Abstract:
The present invention relates to an image processing apparatus, an image processing method, and a program with which processed images at the time of applying a plurality of different image processings on one moving image can be easily compared.Image processing units 213-1 to 213-3 execute a predetermined image processing on an input image supplied from an image distribution unit 212 at the same time and supply processed images which are the images after the processing to an image synthesis unit 214. The image synthesis unit 214 uses the input image and the three types of the processed images to generate a synthesized image to be supplied to an image presentation unit 215. Also, the image synthesis unit 214 supplies a main image which is an image functioning as a principal among a plurality of images used for the synthesized image to an image recording unit 216. The present invention can be, for example, to an image processing apparatus configured to apply a plurality of different image processings on the moving image.
Abstract:
A double-stranded nucleic acid molecule for suppressing the expression of at least one of COX7RP and Efp genes which includes (a) a sense strand which includes a nucleotide sequence corresponding to a target sequence indicated by any one of SEQ ID Nos.: 1 to 38 and (b) an antisense strand which includes a nucleotide sequence complementary to that of the sense strand specified in (a); a cancer cell proliferation inhibitor with the double-stranded nucleic acid molecule and against at least one of uterine, breast and bladder cancer cells; and a pharmaceutical agent with the cancer cell proliferation inhibitor and against at least one of uterine, breast and bladder cancers.
Abstract translation:用于抑制COX7RP和Efp基因中的至少一种表达的双链核酸分子,其包括(a)有义链,其包含对应于由SEQ ID NO:1至 38和(b)反义链,其包含与(a)中规定的有义链的核苷酸序列互补的核苷酸序列; 具有双链核酸分子和针对子宫,乳腺和膀胱癌细胞中的至少一个的癌细胞增殖抑制剂; 以及具有癌细胞增殖抑制剂和针对子宫,乳腺和膀胱癌中的至少一种的药剂。
Abstract:
An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group or a C1-6 alkoxy C1-6 alkyl group; R2 represents a hydrogen atom, a C1-6 alkyl group, an amino group or a di C1-6 alkylamino group; one of X and Y is a nitrogen atom while the other is a nitrogen atom or an oxygen atom; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom, or 1 or 2 C1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, an oxygen atom, a sulfur atom, —CH2O—, —OCH2—, —NH—, —CH2NH—, —NHCH2—, —CH2S—, or —SCH2—; R3 represents a hydrogen atom, a halogen atom, a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, a 5- or 6-member heteroaryl group, or 5- or 6-member non-aromatic heterocyclic group which may have 1 or 2 substituents; and R4 represents a hydrogen atom or a halogen atom.
Abstract:
The present invention provides compounds which are useful as safe substitutes for the organotin reagent used in coupling reaction for the oxymethylation of aromatic rings, such as alkoxymethylation or hydroxymethylation, with a palladium catalyst and which can dispense with chromatographic purification with silica gel in the production and are suitable for mass production; and compounds applicable even to the oxymethylation of aromatic ring substrates which do not permit coupling reaction by conventional technique or have low reactivity.
Abstract:
A grand piano has action units for driving hammers to rotate toward strings, and each action unit is equipped with a repetition mechanism; the repetition mechanism has an elastic guide plate instead of a repetition lever and a repetition spring; and the elastic guide plate per se is deformed after contact with a drop screw, and returns to the initial position for permitting a pianist to play a music tune through repetition of key when the pianist releases the depressed key, whereby the action unit becomes simpler in structure than the conventional action unit.
Abstract:
An adsorption heat pump is provided in which water vapor can be efficiently adsorbed and desorbed using a heat source having a lower temperature than ones heretofore in use because the pump employs an adsorbent which has a large difference in water adsorption amount in adsorption/desorption and can be regenerated (release the adsorbate) at a low temperature.The invention provides an adsorption heat pump which comprises an adsorbate, an adsorption/desorption part having an adsorbent for adsorbate adsorption/desorption, a vaporization part for adsorbate vaporization which has been connected to the adsorption/desorption part, and a condensation part for adsorbate condensation which has been connected to the adsorption/desorption part, wherein the adsorbent, when examined at 25° C., gives a water vapor adsorption isotherm which, in the relative vapor pressure range of from 0.05 to 0.30, has a relative vapor pressure region in which a change in relative vapor pressure of 0.15 results in a change in water adsorption amount of 0.18 g/g or larger.
Abstract:
Keys of an acoustic piano require balancers for cancellation of a part of self weight of the action units/hammers; however, the balancers are liable to be dropped off due to the aged deterioration of the wooden bars; in order to keep the balancers stable in the keys against the aged deterioration, the balancer is plastically deformed so as to bite into the wooden bar, the balancer, which is formed with thorns, is rotated so as to make the thorns bite into the wooden bar, the balancer is shaped into a configuration different from the holes so as to exert resilient force on the inner surface in a direction in parallel to the grain of wood, or the balancer is inserted into a constricted hole so as to strongly exert the resilient force on the inner surface, thereby being prevented from the dropping off from the keys.
Abstract:
A plurality of strings are stretched over a frame, constituting an overall framework of a body of a piano, with their respective rear-end engaging rings engaged by corresponding pins provided on the frame. There is also provided a string-bounding preventing member that, in case any one of the strings snaps or breaks, prevents the broken string from disengaging from the corresponding pin to bound violently away from the pin. The string-bounding preventing member is, for example, a strap member that is passed through the respective engaging rings to thereby connect together the strings. The string-bounding preventing member allows the broken string to be left connected with the other strings and hence stay in place on the frame without bounding.
Abstract:
A thin film transistor has a structure capable of decreasing deterioration in Vgs-Ids characteristics. The thin film transistor has a source region composed of an N-type impurity-diffused region, a drain region, and a gate electrode, and a channel region formed directly below the gate electrode. To the source region and the drain region are connected a source electrode and a drain electrode, respectively, through a plurality of contact holes. In the channel region are formed a plurality of P-type impurity-diffused regions at constant intervals.
Abstract:
The present invention relates to a compound of the formula [I]: wherein R1 is lower alkyl or hydroxy(lower)alkyl, and R2 is hydrogen or amino protecting group, or R1 and R2 are bonded together and form lower alkylene; R is -A-R6 wherein A is bond, —NHCO—(CH2CO)n—, lower alkylene, —NH—CO—CO— or the like, and R6 is wherein R7, R8, R9 and R10 are independently amino, guanidino, amidino or the like; R4 is carboxy or protected carboxy; and R5 is amino or protected amino, or a pharmaceutically acceptable salt thereof, a process for preparing a compound of the formula [I], and a pharmaceutical composition comprising a compound of the formula [I] in admixture with a pharmaceutically acceptable carrier.