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The hard-to-cut material nickel-base Inconel-718 is used in large quantities in the aerospace industry and defense industry because the Inconel-718 has good mechanical strength at high temperatures, but the tool is likely to wear in the cutting processes. In this study, chip color and features were employed to predict tool lives because the chips are the closest to the cutting tool in the shear zone during the cutting processes, which can more authentically reflect the phenomenon of tool wear. The changes in chip color and geometric shape were extracted and digitized, and the prediction method employed a two-stage model. In Stage 1, a convolutional neural network (CNN) was used for chip condition classification and validation, and in Stage 2, back propagation neural network (BP) was employed to predict the tool wear. The result showed that when the Google-Net and ResNet50 network models were adopted for CNN chip feature recognition, with the confusion matrix of multi-classification for validation, the recognition precisions were 66.7% and 88.9%, respectively. The modeling and prediction were performed in the BP neural network; the chip chromaticity, chip thickness, and chip width were employed as input features, and the precision was enhanced by multi-fusion features. Finally, the mean absolute percentage error values for heavy cutting were 17.11%, medium cutting at 5.45%, and small cutting at 9.02%, indicating that the CNN-BP prediction model has good forecast accuracy, thus providing a new model prediction form for tool life. [ABSTRACT FROM AUTHOR]

Objective: This study aimed to summarize the magnetic resonance imaging (MRI) and computed tomography (CT) features of the central nervous system (CNS) in children with Hoyeraal‐Hreidarsson syndrome. Methods: The imaging and clinical data of four children diagnosed with Hoyeraal‐Hreidarsson syndrome by clinical and laboratory tests in the Guangzhou Women and Children's Medical Center were gathered and analyzed retrospectively. The clinical manifestations and CNS imaging features of Hoyeraal‐Hreidarsson syndrome were summarized based on our results and a literature review. Results: Our results showed that delayed development, skin pigmentation, nail/toenail dystrophy, thrombocytopenia, and anemia are the most observed clinical presentations of Hoyeraal‐Hreidarsson syndrome. Important findings on CNS imaging showed that all patients had cerebellar hypoplasia, delayed myelination, hydrocephalus, brain atrophy, and calcification. The gene mutations in all cases were consistent with those of dyskeratosis congenita, including TINF2 mutations in three cases and DKC1 mutations in one case. Conclusion: Hoyeraal‐Hreidarsson syndrome is a severe variant of dyskeratosis congenita. Both DKC1 and TINF2 mutations can lead to the phenotypes of Hoyeraal‐Hreidarsson syndrome. In our study, CNS imaging revealed that cerebellar hypoplasia has an important diagnostic value for Hoyeraal‐Hreidarsson syndrome while delayed myelination, calcification of the parenchyma, brain atrophy, and hydrocephalus are also important findings on CNS imaging. Combining imaging features with clinical and laboratory indicators can assist the diagnosis of Hoyeraal‐Hreidarsson syndrome. [ABSTRACT FROM AUTHOR]

Background: Intracranial infections with Corynebacterium striatum (C. striatum) have been described sporadically in the literature over the last two decades. However, C. striatum meningitis combined with multiple abscesses has not been published before.Case Presentation: In this report, we describe the clinical and imaging findings in a 54-year-old woman with meningitis caused by C. striatum and combined with suspected brain and lung abscesses. This patient who underwent multiple fractures and a recent cut presented with headache and paraphasia. C. striatum was isolated in cerebrospinal fluid and supposedly transmitted from the skin purulent wound through blood. The patient was treated with intravenous vancomycin and had a transient improvement, but died finally. Multiple abscesses, especially in the brain, could be a reason to explain her conditions were deteriorating rapidly.Conclusions: Note that C. striatum can cause life-threatening infections. Early identification and diagnosis, early administration of antibiotics to which the bacterium is susceptible, and treatment of complications will be beneficial in patients with C. striatum-related infection. [ABSTRACT FROM AUTHOR]

Granulites and eclogites are useful for revealing the thermal and tectonic evolution of orogens. Early Palaeozoic granulites and associated eclogites in the East Kunlun Orogenic Belt (EKOB) display contrasting metamorphic age. Such asynchronous granulite–eclogite associations have rarely been reported, and the geological significance of their existence remains to be further explored. In this study, petrological and geochronological techniques were used to investigate two felsic and two mafic granulites collected from the Qingshuiquan area in the eastern section of the EKOB. These rocks record similar P–T paths, which are characterized by a peak stage within suprasolidus and high‐pressure (HP) granulite facies conditions (750–832°C and 10.1–12.0 kbar), followed by an initial decompression and cooling stage to subsolidus conditions (600–748°C and 6.5–8.6 kbar), and then a stage of further retrogression under greenschist facies conditions. The protoliths to these granulites are of volcanic and sedimentary origin and suggested to be a component of the continental basement unit. Metamorphic P–T paths indicate that these rocks experienced peak metamorphism at a depth of ~40 km, then cooling and uplift to a depth of ~25 km, and eventually experienced low‐grade retrogression at shallow crustal levels. Cathodoluminescence images and compositional data demonstrate that the zircons in these rocks are of metamorphic origin and they crystallized at or near peak conditions. SIMS U–Pb dating of representative zircon grains yield concordant metamorphic ages of c. 490–520 Ma, with a peak value of 505 Ma on the probability density curve. These ages are similar to other 480–530 Ma ages typically retrieved from EKOB granulites and associated rocks, and are markedly older than the 400–450 Ma ages retrieved from eclogites and their host rocks. The HP granulites and eclogites of the EKOB do not show overprinting relationships. Such asynchronous characteristics imply that the two rock types formed in distinct tectonic settings and at different stages of a protracted subduction–collision process. The studied granulites are suggested to have formed in the root of a continental arc during a stage of Proto‐Tethys Ocean subduction. The formation of the eclogites could be attributed to subsequent deep continental subduction. [ABSTRACT FROM AUTHOR]

