2,681 research outputs found
An Energy-Efficient ECC Processor of UHF RFID Tag for Banknote Anti-Counterfeiting
In this paper, we present the design and analysis of an energy-efficient 163-b elliptic curve cryptographic (ECC) processor suitable for passive ultrahigh frequency (UHF) radio frequency identification (RFID) tags that are usable for banknote authentication and anti-counterfeiting. Even partial public key cryptographic functionality has long been thought to consume too much power and to be too slow to be usable in passive UHF RFID systems. Utilizing a low-power design strategy with optimized register file management and an architecture based on the López-Dahab Algorithm, we designed a low-power ECC processor that is used with a modified ECC-DH authentication protocol. The ECC-DH authentication protocol is compatible with the ISO/IEC 18000-63 (“Gen2”) passive UHF RFID protocol. The ECC processor requires 12 145 gate equivalents. The ECC processor consumes 5.04 nJ/b at a frequency of 960 kHz when implemented in a 0.13-μm standard CMOS process. The tag identity authentication function requires 30 600 cycles to complete all scalar multiplication operations. This size, speed, and power of the ECC processor makes it practical to use within a passive UHF RFID tag and achieve up to 1500 banknote authentications per minute, which is sufficient for use in the fastest banknote counting machines
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompaction
BACKGROUND: Defects of cytoarchitectural proteins can cause left ventricular noncompaction, which is often associated with conduction system diseases. We have previously identified a p.D117N mutation in the LIM domain-binding protein 3-encoding Z-band alternatively spliced PDZ motif gene (ZASP) in a patient with left ventricular noncompaction and conduction disturbances. We sought to investigate the role of p.D117N mutation in the LBD3 NM_001080114.1 isoform (ZASP1-D117N) for the regulation of cardiac sodium channel (Na(v)1.5) that plays an important role in the cardiac conduction system.
METHODS AND RESULTS: Effects of ZASP1-wild-type and ZASP1-D117N on Na(v)1.5 were studied in human embryonic kidney-293 cells and neonatal rat cardiomyocytes. Patch-clamp study demonstrated that ZASP1-D117N significantly attenuated I(Na) by 27% in human embryonic kidney-293 cells and by 32% in neonatal rat cardiomyocytes. In addition, ZASP1-D117N rightward shifted the voltage-dependent activation and inactivation in both systems. In silico simulation using Luo-Rudy phase 1 model demonstrated that altered Na(v)1.5 function can reduce cardiac conduction velocity by 28% compared with control. Pull-down assays showed that both wild-type and ZASP1-D117N can complex with Na(v)1.5 and telethonin/T-Cap, which required intact PDZ domains. Immunohistochemical staining in neonatal rat cardiomyocytes demonstrates that ZASP1-D117N did not significantly disturb the Z-line structure. Disruption of cytoskeletal networks with 5-iodonaphthalene-1-sulfonyl homopiperazine and cytochalasin D abolished the effects of ZASP1-D117N on Na(v)1.5.
CONCLUSIONS: ZASP1 can form protein complex with telethonin/T-Cap and Na(v)1.5. The left ventricular noncompaction-specific ZASP1 mutation can cause loss of function of Na(v)1.5, without significant alteration of the cytoskeletal protein complex. Our study suggests that electric remodeling can occur in left ventricular noncompaction subject because of a direct effect of mutant ZASP on Na(v)1.5
Measurement of the Inclusive Charm Cross Section at 4.03 GeV and 4.14 GeV
The cross section for charmed meson production at and 4.14
GeV has been measured with the Beijing Spectrometer. The measurement was made
using 22.3 of data collected at 4.03 GeV and 1.5
of data collected at 4.14 GeV. Inclusive observed cross sections for
the production of charged and neutral D mesons and momentum spectra are
presented. Observed cross sections were radiatively corrected to obtain tree
level cross sections. Measurements of the total hadronic cross section are
obtained from the charmed meson cross section and an extrapolation of results
from below the charm threshold.Comment: 11 pages, 13 figures. The top level tex file is paper.tex. It builds
the paper from other tex files in this .tar and the .eps file
Measurement of the Total Cross Section for Hadronic Production by e+e- Annihilation at Energies between 2.6-5 Gev
Using the upgraded Beijing Spectrometer (BESII), we have measured the total
cross section for annihilation into hadronic final states at
center-of-mass energies of 2.6, 3.2, 3.4, 3.55, 4.6 and 5.0 GeV. Values of ,
, are determined.Comment: Submitted to Phys. Rev. Let
Measurements of the Cross Section for e+e- -> hadrons at Center-of-Mass Energies from 2 to 5 GeV
We report values of for 85 center-of-mass energies between
2 and 5 GeV measured with the upgraded Beijing Spectrometer at the Beijing
Electron-Positron Collider.Comment: 5 pages, 3 figure
Study of the P-wave charmonium state \chi_{cJ} in \psi(2S) decays
The processes , and have been studied using a sample of produced
decays. We determine the total width of the to be
MeV. We present the first
measurement of the branching fraction , where the first error is statistical and the
second one systematic. Branching fractions of and
are also reported.Comment: 10 pages, revtex, 3 figures, 2 table
First Measurement of the Branching Fraction of the Decay psi(2S) --> tau tau
The branching fraction of the psi(2S) decay into tau pair has been measured
for the first time using the BES detector at the Beijing Electron-Positron
Collider. The result is ,
where the first error is statistical and the second is systematic. This value,
along with those for the branching fractions into e+e- and mu+mu of this
resonance, satisfy well the relation predicted by the sequential lepton
hypothesis. Combining all these values with the leptonic width of the resonance
the total width of the psi(2S) is determined to be keV.Comment: 9 pages, 2 figure
A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms
We describe a genetic variation map for the chicken genome containing 2.8 million single-nucleotide polymorphisms ( SNPs). This map is based on a comparison of the sequences of three domestic chicken breeds ( a broiler, a layer and a Chinese silkie) with that of their wild ancestor, red jungle fowl. Subsequent experiments indicate that at least 90% of the variant sites are true SNPs, and at least 70% are common SNPs that segregate in many domestic breeds. Mean nucleotide diversity is about five SNPs per kilobase for almost every possible comparison between red jungle fowl and domestic lines, between two different domestic lines, and within domestic lines - in contrast to the notion that domestic animals are highly inbred relative to their wild ancestors. In fact, most of the SNPs originated before domestication, and there is little evidence of selective sweeps for adaptive alleles on length scales greater than 100 kilobases
Pairing symmetry and properties of iron-based high temperature superconductors
Pairing symmetry is important to indentify the pairing mechanism. The
analysis becomes particularly timely and important for the newly discovered
iron-based multi-orbital superconductors. From group theory point of view we
classified all pairing matrices (in the orbital space) that carry irreducible
representations of the system. The quasiparticle gap falls into three
categories: full, nodal and gapless. The nodal-gap states show conventional
Volovik effect even for on-site pairing. The gapless states are odd in orbital
space, have a negative superfluid density and are therefore unstable. In
connection to experiments we proposed possible pairing states and implications
for the pairing mechanism.Comment: 4 pages, 1 table, 2 figures, polished versio
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