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基于FCM算法的零件簇编码分析 被引量:1
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作者 张太华 顾新建 《中国机械工程》 EI CAS CSCD 北大核心 2007年第21期2585-2588,共4页
给出一个基于模糊c-平均(FCM)算法的零件簇聚类分析的过程模型来描述分析过程;构造了适合于零件簇聚类分析的FCM算法,该方法考虑了零件簇对象特征之间的模糊关系和各零件对象特征聚类中心之间的距离,无需设计权重系数;通过实例进行了聚... 给出一个基于模糊c-平均(FCM)算法的零件簇聚类分析的过程模型来描述分析过程;构造了适合于零件簇聚类分析的FCM算法,该方法考虑了零件簇对象特征之间的模糊关系和各零件对象特征聚类中心之间的距离,无需设计权重系数;通过实例进行了聚类分析,并与模糊聚类和k-平均聚类两种方法进行比较,证明该FCM算法是有效的。 展开更多
关键词 大批量定制 零件编码 FCM算法 比较分析
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基于Inter-Flow网络编码的多Sink无线传感器网络Anycast路由 被引量:7
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作者 仝杰 杜治高 钱德沛 《计算机研究与发展》 EI CSCD 北大核心 2014年第1期161-172,共12页
以最大化时间驱动型传感器网络的生命周期为目标,基于Inter-Flow网络编码,提出了多Sink环境下编码感知的交叉路径任播路由协议CodeMesh.首先分析多跳无线网络下单播流间编码条件,提出并证明了多Sink任播网络模型下的编码规则;进而提出... 以最大化时间驱动型传感器网络的生命周期为目标,基于Inter-Flow网络编码,提出了多Sink环境下编码感知的交叉路径任播路由协议CodeMesh.首先分析多跳无线网络下单播流间编码条件,提出并证明了多Sink任播网络模型下的编码规则;进而提出多流编码簇的概念,以及确定编码簇个数和优化编码簇成员的方法;定义了统一量化编码和非编码路径代价,并综合链路质量、负载平衡和编码收益的路由度量;最后设计了兼具反应式源路由和主动式路由特点的任播编码路由协议.CodeMesh充分利用Sink节点丰富的计算和通信资源,将路由优化与重构、路由更新与维护与周期性数据收集过程相结合,大大降低了路由开销.部署于实验床平台的实验结果表明,CodeMesh能够有效寻找到具有最多编码机会的路径,从而减少数据传输次数,提高网络传输效率,同时平衡节点负载和能耗,延长整个网络的生存时间. 展开更多
关键词 无线传感器网络 多Sink 流间网络编码 编码簇 任播路由
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结肠癌组织中lncRNA HOXA-AS3、miR-29b表达变化及意义
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作者 陈超 徐俊 +2 位作者 李幸 刘畅 熊非 《山东医药》 CAS 2023年第19期50-53,共4页
目的探讨结肠癌组织中长链非编码RNA同源框A簇反义-RNA3(lncRNA HOXA-AS3)、微小RNA-29b(miR-29b)的表达变化及临床意义。方法选取105例结肠癌患者,术中取癌组织及癌旁组织。用实时荧光定量PCR法检测组织中lncRNA HOXA-AS3、miR-29b表达... 目的探讨结肠癌组织中长链非编码RNA同源框A簇反义-RNA3(lncRNA HOXA-AS3)、微小RNA-29b(miR-29b)的表达变化及临床意义。方法选取105例结肠癌患者,术中取癌组织及癌旁组织。用实时荧光定量PCR法检测组织中lncRNA HOXA-AS3、miR-29b表达,分析二者表达的相关性及与病理参数的关系。随访3年,统计患者生存情况,根据结肠癌组织中lncRNA HOXA-AS3、miR-29b表达均值分为lncRNA HOXA-AS3高表达组(≥2.08,n=60)及低表达组(<2.08,n=45),miR-29b高表达组(≥1.08,n=52)及低表达组(<1.08,n=53),分析lncRNA HOXA-AS3、miR-29b表达水平与患者总生存率的关系。结果与癌旁组织比较,结肠癌组织中lncRNA HOXA-AS3表达高、miR-29b表达低(P均<0.05)。Pearson相关分析结果显示,结肠癌组织中lncRNA HOXA-AS3与miR-29b表达呈负相关(r=-0.741,P<0.05)。结肠癌组织中lncRNA HOXA-AS3、miR-29b表达与肿瘤侵犯浆膜、TNM分期和淋巴结转移有关(P均<0.05),与性别、年龄、肿瘤最大径、分化程度无关(P均>0.05)。105例结肠癌患者3年总生存率为80.95%(85/105),lncRNA HOXA-AS3高表达组总生存率低于其低表达组(P均<0.05),miR-29b高表达组总生存率高于其低表达组(P均<0.05)。结论结肠癌组织中lncRNA HOXA-AS3高表达,miR-29b低表达;二者可能共同参与结肠癌发生、发展,且与预后有关。 展开更多
关键词 结肠癌 长链非编码RNA同源框A反义RNA3 微小RNA-29b 病理参数 预后
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Characterization of a S-locus-related Receptor-like Kinase Cluster in Rice Chromosome 4 被引量:1
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作者 雷海燕 周波 +1 位作者 洪国藩 韩斌 《Acta Botanica Sinica》 CSCD 2002年第11期1346-1350,共5页
