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41.
根据目前地基平板载荷试验中存在的一些问题.提出一些建议供工程检测人员及规范制定单位参考. 相似文献
42.
This paper presents closed-form solution for buckling analysis of orthotropic plates using two variable refined plate theory. The theory accounts for a quadratic variation of the transverse shear strains across the thickness, and satisfies the zero traction boundary conditions on the top and bottom surfaces of the plate without using shear correction factors. Governing equations are derived from the principle of minimum total potential energy. The closed-form solutions of rectangular plates with two opposite edges simply supported and the other two edges having arbitrary boundary conditions are obtained by applying the state space approach to the Levy-type solution. Comparison studies are performed to verify the validity of the present results. The effects of boundary condition, loading condition, and variations of modulus ratio, aspect ratio, and thickness ratio on the critical buckling load of orthotropic plates are investigated and discussed in detail. 相似文献
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对传统的3B编程方法进行了新的探索和实践,在传统的3B手工编程的基础上总结出了易掌握、不易出错、高效的编程技巧即“终-终-终”;“起-终-起”的方法。通过比较教学证实,它是一种高效实用的新方法。 相似文献
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Aashish Soni Xiaolu Duan Martin Stuschke George Iliakis 《International journal of molecular sciences》2022,23(14)
The intra-S-phase checkpoint was among the first reported cell cycle checkpoints in mammalian cells. It transiently slows down the rate of DNA replication after DNA damage to facilitate repair and thus prevents genomic instability. The ionizing radiation (IR)-induced intra-S-phase checkpoint in mammalian cells is thought to be mainly dependent upon the kinase activity of ATM. Defects in the intra-S-phase checkpoint result in radio-resistant DNA synthesis (RDS), which promotes genomic instability. ATM belongs to the PI3K kinase family along with ATR and DNA-PKcs. ATR has been shown to be the key kinase for intra-S-phase checkpoint signaling in yeast and has also been implicated in this checkpoint in higher eukaryotes. Recently, contributions of DNA-PKcs to IR-induced G2-checkpoint could also be established. Whether and how ATR and DNA-PKcs are involved in the IR-induced intra-S-phase checkpoint in mammalian cells is incompletely characterized. Here, we investigated the contributions of ATM, ATR, and DNA-PKcs to intra-S-phase checkpoint activation after exposure to IR of human and hamster cells. The results suggest that the activities of both ATM and ATR are essential for efficient intra-S-phase checkpoint activation. Indeed, in a wild-type genetic background, ATR inhibition generates stronger checkpoint defects than ATM inhibition. Similar to G2 checkpoint, DNA-PKcs contributes to the recovery from the intra-S-phase checkpoint. DNA-PKcs–deficient cells show persistent, mainly ATR-dependent intra-S-phase checkpoints. A correlation between the degree of DSB end resection and the strength of the intra-S-phase checkpoint is observed, which again compares well to the G2 checkpoint response. We conclude that the organization of the intra-S-phase checkpoint has a similar mechanistic organization to that of the G2 checkpoint in cells irradiated in the G2 phase. 相似文献
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研究锥盘淬火变形的原因,改进设计限形淬火压具,使薄壁件锥盘的淬火变形报废率由25%下降到5%以下,经济效益和社会效益十分显著。 相似文献
49.
Yongjie Liu Dan Li Shengquan Zhang Liping Zhang Jie Gong Yanhong Li Jiamin Chen Fengting Zhang Xiangzheng Liao Zhaobo Chen Yongbo Wang Binshuang Pang Jinxiu Ma Xianchao Chen Jiangang Gao Changping Zhao Shiqing Gao 《International journal of molecular sciences》2022,23(15)
Temperature-sensitive genic male sterile (TGMS) line Beijing Sterility 366 (BS366) has been utilized in hybrid breeding for a long time, but the molecular mechanism underlying male sterility remains unclear. Expression arrays, small RNA, and degradome sequencing were used in this study to explore the potential role of miRNA in the cold-induced male sterility of BS366. Microspore observation showed defective cell plates in dyads and tetrads and shrunken microspores at the vacuolated stage. Differential regulation of Golgi vesicle transport, phragmoplast formation, sporopollenin biosynthesis, pollen exine formation, and lipid metabolism were observed between cold and control conditions. Pollen development was significantly represented in the 352 antagonistic miRNA-target pairs in the integrated analysis of miRNA and mRNA profiles. The specific cleavage of ARF17 and TIR1 by miR160 and miR393 were found in the cold-treated BS366 degradome, respectively. Thus, the cold-mediated miRNAs impaired cell plate formation through repression of Golgi vesicle transport and phragmoplast formation. The repressed expression of ARF17 and TIR1 impaired pollen exine formation. The results of this study will contribute to our understanding of the roles of miRNAs in male sterility in wheat. 相似文献
50.