828 research outputs found
Proving AGT conjecture as HS duality: extension to five dimensions
We extend the proof from arXiv:1012.3137, which interprets the AGT relation
as the Hubbard-Stratonovich duality relation to the case of 5d gauge theories.
This involves an additional q-deformation. Not surprisingly, the extension
turns out to be trivial: it is enough to substitute all relevant numbers by
q-numbers in all the formulas, Dotsenko-Fateev integrals by the Jackson sums
and the Jack polynomials by the MacDonald ones. The problem with extra poles in
individual Nekrasov functions continues to exist, therefore, such a proof works
only for \beta = 1, i.e. for q=t in MacDonald's notation. For \beta\ne 1 the
conformal blocks are related in this way to a non-Nekrasov decomposition of the
LMNS partition function into a double sum over Young diagrams.Comment: 18 page
Spectral Duality in Integrable Systems from AGT Conjecture
We describe relationships between integrable systems with N degrees of
freedom arising from the AGT conjecture. Namely, we prove the equivalence
(spectral duality) between the N-cite Heisenberg spin chain and a reduced gl(N)
Gaudin model both at classical and quantum level. The former one appears on the
gauge theory side of the AGT relation in the Nekrasov-Shatashvili (and further
the Seiberg-Witten) limit while the latter one is natural on the CFT side. At
the classical level, the duality transformation relates the Seiberg-Witten
differentials and spectral curves via a bispectral involution. The quantum
duality extends this to the equivalence of the corresponding Baxter-Schrodinger
equations (quantum spectral curves). This equivalence generalizes both the
spectral self-duality between the 2x2 and NxN representations of the Toda chain
and the famous AHH duality
On "Dotsenko-Fateev" representation of the toric conformal blocks
We demonstrate that the recent ansatz of arXiv:1009.5553, inspired by the
original remark due to R.Dijkgraaf and C.Vafa, reproduces the toric conformal
blocks in the same sense that the spherical blocks are given by the integral
representation of arXiv:1001.0563 with a peculiar choice of open integration
contours for screening insertions. In other words, we provide some evidence
that the toric conformal blocks are reproduced by appropriate beta-ensembles
not only in the large-N limit, but also at finite N. The check is explicitly
performed at the first two levels for the 1-point toric functions.
Generalizations to higher genera are briefly discussed.Comment: 10 page
Brezin-Gross-Witten model as "pure gauge" limit of Selberg integrals
The AGT relation identifies the Nekrasov functions for various N=2 SUSY gauge
theories with the 2d conformal blocks, which possess explicit Dotsenko-Fateev
matrix model (beta-ensemble) representations the latter being polylinear
combinations of Selberg integrals. The "pure gauge" limit of these matrix
models is, however, a non-trivial multiscaling large-N limit, which requires a
separate investigation. We show that in this pure gauge limit the Selberg
integrals turn into averages in a Brezin-Gross-Witten (BGW) model. Thus, the
Nekrasov function for pure SU(2) theory acquires a form very much reminiscent
of the AMM decomposition formula for some model X into a pair of the BGW
models. At the same time, X, which still has to be found, is the pure gauge
limit of the elliptic Selberg integral. Presumably, it is again a BGW model,
only in the Dijkgraaf-Vafa double cut phase.Comment: 21 page
Data management for prospective research studies using SASÂź software
<p>Abstract</p> <p>Background</p> <p>Maintaining data quality and integrity is important for research studies involving prospective data collection. Data must be entered, erroneous or missing data must be identified and corrected if possible, and an audit trail created.</p> <p>Methods</p> <p>Using as an example a large prospective study, the Missouri Lower Respiratory Infection (LRI) Project, we present an approach to data management predominantly using SAS software. The Missouri LRI Project was a prospective cohort study of nursing home residents who developed an LRI. Subjects were enrolled, data collected, and follow-ups occurred for over three years. Data were collected on twenty different forms. Forms were inspected visually and sent off-site for data entry. SAS software was used to read the entered data files, check for potential errors, apply corrections to data sets, and combine batches into analytic data sets. The data management procedures are described.</p> <p>Results</p> <p>Study data collection resulted in over 20,000 completed forms. Data management was successful, resulting in clean, internally consistent data sets for analysis. The amount of time required for data management was substantially underestimated.</p> <p>Conclusion</p> <p>Data management for prospective studies should be planned well in advance of data collection. An ongoing process with data entered and checked as they become available allows timely recovery of errors and missing data.</p
Immunoregulatory effects of AFP domains on monocyte-derived dendritic cell function
