells of the immune system. Failure of this epidermal layer of the skin to maintain a competent barrier against pathogens can trigger the activation of allergic immune responses, causing the most common form of skin disease, atopic dermatitis (AD). While mild-to-moderate AD can usually be well controlled by emollient and corticosteroid therapies, some AD patients go on to develop a more treatment-resistant form of chronic AD. The pathophysiological mechanisms of chronic AD are poorly understood, making development of new therapies and management of chronic AD difficult. In this thesis, we develop a mechanistic mathematical model of chronic AD with the aim of elucidating how the complicated disease dynamics of chronic AD emerge as the result of dysregulated interactions between the barrier and immune system. We show how different genotypes can lead to different disease dynamics and propose how various therapies might affect these dynamics. The model we develop is structured as a hybrid dynamical system, consisting of both continuous-valued and discrete-valued components which interact to produce counterintuitive dynamical properties. We develop a series of novel methods designed to elucidate the range of dynamics available in our model. Finally, we investigate how the methods we develop here can be applied to hybrid dynamical systems more broadly.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130658","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:43Z","registered":"2026-06-17T02:30:20Z","published":null,"updated":"2026-06-17T02:30:20Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130653","type":"dois","attributes":{"doi":"10.25560/130653","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130653","identifierType":"URL"}],"creators":[{"name":"Jones, Edmund","nameType":"Personal","givenName":"Edmund","familyName":"Jones","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Non-destructive evaluation of discontinuous creep crack growth in 316H stainless steel"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-12-23","dateType":"Issued"},{"date":"2026-06-16T10:51:01Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Component life assessment is of great importance in the nuclear industry and has become of particular interest during the life extension of advanced gas cooled reactors (AGRs). Creep crack growth (CCG) is a significant failure mode for components in AGRs. Laboratory CCG tests are used to determine CCG laws that are applied to component life assessments. Accurate non-destructive evaluation (NDE) methods are critical for laboratory CCG tests to be valid and useful. The CCG tests currently use direct current potential drop (DCPD) measurement systems to evaluate the crack length. However, there have been concerns about the accuracy of the DCPD method for sizing discontinuous cracks as often found in CCG tests performed on 316H stainless steel. This thesis investigates discontinuous cracking, a characteristic form of creep damage ahead of a stress concentration in 316H stainless steel. This thesis will show that DCPD is not effective at sizing discontinuous creep damage in examples presented in this work the real extent of damage was greater than three times the size predicted using DCPD. This has implications for the accuracy of component life assessments and CCG testing undertaken using DCPD over the past 40 years. This thesis proposes an alternative measurement system to size creep damage during CCG testing. This alternative method uses a temporal Rayleigh wave ultrasound approach. The interaction of Rayleigh waves with different crack like defects is presented, showing the feasibility of a measurement systems using Rayleigh waves. The development of the practical measurement system to size creep damage in compact tension (CT) samples using waveguides is presented. This novel measurement systems performance is shown to outperform DCPD in a CCG test. The Rayleigh wave measurement system predicting the extent of a 1.4 mm discontinuous creep crack within 0.2 mm while DCPD predicted a crack length of 0.4 mm.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130653","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:43Z","registered":"2026-06-17T02:30:19Z","published":null,"updated":"2026-06-17T02:30:19Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130652","type":"dois","attributes":{"doi":"10.25560/130652","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130652","identifierType":"URL"}],"creators":[{"name":"Saunders, Catherine","nameType":"Personal","givenName":"Catherine","familyName":"Saunders","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Advanced single particle characterisation of cargo loading in therapeutic particles"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-09-27","dateType":"Issued"},{"date":"2026-06-16T10:40:00Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Using particles as drug delivery systems offers a flexible modality for improved biostability and controlled release. However, these systems often exhibit compositional and cargo loading heterogeneity, which impacts their biological behaviours. This heterogeneity