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This study investigates the mechanical responses and deformation mechanisms of CoCrFeMnNi high-entropy alloy (HEA) with varying grain size gradients through molecular dynamics simulations, and explores the tension-compression asymmetry of gradient nanograined high-entropy alloy (G-HEA) under different loading conditions. In the early stage of plastic deformation, the normal stress and shear strain of G-HEA both exhibit gradient distribution characteristics under compression and tension. However, as the engineering strain increased, these gradient distribution characteristics gradually diminished and ultimately disappeared. Grain boundary (GB) migration and grain merging are the main GB activities of G-HEA, and fine grains in the soft zone have stronger grain boundary vitality compared to coarse grains in the hard zone. G-HEA exhibits multiple plastic deformation mechanisms, including dislocation slip, deformation twinning, and hexagonal close-packed (HCP) phase transformation. There are both synergy and competition among various deformation mechanisms, which collectively enhance the mechanical properties of materials. This work has found that the differences in GB activities are the main cause of stress and strain asymmetry in G-HEA, while the different nucleation positions of dislocations are the reasons for the asymmetry in dislocation density, yield stress, and average flow stress. In addition, when = 0.32, the yield stress and flow stress of G-HEA both reach their maximum/minimum values, further demonstrating the role of gradient nanostructures in regulating stress and strain distribution. Therefore, the research results of this article provide a theoretical basis for designing G-HEA suitable for different application scenarios.
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http://dx.doi.org/10.1039/d5ra00735f | DOI Listing |
Lab Chip
September 2025
Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.
Traumatic brain injuries (TBIs) are a risk factor for Alzheimer's disease (AD), and share several important pathological features including the development of neurofibrillary tangles (NFT) of tau protein. While this association is well established, the underlying pathogenesis is poorly defined and current treatment options remain limited, necessitating novel methods and approaches. In response we developed "TBI-on-a-chip", an trauma model utilizing murine cortical networks on microelectrode arrays (MEAs), capable of reproducing clinically relevant impact injuries while providing simultaneous morphological and electrophysiological readout.
View Article and Find Full Text PDFVirchows Arch
September 2025
Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Minas Gerais, Av. Antônio Carlos, Pampulha, Belo Horizonte, 31270-901, Brazil.
Plasmablastic lymphoma (PBL) is a rare and aggressive non-Hodgkin lymphoma with a poor prognosis and short survival rates. It is classified as a large B-cell lymphoma subtype, but carries a plasmacytic immunophenotype. Therefore, PBL has pathogenetic overlaps with diffuse large B-cell lymphoma not otherwise specified (DLBCL NOS) and plasma cell neoplasms (PCNs).
View Article and Find Full Text PDFSignal Transduct Target Ther
September 2025
Institute of Neuroscience, Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.
Essential tremor (ET) is a common neurological disease that is characterized by 4-12 Hz kinetic tremors of the upper limbs and high genetic heterogeneity. Although numerous candidate genes and loci have been reported, the etiology of ET remains unclear. A novel ET-related gene was initially identified in a five-generation family via whole-exome sequencing, and other variants were identified in 772 familial ET probands and 640 sporadic individuals via whole-genome sequencing.
View Article and Find Full Text PDFBrain Res
September 2025
Department of Neurology, Shanghai Sixth People's Hospital, Shanghai 200233, China. Electronic address:
Migraine is a complex neurological disorder influenced by multiple genetic susceptibility factors, yet current animal models fail to fully recapitulate its human-specific pathophysiology. In this study, we explored the potential mechanisms underlying migraine by examining functional abnormalities and molecular dysregulation in glutamatergic neurons derived from induced pluripotent stem cells (iPSCs) of migraine patients. As key excitatory cells in the central nervous system, glutamatergic neurons are implicated in migraine through altered excitability, ion channel dysfunction, and dysregulation of nociceptive signaling molecules.
View Article and Find Full Text PDFBiochim Biophys Acta Biomembr
September 2025
Center for Computational and Integrative Biology (CCIB), Rutgers-Camden, Camden, NJ, United States of America; Department of Physics, Rutgers-Camden, Camden, NJ, United States of America. Electronic address:
The Envelope protein (E protein) of SARS-CoVs 1 and 2 has been implicated in the viral budding process and maintaining the spherical shape of the virus, but direct evidence linking the protein to long-range membrane deformation is still lacking. Computational predictions from molecular simulation have offered conflicting results, some showing long-range E-induced membrane curvature and others showing only local deformations. In the present study, we determine the mechanism driving these deformations by modulating the degree of hydrophobic mismatch between protein and membrane.
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