543 research outputs found

    A new sesquiterpene lactone and a new aromatic glycoside from Illicium difengpi

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    AbstractA new sesquiterpene lactone (1) and a new aromatic glycoside (2), together with three known compounds (3–5) were isolated from the stem bark of Illicium difengpi K. I. B et K. I. M. Their structures were determined by spectroscopic methods, including 1D and 2D NMR, HRESIMS, and chemical methods. The absolute configuration of the secondary alcohol in 1 was confirmed by Mosher's method. Compound 2 exhibited significant anti-inflammatory activity with IC50 value of 6.72μmol/L

    12导联动态心电图与冠状动脉造影结果的对比分析

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    Objective:To discuss the value of the 12-lead dynamic electrocardiogram (DCG) in diagnosis of coronary heart disease(CHD) by comparing and analyzing the results between 12-lead DCG and coronary angiography. Methods: 105 patients with suspected CHD undergoing both 12-lead DCG and coronary angiography were analyzed. Results: 105 patients with positive coronary angiography of 46 cases, 59 cases were negative, of which 12 lead DCG showed ischemic ST segment depression in 32 patients, no ST-segment depression in 14 cases, normal coronary angiography in 59 cases of 12-lead DCG showed ischemic ST segment depression in 23 patients, no ST-segment depression in 36 cases. Conclusion:12-lead DCG is one of ideal non-invasive methods in the diagnosis of CHD of ischemic ST segment depression with typical chest pain.It is simple,economic and practical.目的  通过比较分析12导联动态心电图(DCG)与冠状动脉造影结果,探讨12导联DCG对冠心病的临床诊断价值。方法  将105例可疑冠心病患者24h同步12导联DCG与冠状动脉造影结果进行对比分析。结果  105例患者经冠状动脉造影阳性46例,其中32例12导联DCG显示缺血性ST段压低,无ST段压低改变14例;冠状动脉造影正常的59例中12导联DCG显示缺血性ST段压低23例,无ST段压低改变36例。结论  12导联DCG是临床诊断缺血性ST段压低伴典型胸痛的冠心病较为理想的无创性检查方法之一,而且操作简单,价廉、实用

    Autophagy in Plant Pathogenic Fungi

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    Autophagy is a ubiquitous and conserved process in eukaryotic cells from yeasts to mammals. It also appears to play vital roles in plant pathogenic fungi, impacting growth, morphology, development, and pathogenicity. In this chapter, we have introduced a new concept to delineate the role of autophagy in homeostasis of plant pathogenic fungi and in their interaction with host cells, in breach of host barrier, and in the mechanisms of plant fungal infection

    Hippocampal Synaptic and Neural Network Deficits in Young Mice Carrying the Human APOE4 Gene

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    Introduction: Apolipoprotein E4 (APOE4) is a major genetic risk factor for late-onset sporadic Alzheimer disease. Emerging evidence demonstrates a hippocampus-associated learning and memory deficit in aged APOE4 human carriers and also in aged mice carrying human APOE4 gene. This suggests that either exogenous APOE4 or endogenous APOE4 alters the cognitive profile and hippocampal structure and function. However, little is known regarding how Apoe4 modulates hippocampal dendritic morphology, synaptic function, and neural network activity in young mice. Aim: In this study, we compared hippocampal dendritic and spine morphology and synaptic function of young (4 months) mice with transgenic expression of the human APOE4 and APOE3 genes. Methods: Hippocampal dendritic and spine morphology and synaptic function were assessed by neuronal imaging and electrophysiological approaches. Results: Morphology results showed that shortened dendritic length and reduced spine density occurred at hippocampal CA1 neurons in Apoe4 mice compared to Apoe3 mice. Electrophysiological results demonstrated that in the hippocampal CA3-CA1 synapses of young Apoe4 mice, basic synaptic transmission, and paired-pulse facilitation were enhanced but long-term potentiation and carbachol-induced hippocampal theta oscillations were impaired compared to young Apoe3 mice. However, both Apoe genotypes responded similarly to persistent stimulations (4, 10, and 40 Hz for 4 seconds). Conclusion: Our results suggest significant alterations in hippocampal dendritic structure and synaptic function in Apoe4 mice, even at an early age

    Genetic Variations in Plasma Circulating DNA of HBV-Related Hepatocellular Carcinoma Patients Predict Recurrence after Liver Transplantation

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    BACKGROUND: Recurrence prediction of hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) patients undergoing liver transplantation (LT) present a great challenge because of a lack of biomarkers. Genetic variations play an important role in tumor development and metastasis. METHODS: Oligonucleotide microarrays were used to evaluate the genetic characteristics of tumor DNA in 30 HBV-related HCC patients who were underwent LT. Recurrence-related single-nucleotide polymorphism were selected, and their prognostic value was assessed and validated in two independent cohorts of HCC patients (N = 102 and N = 77), using pretransplant plasma circulating DNA. Prognostic significance was assessed by Kaplan-Meier survival estimates and log-rank tests. Multivariate analyses were performed to evaluate prognosis-related factors. RESULTS: rs894151 and rs12438080 were significantly associated with recurrence (P = .003 and P = .004, respectively). Multivariate analyses demonstrated that the co-index of the 2 SNPs was an independent prognostic factor for recurrence (P = .040). Similar results were obtained in the third cohort (N = 77). Furthermore, for HCC patients (all the 3 cohorts) exceeding Milan criteria, the co-index was a prognostic factor for recurrence and survival (P<.001 and P = .002, respectively). CONCLUSIONS: Our study demonstrated first that genetic variations of rs894151 and rs12438080 in pretransplant plasma circulating DNA are promising prognostic markers for tumor recurrence in HCC patients undergoing LT and identify a subgroup of patients who, despite having HCC exceeding Milan criteria, have a low risk of post-transplant recurrence

    Applying hybrid clustering in pulsar candidate sifting with multi-modality for FAST survey

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    Pulsar search is always the basis of pulsar navigation, gravitational wave detection and other research topics. Currently, the volume of pulsar candidates collected by Five-hundred-meter Aperture Spherical radio Telescope (FAST) shows an explosive growth rate that has brought challenges for its pulsar candidate filtering System. Particularly, the multi-view heterogeneous data and class imbalance between true pulsars and non-pulsar candidates have negative effects on traditional single-modal supervised classification methods. In this study, a multi-modal and semi-supervised learning based pulsar candidate sifting algorithm is presented, which adopts a hybrid ensemble clustering scheme of density-based and partition-based methods combined with a feature-level fusion strategy for input data and a data partition strategy for parallelization. Experiments on both HTRU (The High Time Resolution Universe Survey) 2 and FAST actual observation data demonstrate that the proposed algorithm could excellently identify the pulsars: On HTRU2, the precision and recall rates of its parallel mode reach 0.981 and 0.988. On FAST data, those of its parallel mode reach 0.891 and 0.961, meanwhile, the running time also significantly decrease with the increment of parallel nodes within limits. So, we can get the conclusion that our algorithm could be a feasible idea for large scale pulsar candidate sifting of FAST drift scan observation
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