is challenging to characterise with standard analytical techniques, which hinders translation of new formulations to the clinic. Consequently, there is great opportunity to develop advanced techniques to characterise therapeutic particles. In this thesis, several advanced characterisation methods are applied to study cargo loading in a variety of drug delivery systems. One study utilised a recently developed platform, single particle automated Raman trapping analysis (SPARTA), which gives single particle information at the population level. An analysis method was developed herein to determine cargo loading location in vesicles and population heterogeneity. This method allowed detailed characterisation of cargo loading behaviours in a wide range of nanovesicles, including commercial formulations. Another study utilised small angle neutron scattering (SANS) to study bulk-level structural changes in nanostructured lipid nanoparticles (LNP) based on formulation, and protein loading. This was combined with fluorescence correlation spectroscopy (FCS) to examine the connections between LNP formulation, morphology and loading ability. This revealed that protein loading is dictated by the interaction between electrostatic, lipid ordering and sterics. The final study utilised confocal Raman imaging to study changes in drug release and carrier morphology in microparticles for controlled release. A platform was developed to allow repeated measurements on the same microparticles over several weeks, combined with measurement automation for population-level analysis. Taken together, the methods developed and utilised in this thesis allow population-level understanding of cargo loading in therapeutic particles, with single particle detail. This approach is crucial to understanding population heterogeneity, which can support manufacturing quality control, inform regulatory characterisation standards, and aid the prediction of in vivo behaviours, to ultimately advance the translation of future particle-based therapeutics.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130652","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:43Z","registered":"2026-06-17T02:30:18Z","published":null,"updated":"2026-06-17T02:30:18Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130650","type":"dois","attributes":{"doi":"10.25560/130650","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130650","identifierType":"URL"}],"creators":[{"name":"Sahota, Annpreet","nameType":"Personal","givenName":"Annpreet","familyName":"Sahota","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Single-cell nanobiopsy for spatial and temporal profiling of living cells"}],"publisher":"Imperial College London","container":{},"publicationYear":2024,"subjects":[],"contributors":[],"dates":[{"date":"2024-01-17","dateType":"Issued"},{"date":"2026-06-16T10:31:48Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Single-cell analysis is a rapidly growing field that is reshaping our understanding of fundamental biological processes and complex diseases. Subcellular sampling techniques advance from previous single-cell methods as they maintain cells in their standard microenvironment and do not require cell lysis or fixation. These have the potential to profile the single-cell omics of living cells and aid our understanding of intracellular mechanisms. However, many existing subcellular sampling tools involve the aspiration of cytoplasmic fluid, raising questions regarding the viability of cells with repeat sampling. In this work, minimally invasive dielectrophoretic nanoscale tweezers (nanotweezers) are employed for precise sampling of RNA and single mitochondrion in living neurons. With this nanobiopsy tool, biomolecules are trapped directly from cells, avoiding the need to remove large cytoplasmic volumes. The nanotweezer platform is developed to provide spatial and temporal measurements of biomolecules in live single cells. Following optimising the dielectrophoretic trapping capabilities of the nanotweezer, we show that mRNA can be successfully isolated from different compartments of live rat hippocampal neurons with high spatial resolution. Repeat sampling from the same cell with minimal impact on cell viability and the detection of RNAs from individual nanobiopsies is achieved. As a result, the tool is used to study dendritic localisation of mRNAs, including measuring dynamic changes in gene expression in the same living cell. Single mitochondrion extraction from the neurites of single neurons is also presented, alongside developing methods for single mitochondrion analysis. Finally, the effects of α-synuclein on single-cell mitochondrial expression are investigated, where we demonstrate the removal of mitochondria from the same living neuron before and after treatment. This work shows promising results for future expansion of the tool for dynamic and precise spatial quantification of biomolecules in single cells which could ultimately have significant implications in spatial transcriptomics, deciphering cellular mechanics, and tracking disease.