522 research outputs found

    Organizational Values Perceived as Evident Among Ohio State University Extension Personnel

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    The study reported here sought to determine the perceived evidence of organizational values and compare the perceived organizational values of Ohio State University Extension personnel. It investigated the organizational values according to the levels of perceived extremely evident and extremely valued. The top five values perceived as extremely evident were: unbiased delivery of information, research-based programs, honesty/integrity in our work, an emphasis on excellence in educational programming, and helping people help themselves (range: 46.4% - 50.4%). The findings provide direction for OSU Extension to develop strong organizational values and target values not being expressed in the work environment

    Results of a Pilot Walking School Bus Program to Prevent Obesity in Hispanic Elementary School Children

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    Thirty-three percent of children, 6-11years, in the US are overweight or obese.1 Walking to school is an affordable mode of transportation that may help reduce this high prevalence of childhood obesity.2 The Walking School Bus (WSB) is an innovative program designed to cut down on traffic congestion while providing a safe way to walk children to school.3 We are aware of no published studies examining the impact of this specific program on obesity prevention. In addition, low-income and minority neighborhoods have been underrepresented in the walkability literature.4 Therefore, we tested the feasibility of a modified WSB program in a low-income minority neighborhood as a strategy to prevent childhood obesity

    Age related diffusion and tractography changes in typically developing pediatric cervical and thoracic spinal cord

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    Background and objective: Diffusion tensor imaging (DTI) and diffusion tensor tractography (DTT) are two techniques that can measure white matter integrity of the spinal cord. Recently, DTI indices have been shown to change with age. The purpose of this study is (a) to evaluate the maturational states of the entire pediatric spinal cord using DTI and DTT indices including fractional anisotropy (FA), mean diffusivity (MD), mean length of white matter fiber tracts and tract density and (b) to analyze the DTI and DTT parameters along the entire spinal cord as a function of spinal cord levels and age. Method: A total of 23 typically developing (TD) pediatric subjects ranging in age from 6 to 16 years old (11.94 ± 3.26 (mean ± standard deviation), 13 females and 10 males) were recruited, and scanned using 3.0 T MR scanner. Reduced FOV diffusion tensor images were acquired axially in the same anatomical location prescribed for the T2-weighted images to cover the entire spinal cord (C1-mid L1 levels). To mitigate motion induced artifacts, diffusion directional images were aligned with the reference image (b0) using a rigid body registration algorithm performed by in-house software developed in Matlab (MathWorks, Natick, Massachusetts). Diffusion tensor maps (FA and MD) and streamline deterministic tractography were then generated from the motion corrected DTI dataset. DTI and DTT parameters were calculated by using ROIs drawn to encapsulate the whole cord along the entire spinal cord by an independent board certified neuroradiologist. These indices then were compared between two age groups (age group A = 6–11 years (n = 11) and age group B = 12–16 years (n = 12)) based on similar standards and age definitions used for reporting spinal cord injury in the pediatric population. Standard least squared linear regression based on a restricted maximum likelihood (REML) method was used to evaluate the relationship between age and DTI and DTT parameters. Results: An increase in FA (group A = 0.42 ± 0.097, group B = 0.49 ± 0.116), white matter tract density (group A = 368.01 ± 236.88, group B = 440.13 ± 245.24) and mean length of fiber tracts (group A = 48.16 ± 20.48 mm, group B = 60.28 ± 23.87 mm) and a decrease in MD (group A = 1.06 ± 0.23 × 10−3 mm2/s, group B = 0.82 ± 0.24 × 10−3 mm2/s) were observed with age along the entire spinal cord. Statistically significant increases have been shown in FA (p = 0.004, R2 = 0.57), tract density (p = 0.0004, R2 = 0.58), mean length of fiber tracts (p \u3c 0.001, R2 = 0.5) and a significant decrease has been shown in MD (p = 0.002, R2 = 0.59) between group A and group B. Also, it has been shown DTI and DTT parameters vary along the spinal cord as a function of intervertebral disk and mid-vertebral body level. Conclusion: This study provides an initial understanding of age related changes of DTI values as well as DTT metrics of the spinal cord. The results show significant differences in DTI and DTT parameters which may result from decreasing water content, myelination of fiber tracts, and the thickening diameter of fiber tracts during the maturation process. Consequently, when quantitative DTI and DTT of the spinal cord is undertaken in the pediatric population an age and level matched normative dataset should be used to accurately interpret the quantitative results. © 201

