600 MW“W”型火焰锅炉NOx的排放特性

以某电厂1台超临界600 MW”W”火焰锅炉NOx排放量过高为背景,对锅炉炉内燃烧过程进行数值模拟,研究不同负荷、不同煤种及不同配风方式对NOx排放量的影响.研究结果表明:不对称停运前后拱燃烧器会使NOx排放量升高,NOx排放量随燃料中N质量分数增大而增大；当前、后拱上气流或前后墙分级风量不同时,会使得NOx排放量升高.     

一个人类锌指蛋白家族新基因ZFP28的克隆及表达

Krupple型锌指蛋白是一类具有重要功能的转录调节因子，初步克隆了一个新的人类krupple型锌指蛋白基因，经国际基因命我委员会批准命名为ZFP28。此基因长4076个碱基，含8个外显子，在基因组DNA上长18kb。它编码的蛋白质全长868个氨基酸，含1个信号肽，2个KRAB框和14个C2H2型的锌指。Northem Bolt分析表明该基因在人类早期胚胎的各个组织中普遍表达，在肺和肝中的表达水平最强，其结构和表达特征预示着它编码的是一个具DNA结合功能的转录调控因子。     

一种分布式文件系统中位置独立性的解决策略

分布式系统中位置独立性是不容易实现的 ,但它却是系统所期望拥有的一个特性。讨论了分布式文件系统中目录服务的实现 ,给出了一种位置独立性的解决策略     

重介质旋流器分选机理研究

物料分选过程 ,是整个体系能量降低的过程 ,从这一原理出发 ,不同性质的固体颗粒在重介质旋流器中将位于不同的位置 ,使不同性质的固体颗粒得以分离。固体颗粒在重介质旋流器中的运动轨迹大体呈圆锥螺旋线形状 ,实测出的密度线验证了该结论     

The DNA sequence and analysis of human chromosome 13

Chromosome 13 is the largest acrocentric human chromosome. It carries genes involved in cancer including the breast cancer type 2 (BRCA2) and retinoblastoma (RB1) genes, is frequently rearranged in B-cell chronic lymphocytic leukaemia, and contains the DAOA locus associated with bipolar disorder and schizophrenia. We describe completion and analysis of 95.5 megabases (Mb) of sequence from chromosome 13, which contains 633 genes and 296 pseudogenes. We estimate that more than 95.4% of the protein-coding genes of this chromosome have been identified, on the basis of comparison with other vertebrate genome sequences. Additionally, 105 putative non-coding RNA genes were found. Chromosome 13 has one of the lowest gene densities (6.5 genes per Mb) among human chromosomes, and contains a central region of 38 Mb where the gene density drops to only 3.1 genes per Mb.     

Specific precipitins for type XIV pneumococcus polysaccharide fromAbrus precatorius seeds

Zusammenfassung Präzipitine ausAbrus precatorius-Samen scheinen folgende Spezifität zu besitzen: 1. gegen Pneumococcus-Polysaccharide des Typus XIV; 2. gegen die menschlichen blutgruppenspezifischen Substanzen A, B, H und Le^a      

克拉2气田石油地质特征

克拉2气田位于库车拗陷克拉苏构造带中段, 是双重构造中呈串珠状分布的一系列褶皱中的一个局部构造. 含气层系以下白垩统巴什基奇克组砂岩为主, 其次为下第三系库姆格列木群白云岩段和砂砾岩段及下白垩统巴西盖组砂岩. 天然气中甲烷含量大于97%, 属于干气, 气源为侏罗系煤系地层. 克拉2号构造圈闭形成于西域期, 成藏期晚. 下第三系厚层膏盐区域盖层形成的良好封盖条件及其成藏期晚是克拉2大气田得以很好保存的根本原因. 克拉2气田的异常高压是由于西域期来自北部的强烈构造挤压作用而形成的.     

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

Rett syndrome (RTT) is an inherited neurodevelopmental disorder of females that occurs once in 10,000-15,000 births. Affected females develop normally for 6-18 months, but then lose voluntary movements, including speech and hand skills. Most RTT patients are heterozygous for mutations in the X-linked gene MECP2 (refs. 3-12), encoding a protein that binds to methylated sites in genomic DNA and facilitates gene silencing. Previous work with Mecp2-null embryonic stem cells indicated that MeCP2 is essential for mouse embryogenesis. Here we generate mice lacking Mecp2 using Cre-loxP technology. Both Mecp2-null mice and mice in which Mecp2 was deleted in brain showed severe neurological symptoms at approximately six weeks of age. Compensation for absence of MeCP2 in other tissues by MeCP1 (refs. 19,20) was not apparent in genetic or biochemical tests. After several months, heterozygous female mice also showed behavioral symptoms. The overlapping delay before symptom onset in humans and mice, despite their profoundly different rates of development, raises the possibility that stability of brain function, not brain development per se, is compromised by the absence of MeCP2.