41 resultados para Indra


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Sanskrit title at head of title-page.

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The workshop is an activity of the IMIA Working Group ‘Security in Health Information Systems’ (SiHIS). It is focused to the growing global problem: how to protect personal health data in today’s global eHealth and digital health environment. It will review available trust building mechanisms, security measures and privacy policies. Technology alone does not solve this complex problem and current protection policies and legislation are considered woefully inadequate. Among other trust building tools, certification and accreditation mechanisms are dis-cussed in detail and the workshop will determine their acceptance and quality. The need for further research and international collective action are discussed. This workshop provides an opportunity to address a critical growing problem and make pragmatic proposals for sustainable and effective solutions for global eHealth and digital health.

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Cyclic di-GMP (c-di-GMP), a ubiquitous bacterial second messenger, has emerged as a key controller of several biological processes. Numbers of reports that deal with the mechanistic aspects of this second messenger have appeared in the literature. However, the lack of a reporter tag attached to the c-di-GMP at times limits the understanding of further details. In this study, we have chemically coupled N-methylisatoic anhydride (MANT) with c-di-GMP, giving rise to Mant-(c-di-GMP) or MANT-CDG. We have characterized the chemical and physical properties and spectral behavior of MANT-CDG. The fluorescence of MANT-CDG is sensitive to changes in the microenvironment, which helped us study its interaction with three different c-di-GMP binding proteins (a diguanylate cyclase, a phosphodiesterase, and a PilZ domain-containing protein). In addition, we have shown here that MANT-CDG can inhibit diguanylate cyclase activity; however, it is hydrolyzed by c-di-GMP specific phosphodiesterase. Taken together, our data suggest that MANT-CDG behaves like native c-di-GMP, and this study raises the possibility that MANT-CDG will be a valuable research tool for the in vitro characterization of c-di-GMP signaling factors.

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Geopolymers are an alternative binder to portland cement in the manufacture of mortars and concrete, as its three-dimensional aluminosilicate network imparts excellent mechanical properties. Use of geopolymers in place of ordinary portland cement is favored owing to the possible energy and carbon dioxide savings. River sand is another construction industry material that needs development of a sustainable alternate in India. Geopolymerization of fly ash amorphous silica mixtures is employed to produce fine aggregates as a possible replacement to river sand. Geopolymerization of fly ash amorphous silica mixtures in 10M NaOH solution at 100 degrees C for 7days produced fine aggregates termed fly ash geopolymer sand (FAPS)] that had comparable grain size distribution, specific gravity, and improved frictional resistance with river sand. The FAPS particles exhibited more alkaline pH (12.5) and higher total dissolved solids (TDS) concentration (TDS=747 mg/L) in comparison to the river sand specimen (pH=7.9 and TDS=32.5 mg/L). However, when used as fine aggregate in mortar, FAPS-mortar specimens develop similar pH, lower TDS, similar compressive strength, and modulus in relation to river sand-mortar specimens. The experimental results suggest that FAPS particles have the potential to replace river sand in the manufacture of mortar and concrete.

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We have reported previously that the long-term survival of Mycobacterium smegmatis is facilitated by a dual-active enzyme MSDGC-1 (renamed DcpA), which controls the cellular turnover of cyclic diguanosine monophosphate (c-di-GMP). Most mycobacterial species possess at least a single copy of a DcpA orthologue that is highly conserved in terms of sequence similarity and domain architecture. Here, we show that DcpA exists in monomeric and dimeric forms. The dimerization of DcpA is due to non-covalent interactions between two protomers that are arranged in a parallel orientation. The dimer shows both synthesis and hydrolysis activities, whereas the monomer shows only hydrolysis activity. In addition, we have shown that DcpA is associated with the cytoplasmic membrane and exhibits heterogeneous cellular localization with a predominance at the cell poles. Finally, we have also shown that DcpA is involved in the change in cell length and colony morphology of M. smegmatis. Taken together, our study provides additional evidence about the role of the bifunctional protein involved in c-di-GMP signalling in M. smegmatis.

