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1,494 result(s) for "Kubota, M."
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Large anisotropic deformation of skyrmions in strained crystal
Uniaxial strain as small as 0.3% in FeGe thin films can induce large anisotropic deformation of magnetic skyrmions and their crystal lattice hosted in the material. Mechanical control of magnetism is an important and promising approach in spintronics. To date, strain control has mostly been demonstrated in ferromagnetic structures by exploiting a change in magnetocrystalline anisotropy. It would be desirable to achieve large strain effects on magnetic nanostructures. Here, using in situ Lorentz transmission electron microscopy, we demonstrate that anisotropic strain as small as 0.3% in a chiral magnet of FeGe induces very large deformations in magnetic skyrmions 1 , 2 , as well as distortions of the skyrmion crystal lattice on the order of 20%. Skyrmions are stabilized by the Dzyaloshinskii–Moriya interaction 3 , 4 , originating from a chiral crystal structure. Our results show that the change in the modulation of the strength of this interaction is amplified by two orders of magnitude with respect to changes in the crystal lattice due to an applied strain. Our findings may provide a mechanism to achieve strain control of topological magnetic structures based on the Dzyaloshinskii–Moriya interaction.
Microwave magnetoelectric effect via skyrmion resonance modes in a helimagnetic multiferroic
Magnetic skyrmion, a topologically stable spin-swirling object, can host emergent electromagnetism, as exemplified by the topological Hall effect and electric-current-driven skyrmion motion. To achieve efficient manipulation of nano-sized functional spin textures, it is imperative to exploit the resonant motion of skyrmions, analogously to the role of the ferromagnetic resonance in spintronics. The magnetic resonance of skyrmions has recently been detected with oscillating magnetic fields at 1–2 GHz, launching a search for new skyrmion functionality operating at microwave frequencies. Here we show a microwave magnetoelectric effect in resonant skyrmion dynamics. Through microwave transmittance spectroscopy on the skyrmion-hosting multiferroic crystal Cu 2 OSeO 3 combined with theoretical simulations, we reveal nonreciprocal directional dichroism (NDD) at the resonant mode, that is, oppositely propagating microwaves exhibit different absorption. The microscopic mechanism of the present NDD is not associated with the conventional Faraday effect but with the skyrmion magnetoelectric resonance instead, suggesting a conceptually new microwave functionality. Magnetic skyrmions are topologically stable swirls in a spin structure. Here, the authors demonstrate new ways of controlling them by showing that the absorption of an electromagnetic wave by a skyrmion depends on the direction of incidence and that the resonance modes respond to a magnetic field.
Depression-like episodes in mice harboring mtDNA deletions in paraventricular thalamus
Depression is a common debilitating human disease whose etiology has defied decades of research. A critical bottleneck is the difficulty in modeling depressive episodes in animals. Here, we show that a transgenic mouse with chronic forebrain expression of a dominant negative mutant of Polg1 , a mitochondrial DNA (mtDNA) polymerase, exhibits lethargic behavioral changes, which are associated with emotional, vegetative and psychomotor disturbances, and response to antidepression drug treatment. The results suggested a symptomatic similarity between the lethargic behavioral change that was recurrently and spontaneously experienced by the mutant mice and major depressive episode as defined by DSM-5. A comprehensive screen of mutant brain revealed a hotspot for mtDNA deletions and mitochondrial dysfunction in the paraventricular thalamic nucleus (PVT) with similar defects observed in postmortem brains of patients with mitochondrial disease with mood symptoms. Remarkably, the genetic inhibition of PVT synaptic output by Cre-loxP-dependent expression of tetanus toxin triggered de novo depression-like episodes. These findings identify a novel preclinical mouse model and brain area for major depressive episodes with mitochondrial dysfunction as its cellular mechanism.
Three-dimensional constraint-based void-growth model for high temperature hydrogen attack
High temperature hydrogen attack (HTHA) is degradation of steels exposed to hydrogen gas at high temperatures and pressures. Hydrogen in steels reacts with carbon from carbides to produce methane gas bubbles typically on grain boundaries which grow and coalesce, leading to loss of strength and fracture toughness. Current design practice against HTHA is based on the Nelson curves which define the conditions for safe operation in a temperature/hydrogen-partial-pressure diagram. Nelson curves are phenomenological in nature and do not account for the underlying failure mechanism(s), material microstructure, carbide stability, and applied stresses. In light of experimental evidence of predominant cavitation ahead of cracks reported by Martin et al. (Acta Mater 140:300–304, 2017), it is expected that void growth is accelerated by the triaxial stresses associated with microstructural flaws. To this end, we propose a three-dimensional, axisymmetric, constraint-based void-growth model extending the “one-dimensional” model of Dadfarnia et al. (Int J Fract 219:1–17, 2019). The present model is shown to yield satisfactory agreement with the available experimental data from hydrogen attack of 2¼Cr–1Mo steel at temperatures ranging from 500 to 600 °C. In addition, the model is used to construct Nelson type curves in the temperature/hydrogen-partial-pressure diagram. These curves represent failure times for given applied stresses and triaxiality. The proposed methodology can be viewed as providing a step toward improving the current design practice against HTHA while maintaining the simplicity of the original Nelson curve approach.
