Panebra, A., S.-X. Ma, L.-W. Zhai, X.-T. Wang, S. G. Rhee, and S. Khurana. Regulation of phospholipase C-g1 by the actin-regulatory protein villin. Am J Physiol Cell Physiol 281: C1046–C1058, 2001.—The actin-regulatory protein villin is tyrosine phosphorylated and associates with phospholipase C-g1 (PLC-g1) in the brush border of intestinal epithelial cells. To study the mechanism of villin-ass...

Given two graphs G1 and G2, the planar Ramsey number PR(G1, G2) is the smallest integer n such that every planar graph on n vertices either contains a copy of G1 or its complement contains a copy of G2. So far, the planar Ramsey numbers have been determined, when both, G1 and G2 are complete graphs or both are cycles. By combining computer search with some theoretical results, in this paper we ...

We prove that the strong product G1 G2 of G1 and G2 is Z3-flow contractible if and only if G1 G2 is not T K2, where T is a tree (we call T K2 a K4-tree). It follows that G1 G2 admits an NZ 3-flow unless G1 G2 is a K4-tree. We also give a constructive proof that yields a polynomial algorithm whose output is an NZ 3-flow if G1 G2 is not a K4-tree, and an NZ 4-flow otherwise. 2009 Wiley Periodical...

We discuss G smoothness conditions for rectangular and triangular Gregory patches. We then incorporate these G conditions into a surface fitting algorithm. Knowledge of the patch type is inconsequential to the formulation of the G conditions, hence the term agnostic G Gregory surfaces. 2012 Elsevier Inc. All rights reserved.

For locally compact groups Gi, i = 1, 2, · · · , n, let CB(G1, · · · , Gn) denote the Banach space of completely bounded multilinear forms on C0(G1)×· · ·×C0(Gn) in the completely bounded norm. CB(G1, · · · , Gn) has the structure of a Banach ∗-algebra under a multiplication and adjoint operation which agree with the convolution structure on the measure algebra M(G1 ×· · ·×Gn). If the Gi are al...

We apply the averaging method of first order to study maximum number limit cycles ordinary differential systems form ¨x + x = ε (f1(x, y)y f2 (x, y)) , ¨y y (g1(x, y)x g2 where f1(x, y) and g1(x, are real cubic polynomials; f2(x, g2(x, quadratic polynomials. Furthermore is a small parameter.

where Ni are known nonlinear functionals, g = (g1, · · · , gr) are unknown functions, and 2i iid ∼ N(0, σ) are random errors. Without loss of generality, we assume that r = 2. As in O’Sullivan (1990), we express design points x explicitly in the functional Ni: Ni(g1, g2) = η(g1, g2; xi), where η is a known nonlinear functional. In the following sections, η(g1, g2; x) is sometimes also represent...

Background: The combination of doxorubicin (DOX) with paclitaxel (PTX) effectively treats breast cancer (BC). However,DOX-associated cardiotoxicity (CTX) is aggravated by the use PTX. Consensus lacking about which drug sequence involves most CTX. Objectives: To evaluate whether DOX followed PXT or reverse has greatest cardiotoxic potential in treatment BC. Methods: Prospective study women prima...

Let α(G) and β(G) be the independent number and vertex covering number of G, respectively. The Kronecker Product G1 ⊗ G2 of graph of G1 and G2 has vertex set V (G1 ⊗ G2) = V (G1) × V (G2) and edge set E(G1 ⊗ G2) = {(u1v1)(u2v2)|u1u2 ∈ E(G1) and v1v2 ∈ E(G2)}. In this paper, let G is a simple graph with order p, we prove that, α(Km,n⊗G)= max {(m+n)α(G),p max{m,n}} and β(Km,n⊗G) =min {(m + n)β(G)...

Definitive identification of the species in the Burkholderia cepacia complex by routine clinical microbiology methods is difficult. Phenotypic tests to identify B. multivorans and B. vietnamiensis have been established; more recent work indicates B. stabilis may also be identified by growth characteristics and biochemical tests. However, attempts to identify genomovars I and III have, thus far,...