Near- and far-field expansions for stationary solutions of Poisson--Nernst--Planck equations

This work is concerned with the stationary Poisson--Nernst--Planck equation with a large parameter which describes a huge number of ions occupying an electrolytic region. Firstly, we focus on the model with a single specie of positive charges in one-dimensional bounded domains due to the assumption that these ions are transported in the same direction along a tubular-like mircodomain. We show that the solution asymptotically blows up in a thin region attached to the boundary, and establish the refined "near-field" and "far-field" expansions for the solutions with respect to the parameter. Moreover, we obtain the boundary concentration phenomenon of the net charge density, which mathematically confirms the physical description that the non-neutral phenomenon occurs near the charged surface. In addition, we revisit a nonlocal Poisson--Boltzmann model for monovalent binary ions and establish a novel comparison for these two models

The Impact of Individual Characteristics, Personality Traits, Perceived Risk on Young People's Intention to Participate in Overseas Working Holiday

AbstractThis paper analyzes whether individual characteristics, personality traits, and perceived risk will affect young people's intention to participate in overseas working holiday, and taking the three countries of Australia, the United States, and the United Kingdom as examples. The sample consists of young people and students at numerous universities and colleges, with ages ranging from 18 to 31. A total of 350 questionnaires were issued, and 204 valid questionnaires were recovered, with a return rate of 58.2%. Multiple regression was used to test hypotheses. The research results indicate that the factors influencing young people's intention to take working holiday in different countries were not entirely the same. It is found that age, work experience, neuroticism, extroversion, openness to experience, agreeableness, environmental and social risk, and agent and workplace risk may influence intention to participate in overseas working holiday. The research implications and recommendations are also presented

Peritoneal metastatic adenocarcinoma possibly due to a gastric duplication cyst: a case report and literature review

BACKGROUND: Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare. CASE PRESENTATION: During a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cystic lesion with no enhancement. Laparoscopic surgery showed a 10 × 10 cm cyst adhering to the gastric corpus. However, attempts to remove the lesion en bloc were unsuccessful, and the ruptured cyst had contaminated the peritoneal cavity. Gastric duplication was diagnosed from microscopic examination of the cyst. Seven months later, the patient suffered a progressive increase in ascites, and repeated cytological analysis showed small nests of adenocarcinoma cells, with primary lesion unknown. Diagnostic laparoscopy showed multiple white nodules scattered over the surface of the liver, greater omentum, and peritoneum. Biopsy of the omental nodules confirmed adenocarcinoma, while carcinomatosis was diagnosed in the peritoneum. CONCLUSIONS: Clinical presentation and chronological developments indicated that the malignancy probably originated from the gastric duplication cyst. This case highlights the importance of accurate preoperative diagnosis and optimal surgical management for gastric duplication as well as considering the potential existence of malignant transformation during surgical evaluation of adult patients with gastric duplication cysts

Higgs boson decays to BcB_c meson in the fragmentation-function approach

In the paper, we present a calculation of the decay widths for the Higgs boson decays to the $B_c$, $B_c^*$, $B_c(2^1S_0)$ and $B_c^*(2^3S_1)$ mesons using the fragmentation-function approach. In the calculation, the fragmentation functions up to order $\alpha_s^3$ based on the nonrelativistic QCD factorization theory are used, and the decay widths for $H\to Q+X$ and $H \to g+X$ at the partonic level are calculated up to order $\alpha_s$. The large logarithms of $m_H^2/m_{Bc}^2$ are resummed up to next-to-leading logarithmic accuracy by solving the evolution equations for the running quark masses and the fragmentation functions. Compared to the leading-order decay widths based on the nonrelativistic QCD approach, the decay widths based on the fragmentation-function approach that include the higher-order QCD corrections are reduced significantly. Our numerical results show that there are about $1.2\times 10^5$ $B_c$ events via the Higgs decays to be produced at the HL-LHC with $3ab^{-1}$, and about $1.6\times 10^6$ $B_c$ events via the Higgs decays to be produced at the HE-LHC with $15ab^{-1}$.Comment: 12 pages, 9 figure

The nucleolar protein NIFK promotes cancer progression via CK1α/β-catenin in metastasis and Ki-67-dependent cell proliferation.