High-fat diet (HFD) is known to promote atherosclerosis which accelerates the development of atherosclerotic cardiovascular diseases. Vascular dysfunction characterized by inflammation and lipid accumulation is common in atherosclerosis caused by HFD. The specific effects of HFD on blood vessels and the underlying mechanisms need to be further clarified. Toll-like receptor 4 (TLR4) is a key contributing factor in atherosclerosis and TLR4 deficiency protects vascular smooth muscle cells against inflammatory responses and lipid accumulation in vitro . However, the physiological significance of TLR4 signaling in HFD-induced changes is unknown. In this study, we observed that HFD feeding increased body weight, circulating inflammatory cytokines and lipid accumulation in the aorta of wild-type mice but apart from increasing body weight, did not affect the TLR4 knockout mice. TLR4 expression increased significantly in the arterial walls after receiving HFD treatment, while that of the co-localizing PPARγ and ABCG1 markedly decreased. TLR4 deficiency reversed the HFD-induced attenuation of PPARγ and ABCG1. In conclusion, TLR4 mediates HFD induced increase in body weight, inflammation and aortic lipid accumulation through, at least partly, the PPARγ/ABCG1 signaling pathway. Therefore, interfering with TLR4 signaling is a viable therapeutic option in diet induced atherosclerosis. [ABSTRACT FROM AUTHOR]

The phenotypic modulation of contractile vascular smooth muscle cell (VSMC) is widely accepted as the pivotal process in the arterial remodeling induced by hypertension. This study aimed to investigate the potential role of transient receptor potential vanilloid type 1 (TRPV1) on regulating VSMC plasticity and intracranial arteriole remodeling in hypertension. Spontaneously hypertensive rats (SHR), Wistar-Kyoto (WKY) rats and TRPV1 mice on a C57BL/6J background were used. By microscopic observation of the histopathological sections of vessels from hypertensive SHR and age-matched normotensive WKY control rats, we found that hypertension induced arterial remodeling. Decreased α-smooth muscle actin (α-SMA) and SM22α while increased osteopontin (OPN) were observed in aorta and VSMCs derived from SHR compared with those in WKY, and VSMCs derived from SHR upregulated inflammatory factors. TRPV1 activation by capsaicin significantly increased expression of α-SMA and SM22α, reduced expression of OPN, retarded proliferative and migratory capacities and inhibited inflammatory status in VSMCs from SHR, which was counteracted by TRPV1 antagonist 5′-iodoresiniferatoxin (iRTX) combined with capsaicin. TRPV1 activation by capsaicin ameliorated intracranial arteriole remodeling in SHR and deoxycorticosterone acetate (DOCA)-salt hypertensive mice. However, the attenuation of arteriole remodeling by capsaicin was not observed in TRPV1 mice. Furthermore, TRPV1 activation significantly decreased the activity of PI3K and phosphorylation level of Akt in SHR-derived VSMCs. Taken together, we provide evidence that TRPV1 activation by capsaicin attenuates intracranial arteriole remodeling through inhibiting VSMC phenotypic modulation during hypertension, which may be at least partly attributed to the suppression PI3K/Akt signaling pathway. These findings highlight the prospect of TRPV1 in prevention and treatment of hypertension. [ABSTRACT FROM AUTHOR]

The formation of fat-laden foam cells, contributing to the fatty streaks of the plaques of atheroma, is the critical early process in atherosclerosis. The previous study demonstrated that vascular smooth muscle cells (VSMCs) contain a much larger burden of the excess cholesterol in comparison with monocyte-derived macrophages in human coronary atherosclerosis, as the main origin of foam cells. It is noteworthy that VSMC-derived foam cells are deposited in subintima but not media, where VSMCs normally deposit in. Therefore, migration from media to intima is an indispensable step for a VSMC to accrue neutral lipids and form foam cell. Whether this migration occurs paralleled with or prior to the formation of foam cell is still unclear. Herein, the present study was designed to test the VSMC migratory capability in the process of foam cell formation induced by oxidized low-density lipoprotein (oxLDL). In conclusion, we provide evidence that oxLDL induces the VSMC-derived foam cells formation with increased migration ability and MMP-9 expression, which were partly attributed to the impaired SIRT1 and enhanced nuclear factor-kappa B (NF-κB) activity. As activation of transient receptor potential vanilloid type 1 (TRPV1) has been reported to have anti-atherosclerotic effects, we investigated its role in oxLDL-treated VSMC migration. It is found that activating TRPV1 by capsaicin inhibits VSMC foam cell formation and the accompanied migration through rescuing the SIRT1 and suppressing NF-κB signaling. The present study provides evidence that SIRT1 may be a promising intervention target of atherosclerosis, and raises the prospect of TRPV1 in prevention and treatment of atherosclerosis. [ABSTRACT FROM AUTHOR]

Increasing evidence showed that abnormal proliferation and migration of vascular smooth muscle cells (VSMCs) are common event in the pathophysiology of many vascular diseases, including atherosclerosis and restenosis after angioplasty. Among the underlying mechanisms, oxidative stress is one of the principal contributors to the proliferation and migration of VSMCs. Oxidative stress occurs as a result of persistent production of reactive oxygen species (ROS). Recently, the protective effects of peroxisome proliferator-activated receptor γ (PPARγ) against oxidative stress/ROS in other cell types provide new insights to inhibit the suggests that PPARγ may regulate VSMCs function. However, it remains unclear whether activation of PPARγ can attenuate oxidative stress and further inhibit VSMC proliferation and migration. In this study, we therefore investigated the effect of PPARγ on inhibiting VSMC oxidative stress and the capability of proliferation and migration, and the potential role of mitochondrial uncoupling protein 2 (UCP2) in oxidative stress. It was found that platelet derived growth factor-BB (PDGF-BB) induced VSMC proliferation and migration as well as ROS production; PPARγ inhibited PDGF-BB-induced VSMC proliferation, migration and oxidative stress; PPARγ activation upregulated UCP2 expression in VSMCs; PPARγ inhibited PDGF-BB-induced ROS in VSMCs by upregulating UCP2 expression; PPARγ ameliorated injury-induced oxidative stress and intimal hyperplasia (IH) in UCP2-dependent manner. In conclusion, our study provides evidence that activation of PPARγ can attenuate ROS and VSMC proliferation and migration by upregulating UCP2 expression, and thus inhibit IH following carotid injury. These findings suggest PPARγ may represent a prospective target for the prevention and treatment of IH-associated vascular diseases. [ABSTRACT FROM AUTHOR]

