800MPa级别以上含钛低碳贝氏体钢的开发

800MPa级别含钛低碳贝氏体钢因为其经济性的成分设计,在加热制度、轧后冷却工艺上与一般低碳贝氏体钢有一定差别。介绍了该钢种的开发过程与工艺要点。     

对主成分分析在搅拌桩质量检测的评判研究

简述了桩身质量检测的常用方法及评判标准,采用主成分分析原理与关联度分析原理,结合搅拌桩检测资料,对影响桩身质量的因素进行了分析研究,得出了一些有价值的结论,对搅拌桩检测方法及评判标准的改进与完善具有参考意义.     

基于划分DBSCAN算法的小区载频配置优化

为了充分利用无线网络资源,提升无线网络质量,充分利用了DBSCAN（Density Based Spatial Clustering of Applications with Noise）算法的优点,提出基于划分DBSCAN算法的话务量异常小区的检测方法,并通过对现网大量话务数据的统计分析,找出小区载频配置数和最佳话务量之间的关系。对话务量异常、拥塞率高的小区进行载频配置优化,并对城市小区网络优化有一定的指导意义。     

A Single Injection of NTG-101 Reduces the Expression of Pain-Related Neurotrophins in a Canine Model of Degenerative Disc Disease

Background: Tissue sources of pain emanating from degenerative discs remains incompletely understood. Canine intervertebral discs (IVDs) were needle puncture injured, 4-weeks later injected with either phosphate-buffered saline (PBS) or NTG-101, harvested after an additional fourteen weeks and then histologically evaluated for the expression of NGFr, BDNF, TrkB and CALCRL proteins. Quantification was performed using the HALO automated cell-counting scoring platform. Immunohistochemical analysis was also performed on human IVD tissue samples obtained from spinal surgery. Immunohistochemical analysis and quantification of neurotrophins and neuropeptides was performed using an in vivo canine model of degenerative disc disease and human degenerative disc tissue sections. Discs injected with NTG-101 showed significantly lower levels of Nerve Growth Factor receptor (NGFr/TrkA, p = 0.0001), BDNF (p = 0.009), TrkB (p = 0.002) and CALCRL (p = 0.008) relative to PBS injections. Human IVD tissue obtained from spinal surgery due to painful DDD show robust expression of NGFr, BDNF, TrkB and CALCRL proteins. A single intradiscal injection of NTG-101 significantly inhibits the expression of NGFr, BDNF, TrkB and CALCRL proteins in degenerative canine IVDs. These results strongly suggest that NTG-101 inhibits the development of neurotrophins that are strongly associated with painful degenerative disc disease and may have profound effects upon the management of patients living with discogenic pain.     

硫酸钾尾液冷冻回收高硫钾比矿物工艺研究

以硫酸钾尾液为原料,研究低温冷冻回收高硫钾比矿物合理的工艺技术路线,探寻适宜的贮存条件,为加工车间夏季高温生产硫酸钾提供优质高硫钾比原料.在低温下进行冷冻试验,根据冷冻结晶矿物产率及其干基组分确定适宜的冷冻温度为-15～5℃,冷冻制得的结晶矿物硫钾比均在3.0～5.1,符合夏季生产硫酸钾所需原料硫钾比>2.5的要求.高...     

应用水化硅酸盐纳米粉体制备块体材料

以磨细生石灰和硅质原料的混合物为前驱物,采用动态水热合成方法制备了水化硅酸盐纳米粉体.借助SEM、TEM及氮吸附等测试方法,分析了制得的水化硅酸盐粉体的形貌、粒径和比表面积.将制得的水化硅酸盐纳米粉体压制成块状固体.采用正交设计方法研究了成型压力、水泥掺量、纤维掺量、聚合物掺量等因素对块体材料力学性能的影响.结果表明:由该粉体压制成的块体材料立即具有强度和耐水性,且表观密度低;成型压力是影响其力学性能最显著的因素.     

