324 research outputs found
Entangling power and operator entanglement in qudit systems
We establish the entangling power of a unitary operator on a general
finite-dimensional bipartite quantum system with and without ancillas, and give
relations between the entangling power based on the von Neumann entropy and the
entangling power based on the linear entropy. Significantly, we demonstrate
that the entangling power of a general controlled unitary operator acting on
two equal-dimensional qudits is proportional to the corresponding operator
entanglement if linear entropy is adopted as the quantity representing the
degree of entanglement. We discuss the entangling power and operator
entanglement of three representative quantum gates on qudits: the SUM, double
SUM, and SWAP gates.Comment: 8 pages, 1 figure. Version 3: Figure was improved and the MS was a
bit shortene
Strongly focused light beams interacting with single atoms in free space
We construct 3-D solutions of Maxwell's equations that describe Gaussian
light beams focused by a strong lens. We investigate the interaction of such
beams with single atoms in free space and the interplay between angular and
quantum properties of the scattered radiation. We compare the exact results
with those obtained with paraxial light beams and from a standard input-output
formalism. We put our results in the context of quantum information processing
with single atoms.Comment: 9 pages, 9 figure
Holonomic quantum gates: A semiconductor-based implementation
We propose an implementation of holonomic (geometrical) quantum gates by
means of semiconductor nanostructures. Our quantum hardware consists of
semiconductor macroatoms driven by sequences of ultrafast laser pulses ({\it
all optical control}). Our logical bits are Coulomb-correlated electron-hole
pairs (excitons) in a four-level scheme selectively addressed by laser pulses
with different polarization. A universal set of single and two-qubit gates is
generated by adiabatic change of the Rabi frequencies of the lasers and by
exploiting the dipole coupling between excitons.Comment: 10 Pages LaTeX, 10 Figures include
Entanglement capability of self-inverse Hamiltonian evolution
We determine the entanglement capability of self-inverse Hamiltonian
evolution, which reduces to the known result for Ising Hamiltonian, and
identify optimal input states for yielding the maximal entanglement rate. We
introduce the concept of the operator entanglement rate, and find that the
maximal operator entanglement rate gives a lower bound on the entanglement
capability of a general Hamiltonian.Comment: 4 pages, no figures. Version 3: small change
Universal quantum gates based on a pair of orthogonal cyclic states: Application to NMR systems
We propose an experimentally feasible scheme to achieve quantum computation
based on a pair of orthogonal cyclic states. In this scheme, quantum gates can
be implemented based on the total phase accumulated in cyclic evolutions. In
particular, geometric quantum computation may be achieved by eliminating the
dynamic phase accumulated in the whole evolution. Therefore, both dynamic and
geometric operations for quantum computation are workable in the present
theory. Physical implementation of this set of gates is designed for NMR
systems. Also interestingly, we show that a set of universal geometric quantum
gates in NMR systems may be realized in one cycle by simply choosing specific
parameters of the external rotating magnetic fields. In addition, we
demonstrate explicitly a multiloop method to remove the dynamic phase in
geometric quantum gates. Our results may provide useful information for the
experimental implementation of quantum logical gates.Comment: 9 pages, language revised, the publication versio
Adiabatic evolution of a coupled-qubit Hamiltonian
We present a general method for studying coupled qubits driven by
adiabatically changing external parameters. Extended calculations are provided
for a two-bit Hamiltonian whose eigenstates can be used as logical states for a
quantum CNOT gate. From a numerical analysis of the stationary Schroedinger
equation we find a set of parameters suitable for representing CNOT, while from
a time-dependent study the conditions for adiabatic evolution are determined.
Specializing to a concrete physical system involving SQUIDs, we determine
reasonable parameters for experimental purposes. The dissipation for SQUIDs is
discussed by fitting experimental data. The low dissipation obtained supports
the idea that adiabatic operations could be performed on a time scale shorter
than the decoherence time.Comment: 10 pages, 4 figures, to be pub.in Phys Rev
Mutation update for the SATB2 gene
SATB2-associated syndrome (SAS) is an autosomal dominant neurodevelopmental disorder caused by alterations in the SATB2 gene. Here we present a review of published pathogenic variants in the SATB2 gene to date and report 38 novel alterations found in 57 additional previously unreported individuals. Overall, we present a compilation of 120 unique variants identified in 155 unrelated families ranging from single nucleotide coding variants to genomic rearrangements distributed throughout the entire coding region of SATB2. Single nucleotide variants predicted to result in the occurrence of a premature stop codon were the most commonly seen (51/120=42.5%) followed by missense variants (31/120=25.8%). We review the rather limited functional characterization of pathogenic variants and discuss current understanding of the consequences of the different molecular alterations. We present an expansive phenotypic review along with novel genotype-phenotype correlations. Lastly, we discuss current knowledge on animal models and present future prospects. This review should help provide better guidance for the care of individuals diagnosed with SAS
Psychosocial Treatment of Children in Foster Care: A Review
A substantial number of children in foster care exhibit psychiatric difficulties. Recent epidemiologi-cal and historical trends in foster care, clinical findings about the adjustment of children in foster care, and adult outcomes are reviewed, followed by a description of current approaches to treatment and extant empirical support. Available interventions for these children can be categorized as either symptom-focused or systemic, with empirical support for specific methods ranging from scant to substantial. Even with treatment, behavioral and emotional problems often persist into adulthood, resulting in poor functional outcomes. We suggest that self-regulation may be an important mediat-ing factor in the appearance of emotional and behavioral disturbance in these children
AD51B in Familial Breast Cancer
Common variation on 14q24.1, close to RAD51B, has been associated with breast cancer: rs999737 and rs2588809 with the risk of female breast cancer and rs1314913 with the risk of male breast cancer. The aim of this study was to investigate the role of RAD51B variants in breast cancer predisposition, particularly in the context of familial breast cancer in Finland. We sequenced the coding region of RAD51B in 168 Finnish breast cancer patients from the Helsinki region for identification of possible recurrent founder mutations. In addition, we studied the known rs999737, rs2588809, and rs1314913 SNPs and RAD51B haplotypes in 44,791 breast cancer cases and 43,583 controls from 40 studies participating in the Breast Cancer Association Consortium (BCAC) that were genotyped on a custom chip (iCOGS). We identified one putatively pathogenic missense mutation c.541C>T among the Finnish cancer patients and subsequently genotyped the mutation in additional breast cancer cases (n = 5259) and population controls (n = 3586) from Finland and Belarus. No significant association with breast cancer risk was seen in the meta-analysis of the Finnish datasets or in the large BCAC dataset. The association with previously identified risk variants rs999737, rs2588809, and rs1314913 was replicated among all breast cancer cases and also among familial cases in the BCAC dataset. The most significant association was observed for the haplotype carrying the risk-alleles of all the three SNPs both among all cases (odds ratio (OR): 1.15, 95% confidence interval (CI): 1.11–1.19, P = 8.88 x 10−16) and among familial cases (OR: 1.24, 95% CI: 1.16–1.32, P = 6.19 x 10−11), compared to the haplotype with the respective protective alleles. Our results suggest that loss-of-function mutations in RAD51B are rare, but common variation at the RAD51B region is significantly associated with familial breast cancer risk
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