<p>Abstract</p> <p>Background</p> <p>Alpha-fetoprotein (AFP) is a tumor-associated glycoprotein that functions in regulation of both ontogenic and oncogenic growth. Recent study showed that AFP can induce apoptosis or impair monocyte-derived dendritic cell (MDDC) function. However, it is still unclear which AFP domain (D-AFP) plays major role in this function.</p> <p>Results</p> <p>As expected monocytes cultured in the presence of Granulocyte Macrophage-Colony Stimulating Factor (GM-CSF) and Interleukin-4 (IL-4) developed into MDDC. Up-regulation of HLA-DR and CD11c as well as loss of CD14 molecules could be observed. Full length AFP (FL-AFP), domain 2 AFP (D2-AFP) and D3-AFP, but not D1-AFP, significantly inhibited the expression of HLA-DR<sup>high</sup>/CD11c<sup>high </sup>and CD80<sup>+</sup>/CD86<sup>high </sup>molecules. In contrast, CD83 expression was substantially down-regulated in all samples. Expression of CD40 was significantly suppressed by FL-AFP but not by any D-AFPs. Finally, both FL-AFP and D-AFP impaired the MDDC ability to secrete IL-12 (p70).</p> <p>Conclusions</p> <p>D2- and D3- but not D1-AFP extensively suppresses the MDDC function. All the recombinant AFP proteins impaired the ability of MDDC to secrete IL-12.</p
Can type of school be used as an alternative indicator of socioeconomic status in dental caries studies? A cross-sectional study
<p>Abstract</p> <p>Background</p> <p>Despite the importance of collecting individual data of socioeconomic status (SES) in epidemiological oral health surveys with children, this procedure relies on the parents as respondents. Therefore, type of school (public or private schools) could be used as an alternative indicator of SES, instead of collecting data individually. The aim of this study was to evaluate the use of the variable type of school as an indicator of socioeconomic status as a substitute of individual data in an epidemiological survey about dental caries in Brazilian preschool children.</p> <p>Methods</p> <p>This study followed a cross-sectional design, with a random sample of 411 preschool children aged 1 to 5 years, representative of CatalĂŁo, Brazil. A calibrated examiner evaluated the prevalence of dental caries and parents or guardians provided information about several individual socioeconomic indicators by means of a semi-structured questionnaire. A multilevel approach was used to investigate the association among individual socioeconomic variables, as well as the type of school, and the outcome.</p> <p>Results</p> <p>When all significant variables in the univariate analysis were used in the multiple model, only mother's schooling and household income (individual socioeconomic variables) presented significant associations with presence of dental caries, and the type of school was not significantly associated. However, when the type of school was used alone, children of public school presented significantly higher prevalence of dental caries than those enrolled in private schools.</p> <p>Conclusions</p> <p>The type of school used as an alternative indicator for socioeconomic status is a feasible predictor for caries experience in epidemiological dental caries studies involving preschool children in Brazilian context.</p
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Combination of Ginsenosides Rb2 and Rg3 Promotes Angiogenic Phenotype of Human Endothelial Cells via PI3K/Akt and MAPK/ERK Pathways.
Shexiang Baoxin Pill (SBP) is an oral formulation of Chinese materia medica for the treatment of angina pectoris. It displays pleiotropic roles in protecting the cardiovascular system. However, the mode of action of SBP in promoting angiogenesis, and in particular the synergy between its constituents is currently not fully understood. The combination of ginsenosides Rb2 and Rg3 were studied in human umbilical vein endothelial cells (HUVECs) for their proangiogenic effects. To understand the mode of action of the combination in more mechanistic detail, RNA-Seq analysis was conducted, and differentially expressed genes (DEGs), pathway analysis and Weighted Gene Correlation Network Analysis (WGCNA) were applied to further identify important genes that a play pivotal role in the combination treatment. The effects of pathway-specific inhibitors were observed to provide further support for the hypothesized mode of action of the combination. Ginsenosides Rb2 and Rg3 synergistically promoted HUVEC proliferation and tube formation under defined culture conditions. Also, the combination of Rb2/Rg3 rescued cells from homocysteine-induced damage. mRNA expression of CXCL8, CYR61, FGF16 and FGFRL1 was significantly elevated by the Rb2/Rg3 treatment, and representative signaling pathways induced by these genes were found. The increase of protein levels of phosphorylated-Akt and ERK42/44 by the Rb2/Rg3 combination supports the notion that it promotes endothelial cell proliferation via the PI3K/Akt and MAPK/ERK signaling pathways. The present study provides the hypothesis that SBP, via ginsenosides Rb2 and Rg3, involves the CXCR1/2 CXCL8 (IL8)-mediated PI3K/Akt and MAPK/ERK signaling pathways in achieving its proangiogenic effects
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