576 research outputs found

    Kreck-Stolz invariants for quaternionic line bundles

    No full text

    Scalar curvature estimates for compact symmetric spaces

    Get PDF
    We establish extremality of Riemannian metrics g with non-negative curvature operator on symmetric spaces M=G/K of compact type with rk(G)-rk(K)\le 1. Let g' be another metric with scalar curvature k', such that g'\ge g on 2-vectors. We show that k'\ge k everywhere on M implies k'=k. Under an additional condition on the Ricci curvature of g, k'\ge k even implies g'=g. We also study area-non-increasing spin maps onto such Riemannian manifolds.Comment: 13 pages, LaTeX, uses amsar

    Vafa-Witten Estimates for Compact Symmetric Spaces

    Full text link
    We give an optimal upper bound for the first eigenvalue of the untwisted Dirac operator on a compact symmetric space G/H with rk G-rk H\le 1 with respect to arbitrary Riemannian metrics. We also prove a rigidity statement.Comment: LaTeX, 11 pages. V2: Rigidity statement added, minor changes. To appea

    Instantaneous modulations in time-varying complex optical potentials

    Get PDF
    We study the impact of a spatially homogeneous yet non-stationary dielectric permittivity on the dynamical and spectral properties of light. Our choice of potential is motivated by the interest in PT-symmetric systems as an extension of quantum mechanics. Because we consider a homogeneous and non-stationary medium, PT symmetry reduces to time-reversal symmetry in the presence of balanced gain and loss. We construct the instantaneous amplitude and angular frequency of waves within the framework of Maxwell's equations and demonstrate the modulation of light amplification and attenuation associated with the well-defined temporal domains of gain and loss, respectively. Moreover, we predict the splitting of extrema of the angular frequency modulation and demonstrate the associated shrinkage of the modulation period. Our theory can be extended for investigating similar time-dependent effects with matter and acoustic waves in PT-symmetric structures.Comment: 13 pages, 4 figure

    Platelet Apoptosis in Adult Immune Thrombocytopenia: Insights into the Mechanism of Damage Triggered by Auto-antibodies

    Get PDF
    Mechanisms leading to decreased platelet count in immune thrombocytopenia (ITP) are heterogeneous. This study describes increased platelet apoptosis involving loss of mitochondrial membrane potential (ΔΨm), caspase 3 activation (aCasp3) and phosphatidylserine (PS) externalization in a cohort of adult ITP patients. Apoptosis was not related to platelet activation, as PAC-1 binding, P-selectin exposure and GPIb-IX internalization were not increased. Besides, ITP platelets were more sensitive to apoptotic stimulus in terms of aCasp3. Incubation of normal platelets with ITP plasma induced loss of ΔΨm, while PS exposure and aCasp3 remained unaltered. The increase in PS exposure observed in ITP platelets could be reproduced in normal platelets incubated with ITP plasma by adding normal CD3+ lymphocytes to the system as effector cells. Addition of leupeptin -a cathepsin B inhibitor- to this system protected platelets from apoptosis. Increased PS exposure was also observed when normal platelets and CD3+ lymphocytes were incubated with purified IgG from ITP patients and was absent when ITP plasma was depleted of auto-antibodies, pointing to the latter as responsible for platelet damage. Apoptosis was present in platelets from all patients carrying anti-GPIIb-IIIa and anti-GPIb auto-antibodies but was absent in the patient with anti-GPIa-IIa auto-antibodies. Platelet damage inversely correlated with platelet count and decreased during treatment with a thrombopoietin receptor agonist. These results point to a key role for auto-antibodies in platelet apoptosis and suggest that antibody-dependent cell cytotoxicity is the mechanism underlying this phenomenon.Fil: Goette, Nora Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Glembotsky, Ana Claudia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Lev, Paola Roxana. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Grodzielski, Matías. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Contrufo, Geraldine. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Pierdominici, Marta S.. Departamento de Hematología, Hospital Ramos Mejía, Buenos Aires, Argentina; ArgentinaFil: Espasandin, Yesica Romina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Riveros, Dardo Alberto. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; ArgentinaFil: García, Alejandro Jorge. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; ArgentinaFil: Molinas, Felisa Concepción. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Heller, Paula Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; ArgentinaFil: Marta, Rosana Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Médicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Médicas; Argentin

    The European Network for Translational Research in Atrial Fibrillation (EUTRAF): objectives and initial results.

    Get PDF
    Atrial fibrillation (AF) is the most common sustained arrhythmia in the general population. As an age-related arrhythmia AF is becoming a huge socio-economic burden for European healthcare systems. Despite significant progress in our understanding of the pathophysiology of AF, therapeutic strategies for AF have not changed substantially and the major challenges in the management of AF are still unmet. This lack of progress may be related to the multifactorial pathogenesis of atrial remodelling and AF that hampers the identification of causative pathophysiological alterations in individual patients. Also, again new mechanisms have been identified and the relative contribution of these mechanisms still has to be established. In November 2010, the European Union launched the large collaborative project EUTRAF (European Network of Translational Research in Atrial Fibrillation) to address these challenges. The main aims of EUTRAF are to study the main mechanisms of initiation and perpetuation of AF, to identify the molecular alterations underlying atrial remodelling, to develop markers allowing to monitor this processes, and suggest strategies to treat AF based on insights in newly defined disease mechanisms. This article reports on the objectives, the structure, and initial results of this network

    Spillovers of Prosocial Motivation: Evidence from an Intervention Study on Blood Donors

    Get PDF
    Spillovers of prosocial motivation can enhance the provision of public goods, and have implications for the cost-benefit analysis of policy interventions. We analyze a large-scale intervention among dyads of pre- registered blood donors. A quasi-random phone call provides the instrument for identifying endogenous and exogenous social interaction. The phone call has a strong effect on the recipient's propensity to donate. Between 40% and 44% of that behavioral impulse is transmitted within dyads due to motivational spillovers. This creates a significant social multiplier to policy interventions, with estimates ranging between 1.6 and 1.8. There is no evidence for exogenous social interaction
    corecore