Mitsubishi

About: Mitsubishi is a company organization based out in Tokyo, Japan. It is known for research contribution in the topics: Signal & Layer (electronics). The organization has 53115 authors who have published 54821 publications receiving 870150 citations. The organization is also known as: Mitsubishi Group of Companies & Mitsubishi Companies.

Arx homeobox gene is essential for development of mouse olfactory system.

Abstract: The olfactory system provides an excellent model in which to study cell proliferation, migration, differentiation, axon guidance, dendritic morphogenesis, and synapse formation. We report here crucial roles of the Arx homeobox gene in the developing olfactory system by analyzing its mutant phenotypes. Arx protein was expressed strongly in the interneurons and weakly in the radial glia of the olfactory bulb, but in neither the olfactory sensory neurons nor bulbar projection neurons. Arx-deficient mice showed severe anatomical abnormalities in the developing olfactory system: (1) size reduction of the olfactory bulb, (2) reduced proliferation and impaired entry into the olfactory bulb of interneuron progenitors, (3) loss of tyrosine hydroxylase-positive periglomerular cells, (4) disorganization of the layer structure of the olfactory bulb, and (5) abnormal axonal termination of olfactory sensory neurons in an unusual axon-tangled structure, the fibrocellular mass. Thus, Arx is required for not only the proper developmental processes of Arx-expressing interneurons, but also the establishment of functional olfactory neural circuitry by affecting Arx-non-expressing sensory neurons and projection neurons. These findings suggest a likely role of Arx in regulating the expression of putative instructive signals produced in the olfactory bulb for the proper innervation of olfactory sensory axons.

Spread-spectrum signal receiving method and spread-spectrum signal receiving apparatus

Abstract: A spread-spectrum signal receiving method and apparatus in which a correlation operation is performed for obtaining a correlation between a base-band component of a received spread-spectrum signal and a spread code, so as to demodulate the received signal. In the method, a correlation operation between the spread code and the base-band component, and a correlation operation at a timing equal to a timing difference between the spread code and the base-band component in the former correlation operation step, the timing difference being 1/2 of a spread-code interval, are performed. Then, based on results obtained in these correlation operations, a correlation operation result at the timing point where a timing difference between the spread code and the base-band component is less than 1/2 of the spread-code interval, is estimated.

Dual-tagging gene trap of novel genes in Drosophila melanogaster.

Abstract: A gene-trap system is established for Drosophila. Unlike the conventional enhancer-trap system, the gene-trap system allows the recovery only of fly lines whose genes are inactivated by a P-element insertion, i.e., mutants. In the gene-trap system, the reporter gene expression reflects precisely the spatial and temporal expression pattern of the trapped gene. Flies in which gene trap occurred are identified by a two-step screening process using two independent markers, mini-w and Gal4, each indicating the integration of the vector downstream of the promoter of a gene (dual tagging). mini-w has its own promoter but lacks a polyadenylation signal. Therefore, mini-w mRNA is transcribed from its own promoter regardless of the vector integration site in the genome. However, the eyes of flies are not orange or red unless the vector is incorporated into a gene enabling mini-w to be spliced to a downstream exon of the host gene and polyadenylated at the 39 end. The promoter-less Gal4 reporter is expressed as a fusion mRNA only when it is integrated downstream of the promoter of a host gene. The exons of trapped genes can be readily cloned by vectorette RT-PCR, followed by RACE and PCR using cDNA libraries. Thus, the dual-tagging gene- trap system provides a means for (i) efficient mutagenesis, (ii) unequivocal identification of genes responsible for mutant phenotypes, (iii) precise detection of expression patterns of trapped genes, and (iv) rapid cloning of trapped genes.

Optical recording and reproducing apparatus for tracking wobbling guide grooves

Abstract: An optical recording and reproducing apparatus uses a laser to form one or more spots on an information recording medium preformatted with wobbling guide grooves, and detects tracking error. If the differential push-pull method of detecting tracking error is used, a center spot is flanked by satellite spots distant by an odd multiple of half time repeating period of tile wobble. If tile three-beam method is used, the distance is an odd multiple of one-fourth the repeating period of the wobble. If the push-pull method is used, a split photodetector generates a pair of electrical signals. The sum and difference of these signals are filtered, then synchronously detected, and the result is combined with the difference signal to generate a corrected tracking error signal.

Process for preparing laminated resin product

Abstract: In a process for preparing a laminated resin product by melt-laminating (1) a modified polyolefin composition with (2) a polyester, a polyamide or a hydrolyzed copolymer of ethylenevinylacetate, the improvement comprising using as the modified polyolefin a modified polyolefin composition which comprises a mixture of 60 - 97 wt.% of a polyolefin which polyolefin comprises from 0.1 to 100 wt.% of a polyolefin modified with an unsaturated acid or anhydride content is from 0.01 to 10 wt.% of the total polyolefin content and wherein an unmodified polyolefin comprises from 99.9 to 0 wt.% of the total polyolefin content with 40 - 3 wt.% of a rubber component having 40 - 140 of Mooney viscosity 50 ML 1 + 4 (100° C) and the product so produced.