1,718 research outputs found

    Internationalization propensity in family-controlled public firms in emerging markets: The effects of family ownership, governance, and top management team heterogeneity

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    Internationalization propensity is a growing issue faced by family firms. This study contributes to the family business literature by developing a conceptual framework that can identify the family and managerial determinants that affect the extensiveness of internationalization. Drawing on the socioemotional wealth and upper echelon perspectives, it empirically examines the association among family heterogeneity (i.e., family participation is heterogeneous in terms of ownership and governance oversight), top management team (TMT) heterogeneity (i.e., the TMT’s background is heterogeneous in terms of its overseas education and industry experience), and internationalization propensity in publicly traded enterprises. The analysis of data collected from 105 public firms in Taiwan shows that active family participation in ownership and governance oversight and TMT overseas industry experience heterogeneity are significantly and positively associated with internationalization propensity. However, family ownership is found to be significantly but negatively associated with internationalization propensity. We finally discuss the implications of the presented findings for practitioners and organizational theorists

    Turning a native or corroded Mg alloy surface into an anti-corrosion coating in excited CO2

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    Despite their energy-efficient merits as promising light-weight structural materials, magnesium (Mg) based alloys suffer from inadequate corrosion resistance. One primary reason is that the native surface film on Mg formed in air mainly consists of Mg(OH)2 and MgO, which is porous and unprotective, especially in humid environments. Here, we demonstrate an environmentally benign method to grow a protective film on the surface of Mg/Mg alloy samples at room temperature, via a direct reaction of already-existing surface film with excited CO2. Moreover, for samples that have been corroded obviously on surface, the corrosion products can be converted directly to create a new protective surface. Mechanical tests show that compared with untreated samples, the protective layer can elevate the yield stress, suppress plastic instability and prolong compressive strains without peeling off from the metal surface. This environmentally friendly surface treatment method is promising to protect Mg alloys, including those already-corroded on the surface.China. Ministry of Science and Technology. National Key Research and Development Program (No. 2017YFB0702001)National Natural Science Foundation of China (51621063)National Natural Science Foundation of China (51601141)National Natural Science Foundation of China ( 51401239)Shaanxi Sheng (China). Science and Technology Department (2016KTZDGY-04-03)Shaanxi Sheng (China). Science and Technology Department (2016KTZDGY-04-04)China Postdoctoral Science Foundation (2016M600788)China University of Petroleum. Science Foundation (No. 2462018BJC005)China University of Petroleum. Science Foundation (C201603)National Science Foundation (U.S.) (ECCS-1610806

    Robust optimal dispatching model and a benefit allocation strategy for rural novel virtual power plants incorporating biomass waste energy conversion and carbon cycle utilization

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    To optimize the utilization of rural biomass waste resources (e.g., straw and solid waste), biomass waste energy conversion (BWEC) and carbon cycle utilization (CCU) are integrated into a traditional virtual power plant, i.e., a rural BWEC-CCU-based virtual power plant. Furthermore, a fuzzy robust two-stage dispatching optimal model for the BWEC-CCU-based virtual power plant is established considering the non-determinacy from a wind power plant (WPP) and photovoltaic (PV) power. The scheduling model includes the day-ahead deterministic dispatching model and real-time uncertainty dispatching model. Among them, in the day-ahead dispatching phase, the dispatching plan is formulated with minimum operating cost and carbon emission targets. In the real-time dispatching phase, the optimal dispatching strategy is formulated aiming at minimum deviation adjustment cost by applying the Latin hypercube sampling method. The robust stochastic theory is used to describe the uncertainty. Third, in order to achieve optimal distribution of multi-agent cooperation benefits, a benefit distribution strategy based on Nash negotiation is designed considering the three-dimensional interfering factor of the marginal benefit contribution, carbon emission contribution, and deviation risk. Finally, a rural distribution network in Jiangsu province, China, is selected for case analysis, and the results show that 1) the synergistic optimal effect of BWEC and CCU is obvious, and the operation cost and deviation adjustment cost could decrease by 26.21% and 39.78%, respectively. While the capacity ratio of WPP + PV, BWEC, and CCU is 5:3:2, the dispatching scheme is optimum. 2) This scheduling model can be used to formulate the optimal scheduling scheme. Compared with the robust coefficient Γ = 0, when Γ = 1, the WPP and PV output decreased by 15.72% and 15.12%, and the output of BWEC and CCU increased by 30.7% and 188.19%, respectively. When Γ∈ (0.3, 0.9), the growth of Γ has the most direct impact on the dispatching scheme. 3) The proposed benefit equilibrium allocation strategy can formulate the most reasonable benefit allocation plan. Compared with the traditional benefit allocation strategy, when the proposed method is used, the benefit share of the WPP and PV reduces by 5.2%, and the benefit share of a small hydropower station, BWEC, and CCU increases by 1.7%, 9.7%, and 3.8%, respectively. Overall, the proposed optimal dispatching and benefit allocation strategy could improve the aggregated utilization of rural biomass waste resources and distributed energy resources while balancing the benefit appeal of different agents

    DNA Methylation and Gene Expression of Matrix Metalloproteinase 9 Gene in Deficit and Non-deficit Schizophrenia

