1,013 research outputs found

    The safety and efficacy of using moxibustion and or acupuncture for cancer-related insomnia: A systematic review and meta-analysis of randomised controlled trials

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    Introduction: This study aimed to synthesise the best available evidence on the safety and efficacy of using moxibustion and/or acupuncture to manage cancer-related insomnia (CRI). Methods: The PRISMA framework guided the review. Nine databases were searched from its inception to July 2020, published in English or Chinese. Randomised clinical trials (RCTs) of moxibustion and or acupuncture for the treatment of CRI were selected for inclusion. Methodological quality was assessed using the method suggested by the Cochrane collaboration. The Cochrane Review Manager was used to conduct a meta-analysis. Results: Fourteen RCTs met the eligibility criteria. Twelve RCTs used the Pittsburgh Sleep Quality Index (PSQI) score as continuous data and a meta-analysis showed positive effects of moxibustion and or acupuncture (n = 997, mean difference (MD) = −1.84, 95% confidence interval (CI) = −2.75 to −0.94, p < 0.01). Five RCTs using continuous data and a meta-analysis in these studies also showed significant difference between two groups (n = 358, risk ratio (RR) = 0.45, 95% CI = 0.26–0.80, I2 = 39%). Conclusion: The meta-analyses demonstrated that moxibustion and or acupuncture showed a positive effect in managing CRI. Such modalities could be considered an add-on option in the current CRI management regimen

    Cloning and functional characterization of a complex endo-beta-1,3-glucanase from Paenibacillus sp

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    A beta-1,3-glucanase gene, encoding a protein of 1,793 amino acids, was cloned from a strain of Paenibacillus sp. in this study. This large protein, designated as LamA, consists of many putative functional units, which include, from N to C terminus, a leader peptide, three repeats of the S-layer homologous module, a catalytic module of glycoside hydrolase family 16, four repeats of the carbohydrate-binding module of family CBM_4_9, and an analogue of coagulation factor Fa5/8C. Several truncated proteins, composed of the catalytic module with various organizations of the appended modules, were successfully expressed and characterized in this study. Data indicated that the catalytic module specifically hydrolyze beta-1,3- and beta-1,3-1,4-glucans. Also, laminaritriose was the major product upon endolytic hydrolysis of laminarin. The CBM repeats and Fa5/8C analogue substantially enhanced the hydrolyzing activity of the catalytic module, particularly toward insoluble complex substrates, suggesting their modulating functions in the enzymatic activity of LamA. Carbohydrate-binding assay confirmed the binding capabilities of the CBM repeats and Fa5/8C analogue to beta-1,3-, beta-1,3-1,4-, and even beta-1,4-glucans. These appended modules also enhanced the inhibition effect of the catalytic module on the growth of Candida albicans and Rhizoctonia solani

    On the Perturbative Nature of Color Superconductivity

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    Color superconductivity is a possible phase of high density QCD. We present a systematic derivation of the transition temperature, T_C, from the QCD Lagrangian through study of the di-quark proper vertex. With this approach, we confirm the dependence of T_C on the coupling g, namely TCμg5eκ/gT_C \sim \mu g^{-5} e^{-\kappa/g}, previously obtained from the one-gluon exchange approximation in the superconducting phase. The diagrammatic approach we employ allows us to examine the perturbative expansion of the vertex and the propagators. We find an additional O(1) contribution to the prefactor of the exponential from the one-loop quark self energy and that the other one-loop radiative contributions and the two gluon exchange vertex contribution are subleading.Comment: 13 pages, 3 figures, revtex, details and discussion expande

    An improved geometric inequality via vanishing moments, with applications to singular Liouville equations

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    We consider a class of singular Liouville equations on compact surfaces motivated by the study of Electroweak and Self-Dual Chern-Simons theories, the Gaussian curvature prescription with conical singularities and Onsager's description of turbulence. We analyse the problem of existence variationally, and show how the angular distribution of the conformal volume near the singularities may lead to improvements in the Moser-Trudinger inequality, and in turn to lower bounds on the Euler-Lagrange functional. We then discuss existence and non-existence results.Comment: some references adde

    Microstructure and Optical Properties of Tantalum Modified TiO2 Thin Films Prepared by the Sol-Gel Process

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    Tantalum doped TiO2 thin films ((TiO2)(1-x) (Ta2O5)(x), x = 0, 0.1%, 0.3%, 0.5%, 0.8%) were prepared on ITO-coated substrates by means of the sol gel method and spin coating technology followed by rapid thermal annealing treatment (RTA). The effects of various processing parameters, including Ta content (x = 0-0.8%) and annealing temperature, on the growth and properties of thin films were investigated. Structural characteristics by X-ray diffraction analysis indicated that the doping of Ta2O5 in the TiO2 without change the anatase structure of TiO2 thin films. The optical transmittance of (TiO2)(1-x) (Ta2O5) thin films decrease from 50% down to 20% with increasing the Ta2O5 concentrations from x = 0.00 to x = 0.8%. The absorption coefficient shows energy gap were decreased with increasing Ta2O5 content from 2.932 eV for x = 0.00 to 2.717 eV for x = 0.8%. Doping TiO2 with Ta2O5 can lower its band gap and shift its optical response to the visible region

    CD30-redirected chimeric antigen receptor T cells target CD30+ and CD30- embryonal carcinoma via antigen-dependent and fas/fasl interactions

