234 research outputs found

    Fine and Large Coulomb Diamonds in a Silicon Quantum Dot

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    We experimentally study the transport properties of silicon quantum dots (QDs) fabricated from a highly doped n-type silicon-on-insulator wafer. Low noise electrical measurements using a low temperature complementary metal-oxide-semiconductor (LTCMOS) amplifier are performed at 4.2 K in liquid helium. Two series of Coulomb peaks are observed: long-period oscillations and fine structures, and both of them show clear source drain voltage dependence. We also observe two series of Coulomb diamonds having different periodicity. The obtained experimental results are well reproduced by a master equation analysis using a model of double QDs coupled in parallel.Comment: 5 pages, 4 figures, to appear in Jpn. J. Appl. Phy

    AnoA: A Framework For Analyzing Anonymous Communication Protocols

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    Anonymous communication (AC) protocols such as the widely used Tor network have been designed to provide anonymity over the Internet to their participating users. While AC protocols have been the subject of several security and anonymity analyses in the last years, there still does not exist a framework for analyzing complex systems, such as Tor, and their different anonymity properties in a unified manner. In this work we present AnoA: a generic framework for defining, analyzing, and quantifying anonymity properties for AC protocols. In addition to quantifying the (additive) advantage of an adversary in an indistinguishability-based definition, AnoA uses a multiplicative factor, inspired from differential privacy. AnoA enables a unified quantitative analysis of well-established anonymity properties, such as sender anonymity, sender unlinkability, and relationship anonymity. AnoA modularly specifies adversarial capabilities by a simple wrapper-construction, called adversary classes. We examine the structure of these adversary classes and identify conditions under which it suffices to establish anonymity guarantees for single messages in order to derive guarantees for arbitrarily many messages. We coin this condition single-challenge reducability. This then leads us to the definition of Plug\u27n\u27Play adversary classes (PAC), which are easy to use, expressive, and single-challenge reducable. Additionally, we show that our framework is compatible with the universal composability (UC) framework. Leveraging a recent security proof about Tor, we illustrate how to apply AnoA to a simplified version of Tor against passive adversaries

    p45 NF-E2 regulates syncytiotrophoblast differentiation by post-translational GCM1 modifications in human intrauterine growth restriction

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    AbstractPlacental insufficiency jeopardizes prenatal development, potentially leading to intrauterine growth restriction (IUGR) and stillbirth. Surviving fetuses are at an increased risk for chronic diseases later in life. IUGR is closely linked with altered trophoblast and placental differentiation. However, due to a paucity of mechanistic insights, suitable biomarkers and specific therapies for IUGR are lacking. The transcription factor p45 NF-E2 (nuclear factor erythroid derived 2) has been recently found to regulate trophoblast differentiation in mice. The absence of p45 NF-E2 in trophoblast cells causes IUGR and placental insufficiency in mice, but mechanistic insights are incomplete and the relevance of p45 NF-E2 for human syncytiotrophoblast differentiation remains unknown. Here we show that p45 NF-E2 negatively regulates human syncytiotrophoblast differentiation and is associated with IUGR in humans. Expression of p45 NF-E2 is reduced in human placentae complicated with IUGR compared with healthy controls. Reduced p45 NF-E2 expression is associated with increased syncytiotrophoblast differentiation, enhanced glial cells missing-1 (GCM1) acetylation and GCM1 desumoylation in IUGR placentae. Induction of syncytiotrophoblast differentiation in BeWo and primary villous trophoblast cells with 8-bromo-adenosine 3′,5′-cyclic monophosphate (8-Br-cAMP) reduces p45 NF-E2 expression. Of note, p45 NF-E2 knockdown is sufficient to increase syncytiotrophoblast differentiation and GCM1 expression. Loss of p45 NF-E2 using either approach resulted in CBP-mediated GCM1 acetylation and SENP-mediated GCM1 desumoylation, demonstrating that p45 NF-E2 regulates post-translational modifications of GCM1. Functionally, reduced p45 NF-E2 expression is associated with increased cell death and caspase-3 activation in vitro and in placental tissues samples. Overexpression of p45 NF-E2 is sufficient to repress GCM1 expression, acetylation and desumoylation, even in 8-Br-cAMP exposed BeWo cells. These results suggest that p45 NF-E2 negatively regulates differentiation and apoptosis activation of human syncytiotrophoblast by modulating GCM1 acetylation and sumoylation. These studies identify a new pathomechanism related to IUGR in humans and thus provide new impetus for future studies aiming to identify new biomarkers and/or therapies of IUGR.</jats:p
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