Abstract: A silver halide color photographic light-sensitive material having blue-, green-, and red-sensitive silver halide emulsion layers contains a pyrazoloazole-type compound which releases a development inhibitor in at least one layer and contains an acylacetamide-type yellow coupler having a novel acyl group in at least one layer.

Abstract: A seat apparatus used by a worker when effecting a job on an automobile is disclosed. The seat apparatus includes: a two-axis support device located above a horizontal feed path of an automobile body, for supporting a suspension carriage such that the carriage is movable in a substantially horizontal plane; a hanger arm attached to the suspension carriage; and a seat member provided on a lower end portion of the hanger arm which can enter the automobile body through its side opening, in a direction perpendicular to the feed path of the body. The seat member on which the worker sits is movable with the suspension carriage in the direction perpendicular to the feed path, and is thus selectively located in a retracted position outside the automobile body, or a working position inside the automobile body, at which the worker is able to effect the job.

Abstract: The present invention discloses a quinoline derivative and salt thereof of the following general formula: ##STR1## (wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and n have the same meanings as defined above). Such a derivative is useful as an antiulcer agent.

Abstract: The invention relates to an improved process for producing a rubber-modified styrene resin, and a rubber-modified styrene resin composition resulting therefrom, such resin having improved mechanical strength, impact resistance and high gloss, such being accomplished by producing a rubber-modified styrene resin containing substantially no rubber particle having a density of not higher than 0.96 gm/cm.sup.3 at 25.degree. C.

Abstract: A growth promoter for Bifidobacterium species comprising gourd food, from yugao gourd, as active ingredient is provided. The growth promoter has a more selective and more marked growth-promoting effect than conventional bifidus factors.

Abstract: Human blood coagulation factor XIII allows the prevention of intraventricular hemorrhage when administered to premature infants, preferably by intravenous injections.

Abstract: A post-acceleration detector for a mass spectrometer comprises a conversion electrode bombarded by an ion beam thereby emitting charged particles having a polarity opposite to that of the ion beam, a charged particle detector amplifying and detecting the charged particles, and a mechanism for moving the conversion electrode relative to the charged particle detector according to the energy of the ion beam.

Abstract: A hydroquinoline compound of the formula (1): ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, A, l, m and n are as defined or its pharmaceutically acceptable salt, composition containing the compound and processes for preparing same are disclosed. The compound is useful as an antiulcer agent.

Abstract: Novel tetrahydroquinoline derivatives and salts thereof and novel imidazopyridine derivatives and salts thereof, both having excellent anti-peptic ulcer activities, and are useful as treating agents for peptic ulcers such as gastric ulcer, duodenum ulcer and the like.

Abstract: A process is disclosed which prepares a low pressure mercury vapor discharge lamp having a bulb and an end plate connected to the bottom of the bulb. The steps involve the application of an adhesive on one surface of the end plate, and the subsequent insertion of an exhaust tube into the end plate in such a way that an enlarged diameter portion of the exhust tube has an adhesive formed on this portion. As a result of the location and the structure of the steps, it is possible to provide a single step method of heating which functions to perform the essential bonding of all parts.

Abstract: Tetrazole derivatives of the formula: ##STR1## wherein R.sup.1 is an optional defined substituent; A is sulfur or a lower alkylene-thio, l is 0 or 1; B is a lower alkylene; R.sup.2 is hydroxy, a lower alkoxy, or a group: ##STR2## wherein R.sup.3 and R.sup.4 are optional defined substituents, or the R.sup.3 or R.sup.4 may combine together with the nitrogen atom to which they are joined to form a defined heterocyclic group, and a pharmaceutically acceptable salt thereof, which have prophylactic or therapeutic activities against peptic and/or duodenal ulcers and also anti-inflammatory activity and are useful as an anti-ulcer or anti-inflammatory drug; processes for the preparation of the tetrazole derivatives; and pharmaceutical compositon containing said tetrazole derivatives.

Abstract: Novel tetrahydroquinoline derivatives and salts thereof and novel imidazopyridine derivatives and salts thereof, both having excellent anti-peptic ulcer activities, and are useful as treating agents for peptic ulcers such as gastric ulcer, duodenum ulcer and the like.

Abstract: A low pressure mercury vapor discharge lamp forms an electric discharge path by the use of a bulb placed on an end plate and the bulb is formed by a process which results in the connecting outer side surfaces of juxtaposed glass tubes through communication holes formed in the outer side surfaces respectively. The process involves placing the juxtaposed glass tubes so that their outer surfaces are opposed in a contacting state. A portion of each of the glass tubes is heated in order to form a communication hole through the utilization of a burner inserted through an open end into the interior of each of the glass tubes in order to cause fusion of that particular portion in each tube to thereby form the communication hole by wind pressure.