    MAPPFinder: using Gene Ontology and GenMAPP to create a global gene-expression profile from microarray data

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    MAPPFinder is a tool that creates a global gene-expression profile across all areas of biology by integrating the annotations of the Gene Ontology (GO) Project with the free software package GenMAPP . The results are displayed in a searchable browser, allowing the user to rapidly identify GO terms with over-represented numbers of gene-expression changes. Clicking on GO terms generates GenMAPP graphical files where gene relationships can be explored, annotated, and files can be freely exchanged

    Challenges in editing late nineteenth-and early twentieth-century prose fiction: what is editorial “completeness”?

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    Guy, Scott, Conklin, and Carrol join forces to analyze controversial questions about multi-volume variorum editions of late nineteenth- and early twentieth-century writers such as Wilde, Conrad, Woolf, James, and Wyndam Lewis. What prompted such ambitious, costly editions that take years to complete? How do editors plan to compete with the many popular and scholarly editions readily available? Controversy has also emerged about the readership for these projects and how editorial principles have changed. At center is the thorny question of the role of an editor's value judgments and the "completeness" of an edition. On what grounds can a variorum edition claim to be "definitive"? Is there a better means of determining the "meaningfulness" of textual variants than a reliance on editorial judgment alone? Guy and company offer a timely consideration of variorum editions, the kinds of textual data such editorial scholarship provides and its relevance to literary critical judgments

    The role of empirical methods in investigating readers’ constructions of authorial creativity in literary reading

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    The popularity of literary biographies and the importance publishers place on author publicity materials suggest the concept of an author’s creative intentions is important to readers’ appreciation of literary works. However, the question of how this kind of contextual information informs literary interpretation is contentious. One area of dispute concerns the extent to which readers’ constructions of an author’s creative intentions are text-centred and therefore can adequately be understood by linguistic evidence alone. The current study shows how the relationship between linguistic and contextual factors in readers’ constructions of an author’s creative intentions may be investigated empirically. We use eye-tracking to determine whether readers’ responses to textual features (changes to lexis and punctuation) are affected by prior, extra-textual prompts concerning information about an author’s creative intentions. We showed participants pairs of sentences from Oscar Wilde and Henry James while monitoring their eye movements. The first sentence was followed by a prompt denoting a different attribution (Authorial, Editorial/Publisher and Typographic) for the change that, if present, would appear in the second sentence. After reading the second sentence, participants were asked whether they had detected a change and, if so, to describe it. If the concept of an author’s creative intentions is implicated in literary reading this should influence participants’ reading behaviour and ability to accurately report a change based on the prompt. The findings showed that readers’ noticing of textual variants was sensitive to the prior prompt about its authorship, in the sense of producing an effect on attention and re-reading times. But they also showed that these effects did not follow the pattern predicted of them, based on prior assumptions about readers’ cultures. This last finding points to the importance, as well as the challenges, of further investigating the role of contextual information in readers’ constructions of an author’s creative intentions

    Identifying genetic networks underlying myometrial transition to labor

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    BACKGROUND: Early transition to labor remains a major cause of infant mortality, yet the causes are largely unknown. Although several marker genes have been identified, little is known about the underlying global gene expression patterns and pathways that orchestrate these striking changes. RESULTS: We performed a detailed time-course study of over 9,000 genes in mouse myometrium at defined physiological states: non-pregnant, mid-gestation, late gestation, and postpartum. This dataset allowed us to identify distinct patterns of gene expression that correspond to phases of myometrial 'quiescence', 'term activation', and 'postpartum involution'. Using recently developed functional mapping tools (HOPACH (hierarchical ordered partitioning and collapsing hybrid) and GenMAPP 2.0), we have identified new potential transcriptional regulatory gene networks mediating the transition from quiescence to term activation. CONCLUSIONS: These results implicate the myometrium as an essential regulator of endocrine hormone (cortisol and progesterone synthesis) and signaling pathways (cyclic AMP and cyclic GMP stimulation) that direct quiescence via the transcripitional upregulation of both novel and previously associated regulators. With term activation, we observe the upregulation of cytoskeletal remodeling mediators (intermediate filaments), cell junctions, transcriptional regulators, and the coordinate downregulation of negative control checkpoints of smooth muscle contractile signaling. This analysis provides new evidence of multiple parallel mechanisms of uterine contractile regulation and presents new putative targets for regulating myometrial transformation and contraction