Despite advancements in diagnosis and treatment of cardiovascular diseases (CVDs), the morbidity and mortality of CVDs are still rising. Atherosclerosis is a chronic inflammatory disease contributing to multiple CVDs. Considering the complexity and severity of atherosclerosis, it is apparent that exploring the mechanisms of atherosclerotic formation and seeking new therapies for patients with atherosclerosis are required to overcome the heavy burden of CVDs on the quality and length of life of the global population. Vascular smooth muscle cells (VSMCs) play a dominant role in functional and structural changes of the arterial walls in response to atherogenic factors. Therefore, improvement of VSMC functions will slow down the development of atherosclerosis to a large extent. Given its protective performances on regulation of cholesterol metabolism and inflammatory responses, SIRT1 has long been known as an anti-atherosclerosis factor. In this review, we focus on the effects of SIRT1 on VSMC functions and thereby the development of atherosclerosis. [ABSTRACT FROM AUTHOR]

The fully differentiated medial vascular smooth muscle cells (VSMCs) of mature vessels keep quiescent and contractile. However, VSMC can exhibit the plasticity in phenotype switching from a differentiated and contractile phenotype to a dedifferentiated state in response to alterations in local environmental cues, which is called phenotypic modulation or switching. Distinguishing from its differentiated state expressing more smooth muscle (SM)-specific/selective proteins, the phenotypic modulation in VSMC is characterized by an increased rate of proliferation, migration, synthesis of extracellular matrix proteins and decreased expression of SM contractile proteins. Although it has been well demonstrated that phenotypic modulation of VSMC contributes to the occurrence and progression of many proliferative vascular diseases, little is known about the details of the molecular mechanisms of VSMC phenotypic modulation. Growing evidence suggests that variety of molecules including microRNAs, cytokines and biochemical factors, membrane receptors, ion channels, cytoskeleton and extracellular matrix play important roles in controlling VSMC phenotype. The focus of the present review is to provide an overview of potential molecular mechanisms involved in VSMC phenotypic modulation in recent years. To clarify VSMC differentiation and phenotypic modulation mechanisms will contribute to producing cell-based therapeutic interventions for aberrant VSMC differentiation-related diseases. [ABSTRACT FROM AUTHOR]

The transient receptor potential vanilloid type 1 (TRPV1) channel, a ligand-gated cation channel of the TRP subfamily, can be activated by multiple stimuli, including capsaicin. Currently, cumulative studies have demonstrated an interesting link between TRPV1 and cardiovascular diseases, including hypertension. Additionally, the protective effect of TRPV1 against hypertension and its related disorders has been proved to be partly involved with the improved action of vascular smooth muscle cells (VSMCs). This review focuses on the current knowledge of TRPV1 in improving VSMC function and attenuating hypertension. [ABSTRACT FROM AUTHOR]

Several epidemiologic studies have evaluated the association between intercellular adhesion molecule-1 (ICAM-1) gene K469E polymorphism and stroke, but the results were inconsistent. The present meta-analysis was performed to investigate the relationship between K469E polymorphism and stroke in the Chinese population. A comprehensive search for related studies from the electronic databases of PubMed, Embase, Web of Science, CBMdisc and CNKI as well as a manual search of the references of identified articles was performed. Data were extracted to calculate for allelic, additive, dominant and recessive models using pooled odds ratios (ORs) along with 95% confidence intervals (CIs) by Review Manager 5.0 and Stata 11.0. Different effect models, subgroup analysis, sensitivity analysis, publication bias and power calculations were used to improve the comprehensive analysis. Finally, a total of 12 studies containing 1593 cases and 1555 controls were included in the final meta-analysis. No evidence of significant association between ICAM-1 gene K469E polymorphism and stroke was found in all four models (allelic model: OR = 1.07, 95%CI = 0.78-1.47; additive model: OR = 1.21, 95% CI = 0.67-2.16 (EE vs. KK); OR = 1.04, 95%CI = 0.75-1.45 (EK vs. KK); dominant model: OR = 1.07, 95% CI = 0.73-1.56; and recessive model: OR = 1.18, 95% CI = 0.77-1.83, respectively) based on the overall population, as well as subgroup analysis and sensitivity analysis. In conclusion, the present meta-analysis showed no evidence of significant association between ICAM-1 gene K469E polymorphism and stroke in the Chinese population. Nonetheless, this conclusion should be interpreted cautiously due to the low statistical power and considerable heterogeneity. Therefore, larger sample-size studies with homogeneous cases and well-matched controls are needed to further address this correlation. [ABSTRACT FROM AUTHOR]

