Proof of the Double Bubble Conjecture in R^n

The least-area hypersurface enclosing and separating two given volumes in R^n is the standard double bubble.Comment: 20 pages, 22 figure

Saari's homographic conjecture for planar equal-mass three-body problem in Newton gravity

Saari's homographic conjecture in N-body problem under the Newton gravity is the following; configurational measure \mu=\sqrt{I}U, which is the product of square root of the moment of inertia I=(\sum m_k)^{-1}\sum m_i m_j r_{ij}^2 and the potential function U=\sum m_i m_j/r_{ij}, is constant if and only if the motion is homographic. Where m_k represents mass of body k and r_{ij} represents distance between bodies i and j. We prove this conjecture for planar equal-mass three-body problem. In this work, we use three sets of shape variables. In the first step, we use \zeta=3q_3/(2(q_2-q_1)) where q_k \in \mathbb{C} represents position of body k. Using r_1=r_{23}/r_{12} and r_2=r_{31}/r_{12} in intermediate step, we finally use \mu itself and \rho=I^{3/2}/(r_{12}r_{23}r_{31}). The shape variables \mu and \rho make our proof simple

Puzzles in BB physics

I discuss some puzzles observed in exclusive $B$ meson decays, concentrating on the large difference between the direct CP asymmetries in the $B^0\to \pi^\mp K^\pm$ and $B^\pm\to \pi^0 K^\pm$ modes, the large $B^0\to\pi^0\pi^0$ branching ratio, and the large deviation of the mixing-induced CP asymmetries in the $b\to sq\bar q$ penguins from those in the $b\to c\bar c s$ trees.Comment: 6 pages, 1 figure, talk presented at the 9th Workshop on High Energy Physics Phenomenology, Bhubaneswar, Orissa, India, Jan. 3-14, 2006; reference adde

Rigidity of minimal surfaces in S 3

Isometric deformations of compact minimal surfaces in the standard three-sphere are studied. It is shown that a given surface admits only finitely many noncongruent minimal immersions into S 3 with the same first fundamental form.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/46646/1/229_2005_Article_BF01258661.pd

Perturbative QCD factorization of πγ∗→γ(π)\pi \gamma^*\to \gamma(\pi) and B→γ(π)lνˉB\to \gamma(\pi)l\bar \nu

We prove factorization theorem for the processes $\pi\gamma^*\to\gamma$ and $\pi\gamma^*\to\pi$ to leading twist in the covariant gauge by means of the Ward identity. Soft divergences cancel and collinear divergences are grouped into a pion wave function defined by a nonlocal matrix element. The gauge invariance and universality of the pion wave function are confirmed. The proof is then extended to the exclusive $B$ meson decays $B\to\gamma l\bar\nu$ and $B\to\pi l\bar\nu$ in the heavy quark limit. It is shown that a light-cone $B$ meson wave function, though absorbing soft dynamics, can be defined in an appropriate frame. Factorization of the $B\to\pi l\bar\nu$ decay in $k_T$ space, $k_T$ being parton transverse momenta, is briefly discussed. We comment on the extraction of the leading-twist pion wave function from experimental data.Comment: 21 pages in Latex file, version to appear in Phys. Rev.

Procjena cito-/genotoksičnosti irinotekana u V79-stanicama primjenom komet-testa, mikronukleus-testa i testa kromosomskih aberacija

Irinotecan is a topoisomerase I interactive agent, widely used in the treatment of metastatic colorectal cancer. The genotoxic effects of the maximum single dose (18 μg mL-1), recommended monotherapy dose (9 μg mL-1), and recommended combined therapy dose (4.5 μg mL-1) of irinotecan were studied on V79 cells using the comet assay, chromosome aberration assay, and micronucleus test. The cells were treated with irinotecan for 2 h or 24 h. The statistical signifi cance of the results was determined using the one-way ANOVA test and a nonparametric Mann Whitney U test. The comet assay did not show dose-dependent or time-dependent effects. The chromosome aberration analysis showed large DNA rearrangements, i.e., chromosome exchanges. Although the exposed cultures showed a signifi cant increase in micronucleated cells in respect to control, no dose-dependent relation was established among the treated cultures. Timedependent effect was also not observed.Irinotekan je citotoksični lijek koji inhibira enzim DNA-topoizomerazu I. U širokoj je primjeni u terapiji metastatskog karcinoma kolona i rektuma. U uvjetima in vitro primjenom komet-testa, analize kromosomskih aberacija i mikronukleus-testa na V79-stanicama istražili smo genotoksični učinak maksimalne pojedinačne doze (18 μg mL-1), preporučene monoterapijske doze (9 μg mL-1) i preporučene doze irinotekana za kombiniranu terapiju (4,5 μg mL-1). Kulture stanica bile su tretirane irinotekanom 2 h i 24 h. Statistička značajnost određivana je jednosmjernim ANOVA-testom i neparametrijskim Mann Whitneyevim U-testom. Komet-testom nije utvrđen učinak koncentracije i/ili vremena izloženosti. Analiza kromosomskih aberacija pokazala je prisutnost izmjena kromatida, tj. porast broja triradijusa i tetraradijusa. Iako je u kulturama stanica izloženi irinotekanu opažen značajan porast broja mikronukleusa u odnosu na kontrolu, nije uočena ovisnost o dozi lijeka ni o vremenu izloženosti u opisanim eksperimentalnim uvjetima. Dobiveni rezultati upućuju na genotoksičnost irinotekana za V79-stanice. Nijednom od primijenjenih metoda nije utvrđena ovisnost učinka irinotekana o vremenu ili dozi