60 research outputs found
Unitary Fermi gas, epsilon expansion, and nonrelativistic conformal field theories
We review theoretical aspects of unitary Fermi gas (UFG), which has been
realized in ultracold atom experiments. We first introduce the epsilon
expansion technique based on a systematic expansion in terms of the
dimensionality of space. We apply this technique to compute the thermodynamic
quantities, the quasiparticle spectrum, and the critical temperature of UFG. We
then discuss consequences of the scale and conformal invariance of UFG. We
prove a correspondence between primary operators in nonrelativistic conformal
field theories and energy eigenstates in a harmonic potential. We use this
correspondence to compute energies of fermions at unitarity in a harmonic
potential. The scale and conformal invariance together with the general
coordinate invariance constrains the properties of UFG. We show the vanishing
bulk viscosities of UFG and derive the low-energy effective Lagrangian for the
superfluid UFG. Finally we propose other systems exhibiting the nonrelativistic
scaling and conformal symmetries that can be in principle realized in ultracold
atom experiments.Comment: 44 pages, 15 figures, contribution to Lecture Notes in Physics
"BCS-BEC crossover and the Unitary Fermi Gas" edited by W. Zwerge
A calculation of the QCD phase diagram at finite temperature, and baryon and isospin chemical potentials
We study the phases of a two-flavor Nambu-Jona-Lasinio model at finite
temperature , baryon and isospin chemical potentials:
, . This study
completes a previous analysis where only small isospin chemical potentials
were consideredComment: 21 pages, 13 figures included, two more refernces adde
Phase structures of strong coupling lattice QCD with finite baryon and isospin density
Quantum chromodynamics (QCD) at finite temperature (T), baryon chemical
potential (\muB) and isospin chemical potential (\muI) is studied in the strong
coupling limit on a lattice with staggered fermions. With the use of large
dimensional expansion and the mean field approximation, we derive an effective
action written in terms of the chiral condensate and pion condensate as a
function of T, \muB and \muI. The phase structure in the space of T and \muB is
elucidated, and simple analytical formulas for the critical line of the chiral
phase transition and the tricritical point are derived. The effects of a finite
quark mass (m) and finite \muI on the phase diagram are discussed. We also
investigate the phase structure in the space of T, \muI and m, and clarify the
correspondence between color SU(3) QCD with finite isospin density and color
SU(2) QCD with finite baryon density. Comparisons of our results with those
from recent Monte Carlo lattice simulations on finite density QCD are given.Comment: 18 pages, 6 figures, revtex4; some discussions are clarified, version
to appear in Phys. Rev.
Josephson current in s-wave superconductor / Sr_2RuO_4 junctions
The Josephson current between an s-wave and a spin-triplet superconductor
SrRuO (SRO) is studied theoretically. In spin-singlet / spin-triplet
superconductor junctions, there is no Josephson current proportional to in the absence of the spin-flip scattering near junction interfaces,
where is a phase-difference across junctions. Thus a dominant term of
the Josephson current is proportional to . The spin-orbit
scattering at the interfaces gives rise to the Josephson current proportional
to , which is a direct consequence of the chiral paring symmetry in
SRO
Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry.
BACKGROUND: The Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. METHODS AND RESULTS: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012-2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P < 0.001). Diabetes and coronary artery disease (CAD) were prevalent in 36.2% and 28.1% of patients as compared with global prevalence of 22.2% and 21.6%, respectively (P < 0.001 for both). Antiplatelet therapy was the most common antithrombotic treatment in India. With increasing stroke risk, however, patients were more likely to receive oral anticoagulant therapy [mainly vitamin K antagonist (VKA)], but average international normalized ratio (INR) was lower among Indian patients [median INR value 1.6 (interquartile range {IQR}: 1.3-2.3) versus 2.3 (IQR 1.8-2.8) (P < 0.001)]. Compared with other countries, patients from India had markedly higher rates of all-cause mortality [7.68 per 100 person-years (95% confidence interval 6.32-9.35) vs 4.34 (4.16-4.53), P < 0.0001], while rates of stroke/systemic embolism and major bleeding were lower after 1 year of follow-up. CONCLUSION: Compared to previously published registries from India, the GARFIELD-AF registry describes clinical profiles and outcomes in Indian patients with AF of a different etiology. The registry data show that compared to the rest of the world, Indian AF patients are younger in age and have more diabetes and CAD. Patients with a higher stroke risk are more likely to receive anticoagulation therapy with VKA but are underdosed compared with the global average in the GARFIELD-AF. CLINICAL TRIAL REGISTRATION-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362
Redesign of yeast Cu,Zn-superoxide dismutase: Probing the structure-function relationship and designing mimics of other metalloenzymes
57 Sequential Progression of Aberrant Methylation in Cancer-Related Genes in Various Stages of Human Hepatocarcinogenesis
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