Background: The association between methylenetetrahydrofolate reductase (MTHFR) gene A1298C polymorphism and adult stroke remains controversial. The present article was designed to clarify this relationship through pooled analysis of the numerous epidemiological studies focusing on this association. Methods: We comprehensively searched all published papers in electronic database including PubMed, Embase, Web of Science, Chinese Biomedical Literature on disc (CBMdisc) and China National Knowledge Infrastructure (CNKI) up to 2013. The pooled odds ratios (ORs) with 95% confidence intervals (CIs) for allelic (C allele vs. A allele), additive (CC vs. AA), dominant (CC+AC vs. AA), and recessive (CC vs. AA+AC) models were calculated. Subgroup and sensitivity analyses were performed to detect the heterogeneity and examine the reliability of results, respectively. Begg's funnel plots and Egger's regression test were used to assess the potential publication bias. Results: A total of fifteen studies containing 2,361 cases and 2,653 controls were included in the final meta-analysis. The combined results of overall analysis showed that there was significant association between MTHFR gene A1298C polymorphism and adult stroke (allelic model: OR = 1.36, 95% CI = 1.11-1.67; additive model: OR = 1.88, 95% CI = 1.12-3.18; dominant model: OR = 1.33, 95% CI = 1.08-1.65 and recessive model: OR = 1.77, 95% CI = 1.07-2.94, respectively). On subgroup analysis by ethnicity of study population, significant association was shown in meta-analysis based on Asian population (allelic model: OR = 1.40, 95% CI = 1.19-1.65; additive model: OR = 2.58, 95% CI = 1.34-4.96; dominant model: OR = 1.44, 95% CI = 1.20-1.73 and recessive model: OR = 2.12, 95% CI = 1.20-3.76, respectively), but not in Caucasian population (allelic model: OR = 1.30, 95% CI = 0.93-1.82; additive model: OR = 1.65, 95% CI = 0.81-3.33; dominant model: OR = 1.17, 95% CI = 0.86-1.61 and recessive model: OR = 1.70, 95% CI = 0.83-3.50, respectively). In addition, the heterogeneity was effectively removed or decreased by limiting the included studies with population of Asian ethnicity. Furthermore, the corresponding pooled ORs were not materially changed in all genetic models of meta-analysis after limiting the included studies with population-based controls. However, except the recessive model, publication bias presented in the allelic, additive, dominant models identified by the Begg's funnel plots and Egger's regression test. Conclusions: In conclusion, the overall analysis suggests that MTHFR gene A1298C polymorphism plays an important role in the development of adult stroke. Genotype CC of MTHFR-1298A/C could increase the risk of stroke and may act as a predictor for clinical evaluation, especially in the Asian population. More studies with large-scale and different ethnicities are required to further confirm our findings. © 2014 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

A variety of epidemiological studies have evaluated the association between methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and cerebrovascular disease, but the results were inconsistent. The present meta-analysis was therefore performed to investigate the relationship between C677T polymorphism and cerebrovascular disease in Chinese population. Systematically searching for related studies from PubMed, Embase, Web of Science, CBMdisc and CNKI databases up to 20 September 2013 and manual searching of the reference lists of identified articles was performed. Information was extracted to calculate for the additive, dominant, and recessive models using the pooled odds ratios (ORs) along with 95 % confidence intervals (CIs), using Review Manager 5.0, STATA 11.0 and SPSS 17. Logistic regression, fixed or random effects model, subgroup analysis, sensitivity analysis, meta-regression analysis and publication bias were conducted to improve the comprehensive analysis. A total of 68 case-control studies containing 7,990 cases and 6,941 controls were included in the final meta-analysis. Evidence of significant association between C677T polymorphism and risk of cerebrovascular disease was found in all three genetic models (additive model OR 1.472, 95 % CI 1.368-1.585, P < 0.001 (CT vs. CC); OR 1.819, 95 % CI 1.666-1.985, P < 0.001 (TT vs. CC); dominant model OR 1.77, 95 % CI 1.57-1.98, p < 0.00001; and recessive model OR 1.54, 95 % CI 1.39-1.71, p < 0.00001, respectively) based on the overall population. In addition, the results were verified by the subgroup analysis and sensitivity analysis. The present meta-analysis suggests that MTHFR gene C677T polymorphism is significantly associated with increased risk of cerebrovascular disease. TT genotype may act as an independent risk factor for cerebrovascular disease in Chinese population. [ABSTRACT FROM AUTHOR]

The three types of low mature organic-rich samples from US Green River shale (Type I kerogen), Woodford shale (Type II kerogen), and China Pearl River Mouth Basin( Type III kerogen) were chosen as the initial samples for pyrolysis simulation on hydrocarbon generation. A pyrolysis system of sealed gold tubes in high pressure vessels was employed to conduct pyrolysis experiments at two heating rates of 20 °C/h and 2 °C/h under a constant confining pressure of 24. 1 MPa. The yields of gaseous hydrocarbons (C1-5) and liquid hydrocarbons (C6-14 and C14+), and the carbon isotopic compositions of gaseous hydrocarbons (C1-C4) were measured to reveal the generation mechanism of shale gas. The results show that the organic matter conversion from organic-rich shales to oil and gas can be divided into three stages: oil generation, gas generation from oil secondary cracking and gaseous hydrocarbons cracking. At the stage of oil generation by the thermal decomposition of primary kerogen, the yields of liquid hydrocarbons increase rapidly with the increase of temperature, and reach the peak values at approximately 0. 9%- 1.1% Ro, whereas gaseous hydrocarbons show low yields. At the stage of oil secondary cracking, gaseous hydrocarbons increase rapidly in the yields associated with the decreases in the yield of liquid hydrocarbons. At the stage of gaseous hydrocarbons cracking, the gas yields increase slightly, whereas gas is getting drier and enriches in CH4. The carbon isotopes of gaseous hydrocarbons vary from heavier to lighter with the increase of temperature, and reach the lightest values before the end of oil cracking, and then become heavier. The partial reversals of carbon isotopic compositions of gaseous hydrocarbons at the stage of oil cracking is observed for Type I shale, i. e., δ13C1<δ13C2<δ13nC4. The results also suggest that shale gas is mainly derived from kerogen primary cracking and oil and gas secondary cracking, and shale gas content is constrained by the organic matter type and thermal maturity, and the Type I shale has the highest gas yield. The partial reversal distributions of carbon isotopic compositions of gaseous hydrocarbons in shale gas could be caused by oil secondary cracking, or the mixing of gaseous hydrocarbons from different stages of thermal maturation. [ABSTRACT FROM AUTHOR]

The reaction of N-diphenylphosphinoyl imines 1 with [3-(trimethylsilyl)allyl]dimethylsulfonium bromide (5) in the presence of Nail at room temperature predominantly gave trans-vinylaziridines 4. On the other hand, cis-vinylaziridines 4 were the main products when the preformed ylide prepared from the reaction of [3-(trimethylsilyl)allyl]diphenylsulfonium perchlorate (6) was reacted with the same imines 1 at low temperature, trans-Aziridines were also obtained when imines 1 and sulfinimines 9 were reacted with N,N-dimethylacetamide-2-dimethylsulfonium bromide (7) in the presence of a base, respectively. A mechanistic study showed that the stereochemistry of these reactions was controlled by the reactivity of the imines and ylides. A higher reactivity of imines and ylides favors the formation of cis-aziridines, whereas a lower reactivity leads to trans-products. [ABSTRACT FROM AUTHOR]

Presents a mutagenic analysis of the RRE, the target sequence for the Rev protein of HIV-1, that directly compares the functional efficiency of the two alternative structures using an ex vivo transfection/expression system. Contributions of the original and alternative structures to the functioning of RRE construct; Functional equivalence and relevance of the two structures.