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130650","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-17T02:01:43Z","registered":"2026-06-17T02:30:16Z","published":null,"updated":"2026-06-17T02:30:16Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130635","type":"dois","attributes":{"doi":"10.25560/130635","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130635","identifierType":"URL"}],"creators":[{"name":"Al-Sulaiti, Mohammed","nameType":"Personal","givenName":"Mohammed","familyName":"Al-Sulaiti","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Conceptualizing a climate change legislative framework in Qatar based on the capacity of existing environmental legislation: an exploratory and explanatory study"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-11-27","dateType":"Issued"},{"date":"2026-06-15T15:18:45Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"This PhD thesis focuses on examining and interpreting various pieces of environmental legislation in order to conceptualize the climate legislation mechanism in Qatar. The main research methodology employed in this study involves doctrinal analysis of environmental legislation and content analysis of national development plans, particularly the environmental pillar. The study utilizes an analysis of the existing environmental legislation as well as the environmental section of national development plans. The analysis includes the consideration of several legal documents such as laws, decree laws, Emiri Decrees, Emiri Resolutions, Decrees, Council of Ministers Resolutions, Prime Minister Resolutions, and Ministerial Resolutions. The main findings of this thesis highlight that while Qatar currently lacks a specific climate change law, there are elements that could be utilized to develop such a law. The study suggests that building a legislative framework for climate change could help avoid the irregular development that has been observed in environmental legislation in Qatar. Thus, this thesis proposes a legislative framework for climate change based on legislative policy and legislative drafting. It also legally codifies the content of the NCCAP, specifically focusing on reducing GHG emissions by 25% by 2030. By aligning with Qatar’s international obligations, such as the Nationally Determined Contributions (NDC) submission to the United Nations Framework Convention on Climate Change (UNFCCC), the proposed legal text becomes more acceptable.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130635","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:45Z","registered":"2026-06-16T02:30:22Z","published":null,"updated":"2026-06-17T02:01:43Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130633","type":"dois","attributes":{"doi":"10.25560/130633","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130633","identifierType":"URL"}],"creators":[{"name":"Dewé, Tamsin","nameType":"Personal","givenName":"Tamsin","familyName":"Dewé","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Modelling the relationship between antibiotic consumption and resistance in heterogeneous populations"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-09-01","dateType":"Issued"},{"date":"2026-06-15T15:13:08Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Antibiotic resistance occurs when bacteria can withstand treatment with antibiotics designed to kill them or inhibit their growth, and has been identified as a major threat to global health. Mathematical and statistical models can help us understand the epidemiology and evolution of resistance, but there are important features that are not well captured by existing models. In particular, the coexistence of antibiotic-resistant and sensitive bacterial strains at intermediate frequencies is persistently observed across a wide range of bacterial and host populations, resistance mechanisms, and rates of antibiotic treatment. In this research, an agent-based model of multi-strain bacterial populations was developed, with a novel competition mechanism that enables coexistence of resistant and sensitive bacteria across a wide range of parameters. Results from this model also demonstrated the influence of bacterial population structure, in addition to antibiotic consumption, in shaping resistance in heterogeneous populations. The model was then used to examine the influence of horizontal gene transfer on resistance dynamics, and determine the conditions for sustaining coexistence when resistance is mobile. Likelihood-free inference was used to estimate model parameters, which enabled simulations that mirrored the heterogeneity of an observed bacterial population. As a counterpart to this model of resistance carriage in commensal organisms, a statistical model of resistance in clinical isolates was compared to antibiotic consumption data from veterinary and medical settings across Europe. Results from this analyses supported the importance of antibiotic consumption as a driver of resistance in organisms causing disease; however, they also showed that this relationship is affected by other factors. Taken together, the results of this research underline the importance of a One Health approach, and good antibiotic stewardship, in controlling antibiotic resistance. However, they also imply that more specific interventions are not necessarily transferable to different contexts.