Abstract: The invention provides resonant vibratory sensors to render such resonant vibratory sensors more beneficial than conventional MEMS-based and non-MEMS-based resonant vibratory sensors for various usage applications, such as portable applications requiring navigation-grade performance. The resonant vibratory sensors include as examples an oscillator, a vibratory gyroscope and a vibratory accelerometer. In one embodiment, the resonant vibratory sensor is a disk resonator gyroscope. The improved resonant vibratory sensors employ materials having an ultra low thermal expansion coefficient, which provides an improved thermoelastic quality factor.

Abstract: A device for measuring a flow of a fluid is provided. The device includes a base, a channel, and at least two electronic circuits. The channel is mounted on the base, flowing the fluid therein and having at least two sections, and the at least two electronic circuits are electrically connected to the respective at least two sections, detecting a respective variation signal corresponding to the respective at least two sections so as to obtain the flow according to the respective variation signal.

Abstract: Disclosed are an optical fuse and a device for fabricating such an optical fuse. The optical fuse comprises a medium constituting a structure in which a light-emitting end of a first optical waveguide is coupled to a light-incident end of a second optical waveguide across the medium, and a light-absorbing body adapted to absorb the light. The medium is transparent to light passing through the structure, and the light-absorbing body is disposed in contact with an outer peripheral surface of the medium in such a manner as to allow a part of light emitted from the light-emitting end into the medium to reach the light-absorbing body. The optical-fuse fabricating device comprises a pair of first and second support members formed, respectively, with first and second through-holes for supporting an optical fiber, and a beam member mechanically connecting the first and second support member together.

Abstract: An interferometric method including: generating a variable frequency source beam; from the source beam, generating a collimated beam propagating at an angle ? relative to an optical axis; introducing the collimated beam into an interferometer that includes a reference object and a measurement object, wherein at least a portion of the collimated beam interacts with the reference object to generate a reference beam, at least a portion of the collimated beam interacts with the measurement object to generate a return measurement beam, and the reference beam and the return measurement beam are combined to generate a combined beam; causing the angle ? to have a first value and at a later time a second value that is different from the first value; and causing the variable frequency F to have a first value that corresponds to the first value of the angle ? and at the later time to have a second value that corresponds to the first value of the angle ?.

Abstract: A field emission display (FED) device, which includes a top substrate, a bottom substrate, and an intermediate plate set located between the top substrate and the bottom substrate. The top substrate has a phosphor layer and an anode. The bottom substrate has a cathode, and an electron emitter. The intermediate plate set has a metal plate with multiple holes, an insulating layer with multiple holes, and a gate layer. In the FED device, the insulating layer is located between the gate layer and the metal plate for electrical insulation, and the gate layer has a gap from the bottom substrate. Thus, the processing steps prepared for the bottom substrate can be reduced to thereby prevent the electron emitters from damage. The number of electrons bombarding on the phosphor layer is effectively increased to thereby increase the brightness and color contrast on pixels.

Abstract: An isoflavone derivative of tectorigenin compound as shown in formula (II), its preparation method and the antiviral medicine containing it as an effective constituent. The compound structure is shown as follows: Where:: R1 is H, NH2 or SO3M; R2 is OR?; R3 is H or —CH2NR?; where R? is H, —CH2COONa or —CH2CH2NMe2; NR? is or —NMe2; M is H, Na, K or N+H (CH2CH2OH)3.

Abstract: The invention provides a T2D mouse comprising a progeny from mating a C57BL/6 mouse and a DBA/2 mouse and exhibiting a blood glucose level of at least about 200 mg/dl, wherein the mouse is a non-human mammalian model predictive of human type 2 diabetes. The T2D mouse also can exhibit impairment of glucose tolerance, normal or increased insulin production, impaired adipocyte or muscle glucose transport or decreased expression of at least one polypeptide involved in insulin action. Further provided is a method of producing a non-human mammal predictive of type 2 diabetes. The method includes mating a C57BL/6 mouse with a DBA/2 mouse, and backing crossing offspring of the mating with a parental DBA/2 mouse to produce a progeny exhibiting a blood glucose level of at least about 200 mg/dl that is predictive of human type 2 diabetes. A method of screening for a therapeutic agent for use in treating type 2 diabetes also is provided.

Abstract: It is an object of the present invention to provide an optical recording disc which can record data constituted by a recording mark train including recording marks and blank regions neighboring recording marks therein and reproduce the data therefrom in a desired manner even in the case where the lengths of a recording mark and a blank region between neighboring recording marks are shorter than the resolution limit and whose storage capacity can be markedly increased and a method for manufacturing such an optical recording disc.

Abstract: The invention provides a method of forming, on a substrate, a thin film of a perovskite type oxide in which at least either of a site A and a site B is constituted of plural elements and the plural elements in at least either site include elements different in valence number within such site, the method including steps of dividing the elements belonging to the site A and the site B in plural groups in such a manner that the elements different in valence number belong to a same group, and supplying the substrate with raw materials containing the elements belonging to such respective groups in respectively different steps.

Abstract: A LCD device and a manufacturing method thereof are disclosed. The LCD is characteristic of the electrode layer having no alignment layer disposed thereon. On this structure, the electrode layer of the positive and negative electrodes are adjacent to the liquid crystal molecules in the liquid crystal layer, and the electric field produced therebetween and also the structure for isolating the alignment layer in this region can avoid the disclination of the liquid crystal molecules caused by the transverse electric field produced between the electrodes so as to improve the optical efficiency of the LCD device. The manufacturing steps thereof includes providing a first substrate and a second substrate, forming a second alignment layer and a patterned second electrode layer on the second substrate simultaneously or sequentially, injecting liquid crystal to form a liquid crystal layer, and fabricating to form a liquid crystal display cell.

