354 research outputs found

    Motivators for student academic dishonesty at a medium sized university in Alberta, Canada: Faculty and student perspectives

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    Academic misconduct describes a complex set of behaviours with many reported motivating factors. However, most research investigating the motivating factors behind academic misconduct has been conducted on American college students. To assess academic misconduct at our mid-sized university in Alberta, Canada, we conducted focus groups with students and faculty to further explore the motivational factors underlying academic misconduct. We conducted a thematic analysis on the interview responses in which two thematic categories of motivations arose: dispositional (or psychological) factors and situational (or contextual) factors. Both student and faculty participants reported a variety of motivating factors for academic misconduct, including but not limited to dispositional aspects, such as attitudes concerning academic misconduct or a lack of understanding, as well as contextual factors, such as taking a full course load and familial pressure. However, unlike their American counterparts, our participants did not discuss the impact that their peers have on motivating academic misconduct. We add our results to the growing body of research which focuses on identifying and analyzing Canadian trends in academic misconduct research

    Bibliometric analysis of authorship trends and collaboration dynamics over the past three decades of BONE's publication history

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    The existence of a gender gap in academia has been a hotly debated topic over the past several decades. It has been argued that due to the gender gap, it is more difficult for women to obtain higher positions. Manuscripts serve as an important measurement of one's accomplishments within a particular field of academia. Here, we analyzed, over the past 3 decades, authorship and other trends in manuscripts published in BONE, one of the premier journals in the field of bone and mineral metabolism. For this study, one complete year of manuscripts was evaluated (e.g. 1985, 1995, 2005, 2015) for each decade. A bibliometric analysis was then performed of authorship trends for those manuscripts. Analyzed fields included: average number of authors per manuscript, numerical position of the corresponding author, number of institutions collaborating on each manuscript, number of countries involved with each manuscript, number of references, and number of citations per manuscript. Each of these fields increased significantly over the 30-year time frame (p < 10− 6). The gender of both the first and corresponding authors was identified and analyzed over time and by region. There was a significant increase in the percentage of female first authors from 23.4% in 1985 to 47.8% in 2015 (p = 0.001). The percentage of female corresponding authors also increased from 21.2% in 1985 to 35.4% in 2015 although it was not significant (p = 0.07). With such a substantial emphasis being placed on publishing in academic medicine, it is crucial to comprehend the changes in publishing characteristics over time and geographical region. These findings highlight authorship trends in BONE over time as well as by region. Importantly, these findings also highlight where challenges still exist

    Genetic Predisposition of Atherosclerotic Cardiovascular Disease in Ancient Human Remains

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    Background: Several computed tomographic studies have shown the presence of atherosclerosis in ancient human remains. However, while it is important to understand the development of atherosclerotic cardiovascular disease (ASCVD), genetic data concerning the prevalence of the disease-associated single nucleotide polymorphisms (SNPs) in our ancestors are scarce. Objective: For a better understanding of the role of genetics in the evolution of ASCVD, we applied an enrichment capture sequencing approach to mummified human remains from different geographic regions and time periods. Methods: Twenty-two mummified individuals were analyzed for their genetic predisposition of ASCVD. Next-generation sequencing methods were applied to ancient DNA (aDNA) samples, including a novel enrichment approach specifically designed to capture SNPs associated with ASCVD in genome-wide association studies of modern humans. Findings: Five out of 22 ancient individuals passed all filter steps for calculating a weighted polygenic risk score (PRS) based on 87 SNPs in 56 genes. PRSs were correlated to scores obtained from contemporary people from around the world and cover their complete range. The genetic results of the ancient individuals reflect their phenotypic results, given that the only two mummies showing calcified atherosclerotic arterial plaques on computed tomography scans are the ones exhibiting the highest calculated PRSs. Conclusions: These data show that alleles associated with ASCVD have been widespread for at least 5,000 years. Despite some limitations due to the nature of aDNA, our approach has the potential to lead to a better understanding of the interaction between environmental and genetic influences on the development of ASCVD

    The Vehicle, Fall 1991

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    Table of Contents ImprovisationAmy Schmitzerpage 5-6 Courthouse ClockAnthony Smithpage 7 The PaintingAngie Gallionpage 8 Empty MoonVictoria Bennettpage 9 ClarissaLaura Durnellpage 10 untitledNancy Jamespage 11 Imprisoned (photo)Dan Kooncepage 12 I Hit Mother Nature with My Ten SpeedJohn Haywardpage 13 The Realm of MotherJennifer Moropage 14-16 untitled (drawing)Mark Randallpage 20 With Purity and PerversionBret Evangelistapage 21 O\u27Hare AirportAnthony Smithpage 22 morgen, my desolationtravis mcdadepage 22-23 Ever GreenChris Rosenstockpage 24 JigsawThomas D. Schnarrepage 25-26 Notes on the Egyptian ExhibitVictoria Bennettpage 27 Moving OnChristina Roypage 28 weep my inquisitive hearttravis mcdadepage 29-30 Dance (drawing)Tim Cullotonpage 31 Roots of the OakThomas D. Schnarrepage 32-33 god\u27s suicideLiam Burkepage 34 The Poa TreeSheila Taylorpage 35https://thekeep.eiu.edu/vehicle/1056/thumbnail.jp

    Cluster M Mycobacteriophages Bongo, PegLeg, and Rey with Unusually Large Repertoires of tRNA Isotopes

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    Genomic analysis of a large set of phages infecting the common hostMycobacterium smegmatis mc2155 shows that they span considerable genetic diversity. There are more than 20 distinct types that lack nucleotide similarity with each other, and there is considerable diversity within most of the groups. Three newly isolated temperate mycobacteriophages, Bongo, PegLeg, and Rey, constitute a new group (cluster M), with the closely related phages Bongo and PegLeg forming subcluster M1 and the more distantly related Rey forming subcluster M2. The cluster M mycobacteriophages have siphoviral morphologies with unusually long tails, are homoimmune, and have larger than average genomes (80.2 to 83.7 kbp). They exhibit a variety of features not previously described in other mycobacteriophages, including noncanonical genome architectures and several unusual sets of conserved repeated sequences suggesting novel regulatory systems for both transcription and translation. In addition to containing transfer-messenger RNA and RtcB-like RNA ligase genes, their genomes encode 21 to 24 tRNA genes encompassing complete or nearly complete sets of isotypes. We predict that these tRNAs are used in late lytic growth, likely compensating for the degradation or inadequacy of host tRNAs. They may represent a complete set of tRNAs necessary for late lytic growth, especially when taken together with the apparent lack of codons in the same late genes that correspond to tRNAs that the genomes of the phages do not obviously encode
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