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Bacteria have evolved to survive the ever-changing environment using intriguing mechanisms of quorum sensing (QS). Very often, QS facilitates formation of biofilm to help bacteria to persist longer and the formation of such biofilms is regulated by c-di-GMP. It is a well-known second messenger also found in mycobacteria. Several methods have been developed to study c-di-GMP signaling pathways in a variety of bacteria. In this review, we have attempted to highlight a connection between c-di-GMP and biofilm formation and QS in mycobacteria and several methods that have helped in better understanding of c-di-GMP signaling. (c) 2014 IUBMB Life, 66(12):823-834, 2014

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We show using detailed magnetic and thermodynamic studies and theoretical calculations that the ground state of Ba3ZnIr2O9 is a realization of a novel spin-orbital liquid state. Our results reveal that Ba3ZnIr2O9 with Ir5+ (5d(4)) ions and strong spin-orbit coupling (SOC) arrives very close to the elusive J = 0 state but each Ir ion still possesses a weak moment. Ab initio density functional calculations indicate that this moment is developed due to superexchange, mediated by a strong intradimer hopping mechanism. While the Ir spins within the structural Ir2O9 dimer are expected to form a spin-orbit singlet state (SOS) with no resultant moment, substantial frustration arising from interdimer exchange interactions induce quantum fluctuations in these possible SOS states favoring a spin-orbital liquid phase down to at least 100 mK.

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Seit der Entdeckung der Methyltransferase 2 als hoch konserviertes und weit verbreitetes Enzym sind zahlreiche Versuche zur vollständigen Charakterisierung erfolgt. Dabei ist die biologische Funktion des Proteins ein permanent umstrittener Punkt. In dieser Arbeit wird dnmA als sensitiver Oszillator bezüglich des Zellzyklus und weiterer Einflüsse gezeigt. Insgesamt liegt der Hauptfokus auf der Untersuchung der in vivo Charakterisierung des Gens, der endogenen subzellulären Verteilung, sowie der physiologischen Aufgaben des Proteins in vivo in D. discoideum. Um Hinweise auf Signalwege in vivo zu erhalten, in denen DnmA beteiligt ist, war es zunächst notwendig, eine detaillierte Analyse des Gens anzufertigen. Mit molekularbiologisch äußerst sensitiven Methoden, wie beispielsweise Chromatin‐IP oder qRT‐PCR, konnte ein vollständiges Expressionsprofil über den Zell‐ und Lebenszyklus von D. discoideum angelegt werden. Besonders interessant sind dabei die Ergebnisse eines ursprünglichen Wildtypstammes (NC4), dessen dnmA‐Expressionsprofil quantitativ von anderen Wildtypstämmen abweicht. Auch auf Proteinebene konnten Zellzyklus‐abhängige Effekte von DnmA bestimmt werden. Durch mikroskopische Untersuchungen von verschiedenen DnmA‐GFP‐Stämmen wurden Lokalisationsänderungen während der Mitose gezeigt. Weiterhin wurde ein DnmA‐GFP‐Konstrukt unter der Kontrolle des endogenen Promotors generiert, wodurch das Protein in der Entwicklung eindeutig als Zelltypus spezifisches Protein, nämlich als Präsporen‐ bzw. Sporenspezifisches Protein, identifiziert werden konnte. Für die in vivo Analyse der katalytischen Aktivität des Enzyms konnten nun die Erkenntnisse aus der Charakterisierung des Gens bzw. Proteins berücksichtigt werden, um in vivo Substratkandidaten zu testen. Es zeigte sich, dass von allen bisherigen Substrat Kandidaten lediglich die tRNA^Asp als in vivo Substrat bestätigt werden konnte. Als besondere Erkenntnis konnte hierbei ein quantitativer Unterschied des Methylierungslevels zwischen verschiedenen Wildtypstämmen detektiert werden. Weiterhin wurde die Methylierung sowie Bindung an einen DNA‐Substratkandidaten ermittelt. Es konnte gezeigt werden, dass DnmA äußerst sequenzspezifisch mit Abschnitten des Retrotransposons DIRS‐1 in vivo eine Bindung eingeht. Auch für den Substrakandidaten snRNA‐U2 konnte eine stabile in vitro Komplexbildung zwischen U2 und hDnmt2 gezeigt werden. Insgesamt erfolgte auf Basis der ermittelten Expressionsdaten eine erneute Charakterisierung der Aktivität des Enzyms und der Substrate in vivo und in vitro.

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Este estudio de caso se enfoca en identificar cuales fueron los factores que motivaron la participación de los partidos kurdos PDK y UPK en la invasión a Irak 2003 – 2009. Con base en los supuestos teóricos de autores realistas K.Waltz, M. Ayoob y liberales y R. Keohane y J. Nye, se estudian las dinámicas y las interacciones que permitieron establecer un acercamiento con los Estados Unidos con un énfasis específico en los intereses políticos de los partidos kurdos. El kurdistán iraquí llega a ser el área clave para el acercamiento de la potencia a la zona y los intereses políticos permitieron establecer un escenario de cooperación e interdependencia, incrementando tanto la participación como la autonomía de los kurdos en las dinámicas del país y de la región.