Abstract: In a communication system, subchannel state information for a plurality of user equipments (UEs) are collected, and a plurality of subchannel state prediction parameter values for the respective UEs are calculated using the subchannel state information. In addition, the communication system allocates at least one subchannel among the plurality of subchannels to a first UE having the highest priority. Subsequently, the communication system determines whether to allocate additional power to the at least one subchannel based on the plurality of subchannel state prediction parameter values, and allocates additional power to a subchannel that needs the additional power among the at least one subchannel.

Abstract: The invention relates to an improved method for agrobacterium transformation and regeneration of plants. The inventive method is characterized in that it consists in sequentially preparing, inoculating and co-cultivating explants. The preparation of each subsequent lot of plants is carried out after a time interval for transforming plant cells and forming an induced resistance with respect to abiotic and biotic stresses in a leaf discs, thereby making it possible to reduce a necrosis degree and the number of somaclonal variations of the transgenic plants.

Abstract: The present invention is a hair graft derived from a plucked hair comprising a plucked hair having adhered epidermal stem cells and associated follicular dermal cells. The present invention also includes methods of making a hair graft, methods of implanting a hair graft and methods of identifying inductive follicular dermal cells.

Abstract: The present invention relates, e.g., to a minimal set of protein-coding genes which provides the information required for replication of a free-living organism in a rich bacterial culture medium, wherein (1) the gene set does not comprise the 101 genes listed in Table 2; and/or wherein (2) the gene set comprises the 381 protein-coding genes listed in Table 3 and, optionally, one of more of: a set of three genes encoding ABC transporters for phosphate import (genes MG410, MG411 and MG412; or genes MG289, MG290 and MG291); the lipoprotein-encoding gene MG185 or MG260; and/or the glycerophosphoryl diester phosphodiesterase gene MG293 or MG385.

Abstract: A composite structure body obtained through a plurality of processes including forming composite fine particles by way of a process in which a surface of the fine particles of a brittle material is coated with another brittle material; then by bombarding the composite fine particles against a surface of a substrate at high velocities, an anchor portion biting the substrate surface is formed; the composite fine particles are simultaneously distorted and fractured by impact of the bombardment; mutual rejoining of the composite fine particles is made through intermediary of a newly generated active surface formed by the distortion or fracture; and thereby forming a structure body in which crystals and/or microstructures of the brittle materials are dispersed above the anchor portion; and a pre-processing which includes imparting internal distortion to the brittle material fine particles.

Abstract: The object of the present invention is to provide a sample assay structure in a microfluidic chip for quantitative analysis which comprises a sample inlet port for inputting a testing sample; an analyte detection region, coupled to the sample inlet port, consisting of at least one microfluidic channel, in which a plurality of immobilized substances capable of reacting with the analyte are placed; and a fluid driving device, capable of controlling the speed of the flow of the test sample through the analyte detection region, allowing the quantity of the analyte be indicated by the length of the portion of the microfluidic channel where the analyte reacted with the immobilized substances.

Abstract: A flip-chip light emitting device and a method of manufacturing thereof are provided. The flip-chip nitride light emitting device includes a substrate, an n type clad layer, an active layer, a p type clad layer, a multi ohmic contact layer, and a reflective layer, which are stacked in this order, wherein the multi ohmic contact layer is obtained by repeatedly stacking at least one stack unit of a reforming metal layer and a transparent conductive thin film, and wherein the reforming metal layer mainly contains silver (Ag). According to the flip-chip light emitting device and the method of manufacturing thereof, since the ohmic contact characteristics associated with a p type clad layer can be improved, it is possible to increase wire bonding efficiency and yield in a packaging process. In addition, since a low non-contact resistance and a good current-voltage characteristic can be obtained, it is possible to improve light emitting efficiency and to expand life time of the flip-chip light emitting device.

Abstract: A micro device for cell culture is disclosed, which cooperates with a fluid and includes: a top plate having an inlet port; a orifice plate having a plurality of orifices; a culture plate having a plurality of culture wells and a plurality of injection ports; and a bottom plate having at least one collecting well and at least one collecting flow channel, wherein, the culture plate is placed between the orifice plate and the bottom plate. The collecting flow channel connects to all regulating orifices in the culture wells and guides the fluid from the culture wells, then receives the fluid in the collecting well. The fluid flows into the orifice plate from the inlet port of the top plate, and then diversifies into the culture plate, then arrives at each culture well by way of the injection ports, and finally collects in the collecting well of the bottom plate.

Abstract: In a method comprising comparing a solid phase carrier extract 1 obtained by pre-treating a sample with a ligand-immobilized solid phase carrier and a solid phase carrier extract 2 obtained by treating the pretreated sample again with a ligand-immobilized solid phase carrier in terms of the proteins contained therein, and identifying a protein whose content is remarkably decreased in the extract 2 compared to the extract 1, 1) the problem of the solubility of subject ligand, 2) the problem of the non-specific protein-denaturing effect of the subject ligand added, and the like, which have been problematic in antagonism experiments in target search using an affinity resin, have been solved.

Abstract: The present invention discloses methods of labeling Fc portions of antibodies, or fusion proteins incorporating Fc portions of antibodies, so that they can be used in immunostaining or immunolabeling procedures. A wide variety of labels can be used. A linker can be used between the label and the protein to be labeled, allowing for flexibility in labeling. A large variety of coupling reactions can be used to generate the labeled protein molecule, The protein molecule to be labeled can be part of a larger fusion protein. The labeled protein molecules can be used in immunostaining and immunolabeling procedures but also in in vivo applications for therapy and diagnostic imaging.