MicroRNA Expression in Clear Cell Renal Cell Carcinoma Cell Lines and Tumor Biopsies: Potential Therapeutic Targets

This study was carried out to quantitate the expression levels of microRNA-17, -19a, -34a, -155, and -210 (miRs) expressed in nine clear cell renal cell carcinoma (ccRCC) and one chromophobe renal cell carcinoma cell line with and without sarcomatoid differentiation, and in six primary kidney tumors with matching normal kidney tissues. The data in the five non-sarcomatoid ccRCC cell lines—RC2, CAKI-1, 786-0, RCC4, and RCC4/VHL—and in the four ccRCC with sarcomatoid differentiation—RCJ41T1, RCJ41T2, RCJ41M, and UOK-127—indicated that miR-17 and -19a were expressed at lower levels relative to miR-34a, -155, and -210. Compared with RPTEC normal epithelial cells, miR-34a, miR-155, and miR-210 were expressed at higher levels, independent of the sarcomatoid differentiation status and hypoxia-inducible factors 1α and 2α (HIFs) isoform expression. In the one chromophobe renal cell carcinoma cell line, namely, UOK-276 with sarcomatoid differentiation, and expressing tumor suppressor gene TP53, miR-34a, which is a tumor suppressor gene, was expressed at higher levels than miR-210, -155, -17, and -19a. The pilot results generated in six tumor biopsies with matching normal kidney tissues indicated that while the expression of miR-17 and -19a were similar to the normal tissue expression profile, miR-210, -155, -and 34a were expressed at a higher level. To confirm that differences in the expression levels of the five miRs in the six tumor biopsies were statistically significant, the acquisition of a larger sample size is required. Data previously generated in ccRCC cell lines demonstrating that miR-210, miR-155, and HIFs are druggable targets using a defined dose and schedule of selenium-containing molecules support the concept that simultaneous and concurrent downregulation of miR-210, miR-155, and HIFs, which regulate target genes associated with increased tumor angiogenesis and drug resistance, may offer the potential for the development of a novel mechanism-based strategy for the treatment of patients with advanced ccRCC.     

Norovirus Intestinal Infection and Lewy Body Disease in an Older Patient with Acute Cognitive Impairment

We present a case report on an older woman with unspecific symptoms and predominant long-term gastrointestinal disturbances, acute overall health deterioration with loss of autonomy for daily activities, and cognitive impairment. Autopsy revealed the presence of alpha-synuclein deposits spread into intestinal mucosa lesions, enteric plexuses, pelvic and retroperitoneal nerves and ganglia, and other organs as well as Lewy pathology in the central nervous system (CNS). Moreover, we isolated norovirus from the patient, indicating active infection in the colon and detected colocalization of norovirus and alpha-synuclein in different regions of the patient’s brain. In view of this, we report a concomitant norovirus infection with synthesis of alpha-synuclein in the gastrointestinal mucosa and Lewy pathology in the CNS, which might support Braak’s hypothesis about the pathogenic mechanisms underlying synucleinopathies.     

型煤气化试烧小结

介绍焦炭炉改型煤和富氧气化的工艺试验。总结试验中存在的问题,提出相应的改进措施。改烧型煤后可缓解焦炭原料来源紧张、价格高的问题。     

Pathogenic Impact of α-Synuclein Phosphorylation and Its Kinases in α-Synucleinopathies

α-Synuclein is a protein with a molecular weight of 14.5 kDa and consists of 140 amino acids encoded by the SNCA gene. Missense mutations and gene duplications in the SNCA gene cause hereditary Parkinson’s disease. Highly phosphorylated and abnormally aggregated α-synuclein is a major component of Lewy bodies found in neuronal cells of patients with sporadic Parkinson’s disease, dementia with Lewy bodies, and glial cytoplasmic inclusion bodies in oligodendrocytes with multiple system atrophy. Aggregated α-synuclein is cytotoxic and plays a central role in the pathogenesis of the above-mentioned synucleinopathies. In a healthy brain, most α-synuclein is unphosphorylated; however, more than 90% of abnormally aggregated α-synuclein in Lewy bodies of patients with Parkinson’s disease is phosphorylated at Ser129, which is presumed to be of pathological significance. Several kinases catalyze Ser129 phosphorylation, but the role of phosphorylation enzymes in disease pathogenesis and their relationship to cellular toxicity from phosphorylation are not fully understood in α-synucleinopathy. Consequently, this review focuses on the pathogenic impact of α-synuclein phosphorylation and its kinases during the neurodegeneration process in α-synucleinopathy.