1,288 research outputs found

    Scale Invariant O(g4)O(g^4) Lipatov Kernels at Non-Zero Momentum Transfer

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    We summarize recent work on the evaluation of the scale invariant next-to-leading order Lipatov kernel, constructed via transverse momentum diagrams. At zero momentum transfer the square of the leading-order kernel appears together with an additional component, now identified as a new partial-wave amplitude, having a separate, holomorphically factorizable, spectrum. We present a simplified expression for the full kernel at non-zero momentum transfer and give a complete analysis of its infrared properties. We also construct a non-forward extension of the new amplitude which is infra-red finite and satifies Ward identity constraints. We conjecture that this new kernel has the conformal invariance properties corresponding to the holomorphic factorization of the forward spectrum.Comment: 26 pages in latex, 4 uu-encoded ps-fig

    Frobenius Splittings

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    We give a gentle introduction to Frobenius splittings. Then we recall a few results that have been obtained with the method.Comment: 21 pages, typos correcte

    The ATF6-Met [67] Val substitution is associated with increased plasma cholesterol levels

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    Objective— Activating transcription factor 6 (ATF6) is a sensor of the endoplasmic reticulum stress response and regulates expression of several key lipogenic genes. We used a 2-stage design to investigate whether ATF6 polymorphisms are associated with lipids in subjects at increased risk for cardiovascular disease (CVD). Methods and Results— In stage 1, 13 tag-SNPs were tested for association in Dutch samples ascertained for familial combined hyperlipidemia (FCHL) or increased risk for CVD (CVR). In stage 2, we further investigated the SNP with the strongest association from stage 1, a Methionine/Valine substitution at amino-acid 67, in Finnish FCHL families and in subjects with CVR from METSIM, a Finnish population-based cohort. The combined analysis of both stages reached region-wide significance (P=9x10–4), but this association was not seen in the entire METSIM cohort. Our functional analysis demonstrated that Valine at position 67 augments ATF6 protein and its targets Grp78 and Grp94 as well as increases luciferase expression through Grp78 promoter. Conclusions— A common nonsynonymous variant in ATF6 increases ATF6 protein levels and is associated with cholesterol levels in subjects at increased risk for CVD, but this association was not seen in a population-based cohort. Further replication is needed to confirm the role of this variant in lipids. We report the association of the ATF6-methionine [67]valine amino-acid substitution with plasma cholesterol levels. Association analyses in 2674 subjects and functional data suggest that the ATF6 gene may influence cholesterol levels in subjects at increased risk to develop cardiovascular disease

    Two-Loop Polarization Contributions to Radiative-Recoil Corrections to Hyperfine Splitting in Muonium

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    We calculate radiative-recoil corrections of order α2(Zα)(m/M)EF\alpha^2(Z\alpha)(m/M)E_F to hyperfine splitting in muonium generated by the diagrams with electron and muon polarization loops. These corrections are enhanced by the large logarithm of the electron-muon mass ratio. The leading logarithm cubed and logarithm squared contributions were obtained a long time ago. The single-logarithmic and nonlogarithmic contributions calculated here improve the theory of hyperfine splitting, and affect the value of the electron-muon mass ratio extracted from the experimental data on the muonium hyperfine splitting.Comment: 15 pages, 11 figure

    Quantum Electrodynamics of the Helium Atom

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    Using singlet S states of the helium atom as an example, I describe precise calculation of energy levels in few-electron atoms. In particular, a complete set of effective operators is derived which generates O(m*alpha^6) relativistic and radiative corrections to the Schr"odinger energy. Average values of these operators can be calculated using a variational Schr"odinger wave function.Comment: 23 pages, revte