Studies the sequence specificity in the higher-order interaction of the HIV-1 Rev protein with its RRE target sequence. Role of RNA-contained information in higher-order binding; Interaction of Rev protein with the primary Rev binding domain; REV's recognition of sequence-specific information in the RRE.

U(1)X SSM is the extension of the minimal supersymmetric standard model (MSSM) and its local gauge group is SU(3)C× SU(2)L× U(1)Y× U(1)X. To obtain this model, three singlet new Higgs superfields and right-handed neutrinos are added to MSSM. In the framework of U(1)XSSM, we study the Higgs mass and take the lightest CP-even sneutrino as a cold dark matter candidate. For the lightest CP-even sneutrino, the relic density and the cross section for dark matter scattering off nucleon are both researched. In suitable parameter space of the model, the numerical results satisfy the constraints of the relic density and the cross section with the nucleon. [ABSTRACT FROM AUTHOR]

An alginate lyase producing bacterial strain, Cobetia sp. WG-007, was isolated and identified from rotting seaweed. The alginate lyase, Aly-W02, was purified by procedures of ultrafiltration, Q-Sepharose Fast Flow, Phenyl Sepharose 6 Fast Flow, and Superdex-G100 with specific activity of 21,285.5 U/mg. Aly-W02 had an apparent molecular mass of 35 kDa. It exhibited maximum activity at 45 °C in 50 mM sodium phosphate buffer (pH 8.5). This alginate lyase was stable in the pH range of 6.0-8.5. Among the tested metal ions, the addition of K+, Na+, and Mg2+ ions can enhance the enzyme activities, while Ba2+, Ni+, Cu2+, Mn2+, Zn2+, Ag+, and ethylenediaminetetraacetic acid decreased the activities. It displayed high salt-tolerant ability; 0.8 M NaCl or 1.5 M KCl significantly enhanced the enzyme activity. Furthermore, Aly-W02 mainly released disaccharide, trisaccharide, and tetrasaccharid from alginate. It showed potential in producing low molecular weight alginate oligosaccharides. [ABSTRACT FROM AUTHOR]

Exact solutions of the Navier-Stokes equations between two infinite planes are considered, where the velocity components parallel to the planes depend linearly on two spatial coordinates, and the third component depends only on the coordinate perpendicular to the planes. A class of unsteady exact solutions is found in this form with spiral or elliptical oscillation as an eigenmode of exponential time dependence, which can be arbitrarily superposed, while the pressure and boundary conditions remain unchanged. As a specific case, the flow between two infinite rotating disks is considered, and the corresponding eigenvalue problems are numerically investigated. Multiple solutions have been taken into account under axisymmetric and non-axisymmetric distributions of pressure. The eigenvalues, which are dependent on the Reynolds number, the rotation ratio, and the pressure parameter ratio, are calculated, and the phase diagrams containing neutral curves are presented. It is shown that some axisymmetric flows between two parallel rotating disks can be associated with an added periodic oscillation at low frequency proportional to the rotation ratio and with arbitrarily large amplitude. [ABSTRACT FROM AUTHOR]

The aqueous solution of polyacrylamide serves as reagent, catalyst, and reaction medium. [ABSTRACT FROM AUTHOR]

• The gneisses record two period metamorphic events as Neoproterozoic and early Paleozoic metamorphism. • 920–929 Ma from granitic gneisses and ca. 0.9 Ga from paragneisses represent the Neoproterozoic tectono-thermal event. • The early Paleozoic metamorphic ages given by the rim domains of zircons from gneiss samples record the the UHP-HP metamorphic evolution in EKO. The East Kunlun Orogen (EKO) is a long-lived accretionary orogenic belt that records the Paleozoic–Mesozoic amalgamation processes of the East Asia continent. The belt consists mainly of various kinds of gneisses with minor amounts of eclogite and garnet amphibolite occurring as lenses. We report zircon U–Pb ages and Hf–O isotopic compositions for the granitic gneisses and paragneisses in the Xiarihamu area near Golmud in Qinghai Province, to investigate the metamorphic history and evolution of the orogenic belt. For the granitic gneisses, zircon U–Pb chronology reveals a Neoproterozoic magmatic event and an early Paleozoic metamorphic event. The magmatic crystallization ages of the two granitic gneisses are 920 ± 6 and 929 ± 2 Ma, and yield ε Hf (t) values of −8.4 to 1.7 and δ18O values of 7.94–11.19‰, suggesting their derivation mainly from continental crustal materials. The detrital zircons from the paragneisses record a Neoproterozoic metamorphic event and a Paleozoic metamorphic event. Most of the detrital zircons from the two paragneiss samples yielded ages of 2.1–0.9 Ga, indicating that the sources of the sediment were formed mainly during the Neoproterozoic to Paleoproterozoic. These Neoproterozoic magmatic and metamorphic events suggest that the EKO underwent a Neoproterozoic tectonothermal event that was related to the assembly of the Rodinia supercontinent. The similar tectonic histories of the EKO and North Qaidam belt (NQB) indicate they were probably part of a single tectonic unit during the Neoproterozoic. Some of the zircons have metamorphic overgrowth rims yielding two stages of Paleozoic metamorphic ages of ca. 440 Ma (438 ± 2 Ma) and ca. 420 Ma (419 ± 6 Ma, 416 ± 6 Ma, and 423 ± 6 Ma). Combined the discover of high-pressure mineral inclusions (jadeite + quartz) in these rims with the results in previous studies, the ages of these rims (ca. 440 Ma and ca. 420 Ma) are suggested to represent of HP-UHP metamorphism of the EKO. These age data imply that the gneisses in this study might share common early Paleozoic metamorphic event with the HP–UHP eclogites in the EKO. [ABSTRACT FROM AUTHOR]