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130633","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:44Z","registered":"2026-06-16T02:30:20Z","published":null,"updated":"2026-06-17T02:01:42Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130634","type":"dois","attributes":{"doi":"10.25560/130634","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130634","identifierType":"URL"}],"creators":[{"name":"Guo, Jia","nameType":"Personal","givenName":"Jia","familyName":"Guo","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Lanthanum nickel oxide based double perovskites and their exsolution phenomena"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-10-24","dateType":"Issued"},{"date":"2026-06-15T15:15:49Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"The increasing energy demand and the need to reduce greenhouse gas emissions are driving a transition to renewable energy sources. Solid-oxide cells (SOCs) offer promise for integrating intermittent renewables into the grid, yet current fuel electrode materials, exemplified by Ni cermet, face limitations including degradation and poisoning. A novel approach called 'exsolution,' involving the creation of metal nanoparticle-decorated oxides, is gaining traction for its potential to improve SOCs by producing stable and efficient electrode materials. This thesis investigates double perovskite materials as potential fuel electrodes due to their favourable electrochemical properties and unique exsolution behaviour. Specifically, lanthanum nickel ruthenates (LaxNiRuO6-y, x = 2, 1.9,1.85) and ruthenium-doped lanthanum nickel titanates (LaxNiTi0.9Ru0.1O6-δ, x = 2, 1.85) were studied. A-site deficiency was found to facilitate exsolution. Notably, A-site deficient lanthanum nickel ruthenate (La1.85NiRuO6-y) exhibited exsolution of Ni and Ru cations at relatively low temperatures, with particle size increasing at higher temperatures. In this study, La1.85NiRuO6-y underwent exsolution of Ni and Ru cations at 450°C, with separate B-site cation exsolution initiating at lower temperatures (300~360°C). In-situ microscopy and electrochemical analysis confirmed rapid exsolution at 450°C, resulting in enhanced electrochemical performance in single cells test due to the exsolution of Ni-Ru bimetallic nanoparticles. A-site deficient ruthenium-doped lanthanum nickel titanates (La1.85NiTi0.9Ru0.1O6-δ) displayed exsolution of Ni nanoparticles over a wide temperature range, contrasting with Ru cations, which required extremely high temperatures for exsolution. The thesis proposes a critical temperature range (400-450°C) influencing exsolution behaviour. Additionally, attempts to replace exsolved cations with infiltrated iron cations showed enhanced exsolution of Ni-Ru alloy nanoparticles. In summary, this thesis extensively examines double perovskite materials as fuel electrodes for SOCs, emphasizing their exsolution behaviours. It illuminates exsolution in B-site ordered double perovskites with varied cation properties and proposes metal nanoparticle-decorated lanthanum nickel ruthenates and titanates as promising SOC fuel electrode candidates.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130634","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:44Z","registered":"2026-06-16T02:30:21Z","published":null,"updated":"2026-06-17T02:01:42Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130632","type":"dois","attributes":{"doi":"10.25560/130632","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130632","identifierType":"URL"}],"creators":[{"name":"Tagliaferri, Stefano","nameType":"Personal","givenName":"Stefano","familyName":"Tagliaferri","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Direct ink writing of aqueous electrochemical energy storage devices"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-08-01","dateType":"Issued"},{"date":"2026-06-15T15:11:32Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Electrochemical energy storage devices (EESDs) will play a key role in the future development of portable and wearable electronics. The current manufacturing methods for EESDs rely on toxic and flammable solvents, raising concerns about user safety and environmental sustainability. Energy storage devices containing aqueous electrolytes are intrinsically safer; however, their low energy density and cycle life hinder commercialization. Direct Ink Writing (DIW) is a 3D printing technique emerging as a promising manufacturing method for customizable EESDs with tailored size and enhanced performance. Inks for DIW can be formulated using water and environmentally sustainable solvents. Additionally, 3D printed EESDs present superior surface-to-volume ratios and high loading of active material, overcoming the energy density limitations of aqueous EESDs and the low rate capability of thick electrodes. DIW has the capability to print a broad range of materials, enabling the fabrication of electrodes, electrolyte and passive components in the same manufacturing process. Nonetheless, the composition of the inks for