热处理工艺对触变成形AZ91D镁合金组织的影响

对触变成形AZ91D镁合金在不同热处理条件下的时效组织进行了研究,结果表明:随着固溶温度的增加,第二相具有较大的时效析出速度,并且析出数量较多.经415 ℃、24 h固溶处理后的试样在时效处理过程中,第二相有两种析出方式:连续与不连续析出.在180 ℃没有连续析出,温度高于200 ℃后两种方式交替进行.时效处理温度越高,第二相析出的速度越快.同时也使得连续析出在很短时间内就开始发生,并且在晶粒内部与不连续析出互相交织在一起进行.     

Bernoulli多项式与幂和多项式的关系

研究了Bernoulli多项式与幂和多项式的关系,给出了用幂和表示Bernoulli多项式的一个公式,得到了关于Bernoulli多项式的形式上非常对称的两个恒等式.     

外加轴向磁场对短路过渡的影响

为提高短路过渡频率、减少焊接飞溅,分别通过施加直流与交变轴向磁场,研究了轴向磁场对短路过渡的影响规律,分析了高速摄像、电流电压信号以及熔滴在磁场作用下的短路过渡受力情况.结果表明:当直流磁场励磁电流为4 A时,短路过渡频率达到最大值;当交流磁场励磁电流为9 A、磁场频率为100 Hz时,短路过渡频率达到最大值,这与电流...     

低雷诺数对某型涡扇发动机稳定性影响及扩稳调节规律分析研究

在高空、低速飞行时,雷诺数对发动机性能和稳定性有较大的影响.本文计算分析了飞行高度H=20 km、飞行速度Ma=0.7时,雷诺数对某型涡扇发动机性能和稳定性的影响,在此基础上,提出了为扩大发动机工作稳定性而应采取的调节规律.     

Interleukin-33 stimulates formation of functional osteoclasts from human CD14+ monocytes

Interleukin (IL)-33 is a recently described pro-inflammatory cytokine. Here we demonstrate IL-33 as a regulator of functional osteoclasts (OCs) from human CD14⁺ monocytes. IL-33 stimulates formation of tartrate-resistant acid phosphatase (TRAP)⁺ multinuclear OCs from monocytes. This action was suppressed by anti-ST2 antibody, suggesting that IL-33 acts through its receptor ST2, but not by the receptor activator of NF-κB ligand (RANKL) decoy, osteoprotegerin, or anti-RANKL antibody. IL-33 stimulated activating phosphorylations of signaling molecules in monocytes that are critical for OC development. These included Syk, phospholipase Cγ2, Gab2, MAP kinases, TAK-1, and NF-κB. IL-33 also enhanced expression of OC differentiation factors including TNF-α receptor-associated factor 6 (TRAF6), nuclear factor of activated T cells cytoplasmic 1, c-Fos, c-Src, cathepsin K, and calcitonin receptor. IL-33 eventually induced bone resorption. This study suggests that the osteoclastogenic property of IL-33 is mediated through TRAF6 as well as the immunoreceptor tyrosine-based activation motif-dependent Syk/PLCγ pathway in human CD14⁺ monocytes.     

接触网抗风可靠性研究现状及展望

介绍了接触网抗风可靠性研究的国内外现状;并分析了接触网风荷载作用下的失效形式、抗风可靠性的安全界限和破坏准则;对存在的难点及研究方向提出了几点建议。     

嫁接用苗生长状态无损测量技术的研究

利用机器视觉技术对蔬菜幼苗的生长特征信息进行了无损检测,该研究技术是定量化研究植物生长规律的关键技术之一,并为蔬菜自动化生产过程中的嫁接、移栽、间苗等作业提供必要的技术理论依据.该研究通过在温室内设计了一套计算机视觉系统,对多株群体蔬菜苗的生长进行了长时间、连续、快速的无损检测,并利用VB6.0编制了图像处理软件,提取了蔬菜幼苗的外部形态特征,经过图像处理软件分析得到蔬菜幼苗的日生长变化规律,发现蔬菜苗在夜间的生长率明显高于白天.研究表明,采用机器视觉及图像处理技术可以快速、准确地监测出蔬菜幼苗的外部形态特征量,能够对蔬菜生长状态进行直观测量,实现对蔬菜幼苗生长规的定量化研究,为蔬菜生产过程中相关作业的自动化提供可靠的理论依据.     

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

RNA exosomes are multi-subunit complexes conserved throughout evolution and are emerging as the major cellular machinery for processing, surveillance and turnover of a diverse spectrum of coding and noncoding RNA substrates essential for viability. By exome sequencing, we discovered recessive mutations in EXOSC3 (encoding exosome component 3) in four siblings with infantile spinal motor neuron disease, cerebellar atrophy, progressive microcephaly and profound global developmental delay, consistent with pontocerebellar hypoplasia type 1 (PCH1; MIM 607596). We identified mutations in EXOSC3 in an additional 8 of 12 families with PCH1. Morpholino knockdown of exosc3 in zebrafish embryos caused embryonic maldevelopment, resulting in small brain size and poor motility, reminiscent of human clinical features, and these defects were largely rescued by co-injection with wild-type but not mutant exosc3 mRNA. These findings represent the first example of an RNA exosome core component gene that is responsible for a human disease and further implicate dysregulation of RNA processing in cerebellar and spinal motor neuron maldevelopment and degeneration.     

Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder

Transitional cell carcinoma (TCC) is the most common type of bladder cancer. Here we sequenced the exomes of nine individuals with TCC and screened all the somatically mutated genes in a prevalence set of 88 additional individuals with TCC with different tumor stages and grades. In our study, we discovered a variety of genes previously unknown to be mutated in TCC. Notably, we identified genetic aberrations of the chromatin remodeling genes (UTX, MLL-MLL3, CREBBP-EP300, NCOR1, ARID1A and CHD6) in 59% of our 97 subjects with TCC. Of these genes, we showed UTX to be altered substantially more frequently in tumors of low stages and grades, highlighting its potential role in the classification and diagnosis of bladder cancer. Our results provide an overview of the genetic basis of TCC and suggest that aberration of chromatin regulation might be a hallmark of bladder cancer.