Precise comparison of the Gaussian expansion method and the Gamow shell model

We perform a detailed comparison of results of the Gamow Shell Model (GSM) and the Gaussian Expansion Method (GEM) supplemented by the complex scaling (CS) method for the same translationally-invariant cluster-orbital shell model (COSM) Hamiltonian. As a benchmark test, we calculate the ground state $0^{+}$ and the first excited state $2^{+}$ of mirror nuclei $^{6}$He and $^{6}$Be in the model space consisting of two valence nucleons in $p$-shell outside of a $^{4}$He core. We find a good overall agreement of results obtained in these two different approaches, also for many-body resonances.Comment: 8 pages, 7 figures. Submitted to PR

Integration of the Rural Roads database in Thailand with the parallel computing environment

We present a solution to integrate the database of the Department of Rural Roads (DRR) in Thailand and to utilize the date on the environment of the parallel computing. We define and classify the usage of the data according to the level of the collaboration for different sources. For the user interface of the integration, we provide a web-based environment with the technique of the HTML5

The Bayesian Optimal Algorithm for Query Refinement in Information Retrieval

Summary To realize more efficient information retrieval it is critical to improve the user's original query, because novice users can not be expected to formulate precise and effective queries. Queries can often be improved by adding extra terms that appear in relevant documents but which were not included in the original query. This is called query expansion. Query refinement, a variant of query expansion, interactively recommends new terms related to the original query. Because previous research did not offer any criterion to guarantee optimality, this paper proposes an optimal algorithm for query refinement with reference to the Bayes criterion

A-band methyl halide dissociation via electronic curve crossing as studied by electron energy loss spectroscopy

Excitation of the A-band low-lying electronic states in the methyl halides, CH3I, CH3Br, CH3Cl, and CH3F, has been investigated for the (n→σ∗) transitions, using electron energy loss spectroscopy (EELS) in the range of 3.5–7.5 eV. For the methyl halides, CH3I, CH3Br, and CH3Cl, three components of the Q complex (3Q1, 3Q0, and 1Q1) were directly observed, with the exception of methyl fluoride, in the optically forbidden EELS experimental conditions of this investigation. The effect of electronic-state curve crossing emerged in the transition probabilities for the 3Q0 and 1Q1 states, with spin-orbit splitting observed and quantified against results from recent ab initio studies

SNAIL2 contributes to tumorigenicity and chemotherapy resistance in pancreatic cancer by regulating IGFBP2

Pancreatic cancer has an extremely poor prognosis because of its resistance to conventional therapies. Cancer stem cell (CSC)-targeted therapy is considered a promising approach for this disease. Epithelial-mesenchymal transition-inducing transcription factors (EMT-TFs) contribute to CSC properties in some solid tumors; however, this mechanism has not been fully elucidated in pancreatic cancer. Zinc finger protein, SNAIL2 (also known as SLUG), is a member of the SNAIL superfamily of EMT-TFs and is commonly overexpressed in pancreatic cancer. Patients exhibiting high SNAIL2 expression have a poor prognosis. In this study, we showed that the suppression of SNAIL2 expression using RNA interference decreased tumorigenicity in vitro (sphere formation assay) and in vivo (xenograft assay) in 2 pancreatic cancer cell lines, KLM1 and KMP5. In addition, SNAIL2 suppression resulted in increased sensitivity to gemcitabine and reduced the expression of CD44, a pancreatic CSC marker. Moreover, experiments on tumor spheroids established from surgically resected pancreatic cancer tissues yielded similar results. A microarray analysis revealed that the mechanism was mediated by insulin-like growth factor (IGF) binding protein 2. These results indicate that IGFBP2 regulated by SNAIL2 may represent an effective therapeutic target for pancreatic cancer