66 research outputs found

    What data characteristics are needed for data reuse in the domain of social sciences in Korea?

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    With the benefits of data sharing and reuse, data reuse have been promoted in various domains. While there are practices and discussions regarding data sharing and reuse, we still have little knowledge on what characteristics of data impact decisions on data reuse. In this sense, we aim to explore data characteristics in the context of data reuse within the domain of social sciences in Korea. For the purpose of this study, we conducted in-depth interviews with twelve re-searchers in the field of social science in terms of six dimensions: data producer, country/language, data type/collection method, procedure, accessibility, size/currency. For the producer dimension, social scientists preferred data that have been produced by an institution rather than an individual researcher. In language used in the data sets, English were more favored because researchers preferred English than any other languages. In terms of data type, quantitative and survey data types are preferred. For the procedure of data, researchers preferred original raw data with plenty of metadata and demographic information for analysis. For accessibility, there was less preference for restricted data. Lastly, for size/currency, researchers showed a preference for big size data and current data. These preliminary findings can provide better understanding about data reuse and guide improved data reuse services

    Measuring the maturity of open access: a preliminary study

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    Open access is an important part of scholarly communication, and it has been a global phenomenon. The growth of open access brings several signif-icant benefits to the general public as well as researchers, ultimately leads to the advancement of science. For the continuous growth and development of open access, it is necessary to measure the degree of maturity of open ac-cess. However, there is not much discussion about the assessment frame-work for open access. This study aims to propose an assessment framework of open access maturity. For the purpose of this study, we conducted an analysis with a total of 24 literatures relevant to the digital maturity, the ma-turity of open data/open science, and major open access initiatives. For digi-tal maturity, 18 articles were analyzed: 10 articles for generic purpose model, and 8 articles for industry-specific model. In addition, three articles on the maturity of open data/open science were analyzed and three major open ac-cess initiatives. In preliminary analysis results, three dimensions with 13 be-longing items were proposed for measuring the maturity of open access. Three dimensions are OA Policy, OA capability, and Openness quality. For OA policy, there are three items such as OA policy document, OA govern-ance, and OA strategy. For OA Capability, finance for OA, people for OA, culture for OA, and collaboration for OA are proposed. For Openness Quali-ty dimension, six items are suggested: submission and review, author rights, user rights, findability, accessibility, and monitoring

    The associations of continuity of care with inpatient, outpatient, and total medical care costs among older adults with urinary incontinence

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    Introduction Urinary incontinence is a significant health problem with considerable social and economic consequences among older adults. The objective of this study was to investigate the financial impact of continuity of care (CoC) among older urinary incontinence patients in South Korea. Methods We used the NHIS-Senior cohort patient data between January 1, 2010, and December 31, 2010. Patients who were diagnosed with urinary incontinence in 2010 were included. Operational definition of CoC included referrals, number of providers, and number of visits. A generalized linear model (GLM) with Ī³-distributed errors and the log link function was used to examine the relationship between health cost and explanatory variables. Additionally, we conducted a two-part model analysis for inpatient cost. Marginal effect was calculated. Results Higher CoC was associated with a decrease in total medical cost (-0.63, Pā€‰<ā€‰.0001) and in outpatient costs (-0.28, Pā€‰<ā€‰.001). Higher Charlson Comorbidity Index (CCI) score was a significant predictor for increasing total medical cost (0.59, Pā€‰<ā€‰.0001) and outpatient cost (0.22, Pā€‰<ā€‰.0001). Higher CoC predict a reduced medical cost of 360.93forinpatientcost(Pā€‰=ā€‰0.044)and360.93 for inpatient cost (Pā€‰=ā€‰0.044) and 23.91 for outpatient cost (Pā€‰=ā€‰0.008) per patient. Conclusion Higher CoC was associated with decrease in total medical costs among older UI patients. Policy initiatives to promote CoC of older UI patients in the community setting could lead to greater financial sustainability of public health insurance in South Korea.This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors

    International Implementation of Digital Library Software/Platforms

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    Presented at the ASIS&T Annual Meeting, Vancouver BC, Canada, November 11, 2009.This panel will present an overview of adoption and implementation of digital library software/platforms and standards with an international perspective. Decision factors in adoption of particular software/platform and standards are reviewed. Impact of organizational, social, legal, and cultural factors are highlighted

    Opposing Regulation of PROX1 by Interleukin-3 Receptor and NOTCH Directs Differential Host Cell Fate Reprogramming by Kaposi Sarcoma Herpes Virus

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    Lymphatic endothelial cells (LECs) are differentiated from blood vascular endothelial cells (BECs) during embryogenesis and this physiological cell fate specification is controlled by PROX1, the master regulator for lymphatic development. When Kaposi sarcoma herpes virus (KSHV) infects host cells, it activates the otherwise silenced embryonic endothelial differentiation program and reprograms their cell fates. Interestingly, previous studies demonstrated that KSHV drives BECs to acquire a partial lymphatic phenotype by upregulating PROX1 (forward reprogramming), but stimulates LECs to regain some BEC-signature genes by downregulating PROX1 (reverse reprogramming). Despite the significance of this KSHV-induced bidirectional cell fate reprogramming in KS pathogenesis, its underlying molecular mechanism remains undefined. Here, we report that IL3 receptor alpha (IL3RĪ±) and NOTCH play integral roles in the host cell type-specific regulation of PROX1 by KSHV. In BECs, KSHV upregulates IL3RĪ± and phosphorylates STAT5, which binds and activates the PROX1 promoter. In LECs, however, PROX1 was rather downregulated by KSHV-induced NOTCH signal via HEY1, which binds and represses the PROX1 promoter. Moreover, PROX1 was found to be required to maintain HEY1 expression in LECs, establishing a reciprocal regulation between PROX1 and HEY1. Upon co-activation of IL3RĪ± and NOTCH, PROX1 was upregulated in BECs, but downregulated in LECs. Together, our study provides the molecular mechanism underlying the cell type-specific endothelial fate reprogramming by KSHV

    Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia

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    SPONASTRIME dysplasia is a rare, recessive skeletal dysplasia characterized by short stature, facial dysmorphism, and aberrant radiographic findings of the spine and long bone metaphysis. No causative genetic alterations for SPONASTRIME dysplasia have yet been determined. Using whole-exome sequencing (WES), we identified bi-allelic TONSL mutations in 10 of 13 individuals with SPONASTRIME dysplasia. TONSL is a multi-domain scaffold protein that interacts with DNA replication and repair factors and which plays critical roles in resistance to replication stress and the maintenance of genome integrity. We show here that cellular defects in dermal fibroblasts from affected individuals are complemented by the expression of wild-type TONSL. In addition, in vitro cell-based as-says and in silico analyses of TONSL structure support the pathogenicity of those TONSL variants. Intriguingly, a knock-in (KI) Tonsl mouse model leads to embryonic lethality, implying the physiological importance of TONSL. Overall, these findings indicate that genetic variants resulting in reduced function of TONSL cause SPONASTRIME dysplasia and highlight the importance of TONSL in embryonic development and postnatal growth.Peer reviewe
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