Permian (260-290 Ma) mafic dyke swarms in the northern of Xinjiang widely develop in West Junggar, Turpan-Hami Basin, East Tianshan, West Tianshan and the northeast margin of Tarim. The formation age of mafic dyke swarm is similar to that of Tarim large igneous provinces. The correlations between contents of major elements and MgO of mafic dyke swarms are obvious. Mafic dykes are enriched in large ion lithophile elements (Rb, Ba, Sr, etc.) and light rare earth elements (LREE), and depleted in high field strength element (Nb, Ta, Ti, etc.), and there is no obvious Eu anomaly, the characteristics are similar to island arc magma. εNd(t) values of mafic dykes are -11.25-7.86, and the initial N(87Sr)/N(86Sr) values are 0.703-0.710. Mafic dyke swarms in West Tianshan are depleted in LREE, and those in the northeast margin of Tarim are depleted in Sr. The magma of Permian mafic dyke swarm in the northern of Xinjiang is probably originated from enriched asthenosphere mantle source, and experiences different degrees of contamination of crust materials or metasomatic lithospheric mantle with subduction in the process of magmatic evolution. The dykes in West Junggar, East Tianshan, West Tianshan and Turpan-Hami Basin experience the contamination of lithospheric mantle with metasomatism of fluids from plate subduction; the mafic dykes in East Tianshan and the northeast margin of Tarim experience obvious contamination of crustal materials in the process of magmatic evolution. The Permian mafic dyke swarms in the northern of Xinjiang could be the products of mantle plume magmatism in different processes of evolution. [ABSTRACT FROM AUTHOR]

Single ventricle (SV) physiology is associated with growth retardation in children. The nutritional status of pediatric patients with SV undergoing a bidirectional Glenn (BDG) procedure vitally affects the feasibility of the next operation stages. To explore the nutritional status and to identify specific anthropometric parameters relevant to short-term surgical outcomes in children with SV after the BDG procedure, this study included 151 patients who underwent the BDG procedure. Anthropometric assessments and Infant and Child Feeding Index (ICFI) scores were used to evaluate nutritional status. There was a significant statistical correlation between ICFI and malnutrition in both the height-for-age Z-score (HAZ) and weight-for-age Z-score (WAZ) groups (P < 0.05). The clinical data, including ventilation time, nosocomial infection presence, pressure injury presence, peritoneal dialysis status, and total intensive care unit days, after BDG surgery were significantly different among the HAZ groups (P < 0.05), while nosocomial infection was different among the WAZ groups (P < 0.05). Children after BDG procedure had a high incidence of malnutrition, in addition to disease factors, the type and frequency of dietary intake were also important factors leading to worse clinical outcomes during hospitalization. Therefore, it is vital to maintain an optimal nutritional status in infants with SV who are undergoing a series of surgical procedures. [ABSTRACT FROM AUTHOR]

A new bis- N -heterocyclic carbene palladium complex, (C13H9N2F2)2PdCl2, is synthesized by a three-step reaction and characterized by 1H NMR and 13C NMR spectroscopy as well as by X-ray crystallography. This new bis- N -heterocyclic carbene palladium complex has excellent stability and is capable of efficiently catalyzing the Mizoroki–Heck coupling reaction of aryl halides with acrylates. [ABSTRACT FROM AUTHOR]

• The phosphate cement was used to produce fiber-reinforced inorganic polymer (FRiP) composites. • The FRiP composites achieved excellent bonding performance with concrete substrate. • The FRiP composites exhibited significantly improved fire resistance compared to FRP composites. Fiber reinforced polymer (FRP) composites have been widely used for strengthening of concrete structures for many years. A critical concern for the FRP strengthening technology is the fire resistance. In this study, phosphate cement-based fiber-reinforced inorganic polymer (FRiP) composites were used to replace conventional fiber-reinforced polymer (FRP) composites to strengthen concrete beams for improved fire resistance. The performances of FRiP composites, FRiP-to-concrete interfaces and FRiP-strengthened concrete beams were examined both before and after fire exposure. It was demonstrated that the phosphate cement-based FRiP composites can significantly enhance the mechanical strength of the concrete beams. In addition, they exhibit much improved fire resistance as compared to the epoxy-based FRP composites. [ABSTRACT FROM AUTHOR]

In this study, we determined the number of peripheral blood circulating tumor cells (CTCs) pre- and post-NK in patients with stage IV non- small cell lung cancer (NSCLC) as a reference for understanding the relevance of any changes to the efficacy of NK cells therapy. The patients were given one to three courses of immunotherapy. CTC numbers and CTC-related gene expression were measured in the peripheral blood of 31 patients with stage IV NSCLC at 1 day before and 7 and 30 d after NK cells therapy using magnetic activated cell sorting (MACS) and fluorescence activated cell sorting (FACS) combined with real-time quantitative PCR (RT-qPCR). Throughout the research, fever was the most common reaction (34.6%). The number of CTCs was 18.11 ± 5.813, 15.13 ± 5.984 and 10.32 ± 5.623, respectively, and this decreased significantly over time. ΔCt values for the CTC-related genes CEA, MAGE-3 and CK18 increased significantly after NK cells infusion. The expression of CEA, CK18 and MAGE-3 decreased significantly with time after NK. CTC was a useful biomarker for evaluating the efficacy of NK cells therapy on stage IV NSCLC. [ABSTRACT FROM AUTHOR]

