477 research outputs found

    Hodge metrics and positivity of direct images

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    Building on Fujita-Griffiths method of computing metrics on Hodge bundles, we show that the direct image of an adjoint semi-ample line bundle by a projective submersion has a continuous metric with Griffiths semi-positive curvature. This shows that for every holomorphic semi-ample vector bundle EE on a complex manifold, and every positive integer kk, the vector bundle SkEdetES^kE\otimes\det E has a continuous metric with Griffiths semi-positive curvature. If EE is ample on a projective manifold, the metric can be made smooth and Griffiths positive.Comment: revised and expanded version of "A positivity property of ample vector bundles

    Solvothermal nanoYAG synthesis: Mechanism and particle growth kinetics

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    This paper was accepted for publication in the journal Journal of Supercritical Fluids and the definitive published version is available at http://dx.doi.org/10.1016/j.supflu.2015.09.031NanoYAG particles with spherical morphology have been synthesised using a solvothermal method; a structure sensitive reaction, where the chemical reaction and the particle growth kinetics are interdependent. It has been observed that the primary YAG particles agglomerated into ∼30 nm clusters via a self-assembled Ostwald ripening process along (2 1 1) planes, separated by a distance of ∼0.49 nm, at 270 °C and 2.0 MPa for 2 h. These nanoclusters coalesced into single nanoparticles of ∼30 nm in size and exhibited a smaller inter planar distance of ∼0.26 nm, corresponding to the (4 2 0) planes, when synthesized at 300 °C and 8.5 MPa for 2 h. in addition, the solvent 1,4-butanediol transformed into 1,4-diacetoxybutane, this will have undergone esterification by reacting with the terminal acetate groups cleaved from the precursor, yttrium acetate. The proposed mechanism based on the analytical evidence suggests that a complete dissolution of precursors facilitated the structural re-arrangement of atoms within the planes and lead to a significantly higher degree of crystallinity. Moreover, once the particles with (4 2 0) planes had formed, they were no longer involved in facile coalescence along their preferential planes due to their lower interfacial energy compared to the (2 1 1) planes. This led to control of the particle morphology and with little agglomeration occurring in the final nanopowder

    Graphdti: A Robust Deep Learning Predictor Of Drug-Target Interactions From Multiple Heterogeneous Data

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    Traditional techniqueset identification, we developed GraphDTI, a robust machine learning framework integrating the molecular-level information on drugs, proteins, and binding sites with the system-level information on gene expression and protein-protein interactions. In order to properly evaluate the performance of GraphDTI, we compiled a high-quality benchmarking dataset and devised a new cluster-based cross-validation p to identify macromolecular targets for drugs utilize solely the information on a query drug and a putative target. Nonetheless, the mechanisms of action of many drugs depend not only on their binding affinity toward a single protein, but also on the signal transduction through cascades of molecular interactions leading to certain phenotypes. Although using protein-protein interaction networks and drug-perturbed gene expression profiles can facilitate system-level investigations of drug-target interactions, utilizing such large and heterogeneous data poses notable challenges. To improve the state-of-the-art in drug targrotocol. Encouragingly, GraphDTI not only yields an AUC of 0.996 against the validation dataset, but it also generalizes well to unseen data with an AUC of 0.939, significantly outperforming other predictors. Finally, selected examples of identified drug-target interactions are validated against the biomedical literature. Numerous applications of GraphDTI include the investigation of drug polypharmacological effects, side effects through off-target binding, and repositioning opportunities

    On the canonical map of surfaces with q>=6

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    We carry out an analysis of the canonical system of a minimal complex surface of general type with irregularity q>0. Using this analysis we are able to sharpen in the case q>0 the well known Castelnuovo inequality K^2>=3p_g+q-7. Then we turn to the study of surfaces with p_g=2q-3 and no fibration onto a curve of genus >1. We prove that for q>=6 the canonical map is birational. Combining this result with the analysis of the canonical system, we also prove the inequality: K^2>=7\chi+2. This improves an earlier result of the first and second author [M.Mendes Lopes and R.Pardini, On surfaces with p_g=2q-3, Adv. in Geom. 10 (3) (2010), 549-555].Comment: Dedicated to Fabrizio Catanese on the occasion of his 60th birthday. To appear in the special issue of Science of China Ser.A: Mathematics dedicated to him. V2:some typos have been correcte

    Probabilistic Algorithmic Knowledge

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    The framework of algorithmic knowledge assumes that agents use deterministic knowledge algorithms to compute the facts they explicitly know. We extend the framework to allow for randomized knowledge algorithms. We then characterize the information provided by a randomized knowledge algorithm when its answers have some probability of being incorrect. We formalize this information in terms of evidence; a randomized knowledge algorithm returning ``Yes'' to a query about a fact \phi provides evidence for \phi being true. Finally, we discuss the extent to which this evidence can be used as a basis for decisions.Comment: 26 pages. A preliminary version appeared in Proc. 9th Conference on Theoretical Aspects of Rationality and Knowledge (TARK'03

    Analytic curves in algebraic varieties over number fields

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    We establish algebraicity criteria for formal germs of curves in algebraic varieties over number fields and apply them to derive a rationality criterion for formal germs of functions, which extends the classical rationality theorems of Borel-Dwork and P\'olya-Bertrandias valid over the projective line to arbitrary algebraic curves over a number field. The formulation and the proof of these criteria involve some basic notions in Arakelov geometry, combined with complex and rigid analytic geometry (notably, potential theory over complex and pp-adic curves). We also discuss geometric analogues, pertaining to the algebraic geometry of projective surfaces, of these arithmetic criteria.Comment: 55 pages. To appear in "Algebra, Arithmetic, and Geometry: In Honor of Y.i. Manin", Y. Tschinkel & Yu. Manin editors, Birkh\"auser, 200

    The use of Raman spectroscopy to differentiate between different prostatic adenocarcinoma cell lines

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    Raman spectroscopy (RS) is an optical technique that provides an objective method of pathological diagnosis based on the molecular composition of tissue. Studies have shown that the technique can accurately identify and grade prostatic adenocarcinoma (CaP) in vitro. This study aimed to determine whether RS was able to differentiate between CaP cell lines of varying degrees of biological aggressiveness. Raman spectra were measured from two well-differentiated, androgen-sensitive cell lines (LNCaP and PCa 2b) and two poorly differentiated, androgen-insensitive cell lines (DU145 and PC 3). Principal component analysis was used to study the molecular differences that exist between cell lines and, in conjunction with linear discriminant analysis, was applied to 200 spectra to construct a diagnostic algorithm capable of differentiating between the different cell lines. The algorithm was able to identify the cell line of each individual cell with an overall sensitivity of 98% and a specificity of 99%. The results further demonstrate the ability of RS to differentiate between CaP samples of varying biological aggressiveness. RS shows promise for application in the diagnosis and grading of CaP in clinical practise as well as providing molecular information on CaP samples in a research setting

    The Future of Biologic Agents in the Treatment of Sjögren’s Syndrome

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    The gain in knowledge regarding the cellular mechanisms of T and B lymphocyte activity in the pathogenesis of Sjögren’s syndrome (SS) and the current availability of various biological agents (anti-TNF-α, IFN- α, anti-CD20, and anti-CD22) have resulted in new strategies for therapeutic intervention. In SS, various phase I and II studies have been performed to evaluate these new strategies. Currently, B cell-directed therapies seem to be more promising than T cell-related therapies. However, large, randomized, placebo-controlled clinical trials are needed to confirm the promising results of these early studies. When performing these trials, special attention has to be paid to prevent the occasional occurrence of the severe side effects
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