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Search Results: 1 - 10 of 2867 matches for " Akira Nishiyama "
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Entropy Production in Gluodynamics in temporal axial gauge in 2+1 dimensions
Akihiro Nishiyama,Akira Ohnishi
Physics , 2010, DOI: 10.1143/PTP.125.775
Abstract: Entropy production in non-Abelian gauge theory is discussed in the limit of vanishing classical fields. Based on the Kadanoff-Baym equation with the leading order self-energy in the temporal axial gauge, the kinetic entropy is introduced and is proven to increase for a given self-energy. Numerical simulation of the Kadanoff-Baym equation for the non-Abelian gauge theory is performed in 2+1 dimensions. Starting from anisotropic distribution in momentum space, relaxation to isotropic distribution proceeds and the entropy is produced due to off-shell scattering of massive transverse polarization mode as expected from the proof of the H-theorem.
Myocardial Segmentation of Area at Risk Based on Coronary Computed Tomography Angiography and Voronoi Diagram in Comparison with Magnetic Resonance Perfusion Imaging  [PDF]
Naoki Fukuyama, Teruhito Kido, Akira Kurata, Yuki Tanabe, Tomoyuki Kido, Takahiro Yokoi, Ryo Ogawa, Hikaru Nishiyama, Teruyoshi Uetani, Teruhito Mochizuki
Open Journal of Radiology (OJRad) , 2017, DOI: 10.4236/ojrad.2017.71002
Abstract: Purpose: To assess the clinical feasibility of automated segmentation of the myocardial area at risk (MAAR) using coronary computed tomography angiography (CT-MAAR), as compared to stress magnetic resonance myocardial perfusion imaging (MR-MPI). Materials and Methods: Thirty patients who underwent coronary computed tomography angiography (CTA) and stress MR-MPI were retrospectively evaluated. The myocardial territory of the left ventricle (LV) distal to coronary artery stenosis (≥50% or ≥70% stenosis on coronary CTA) was three-dimensionally quantified using a Voronoi diagram. The ratio of all stenosis-related territories to the LV volume was defined as CT-MAAR (%-LV volume). The proportion of segments with perfusion defects in stress MR-MPI to the total of 16 segments (range: 0% - 100%; with a 6.3%-interval scale) was defined as the reference. Correlation was assessed using Spearman’s test. The capability of CT-MAAR to predict the ischemic burden was assessed. Results: Stress MR-MPI depicted a median ischemic burden of 25.2% (range: 18.9% - 44.1%) in 30 patients without myocardial infarction. When CTA stenosis criteria of ≥50% (n = 30) and ≥70% (n = 27) were applied to estimate CT-MAAR, the median CT-MAAR values were 48.2% (31.6% - 64.3%) and 32.5% (23.7% - 51.9%), respectively. The correlations between the CT-MAAR values and the MR-based ischemic burden were significant (0.73 and 0.97 for ≥50% and ≥70% stenosis, respectively). CT-MAAR predicted the MR-based ischemic burden within ±1 segment of %-LV (6.3%) in 40% (12/30) of patients with ≥50% stenosis, and in 81.5% (22/27) of patients with ≥70% stenosis. Conclusions: Comprehensive assessment of resting coronary CTA combined with Voronoi diagram-based myocardial segmentation may help predict the myocardial ischemic burden in patients with severe coronary CTA stenosis.
Activation of JNK Triggers Release of Brd4 from Mitotic Chromosomes and Mediates Protection from Drug-Induced Mitotic Stress
Akira Nishiyama, Anup Dey, Tomohiko Tamura, Minoru Ko, Keiko Ozato
PLOS ONE , 2012, DOI: 10.1371/journal.pone.0034719
Abstract: Some anti-cancer drugs, including those that alter microtubule dynamics target mitotic cells and induce apoptosis in some cell types. However, such drugs elicit protective responses in other cell types allowing cells to escape from drug-induced mitotic inhibition. Cells with a faulty protective mechanism undergo defective mitosis, leading to genome instability. Brd4 is a double bromodomain protein that remains on chromosomes during mitosis. However, Brd4 is released from mitotic chromosomes when cells are exposed to anti-mitotic drugs including nocodazole. Neither the mechanisms, nor the biological significance of drug-induced Brd4 release has been fully understood. We found that deletion of the internal C-terminal region abolished nocodazole induced Brd4 release from mouse P19 cells. Furthermore, cells expressing truncated Brd4, unable to dissociate from chromosomes were blocked from mitotic progression and failed to complete cell division. We also found that pharmacological and peptide inhibitors of the c-jun-N-terminal kinases (JNK) pathway, but not inhibitors of other MAP kinases, prevented release of Brd4 from chromosomes. The JNK inhibitor that blocked Brd4 release also blocked mitotic progression. Further supporting the role of JNK in Brd4 release, JNK2–/– embryonic fibroblasts were defective in Brd4 release and sustained greater inhibition of cell growth after nocodazole treatment. In sum, activation of JNK pathway triggers release of Brd4 from chromosomes upon nocodazole treatment, which mediates a protective response designed to minimize drug-induced mitotic stress.
