An efficient spatio-temporal data structure for multi version managemeng of engineering drawings

In the engineering database system，multiple versions of a design including engineering drawings should be managed efficiently. The paper proposes an efficient spatial data structure，that is an expansion of the R-tree and HR-tree，for version management of engineering drawings. A novel mechanism to manage the difference between drawings is introduced to the HR-tree to eliminate redundant duplications and to reduce the amount of storage required for the data structurr. Data management mechanism and structural properties of our data structure called the MVR+-tree are described.     

The effects of microinjection of carbachol or hemicholinium into the amygdala on the levels of plasma and adrenal corticosterone in rats

Summary Microinjection of 0.4 g of carbachol into the amygdala caused a rise of corticosterone (CS) in the morning, when the prestimulating level of CS was lower. But the same procedure with a larger dose had no effect in the afternoon, when the prestimulating level of CS was higher.     

Two new species of eyeless amphipods from a coastal area in Japan (Crustacea: Amphipoda: Hadziidae,Melitidae), with reinstatement of the genus Paraniphargus Tattersall, 1925

Two new species of eyeless amphipods are described from coastal Japan. Dulzura projecta sp. nov. (Hadziidae) was collected under large stones and in coarse sand from Osaka to Mie Prefectures. Dulzura projecta can be distinguished from the other Dulzura species by the distinct projection on article 1 of the male pleopod 3 inner ramus and the very long carpus of male gnathopod 1. Paraniphargus shiosai sp. nov. (Melitidae) was collected in coarse sand from Mie Prefecture, and can be differentiated from the other two species in the genus by the dorsal teeth on the pleonites, the smaller coxa 4 with shallow excavation and the shorter antenna 1 flagellum. Paraniphargus is reinstated as a distinct genus, following observation of the gnathopods, which revealed sexual monomorphism between males and females.     

Inkjet printing of single-crystal films

The use of single crystals has been fundamental to the development of semiconductor microelectronics and solid-state science. Whether based on inorganic or organic materials, the devices that show the highest performance rely on single-crystal interfaces, with their nearly perfect translational symmetry and exceptionally high chemical purity. Attention has recently been focused on developing simple ways of producing electronic devices by means of printing technologies. 'Printed electronics' is being explored for the manufacture of large-area and flexible electronic devices by the patterned application of functional inks containing soluble or dispersed semiconducting materials. However, because of the strong self-organizing tendency of the deposited materials, the production of semiconducting thin films of high crystallinity (indispensable for realizing high carrier mobility) may be incompatible with conventional printing processes. Here we develop a method that combines the technique of antisolvent crystallization with inkjet printing to produce organic semiconducting thin films of high crystallinity. Specifically, we show that mixing fine droplets of an antisolvent and a solution of an active semiconducting component within a confined area on an amorphous substrate can trigger the controlled formation of exceptionally uniform single-crystal or polycrystalline thin films that grow at the liquid-air interfaces. Using this approach, we have printed single crystals of the organic semiconductor 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C(8)-BTBT) (ref. 15), yielding thin-film transistors with average carrier mobilities as high as 16.4?cm(2)?V(-1)?s(-1). This printing technique constitutes a major step towards the use of high-performance single-crystal semiconductor devices for large-area and flexible electronics applications.     

A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition

Disruption of histone acetylation patterns is a common feature of cancer cells, but very little is known about its genetic basis. We have identified truncating mutations in one of the primary human histone deacetylases, HDAC2, in sporadic carcinomas with microsatellite instability and in tumors arising in individuals with hereditary nonpolyposis colorectal cancer syndrome. The presence of the HDAC2 frameshift mutation causes a loss of HDAC2 protein expression and enzymatic activity and renders these cells more resistant to the usual antiproliferative and proapoptotic effects of histone deacetylase inhibitors. As such drugs may serve as therapeutic agents for cancer, our findings support the use of HDAC2 mutational status in future pharmacogenetic treatment of these individuals.     

Genome assembly comparison identifies structural variants in the human genome

Numerous types of DNA variation exist, ranging from SNPs to larger structural alterations such as copy number variants (CNVs) and inversions. Alignment of DNA sequence from different sources has been used to identify SNPs and intermediate-sized variants (ISVs). However, only a small proportion of total heterogeneity is characterized, and little is known of the characteristics of most smaller-sized (<50 kb) variants. Here we show that genome assembly comparison is a robust approach for identification of all classes of genetic variation. Through comparison of two human assemblies (Celera's R27c compilation and the Build 35 reference sequence), we identified megabases of sequence (in the form of 13,534 putative non-SNP events) that were absent, inverted or polymorphic in one assembly. Database comparison and laboratory experimentation further demonstrated overlap or validation for 240 variable regions and confirmed >1.5 million SNPs. Some differences were simple insertions and deletions, but in regions containing CNVs, segmental duplication and repetitive DNA, they were more complex. Our results uncover substantial undescribed variation in humans, highlighting the need for comprehensive annotation strategies to fully interpret genome scanning and personalized sequencing projects.