We have identified 14 S _locus glycoprotein (SLG)_related protein kinase genes in a 323 kb contig of rice (Oryza sativa L.) chromosome 4 and we detected the transcription pattern of this gene cluster by reverse tra... We have identified 14 S _locus glycoprotein (SLG)_related protein kinase genes in a 323 kb contig of rice (Oryza sativa L.) chromosome 4 and we detected the transcription pattern of this gene cluster by reverse transcription_polymerase reaction (RT_PCR). RT_PCR results revealed that nine putative genes were transcribed in rice and these genes had the different expression patterns: two genes are expressed predominantly in reproductive tissues while the other seven genes are expressed in both reproductive and vegetative tissues. Analysis of the predicted amino acid sequences demonstrated that the extracellular receptor domains are highly homologous to SLG of Brassica, whereas the cytoplasmic kinase domains contain conserved amino acids present in serine/threonine kinases. 展开更多
关键词 Oryza sativa receptor_like protein kinase S _locus receptor kinase S _locus glycoprotein rice ( Oryza sativa )
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Characterization and Expression Profiling of Genes Encoding the Gibberellin 3-oxidase in Dasypyrum villosum Dwarf Mutant
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作者 Peng CAI Zaijun YANG +1 位作者 Zhengsong PENG Maoqun YU 《Agricultural Science & Technology》 CAS 2017年第9期1585-1589,共5页
Gibberellin 3-oxidase catalyzes the conversion of inactive gibberellin(GA) species into GAs with biological activity and it is subjected to strict developmental controls in the life cycle of a plant. In this study, 33... Gibberellin 3-oxidase catalyzes the conversion of inactive gibberellin(GA) species into GAs with biological activity and it is subjected to strict developmental controls in the life cycle of a plant. In this study, 33 gene sequences, encoding the gibberellin 3-oxidase(GA3ox) from Dasypyrum villosum and its dwarf mutant, were obtained. Each contained a 1 107 bp coding sequence(CDS) that encoded a putative protein containing 369 amino acids. The GA3ox protein showed 77% to 97% homology and shared the major conserved structural domains of GA3ox proteins with rice, sorghum bicolor, oat, barley, and wheat. Sequence alignment showed that there were 20 single nucleotide polymorphisms(SNPs) and 22 Insertion/deletions(In Dels) among these sequences, which could be divided into 2 haplotypes, haplotypes Ⅰ and Ⅱ. Haplotype Ⅰ was found in the wild type and was1 495 bp in length, and haplotype Ⅱ was found in the dwarf mutant and was 1 485 bp in length. The Q-PCR results showed that GA3ox was expressed in the leaves, roots, internodes, and stem nodes, and that there was a significant difference in the transcript level of the GA3ox between the wild type and dwarf mutant. The transcript levels of GA3ox in the leaves at the seedling stage, stem elongation stage and the heading stage, in the root and stem nodes at the stem elongation stage and in the internodes at the heading stage of the wild type, were significantly higher than those in the dwarf mutant. However, GA3ox expression in the rest of the wild type tissues at the 3 stages was slightly higher than or not different from the dwarf mutant.The results suggested that the wild type and mutant allele sequences of GA3ox in D. villosum showed 2 amino acid changes in exons and variations in the lengths of introns or the SNPs in introns, which most probably impaired the function of the enzyme,affected the GA3ox expression level, and eventually gave rise to dwarfing. 展开更多
