289 research outputs found

    Joint Sensing and Communication Optimization in Target-Mounted STARS-Assisted Vehicular Networks: A MADRL Approach

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    The utilization of integrated sensing and communication (ISAC) technology has the potential to enhance the communication performance of road side units (RSUs) through the active sensing of target vehicles. Furthermore, installing a simultaneous transmitting and reflecting surface (STARS) on the target vehicle can provide an extra boost to the reflection of the echo signal, thereby improving the communication quality for in-vehicle users. However, the design of this target-mounted STARS system exhibits significant challenges, such as limited information sharing and distributed STARS control. In this paper, we propose an end-to-end multi-agent deep reinforcement learning (MADRL) framework to tackle the challenges of joint sensing and communication optimization in the considered target-mounted STARS assisted vehicle networks. By deploying agents on both RSU and vehicle, the MADRL framework enables RSU and vehicle to perform beam prediction and STARS pre-configuration using their respective local information. To ensure efficient and stable learning for continuous decision-making, we employ the multi-agent soft actor critic (MASAC) algorithm and the multi-agent proximal policy optimization (MAPPO) algorithm on the proposed MADRL framework. Extensive experimental results confirm the effectiveness of our proposed MADRL framework in improving both sensing and communication performance through the utilization of target-mounted STARS. Finally, we conduct a comparative analysis and comparison of the two proposed algorithms under various environmental conditions

    Quantitative seismic interpretation of rock brittleness based on statistical rock physics

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    Rock brittleness is one of the important properties for fracability evaluation, and it can be represented by different physical properties. The mineralogy-based brittleness index (BIM) builds a simple relationship between mineralogy and brittleness, but it may be ambiguous for rocks with a complex microstructure; whereas the elastic moduli-based brittleness index (BIE) is applicable in the field, but BIE interpretation needs to be constrained by lithofacies information. We have developed a new workflow for quantitative seismic interpretation of rock brittleness: Lithofacies are defined by a criterion combining BIM and BIE for comprehensive brittleness evaluation; statistical rock-physics methods are applied for quantitative interpretation by using inverted elastic parameters; acoustic impedance and elastic impedance are selected as the optimized pair of attributes for lithofacies classification. To improve the continuity and accuracy of the interpreted results, a Markov random field is applied in the Bayesian rule as the spatial constraint. A 2D synthetic test demonstrates the feasibility of the Bayesian classification with a Markov random field. This new interpretation framework is also applied to a shale reservoir formation from China. Comparison analysis indicates that brittle shale sections can be efficiently discriminated from ductile shale sections and tight sand sections by using the inverted elastic parameters

    Attention Diversification for Domain Generalization

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    Convolutional neural networks (CNNs) have demonstrated gratifying results at learning discriminative features. However, when applied to unseen domains, state-of-the-art models are usually prone to errors due to domain shift. After investigating this issue from the perspective of shortcut learning, we find the devils lie in the fact that models trained on different domains merely bias to different domain-specific features yet overlook diverse task-related features. Under this guidance, a novel Attention Diversification framework is proposed, in which Intra-Model and Inter-Model Attention Diversification Regularization are collaborated to reassign appropriate attention to diverse task-related features. Briefly, Intra-Model Attention Diversification Regularization is equipped on the high-level feature maps to achieve in-channel discrimination and cross-channel diversification via forcing different channels to pay their most salient attention to different spatial locations. Besides, Inter-Model Attention Diversification Regularization is proposed to further provide task-related attention diversification and domain-related attention suppression, which is a paradigm of "simulate, divide and assemble": simulate domain shift via exploiting multiple domain-specific models, divide attention maps into task-related and domain-related groups, and assemble them within each group respectively to execute regularization. Extensive experiments and analyses are conducted on various benchmarks to demonstrate that our method achieves state-of-the-art performance over other competing methods. Code is available at https://github.com/hikvision-research/DomainGeneralization.Comment: ECCV 2022. Code available at https://github.com/hikvision-research/DomainGeneralizatio

