248 research outputs found

    Towards High-Precision Parton Distributions from Lattice QCD via Distillation

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    We apply the Distillation spatial smearing program to the extraction of the unpolarized isovector valence PDF of the nucleon. The improved volume sampling and control of excited-states afforded by distillation leads to a dramatically improved determination of the requisite Ioffe-time Pseudo-distribution (pITD). The impact of higher-twist effects is subsequently explored by extending the Wilson line length present in our non-local operators to one half the spatial extent of the lattice ensemble considered. The valence PDF is extracted by analyzing both the matched Ioffe-time Distribution (ITD), as well as a direct matching of the pITD to the PDF. Through development of a novel prescription to obtain the PDF from the pITD, we establish a concerning deviation of the pITD from the expected DGLAP evolution of the pseudo-PDF. The presence of DGLAP evolution is observed once more following introduction of a discretization term into the PDF extractions. Observance and correction of this discrepancy further highlights the utility of distillation in such structure studies

    Toward the Determination of the Gluon Helicity Distribution in the Nucleon from Lattice Quantum Chromodynamics

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    We present the first exploratory lattice quantum chromodynamics (QCD) calculation of the polarized gluon Ioffe-time pseudodistribution in the nucleon. The Ioffe-time pseudodistribution provides a frame-independent and gauge-invariant framework to determine the gluon helicity in the nucleon from first principles. We employ a high-statistics computation using a 323 × 64 lattice ensemble characterized by a 358 MeV pion mass and a 0.094 fm lattice spacing. We establish the pseudodistribution approach as a feasible method to address the proton spin puzzle with successive improvements in statistical and systematic uncertainties anticipated in the future. Within the statistical precision of our data, we find a good comparison between the lattice determined polarized gluon Ioffe-time distribution and the corresponding expectations from the state-of-the-art global analyses. We find a hint for a nonzero gluon spin contribution to the proton spin from the model-independent extraction of the gluon helicity pseudodistribution over a range of Ioffe-time, ν ≲ 9

    Unpolarized Gluon Distribution in the Nucleon From Lattice Quantum Chromodynamics

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    In this study, we present a determination of the unpolarized gluon Ioffe-time distribution in the nucleon from a first principles lattice quantum chromodynamics calculation. We carry out the lattice calculation on a 323 × 64 ensemble with a pion mass of 358 MeV and lattice spacing of 0.094 fm. We construct the nucleon interpolating fields using the distillation technique, flow the gauge fields using the gradient flow, and solve the summed generalized eigenvalue problem to determine the gluonic matrix elements. Combining these techniques allows us to provide a statistically well-controlled Ioffe-time distribution and unpolarized gluon parton distribution function. We obtain the flow time independent reduced Ioffe-time pseudodistribution and calculate the light-cone Ioffe-time distribution and unpolarized gluon distribution function in the MS scheme at μ = 2  GeV, neglecting the mixing of the gluon operator with the quark singlet sector. Finally, we compare our results to phenomenological determinations

    Isolated central nervous system relapse of systemic lymphoma (SCNSL): clinical features and outcome of a retrospective analysis

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    We analyzed clinical outcome of patients with an isolated central nervous system lymphoma (CNSL) relapse after systemic non-Hodgkin’s lymphoma (NHL). All 23 patients with an isolated secondary CNSL (SCNSL) treated at two institutions from 04/2003–12/2007 were included into this analysis. At cerebral relapse, 15/23 patients were treated with a regimen consisting of high-dose methotrexate (Bonn protocol). After a median follow-up of 6.5 months (range 1–68), 15/23 (65%) patients with SCNSL had relapsed or progressed. HD (high-dose)- methotrexate (MTX) chemotherapy according to the Bonn protocol is effective concerning response rates; however, overall survival of patients with SCNSL seems to be impaired in comparison to relapses in primary CNSL (PCNSL)

    Inositol Hexakisphosphate-Induced Autoprocessing of Large Bacterial Protein Toxins

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    Large bacterial protein toxins autotranslocate functional effector domains to the eukaryotic cell cytosol, resulting in alterations to cellular functions that ultimately benefit the infecting pathogen. Among these toxins, the clostridial glucosylating toxins (CGTs) produced by Gram-positive bacteria and the multifunctional-autoprocessing RTX (MARTX) toxins of Gram-negative bacteria have distinct mechanisms for effector translocation, but a shared mechanism of post-translocation autoprocessing that releases these functional domains from the large holotoxins. These toxins carry an embedded cysteine protease domain (CPD) that is activated for autoprocessing by binding inositol hexakisphosphate (InsP6), a molecule found exclusively in eukaryotic cells. Thus, InsP6-induced autoprocessing represents a unique mechanism for toxin effector delivery specifically within the target cell. This review summarizes recent studies of the structural and molecular events for activation of autoprocessing for both CGT and MARTX toxins, demonstrating both similar and potentially distinct aspects of autoprocessing among the toxins that utilize this method of activation and effector delivery
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