关键词 Dasypyrum villosum Gibberellin 3-oxidase Dwarf mutant WHEAT SNP
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METTL3介导的LncRNA MIR99AHG通过抑制miR-136-5p表达诱导卵巢颗粒细胞凋亡的机制研究
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作者 常建芳 孙延庆 《中国计划生育和妇产科》 2024年第6期58-64,共7页
目的 研究LncRNA MIR99AHG(MIR99AHG)在化疗药物导致的卵巢颗粒细胞凋亡中的作用及其潜在的调节机制。方法 采集正常女性和卵巢早衰(premature ovarian failure, POF)患者的卵泡液,检测MIR99AHG表达。将卵巢颗粒细胞KGN分为对照组、顺... 目的 研究LncRNA MIR99AHG(MIR99AHG)在化疗药物导致的卵巢颗粒细胞凋亡中的作用及其潜在的调节机制。方法 采集正常女性和卵巢早衰(premature ovarian failure, POF)患者的卵泡液,检测MIR99AHG表达。将卵巢颗粒细胞KGN分为对照组、顺铂组、顺铂+NC shRNA组、顺铂+sh-MIR99AHG组、顺铂+vector组、顺铂+OE-METTL3组、顺铂+OE-METTL3+OE-MIR99AHG组、顺铂+OE-MIR99AHG组、顺铂+NC mimic组、顺铂+miR-136-5p mimic组及顺铂+sh-MIR99AHG+NC inhibitor组和顺铂+sh-MIR99AHG+miR-136-5p inhibitor组。KGN细胞经相应载体或质粒处理后,采用RIP分析MIR99AHG的m6A修饰水平;在线数据库预测MIR99AHG与miR-136-5p的结合位点,并通过荧光素酶报告基因分析进行验证;采用CCK-8和流式细胞术分析KGN细胞的活力和凋亡水平;ELISA检测Caspase-3酶活性;Western blot检测凋亡相关蛋白BCL-2和Bax表达水平。结果 与正常女性相比,POF患者卵泡液中MIR99AHG表达水平显著上调(P<0.001)。与对照组相比,顺铂处理组KGN细胞中MIR99AHG表达显著上调,METTL3表达及蛋白水平显著下调(P<0.05)。与对照组相比,顺铂处理组KGN细胞活力显著降低,细胞凋亡率显著升高(P<0.05);而与NC shRNA组相比,sh-MIR99AHG组KGN细胞活力显著升高,细胞凋亡率显著降低(P<0.05)。RIP分析发现,Anti-m6A抗体下拉复合物中MIR99AHG显著富集。与vector组相比,OE-METTL3组MIR99AHG的m6A水平显著升高,MIR99AHG mRNA表达水平显著降低(P<0.05);OE-METTL3组KGN细胞活力显著升高,细胞凋亡率显著降低(P<0.05);共转染OE-MIR99AHG可逆转OE-METTL3对KGN细胞活力、凋亡及相关蛋白表达的影响。miR-136-5p与MIR99AHGA存在结合位点,MIR99AHGA负调控miR-136-5p表达。与NC-mimic组相比,miR-136-5p mimic组细胞活力及BCL-2蛋白表达明显升高,细胞凋亡率、Caspase-3酶活性及Bax蛋白表达明显降低(P<0.05)。共转染miR-136-5p inhibitor逆转了sh-MIR99AHG对细胞KGN细胞活力、凋亡及相关蛋白表达的影响(P<0.05)。结论 顺铂诱导MIR99AHG在卵巢颗粒细胞中上调,METTL3通过m6A甲基化修饰抑制MIR99AHG表达,促进MIR99AHG靶标miR-136-5p的上调,从而抑制卵巢颗粒细胞凋亡,改善化疗药物顺铂介导的卵巢早衰。 展开更多
关键词 卵巢颗粒细胞 长链非编码mir-99a-let-7c宿主基因 N6-甲基腺苷修饰 N6腺苷甲基转移酶样3 微小核糖核酸-136-5p
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Scheme for Implementing Controlled Dense Coding with Six-Atom Cluster State in Cavity QED
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作者 李渊华 李翠翠 +2 位作者 王贤平 桑明煌 聂义友 《Communications in Theoretical Physics》 SCIE CAS CSCD 2013年第5期559-562,共4页
We propose an experimentally feasible protocol for implementing controlled dense coding with a six-atom duster state in cavity QED. In the scheme, we investigate that the atoms interact simultaneously with the highly ... We propose an experimentally feasible protocol for implementing controlled dense coding with a six-atom duster state in cavity QED. In the scheme, we investigate that the atoms interact simultaneously with the highly detuned single-mode cavity and the strong classical driving field, and thus our scheme is not sensitive to both the cavity decay and the thermal field, in addition, the four-atom entangled states can be exactly distinguished by performing the single-atom measurements in cavity QED, therefore our scheme might be implemented in a simple way. 展开更多
关键词 quantum information controlled dense coding six-atom cluster state cavity QED
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