30 research outputs found

    Instanton calculus and loop operator in supersymmetric gauge theory

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    We compute the one-point function of the glueball loop operator in the maximally confining phase of supersymmetric gauge theory using instanton calculus. In the maximally confining phase the residual symmetry is the diagonal U(1) subgroup and the localization formula implies that the chiral correlation functions are the sum of the contributions from each fixed point labeled by the Young diagram. The summation can be performed exactly by operator formalism of free fermions, which is also featured in the equivariant Gromov-Witten theory of P^1. By taking the Laplace transformation of the glueball loop operator, we find an exact agreement with the previous results for the generating function (resolvent) of the glueball one-point functions.journal articl

    磁気共鳴法を用いた特殊な場に存在する水の構造解析(第3報)

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    Search for D0-D̅0 Mixing in D0→K+π- Decays and Measurement of the Doubly-Cabibbo-Suppressed Decay Rate

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    MOESM11 of Genome-wide analysis of gene regulation mechanisms during Drosophila spermatogenesis

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    Additional file 11: Table 3. Interplay between meiosis arrest genes. tMAC does not affect the expression of genes encoding tTAFs. Can mutation results in reduced expression of topi, achi, and vis. Additionally, Can peaks are detectable in the immediate vicinity of TSSs of these genes

    MOESM17 of Genome-wide analysis of gene regulation mechanisms during Drosophila spermatogenesis

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    Additional file 17: Fig. 13. The dynamics of Mip40 binding during spermatogenesis, as assayed at varying levels of significance levels for Mip40 peak calling. The same groups of target genes are identified, as those shown in Fig. 5b. A The threshold for peak calling P > 10−3. B The threshold for peak calling P > 10−6.25

    MOESM6 of Genome-wide analysis of gene regulation mechanisms during Drosophila spermatogenesis

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    Additional file 6: Fig. 5. Averaged DamID profiles of Can, Comr, and Mip40 at the TSS of genes. The genes having the peaks of Can, Comr, and Mip40 within 1 kb around their TSS were selected. Then, for each coordinate within this area the normalized number of peaks was calculated. Ordinate–relative abundance of each protein. Black line represents the randomized set of peaks
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