165 research outputs found

    The Iwasawa decomposition and the Bruhat decomposition of the automorphism group on certain exceptional Jordan algebra

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    Let J1\mathcal{J}^1 be the real form of a complex simple Jordan algebra such that the automorphism group is F4(20)\mathrm{F}_{4(-20)}. By using some orbit types of F4(20)\mathrm{F}_{4(-20)} on J1\mathcal{J}^1, for F4(20)\mathrm{F}_{4(-20)}, explicitly, we give the Iwasawa decomposition, the Oshima--Sekiguchi's KϵK_{\epsilon}-Iwasawa decomposition, the Matsuki decomposition, and the Bruhat and Gauss decompositions.Comment: v3, 30 pages, 1 figure, major changes from v2 by separating section 9--14, reformatted, and the title changed to appear in Tsukuba J. of Mat

    Orbit decomposition of Jordan matrix algebras of order three under the automorphism groups

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    The orbit decomposition is given under the automorphism group on the real split Jordan algebra of all hermitian matrices of order three corresponding to any real split composition algebra, or the automorphism group on the complexification, explicitly, in terms of the cross product of H. Freudenthal and the characteristic polynomial.Comment: v2, 32 pages, presentation improved, minor errors corrected, and the title changed as appeared in J. Math. Sci. Univ. Toky

    Development of the Counseling Center Assessment of Psychological Symptoms‐Japanese version: Pilot study

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    There is currently no reliable and valid multidimensional instrument for measuring psychological symptoms among Japanese university students. The purpose of this pilot study was to translate the Counseling Center Assessment of Psychological Symptoms‐62 (CCAPS‐62) into Japanese and evaluate its validity and reliability. Following robust translation procedures, the CCAPS‐Japanese was created. In the validation study, 2,758 undergraduate students from 11 universities (mean age = 19.08 ± 1.85 years) completed the CCAPS‐Japanese. The results of confirmatory factor analysis supported the theoretical eight‐factor structure model of the CCAPS‐Japanese with the exclusion of seven items. The decision to retain/remove items was made by evaluating factor loadings and model fit indices while considering cultural equivalence and structural validity. Using the finalized 55‐item CCAPS‐Japanese, further analyses demonstrated that the eight subscales had acceptable to good internal consistencies (α = .61–.89). Thus, the tool’s validity and reliability were established. The CCAPS‐Japanese may be appropriate for assessing the psychological concerns of Japanese university students.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/153629/1/cpp2412_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/153629/2/cpp2412.pd

    Contrasting Textural and Chemical Signatures of Chromitites in the Mesoarchaean Ulamertoq Peridotite Body, Southern West Greenland

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    Peridotites occur as lensoid bodies within the Mesoarchaean orthogneiss in the Akia terrane of Southern West Greenland. The Ulamertoq peridotite body is the largest of these peridotites hosted within the regional orthogneiss. It consists mainly of olivine, orthopyroxene, and amphibole-rich ultramafic rocks exhibiting metamorphic textural and chemical features. Chromitite layers from different localities in Ulamertoq show contrasting characteristics. In one locality, zoned chromites are hosted in orthopyroxene-amphibole peridotites. Compositional zonation in chromites is evident with decreasing Cr and Fe content from core to rim, while Al and Mg increase. Homogeneous chromites from another locality are fairly uniform and Fe-rich. The mineral chemistry of the major and accessory phases shows metamorphic signatures. Inferred temperature conditions suggest that the zoned chromites, homogeneous chromites, and their hosts are equilibrated at different metamorphic conditions. In this paper, various mechanisms during the cumulus to subsolidus stages are explored in order to understand the origin of the two contrasting types of chromites

    Cesium Implant for Tongue Carcinoma with a Thickness of 1.5 cm or More: Cases Successfully Treated with a Modified Manchester System

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    ∙The authors have no financial conflicts of interest. Purpose: Deciding on treatment carcinoma of the tongue when the tumor has a thickness of 1.5 cm or more is difficult. Surgery often requires wide resection and re-construction, leading to considerable functional impairment. A cesium implant is an attractive option, but according to the Manchester System, a two plane implant is needed. Materials and Methods: According to the textbook, a tumor is sandwiched between the needles, which are implanted at the edge of the tumor. This may cause an unnecessarily high dose to the outer surface of the tongue, which sometimes leads to a persistent ulcer. To avoid this complication, we invented a modified implantation method, and applied the method to five consecutive patients. Results: With a minimum follow-up of 2 years, all primary tumors in 5 consecutive patients have been controlled. No complications occurred in soft tissu

    Isolated congenital megacystis without intestinal obstruction: A mild variant of chronic intestinal pseudoobstruction syndrome?