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    Tumor antigen heterogeneity limits success of chimeric antigen receptor (CAR) T-cell therapies. Embryonal carcinomas (EC) and mixed testicular germ cell tumors (TGCT) containing EC, which are the most aggressive TGCT subtypes, are useful for dissecting this issue as ECs express the CD30 antigen but also containCD30-/dim cells.Wefound that CD30- redirected CAR T cells (CD30.CAR T cells) exhibit antitumor activity in vitro against the human EC cell lines Tera-1, Tera-2, and NCCIT and putative EC stem cells identified by Hoechst dye staining. Cytolytic activity of CD30.CAR T cells was complemented by their sustained proliferation and proinflammatory cytokine production. CD30.CAR T cells also demonstrated antitumor activity in an in vivo xenograft NOD/SCID/gcnull (NSG)mousemodel of metastatic EC.Weobserved that CD30. CAR T cells, while targeting CD30+ EC tumor cells through the CAR (i.e., antigen-dependent targeting), also eliminated surrounding CD30- EC cells in an antigen-independent manner, via a cell-cell contact-dependent Fas/FasL interaction. In addition, ectopic Fas (CD95)expression inCD30+ Fas-ECwas sufficient to improve CD30.CAR T-cell antitumor activity. Overall, these data suggest that CD30.CAR T cells might be useful as an immunotherapy for ECs. Additionally, Fas/FasL interaction between tumor cells and CAR T cells can be exploited to reduce tumor escapedue to heterogeneous antigen expression or to improve CAR T-cell antitumor activity

    Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

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    Background Converging evidence suggests that immune-mediated dysfunction plays an important role in the pathogenesis of frontotemporal dementia (FTD). Although genetic studies have shown that immune-associated loci are associated with increased FTD risk, a systematic investigation of genetic overlap between immune-mediated diseases and the spectrum of FTD-related disorders has not been performed. Methods and findings Using large genome-wide association studies (GWASs) (total n = 192,886 cases and controls) and recently developed tools to quantify genetic overlap/pleiotropy, we systematically identified single nucleotide polymorphisms (SNPs) jointly associated with FTD-related disorders—namely, FTD, corticobasal degeneration (CBD), progressive supranuclear palsy (PSP), and amyotrophic lateral sclerosis (ALS)—and 1 or more immune-mediated diseases including Crohn disease, ulcerative colitis (UC), rheumatoid arthritis (RA), type 1 diabetes (T1D), celiac disease (CeD), and psoriasis. We found up to 270-fold genetic enrichment between FTD and RA, up to 160-fold genetic enrichment between FTD and UC, up to 180- fold genetic enrichment between FTD and T1D, and up to 175-fold genetic enrichment between FTD and CeD. In contrast, for CBD and PSP, only 1 of the 6 immune-mediated diseases produced genetic enrichment comparable to that seen for FTD, with up to 150-fold genetic enrichment between CBD and CeD and up to 180-fold enrichment between PSP and RA. Further, we found minimal enrichment between ALS and the immune-mediated diseases tested, with the highest levels of enrichment between ALS and RA (up to 20-fold). For FTD, at a conjunction false discovery rate < 0.05 and after excluding SNPs in linkage disequilibrium, we found that 8 of the 15 identified loci mapped to the human leukocyte antigen (HLA) region on Chromosome (Chr) 6. We also found novel candidate FTD susceptibility loci within LRRK2 (leucine rich repeat kinase 2), TBKBP1 (TBK1 binding protein 1), and PGBD5 (piggyBac transposable element derived 5). Functionally, we found that the expression of FTD–immune pleiotropic genes (particularly within the HLA region) is altered in postmortem brain tissue from patients with FTD and is enriched in microglia/macrophages compared to other central nervous system cell types. The main study limitation is that the results represent only clinically diagnosed individuals. Also, given the complex interconnectedness of the HLA region, we were not able to define the specific gene or genes on Chr 6 responsible for our pleiotropic signal. Conclusions We show immune-mediated genetic enrichment specifically in FTD, particularly within the HLA region. Our genetic results suggest that for a subset of patients, immune dysfunction may contribute to FTD risk. These findings have potential implications for clinical trials target

    Novel CP-violating Effects in B decays from Charged-Higgs in a Two-Higgs Doublet Model for the Top Quark

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    We explore charged-Higgs cp-violating effects in a specific type III two-Higgs doublet model which is theoretically attractive as it accommodates the large mass of the top quark in a natural fashion. Two new CP-violating phases arise from the right-handed up quark sector. We consider CP violation in both neutral and charged B decays. Some of the important findings are as follows. 1) Large direct-CP asymmetry is found to be possible for B+- to psi/J K+-. 2) Sizable D-anti-D mixing effect at the percent level is found to be admissible despite the stringent constraints from the data on K-anti-K mixing, b to s gamma and B to tau nu decays. 3) A simple but distinctive CP asymmetry pattern emerges in decays of B_d and B_s mesons, including B_d to psi/J K_S, D+ D-, and B_s to D_s+ D_s-, psi eta/eta^prime, psi/J K_S. 4) The effect of D-anti-D mixing on the CP asymmetry in B+- to D/anti-D K+- and on the extraction of the angle gamma of the unitarity triangle from such decays can be significant.Comment: 32 pages, 5 figures, section V.A revised, version to appear in PR

    Single-particle nonlocality and entanglement with the vacuum

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    We propose a single-particle experiment that is equivalent to the conventional two-particle experiment used to demonstrate a violation of Bell's inequalities. Hence, we argue that quantum mechanical nonlocality can be demonstrated by single-particle states. The validity of such a claim has been discussed in the literature, but without reaching a clear consensus. We show that the disagreement can be traced to what part of the total state of the experiment one assigns to the (macroscopic) measurement apparatus. However, with a conventional and legitimate interpretation of the measurement process one is led to the conclusion that even a single particle can show nonlocal properties.Comment: 6 pages, 5 figure
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