333 research outputs found
Masses of ground and excited-state hadrons
We present the first Dyson-Schwinger equation calculation of the light hadron
spectrum that simultaneously correlates the masses of meson and baryon ground-
and excited-states within a single framework. At the core of our analysis is a
symmetry-preserving treatment of a vector-vector contact interaction. In
comparison with relevant quantities the
root-mean-square-relative-error/degree-of freedom is 13%. Notable amongst our
results is agreement between the computed baryon masses and the bare masses
employed in modern dynamical coupled-channels models of pion-nucleon reactions.
Our analysis provides insight into numerous aspects of baryon structure; e.g.,
relationships between the nucleon and Delta masses and those of the
dressed-quark and diquark correlations they contain.Comment: 25 pages, 7 figures, 4 table
Octet magnetic moments and the Coleman-Glashow sum rule violation in the chiral quark model
Baryon octet magnetic moments when calculated within the chiral quark model,
incorporating the orbital angular momentum as well as the quark sea
contribution through the Cheng-Li mechanism, not only show improvement over the
non relativistic quark model results but also gives a non zero value for the
right hand side of Coleman-Glashow sum rule. When effects due to spin-spin
forces between constituent quarks as well as `mass adjustments' due to
confinement are added, it leads to an excellent fit for the case of p,
\Sigma^+, \Xi^o and violation of Coleman-Glashow sum rule, whereas in almost
all the other cases the results are within 5% of the data.Comment: 5 RevTeX pages, accepted for publication in PRD(Rapid Communication
The Influence of an External Chromomagnetic Field on Color Superconductivity
We study the competition of quark-antiquark and diquark condensates under the
influence of an external chromomagnetic field modelling the gluon condensate
and in dependence on the chemical potential and temperature. As our results
indicate, an external chromomagnetic field might produce remarkable qualitative
changes in the picture of the color superconducting (CSC) phase formation. This
concerns, in particular, the possibility of a transition to the CSC phase and
diquark condensation at finite temperature.Comment: 27 pages, RevTex, 8 figures; the version accepted for the publication
in PRD (few references added; new numerical results added; main conclusions
are not changed
Search for the glueball candidates f0(1500) and fJ(1710) in gamma gamma collisions
Data taken with the ALEPH detector at LEP1 have been used to search for gamma
gamma production of the glueball candidates f0(1500) and fJ(1710) via their
decay to pi+pi-. No signal is observed and upper limits to the product of gamma
gamma width and pi+pi- branching ratio of the f0(1500) and the fJ(1710) have
been measured to be Gamma_(gamma gamma -> f0(1500)). BR(f0(1500)->pi+pi-) <
0.31 keV and Gamma_(gamma gamma -> fJ(1710)). BR(fJ(1710)->pi+pi-) < 0.55 keV
at 95% confidence level.Comment: 10 pages, 3 figure
Search for supersymmetry with a dominant R-parity violating LQDbar couplings in e+e- collisions at centre-of-mass energies of 130GeV to 172 GeV
A search for pair-production of supersymmetric particles under the assumption
that R-parity is violated via a dominant LQDbar coupling has been performed
using the data collected by ALEPH at centre-of-mass energies of 130-172 GeV.
The observed candidate events in the data are in agreement with the Standard
Model expectation. This result is translated into lower limits on the masses of
charginos, neutralinos, sleptons, sneutrinos and squarks. For instance, for
m_0=500 GeV/c^2 and tan(beta)=sqrt(2) charginos with masses smaller than 81
GeV/c^2 and neutralinos with masses smaller than 29 GeV/c^2 are excluded at the
95% confidence level for any generation structure of the LQDbar coupling.Comment: 32 pages, 30 figure
A Clinical Report of Bone Regeneration in Maxillofacial Surgery using Bonelike ® Synthetic Bone Graft
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus
Genome wide association studies (GWAS) for fasting glucose (FG) and insulin (FI) have identified common variant signals which explain 4.8% and 1.2% of trait variance, respectively. It is hypothesized that low-frequency and rare variants could contribute substantially to unexplained genetic variance. To test this, we analyzed exome-array data from up to 33,231 non-diabetic individuals of European ancestry. We found exome-wide significant (P<5×10-7) evidence for two loci not previously highlighted by common variant GWAS: GLP1R (p.Ala316Thr, minor allele frequency (MAF)=1.5%) influencing FG levels, and URB2 (p.Glu594Val, MAF = 0.1%) influencing FI levels. Coding variant associations can highlight potential effector genes at (non-coding) GWAS signals. At the G6PC2/ABCB11 locus, we identified multiple coding variants in G6PC2 (p.Val219Leu, p.His177Tyr, and p.Tyr207Ser) influencing FG levels, conditionally independent of each other and the non-coding GWAS signal. In vitro assays demonstrate that these associated coding alleles result in reduced protein abundance via proteasomal degradation, establishing G6PC2 as an effector gene at this locus. Reconciliation of single-variant associations and functional effects was only possible when haplotype phase was considered. In contrast to earlier reports suggesting that, paradoxically, glucose-raising alleles at this locus are protective against type 2 diabetes (T2D), the p.Val219Leu G6PC2 variant displayed a modest but directionally consistent association with T2D risk. Coding variant associations for glycemic traits in GWAS signals highlight PCSK1, RREB1, and ZHX3 as likely effector transcripts. These coding variant association signals do not have a major impact on the trait variance explained, but they do provide valuable biological insights
Baseline ‘state anxiety’ influences HPA-axis sensitivity to one sham-controlled HF-rTMS session applied to the right dorsolateral prefrontal cortex
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