From the Cooper problem to canted supersolids in Bose-Fermi mixtures

We calculate the phase diagram of the Bose-Fermi Hubbard model on the 3d cubic lattice at fermionic half filling and bosonic unit filling by means of single-site dynamical mean-field theory. For fast bosons, this is equivalent to the Cooper problem in which the bosons can induce s-wave pairing between the fermions. We also find miscible superfluid and canted supersolid phases depending on the interspecies coupling strength. In contrast, slow bosons favor fermionic charge density wave structures for attractive fermionic interactions. These competing instabilities lead to a rich phase diagram within reach of cold gas experiments.Comment: 5 pages, 4 figures; replaced with published versio

Regularization of Diagrammatic Series with Zero Convergence Radius

The divergence of perturbative expansions for the vast majority of macroscopic systems, which follows from Dyson's collapse argument, prevents Feynman's diagrammatic technique from being directly used for controllable studies of strongly interacting systems. We show how the problem of divergence can be solved by replacing the original model with a convergent sequence of successive approximations which have a convergent perturbative series. As a prototypical model, we consider the zero-dimensional $\vert \psi \vert^4$ theory.Comment: 4 pages, 3 figure

Dynamical mean field solution of the Bose-Hubbard model

We present the effective action and self-consistency equations for the bosonic dynamical mean field (B-DMFT) approximation to the bosonic Hubbard model and show that it provides remarkably accurate phase diagrams and correlation functions. To solve the bosonic dynamical mean field equations we use a continuous-time Monte Carlo method for bosonic impurity models based on a diagrammatic expansion in the hybridization and condensate coupling. This method is readily generalized to bosonic mixtures, spinful bosons, and Bose-Fermi mixtures.Comment: 10 pages, 3 figures. includes supplementary materia

Bosons Confined in Optical Lattices: the Numerical Renormalization Group revisited

A Bose-Hubbard model, describing bosons in a harmonic trap with a superimposed optical lattice, is studied using a fast and accurate variational technique (MF+NRG): the Gutzwiller mean-field (MF) ansatz is combined with a Numerical Renormalization Group (NRG) procedure in order to improve on both. Results are presented for one, two and three dimensions, with particular attention to the experimentally accessible momentum distribution and possible satellite peaks in this distribution. In one dimension, a comparison is made with exact results obtained using Stochastich Series Expansion.Comment: 10 pages, 15 figure

A randomised, double-blind, double-dummy comparative study of gatifloxacin with clarithromycin in the treatment of community-acquired pneumonia

ABSTRACTEligible patients were randomised in this multicentre, randomised, double-blind, double-dummy parallel-group study in a ratio of 1:1 to either gatifloxacin 400 mg once-daily for 5–14 days plus matching placebo, or clarithromycin 500 mg twice-daily for 5–14 days. The primary outcome measure was clinical response (clinical cure plus improvement) at the end of treatment. Secondary endpoints were clinical response at end of study, clinical cure at end of treatment and end of study, bacteriological response at end of treatment and end of study, and treatment duration. The overall clinical response was similar in the two treatment groups, with 92.2% of gatifloxacin-treated patients cured or improved at the end of treatment, compared with 93.1% of those receiving clarithromycin. Corresponding bacteriological response rates (eradication plus presumed eradication) were 96.7% and 87.5%, respectively. The study drugs were well-tolerated, with nausea (gatifloxacin) and bitter taste (clarithromycin) being the only treatment-related adverse events with a frequency of >5%. No patients experienced phototoxicity, hepatic or renal dysfunction, tendonitis or crystalluria. Oral gatifloxacin 400 mg once-daily appeared to be a safe and effective alternative to clarithromycin in the treatment of community-acquired pneumonia

How does an interacting many-body system tunnel through a potential barrier to open space?

The tunneling process in a many-body system is a phenomenon which lies at the very heart of quantum mechanics. It appears in nature in the form of alpha-decay, fusion and fission in nuclear physics, photoassociation and photodissociation in biology and chemistry. A detailed theoretical description of the decay process in these systems is a very cumbersome problem, either because of very complicated or even unknown interparticle interactions or due to a large number of constitutent particles. In this work, we theoretically study the phenomenon of quantum many-body tunneling in a more transparent and controllable physical system, in an ultracold atomic gas. We analyze a full, numerically exact many-body solution of the Schr\"odinger equation of a one-dimensional system with repulsive interactions tunneling to open space. We show how the emitted particles dissociate or fragment from the trapped and coherent source of bosons: the overall many-particle decay process is a quantum interference of single-particle tunneling processes emerging from sources with different particle numbers taking place simultaneously. The close relation to atom lasers and ionization processes allows us to unveil the great relevance of many-body correlations between the emitted and trapped fractions of the wavefunction in the respective processes.Comment: 18 pages, 4 figures (7 pages, 2 figures supplementary information

