1,753 research outputs found

    A Cyber-War Between Bots: Human-Like Attackers are More Challenging for Defenders than Deterministic Attackers

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    Adversary emulation is commonly used to test cyber defense performance against known threats to organizations. However, designing attack strategies is an expensive and unreliable manual process, based on subjective evaluation of the state of a network. In this paper, we propose the design of adversarial human-like cognitive models that are dynamic, adaptable, and have the ability to learn from experience. A cognitive model is built according to the theoretical principles of Instance-Based Learning Theory (IBLT) of experiential choice in dynamic tasks. In a simulation experiment, we compared the predictions of an IBL attacker with a carefully designed efficient but deterministic attacker attempting to access an operational server in a network. The results suggest that an IBL cognitive model that emulates human behavior can be a more challenging adversary for defenders than the carefully crafted optimal attack strategies. These insights can be used to inform future adversary emulation efforts and cyber defender training

    Towards Prediction of Financial Crashes with a D-Wave Quantum Computer

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    Prediction of financial crashes in a complex financial network is known to be an NP-hard problem, i.e., a problem which cannot be solved efficiently with a classical computer. We experimentally explore a novel approach to this problem by using a D-Wave quantum computer to obtain financial equilibrium more efficiently. To be specific, the equilibrium condition of a nonlinear financial model is embedded into a higher-order unconstrained binary optimization (HUBO) problem, which is then transformed to a spin-1/21/2 Hamiltonian with at most two-qubit interactions. The problem is thus equivalent to finding the ground state of an interacting spin Hamiltonian, which can be approximated with a quantum annealer. Our experiment paves the way to study quantitative macroeconomics, enlarging the number of problems that can be handled by current quantum computers

    12-h clock regulation of genetic information flow by XBP1s

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    © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Pan, Y., Ballance, H., Meng, H., Gonzalez, N., Kim, S., Abdurehman, L., York, B., Chen, X., Schnytzer, Y., Levy, O., Dacso, C. C., McClung, C. A., O'Malley, B. W., Liu, S., & Zhu, B. 12-h clock regulation of genetic information flow by XBP1s. Plos Biology, 18(1), (2020): e3000580, doi:10.1371/journal.pbio.3000580.Our group recently characterized a cell-autonomous mammalian 12-h clock independent from the circadian clock, but its function and mechanism of regulation remain poorly understood. Here, we show that in mouse liver, transcriptional regulation significantly contributes to the establishment of 12-h rhythms of mRNA expression in a manner dependent on Spliced Form of X-box Binding Protein 1 (XBP1s). Mechanistically, the motif stringency of XBP1s promoter binding sites dictates XBP1s’s ability to drive 12-h rhythms of nascent mRNA transcription at dawn and dusk, which are enriched for basal transcription regulation, mRNA processing and export, ribosome biogenesis, translation initiation, and protein processing/sorting in the Endoplasmic Reticulum (ER)-Golgi in a temporal order consistent with the progressive molecular processing sequence described by the central dogma information flow (CEDIF). We further identified GA-binding proteins (GABPs) as putative novel transcriptional regulators driving 12-h rhythms of gene expression with more diverse phases. These 12-h rhythms of gene expression are cell autonomous and evolutionarily conserved in marine animals possessing a circatidal clock. Our results demonstrate an evolutionarily conserved, intricate network of transcriptional control of the mammalian 12-h clock that mediates diverse biological pathways. We speculate that the 12-h clock is coopted to accommodate elevated gene expression and processing in mammals at the two rush hours, with the particular genes processed at each rush hour regulated by the circadian and/or tissue-specific pathways.This study was supported by the American Diabetes Association junior faculty development award 1-18-JDF-025 to B.Z., by funding from National Institute of Health HD07879 and 1P01DK113954 to B.W.O, by funding from National Science Foundation award 1703170 to C.C.D. and B.Z., and by funding from Brockman Foundation to C.C.D and B.W.O. This work was further supported by the UPMC Genome Center with funding from UPMC’s Immunotherapy and Transplant Center. This research was supported in part by the University of Pittsburgh Center for Research Computing through the resources provided. Research reported in this publication was further supported by the National Institute of Diabetes And Digestive And Kidney Diseases of the National Institutes of Health under award number P30DK120531 to Pittsburgh Liver Research Center, in which both S.L. and B.Z. are members. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