Abstract: Both legs (1a, 1b) of a U-shaped bulb are brought into a mutually contacting state or are opposed to each other with a space of gap (31) and end parts (1a', 1b') of the legs are directly put on an end plate (10) so as to form an electric discharge path in the U-shaped bulb. Since the legs (1a, 1b) are in contact with each other within limit of elastic deformation of a connecting part (2a) of the bulb (1), breakage of the bulb is avoidable even when an external force is applied to the bulb so as to bring the legs (1a, 1b) closer.

Abstract: Novel oxindole derivative and salt thereof represented by the general formula, ##STR1## wherein R.sup.1 is a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a phenyl-lower alkyl group; R.sup.2 is a hydrogen atom or a lower alkyl group; R.sup.3 is a hydrogen atom, a cycloalkylcarbonyl group, a benzoyl group which may have 1 to 3 substituents selected from the group consisting of a halogen atom, a lower alkyl group and a lower alkoxy group on the phenyl ring, or a phenyl-lower alkanoyl group which may have halogen atoms as the substituents on the phenyl ring; provided that when R.sup.4 is a hydrogen atom, then R.sup.3 should be neither a hydrogen atom nor a lower alkyl group.The novel oxindole derivative and salt thereof possesses anti-peptic ulcer effects and are useful as anti-peptic ulcer agents.

Abstract: When AC voltages in-phase to each other are superposed on the DC voltages applied to a pair of opposing electrodes of a quadrupole lens, the waveform of the intensity of the ion beam is disturbed only if the central orbit of ions is deviated from the center of the quadrupole lens. In view of this, adjustment of the central orbit of ions is facilitated with the help of variations in the waveform of the intensity of the ion beam while superposing the AC voltages in-phase to each other on the DC voltages applied thereto.

Abstract: Tetrazole derivatives of the formula: ##STR1## wherein R.sup.1 is an optional defined substituent; A is sulfur or a lower alkylene-thio, l is 0 or 1; B is a lower alkylene; R.sup.2 is hydroxy, a lower alkoxy, or a group: ##STR2## wherein R.sup.3 and R.sup.4 are optional defined substituents, or the R.sup.3 and R.sup.4 may combine together with the nitrogen atom to which they are joined to form a defined heterocyclic group, and a pharmaceutically acceptable salt thereof, which have prophylactic or therapeutic activities against peptic and/or duodenal ulcers and also anti-inflammatory activity and are useful as an anti-ulcer or anti-inflammatory drug; processes for the preparation of the tetrazole derivatives; and pharmaceutical composition containing said tetrazole derivatives.

Abstract: A glass fiber-reinforced heat resistant resin composition which comprises:from 5 to 90% by weight of a pelletized polymer (A) obtained by suspension-polymerizing a vinyl aromatic monomer optionally together with an unsaturated nitrile monomer and a vinyl monomer copolymerizable therewith, in the presence of chopped glass fiber strands, and comprising from 50 to 90% by weight of the chopped glass fiber strands and from 50 to 10% by weight of a resin component consisting essentially of from 40 to 100% of residues of the vinyl aromatic monomer, from 0 to 60% of residues of the unsaturated nitrile monomer and from 0 to 30% of residues of the copolymerizable vinyl monomer;from 95 to 10% by weight of a polymer (B) comprising from 10 to 50% of residues of a maleimide monomer, from 90 to 50% of residues of a vinyl aromatic monomer, from 0 to 10% of residues of maleic anhydride and from 0 to 30% of residues of a vinyl monomer copolymerizable therewith.

Abstract: Disclosed are carbostyril derivatives and their salts of the formulas ##STR1## The compounds have anti-peptic ulcer effects, and are useful as a treating agent for curing peptic ulcers in the digestive system, such as ulcers in the stomach and in the duodenum. The compounds particularly have prophylaxis and curing effects for treating chronic ulcers, for example experimental acetic acid-induced ulcers and cautery ulcers, with both low toxicity and few side-effects. Also disclosed are processes for preparing the compounds and for preparing pharmaceutical compositions containing them.

Abstract: Disclosed are carbostyril derivatives and their salts of the formulas ##STR1## The compounds have anti-peptic ulcer effects, and are useful as a treating agent for curing peptic ulcers in the digestive system, such as ulcers in the stomach and in the duodenum. The compounds particularly have prophylaxis and curing effects for treating chronic ulcers, for example experimental acetic acid-induced ulcers and cautery ulcers, with both low toxicity and few side-effects. Also disclosed are processes for preparing the compounds and for preparing pharmaceutical compositions containing them.