Exact out-of-time-ordered correlation functions for an interacting lattice fermion model

Exact solutions for local equilibrium and nonequilibrium out-of-time-ordered correlation (OTOC) functions are obtained for a lattice fermion model with on-site interactions, namely, the Falicov-Kimball (FK) model, in the large dimensional and thermodynamic limit. Our approach is based on the nonequilibrium dynamical mean-field theory generalized to an extended Kadanoff-Baym contour. We find that the density-density OTOC is most enhanced at intermediate coupling around the metal-insulator phase transition. In the high-temperature limit, the OTOC remains nontrivially finite and interaction dependent, even though dynamical charge correlations probed by an ordinary response function are completely suppressed. We propose an experiment to measure OTOCs of fermionic lattice systems including the FK and Hubbard models in ultracold atomic systems

CIT-5: a high-silica zeolite with 14-ring pores

The synthesis and structure of a new zeolite, CIT-5 (California Institute of Technology Number Five), is described, which possesses one-dimensional pores comprised of 14 T-atoms (tetrahedrally coordinated silicon or aluminium atoms)

Collective Excitations and Nonequilibrium Phase Transition in Dissipative Fermionic Superfluids

We predict a new mechanism to induce collective excitations of a fermionic superfluid via sudden switch-on of two-body loss, for which we extend the BCS theory to fully incorporate quantum jumps. We find that such dissipation induces an amplitude oscillation of the superfluid order parameter accompanied by chirped phase rotation, which highlights the role of dissipation in a superfluid as a consequence of particle loss. We demonstrate that when the dissipation is introduced to one of the two superfluids coupled via a Josephson junction, it gives rise to a relative-phase mode analogous to the Leggett mode, which can be detected from time evolution of the Josephson current. We find that the coupled system exhibits a nonequilibrium dissipative phase transition characterized by the vanishing dc Josephson current. The dissipation-induced collective modes can be realized with ultracold fermionic atoms undergoing inelastic collisions.Comment: 13 pages, 7 figure

Survival simulation of hepatocellular carcinoma derived from follow-up studies of 450 patients.

A simulation model to predict the survival probability of individual patients with hepatocellular carcinoma (HCC) after therapy was derived from the results of various therapies and follow-up studies of 450 HCC patients. Twenty-two prognostically important variables were analyzed by Cox's proportional hazards model. The 9 significant variables that were extracted were used to build the simulation. In this model, S(t), the expected estimated survival rate for individual patient at time t (month), is calculated by the following equation: S(t) = (exp (-0.03655t) (exp [0.9479 ([portal vein invasion]-0.222) + 0.3846 ([tumor number]-2.00) + 0.2578 ([tumor size]-3.231) + 0.0742 ([loge AFP]-5.647) + 0.8184 ([metastasis]-0.036) + 0.2810 ([Child's class]-1.689)-0.7088 ([transcatheter arterial embolization]-0.578)-0.9746 ([percutaneous ethanol injection]-0.153)-0.5377 ([hepatectomy]-0.109)]) The validity of the model was assessed using a split-sample technique. This paper does not discuss the superiority or inferiority of the therapies, because some selection bias for prognostic factors among the therapies can not be completely excluded. But this model is proposed as a practical model to predict the survival of patients with HCC.</p

Biologic markers in prostatic intraepithelial neoplasia: immunohistochemical and cytogenetic analyses

Objective:We evaluated the biological properties of High-grade prostatic intraepithelial neoplasia (PIN) by immunohistochemistry and fluorescence in situ hybridization (FISH) analysis in relation to normal tissue and carcinoma lesions. Materials and Methods:Immunohistochemical staining and FISH were performed on23formalin-fixed radical prostatectomy specimens taken from patients with PIN. Assays were performed using MIB-1, chromogranin A (CGA) and an anti-androgen receptor antibody (AR). A centromere probe for chromosome8was used to test for aneuploidy. Results:The MIB-1index of cancerous specimens (16.2±10.5%) was significantly higher than that of benign (1.9±1.6%, p<0.0001) or PIN (4.0±4.5%, p<0.0001) specimens. The percentage of CGA positive cells was significantly lower in normal tissue (1.2±1.8%) than in PIN (3.5±2.9%, p=0.012) or carcinoma (5.4±4.9%, p=0.005) lesions. Positive staining for AR was consistently observed in the nuclei of both benign and malignant epithelial cells, but positive cytoplasmic staining was also seen in PIN epithelial cells. No significant difference in FISH detected anomalies were found between PIN and carcinoma specimens. Conclusions:Our studies concerning proliferative activity, NE differentiation and chromosomal anomalies of prostatic specimens support the hypothesis that PIN is a biologically intermediate stage in the pathogenesis of prostatic carcinoma. The cellular distribution of AR was altered in PIN cells, but the role of AR in PIN is not yet clear