6,672 research outputs found

    UMSL Bulletin 2023-2024

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    The 2023-2024 Bulletin and Course Catalog for the University of Missouri St. Louis.https://irl.umsl.edu/bulletin/1088/thumbnail.jp

    Graduate Catalog of Studies, 2023-2024

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    The Sound of Bass Culture(s): Heaviness, Blackness, and Ubiquitous Bass

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    Bass culture describes the shared affinity for excessive low frequency aesthetics. During the 2000s and 2010s, discussion of the term first emerged within the context of bass-centric Afrodiasporic popular music genres such as hip-hop, EDM, dancehall, and reggaeton. In this thesis, I theorize sonic elements of bass prominence through the concept of heaviness—a multidimensional timbral definition that extends beyond mere prescriptions of lowness and loudness. Historicizing bass centricity, I discuss Jamaican music during the 1950s and ‘60s where sound system practices contributed to the codification of bass as a sign of Blackness. Looking to the future, I present the concept of ubiquitous bass—the omnipresence of low-end frequencies now available in the latest developments of portable listening devices. Though a case study of Beats headphones, I argue that increased accessibility of heavy bass in virtual experiences marks a significant shift from established accounts of low-end theory

    Proceedings of the 10th International congress on architectural technology (ICAT 2024): architectural technology transformation.

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    The profession of architectural technology is influential in the transformation of the built environment regionally, nationally, and internationally. The congress provides a platform for industry, educators, researchers, and the next generation of built environment students and professionals to showcase where their influence is transforming the built environment through novel ideas, businesses, leadership, innovation, digital transformation, research and development, and sustainable forward-thinking technological and construction assembly design

    3D COACHING: SPORTS BIOMECHANICAL ANALYSIS OF COLLEGIATE ATHLETICS (TRACK & FIELD)

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    Athletic (Track & Field) championships have showcased globally the great strength, power, and speed of athletes in a myriad of disciplines. Notably over the last 30 years, steady improvements in championship performances have intrigued the Athletics community—athletes, coaches, spectators—sparking interest to look further into how this caliber of athletes perform and what the training demands are to continue the pace of progress. Coaches, by nature, focus on what is familiar to them until the next ‘phenomenon’ in development and training becomes recognizable. In consequence, sports science research sources are perceived with complexity, and unused or misused by the Athletic community. Efforts led by leading sports scientists have been made in the live capture of world-class competitors during world championships to better understand, discuss, and use science within the current state of Athletics in published biomechanical reports. Although athletes have a critical role in whether achievements are met, coaching efforts are to serve the athlete's needs within the demands of each discipline. Balancing what an athlete can do biomechanically and the mechanism within a discipline is the challenge. Coaches often turn to the experiences that have built their coaching philosophy for guidance on the best approaches. With a focus on the NCAA collegiate championship, this project served as a biomechanical-driven evidence-based collection to better understand championship performance. The results justified achieving season-best sprint times and jump marks for higher seeding purposes. Furthermore, results underscored the high individuality in step characteristics during the development of acceleration and velocity of sprinters and jumpers. NCAA championships feature arguably the best collegiate and world-class competitors in Athletics. When the coaching and scientific views are taken into consideration at this level, an improved attempt at defining and appropriately applying mechanical principles to the technique and skills used can be established. Assessing kinematic parameters captured during these championships provides insight into biomechanical contributions in performances for coaches to evaluate and improve training design that will shape an athlete’s performance. An opportunity is available to add to the sports science narratives on the mechanics of Athletic disciplines using a biomechanics lens to magnify the coaches’ eye

    Understanding local neuromuscular mechanisms that explain the efficacy of interventions for patellofemoral pain