A survey of influence of work environment on temporomandibular disorders-related symptoms in Japan
Akira Nishiyama, Koji Kino, Masashi Sugisaki, Kaori Tsukagoshi
Head & Face Medicine , 2012, DOI: 10.1186/1746-160x-8-24
Abstract: Our study subjects comprised of 1,969 employees from the same Japanese company. The subjects were assessed using a questionnaire that covered both TRS and the work environment. TRS were measured from 4 items on the questionnaire. The work environment factors recorded were the daily mean duration of personal computer use, driving, precise work, commuting, time spent at home before going to bed, sleeping, attending business meetings, and performing physical labor. Statistical analysis was performed using t-tests, Chi-square tests, and logistic regression analyses. A result with P?<?0.05 was considered statistically significant.The median total score on the 4 items used to assess TRS was 5 (25%?=?4, 75%?=?7). Two groups were defined such that the participants scoring ≤7 were assigned to the low-TRS group and those scoring ≥8, to the high-TRS group. The high-TRS group constituted 22.6% of the subjects. Logistic regression analyses indicated that female gender and extended periods of computer use were significant contributors to the manifestation of TRS.This questionnaire-based study showed that gender and computer use time was associated with the prevalence of TRS in this working population. Thus, evaluation of ergonomics is suggested for TMD patients.The term “temporomandibular disorders (TMD)” encompasses a number of clinical conditions that involve the temporomandibular joint, the masticatory muscles, or both [1]. The prevalence of TMD in the general population has been reported to be 5%–12% [2,3]. Since the 1970s, TMD has been proposed to have a multifactorial etiology in which various contributing factors are responsible for the pain and dysfunction [4,5]. These factors include structural conditions, psychological morbidity, and behavioral problems such as parafunctional habits [6,7].Sugisaki et al. [8] reported that the prevalence of TMD-related symptoms (TRS) was higher in working population (approximately 17–18%) than in the general population (5–12%). They attr
Identification of a 4-Deoxy-l-erythro-5-hexoseulose Uronic Acid Reductase, FlRed, in an Alginolytic Bacterium Flavobacterium sp. Strain UMI-01
Akira Inoue,Ryuji Nishiyama,Shogo Mochizuki,Takao Ojima
Marine Drugs , 2015, DOI: 10.3390/md13010493
Abstract: In alginate-assimilating bacteria, alginate is depolymerized to unsaturated monosaccharide by the actions of endolytic and exolytic alginate lyases (EC and EC The monosaccharide is non-enzymatically converted to 4-deoxy-l-ery thro-5-hexoseulose uronic acid (DEH), then reduced to 2-keto-3-deoxy-d-gluconate (KDG) by a specific reductase, and metabolized through the Entner–Doudoroff pathway. Recently, the NADPH-dependent reductase A1-R that belongs to short-chain dehydrogenases/reductases (SDR) superfamily was identified as the DEH-reductase in Sphingomonas sp. A1. We have subsequently noticed that an SDR-like enzyme gene, flred, occurred in the genome of an alginolytic bacterium Flavobacterium sp. strain UMI-01. In the present study, we report on the deduced amino-acid sequence of flred and DEH-reducing activity of recombinant FlRed. The deduced amino-acid sequence of flred comprised 254 residues and showed 34% amino-acid identities to that of A1-R from Sphingomonas sp. A1 and 80%–88% to those of SDR-like enzymes from several alginolytic bacteria. Common sequence motifs of SDR-superfamily enzymes, e.g., the catalytic tetrad Asn-Lys-Tyr-Ser and the cofactor-binding sequence Thr-Gly-x-x-x-Gly-x-Gly in Rossmann fold, were completely conserved in FlRed. On the other hand, an Arg residue that determined the NADPH-specificity of Sphingomonas A1-R was replaced by Glu in FlRed. Thus, we investigated cofactor-preference of FlRed using a recombinant enzyme. As a result, the recombinant FlRed (recFlRed) was found to show high specificity to NADH. recFlRed exhibited practically no activity toward variety of aldehyde, ketone, keto ester, keto acid and aldose substrates except for DEH. On the basis of these results, we conclude that FlRed is the NADH-dependent DEH-specific SDR of Flavobacterium sp. strain UMI-01.