    γH2AX foci formation in the absence of DNA damage: Mitotic H2AX phosphorylation is mediated by the DNA-PKcs/CHK2 pathway

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    AbstractPhosphorylated H2AX is considered to be a biomarker for DNA double-strand breaks (DSB), but recent evidence suggests that γH2AX does not always indicate the presence of DSB. Here we demonstrate the bimodal dynamic of H2AX phosphorylation induced by ionizing radiation, with the second peak appearing when G2/M arrest is induced. An increased level of γH2AX occurred in mitotic cells, and this increase was attenuated by DNA-PKcs inactivation or Chk2 depletion, but not by ATM inhibition. The phosphorylation-mimic CHK2-T68D abrogated the attenuation of mitotic γH2AX induced by DNA-PKcs inactivation. Thus, the DNA-PKcs/CHK2 pathway mediates the mitotic phosphorylation of H2AX in the absence of DNA damage

    Acetylcholinesterase-capped Mesoporous Silica Nanoparticles Controlled by the Presence of Inhibitors

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    [EN] Two different acetylcholinesterase (AChE)-capped mesoporous silica nanoparticles (MSNs), S1-AChE and S2-AChE, were prepared and characterized. MSNs were loaded with rhodamine B and the external surface was functionalized with either pyridostigmine derivative P1 (to yield solid S1) or neostigmine derivative P2 (to obtain S2). The final capped materials were obtained by coordinating grafted P1 or P2 with AChE ' s active sites (to give S1-AChE and S2-AChE, respectively). Both materials were able to release rho-damine B in the presence of diisopropylfluorophosphate (DFP) or neostigmine in a concentration-dependent manner via the competitive displacement of AChE through DFP and neostigmine coordination with the AChE ' s active sites. The responses of S1-AChE and S2-AChE were also tested with other enzyme inhibitors and substrates. These studies suggest that S1-AChE nanoparticles can be used for the selective detection of nerve agent simulant DFP and paraoxon.Financial support from the Spanish Government and FEDER funds (Project MAT2015‐64139‐C4‐1‐R, AGL2015‐70235‐C2‐2‐R) and the Generalitat Valencia (Project PROMETEOII/2014/047) is gratefully acknowledged. Ll. P. is grateful to the Universitat Politécnica de Valencia for his grant.Pascual, L.; El Sayed Shehata Nasr, S.; Marcos Martínez, MD.; Martínez-Máñez, R.; Sancenón Galarza, F. (2017). Acetylcholinesterase-capped Mesoporous Silica Nanoparticles Controlled by the Presence of Inhibitors. Chemistry - An Asian Journal. 12(7):775-784. https://doi.org/10.1002/asia.201700031S775784127Alberti, S., Soler-Illia, G. J. A. A., & Azzaroni, O. (2015). Gated supramolecular chemistry in hybrid mesoporous silica nanoarchitectures: controlled delivery and molecular transport in response to chemical, physical and biological stimuli. Chemical Communications, 51(28), 6050-6075. doi:10.1039/c4cc10414eAznar, E., Oroval, M., Pascual, L., Murguía, J. R., Martínez-Máñez, R., & Sancenón, F. (2016). Gated Materials for On-Command Release of Guest Molecules. Chemical Reviews, 116(2), 561-718. doi:10.1021/acs.chemrev.5b00456Coll, C., Bernardos, A., Martínez-Máñez, R., & Sancenón, F. (2012). Gated Silica Mesoporous Supports for Controlled Release and Signaling Applications. Accounts of Chemical Research, 46(2), 339-349. doi:10.1021/ar3001469Slowing, I. I., Trewyn, B. G., Giri, S., & Lin, V. S.-Y. (2007). Mesoporous Silica Nanoparticles for Drug Delivery and Biosensing Applications. Advanced Functional Materials, 17(8), 1225-1236. doi:10.1002/adfm.200601191Yang, X., Liu, X., Liu, Z., Pu, F., Ren, J., & Qu, X. (2012). Near-Infrared Light-Triggered, Targeted Drug Delivery to Cancer Cells by Aptamer Gated Nanovehicles. Advanced Materials, 24(21), 2890-2895. doi:10.1002/adma.201104797Descalzo, A. 