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    Patellofemoral pain (PFP) is a common and persistent knee pain complaint among all age ranges, especially highly active people. Multiple approaches have been used to understand symptom persistence, including identifying a mechanism explaining intervention benefits (i.e. changes in specific deficits in groups that show symptoms’ improvement). Research has been conducted to identify the characteristics associated with PFP, but uncertainty regarding local neuromuscular characteristics remain evident. The thesis aimed to a) identify the local neuromuscular characteristics associated with PFP, b) develop an evidence informed laboratory protocol to detect those characteristics, c) establish protocol reliability and feasibility, and d) identify interventions that can target these neuromuscular characteristics. A systematic review with meta-analysis was completed to identify the neuromuscular characteristics of all muscles that cross the knee in people with PFP compared to uninjured groups. Ten deficits within three neuromuscular domains were found. Within the electromyography (EMG) domain, a delay in Vastus medialis (VM) relative to Vastus lateralis (VL) excitation onset, a high Biceps femoris (BF) mean excitation amplitude, and a lower Hoffman-reflex amplitude of VM were identified. Within the muscle performance domain, lower isometric, concentric, and eccentric extensors peak torque and total work, lower concentric flexors peak torque, and lower rate of torque development (RTD) to reach 30%, 60% and 90% of extensors peak torque were identified. Hamstring tightness was identified within muscle flexibility domain. The systematic review was published and the results used to inform testing protocol development. A second systematic review with meta-analysis was conducted to identify interventions that can target the local deficits associated with PFP. The results indicate that currently an intervention that effectively modifies EMG characteristics cannot be identified. Predominantly, exercise interventions have effects on strength and flexibility in PFP. Specifically, hip and knee targeted exercises are found to have a potential mechanism of benefit through both characteristics categories. A unique approach was introduced within the thesis to develop a deficit-detection protocol based on systematic review results. This approach provided a comprehensive analysis of the protocols from the studies that were included in the meta-analysis. A battery of tests was developed and included; a) VM-VL excitation onset timing in step-up task, b) BF mean excitation amplitude in single-leg triple-hop test, c) isometric, d) concentric and e) eccentric extensors peak torque, f) RTD to 30%, 60% and 90% of isometric peak torque, and hamstrings flexibility. Reliability testing of the deficit-detection protocol was conducted with both uninjured and participants with PFP over two phases. Phase one evaluated the original protocols adapted from the review. Phase two was performed on the EMG and RTD domains to explore the effects of signal processing parameters on reliability, such as; onset detection thresholds modification, unnormalised signals, and the addition of absolute RTD. For the PFP group: reliable results were demonstrated for concentric and eccentric extensors peak torque; RTD of the quadriceps at 25ms, 50ms and 90% of peak torque; and hamstrings flexibility. The uninjured group showed reliable results in: unnormalised BF mean excitation amplitude; all three peak torque tests; RTD to 30% of peak torque and at 150 and 175 milliseconds; and hamstrings flexibility. To establish participant recruitment rate and retention, in addition to the acceptability of the test protocol, a preliminary feasibility study of the deficit-detection protocol was conducted. A sample of 14 participants with PFP were recruited and tested at the Mile-end campus of QMUL before and after a six weeks period. Feasibility results indicate that 25.5% were willing to participate following an online screening process (n=17/55) and 82% met the eligibility criteria following face-to-face assessment (n=14/17). Recruitment rate was 0.5 participants per week and drop-out rate was 35.2% (n=11/17). The results indicate that the protocol did not meet all a-priori feasibility criteria, but the results can inform future research planning. The thesis has successfully identified local deficits associated with PFP, developed a test protocol that demonstrates reliability in evaluating these deficits and assessed the feasibility of the protocol in individuals with PFP. Interventions to cause change within these local deficits have been identified, with gap maps demonstrating where further research is required to better align the mechanisms of treatment effects with specific deficits associated with PFP