Expanding perfect fluid generalizations of the C-metric

We reexamine Petrov type D gravitational fields generated by a perfect fluid with spatially homogeneous energy density and in which the flow lines form a timelike non-shearing and non-rotating congruence. It is shown that the anisotropic such spacetimes, which comprise the vacuum C-metric as a limit case, can have \emph{non-zero} expansion, contrary to the conclusion in the original investigation by Barnes (Gen. Rel. Grav. 4, 105 (1973)). This class consists of cosmological models with generically one and at most two Killing vectors. We construct their line element and discuss some important properties. The methods used in this investigation incite to deduce testable criteria regarding shearfree normality and staticity op Petrov type $D$ spacetimes in general, which we add in an appendix.Comment: 16 pages, extended and amended versio

Relation between telomerase activity, hTERT and telomere length for intracranial tumours

Human linear chromosomes are capped by specialized DNA-protein structures called telomeres. The present study analysed the telomerase activity, hTERT protein and telomere length in meningiomas and gliomas in relation to their WHO grading. Fifty-three freshly dissected tumour biopsies were analysed for telomerase activity, hTERT protein expression and telomere length. Telomerase activity was examined in 41 of the 53 biopsies. Telomerase activity was detected in 3 of 35 (8.6%) screened meningiomas (I benign, 1 atypical and I malignant meningioma). For hTERT expression, 56.4% of meningiomas were positive with a mean labelling index (hTERT LI) of 31.3% (SD=26.5) for the hTERT positive meningiomas. The mean telomere length for meningiomas was 6.983 kb (SD=1.969). For gliomas, no active telomerase was detected in 2 low-grade astrocytomas, whereas three of the four screened glioblastomas were positive for telomerase activity. The only hTERT protein positive astrocytoma had a mean labelling index of 9.0%. On the other hand, the hTERT LI for glioblastomas was 53.6% (SD=28.0). The two low-grade astrocytomas had a telomere length of 14.310 and 9.236 kb. The anaplastic astrocytoma had a telomere length of 4.903 kb and the glioblastomas 5.767 kb (SD=2.042). The normal meningeal and neuronal tissue is negative for telomerase activity and hTERT. The length was +/- 10.000 kb. These results indicate that telomere shortening may be a critical step in pathogenesis of atypical and malignant meningiomas and gliomas. Critical telomere shortening in vitro was shown to activate telomerase

Dynamical mean-field theory for bosons

We discuss the recently developed bosonic dynamical mean-field (B-DMFT) framework, which maps a bosonic lattice model onto the selfconsistent solution of a bosonic impurity model with coupling to a reservoir of normal and condensed bosons. The effective impurity action is derived in several ways: (i) as an approximation to the kinetic energy functional of the lattice problem, (ii) using a cavity approach, and (iii) by using an effective medium approach based on adding a one-loop correction to the selfconsistently defined condensate. To solve the impurity problem, we use a continuous-time Monte Carlo algorithm based on a sampling of a perturbation expansion in the hybridization functions and the condensate wave function. As applications of the formalism we present finite temperature B-DMFT phase diagrams for the bosonic Hubbard model on a 3d cubic and 2d square lattice, the condensate order parameter as a function of chemical potential, critical exponents for the condensate, the approach to the weakly interacting Bose gas regime for weak repulsions, and the kinetic energy as a function of temperature.Comment: 26 pages, 19 figure

Immunotherapy for neuroblastoma using syngeneic fibroblasts transfected with IL-2 and IL-12

Cytokine-modified tumour cells have been used in clinical trials for immunotherapy of neuroblastoma, but primary tumour cells from surgical biopsies are difficult to culture. Autologous fibroblasts, however, are straightforward to manipulate in culture and easy to transfect using nonviral or viral vectors. Here we have compared the antitumour effect of fibroblasts and tumour cells transfected ex vivo to coexpress interleukin-2 (IL-2) and IL-12 in a syngeneic mouse model of neuroblastoma. Coinjection of cytokine-modified fibroblasts with Neuro-2A tumour cells abolished their in vivo tumorigenicity. Treatment of established tumours with three intratumoral doses of transfected fibroblasts showed a significant therapeutic effect with reduced growth or complete eradication of tumours in 90% of mice, associated with extensive leukocyte infiltration. Splenocytes recovered from vaccinated mice showed enhanced IL-2 production following Neuro-2A coculture, and increased cytotoxicity against Neuro-2A targets compared with controls. Furthermore, 100% of the tumour-free mice exhibited immune memory against tumour cells when rechallenged three months later. The potency of transfected fibroblasts was equivalent to that of tumour cells in all experiments. We conclude that syngeneic fibroblasts cotransfected with IL-2 and IL-12 mediate therapeutic effects against established disease, and are capable of generating immunological memory. Furthermore, as they are easier to recover and manipulate than autologous tumour cells, fibroblasts provide an attractive alternative immunotherapeutic strategy for the treatment of neuroblastoma