Specific HLA genotypes confer susceptibility to acute necrotizing encephalopathy
Acute necrotizing encephalopathy (ANE) is a rare and severe syndrome of acute encephalopathy triggered by viral infections. Cytokine storm is considered as the main pathogenetic mechanism of ANE. ANE is prevalent in East Asia, suggesting the association of host genetic factors. To elucidate the genetic background of Japanese ANE, we examined genotypes of human leukocyte antigen ( HLA ) -A, C, B, DRB1, DQB1 and DPB1 in 31 patients. Significant positive association was observed in both the allele frequency and positivity of DRB1*09:01 ( P =0.043 and 0.025, respectively), as well as those of DQB1*03:03 ( P =0.034 and 0.026, respectively). The carrier frequency of DRB1*09:01 and DQB1*03:03 alleles was higher in the patients (45.16%) than in controls (28.57%). These alleles are more common in East Asian than in European populations, and are reportedly associated with various autoimmune diseases in Japanese patients. Our data provide further evidence that altered immune response based on individual HLA genotypes may contribute to ANE pathogenesis.
Phytophagy of the predator Podisus nigrispinus (Dallas, 1851) (Hemiptera: Pentatomidae) fed on prey and Brassicaceae
Abstract The purpose of this study was to investigate the development and reproduction of the zoophytophagous predator Podisus nigrispinus (Dallas) (Heteroptera: Pentatomidae) fed kale, broccoli and cabbage affects its. Nymphs and adults of this predator were fed on larvae of Plutella xylostella (L.) (Lepidoptera: Plutellidae) as prey with kale, cabbage, or broccoli. In the nymph period, the duration and prey consumption were similar with all the Brassicacea cultivar. However, nymph viability was higher for predators with broccoli leaves. The mean weight of 5th-instar nymphs, newly emerged females and the sex ratio were similar among the Brassicacea cultivars, while newly emerged males were heavier with kale and broccoli leaves. The supply of broccoli leaves resulted in greater oviposition, higher number of eggs per egg mass and longer longevity of P. nigrispinus males and females. Furthermore, the consumption of P. xylostella larvae by adult predators was higher with these cultivars. The net reproductive rate (R0) and mean generation time (T) were highest for predators with prey and broccoli leaves. The reproductive parameters of P. nigrispinus were enhanced when fed on P. xylostella larvae with and broccoli leaves, which can be an alternative diet in laboratory rearing of this predator. Resumo O objetivo deste estudo foi verificar o desenvolvimento e reprodução do zoofitófago Podisus nigrispinus (Dallas) (Heteroptera: Pentatomidae) em couve, brócolis e repolho. Ninfas e adultos deste predador foram alimentados com lagartas de Plutella xylostella (L.) (Lepidoptera: Plutellidae) como presa e receberam folhas de couve, repolho ou brócolis. Durante o período ninfal, a duração do período e o consumo de presas foram semelhantes com as diferentes cultivares de brassicácea. Porém, a viabilidade ninfal foi maior para predadores com folhas de brócolis. O peso de ninfas de quinto instar e de fêmeas recém-emergidas e a razão sexual de P. nigrispinus foram semelhantes entre as cultivares de brassicáceas, enquanto que o peso de machos recém-emergidos foi maior com folhas de couve e brócolis. Folhas de brócolis proporcionaram maiores número de oviposições, ovos por postura e longevidade de machos e fêmeas de P. nigrispinus. Além disso, o consumo de lagartas de P. xylostella por adultos desse predador fora maiores com esta cultivar. A taxa líquida de reprodução (R0) e o tempo médio de geração (T) foram maiores para predadores com presa e folhas de brócolis. Podisus nigrispinus alimentados com lagartas de P. xylostella e folhas de brócolis apresentaram melhores parâmetros reprodutivos, podendo ser uma alternativa para a criação deste predador em laboratório.
Mice with cleavage-resistant N-cadherin exhibit synapse anomaly in the hippocampus and outperformance in spatial learning tasks
N-cadherin is a homophilic cell adhesion molecule that stabilizes excitatory synapses, by connecting pre- and post-synaptic termini. Upon NMDA receptor (NMDAR) activation by glutamate, membrane-proximal domains of N-cadherin are cleaved serially by a-disintegrin-and-metalloprotease 10 (ADAM10) and then presenilin 1(PS1, catalytic subunit of the γ-secretase complex). To assess the physiological significance of the initial N-cadherin cleavage, we engineer the mouse genome to create a knock-in allele with tandem missense mutations in the mouse N-cadherin/Cadherin-2 gene ( Cdh2 R714G, I715D , or GD) that confers resistance on proteolysis by ADAM10 (GD mice). GD mice showed a better performance in the radial maze test, with significantly less revisiting errors after intervals of 30 and 300 s than WT, and a tendency for enhanced freezing in fear conditioning. Interestingly, GD mice reveal higher complexity in the tufts of thorny excrescence in the CA3 region of the hippocampus. Fine morphometry with serial section transmission electron microscopy (ssTEM) and three-dimensional (3D) reconstruction reveals significantly higher synaptic density, significantly smaller PSD area, and normal dendritic spine volume in GD mice. This knock-in mouse has provided in vivo evidence that ADAM10-mediated cleavage is a critical step in N-cadherin shedding and degradation and involved in the structure and function of glutamatergic synapses, which affect the memory function.