    Multidisciplinary perspectives on Artificial Intelligence and the law

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    This open access book presents an interdisciplinary, multi-authored, edited collection of chapters on Artificial Intelligence (‘AI’) and the Law. AI technology has come to play a central role in the modern data economy. Through a combination of increased computing power, the growing availability of data and the advancement of algorithms, AI has now become an umbrella term for some of the most transformational technological breakthroughs of this age. The importance of AI stems from both the opportunities that it offers and the challenges that it entails. While AI applications hold the promise of economic growth and efficiency gains, they also create significant risks and uncertainty. The potential and perils of AI have thus come to dominate modern discussions of technology and ethics – and although AI was initially allowed to largely develop without guidelines or rules, few would deny that the law is set to play a fundamental role in shaping the future of AI. As the debate over AI is far from over, the need for rigorous analysis has never been greater. This book thus brings together contributors from different fields and backgrounds to explore how the law might provide answers to some of the most pressing questions raised by AI. An outcome of the Católica Research Centre for the Future of Law and its interdisciplinary working group on Law and Artificial Intelligence, it includes contributions by leading scholars in the fields of technology, ethics and the law.info:eu-repo/semantics/publishedVersio

    Identifying alterations in adipose tissue-derived islet GPCR peptide ligand mRNAs in obesity: implications for islet function

