720 research outputs found

    Data-Intensive Computing in the 21st Century

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    The deluge of data that future applications must processā€”in domains ranging from science to business informaticsā€”creates a compelling argument for substantially increased R&D targeted at discovering scalable hardware and software solutions for data-intensive problems

    RuleCNL: A Controlled Natural Language for Business Rule Specifications

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    Business rules represent the primary means by which companies define their business, perform their actions in order to reach their objectives. Thus, they need to be expressed unambiguously to avoid inconsistencies between business stakeholders and formally in order to be machine-processed. A promising solution is the use of a controlled natural language (CNL) which is a good mediator between natural and formal languages. This paper presents RuleCNL, which is a CNL for defining business rules. Its core feature is the alignment of the business rule definition with the business vocabulary which ensures traceability and consistency with the business domain. The RuleCNL tool provides editors that assist end-users in the writing process and automatic mappings into the Semantics of Business Vocabulary and Business Rules (SBVR) standard. SBVR is grounded in first order logic and includes constructs called semantic formulations that structure the meaning of rules.Comment: 12 pages, 7 figures, Fourth Workshop on Controlled Natural Language (CNL 2014) Proceeding

    Tumor cell migration is inhibited by a novel therapeutic strategy antagonizing the alpha-7 receptor

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    A 14mer peptide (T14) derived from the C-terminus of acetylcholinesterase (AChE) selectively activates metastatic breast cancer cells via the alpha-7 nicotinic receptor (Ī±7 nAChR). This naturally occurring peptide is also present in brain, is elevated in Alzheimerā€™s disease, and is antagonised by a cyclized variant (NBP-14). Here we investigated the effects of NBP-14 in six different cancer cell lines, primary leukemia B-cells and normal B-cells. All cells tested expressed Ī±7 nAChR, intracellular and extracellular T14. However, NBP-14 showed low toxicity and weak antiproliferative effects in the majority of the cell lines and was even less toxic in normal B-cells when compared to primary chronic lymphocytic leukemia cells (P < 0.001). Given the potential role of T14 peptide in metastasis, we next investigated the effects of NBP-14 on tumor cell migration, where it caused a dose-dependent reduction. The extent of NBP-14 inhibition positively correlated with the migration of the cells (r2 = 0.45; P = 0.06). Furthermore, NBP-14 preferentially inhibited the migration of primary leukemia cells when compared with normal B-cells (P = 0.0002); when the normal B-cell data was excluded, this correlation was strengthened (r2 = 0.80; P = 0.006). Importantly, the constitutive Ī±7 nAChR expression positively correlated with intracellular T14 levels (r2 = 0.91; P = 0.0003) and inversely correlated with extracellular T14 levels in the cell culture supernatants (r2 = āˆ’0.79; P = 0.034). However, in the presence of NBP-14, Ī±7 nAChR expression was reduced (P = 0.04) and the most migratory cells showed the largest reduction in expression. In conclusion, NBP-14-mediated antagonism of the Ī±7 nAChR offers a novel therapeutic strategy with the potential to inhibit tumor cell migration

    Development of a readiness ruler for use with alcohol brief interventions

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    Background A quick method of assessing readiness to change was needed for a major study of implementing screening and alcohol brief intervention in England. For this purpose, a Readiness Ruler that had been validated among a sample of male college students in the USA was adapted and applied to a sample of excessive drinkers in a general medical practice located in a deprived area of Gateshead, England. Methods 72 participants identified as excessive drinkers by health professionals completed a single-item Readiness Ruler, the 12-item Readiness to Change Questionnaire (RCQ) and the AUDIT questionnaire. Results In terms of concurrent validity, the relationships between the Readiness Ruler, on the one hand, and either stage of change allocation or a dimensional score derived from the RCQ, on the other hand, were highly significant but weaker than expected. When patients who endorsed the ā€œmaintenanceā€ point on the Readiness Ruler were excluded from the analysis, the above relationships were considerably strengthened for reasons that are discussed. On this basis and with another small change, a final Readiness Ruler was developed. Conclusion If the validity of the Readiness Ruler is confirmed in subsequent research, a quick and simple way of measuring readiness to change will be available for research or clinical work with alcohol brief interventions
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