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Accounts of Chemical Research, 44(10), 903-913. doi:10.1021/ar200018xVallet-Regí, M., Balas, F., & Arcos, D. (2007). Mesoporous Materials for Drug Delivery. Angewandte Chemie International Edition, 46(40), 7548-7558. doi:10.1002/anie.200604488Vallet-Regí, M., Balas, F., & Arcos, D. (2007). Mesoporöse Materialien für den Wirkstofftransport. Angewandte Chemie, 119(40), 7692-7703. doi:10.1002/ange.200604488Sancenón, F., Pascual, L., Oroval, M., Aznar, E., & Martínez-Máñez, R. (2015). Gated Silica Mesoporous Materials in Sensing Applications. ChemistryOpen, 4(4), 418-437. doi:10.1002/open.201500053Radhakrishnan, K., Tripathy, J., Gnanadhas, D. P., Chakravortty, D., & Raichur, A. M. (2014). Dual enzyme responsive and targeted nanocapsules for intracellular delivery of anticancer agents. RSC Adv., 4(86), 45961-45968. doi:10.1039/c4ra07815bPatel, K., Angelos, S., Dichtel, W. R., Coskun, A., Yang, Y.-W., Zink, J. I., & Stoddart, J. F. (2008). Enzyme-Responsive Snap-Top Covered Silica Nanocontainers. Journal of the American Chemical Society, 130(8), 2382-2383. doi:10.1021/ja0772086De la Torre, C., Mondragón, L., Coll, C., Sancenón, F., Marcos, M. D., Martínez-Máñez, R., … Orzáez, M. (2014). Cathepsin-B Induced Controlled Release from Peptide-Capped Mesoporous Silica Nanoparticles. Chemistry - A European Journal, 20(47), 15309-15314. doi:10.1002/chem.201404382Agostini, A., Mondragón, L., Pascual, L., Aznar, E., Coll, C., Martínez-Máñez, R., … Gil, S. (2012). Design of Enzyme-Mediated Controlled Release Systems Based on Silica Mesoporous Supports Capped with Ester-Glycol Groups. Langmuir, 28(41), 14766-14776. doi:10.1021/la303161eCandel, I., Aznar, E., Mondragón, L., Torre, C. de la, Martínez-Máñez, R., Sancenón, F., … Parra, M. (2012). Amidase-responsive controlled release of antitumoral drug into intracellular media using gluconamide-capped mesoporous silica nanoparticles. Nanoscale, 4(22), 7237. doi:10.1039/c2nr32062bMas, N., Agostini, A., Mondragón, L., Bernardos, A., Sancenón, F., Marcos, M. D., … Pérez-Payá, E. (2012). Enzyme-Responsive Silica Mesoporous Supports Capped with Azopyridinium Salts for Controlled Delivery Applications. Chemistry - A European Journal, 19(4), 1346-1356. doi:10.1002/chem.201202740Bernardos, A., Aznar, E., Marcos, M. D., Martínez-Máñez, R., Sancenón, F., Soto, J., … Amorós, P. (2009). Enzyme-Responsive Controlled Release Using Mesoporous Silica Supports Capped with Lactose. Angewandte Chemie International Edition, 48(32), 5884-5887. doi:10.1002/anie.200900880Bernardos, A., Aznar, E., Marcos, M. D., Martínez-Máñez, R., Sancenón, F., Soto, J., … Amorós, P. (2009). Enzyme-Responsive Controlled Release Using Mesoporous Silica Supports Capped with Lactose. Angewandte Chemie, 121(32), 5998-6001. doi:10.1002/ange.200900880Zhu, Y., Meng, W., & Hanagata, N. (2011). Cytosine-phosphodiester-guanine oligodeoxynucleotide (CpG ODN)-capped hollow mesoporous silica particles for enzyme-triggered drug delivery. Dalton Transactions, 40(39), 10203. doi:10.1039/c1dt11114kAgostini, A., Mondragón, L., Bernardos, A., Martínez-Máñez, R., Marcos, M. D., Sancenón, F., … Murguía, J. R. (2012). Targeted Cargo Delivery in Senescent Cells Using Capped Mesoporous Silica Nanoparticles. Angewandte Chemie International Edition, 51(42), 10556-10560. doi:10.1002/anie.201204663Agostini, A., Mondragón, L., Bernardos, A., Martínez-Máñez, R., Marcos, M. D., Sancenón, F., … Murguía, J. R. (2012). Targeted Cargo Delivery in Senescent Cells Using Capped Mesoporous Silica Nanoparticles. Angewandte Chemie, 124(42), 10708-10712. doi:10.1002/ange.201204663Aznar, E., Villalonga, R., Giménez, C., Sancenón, F., Marcos, M. D., Martínez-Máñez, R., … Amorós, P. (2013). Glucose-triggered release using enzyme-gated mesoporous silica nanoparticles. Chemical Communications, 49(57), 6391. doi:10.1039/c3cc42210kChen, M., Huang, C., He, C., Zhu, W., Xu, Y., & Lu, Y. (2012). A