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    Megacystis is frequently involved with chronic intestinal pseudoobstruction syndrome; however, isolated megacystis without intestinal obstruction is extremely rare. We present the case of a female patient with isolated congenital megacystis without severe intestinal obstruction. In this case, barium enema did not reveal any significant findings; however, histologic evaluation of her rectum showed hypoganglionosis of the submucous and myenteric plexuses. These findings indicate that this case may be a mild variant of chronic intestinal pseudoobstruction syndrome. The presence of megacystis should alert the physician to the possibility of chronic intestinal pseudoobstruction syndrome. © 2011 Elsevier Inc. All rights reserved

    PETREL for Astrophysics and Carbon Business

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    A multi-purpose 50kg class microsatellite hosting astrophysical mission and earth remote sensing, PETREL , will be launched in 2023. In the night side, PETREL observe the ultra-violet sky with a wide-field telescope covering 50 deg^2 for surveying transient objects related to supernovae, tidal disruption events, and gravitational wave events. Our UV telescope can detect the early phase UV emission from a neutron star merger occurred within 150 Mpc. In addition to the satellite observation, PETREL sends a detection alert including the coordinate and brightness of the UV transient to the ground via the real time communication network within several minutes after detection to conduct follow-up observations with the collaborating ground based observatories over the world. In the day side, PETREL observes the surface of the earth by using the tunable multi-spectral cameras and a ultra-compact hyperspectral camera. Our potential targets are the tropical forests (Green Carbon) and coastal zones (Blue Carbon) in the tropical areas to evaluating the global biological carbon strages. For this purpose PETREL will conduct multiple scale mapping collaborating with drones and small aircraft not only satellite. The obtained data will be used for academical research and for business applications. The technical difficulty of this satellite is that carries out multi-purpose with different requirements, such as astronomical observations which requires a quite high attitude stability and the earth observations requiring a high pointing accuracy, with limited resources. If it is possible, a novel small satellite system or a business style can be realized that can share the payload with academia and industry. PETREL has been adopted as Innovative Satellite Technology Demonstration Program No.3 led by JAXA, and development is underway with the aim of launching in FY2023

    Prescreening based on the presence of CT-scan abnormalities and biomarkers (KL-6 and SP-D) may reduce severe radiation pneumonitis after stereotactic radiotherapy

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    <p>Abstract</p> <p>Purpose</p> <p>To determine the risk factors of severe radiation pneumonitis (RP) after stereotactic body radiation therapy (SBRT) for primary or secondary lung tumors.</p> <p>Materials and methods</p> <p>From January 2003 to March 2009, SBRT was performed on 117 patients (32 patients before 2005 and 85 patients after 2006) with lung tumors (primary = 74 patients and metastatic/recurrent = 43 patients) in our institution. In the current study, the results on cases with severe RP (grades 4-5) were evaluated. Serum Krebs von den Lungen-6 (KL-6) and serum Surfactant protein-D (SP-D) were used to predict the incidence of RP. A shadow of interstitial pneumonitis (IP) on the CT image before performing SBRT was also used as an indicator for RP. Since 2006, patients have been prescreened for biological markers (KL-6 & SP-D) as well as checking for an IP-shadow in CT.</p> <p>Results</p> <p>Grades 4-5 RP was observed in nine patients (7.7%) after SBRT and seven of these cases (6.0%) were grade 5 in our institution. A correlation was found between the incidence of RP and higher serum KL-6 & SP-D levels. IP-shadow in patient's CT was also found to correlate well with the severe RP. Severe RP was reduced from 18.8% before 2005 to 3.5% after 2006 (<it>p </it>= 0.042). There was no correlation between the dose volume histogram parameters and these severe RP patients.</p> <p>Conclusion</p> <p>Patients presenting with an IP shadow in the CT and a high value of the serum KL-6 & SP-D before SBRT treatment developed severe radiation pneumonitis at a high rate. The reduction of RP incidence in patients treated after 2006 may have been attributed to prescreening of the patients. Therefore, pre-screening before SBRT for an IP shadow in CT and serum KL-6 & SP-D is recommended in the management and treatment of patients with primary or secondary lung tumors.</p

    Monkeys mutant for PKD1 recapitulate human autosomal dominant polycystic kidney disease.

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    Autosomal dominant polycystic kidney disease (ADPKD) caused by PKD1 mutations is one of the most common hereditary disorders. However, the key pathological processes underlying cyst development and exacerbation in pre-symptomatic stages remain unknown, because rodent models do not recapitulate critical disease phenotypes, including disease onset in heterozygotes. Here, using CRISPR/Cas9, we generate ADPKD models with PKD1 mutations in cynomolgus monkeys. As in humans and mice, near-complete PKD1 depletion induces severe cyst formation mainly in collecting ducts. Importantly, unlike in mice, PKD1 heterozygote monkeys exhibit cyst formation perinatally in distal tubules, possibly reflecting the initial pathology in humans. Many monkeys in these models survive after cyst formation, and cysts progress with age. Furthermore, we succeed in generating selective heterozygous mutations using allele-specific targeting. We propose that our models elucidate the onset and progression of ADPKD, which will serve as a critical basis for establishing new therapeutic strategies, including drug treatments
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