2,995 research outputs found
Towards multi-scale dynamics on the baryonic branch of Klebanov-Strassler
We construct explicitly a new class of backgrounds in type-IIB supergravity
which generalize the baryonic branch of Klebanov-Strassler. We apply a
solution-generating technique that, starting from a large class of solutions of
the wrapped-D5 system, yields the new solutions, and then proceed to study in
detail their properties, both in the IR and in the UV. We propose a simple
intuitive field theory interpretation of the rotation procedure and of the
meaning of our new solutions within the Papadopoulos-Tseytlin ansatz, in
particular in relation to the duality cascade in the Klebanov-Strassler
solution. The presence in the field theory of different VEVs for operators of
dimensions 2, 3 and 6 suggests that this is an important step towards the
construction of the string dual of a genuinely multi-scale (strongly coupled)
dynamical model.Comment: 37 pages, 7 figures. References added, version to appear in JHE
Ego-Splitting and the Transcendental Subject. Kant’s Original Insight and Husserl’s Reappraisal
In this paper, I contend that there are at least two essential traits that commonly define being an I: self-identity and self-consciousness. I argue that they bear quite an odd relation to each other in the sense that self-consciousness seems to jeopardize self-identity. My main concern is to elucidate this issue within the range of the transcendental philosophies of Immanuel Kant and Edmund Husserl. In the first section, I shall briefly consider Kant’s own rendition of the problem of the Egosplitting. My reading of the Kantian texts reveals that Kant himself was aware of this phenomenon but eventually deems it an unexplainable fact. The second part of the paper tackles the same problematic from the standpoint of Husserlian phenomenology. What Husserl’s extensive analyses on this topic bring to light is that the phenomenon of the Ego-splitting constitutes the bedrock not only of his thought but also of every philosophy that works within the framework of transcendental thinking
Inferring stabilizing mutations from protein phylogenies : application to influenza hemagglutinin
One selection pressure shaping sequence evolution is the requirement that a protein fold with sufficient stability to perform its biological functions. We present a conceptual framework that explains how this requirement causes the probability that a particular amino acid mutation is fixed during evolution to depend on its effect on protein stability. We mathematically formalize this framework to develop a Bayesian approach for inferring the stability effects of individual mutations from homologous protein sequences of known phylogeny. This approach is able to predict published experimentally measured mutational stability effects (ΔΔG values) with an accuracy that exceeds both a state-of-the-art physicochemical modeling program and the sequence-based consensus approach. As a further test, we use our phylogenetic inference approach to predict stabilizing mutations to influenza hemagglutinin. We introduce these mutations into a temperature-sensitive influenza virus with a defect in its hemagglutinin gene and experimentally demonstrate that some of the mutations allow the virus to grow at higher temperatures. Our work therefore describes a powerful new approach for predicting stabilizing mutations that can be successfully applied even to large, complex proteins such as hemagglutinin. This approach also makes a mathematical link between phylogenetics and experimentally measurable protein properties, potentially paving the way for more accurate analyses of molecular evolution
Machine-Part cell formation through visual decipherable clustering of Self Organizing Map
Machine-part cell formation is used in cellular manufacturing in order to
process a large variety, quality, lower work in process levels, reducing
manufacturing lead-time and customer response time while retaining flexibility
for new products. This paper presents a new and novel approach for obtaining
machine cells and part families. In the cellular manufacturing the fundamental
problem is the formation of part families and machine cells. The present paper
deals with the Self Organising Map (SOM) method an unsupervised learning
algorithm in Artificial Intelligence, and has been used as a visually
decipherable clustering tool of machine-part cell formation. The objective of
the paper is to cluster the binary machine-part matrix through visually
decipherable cluster of SOM color-coding and labelling via the SOM map nodes in
such a way that the part families are processed in that machine cells. The
Umatrix, component plane, principal component projection, scatter plot and
histogram of SOM have been reported in the present work for the successful
visualization of the machine-part cell formation. Computational result with the
proposed algorithm on a set of group technology problems available in the
literature is also presented. The proposed SOM approach produced solutions with
a grouping efficacy that is at least as good as any results earlier reported in
the literature and improved the grouping efficacy for 70% of the problems and
found immensely useful to both industry practitioners and researchers.Comment: 18 pages,3 table, 4 figure
Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia
Recent advances in DNA sequencing have enabled mapping of genes for monogenic traits in families with small pedigrees and even in unrelated cases. We report the identification of disease-causing mutations in a rare, severe, skeletal dysplasia, studying a family of two healthy unrelated parents and two affected children using whole-exome sequencing. The two affected daughters have clinical and radiographic features suggestive of anauxetic dysplasia (OMIM 607095), a rare form of dwarfism caused by mutations of RMRP. However, mutations of RMRP were excluded in this family by direct sequencing. Our studies identified two novel compound heterozygous loss-of-function mutations in POP1, which encodes a core component of the RNase mitochondrial RNA processing (RNase MRP) complex that directly interacts with the RMRP RNA domains that are affected in anauxetic dysplasia. We demonstrate that these mutations impair the integrity and activity of this complex and that they impair cell proliferation, providing likely molecular and cellular mechanisms by which POP1 mutations cause this severe skeletal dysplasia
Universal corrections to entanglement entropy of local quantum quenches
We study the time evolution of single interval Renyi and entanglement entropies following local quantum quenches in two dimensional conformal field theories at finite temperature for which the locally excited states have a finite temporal width, \epsilon. We show that, for local quenches produced by the action of a conformal primary field, the time dependence of Renyi and entanglement entropies at order \epsilon^2 is universal. It is determined by the expectation value of the stress tensor in the replica geometry and proportional to the conformal dimension of the primary field generating the local excitation. We also show that in CFTs with a gravity dual, the \epsilon^2 correction to the holographic entanglement entropy following a local quench precisely agrees with the CFT prediction. We then consider CFTs admitting a higher spin symmetry and turn on a higher spin chemical potential \mu. We calculate the time dependence of the order \epsilon^2 correction to the entanglement entropy for small \mu, and show that the contribution at order \mu^2 is universal. We verify our arguments against exact results for minimal models and the free fermion theory
Filarial Lymphedema Is Characterized by Antigen- Specific Th1 and Th17 Proinflammatory Responses and a Lack of Regulatory T Cells
Background: Lymphatic filariasis can be associated with development of serious pathology in the form of lymphedema,
hydrocele, and elephantiasis in a subset of infected patients.