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    The biological pathology of deficit schizophrenia (DS) remains unclear. Matrix metalloproteinase 9 (MMP9) might be associated with neural plasticity and glutamate regulation, involved in schizophrenia pathogenesis. This study explores gene expression and DNA methylation of MMP9 in peripheral blood mononuclear cells (PBMCs) and their relationship with clinical symptoms in DS and non-deficit schizophrenia (NDS). Pyrosequencing was used to determine DNA methylation at CpG sites in exon 4 and exon 5 of MMP9 in 51 DS patients, 53 NDS patients and 50 healthy subjects (HC). RT-qPCR was used to detect MMP9 expression. Clinical symptoms were assessed by BPRS, SANS and SAPS scales. MMP9 expression in PBMCs was significantly higher in DS than NDS and HC subjects. Compared to NDS patients, DS patients had significantly lower DNA methylation at individual CpG sites in exon 4 and exon 5 of MMP9. Correlation analysis showed that DNA methylation in exon 4 was negatively correlated with gene expression in DS group. Positive correlation was found between MMP9 expression and negative symptoms in total schizophrenic patients. The social amotivation factor of SANS and negative syndrome of BPRS was negatively correlated with DNA methylation of CpG5-1 in DS patients but not in NDS patients. DS patients showed a specific abnormality of peripheral MMP9 expression and DNA methylation, indicating a pathological mechanism underlying DS as a specific subgroup of schizophrenia

    Effects of 24-week treatment with acarbose on glucagon-like peptide 1 in newly diagnosed type 2 diabetic patients: a preliminary report

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    BACKGROUND: Treatment with the alpha-glucosidase inhibitor (AGI) acarbose is associated with a significant reduction the risk of cardiovascular events. However, the underlying mechanisms of this effect are unclear. AGIs were recently suggested to participate in stimulating glucagon-like peptide 1 (GLP-1) secretion. We therefore examined the effects of a 24-week treatment of acarbose on endogenous GLP-1, nitric oxide (NO) levels, nitric oxide synthase (NOS) activity, and carotid intima-media thickness (CIMT) in newly diagnosed patients with type 2 diabetes (T2D). METHODS: Blood was drawn from 24 subjects (14 male, 10 female, age: 50.7 ± 7.36 years, BMI: 26.64 ± 3.38 kg/m(2), GHbA1c: 7.00 ± 0.74%) with drug-naïve T2D at 0 and 120 min following a standard mixed meal for the measurements of active GLP-1, NO and NOS. The CIMT was measured prior to and following 24 weeks of acarbose monotherapy (mean dose: 268 mg daily). RESULTS: Following 24 weeks of acarbose treatment, both fasting and postprandial plasma GLP-1 levels were increased. In patients with increased postprandial GLP-1 levels, serum NO levels and NOS activities were also significantly increased and were positively related to GLP-1 levels. Although the CIMT was not significantly altered following treatment with acarbose, a decreased CIMT was negatively correlated with increased GLP-1 levels. CONCLUSIONS: Twenty-four weeks of acarbose monotherapy in newly diagnosed patients with T2D is associated with significantly increased levels of both fasting and postprandial GLP-1 as well as significantly increased NO levels and NOS activity for those patients in whom postprandial GLP-1 levels were increased. Therefore, the benefits of acarbose on cardiovascular risk may be related to its stimulation of GLP-1 secretion

    Therapeutic Effect of Repurposed Temsirolimus in Lung Adenocarcinoma Model

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    Lung cancer is one of the major cause of cancer-related deaths worldwide. The poor prognosis and resistance to both radiation and chemotherapy urged the development of potential targets for lung cancer treatment. In this study, using a network-based cellular signature bioinformatics approach, we repurposed a clinically approved mTOR inhibitor for renal cell carcinomans, temsirolimus, as the potential therapeutic candidate for lung adenocarcinoma. The PI3K-AKT-mTOR pathway is known as one of the most frequently dysregulated pathway in cancers, including non-small-cell lung cancer. By using a well-documented lung adenocarcinoma mouse model of human pathophysiology, we examined the effect of temsirolimus on the growth of lung adenocarcinoma in vitro and in vivo. In addition, temsirolimus combined with reduced doses of cisplatin and gemcitabine significantly inhibited the lung tumor growth in the lung adenocarcinoma mouse model compared with the temsirolimus alone or the conventional cisplatin–gemcitabine combination. Functional imaging techniques and microscopic analyses were used to reveal the response mechanisms. Extensive immunohistochemical analyses were used to demonstrate the apparent effects of combined treatments on tumor architecture, vasculature, apoptosis, and the mTOR-pathway. The present findings urge the further exploration of temsirolimus in combination with chemotherapy for treating lung adenocarcinoma

    Liver-targeting MRI contrast agent based on galactose functionalized o-carboxymethyl chitosan

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    Commercial gadolinium (Gd)-based contrast agents (GBCAs) play important role in clinical diagnostic of hepatocellular carcinoma, but their diagnostic efficacy remained improved. As small molecules, the imaging contrast and window of GBCAs is limited by low liver targeting and retention. Herein, we developed a liver-targeting gadolinium (Ⅲ) chelated macromolecular MRI contrast agent based on galactose functionalized o-carboxymethyl chitosan, namely, CS-Ga-(Gd-DTPA)n, to improve hepatocyte uptake and liver retention. Compared to Gd-DTPA and non-specific macromolecular agent CS-(Gd-DTPA)n, CS-Ga-(Gd-DTPA)n showed higher hepatocyte uptake, excellent cell and blood biocompatibility in vitro. Furthermore, CS-Ga-(Gd-DTPA)n also exhibited higher relaxivity in vitro, prolonged retention and better T1-weighted signal enhancement in liver. At 10 days post-injection of CS-Ga-(Gd-DTPA)n at a dose of 0.03 mM Gd/Kg, Gd had a little accumulation in liver with no liver function damage. The good performance of CS-Ga-(Gd-DTPA)n gives great confidence in developing liver-specifc MRI contrast agents for clinical translation
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