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面向CAE分析的几何模型自动简化技术综述 被引量:9
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作者 曹伟娟 《计算机辅助设计与图形学学报》 EI CSCD 北大核心 2017年第3期406-418,共13页
通过分析面向CAE分析的几何模型自动简化中的关键技术问题,分别针对细节抑制、降维、对称简化、装配体简化以及简化影响评估,介绍了该领域的主要研究进展和代表性成果,并对需要解决的难点问题进行了讨论.
关键词 CAE 细节抑制 降维 对称 装配体 简化影响
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Inhibiting Effect of Lobenzarit Disodium on the Inter-leukin-1 Activity in Normal and in Adjuvant ArthritisKats and on the H_2O_2 Release from Rat Peritoneal Macro-phages
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作者 李卫东 林志彬 《Journal of Chinese Pharmaceutical Sciences》 CAS 1995年第3期131-135,共5页
The effects of Lobenzarit disodium (CCA) upon the activity of interleukin-1(IL-1) of peritoneal macrophages(PMΦ)in normal and in adjuvant arthritis AA) rats and on the release of hydrogen peroxide(H_2O_2)of rat perit... The effects of Lobenzarit disodium (CCA) upon the activity of interleukin-1(IL-1) of peritoneal macrophages(PMΦ)in normal and in adjuvant arthritis AA) rats and on the release of hydrogen peroxide(H_2O_2)of rat peritoneal macrophages were studied. CCA 10~200 μg/ml could inhibit IL-1activity in normal rat in vitro;CCA 10 and 50 mg/kg could depress the level of increased IL-1 in AA rats in vivo;CCA 5~100μg/ml could inhibit the release of H_2O_2 from rat PMΦin vitro.The results suggest that these effects could be one of the mechanisms of anti-inflammatory action of CCA. 展开更多
关键词 Lobenzarit disodium INTERLEUKIN-1 Hydrogen peroxide Peritoneal macrophage Anti-inflammatory effect
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BIM模型在信号运维系统中的轻量化研究 被引量:6
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作者 白雪 任晨宇 朱超平 《铁道通信信号》 2020年第5期52-54,58,共4页
在铁路信号系统运维过程中,由于BIM模型中包含有建设阶段的信息,造成系统数据冗杂、交互时间长,又由于信号设备种类繁多、布局分散,导致系统规模庞大,无形中降低了工作效率.本文对BIM模型进行轻量化方法研究,提出采用细节面片抑制法对... 在铁路信号系统运维过程中,由于BIM模型中包含有建设阶段的信息,造成系统数据冗杂、交互时间长,又由于信号设备种类繁多、布局分散,导致系统规模庞大,无形中降低了工作效率.本文对BIM模型进行轻量化方法研究,提出采用细节面片抑制法对模型进行处理,以达到使BIM模型轻量化的目的,取得良好效果. 展开更多
关键词 建筑信息模型 轻量化 细节面片抑制 措施
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Correlation between expression of gastrin, somatostatin and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma 被引量:27
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作者 Jia-DingMao PeiWu +3 位作者 Xiang-HouXia Ji-QunHu Wen-BinHuang Guo-QiangXu 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第5期721-725,共5页
AIM: To explore the correlation between expression of somatostatin (SS), gastrin (GAS) and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma.METHODS: Sixty-two large intestine cancer tissue samples... AIM: To explore the correlation between expression of somatostatin (SS), gastrin (GAS) and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma.METHODS: Sixty-two large intestine cancer tissue samples were randomly and retrospectively selected from patients with large intestine carcinoma. Immunohistochemical staining for bcl-2, bax, GAS, SS was performed according to the standard streptavidin-biotin-peroxidase (S-P) method.According to the semi-quantitative integral evaluation, SS and GAS were divided into three groups as follows. Scores1-3 were defined as the low expression group, 4-8 as the intermediate expression group, 9-16 as the high expression group. Bax and bcl-2 protein expressions in different GAS and SS expression groups of large intestine carcinoma were assessed.RESULTS: The positive expression rate of bax had a prominent difference between SS and GAS high, intermediate and low expression groups (P<0.05, x2ss = 9.246; P<0.05,x2GAS = 6.981). The positive expression rate of bax in SS high (80.0%, 8/10) and intermediate (76.5%, 13/17)expression groups was higher than that in low expression group (40.0%, 14/35) (P<0.05, x2high vs low = 5.242; P<0.05,x2middle vs low = 6.097). The positive expression rate of bax in GAS high expression group (27.3%, 3/8) was lower than that in low expression group (69.4%, 25/36) (P<0.05,x2 = 4.594). However, bax expression in GAS intermediate expression group (46.7%, 7/15) was lower than that in low expression group, but not statistically significant. The positive expression rate of bcl-2 had a prominent difference between SS and GAS high, intermediate and low expression groups (P<0.05, x2ss = 7.178; P<0.05, x2GAS = 13.831). The positive expression rate of bcl-2 in GAS high (90.9%, 10/11)and intermediate (86.7%, 13/15) expression groups was higher than that in low expression group (44.4%, 16/36)(P<0.05,x2high vs low = 5.600; P<0.05, x2 middle vs low = 7.695).However, the positive expression rate of bcl-2 in SS high (40.0%, 4/10) and intermediate (47.1%, 8/9) expression groups was lower than that in low expression group (77.1%, 27/35)(P<0.05, x2 high vs low = 4.710; P<0.05, x2 middle vs low = 4.706).There was a significant positive correlation between the integral ratio of GAS to SS and the integral of bcl-2 (P<0.01,r=0.340). However, there was a negative correlation between the integral ratio of GAS to the SS and bax the integral of (P<0.05, r = -0.299).CONCLUSION: The regulation and control of gastrin,somatostatin in cell apoptosis of large intestine carcinoma may be directly related to the abnormal expression of bcl-2, bax. 展开更多
关键词 Large intestine carcinoma GASTRIN SOMATOSTATIN bcl-2 gene Bax gene APOPTOSIS
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A microRNA encoded by HSV-1 inhibits a cellular transcriptional repressor of viral immediate early and early genes 被引量:6
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作者 WU WenJuan GUO ZhongPing +6 位作者 ZHANG XueMei GUO Lei LIU LongDing LIAO Yun WANG JingJing WANG LiChun LI QiHan 《Science China(Life Sciences)》 SCIE CAS 2013年第4期373-383,共11页
Viral microRNAs are one component of the RNA interference phenomenon generated during viral infection. They were first identified in the Herpesviridae family, where they were found to regulate viral mRNA translation. ... Viral microRNAs are one component of the RNA interference phenomenon generated during viral infection. They were first identified in the Herpesviridae family, where they were found to regulate viral mRNA translation. In addition, prior work has suggested that Kaposi's sarcoma-associated herpesvirus (KSHV) is capable of regulating cellular gene transcription by miRNA. We demonstrate that a miRNA, hsvl-mir-H27, encoded within the genome of herpes simplex virus 1 (HSV-1), targets the mRNA of the cellular transcriptional repressor Kelch-like 24 (KLHL24) that inhibits transcriptional efficiency of viral imme- diate-early and early genes. The viral miRNA is able to block the expression of KLHL24 in cells infected by HSV-1. Our dis- covery reveals an effective viral strategy for evading host cell defenses and supporting the efficient replication and prolifera- tion of HSV- 1. 展开更多
关键词 herpes simplex virus I (HSV-1) microRNAs (miRNAs) cellular transcriptional repressor Kelch-like 24
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