DIW must be carefully designed to achieve structures with the desired geometry and functional properties. Therefore, in this work we investigated new ink formulations for the manufacturing of aqueous EESDs using DIW, with specific focus on aqueous graphene supercapacitors, zinc hybrid capacitors and zinc ion batteries. The printability of the inks was optimized to fabricate electrochemically-active structures with the desired degree of geometric complexity. We demonstrated that 3D printed graphene and zinc electrodes achieve superior energy density, rate capability and stability in aqueous supercapacitors and zinc hybrid capacitors. Additionally, we shed light into the charge storage and ageing mechanisms of 3D printed electrodes for aqueous supercapacitors and zinc ion batteries, using a combination of physical and electrochemical characterization tools. Finally, we successfully demonstrated an all-printed zinc-ion battery, combining interdigitated zinc anodes and manganese oxide cathodes with printable gel electrolytes.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130632","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:44Z","registered":"2026-06-16T02:30:19Z","published":null,"updated":"2026-06-17T02:01:41Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130630","type":"dois","attributes":{"doi":"10.25560/130630","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130630","identifierType":"URL"}],"creators":[{"name":"Chen, Kaili","nameType":"Personal","givenName":"Kaili","familyName":"Chen","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Engineering catalytic gold nanoclusters and nanovesicles for detection of disease"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-10-01","dateType":"Issued"},{"date":"2026-06-15T15:09:28Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Timely and accurate disease detection is a crucial first step in effective disease management, including personalised medicine treatments. Point-of-care (PoC) diagnostics offer numerous advantages, such as user-friendliness, speed, and cost-effectiveness, making them valuable in resource-limited settings. Nevertheless, their limited test offerings often result in lower sensitivity and specificity when compared to laboratory-based diagnostics. To address this limitation, this thesis focuses on leveraging ultra-small renal clearable gold nanoclusters (AuNCs) as the foundation for developing straightforward, sensitive and cost-effective biosensors for in vivo disease monitoring. These NCs possess several benefits, including biocompatibility and the ability to be readily eliminated from the body. In this thesis, the catalytic activity of NCs for signal amplification was optimised firstly while ensuring they retain their renal clearable size, which aimed to enhance the sensitivity of biosensors and guarantee renal clearance for in vivo sensing. The second aim focuses on creating an enzyme-responsive biosensor for the rapid and sensitive detection of malaria infection while malaria remains a substantial global health challenge, particularly in developing nations. The final project involves encapsulating nanoclusters within liposomes to create a biosensor tailored for the detection of bacterial infections. This innovative biosensor holds the potential to revolutionise the diagnosis of bacterial infections. In conclusion, this PhD research thesis represents an important step towards the development of biosensors for in vivo disease detection using ultra-small renal clearable gold nanoclusters. The successful development of these biosensors could have a significant impact on global health, enabling early detection and treatment of diseases, improving patient outcomes, and reducing healthcare costs.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130630","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:43Z","registered":"2026-06-16T02:30:18Z","published":null,"updated":"2026-06-17T02:01:41Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130629","type":"dois","attributes":{"doi":"10.25560/130629","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130629","identifierType":"URL"}],"creators":[{"name":"Li, Edmond Chun Man","nameType":"Personal","givenName":"Edmond Chun Man","familyName":"Li","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"A unity in fragments: understanding stakeholder perceptions of electronic health record systems interoperability and its impact on care delivery in NHS England"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-10-01","dateType":"Issued"},{"date":"2026-06-15T15:06:53Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Despite the growing prevalence of health information technologies such as Electronic Health Records (EHR) in England, the inability of patients’ clinical information to be easily accessed and shared between different healthcare providers continues to pose a significant challenge to clinician productivity, patient safety, and care quality. Considering these shortcomings, dedicated efforts to understanding how difficulties with EHR interoperability manifest in the English National Health Service (NHS) have seldom been undertaken. Using