PPAR gamma pro12Ala polymorphism and type 2 diabetes: a study in a spanish cohort

Type 2 diabetes (T2D) is a disease whose occurrence is increasing prevalent in westernized civilizations and is responsible for the proliferation in the morbidity and total mortality of patients with cardiovascular diseases, worldwide. However, the complexity in the treatment and prevention of T2D arises from the intricacy of the many physical and biological factors involved in its etiology. Impaired pathways for insulin signaling have been implicated as one the many factors in the development of T2D Individual peroxisome proliferator-activated receptors (PPARs) have previously exhibited associations with alterations of lipid profiles, fat tissue and T2D and displayed complications derived from high levels of glucose. However, PPARgamma has not yet been associated with the development or developmental pathways of T2D. We performed an observational study a Spanish cohort in order to better understand the association between the SNP PPARgamma polymorphism Pro12Ala in our patients and the incidence of T2D and other cardiovascular complications. We study did not find a statistically significant relationship between the Pro12Ala and T2D development in our cohort, future observations will help us to know the association with vascular disease in patients with T2D

Marginal Fermi liquid behavior from 2d Coulomb interaction

A full, nonperturbative renormalization group analysis of interacting electrons in a graphite layer is performed, in order to investigate the deviations from Fermi liquid theory that have been observed in the experimental measures of a linear quasiparticle decay rate in graphite. The electrons are coupled through Coulomb interactions, which remain unscreened due to the semimetallic character of the layer. We show that the model flows towards the noninteracting fixed-point for the whole range of couplings, with logarithmic corrections which signal the marginal character of the interaction separating Fermi liquid and non-Fermi liquid regimes.Comment: 7 pages, 2 Postscript figure

Evidence of several dipolar quasi-invariants in Liquid Crystals

In a closed quantum system of N coupled spins with magnetic quantum number I, there are about (2I + 1)^N constants of motion. However, the possibility of observing such quasi-invariant (QI) states in solid-like spin systems in Nuclear Magnetic Resonance (NMR) is not a strictly exact prediction. The aim of this work is to provide experimental evidence of several QI, in the proton NMR of small spin clusters, besides those already known Zeeman, and dipolar orders (strong and weak). We explore the spin states prepared with the Jeener-Broekaert pulse sequence by analyzing the time-domain signals yielded by this sequence as a function of the preparation times, in a variety of dipolar networks. We observe that the signals can be explained with two dipolar QIs only within a range of short preparation times. At longer times the time-domain signals have an echo-like behaviour. We study their multiple quantum coherence content on a basis orthogonal to the z-basis and see that such states involve a significant number of correlated spins. Then we show that the whole preparation time-scale can only be reconstructed by assuming the occurrence of multiple QI which we isolate experimentally

Cool dwarfs in wide multiple systems. Paper 6: A curious quintuple system of a compact Sun-like triple and a close pair of an M dwarf and a very cool white dwarf at a wide separation

The system WDS 16329+0315 is an old, nearby quintuple physical system in the thick Galactic disc formed by a close-resolved, triple primary of solar metallicity, namely HD 149162, and a very wide, common proper motion, secondary pair, formed by the mid-M dwarf G-17-23 and the white dwarf LSPM J1633+0311S. We present an exhaustive astrometric and photometric data compilation of the system, including Gaia DR2 parallaxes and proper motions, and the first analysis of the nature of the faintest component. LSPM J1633+0311S (HD 149162 C) is a very cool white dwarf with an effective temperature of only about 5500 K, near the coolest end of the grid of theoretical models.Comment: The Observatory, in press, to appear in December 201

Improved ontology for eukaryotic single-exon coding sequences in biological databases

Indexación: Scopus.Efficient extraction of knowledge from biological data requires the development of structured vocabularies to unambiguously define biological terms. This paper proposes descriptions and definitions to disambiguate the term 'single-exon gene'. Eukaryotic Single-Exon Genes (SEGs) have been defined as genes that do not have introns in their protein coding sequences. They have been studied not only to determine their origin and evolution but also because their expression has been linked to several types of human cancer and neurological/developmental disorders and many exhibit tissue-specific transcription. Unfortunately, the term 'SEGs' is rife with ambiguity, leading to biological misinterpretations. In the classic definition, no distinction is made between SEGs that harbor introns in their untranslated regions (UTRs) versus those without. This distinction is important to make because the presence of introns in UTRs affects transcriptional regulation and post-transcriptional processing of the mRNA. In addition, recent whole-transcriptome shotgun sequencing has led to the discovery of many examples of single-exon mRNAs that arise from alternative splicing of multi-exon genes, these single-exon isoforms are being confused with SEGs despite their clearly different origin. The increasing expansion of RNA-seq datasets makes it imperative to distinguish the different SEG types before annotation errors become indelibly propagated in biological databases. This paper develops a structured vocabulary for their disambiguation, allowing a major reassessment of their evolutionary trajectories, regulation, RNA processing and transport, and provides the opportunity to improve the detection of gene associations with disorders including cancers, neurological and developmental diseases. © The Author(s) 2018. Published by Oxford University Press.https://academic.oup.com/database/article/doi/10.1093/database/bay089/509943