Design and Trial Production of Magnetic Filter for Medical Protein Screening System using High Gradient Magnetic Separation
Biomedicine is indispensable for the treatment of various diseases such as cancer and diabetes mellitus. In particular, antibodies utilized by the immune system are believed to represent the future of medical supplies as they offer an effective treatment for diseases with minor side effects. The development of antibody drugs requires a large-scale, sequential, fast separation, and refinement process for the medical proteins. Thus, in the previous study, we proposed a medical protein screening system that is based on high-gradient magnetic separation using a superconducting magnet. In the proposed system, the protein is specifically attached to the magnetic beads and captured by the magnetic force around a magnetic filter generated by a high magnetic field. In this paper, the behaviour of the magnetic beads was investigated using particle trace simulation coupled with electromagnetic and fluid analyses for three types of commercially available magnetic filters. Simulations were performed using the filter stack intervals and number of filters as design parameters. Finally, we designed the suitable filter for capturing the magnetic beads.
An fMRI Study of the Brain Network Involved in Teeth Tapping in Elderly Adults
Cortical activity during jaw movement has been analyzed using various non-invasive brain imaging methods, but the contribution of orofacial sensory input to voluntary jaw movements remains unclear. In this study, we used functional magnetic resonance imaging (fMRI) to observe brain activities during a simple teeth tapping task in adult dentulous (AD), older dentulous (OD), and older edentulous subjects who wore dentures (OEd) or did not wear dentures (OE) to analyze their functional network connections. (1) To assess the effect of age on natural activation patterns during teeth tapping, a comparison of groups with natural dentition-AD and OD-was undertaken. A general linear model analysis indicated that the major activated site in the AD group was the primary sensory cortex (SI) and motor cortex (MI) ( < 0.05, family wise error corrected). In the OD group, teeth tapping induced brain activity at various foci ( < 0.05, family wise error corrected), including the SI, MI, insula cortex, supplementary motor cortex (SMC)/premotor cortex (PMA), cerebellum, thalamus, and basal ganglia in each group. (2) Group comparisons between the OD and OEd subjects showed decreased activity in the SI, MI, Brodmann's area 6 (BA6), thalamus (ventral posteromedial nucleus, VPM), basal ganglia, and insular cortex ( ¡ 0.005, uncorrected). This suggested that the decreased S1/M1 activity in the OEd group was related to missing teeth, which led to reduced periodontal afferents. (3) A conjunction analysis in the OD and OEd/OE groups revealed that commonly activated areas were the MI, SI, cerebellum, BA6, thalamus (VPM), and basal ganglia (putamen; < 0.05, FWE corrected). These areas have been associated with voluntary movements. (4) Psychophysiological interaction analysis (OEd vs OE) showed that subcortical and cortical structures, such as the MI, SI, DLPFC, SMC/PMA, insula cortex, basal ganglia, and cerebellum, likely function as hubs and form an integrated network that participates in the control of teeth tapping. These results suggest that oral sensory inputs are involved in the control of teeth tapping through feedforward control of intended movements, as well as feedback control of ongoing movements.
Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes
There is no established genetic model of bipolar disorder or major depression, which hampers research of these mood disorders. Although mood disorders are multifactorial diseases, they are sometimes manifested by one of pleiotropic effects of a single major gene defect. We focused on chronic progressive external ophthalmoplegia (CPEO), patients with which sometimes have comorbid mood disorders. Chronic progressive external ophthalmoplegia is a mitochondrial disease, which is accompanied by accumulation of mitochondrial DNA (mtDNA) deletions caused by mutations in nuclear-encoded genes such as POLG (mtDNA polymerase). We generated transgenic mice, in which mutant POLG was expressed in a neuron-specific manner. The mice showed forebrain-specific defects of mtDNA and had altered monoaminergic functions in the brain. The mutant mice exhibited characteristic behavioral phenotypes, a distorted day–night rhythm and a robust periodic activity pattern associated with estrous cycle. These abnormal behaviors resembling mood disorder were worsened by tricyclic antidepressant treatment and improved by lithium, a mood stabilizer. We also observed antidepressant-induced mania-like behavior and long-lasting irregularity of activity in some mutant animals. Our data suggest that accumulation of mtDNA defects in brain caused mood disorder-like mental symptoms with similar treatment responses to bipolar disorder. These findings are compatible with mitochondrial dysfunction hypothesis of bipolar disorder.