    Constitutive Gs activation using a single-construct tetracycline-inducible expression system in embryonic stem cells and mice

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    Abstract Introduction The controlled expression of many genes, including G-protein coupled receptors (GPCRs), is important for delineating gene functions in complex model systems. Binary systems for inducible regulation of transgene expression are widely used in mice. One system is the tTA/TRE expression system, composed of a tetracycline-dependent DNA binding factor and a separate tetracycline operon. However, the requirement for two separate transgenes (one for each tTA or TRE component) makes this system less amenable to models requiring directed cell targeting, increases the risk of multiple transgene integration sites, and requires extensive screening for appropriately-functioning clones. Methods We developed a single, polycistronic tetracycline-inducible expression platform to control the expression of multiple cistrons in mammalian cells. This platform has three basic constructs: regulator, responder, and destination vectors. The modular platform is compatible with both the TetOff (tTA) and TetOn (rtTA) systems. The modular Gateway recombineering-compatible components facilitate rapidly generating vectors to genetically modify mammalian cells. We apply this system to use the elongation factor 1α (EF1α) promoter to drive doxycycline-regulated expression of both the fluorescent marker mCherry and an engineered Gs-coupled GPCR "Rs1" separated by a 2A ribosomal skip site. Results We show that our combined expression construct drives expression of both the mCherry and Rs1 transgenes in a doxycycline-dependent manner. We successfully target the expression construct into the Rosa26 locus of mouse embryonic stem (ES) cells. Rs1 expression in mouse ES cells increases cAMP accumulation via both basal and ligand-induced Gs mechanisms and is associated with increased embryoid body size. Heterozygous mice carrying the Rs1 expression construct showed normal growth and weight, and developed small increases in bone formation that could be observed in the calvaria. Conclusions Our results demonstrate the feasibility of a single-vector strategy that combines both the tTA and TRE tetracycline-regulated components for use in cells and mouse models. Although the EF1α promoter is useful for driving expression in pluripotent cells, a single copy of the EF1α promoter did not drive high levels of mCherry and Rs1 expression in the differentiated tissues of adult mice. These findings indicate that promoter selection is an important factor when developing transgene expression models

    GenMAPP 2: New features and resources for pathway analysis

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    BACKGROUND: Microarray technologies have evolved rapidly, enabling biologists to quantify genome-wide levels of gene expression, alternative splicing, and sequence variations for a variety of species. Analyzing and displaying these data present a significant challenge. Pathway-based approaches for analyzing microarray data have proven useful for presenting data and for generating testable hypotheses. RESULTS: To address the growing needs of the microarray community we have released version 2 of Gene Map Annotator and Pathway Profiler (GenMAPP), a new GenMAPP database schema, and integrated resources for pathway analysis. We have redesigned the GenMAPP database to support multiple gene annotations and species as well as custom species database creation for a potentially unlimited number of species. We have expanded our pathway resources by utilizing homology information to translate pathway content between species and extending existing pathways with data derived from conserved protein interactions and coexpression. We have implemented a new mode of data visualization to support analysis of complex data, including time-course, single nucleotide polymorphism (SNP), and splicing. GenMAPP version 2 also offers innovative ways to display and share data by incorporating HTML export of analyses for entire sets of pathways as organized web pages. CONCLUSION: GenMAPP version 2 provides a means to rapidly interrogate complex experimental data for pathway-level changes in a diverse range of organisms
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