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    In addition to acting as an energy reservoir, white adipose tissue is a vital endocrine organ involved in the modulation of cellular function and the maintenance of metabolic homeostasis through the synthesis and secretion of peptides, known as adipokines. It is known that some of these secretory peptides play important regulatory roles in glycaemic control by acting directly on islet β-cells or on insulin-sensitive tissues. Excess adiposity causes alterations in the circulating levels of some adipokines which, depending on their mode of action, can have pro-inflammatory, pro-diabetic or anti-inflammatory, anti-diabetic properties. Some adipokines that are known to act at β-cells have actions that are transduced by binding to G protein- coupled receptors (GPCRs). This large family of receptors represents ~35% of all current drug targets for the treatment of a wide range of diseases, including type 2 diabetes (T2D). Islets express ~300 GPCRs, yet only one islet GPCR is currently directly targeted for T2D treatment. This deficit represents a therapeutic gap that could be filled by the identification of adipose tissue-derived islet GPCR peptide ligands that increase insulin secretion and overall β-cell function. Thus, by defining their mechanisms of action, there is potential for the development of new pharmacotherapies for T2D. Therefore, this thesis describes experiments which aimed to compare the expression profiles of adipose tissue-derived islet GPCR peptide ligand mRNAs under lean and obese conditions, and to characterise the functional effects of a selected candidate of interest on islet cells. Visceral fat depots were retrieved from high-fat diet-induced and genetically obese mouse models, and from human participants. Fat pads were either processed as whole tissue, or mature adipocyte cells were separated from the stromal vascular fraction (SVF) which contains several other cell populations, including preadipocytes and macrophages. The expression levels of 155 islet GPCR peptide ligand mRNAs in whole adipose tissue or in isolated mature adipocytes were quantified using optimised RNA extraction and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) protocols. Comparisons between lean and obese states in mice models and humans revealed significant modifications in the expression levels of several adipokine mRNAs. As expected, mRNAs encoding the positive control genes, Lep and AdipoQ were quantifiable, with the expression of Lep mRNA increasing and that of AdipoQ mRNA decreasing in obesity. Expression of Ccl4 mRNA, encoding chemokine (C-C motif) ligand 4, was significantly upregulated in whole adipose tissue across all models of obesity compared to their lean counterparts. This coincided with elevated circulating Ccl4 peptide levels. This increase was not replicated in isolated mature adipocytes, indicating that the source of upregulated Ccl4 expression in obesity was the SVF of adipose tissue. Based on this significant increase in Ccl4 mRNA expression within visceral fat and its undetermined effects on β-cell function, Ccl4 was selected for further investigation in MIN6 β-cells and mouse islets. PRESTO-Tango β-arrestin reporter assays were performed to determine which GPCRs were activated by exogenous Ccl4. Experiments using HTLA cells expressing a protease-tagged β- arrestin and transfected with GPCR plasmids of interest indicated that 100ng/mL Ccl4 significantly activated Cxcr1 and Cxcr5, but it was not an agonist at the previously identified Ccl4-target GPCRs Ccr1, Ccr2, Ccr5, Ccr9 and Ackr2. RNA extraction and RT-qPCR experiments using MIN6 β-cells and primary islets from lean mice revealed the expression of Cxcr5 mRNA in mouse islets, but it was absent in MIN6 β-cells. The remaining putative Ccl4 receptors (Ccr1, Ccr2, Ccr5, Ccr9, Cxcr1 and Ackr2) were either absent or present at trace levels in mouse islets and MIN6 β-cells. Recombinant mouse Ccl4 protein was used for functional experiments at concentrations of 5, 10, 50 and 100ng/mL, based on previous reports of biological activities at these concentrations. Trypan blue exclusion testing was initially performed to assess the effect of exogenous Ccl4 on MIN6 β-cell viability and these experiments indicated that all concentrations (5-100ng/mL) were well-tolerated. Since β-cells have a low basal rate of apoptosis, cell death was induced by exposure to the saturated free fatty acid, palmitate, or by a cocktail of pro-inflammatory cytokines (interleukin-1β, tumour necrosis factor-α and interferon-γ). In MIN6 β-cells, Ccl4 demonstrated concentration-dependent protective effects against palmitate-induced and cytokine-induced apoptosis. Conversely, while palmitate and cytokines also increased apoptosis of mouse islets, Ccl4 did not protect islets from either inducer. Quantification of bromodeoxyuridine (BrdU) incorporation into β-cell DNA indicated that Ccl4 caused a concentration-dependent reduction in proliferation of MIN6 β-cells in response to 10% fetal bovine serum (FBS). In contrast, immunohistochemical quantification of Ki67-positive mouse islet β-cells showed no differences in β-cell proliferation between control- and Ccl4-treated islets. Whilst the number of β-cells and δ-cells were unaffected, α- cells were significantly depleted by Ccl4 treatment. Exogenous Ccl4 had no effect on nutrient- stimulated insulin secretion from both MIN6 β-cells and primary mouse islets. The 3T3-L1 preadipocyte cell line was used to assess potential Ccl4-mediated paracrine and/or autocrine signalling within adipose tissue. Ccl4 did not alter the mRNA expression of Pparγ, a master regulator of adipocyte differentiation, but did significantly downregulate the mRNA expression of the crucial adipogenic gene, adiponectin. Oil Red O staining and Western blotting were performed to assess lipid accumulation, and insulin and lipolytic signalling, respectively, and these experiments indicated that the observed Ccl4-induced decrease in adiponectin expression failed to correlate with any changes in adipocyte function. In summary, these data demonstrated anti-apoptotic and anti-proliferative actions of the adipokine, Ccl4, on MIN6 β-cells that were not replicated in mouse islets. The absence of any anti-apoptotic, insulin secretory and/or pro-proliferative effects of Ccl4 in islet β-cells suggests that it is unlikely to play a role in regulating β-cell function via crosstalk between adipose tissue and islets. The divergent functional effects highlight that whilst MIN6 cells are a useful primary β-cell surrogate for some studies, primary islets should always be used to confirm physiological relevance. On the other hand, significant α-cell depletion following Ccl4 treatment suggests a cell-specific function within the islets. Furthermore, Ccl4 impaired adiponectin mRNA expression in adipocytes, although, how adipocyte function is affected as a result requires further investigation. Collectively, these data have contributed increased understanding of the role of obesity in modifying the expression of adipose tissue-derived islet GPCR peptide ligands

    UMSL Bulletin 2022-2023

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    The 2022-2023 Bulletin and Course Catalog for the University of Missouri St. Louis.https://irl.umsl.edu/bulletin/1087/thumbnail.jp
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