Methods and Findings: To elucidate the role of CD4+ T cell subsets in the development of lymphatic pathology, we
examined specific sets of cytokines in individuals with filarial lymphedema in response to parasite antigen (BmA) and
compared them with responses from asymptomatic infected individuals. We also examined expression patterns of Toll-like
receptors (TLR1–10) and Nod-like receptors (Nod1, Nod2, and NALP3) in response to BmA. BmA induced significantly higher
production of Th1-type cytokines—IFN-c and TNF-a—in patients with lymphedema compared with asymptomatic
individuals. Notably, expression of the Th17 family of cytokines—IL-17A, IL-17F, IL-21, and IL-23—was also significantly
upregulated by BmA stimulation in lymphedema patients. In contrast, expression of Foxp3, GITR, TGFb, and CTLA-4, known
to be expressed by regulatory T cells, was significantly impaired in patients with lymphedema. BmA also induced
significantly higher expression of TLR2, 4, 7, and 9 as well Nod1 and 2 mRNA in patients with lymphedema compared with
asymptomatic controls.
Conclusion: Our findings implicate increased Th1/Th17 responses and decreased regulatory T cells as well as regulation of
Toll- and Nod-like receptors in pathogenesis of filarial lymphedema
Local quenches and quantum chaos from higher spin perturbations
We study local quenches in 1+1 dimensional conformal field theories at large-c by operators carrying higher spin charge. Viewing such states as solutions in Chern-Simons theory, representing infalling massive particles with spin-three charge in the BTZ back- ground, we use the Wilson line prescription to compute the single-interval entanglement entropy (EE) and scrambling time following the quench. We find that the change in EE is finite (and real) only if the spin-three charge q is bounded by the energy of the perturbation E, as |q|/c < E^2/c^2. We show that the Wilson line/EE correlator deep in the quenched regime and its expansion for small quench widths overlaps with the Regge limit for chaos of the out-of-time-ordered correlator. We further find that the scrambling time for the two- sided mutual information between two intervals in the thermofield double state increases with increasing spin-three charge, diverging when the bound is saturated. For larger values of the charge, the scrambling time is shorter than for pure gravity and controlled by the spin-three Lyapunov exponent 4π/β. In a CFT with higher spin chemical potential, dual to a higher spin black hole, we find that the chemical potential must be bounded to ensure that the mutual information is a concave function of time and entanglement speed is less than the speed of light. In this case, a quench with zero higher spin charge yields the same Lyapunov exponent as pure Einstein gravity
Baseline natural killer and T cell populations correlation with virologic outcome after regimen simplification to atazanavir/ritonavir alone (ACTG 5201)
Objectives: Simplified maintenance therapy with ritonavir-boosted atazanavir (ATV/r) provides an alternative treatment option for HIV-1 infection that spares nucleoside analogs (NRTI) for future use and decreased toxicity. We hypothesized that the level of immune activation (IA) and recovery of lymphocyte populations could influence virologic outcomes after regimen simplification. Methods: Thirty-four participants with virologic suppression ≥48 weeks on antiretroviral therapy (2 NRTI plus protease inhibitor) were switched to ATV/r alone in the context of the ACTG 5201 clinical trial. Flow cytometric analyses were performed on PBMC isolated from 25 patients with available samples, of which 24 had lymphocyte recovery sufficient for this study. Assessments included enumeration of T-cells (CD4/CD8), natural killer (NK) (CD3+CD56 +CD16+) cells and cell-associated markers (HLA-DR, CD's 38/69/94/95/158/279). Results: Eight of the 24 patients had at least one plasma HIV-1 RNA level (VL) <50 copies/mL during the study. NK cell levels below the group median of 7.1% at study entry were associated with development of VL <50 copies/mL following simplification by regression and survival analyses (p = 0.043 and 0.023), with an odds ratio of 10.3 (95% CI: 1.92-55.3). Simplification was associated with transient increases in naïve and CD25+ CD4+ T-cells, and had no impact on IA levels. Conclusions: Lower NK cell levels prior to regimen simplification were predictive of virologic rebound after discontinuation of nucleoside analogs. Regimen simplification did not have a sustained impact on markers of IA or T lymphocyte populations in 48 weeks of clinical monitoring. Trial Registration: ClinicalTrials.gov NCT00084019
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