旅华日本、韩国游客旅游特征及偏好研究

以2004年在北京、上海、广州、桂林、昆明和西安6个热点旅游城市进行的随机抽样调查数据为依据,运用旅游地理学基本原理、心理学分析和比较分析等研究方法,从人口统计、旅游活动及偏好等方面对旅华日本和韩国游客进行了定性和定量的分析,总结出游客基本特征:游客以观光为主要目的,团队多于散客,大部分游客都有1～3次的来华经历;停留时间多为4～7 d;主要目的地是北京、上海和西安;偏好民俗文化类活动和中国传统工艺品.同时通过对比揭示两国游客的共性和差异,并提出一些建议,希望对进一步拓展日韩客源市场提供帮助.     

强化传热生物质燃料热风炉研究

研制出用于粮食及其它农副产品干燥的新型热风炉。此炉型采用生物质燃料洁净燃烧技术及高强化传热技术,具有低污染、高效率、长寿命等优点。     

Long term monitoring of urban subsidence by Permanent Scatterer DInSAR

When using differential SAR interferometry (DInSAR) to monitor the surface deformation over a long time scale, it is often strongly affected by the spatial and temporal decorrelations and atmospheric dishomogeneities. The recently developed Permanent Scatterers (PS) technique proposed by Fertti et al. can overcome these difficulties by interpreting time-series of interferometric phase only at coherent point scatterers. In this study, we apply this PS technique using 25 ERS-1/2 scenes from 1992 to 2000 to monitor the subsidence in Suzhou. By using the linear deformation model, the deformation map in Suzhou urban area over the eight years is obtained. And the calculated results are in good agreement with the measurements of leveling.     

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11

The microtubule-associated protein tau (encoded by MAPT) and several tau kinases have been implicated in neurodegeneration, but only MAPT has a proven role in disease. We identified mutations in the gene encoding tau tubulin kinase 2 (TTBK2) as the cause of spinocerebellar ataxia type 11. Affected brain tissue showed substantial cerebellar degeneration and tau deposition. These data suggest that TTBK2 is important in the tau cascade and in spinocerebellar degeneration.     

光谱辐射标准和计量实验站的建设和研究

介绍了光谱辐射标准和计量光束线（U27）的光学设计、结构和实验站设备，利用透射光栅和AXUV100G探测器系统研究了掠入射分支（SGM）5～140nm的高次谐波情况；给出了研究结果和不同滤片材料对高次谐波的抑制情况，Zr，Si3N4和Al滤片可以有效的抑制5～34nm的高次谐波，MgF2能有效的抑制115～140nm的高次谐波．     

Tissue-specific and reversible RNA interference in transgenic mice

Genetically engineered mice provide powerful tools for understanding mammalian gene function. These models traditionally rely on gene overexpression from transgenes or targeted, irreversible gene mutation. By adapting the tetracycline (tet)-responsive system previously used for gene overexpression, we have developed a simple transgenic system to reversibly control endogenous gene expression using RNA interference (RNAi) in mice. Transgenic mice harboring a tet-responsive RNA polymerase II promoter driving a microRNA-based short hairpin RNA targeting the tumor suppressor Trp53 reversibly express short hairpin RNA when crossed with existing mouse strains expressing general or tissue-specific 'tet-on' or 'tet-off' transactivators. Reversible Trp53 knockdown can be achieved in several tissues, and restoring Trp53 expression in lymphomas whose development is promoted by Trp53 knockdown leads to tumor regression. By leaving the target gene unaltered, this approach permits tissue-specific, reversible regulation of endogenous gene expression in vivo, with potential broad application in basic biology and drug target validation.     

Recombination and linkage disequilibrium in Arabidopsis thaliana

Linkage disequilibrium (LD) is a major aspect of the organization of genetic variation in natural populations. Here we describe the genome-wide pattern of LD in a sample of 19 Arabidopsis thaliana accessions using 341,602 non-singleton SNPs. LD decays within 10 kb on average, considerably faster than previously estimated. Tag SNP selection algorithms and 'hide-the-SNP' simulations suggest that genome-wide association mapping will require only 40%-50% of the observed SNPs, a reduction similar to estimates in a sample of African Americans. An Affymetrix genotyping array containing 250,000 SNPs has been designed based on these results; we demonstrate that it should have more than adequate coverage for genome-wide association mapping. The extent of LD is highly variable, and we find clear evidence of recombination hotspots, which seem to occur preferentially in intergenic regions. LD also reflects the action of selection, and it is more extensive between nonsynonymous polymorphisms than between synonymous polymorphisms.     

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

Opitz-Kaveggia syndrome (also known as FG syndrome) is an X-linked disorder characterized by mental retardation, relative macrocephaly, hypotonia and constipation. We report here that the original family for whom the condition is named and five other families have a recurrent mutation (2881C>T, leading to R961W) in MED12 (also called TRAP230 or HOPA), a gene located at Xq13 that functions as a thyroid receptor-associated protein in the Mediator complex.