830 research outputs found

    Generating Einstein gravity, cosmological constant and Higgs mass from restricted Weyl invariance

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    Recently, it has been pointed out that dimensionless actions in four dimensional curved spacetime possess a symmetry which goes beyond scale invariance but is smaller than full Weyl invariance. This symmetry was dubbed {\it restricted Weyl invariance}. We show that starting with a restricted Weyl invariant action that includes a Higgs sector with no explicit mass, one can generate the Einstein-Hilbert action with cosmological constant and a Higgs mass. The model also contains an extra massless scalar field which couples to the Higgs field (and gravity). If the coupling of this extra scalar field to the Higgs field is negligibly small, this fixes the coefficient of the nonminimal coupling RΦ2R \Phi^2 between the Higgs field and gravity. Besides the Higgs sector, all the other fields of the standard model can be incorporated into the original restricted Weyl invariant action.Comment: 7 pages, no figure

    Artificial Itelligence Teaches Drugs to Target Proteins by Tackling the Induced Folding Problem

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    We explore the possibility of a deep learning (DL) platform that steers drug design to target proteins by inducing binding-competent conformations. We deal with the fact that target proteins are usually not fixed targets but structurally adapt to the ligand in ways that need to be predicted to enable pharmaceutical discovery. In contrast with protein folding predictors, the proposed DL system integrates signals for structural disorder to predict conformations in floppy regions of the target protein that rely on associations with the purposely designed drug to maintain their structural integrity. This is tantamount to solve the drug-induced folding problem within an AI-empowered drug discovery platform. Preliminary testing of the proposed DL platform reveals that it is possible to infer the induced folding ensemble from which a therapeutically targetable conformation gets selected by DL-instructed drug design.Fil: Fernandez, Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentin

    The logistic map and the birth of period-3 cycle

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    The goal of this paper is to present a proof that for the logistic map the period-3 begins at . The third-iterate map is the key for understanding the birth of the period-3 cycle. Any point in a period-3 cycle repeats every three iterates by definition. Such points satisfy the condition ,and they are therefore fixed points of the third-iterate map. This fact and the so called tangent bifurcation for the logistic map, as well as the fixed points definition, are used for finding the value. The algebraic treatment utilizes some properties of symmetric polynomials in three variables. For the purposes of this paper, the bifurcation diagram for the logistic map is also presented, as well as a program in Mathematica for its construction

    Targeted Deletion of PTEN in Kisspeptin Cells Results in Brain Region- and Sex-Specific Effects on Kisspeptin Expression and Gonadotropin Release

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    Kisspeptin-expressing neurons in the anteroventral periventricular nucleus (AVPV) and the arcuate nucleus (ARC) of the hypothalamus relay hormonal and metabolic information to gonadotropin-releasing hormone neurons, which in turn regulate pituitary and gonadal function. Phosphatase and tensin homolog (PTEN) blocks phosphatidylinositol 3-kinase (PI3K), a signaling pathway utilized by peripheral factors to transmit their signals. However, whether PTEN signaling in kisspeptin neurons helps to integrate peripheral hormonal cues to regulate gonadotropin release is unknown. To address this question, we generated mice with a kisspeptin cell-specific deletion of Pten (Kiss-PTEN KO), and first assessed kisspeptin protein expression and gonadotropin release in these animals. Kiss-PTEN KO mice displayed a profound sex and region-specific kisspeptin neuron hyperthrophy. We detected both kisspeptin neuron hyperthrophy as well as increased kisspeptin fiber densities in the AVPV and ARC of Kiss-PTEN KO females and in the ARC of Kiss-PTEN KO males. Moreover, Kiss-PTEN KO mice showed a reduced gonadotropin release in response to gonadectomy. We also found a hyperactivation of mTOR, a downstream PI3K target and central regulator of cell metabolism, in the AVPV and ARC of Kiss-PTEN KO females but not males. Fasting, known to inhibit hypothalamic kisspeptin expression and luteinizing hormone levels, failed to induce these changes in Kiss-PTEN KO females. We conclude that PTEN signaling regulates kisspeptin protein synthesis in both sexes and that its role as a metabolic signaling molecule in kisspeptin neurons is sex-specific

    Dark patterns and consumer vulnerability

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    Dark patterns that manipulate consumer behaviour are now a pervasive feature of digital markets. Depending on the choice architecture utilised, they can affect the perception, behaviour and purchasing patterns of online consumers. Using a novel empirical design, we find strong evidence that individuals across all groups are susceptible to dark patterns, and only weak evidence that user susceptibility is materially affected by commonly used general proxies for consumer vulnerability (such as income, educational attainment or age). Our conclusions provide empirical support for the use of broad restrictions on the use of dark patterns, such as those contained in the EU’s Digital Services Act, that protect all consumer groups. Our study also finds that added friction, in the form of required payment action following successful deployment of dark patterns, reduces their effectiveness. This insight highlights the instances in which dark patterns would be most effective – when no further action is required by the user. Consumer vulnerability is therefore more pronounced when dealing with online providers who store users’ payment details and can rely on a ‘single click’ to complete the purchase
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