    Baryon Resonances

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    In this talk I show recent results on how many excited baryon resonances appear as systems of one meson and one baryon, or two mesons and one baryon, with the mesons being either pseudoscalar or vectors. Connection with experiment is made including a discussion on old predictions and recent results for the photoproduction of the Λ(1405)\Lambda(1405) resonance, as well as the prediction of one 1/2+1/2^+ baryon state around 1920 MeV which might have been seen in the γpK+Λ\gamma p \to K^+ \Lambda reaction.Comment: Talk given at the 10th International Conference on Hypernuclear and Strange Particle Physics, Tokai, Japan, Sptember 200

    Some results on disturbance attenuation for Hamiltonian systems via direct discrete-time design

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    The disturbance attenuation and robust disturbance attenuation problems for Hamiltonian systems in the discrete-time setting are considered and some new results are presented. The new results are derived utilizing the recently presented dissipativity equality obtained by adding the dissipation rate function to the classical dissipativity inequality. A selection of the dissipation rate function yields new results. These results include a condition on the dissipation structure of the system to achieve the desired disturbance attenuation level and gives direct construction of optimal control laws for any desired disturbance attenuation level. The results remove the need to solve Hamilton–Jacobi–Isaacs inequalities

    Obesity-dependent changes in interstitial ECM mechanics promote breast tumorigenesis.

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    Obesity and extracellular matrix (ECM) density are considered independent risk and prognostic factors for breast cancer. Whether they are functionally linked is uncertain. We investigated the hypothesis that obesity enhances local myofibroblast content in mammary adipose tissue and that these stromal changes increase malignant potential by enhancing interstitial ECM stiffness. Indeed, mammary fat of both diet- and genetically induced mouse models of obesity were enriched for myofibroblasts and stiffness-promoting ECM components. These differences were related to varied adipose stromal cell (ASC) characteristics because ASCs isolated from obese mice contained more myofibroblasts and deposited denser and stiffer ECMs relative to ASCs from lean control mice. Accordingly, decellularized matrices from obese ASCs stimulated mechanosignaling and thereby the malignant potential of breast cancer cells. Finally, the clinical relevance and translational potential of our findings were supported by analysis of patient specimens and the observation that caloric restriction in a mouse model reduces myofibroblast content in mammary fat. Collectively, these findings suggest that obesity-induced interstitial fibrosis promotes breast tumorigenesis by altering mammary ECM mechanics with important potential implications for anticancer therapies

    Extensive Chaos in the Nikolaevskii Model

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    We carry out a systematic study of a novel type of chaos at onset ("soft-mode turbulence") based on numerical integration of the simplest one dimensional model. The chaos is characterized by a smooth interplay of different spatial scales, with defect generation being unimportant. The Lyapunov exponents are calculated for several system sizes for fixed values of the control parameter ϵ\epsilon. The Lyapunov dimension and the Kolmogorov-Sinai entropy are calculated and both shown to exhibit extensive and microextensive scaling. The distribution functional is shown to satisfy Gaussian statistics at small wavenumbers and small frequency.Comment: 4 pages (including 5 figures) LaTeX file. Submitted to Phys. Rev. Let

    Phase-space analysis of interacting phantom cosmology

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    We perform a detailed phase-space analysis of various phantom cosmological models, where the dark energy sector interacts with the dark matter one. We examine whether there exist late-time scaling attractors, corresponding to an accelerating universe and possessing dark energy and dark matter densities of the same order. We find that all the examined models, although accepting stable late-time accelerated solutions, cannot alleviate the coincidence problem, unless one imposes a form of fine-tuning in the model parameters. It seems that interacting phantom cosmology cannot fulfill the basic requirement that led to its construction.Comment: 6 figures, use revtex, v2: minor corrections, references added, accepted for publication in JCA

    Recent research on changes in genomic regulation and protein expression in intracerebral haemorrhage

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    Intracerebral haemorrhage (ICH) is a devastating form of stroke that accounts for roughly 10% of all strokes and the effects on those that survive are often debilitating. To date, no suitable therapy exists. Recent work has examined alterations in gene and protein expression after ICH. The focus of this review is to outline the current knowledge of changes in genetic and protein expression after ICH and how those changes may affect the course of brain injury. Both animal and human data are reviewed.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/73607/1/j.1747-4949.2007.00160.x.pd
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