Universal structure of subleading infrared poles at strong coupling

Recently a concise expression for the subleading infrared singularity of dimensional-regularized gauge theories has been proposed. For conformal theories, such relation involves a universal eikonal contribution plus a non-eikonal contribution, related to the subleading term in the anomalous dimension of twist two operators with large spin. In this note we make use of the AdS/CFT correspondence in order to check such conjecture at strong coupling for the case of N=4 SYM.Comment: 13 page

Imidazole and imidazolium antibacterial drugs derived from amino acids

The antibacterial activity of imidazole and imidazolium salts is highly dependent upon their lipophilicity, which can be tuned through the introduction of different hydrophobic substituents on the nitrogen atoms of the imidazole or imidazolium ring of the molecule. Taking this into consideration, we have synthesized and characterized a series of imidazole and imidazolium salts derived from L-valine and L-phenylalanine containing different hydrophobic groups and tested their antibacterial activity against two model bacterial strains, Gram-negative E. coli and Gram-positive B. subtilis. Importantly, the results demonstrate that the minimum bactericidal concentration (MBC) of these derivatives can be tuned to fall close to the cytotoxicity values in eukaryotic cell lines. The MBC value of one of these compounds toward B. subtilis was found to be lower than the IC50 cytotoxicity value for the control cell line, HEK-293. Furthermore, the aggregation behavior of these compounds has been studied in pure water, in cell culture media, and in mixtures thereof, in order to determine if the compounds formed self-assembled aggregates at their bioactive concentrations with the aim of determining whether the monomeric species were in fact responsible for the observed antibacterial activity. Overall, these results indicate that imidazole and imidazolium compounds derived from L-valine and L-phenylalanine—with different alkyl lengths in the amide substitution—can serve as potent antibacterial agents with low cytotoxicity to human cell lines

Comments on operators with large spin

We consider high spin operators. We give a general argument for the logarithmic scaling of their anomalous dimensions which is based on the symmetries of the problem. By an analytic continuation we can also see the origin of the double logarithmic divergence in the Sudakov factor. We show that the cusp anomalous dimension is the energy density for a flux configuration of the gauge theory on $AdS_3 \times S^1$. We then focus on operators in ${\cal N}=4$ super Yang Mills which carry large spin and SO(6) charge and show that in a particular limit their properties are described in terms of a bosonic O(6) sigma model. This can be used to make certain all loop computations in the string theory.Comment: 33 pages, 1 figure,v2:reference to more recent work added, minor correction

Stability of the selfsimilar dynamics of a vortex filament

In this paper we continue our investigation about selfsimilar solutions of the vortex filament equation, also known as the binormal flow (BF) or the localized induction equation (LIE). Our main result is the stability of the selfsimilar dynamics of small pertubations of a given selfsimilar solution. The proof relies on finding precise asymptotics in space and time for the tangent and the normal vectors of the perturbations. A main ingredient in the proof is the control of the evolution of weighted norms for a cubic 1-D Schr\"odinger equation, connected to the binormal flow by Hasimoto's transform.Comment: revised version, 36 page

Rate Theory of Acceleration of Defect Annealing Driven by Discrete Breathers

Siendo un capítulo de libro es un poco estraño que los campos correspondan a una revista. Tal vez, en vez de coordinador/director deberían ser editores, y en vez de editor, editorial. En cambio faltarían campos como volumen y serieNovel mechanisms of defect annealing in solids are discussed, which are based on the large amplitude anharmonic lattice vibrations, a.k.a. intrinsic localized modes or discrete breathers (DBs). A model for amplification of defect annealing rate in Ge by low energy plasma-generated DBs is proposed, in which, based on recent atomistic modelling, it is assumed that DBs can excite atoms around defects rather strongly, giving them energy ≫ kBT for ~100 oscillation periods. This is shown to result in the amplification of the annealing rates proportional to the DB flux, i.e. to the flux of ions (or energetic atoms) impinging at the Ge surface from inductively coupled plasma (ICP)

APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family

BACKGROUND: Severe hypertriglyceridemia (HTG) has been linked to defects in LPL, APOC2, APOA5, LMF1 and GBIHBP1 genes. However, a number of severe HTG cases are probably caused by as yet unidentified mutations. Very high triglyceride plasma levels (>112 mmol/L at diagnosis) were found in two sisters of a Chilean consanguineous family, which is strongly suggestive of a recessive highly penetrant mutation. The aim of this study was to determine the genetic locus responsible for the severe HTG in this family. METHODS: We carried out a genome-wide linkage study with nearly 300,000 biallelic markers (Illumina Human CytoSNP-12 panel). Using the homozygosity mapping strategy, we searched for chromosome regions with excess of homozygous genotypes in the affected cases compared to non-affected relatives. RESULTS: A large homozygous segment was found in the long arm of chromosome 11, with more than 2,500 consecutive homozygous SNP shared by the proband with her affected sister, and containing the APOA5/A4/C3/A1 cluster. Direct sequencing of the APOA5 gene revealed a known homozygous nonsense Q97X mutation (p.Gln97Ter) found in both affected sisters but not in non-affected relatives nor in a sample of unrelated controls. CONCLUSION: The Q97X mutation of the APOA5 gene in homozygous status is responsible for the severe hypertriglyceridemia in this family. We have shown that homozygosity mapping correctly pinpointed the genomic region containing the gene responsible for severe hypertriglyceridemia in this consanguineous Chilean famil

Nonorientable spacetime tunneling

Misner space is generalized to have the nonorientable topology of a Klein bottle, and it is shown that in a classical spacetime with multiply connected space slices having such a topology, closed timelike curves are formed. Different regions on the Klein bottle surface can be distinguished which are separated by apparent horizons fixed at particular values of the two angular variables that eneter the metric. Around the throat of this tunnel (which we denote a Klein bottlehole), the position of these horizons dictates an ordinary and exotic matter distribution such that, in addition to the known diverging lensing action of wormholes, a converging lensing action is also present at the mouths. Associated with this matter distribution, the accelerating version of this Klein bottlehole shows four distinct chronology horizons, each with its own nonchronal region. A calculation of the quantum vacuum fluctuations performed by using the regularized two-point Hadamard function shows that each chronology horizon nests a set of polarized hypersurfaces where the renormalized momentum-energy tensor diverges. This quantum instability can be prevented if we take the accelerating Klein bottlehole to be a generalization of a modified Misner space in which the period of the closed spatial direction is time-dependent. In this case, the nonchronal regions and closed timelike curves cannot exceed a minimum size of the order the Planck scale.Comment: 11 pages, RevTex, Accepted in Phys. Rev.

Conductive films based on composite polymers containing ionic liquids absorbed on crosslinked polymeric ionic-like liquids (SILLPs)

Polymerization of styrenic monomers containing imidazolium subunits in the presence of crosslinking monomers and using ionic liquids (ILs) as porogenic agents provides composite materials with excellent mechanical properties and displaying conductivities that are in the same order of magnitude than those shown by bulk ILs. This approach allows the use of high crosslinking degrees and low IL-loadings without compromising the required properties of the resulting composites. Besides, no appreciable leaching of the bulk IL component is detected.Financial support by Ministerio de Ciencia e Innovacion (CTQ2011-28903-C02-01 and SP-ENE-20120718), Generalitat Valenciana (PROMETEO/2012/020) and Universitat Jaume I (P11B2013-38) is acknowledged.Altava Benito, B.; Compañ Moreno, V.; Andrio Balado, A.; Del Castillo Davila, LF.; Mollá Romano, S.; Burguete, MI.; García-Verdugo Cepeda, E.... (2015). Conductive films based on composite polymers containing ionic liquids absorbed on crosslinked polymeric ionic-like liquids (SILLPs). Polymer. 72:69-81. https://doi.org/10.1016/j.polymer.2015.07.009S69817

Novel splice-affecting variants in CYP27A1 gene in two Chilean patients with Cerebrotendinous Xanthomatosis

Cerebrotendinous Xanthomatosis (CTX), a rare lipid storage disorder, is caused by recessive loss-of-function mutations of the 27-sterol hydroxylase (CYP27A1), producing an alteration of the synthesis of bile acids, with an accumulation of cholestanol. Clinical characteristics include juvenile cataracts, diarrhea, tendon xanthomas, cognitive impairment and other neurological manifestations. Early diagnosis is critical, because treatment with chenodeoxycholic acid may prevent neurological damage. We studied the CYP27A1 gene in two Chilean CTX patients by sequencing its nine exons, exon-intron boundaries, and cDNA from peripheral blood mononuclear cells. Patient 1 is a compound heterozygote for the novel substitution c.256-1G > T that causes exon 2 skipping, leading to a premature stop codon in exon 3, and for the previously-known pathogenic mutation c.1183C > T (p.Arg395Cys). Patient 2 is homozygous for the novel mutation c.1185-1G > A that causes exon 7 skipping and the generation of a premature stop codon in exon 8, leading to the loss of the crucial adrenoxin binding domain of CYP27A1