121 research outputs found
Quantum logic between atoms inside a high Q optical cavity
We propose a protocol for conditional quantum logic between two 4-state atoms
inside a high Q optical cavity. The process detailed in this paper utilizes a
direct 4-photon 2-atom resonant process and has the added advantage of commonly
addressing the two atoms when they are inside the high Q optical cavity.Comment: 8 pages, 3 figs. submitte
Quantum Interference in Superconducting Wire Networks and Josephson Junction Arrays: Analytical Approach based on Multiple-Loop Aharonov-Bohm Feynman Path-Integrals
We investigate analytically and numerically the mean-field
superconducting-normal phase boundaries of two-dimensional superconducting wire
networks and Josephson junction arrays immersed in a transverse magnetic field.
The geometries we consider include square, honeycomb, triangular, and kagome'
lattices. Our approach is based on an analytical study of multiple-loop
Aharonov-Bohm effects: the quantum interference between different electron
closed paths where each one of them encloses a net magnetic flux. Specifically,
we compute exactly the sums of magnetic phase factors, i.e., the lattice path
integrals, on all closed lattice paths of different lengths. A very large
number, e.g., up to for the square lattice, exact lattice path
integrals are obtained. Analytic results of these lattice path integrals then
enable us to obtain the resistive transition temperature as a continuous
function of the field. In particular, we can analyze measurable effects on the
superconducting transition temperature, , as a function of the magnetic
filed , originating from electron trajectories over loops of various
lengths. In addition to systematically deriving previously observed features,
and understanding the physical origin of the dips in as a result of
multiple-loop quantum interference effects, we also find novel results. In
particular, we explicitly derive the self-similarity in the phase diagram of
square networks. Our approach allows us to analyze the complex structure
present in the phase boundaries from the viewpoint of quantum interference
effects due to the electron motion on the underlying lattices.Comment: 18 PRB-type pages, plus 8 large figure
Application of the Hybrid-Maize model for limits to maize productivity analysis in a semiarid environment
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Decline in muscle strength with aging is an important predictor of health trajectory in the elderly. Several factors, including genetics, are proposed contributors to variability in muscle strength. To identify genetic contributors to muscle strength, a meta-analysis of genomewide association studies of handgrip was conducted. Grip strength was measured using a handheld dynamometer in 27 581 individuals of European descent over 65 years of age from 14 cohort studies. Genomewide association analysis was conducted on ~2.7 million imputed and genotyped variants (SNPs). Replication of the most significant findings was conducted using data from 6393 individuals from three cohorts. GWAS of lower body strength was also characterized in a subset of cohorts. Two genomewide significant (P-value< 5 × 10−8) and 39 suggestive (P-value< 5 × 10−5) associations were observed from meta-analysis of the discovery cohorts. After meta-analysis with replication cohorts, genomewide significant association was observed for rs752045 on chromosome 8 (β = 0.47, SE = 0.08, P-value = 5.20 × 10−10). This SNP is mapped to an intergenic region and is located within an accessible chromatin region (DNase hypersensitivity site) in skeletal muscle myotubes differentiated from the human skeletal muscle myoblasts cell line. This locus alters a binding motif of the CCAAT/enhancer-binding protein-β (CEBPB) that is implicated in muscle repair mechanisms. GWAS of lower body strength did not yield significant results. A common genetic variant in a chromosomal region that regulates myotube differentiation and muscle repair may contribute to variability in grip strength in the elderly. Further studies are needed to uncover the mechanisms that link this genetic variant with muscle strength
Genetic Sharing with Cardiovascular Disease Risk Factors and Diabetes Reveals Novel Bone Mineral Density Loci.
Bone Mineral Density (BMD) is a highly heritable trait, but genome-wide association studies have identified few genetic risk factors. Epidemiological studies suggest associations between BMD and several traits and diseases, but the nature of the suggestive comorbidity is still unknown. We used a novel genetic pleiotropy-informed conditional False Discovery Rate (FDR) method to identify single nucleotide polymorphisms (SNPs) associated with BMD by leveraging cardiovascular disease (CVD) associated disorders and metabolic traits. By conditioning on SNPs associated with the CVD-related phenotypes, type 1 diabetes, type 2 diabetes, systolic blood pressure, diastolic blood pressure, high density lipoprotein, low density lipoprotein, triglycerides and waist hip ratio, we identified 65 novel independent BMD loci (26 with femoral neck BMD and 47 with lumbar spine BMD) at conditional FDR < 0.01. Many of the loci were confirmed in genetic expression studies. Genes validated at the mRNA levels were characteristic for the osteoblast/osteocyte lineage, Wnt signaling pathway and bone metabolism. The results provide new insight into genetic mechanisms of variability in BMD, and a better understanding of the genetic underpinnings of clinical comorbidity
Long-range Angular Correlations On The Near And Away Side In P-pb Collisions At √snn=5.02 Tev
7191/Mar294
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Human longevity is heritable, but genome-wide association (GWA) studies have had limited success. Here, we perform two meta-analyses of GWA studies of a rigorous longevity phenotype definition including 11,262/3484 cases surviving at or beyond the age corresponding to the 90th/99th survival percentile, respectively, and 25,483 controls whose age at death or at last contact was at or below the age corresponding to the 60th survival percentile. Consistent with previous reports, rs429358 (apolipoprotein E (ApoE) ε4) is associated with lower odds of surviving to the 90th and 99th percentile age, while rs7412 (ApoE ε2) shows the opposite. Moreover, rs7676745, located near GPR78, associates with lower odds of surviving to the 90th percentile age. Gene-level association analysis reveals a role for tissue-specific expression of multiple genes in longevity. Finally, genetic correlation of the longevity GWA results with that of several disease-related phenotypes points to a shared genetic architecture between health and longevity
Magnetic field dependence of the surface resistance of superconducting tantalum at 35 Gc/s
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