912 research outputs found

    Possible open-charmed pentaquark molecule Ωc(3188)\Omega_c(3188) --- the DΞD \Xi bound state --- in the Bethe-Salpeter formalism

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    We study the SS-wave DΞD\Xi bound state in the Bethe-Salpeter formalism in the ladder and instantaneous approximations. With the kernel generated by the hadronic effective Lagrangian, two open-charmed bound states, which quantum numbers are I=0I=0, JP=(12)−J^P=(\frac{1}{2})^- and I=1I=1, JP=(12)−J^P=(\frac{1}{2})^-, respectively, are predicted as new candidates of hadronic pentaquark molecules in our formalism. If existing, they could contribute to the broad 3188 eV structure near the five new narrow Ωc\Omega_c states observed recently by the LHCb Collaboration.Comment: 8 pages, 4 figures, accepted by Eur. Phys. J.

    A Low-cost, High-impact Node Injection Approach for Attacking Social Network Alignment

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    Social network alignment (SNA) holds significant importance for various downstream applications, prompting numerous professionals to develop and share SNA tools. Unfortunately, these tools can be exploited by malicious actors to integrate sensitive user information, posing cybersecurity risks. While many researchers have explored attacking SNA (ASNA) through a network modification attack way, practical feasibility remains a challenge. This paper introduces a novel approach, the node injection attack. To overcome the problem of modeling and solving within a limited time and balancing costs and benefits, we propose a low-cost, high-impact node injection attack via dynamic programming (DPNIA) framework. DPNIA models ASNA as a problem of maximizing the number of confirmed incorrect correspondent node pairs who have a greater similarity scores than the pairs between existing nodes, making ASNA solvable. Meanwhile, it employs a cross-network evaluation method to identify node vulnerability, facilitating a progressive attack from easy to difficult. Additionally, it utilizes an optimal injection strategy searching method, based on dynamic programming, to determine which links should be added between injected nodes and existing nodes, thereby achieving a high impact for attack effectiveness at a low cost. Experiments on four real-world datasets consistently demonstrate that DPNIA consistently and significantly outperforms various attack baselines

    Protective effects of cysteine analogues on acute myocardial ischemia: novel modulators of endogenous H2S production

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    The current study was designed to evaluate the pharmacologic effects of three novel cysteine-containing compounds: S-propyl-l-cysteine (SPC), S-allyl-l-cysteine (SAC), and S-propargyl-l-cysteine (SPRC) on H(2)S production and antioxidant defenses in an acute myocardial infarction (MI) rat model. The enzymatic activities of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), as well as glutathione redox status and malonaldehyde (MDA) content, also were determined. All three compounds were found to preserve SOD and GPx activities and also tissue GSH levels while reducing the formation of the lipid peroxidation product MDA in ventricular tissues. With immunfluorescence assays, we observed the expression of CSE and Mn-SOD. The morphologic changes of the cardiac cells are seen with both light and electron microscopy. The corresponding pathologic alterations were characterized mainly as loss of adherence between cardiac myocytes and swollen or ruptured mitochondria at the ultrastructural level. Propargylglycine, a selective inhibitor of CSE, abolished the protective effects of each compound used in the current model. Our study provides novel evidence that SPC, SAC, and SPRC have cardioprotective effects in MI by reducing the deleterious effects of oxidative stress by modulating the endogenous levels of H(2)S and preserving the activities of antioxidant defensive enzymes like SOD

    Bis[3-(meth­oxy­carbon­yl)anilinium] hexa­chloridostannate(IV)

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    In the title compound, (NH3C6H4CO2CH3)2[SnCl6], the anions are situated on inversion centers so the asymmetric unit contains one cation and one half-anion. In the crystal, inter­molecular N—H⋯Cl and N—H⋯O hydrogen bonds link the cations and anions into layers parallel to the ac plane. The crystal packing exhibits voids of 37 Å3

    Value of reduced glomerular filtration rate assessment with cardiometabolic index: insights from a population-based Chinese cohort

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    Abstract Background Recent studies have suggested that cardiometabolic index (CMI), a novel estimate of visceral adipose tissue, could be of use in the evaluation of cardiovascular risk factors. However, the potential utility and clinical significance of CMI in the detection of reduced estimated glomerular filtration rate (eGFR) remains uncertain. The purpose of this study was to investigate the usefulness of CMI in assessing reduced eGFR in the general Chinese population. Methods This cross-sectional analysis included 11,578 participants (mean age: 53.8 years, 53.7% females) from Northeast China Rural Cardiovascular Health Study (NCRCHS) of general Chinese population (data collected from January 2013 to August 2013). CMI was calculated by triglyceride to high density lipoprotein cholesterol ratio multiply waist-to-height ratio. Reduced eGFR was defined as eGFR< 60 ml/min per 1.73m2. Multivariate regressions were performed to determine CMI’s association with eGFR value and eGFR reduction, ROC analyses were employed to investigate CMI’s discriminating ability for decreased eGFR. Results The prevalence of reduced eGFR was 1.7% in males and 2.5% in females. CMI was notably more adverse in reduced eGFR groups, regardless of genders. In fully adjusted multivariate linear models, each 1 SD increment of CMI caused 3.150 ml/min per 1.73m2 and 2.411 ml/min per 1.73m2 loss of eGFR before CMI reached 1.210 and 1.520 in males and females, respectively. In logistic regression analyses, per 1 SD increase of CMI brought 51.6% additional risk of reduced eGFR in males while caused 1.347 times of risk in females. After divided into quartiles, people in the top quartile of CMI had higher adjusted ORs of having reduced eGFR, with ORs of 4.227 (1.681, 10.627) and 3.442 (1.685–7.031) for males and females respectively. AUC of CMI was revealed to be 0.633 (0.620–0.646) in males and 0.684 (0.672–0.695) in females. Conclusions Higher CMI was independently associated with greater burden of reduced eGFR, highlighting VAT distribution and dysfunction as a potential mechanism underlying the association of obesity with kidney damage and adverse cardiovascular outcomes. The findings from this study provided important insights regarding the potential usefulness and clinical relevance of CMI in the detection of reduced eGFR among general Chinese population.https://deepblue.lib.umich.edu/bitstream/2027.42/146138/1/12882_2018_Article_1098.pd

    PreQuant: A Task-agnostic Quantization Approach for Pre-trained Language Models

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    While transformer-based pre-trained language models (PLMs) have dominated a number of NLP applications, these models are heavy to deploy and expensive to use. Therefore, effectively compressing large-scale PLMs becomes an increasingly important problem. Quantization, which represents high-precision tensors with low-bit fix-point format, is a viable solution. However, most existing quantization methods are task-specific, requiring customized training and quantization with a large number of trainable parameters on each individual task. Inspired by the observation that the over-parameterization nature of PLMs makes it possible to freeze most of the parameters during the fine-tuning stage, in this work, we propose a novel ``quantize before fine-tuning'' framework, PreQuant, that differs from both quantization-aware training and post-training quantization. PreQuant is compatible with various quantization strategies, with outlier-aware parameter-efficient fine-tuning incorporated to correct the induced quantization error. We demonstrate the effectiveness of PreQuant on the GLUE benchmark using BERT, RoBERTa, and T5. We also provide an empirical investigation into the workflow of PreQuant, which sheds light on its efficacy.Comment: Findings of ACL202
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