    The quotient Unimodular Vector group is nilpotent

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    Jose-Rao introduced and studied the Special Unimodular Vector group SUmr(R)SUm_r(R) and EUmr(R)EUm_r(R), its Elementary Unimodular Vector subgroup. They proved that for r2r \geq 2, EUmr(R)EUm_r(R) is a normal subgroup of SUmr(R)SUm_r(R). The Jose-Rao theorem says that the quotient Unimodular Vector group, SUmr(R)/EUmr(R)SUm_r(R)/EUm_r(R), for r2r \geq 2, is a subgroup of the orthogonal quotient group SO2(r+1)(R)/EO2(r+1)(R)SO_{2(r+1)}(R)/EO_{2(r + 1)}(R). The latter group is known to be nilpotent by the work of Hazrat-Vavilov, following methods of A. Bak; and so is the former. In this article we give a direct proof, following ideas of A. Bak, to show that the quotient Unimodular Vector group is nilpotent of class d=dim(R)\leq d = \dim(R). We also use the Quillen-Suslin theory, inspired by A. Bak's method, to prove that if R=A[X]R = A[X], with AA a local ring, then the quotient Unimodular Vector group is abelian

    Orientifolds and the Refined Topological String

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    We study refined topological string theory in the presence of orientifolds by counting second-quantized BPS states in M-theory. This leads us to propose a new integrality condition for both refined and unrefined topological strings when orientifolds are present. We define the SO(2N) refined Chern-Simons theory which computes refined open string amplitudes for branes wrapping Seifert three-manifolds. We use the SO(2N) refined Chern-Simons theory to compute new invariants of torus knots that generalize the Kauffman polynomials. At large N, the SO(2N) refined Chern-Simons theory on the three-sphere is dual to refined topological strings on an orientifold of the resolved conifold, generalizing the Gopakumar-Sinha-Vafa duality. Finally, we use the (2,0) theory to define and solve refined Chern-Simons theory for all ADE gauge groups

    Learning through social spaces: migrant women and lifelong learning in post-colonial London

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    This article shows how migrant women engage in learning through social spaces. It argues that such spaces are little recognised, and that there are multiple ways in which migrant women construct and negotiate their informal learning through socialising with other women in different informal modes. Additionally, the article shows how learning is shaped by the socio-political, geographical and multicultural context of living in London, outlining ways in which gendered and racialised identities shape, construct and constrain participation in lifelong learning. The article shows that one way in which migrant women resist (post)colonial constructions of difference is by engaging in informal and non-formal lifelong learning, arguing that the benefits are (at least) two-fold. The women develop skills (including language skills) but also use their informal learning to develop what is referred to in this article as 'relational capital'. The article concludes that informal lifelong learning developed through social spaces can enhance a sense of belonging for migrant women

    Male reproductive health and environmental xenoestrogens

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    EHP is a publication of the U.S. government. Publication of EHP lies in the public domain and is therefore without copyright. Research articles from EHP may be used freely; however, articles from the News section of EHP may contain photographs or figures copyrighted by other commercial organizations and individuals that may not be used without obtaining prior approval from both the EHP editors and the holder of the copyright. Use of any materials published in EHP should be acknowledged (for example, "Reproduced with permission from Environmental Health Perspectives") and a reference provided for the article from which the material was reproduced.Male reproductive health has deteriorated in many countries during the last few decades. In the 1990s, declining semen quality has been reported from Belgium, Denmark, France, and Great Britain. The incidence of testicular cancer has increased during the same time incidences of hypospadias and cryptorchidism also appear to be increasing. Similar reproductive problems occur in many wildlife species. There are marked geographic differences in the prevalence of male reproductive disorders. While the reasons for these differences are currently unknown, both clinical and laboratory research suggest that the adverse changes may be inter-related and have a common origin in fetal life or childhood. Exposure of the male fetus to supranormal levels of estrogens, such as diethlylstilbestrol, can result in the above-mentioned reproductive defects. The growing number of reports demonstrating that common environmental contaminants and natural factors possess estrogenic activity presents the working hypothesis that the adverse trends in male reproductive health may be, at least in part, associated with exposure to estrogenic or other hormonally active (e.g., antiandrogenic) environmental chemicals during fetal and childhood development. An extensive research program is needed to understand the extent of the problem, its underlying etiology, and the development of a strategy for prevention and intervention.Supported by EU Contract BMH4-CT96-0314
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