Natural killer (NK) cells are a key component of the innate immune system and play pivotal roles as inflammatory regulators and in tumor surveillance. Human aspartyl β -hydroxylase (HAAH) is a plasma membrane and endoplasmic reticulum protein with hydroxylation activity, which is over-expressed in many malignant neoplasms and can be detected from the sera of tumor patients. HAAH is involved in regulating tumor cell infiltration and metastasis. Escaping from immune surveillance may help tumor cell infiltration and metastasis. However, the effects of HAAH on tumor immune surveillance have not yet been investigated carefully. The present study investigated the potential use of HAAH as an immune regulator of human NK cells. We assessed the effects of recombinant HAAH (r-HAAH) on primary human NK cell morphology, viability, cytotoxicity, apoptosis, receptors expression and cytokine/cytolytic proteins production. Our results demonstrated that r-HAAH negatively affects NK cell activity in a time and dose-dependent manner. It noticeably reduces the viability of the NK cells by increasing apoptosis and necrosis via caspase signaling pathways. Moreover, r-HAAH reduces the NK cell cytotoxicity by inhibiting surface expression of NKG2D, NKp44 and IFN-γ secretion. These findings suggest that one of the ways by which HAAH actively promotes tumor formation and proliferation is by inhibiting NK cell-surveillance activity. [ABSTRACT FROM AUTHOR]

Epidemiological studies have evaluated the association between Toll-like receptor 4 (TLR4) gene Asp299Gly (rs4986790) polymorphism and the risk of ischemic cerebrovascular disease, but the results are inconsistent. In an effort to clarify earlier inconclusive results, a meta-analysis was performed. We searched the PubMed, Web of Science, Embase, Cochrane database, Clinicaltrials.gov, Current Controlled Trials, CNKI, CBMdisc, Chinese Clinical Trial Registry and Google Scholar until up to 20 July 2013. Additionally, hand searching of the references of identified articles was performed. Original observational studies investigating the association between TLR4 gene Asp299Gly polymorphism and ischemic cerebrovascular disease risk were included. All statistical analyses were performed using Stata 11.0. The search strategy identified 1038 potentially relevant articles, seven of which were included in the final meta-analysis, covering a total of 1767 cases and 2785 controls. Overall, no significant association was found between TLR4 gene Asp299Gly polymorphism and ischemic cerebrovascular disease risk (for G allele versus A allele: OR = 0.95, 95% CI = 0.75-1.21, p = 0.69; for G/G+A/G versus A/A: OR = 0.96, 95% CI = 0.75-1.22, p = 0.73). In addition, the similar results were obtained in the sensitivity analysis based on studies with the high quality. In summary, the present meta-analysis indicates that TLR4 gene Asp299Gly polymorphism is not associated with increased ischemic cerebrovascular disease risk. [ABSTRACT FROM AUTHOR]

Highlights: [•] Polysaccharides promote the activities of human NK cells. [•] Simulated microgravity (SMG) conditions decrease the activities of NK cells. [•] NKp30 and cytokines were up-regulated in NK cells by polysaccharides. [•] Polysaccharides can restore the function of NK cells under SMG conditions. [•] Polysaccharides prevented SMG-induced apoptosis and necrosis in NK cells. [ABSTRACT FROM AUTHOR]

Background: Numerous epidemiological studies have evaluated the associations between ATP-binding cassette transporter 1 (ABCA1) R219K (rs2230806) and M883I (rs4149313) polymorphisms and atherosclerosis (AS), but results remain controversial. The purpose of the present study is to investigate whether these two polymorphisms facilitate the susceptibility to AS using a meta-analysis. Methods: PubMed, Embase, Web of Science, Medline, Cochrane database, Clinicaltrials.gov, Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI, Google Scholar and Baidu Library were searched to get the genetic association studies. All statistical analyses were done with Stata 11.0. Results: Forty-seven articles involving 58 studies were included in the final meta-analysis. For the ABCA1 R219K polymorphism, 42 studies involving 12,551 AS cases and 19,548 controls were combined showing significant association between this variant and AS risk (for K allele vs. R allele: OR = 0.77, 95% CI = 0.71–0.84, P<0.01; for K/K vs. R/R: OR = 0.60, 95% CI = 0.51–0.71, P<0.01; for K/K vs. R/K+R/R: OR = 0.69, 95% CI = 0.60–0.80, P<0.01; for K/K+R/K vs. R/R: OR = 0.74, 95% CI = 0.66–0.83, P<0.01). For the ABCA1 M883I polymorphism, 16 studies involving 4,224 AS cases and 3,462 controls were combined. There was also significant association between the variant and AS risk (for I allele vs. M allele: OR = 0.85, 95% CI = 0.77–0.95, P<0.01). Conclusions: The present meta-analysis suggested that the ABCA1 R219K and M883I polymorphisms were associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution. [ABSTRACT FROM AUTHOR]

Abstract: Increasing epidemiological studies have focused on the associations between interleukin-6 (IL-6) gene −174G>C polymorphism and atherosclerotic diseases, but the results are still controversial. This meta-analysis was designed to identify whether this association exists. PubMed, Embase, Web of Science, Cochrane database, Clinicaltrials.gov and Current Controlled Trials, Chinese Clinical Trial Registry, CBMdisc, CNKI and Google Scholar were searched to get the genetic association studies. The crude odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) were used to estimate the association between the IL-6 gene −174G>C polymorphism and atherosclerosis ( AS ) risk. The subgroup analyses were made on the following: ethnicity, atherosclerotic diseases and source of controls. Finally, 50 studies (15,029 cases and 18,485 controls) were included in this meta-analysis. Overall, no significant association was found between the IL-6 gene −174G>C polymorphism and AS risk (for C allele vs. G allele: OR=1.02, 95% CI=0.94–1.11, p =0.64; for C/C vs. G/G: OR=1.01, 95% CI=0.85–1.21, p =0.88; for C/C vs. C/G+G/G: OR=0.97, 95% CI=0.84–1.12, p =0.68; for C/C+C/G vs. G/G: OR=1.07, 95% CI=0.97–1.17, p =0.18). In the subgroup analyses, significant associations were found between the IL-6 gene −174G>C polymorphism and AS in non-Caucasian group (for CC+CG vs. GG: OR=1.22, 95% CI=1.06–1.41, p =0.005), other atherosclerotic diseases group (for C allele vs. G allele: OR =0.75, 95% CI=0.61–0.93, p =0.008; for C/C vs. G/G: OR=0.56, 95% CI=0.38–0.81, p =0.002; for C/C vs. C/G+G/G: OR=0.60, 95% CI=0.45–0.79, p =0.0004) and population-based group (for C allele vs. G allele: OR=1.09, 95% CI=1.00–1.18, p =0.04; for CC+CG vs. GG: OR=1.15, 95% CI=1.04–1.27, p =0.005). In summary, the present meta-analysis suggests that the IL-6 gene −174GC polymorphism is associated with the susceptibility to AS. However, due to the high heterogeneity in the meta-analysis, the results should be interpreted with caution. [Copyright &y& Elsevier]