a multiple-methods approach, this thesis aims to develop a comprehensive understanding of the current state of EHR interoperability and clinical data sharing across the NHS, and its practical effects on routine clinical care through investigating the perceptions and experiences of three key NHS stakeholder groups: healthcare administrators, frontline doctors, and patients. This thesis demonstrates that limited EHR interoperability is a well-recognised problem that remains a significant hurdle to the effective use of healthcare data. Although perceptions towards what interoperability entails and the reasons contributing to its suboptimal state differed between the three stakeholder groups studied, the current state of EHR interoperability remains largely rudimentary, does not meet the expectations of its users, and is detrimental to overall care quality and safety. The need to address limited EHR interoperability will continue to grow in urgency as health systems worldwide increasingly rely on Health Information Technology (HIT) to help meet patients’ evolving care needs and preferences. Doing so will require a fundamental rethinking of how EHR are integrated into our clinical environments, better-coordinated approaches to tackling the multifaceted barriers to achieving interoperability, and continued research efforts to better understand what healthcare providers and patients need from these technologies. Doing so is critical to informing the development of more effective, evidence-based policy solutions to fixing poor EHR interoperability, as the importance and ubiquity of health data continue to grow in the NHS.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130629","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:43Z","registered":"2026-06-16T02:30:17Z","published":null,"updated":"2026-06-17T02:01:41Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}},{"id":"10.25560/130627","type":"dois","attributes":{"doi":"10.25560/130627","identifiers":[{"identifier":"https://hdl.handle.net/10044/1/130627","identifierType":"URL"}],"creators":[{"name":"Williams, Jack","nameType":"Personal","givenName":"Jack","familyName":"Williams","affiliation":["Imperial College London"],"nameIdentifiers":[]}],"titles":[{"title":"Investigation into the function and structure of Peptidyl Arginine Deiminase 6 in early embryonic development"}],"publisher":"Imperial College London","container":{},"publicationYear":2023,"subjects":[],"contributors":[],"dates":[{"date":"2023-12-01","dateType":"Issued"},{"date":"2026-06-15T15:01:03Z","dateType":"Available"}],"language":null,"types":{"ris":"RPRT","bibtex":"article","citeproc":"article-journal","schemaOrg":"ScholarlyArticle","resourceType":"Text","resourceTypeGeneral":"Text"},"relatedIdentifiers":[],"relatedItems":[],"sizes":[],"formats":[],"version":"Open Access","rightsList":[],"descriptions":[{"description":"Peptidyl arginine deiminase 6 (PADI6) is a maternal-effect gene essential for early embryo development and female fertility. Despite its clear biological and clinical significance, the function of PADI6 remains elusive. PADI6 belongs to a family of enzymes, that catalyse the post-translational conversion of arginine to citrulline, however, there is currently no reported catalytic activity of PADI6. The work described in this thesis aimed to expand our understanding of the function of PADI6 in early embryo development, in particular, the question of whether PADI6 has a catalytic function. Using biophysical experiments, I have shown that human PADI6 is dimeric in solution and unlike other PADIs does not bind calcium. We have solved a 2.44 Å X-ray crystal structure of human PADI6, the first high resolution structure of PADI6 to date. Analysis of this structure showed the active site cleft of PADI6 was closed and provided further insight on the structural significance of reported pathogenic PADI6 variants. In search of interacting proteins, I have confirmed interactions with five key early embryonic proteins and shown that these proteins do not have an activating effect on PADI6. Using two mouse models, I have shown that embryonic genome activation (EGA) is defective in embryos from Padi6 knock-out mothers, and that there may be an additional non-essential catalytic function of PADI6 during EGA. Finally, I have shown that knocking out Padi6 in mice has little to no effect on the establishment of the maternal imprinted methylation signature. Together this thesis answers outstanding questions regarding the function of PADI6 and offers new perspectives on its function in early embryonic development.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://spiral.imperial.ac.uk/handle/10044/1/130627","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-06-16T02:01:43Z","registered":"2026-06-16T02:30:15Z","published":null,"updated":"2026-06-17T02:01:40Z"},"relationships":{"client":{"data":{"id":"bl.imperial","type":"clients"}}}}],"meta":{"total":221702,"totalPages":400,"page":1},"links":{"self":"https://api.datacite.org/dois?provider-id=urks\u0026state=findable","next":"https://api.datacite.org/dois?page%5Bnumber%5D=2\u0026page%5Bsize%5D=25\u0026provider-id=urks"}}