Oxidative Stress/Angiotensinogen/Renin-Angiotensin System Axis in Patients with Diabetic Nephropathy
Masumi Kamiyama,Maki Urushihara,Takashi Morikawa,Yoshio Konishi,Masahito Imanishi,Akira Nishiyama,Hiroyuki Kobori
International Journal of Molecular Sciences , 2013, DOI: 10.3390/ijms141123045
Abstract: Although recent studies have proven that renin-angiotensin system (RAS) blockades retard the progression of diabetic nephropathy, the detailed mechanisms of their reno-protective effects on the development of diabetic nephropathy remain uncertain. In rodent models, it has been reported that reactive oxygen species (ROS) are important for intrarenal angiotensinogen (AGT) augmentation in the progression of diabetic nephropathy. However, no direct evidence is available to demonstrate that AGT expression is enhanced in the kidneys of patients with diabetes. To examine whether the expression levels of ROS- and RAS-related factors in kidneys are increased with the progression of diabetic nephropathy, biopsied samples from 8 controls and 27 patients with type 2 diabetes were used. After the biopsy, these patients were diagnosed with minor glomerular abnormality or diabetes mellitus by clinical and pathological findings. The intensities of AGT, angiotensin II (Ang II), 4-hydroxy-2-nonenal (4-HNE), and heme oxygenase-1 (HO-1) were examined by fluorescence in situ hybridization and/or immunohistochemistry. Expression levels were greater in patients with diabetes than in control subjects. Moreover, the augmented intrarenal AGT mRNA expression paralleled renal dysfunction in patients with diabetes. These data suggest the importance of the activated oxidative stress/AGT/RAS axis in the pathogenesis of diabetic nephropathy.
Dielectric Properties of Noncrystalline HfSiON
Masahiro Koike,Tsunehiro Ino,Yuuichi Kamimuta,Masato Koyama,Yoshiki Kamata,Masamichi Suzuki,Yuichiro Mitani,Akira Nishiyama
Physics , 2006, DOI: 10.1103/PhysRevB.73.125123
Abstract: The dielectric properties of noncrystalline hafnium silicon oxynitride (HfSiON) films with a variety of atomic compositions were investigated. The films were deposited by reactive sputtering of Hf and Si in an O, N, and Ar mixture ambient. The bonding states, band-gap energies, atomic compositions, and crystallinities were confirmed by X-ray photoelectron spectroscopy (XPS), reflection electron energy loss spectroscopy (REELS), Rutherford backscattering spectrometry (RBS), and X-ray diffractometry (XRD), respectively. The optical (high-frequency) dielectric constants were optically determined by the square of the reflective indexes measured by ellipsometry. The static dielectric constants were electrically estimated by the capacitance of Au/HfSiON/Si(100) structures. It was observed that low N incorporation in the films led to the formation of only Si-N bonds without Hf-N bonds. An abrupt decrease in band-gap energies was observed at atomic compositions corresponding to the boundary where Hf-N bonds start to form. By combining the data for the atomic concentrations and bonding states, we found that HfSiON can be regarded as a pseudo-quaternary alloy consisting of four insulating components: SiO$_2$, HfO$_2$, Si$_3$N$_4$, and Hf$_3$N$_4$. The optical and static dielectric constants for the films showed a nonlinear dependence on the N concentration, whose behavior can be understood in terms of abrupt Hf-N bond formation.
Diffusion and activation of n-type dopants in germanium
Masahiro Koike,Yoshiki Kamata,Tsunehiro Ino,Daisuke Hagishima,Kosuke Tatsumura,Masato Koyama,Akira Nishiyama
Physics , 2007, DOI: 10.1063/1.2958326
Abstract: The diffusion and activation of $n$-type impurities (P and As) implanted into $p$-type Ge(100) substrates were examined under various dose and annealing conditions. The secondary ion mass spectrometry profiles of chemical concentrations indicated the existence of a sufficiently high number of impurities with increasing implanted doses. However, spreading resistance probe profiles of electrical concentrations showed electrical concentration saturation in spite of increasing doses and indicated poor activation of As relative to P in Ge. The relationships between the chemical and electrical concentrations of P in Ge and Si were calculated, taking into account the effect of incomplete ionization. The results indicated that the activation of P was almost the same in Ge and Si. The activation ratios obtained experimentally were similar to the calculated values, implying insufficient degeneration of Ge. The profiles of P in Ge substrates with and without damage generated by Ge ion implantation were compared, and it was clarified that the damage that may compensate the activated $n$-type dopants has no relationship with the activation of P in Ge.
Periostin Associates with Notch1 Precursor to Maintain Notch1 Expression under a Stress Condition in Mouse Cells
Hideyuki Tanabe,Issei Takayama,Takashi Nishiyama,Masashi Shimazaki,Isao Kii,Minqi Li,Norio Amizuka,Ken-ichi Katsube,Akira Kudo
PLOS ONE , 2012, DOI: 10.1371/journal.pone.0012234
Abstract: Matricellular proteins, including periostin, modulate cell-matrix interactions and cell functions by acting outside of cells.
Delayed Re-Epithelialization in Periostin-Deficient Mice during Cutaneous Wound Healing
Takashi Nishiyama,Isao Kii,Takeshi G. Kashima,Yoshinao Kikuchi,Atsushi Ohazama,Masashi Shimazaki,Masashi Fukayama,Akira Kudo
PLOS ONE , 2012, DOI: 10.1371/journal.pone.0018410
Abstract: Matricellular proteins, including periostin, are important for tissue regeneration.
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