Drinfel'd Realization of Quantum Affine Superalgebra Uq(gl(1∣1))^U_q\hat{(gl(1|1))}

We obtain Drinfel'd's realization of quantum affine superalgebra $U_q\hat{(gl(1|1))}$ based on the super version of RS construction method and Gauss decomposition

Comments on Drinfeld Realization of Quantum Affine Superalgebra Uq[gl(m∣n)(1)]U_q[gl(m|n)^{(1)}] and its Hopf Algebra Structure

By generalizing the Reshetikhin and Semenov-Tian-Shansky construction to supersymmetric cases, we obtain Drinfeld current realization for quantum affine superalgebra $U_q[gl(m|n)^{(1)}]$. We find a simple coproduct for the quantum current generators and establish the Hopf algebra structure of this super current algebra.Comment: Some errors and misprints corrected and a remark in section 4 removed. 12 pages, Latex fil

Elliptic flow of ϕ\phi meson and strange quark collectivity at RHIC

Based on A Multi-Phase Transport (AMPT) model, we have studied the elliptic flow $v_{2}$ of $\phi$ mesons from reconstructed $K^{+}K^{-}$ decay channel at the top Relativistic Heavy Ion Collider energy at Brookhaven National Laboratory. The dependences of $v_{2}$ on transverse momentum $p_T$ and collision centrality are presented and the rescattering effect of $\phi$ mesons in the hadronic phase is also investigated. The results show that experimental measurement of $v_{2}$ for $\phi$ mesons can retain the early collision information before $\phi$ decays and that the $\phi$ $v_2$ value obeys the constituent quark number scaling which has been observed for other mesons and baryons. Our study indicates that the $\phi$ $v_2$ mostly reflects partonic level collectivity developed during the early stage of the nucleus-nucleus collision and the strange and light up/down quarks have developed similar angular anistropy properties at the hadronization.Comment: 5 pages and 5 figures; accepted by Physical Review

Single-cell transcriptomes reveal the mechanism for a breast cancer prognostic gene panel.

The clinical benefits of the MammaPrint® signature for breast cancer is well documented; however, how these genes are related to cell cycle perturbation have not been well determined. Our single-cell transcriptome mapping (algorithm) provides details into the fine perturbation of all individual genes during a cell cycle, providing a view of the cell-cycle-phase specific landscape of any given human genes. Specifically, we identified that 38 out of the 70 (54%) MammaPrint® signature genes are perturbated to a specific phase of the cell cycle. The MammaPrint® signature panel derived its clinical prognosis power from measuring the cell cycle activity of specific breast cancer samples. Such cell cycle phase index of the MammaPrint® signature suggested that measurement of the cell cycle index from tumors could be developed into a prognosis tool for various types of cancer beyond breast cancer, potentially improving therapy through targeting a specific phase of the cell cycle of cancer cells