glucose-responsive controlled release system using glucose oxidase-gated mesoporous silica nanocontainers. Chemical Communications, 48(76), 9522. doi:10.1039/c2cc34290aDíez, P., Sánchez, A., Gamella, M., Martínez-Ruíz, P., Aznar, E., de la Torre, C., … Pingarrón, J. M. (2014). Toward the Design of Smart Delivery Systems Controlled by Integrated Enzyme-Based Biocomputing Ensembles. Journal of the American Chemical Society, 136(25), 9116-9123. doi:10.1021/ja503578bDíez, P., Sánchez, A., Torre, C. de la, Gamella, M., Martínez-Ruíz, P., Aznar, E., … Villalonga, R. (2016). Neoglycoenzyme-Gated Mesoporous Silica Nanoparticles: Toward the Design of Nanodevices for Pulsatile Programmed Sequential Delivery. ACS Applied Materials & Interfaces, 8(12), 7657-7665. doi:10.1021/acsami.5b12645Yang, X., Pu, F., Chen, C., Ren, J., & Qu, X. (2012). An enzyme-responsive nanocontainer as an intelligent signal-amplification platform for a multiple proteases assay. Chemical Communications, 48(90), 11133. doi:10.1039/c2cc36340bDatz, S., Argyo, C., Gattner, M., Weiss, V., Brunner, K., Bretzler, J., … Bein, T. (2016). Genetically designed biomolecular capping system for mesoporous silica nanoparticles enables receptor-mediated cell uptake and controlled drug release. Nanoscale, 8(15), 8101-8110. doi:10.1039/c5nr08163gSun, X., Zhao, Y., Lin, V. S.-Y., Slowing, I. I., & Trewyn, B. G. (2011). Luciferase and Luciferin Co-immobilized Mesoporous Silica Nanoparticle Materials for Intracellular Biocatalysis. Journal of the American Chemical Society, 133(46), 18554-18557. doi:10.1021/ja2080168Liu, P., Wang, X., Hiltunen, K., & Chen, Z. (2015). Controllable Drug Release System in Living Cells Triggered by Enzyme–Substrate Recognition. ACS Applied Materials & Interfaces, 7(48), 26811-26818. doi:10.1021/acsami.5b08914Wang, X., Liu, P., Chen, Z., & Shen, J. (2016). A drug release switch based on protein-inhibitor supramolecular interaction. RSC Advances, 6(30), 25480-25484. doi:10.1039/c6ra03543dRim, H. P., Min, K. H., Lee, H. J., Jeong, S. Y., & Lee, S. C. (2011). pH-Tunable Calcium Phosphate Covered Mesoporous Silica Nanocontainers for Intracellular Controlled Release of Guest Drugs. Angewandte Chemie International Edition, 50(38), 8853-8857. doi:10.1002/anie.201101536Rim, H. P., Min, K. H., Lee, H. J., Jeong, S. Y., & Lee, S. C. (2011). pH-Tunable Calcium Phosphate Covered Mesoporous Silica Nanocontainers for Intracellular Controlled Release of Guest Drugs. Angewandte Chemie, 123(38), 9015-9019. doi:10.1002/ange.201101536Zhao, W., Zhang, H., He, Q., Li, Y., Gu, J., Li, L., … Shi, J. (2011). A glucose-responsive controlled release of insulin system based on enzyme multilayers-coated mesoporous silica particles. Chemical Communications, 47(33), 9459. doi:10.1039/c1cc12740cEl Sayed, S., Milani, M., Milanese, C., Licchelli, M., Martínez-Máñez, R., & Sancenón, F. (2016). Anions as Triggers in Controlled Release Protocols from Mesoporous Silica Nanoparticles Functionalized with Macrocyclic Copper(II) Complexes. Chemistry - A European Journal, 22(39), 13935-13945. doi:10.1002/chem.201601024Tukappa, A., Ultimo, A., de la Torre, C., Pardo, T., Sancenón, F., & Martínez-Máñez, R. (2016). Polyglutamic Acid-Gated Mesoporous Silica Nanoparticles for Enzyme-Controlled Drug Delivery. Langmuir, 32(33), 8507-8515. doi:10.1021/acs.langmuir.6b01715Giménez, C., Climent, E., Aznar, E., Martínez-Máñez, R., Sancenón, F., Marcos, M. D., … Rurack, K. (2014). Über den chemischen Informationsaustausch zwischen gesteuerten Nanopartikeln. Angewandte Chemie, 126(46), 12838-12843. doi:10.1002/ange.201405580De la Torre, C., Agostini, A., Mondragón, L., Orzáez, M., Sancenón, F., Martínez-Máñez, R., … Pérez-Payá, E. (2014). 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    Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