Nucleolar protein interacting with the FHA domain of pKi-67 (NIFK) is a Ki-67-interacting protein. However, its precise function in cancer remains largely uninvestigated. Here we show the clinical significance and metastatic mechanism of NIFK in lung cancer. NIFK expression is clinically associated with poor prognosis and metastasis. Furthermore, NIFK enhances Ki-67-dependent proliferation, and promotes migration, invasion in vitro and metastasis in vivo via downregulation of casein kinase 1α (CK1α), a suppressor of pro-metastatic TCF4/β-catenin signaling. Inversely, CK1α is upregulated upon NIFK knockdown. The silencing of CK1α expression in NIFK-silenced cells restores TCF4/β-catenin transcriptional activity, cell migration, and metastasis. Furthermore, RUNX1 is identified as a transcription factor of CSNK1A1 (CK1α) that is negatively regulated by NIFK. Our results demonstrate the prognostic value of NIFK, and suggest that NIFK is required for lung cancer progression via the RUNX1-dependent CK1α repression, which activates TCF4/β-catenin signaling in metastasis and the Ki-67-dependent regulation in cell proliferation

Relationship of teicoplanin MICs to treatment failure in teicoplanin-treated patients with methicillin-resistant Staphylococcus aureus pneumonia

Background/PurposeThe objective of this study was to determine the predictive value of teicoplanin minimal inhibitory concentrations (MICs) for treatment failure among patients with methicillin-resistant Staphylococcus aureus (MRSA) pneumonia.MethodsIn this study, all patients with ≥1 tracheal aspirates or sputum cultures positive for MRSA admitted to the hospital between April 2011 and September 2011 were reviewed. We enrolled patients who are ≥18 years of age, with a diagnosis of pneumonia, and with a receipt of teicoplanin therapy throughout the course. The relationship between teicoplanin Etest MICs and treatment outcomes of MRSA pneumonia was analyzed to identify the breakpoint of teicoplanin MICs influencing treatment outcomes.ResultsOf the 80 patients enrolled, 31 had a lower teicoplanin MIC level (<2.0 mg/L) and 49 had a higher MIC level (≥2.0 mg/L) for MRSA. The lower MIC group had a higher clinical resolution rate in 14 days [24 (77.4%) vs. 23 (46.9%), p = 0.007] and a lower treatment failure rate at the end of teicoplanin treatment [4 (12.9%) vs. 18 (36.7%), p = 0.020]. A comparison between the treatment success and failure groups showed that the former had a longer duration of teicoplanin use (18.76 ± 10.34vs.12.41 ± 5.65 days; p = 0.014). Results of a multivariate analysis showed that teicoplanin MICs ≥ 2.0 mg/Land shorter duration of teicoplanin therapy were independent risk factors for treatment failure.ConclusionA higher teicoplanin MIC value (≥2.0 mg/L) may predict the treatment failure among patients with teicoplanin-treated MRSA pneumonia

GenEpi: gene-based epistasis discovery using machine learning.

BackgroundGenome-wide association studies (GWAS) provide a powerful means to identify associations between genetic variants and phenotypes. However, GWAS techniques for detecting epistasis, the interactions between genetic variants associated with phenotypes, are still limited. We believe that developing an efficient and effective GWAS method to detect epistasis will be a key for discovering sophisticated pathogenesis, which is especially important for complex diseases such as Alzheimer's disease (AD).ResultsIn this regard, this study presents GenEpi, a computational package to uncover epistasis associated with phenotypes by the proposed machine learning approach. GenEpi identifies both within-gene and cross-gene epistasis through a two-stage modeling workflow. In both stages, GenEpi adopts two-element combinatorial encoding when producing features and constructs the prediction models by L1-regularized regression with stability selection. The simulated data showed that GenEpi outperforms other widely-used methods on detecting the ground-truth epistasis. As real data is concerned, this study uses AD as an example to reveal the capability of GenEpi in finding disease-related variants and variant interactions that show both biological meanings and predictive power.ConclusionsThe results on simulation data and AD demonstrated that GenEpi has the ability to detect the epistasis associated with phenotypes effectively and efficiently. The released package can be generalized to largely facilitate the studies of many complex diseases in the near future

Bioactive Eunicellin-Based Diterpenoids from the Soft Coral Cladiella krempfi

Four new eunicellin-based diterpenoids, krempfielins A–D (1–4), along with two known compounds (5 and 6) have been isolated from a soft coral Cladiella krempfi. The structures of the new metabolites were elucidated by extensive spectroscopic analysis and by comparison with spectroscopic data of related known compounds. Compounds 5 and 6 were shown to exhibit cytotoxicity against a limited panel of cancer cell lines. Furthermore, compounds 2, 3, 5 and 6 were shown to exert significant in vitro anti-inflammatory activity against LPS-stimulated RAW264.7 macrophage cells