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Esta investigación aborda las condiciones bajo las que se llevó a cabo en Colombia, en el primer gobierno del presidente Álvaro Uribe Vélez (2002-2006), la negociación entre el Estado y los grupos paramilitares. Se establecen las características de ese proceso de paz, su correspondencia con modelos tradicionales de negociación y sus alcances sobre el proceso de Desmovilización, Desarme y Reinserción (DDR) de las organizaciones paramilitares.

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España Virtual es un proyecto de I+D, subvencionado por el [CDTI] dentro del programa Ingenio 2010, orientado a la definición de la arquitectura, protocolos y estándares de la futura Internet 3D, con un foco especial en lo relativo a visualización 3D, inmersión en mundos virtuales, interacción entre usuarios y a la introducción de aspectos semánticos, sin dejar de lado el estudio y maduración de las tecnologías para el procesamiento masivo y almacenamiento de datos geográficos. Con una duración de cuatro años, el proyecto está liderado por Elecnor DEIMOS y cuenta con la participación del Centro Nacional de Información Geográfica (IGN/CNIG), Indra Espacio, Androme Ibérica, GeoSpatiumLab, DNX, [Prodevelop], Telefónica I+D y una decena de prestigiosos centros de investigación y universidades nacionales. En este contexto Prodevelop y el Ai2 (Instituto de Automática e Informática Industrial) entran a participar en el proyecto gracias a la Asociación gvSIG con el objetivo de impulsar el desarrollo de la visualización 3D , incorporación de nuevos estándares y mejoras en los ya existentes, así como la evolución de funcionalidades, sobre todo en el ámbito de los servicios remotos y mejoras del rendimiento a través de sistemas de cacheado de datos. También se pretende servir como plataforma para el volcado de resultados en los diferentes activos experimentales realizados por otros socios del proyecto. Para la consecución de objetivos se definen diferentes paquetes de trabajo que va a trabajar sobre nuevos tipos de datos, acceso a datos 3D multirresolución, integración de datos geográficos al vuelo, componentes de visualización 2D, 3D y 4D, algoritmia multirresolución y efectos audiovisuales inmersivos. Concretamente y dentro de estos paquetes de trabajo se presentarán los avances realizados e integrados dentro de gvSIG Desktop v2.0, y otras funcionalidades gvSIG sobre dispositivos móviles

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The human enzyme dihydroorotate dehydrogenase (HsDHODH) has been studied for being a target for development of new antineoplasic and antiproliferative drugs. The synthetic peptide N-t(DH) represents the N-terminal microdomain of this enzyme, responsible for anchoring it to the inner mitochondrial membrane. Also, it is known to harbor quinones that are essential for enzyme catalysis. Here we report structural features of the peptide/membrane interactions obtained by using CD and DEER spectroscopic techniques, both in micelles and in lipid vesicles. The data revealed different peptide conformational states in micelles and liposomes, which could suggest that this microdomain acts in specific regions or areas of the mitochondria, which can be related with the control of the quinone access to the HsDHODH active site. This is the first study to report on conformational changes of the HsDHODH N-terminal microdomain through a combination of CD and DEER spectroscopic techniques.

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The fundamental goal of this thesis is the determination of the isospin dependence of the Ar+Ni fusion-evaporation cross section. Three Ar isotope beams, with energies of about 13AMeV, have been accelerated and impinged onto isotopically enriched Ni targets, in order to produce Pd nuclei, with mass number varying from 92 to 104. The measurements have been performed by the high performance 4pi detector INDRA, coupled with the magnetic spectrometer VAMOS. Even if the results are very preliminary, the obtained fusion-evaporation cross sections behaviour gives a hint at the possible isospin dependence of the fusion-evaporation cross sections.

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To optimize fertility advice in patients with Hodgkin lymphoma (HL) before therapy and during survivorship, information on the impact of chemotherapy is needed. Therefore, we analyzed gonadal functions in survivors of HL.

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An important step in the pathogenesis of multiple sclerosis is adhesion and transmigration of encephalitogenic T cells across brain endothelial cells (EC) which strongly relies on interaction with EC-expressed adhesion molecules. We provide molecular evidence that the transcription factor peroxisome proliferator-activated receptor gamma (PPARgamma) is a negative regulator of brain EC inflammation. The PPARgamma agonist pioglitazone reduces transendothelial migration of encephalitogenic T cells across TNFalpha-stimulated brain EC. This effect is clearly PPARgamma mediated, as lentiviral PPARgamma overexpression in brain EC results in selective abrogation of inflammation-induced ICAM-1 and VCAM-1 upregulation and subsequent adhesion and transmigration of T cells. We therefore propose that PPARgamma in brain EC may be exploited to target detrimental EC-T cell interactions under inflammatory conditions.