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    <p>Abstract</p> <p>Background</p> <p>Conotruncal heart defects (CTDs) are present in 75-85% of patients suffering from the 22q11.2 deletion syndrome. To date, no consistent phenotype has been consistently correlated with the 22q11.2 deletions. Genetic studies have implicated <it>TBX1 </it>as a critical gene in the pathogenesis of the syndrome. The aim of study was to determine the incidence of the 22q11.2 deletion in Chinese patients with CTDs and the possible mechanism for pathogenesis of CTDs.</p> <p>Methods</p> <p>We enrolled 212 patients with CTDs and 139 unrelated healthy controls. Both karyotypic analysis and multiplex ligation-dependent probe amplification were performed for all CTDs patients. Fluorescence <it>in situ </it>hybridization was performed for the patients with genetic deletions and their relatives. The <it>TBX1 </it>gene was sequenced for all patients and healthy controls. The <it>χ</it><sup>2 </sup>and Fisher's exact test were used in the statistical analysis.</p> <p>Results</p> <p>Thirteen of the 212 patients with CTDs (6.13%) were found to have the 22q11.2 deletion syndrome. Of the 13 cases, 11 presented with a hemizygous interstitial microdeletion from <it>CLTCL1 </it>to <it>LZTR1</it>; one presented with a regional deletion from <it>CLTCL1 </it>to <it>DRCR8</it>; and one presented with a regional deletion from <it>CDC45L </it>to <it>LZTR1</it>. There were eight sequence variants in the haploid <it>TBX1 </it>genes of the del22q11 CTDs patients. The frequency of one single nucleotide polymorphism (SNP) in the del22q11 patients was different from that of the non-del patients (<it>P </it>< 0.05), and the frequencies of two other SNPs were different between the non-del CTDs patients and controls (<it>P </it>< 0.05).</p> <p>Conclusions</p> <p>CTDs, especially pulmonary atresia with ventricular septal defect and tetralogy of Fallot, are the most common disorders associated with the 22q11.2 deletion syndrome. Those patients with both CTDs and 22q11.2 deletion generally have a typical or atypical deletion region within the <it>TBX1 </it>gene. Our results indicate that <it>TBX1 </it>genetic variants may be associated with CTDs.</p
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