432 research outputs found
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
Gravitational radiation from gamma-ray bursts as observational opportunities for LIGO and VIRGO
Gamma-ray bursts are believed to originate in core-collapse of massive stars.
This produces an active nucleus containing a rapidly rotating Kerr black hole
surrounded by a uniformly magnetized torus represented by two counter-oriented
current rings. We quantify black hole spin-interactions with the torus and
charged particles along open magnetic flux-tubes subtended by the event
horizon. A major output of Egw=4e53 erg is radiated in gravitational waves of
frequency fgw=500 Hz by a quadrupole mass-moment in the torus. Consistent with
GRB-SNe, we find (i) Ts=90s (tens of s, Kouveliotou et al. 1993), (ii)
aspherical SNe of kinetic energy Esn=2e51 erg (2e51 erg in SN1998bw, Hoeflich
et al. 1999) and (iii) GRB-energies Egamma=2e50 erg (3e50erg in Frail et al.
2001). GRB-SNe occur perhaps about once a year within D=100Mpc. Correlating
LIGO/Virgo detectors enables searches for nearby events and their spectral
closure density 6e-9 around 250Hz in the stochastic background radiation in
gravitational waves. At current sensitivity, LIGO-Hanford may place an upper
bound around 150MSolar in GRB030329. Detection of Egw thus provides a method
for identifying Kerr black holes by calorimetry.Comment: to appear in PRD, 49
A role for XRCC2 gene polymorphisms in breast cancer risk and survival
Background
The XRCC2 gene is a key mediator in the homologous recombination repair of DNA double strand breaks. It is hypothesised that inherited variants in the XRCC2 gene might also affect susceptibility to, and survival from, breast cancer.
Methods
The study genotyped 12 XRCC2 tagging single nucleotide polymorphisms (SNPs) in 1131 breast cancer cases and 1148 controls from the Sheffield Breast Cancer Study (SBCS), and examined their associations with breast cancer risk and survival by estimating ORs and HRs, and their corresponding 95% CIs. Positive findings were further investigated in 860 cases and 869 controls from the Utah Breast Cancer Study (UBCS) and jointly analysed together with available published data for breast cancer risk. The survival findings were further confirmed in studies (8074 cases) from the Breast Cancer Association Consortium (BCAC).
Results
The most significant association with breast cancer risk in the SBCS dataset was the XRCC2 rs3218408 SNP (recessive model p=2.3×10−4, minor allele frequency (MAF)=0.23). This SNP yielded an ORrec of 1.64 (95% CI 1.25 to 2.16) in a two-site analysis of SBCS and UBCS, and a meta-ORrec of 1.33 (95% CI 1.12 to 1.57) when all published data were included. This SNP may mark a rare risk haplotype carried by two in 1000 of the control population. Furthermore, the XRCC2 coding R188H SNP (rs3218536, MAF=0.08) was significantly associated with poor survival, with an increased per-allele HR of 1.58 (95% CI 1.01 to 2.49) in a multivariate analysis. This effect was still evident in a pooled meta-analysis of 8781 breast cancer patients from the BCAC (HR 1.19, 95% CI 1.05 to 1.36; p=0.01).
Conclusions
These findings suggest that XRCC2 SNPs may influence breast cancer risk and survival
Nodulation, arbuscular mycorrhizal colonization and growth of some legumes native from Brazil
Tenure, gender and household structure
Starting with a review of recent literature on gender and housing, this paper goes on to develop a new theory of household structure, in which concepts of gender and generation play a key role. The utility of this theory is then demonstrated in the analysis of data from a survey of households in the City of Salford
Consumo e digestibilidade do feno de capim-braquiária em bovinos de corte sob suplementação com mistura contendo sulfato de amônio, caseína e uréia
The surface detector array of the Telescope Array experiment
The Telescope Array (TA) experiment, located in the western desert of
Utah,USA, is designed for observation of extensive air showers from extremely
high energy cosmic rays. The experiment has a surface detector array surrounded
by three fluorescence detectors to enable simultaneous detection of shower
particles at ground level and fluorescence photons along the shower track. The
TA surface detectors and fluorescence detectors started full hybrid observation
in March, 2008. In this article we describe the design and technical features
of the TA surface detector.Comment: 32 pages, 17 figure
New air fluorescence detectors employed in the Telescope Array experiment
Since 2007, the Telescope Array (TA) experiment, based in Utah, USA, has been
observing ultra high energy cosmic rays to understand their origins. The
experiment involves a surface detector (SD) array and three fluorescence
detector (FD) stations. FD stations, installed surrounding the SD array,
measure the air fluorescence light emitted from extensive air showers (EASs)
for precise determination of their energies and species. The detectors employed
at one of the three FD stations were relocated from the High Resolution Fly's
Eye experiment. At the other two stations, newly designed detectors were
constructed for the TA experiment. An FD consists of a primary mirror and a
camera equipped with photomultiplier tubes. To obtain the EAS parameters with
high accuracies, understanding the FD optical characteristics is important. In
this paper, we report the characteristics and installation of new FDs and the
performances of the FD components. The results of the monitored mirror
reflectance during the observation time are also described in this report.Comment: 44 pages, 23 figures, submitted to NIM-
Definition, aims, and implementation of GA2LEN/HAEi Angioedema Centers of Reference and Excellence
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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