猪血丙种球蛋白的制备工艺研究

报道了运用低温乙醇与明矾吸附、碳吸附相结合，制备猪血丙种球蛋白的工艺，纯度可达９５％以上，回收率达５７％，其他各项指标均达卫生部制定的《中国生物制品规程》标准。     

耐用品动态古诺模型的建立及分析

依据耐用品的市场容量随着时间发生变化的特点,对多个企业同时博弈的动态古诺模型进行修正,建立了适用于耐用品市场的动态古诺模型,并得到新的产量均衡解.通过与合作情形下的最优产量解的比较与分析,得到非合作情形下的产量均衡解和合作情形下的最优产量解都随着阶段数的增加而单调下降,并且前者依旧劣于后者等结论.     

无成本协同效应的横向兼并行为

基于寡头垄断竞争行业,研究了企业横向兼并的获利性和社会福利问题。结果表明:在企业兼并成垄断被排除的情况下,若兼并企业在其内部实施两阶段错开竞争且兼并企业与未参与兼并的企业之间进行Cournot竞争,则一次有利可图的先置兼并行为会引发系列兼并行为。当系列兼并行为发生后,兼并企业可能会陷入"囚徒困境",社会福利与初始的、完全分散的Cournot竞争市场相比可能增加。     

The Ter mutation in the dead end gene causes germ cell loss and testicular germ cell tumours

In mice, the Ter mutation causes primordial germ cell (PGC) loss in all genetic backgrounds. Ter is also a potent modifier of spontaneous testicular germ cell tumour (TGCT) susceptibility in the 129 family of inbred strains, and markedly increases TGCT incidence in 129-Ter/Ter males. In 129-Ter/Ter mice, some of the remaining PGCs transform into undifferentiated pluripotent embryonal carcinoma cells, and after birth differentiate into various cells and tissues that compose TGCTs. Here, we report the positional cloning of Ter, revealing a point mutation that introduces a termination codon in the mouse orthologue (Dnd1) of the zebrafish dead end (dnd) gene. PGC deficiency is corrected both with bacterial artificial chromosomes that contain Dnd1 and with a Dnd1-encoding transgene. Dnd1 is expressed in fetal gonads during the critical period when TGCTs originate. DND1 has an RNA recognition motif and is most similar to the apobec complementation factor, a component of the cytidine to uridine RNA-editing complex. These results suggest that Ter may adversely affect essential aspects of RNA biology during PGC development. DND1 is the first protein known to have an RNA recognition motif directly implicated as a heritable cause of spontaneous tumorigenesis. TGCT development in the 129-Ter mouse strain models paediatric TGCT in humans. This work will have important implications for our understanding of the genetic control of TGCT pathogenesis and PGC biology.     

Genome sequencing in microfabricated high-density picolitre reactors

The proliferation of large-scale DNA-sequencing projects in recent years has driven a search for alternative methods to reduce time and cost. Here we describe a scalable, highly parallel sequencing system with raw throughput significantly greater than that of state-of-the-art capillary electrophoresis instruments. The apparatus uses a novel fibre-optic slide of individual wells and is able to sequence 25 million bases, at 99% or better accuracy, in one four-hour run. To achieve an approximately 100-fold increase in throughput over current Sanger sequencing technology, we have developed an emulsion method for DNA amplification and an instrument for sequencing by synthesis using a pyrosequencing protocol optimized for solid support and picolitre-scale volumes. Here we show the utility, throughput, accuracy and robustness of this system by shotgun sequencing and de novo assembly of the Mycoplasma genitalium genome with 96% coverage at 99.96% accuracy in one run of the machine.     

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

It is well established that autism spectrum disorders (ASD) have a strong genetic component; however, for at least 70% of cases, the underlying genetic cause is unknown. Under the hypothesis that de novo mutations underlie a substantial fraction of the risk for developing ASD in families with no previous history of ASD or related phenotypes--so-called sporadic or simplex families--we sequenced all coding regions of the genome (the exome) for parent-child trios exhibiting sporadic ASD, including 189 new trios and 20 that were previously reported. Additionally, we also sequenced the exomes of 50 unaffected siblings corresponding to these new (n = 31) and previously reported trios (n = 19), for a total of 677 individual exomes from 209 families. Here we show that de novo point mutations are overwhelmingly paternal in origin (4:1 bias) and positively correlated with paternal age, consistent with the modest increased risk for children of older fathers to develop ASD. Moreover, 39% (49 of 126) of the most severe or disruptive de novo mutations map to a highly interconnected β-catenin/chromatin remodelling protein network ranked significantly for autism candidate genes. In proband exomes, recurrent protein-altering mutations were observed in two genes: CHD8 and NTNG1. Mutation screening of six candidate genes in 1,703 ASD probands identified additional de novo, protein-altering mutations in GRIN2B, LAMC3 and SCN1A. Combined with copy number variant (CNV) data, these results indicate extreme locus heterogeneity but also provide a target for future discovery, diagnostics and therapeutics.     

基于公交视角的兰州市城市交通发展策略

从城市路网结构、机动车保有量、跨河交通以及市政工程等方面对交通发展的约束进行了讨论.在此基础上,进一步从线路长度、非直线系数、线网密度、首末站点设置等方面进行了系统分析,认为兰州市公交主要存在公交线路普遍偏长、线路非直线系数过大、线网密度差异大、首末站设置不均衡等问题.据此提出了优化路网结构、发展大容量公共交通、合理规划站点、积极开发水上交通、不断提升管理水平等措施,以期对兰州城市交通的持续健康协调发展和国内其他带状河谷城市发展交通提供决策参考.     

上海公园绿地景观水体透明度影响因子研究

于2010年,以上海市90个公园绿地共107个景观水体为研究对象,通过野外调查与室内分析,探寻水体透明度与光衰减系数的关系,并在此基础上分析影响水体透明度的主要因子.研究结果表明：（1）上海市公园绿地景观水体透明度普遍较低,平均透明度为（0.54±0.24） m,98.31%的水体透明度低于1 m;（2）透明度与光学衰减系数显著负相关,两者之间可建立数学关系式为Kd=0.017+〖SX(〗1.12〖〗ST〖SX)〗;（3）悬浮物是上海城市公园绿地水体透明度的主导影响因子,总磷和铵态氮通过控制浮游藻类的营养水平来影响水体透明度.研究结果为科学合理地评价景观水体水质尤其是水体透明度提供测度,并为水体环境的改善、水生植被的构建及水体的养护管理提供科学依据.