Abstract: A comb ethyl cellulose-g-sodium polyacrylate (EC-g-SPA) was synthesized by atom transfer radical polymerization. The amphiphilic properties of the EC-g-SPA were determined by surface tension measurements. The interactions between EC-g-SPA and the cationic surfactant dodecyl-trimethylammonium bromide (C12TAB) were investigated by surface tension, turbidity, dynamic light scattering and transmission electron microscopy (TEM). The results revealed that the critical aggregate concentration (CAC) of the complexes was 0.8mM. When the C12TAB concentration was lower than the CAC, the hydrodynamic diameter (D h) of the complexes decreased as the surfactant concentration was increased. As the C12TAB concentration was increased above the CAC, the D h initially increased slightly, followed by a sharp decrease. The changes in the sizes and shapes of the aggregates were studied by TEM. The interactions between two species and the structure of the EC-g-SPA/C12TAB complexes were also discussed. [Copyright &y& Elsevier]

Abstract: Human metallothionein-3 (hMT3), also named as human neuronal growth inhibitory factor (hGIF), can inhibit the outgrowth of embryonic cortical neurons in the presence of brain extracts. In order to systematically study the structure–property–reactivity–function relationship of hGIF, our laboratory designed a series of mutants and studied their structure, property, reactivity and functions by a series of chemical and biological tools including UV spectroscopy, CD spectroscopy, NMR, chemical reaction and primary neuronal culture assays. In summary, we concluded that the bioactivity of hGIF was regulated by multiple factors, including the 6CPCP9 motif, an additional threonine insert at sequence position 5, domain–domain interactions, the structure and stability of the metal–thiolate cluster and the linker. Our studies provide more and more evidences which revealed that the bioactivity of hGIF is mainly related to the essential metal release and its characteristic conformation. [Copyright &y& Elsevier]

Abstract: Human metallothionein-3 (hMT3), first isolated and identified as a neuronal growth inhibitory factor (GIF), is a metalloprotein expressed predominantly in brain. However, untill now, the exact mechanism of the bioactivity of hMT3 is still unknown. In order to study the influence of acid–base catalysis on S-nitrosylation of hMT3, we constructed the E23K mutant of hMT3. During the course of bioassay, we found out unexpectedly that mutation at E23 of hMT3 eliminates the neuronal growth inhibitory activity completely. To the best of our knowledge, it is the first report that other residues, besides the TCPCP motif, in the β-domain can alter the bioactivity of hMT3. In order to figure out the causes for the loss of bioactivity of the E23K mutant, the biochemical properties were characterized by UV–vis spectroscopy, CD spectroscopy, pH titration, DTNB reaction, EDTA reaction, and SNOC reaction. All data demonstrated that stability of the metal–thiolate cluster and overall structure of the E23K mutant were not altered too much. However, the reaction of the E23K mutant with SNOC exhibited biphasic kinetics and the mutant protein released zinc ions much faster than hMT3 in the initial step, while hMT3 exhibited single kinetic process. The 2D [1H–15N] HSQC was also employed to characterize structural changes during the reaction of hMT3 with varying mounts of nitric oxide. It was shown that the resonance of Glu23 disappeared at a molar ratio of NO to protein of 4. Based on these results, we suggest that mutation at Glu23 may alter the NO metabolism and/or affect zinc homeostasis in brain, thus altering the neuronal growth inhibitory activity. [Copyright &y& Elsevier]

A series of planar chiral P,N-[2.2]paracyclophane ligands were synthesized and applied in enantioselective palladium-catalyzed allylic alkylation, in which the central chirality of [2.2]paracyclophane is the dominant stereocontrol element. The effect of the substituents attached to the phosphorus atom of these ligands on the yield and stereoselectivity of the reaction was also investigated. [Copyright &y& Elsevier]

Background: The congenital stationary night blindness (CSNB) affects the patients' dim light vision or dark adaption by impairing the normal function of retina. It is a clinically and genetically heterogeneous disorder and can be inherited in an X‐linked, autosomal dominant or autosomal recessive pattern. Several genetic alterations to the genes involved in visual signal transduction of photoreceptors and/or bipolar cells underlie its pathogenesis. Methods: In this study, we used Sanger sequencing and next‐generation sequencing (NGS)‐based gene panel screening to investigate a family of three patients with CSNB inherited in an apparent autosomal dominant pattern. We expected to find out the disease‐causing gene defects carried by this family. Results: We found that the patients in this family did not carry the RHO, GNAT1, or PDE6B mutation, but carried compound heterozygotes mutations of GRM6. Three deleterious GRM6 variants, p.Arg621Ter, p.Gly51Val, and p.Gly464Arg, were found to be co‐segregating with the disease, causing a pseudodominant inheritance of GRM6‐related autosomal recessive complete CSNB. Conclusion: This study presents a rare case of autosomal recessive CSNB (arCSNB) pseudodominant inheritance, which potentially leads us to expand our gene candidate list in future genetic testing for apparent dominant pedigrees. The discovery of the two novel likely pathogenic variants p.Gly51Val and p.Gly464Arg could broaden our knowledge about the genetics of CSNB and provide insights into the structure and function of the GRM6 protein. [ABSTRACT FROM AUTHOR]

via a Pd-catalyzed Heck reaction [ABSTRACT FROM AUTHOR]