55 resultados para Manuel, Juan


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Tesis doctoral originalmente defendida en la Universidad de Deusto el 29-09-2000

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El objetivo principal de este trabajo fin de grado es resaltar las novedades que ha incorporado el Reglamento 1215/2012 en el objetivo de un avance en la consecución de un verdadero espacio judicial europeo con el objeto de potenciar la libre circulación de las resoluciones judiciales en materia civil y mercantil en el ámbito de la Unión Europea. Los dos grandes objetivos de la reforma, la eliminación del exequátur y la extensión de las reglas unificadas de competencia con el propósito de suprimir la remisión a las reglas nacionales cuando el demandado no está domiciliado en un estado miembro, son objeto de estudio y crítica en este trabajo.

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El objetivo del Trabajo de Fin de Grado ha sido combinar tres bloques de análisis: el derecho normativo interno español en materia de derecho internacional privado, el derecho comparado en el marco de la Unión Europea y el derecho europeo (los reglamentos en vigor) y los dos proyectos de reglamento en esta materia actualmente en tramitación. Mediante el trabajo se persigue demostrar la necesidad y oportunidad de que el derecho europeo, sin armonizar sustantivamente las regulaciones de cada estado miembro, utilice las técnicas del derecho internacional para seleccionar el Tribunal competente, designar la ley aplicable reconocimiento y ejecución de decisiones judiciales en materia del derecho de familia internacional y centrándonos en el sector de régimen económico matrimonial en defecto de pacto.

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Single nucleotide-polymorphisms (SNPs) are a source of diversity among human population, which may be responsible for the different individual susceptibility to diseases and/or response to drugs, among other phenotypic traits. Several low penetrance susceptibility genes associated with malignant melanoma (MM) have been described, including genes related to pigmentation, DNA damage repair and oxidative stress pathways. In the present work, we conducted a candidate gene association study based on proteins and genes whose expression we had detected altered in melanoma cell lines as compared to normal melanocytes. The result was the selection of 88 loci and 384 SNPs, of which 314 fulfilled our quality criteria for a case-control association study. The SNP rs6854854 in ANXA5 was statistically significant after conservative Bonferroni correction when 464 melanoma patients and 400 controls were analyzed in a discovery Phase I. However, this finding could not be replicated in the validation phase, perhaps because the minor allele frequency of SNP rs6854854 varies depending on the geographical region considered. Additionally, a second SNP (rs6431588) located on ILKAP was found to be associated with melanoma after considering a combined set of 1,883 MM cases and 1,358 disease-free controls. The OR was 1.29 (95% CI 1.12-1.48; p-value= 4x10(-4)). Both SNPs, rs6854854 in ANXA5 and rs6431588 in ILKAP, show population structure, which, assuming that the Spanish population is not significantly structured, suggests a role of these loci on a specific genetic adaptation to different environmental conditions. Furthermore, the biological relevance of these genes in MM is supported by in vitro experiments, which show a decrease in the transcription levels of ANXA5 and ILKAP in melanoma cells compared to normal melanocytes.

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1 carta (manuscrita) ; 225x330 mm

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[ES] El análisis directo de los ajuares lítico y óseo que se conservan del yacimiento de San juan, nos induce a plantear una hipótesis principal, según la cual la ocupación prehistórica del depósito debió producirse fundamentalmente durante el Aziliense, aunque no puede descartarse un origen anterior, en las últimas fases del Magdaleniense.

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Fecha: 31 de marzo de 1937 / Unidad de ínstalación: Carpeta Rectorado - D-1 / Nº de pág.: 2 (manuscritas)

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Síntesis, caracterización química y estudio estructural de un complejo metalorgánico soportado sobre un polioxovanadato.

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In this paper, inspired by two very different, successful metric theories such us the real view-point of Lowen's approach spaces and the probabilistic field of Kramosil and Michalek's fuzzymetric spaces, we present a family of spaces, called fuzzy approach spaces, that are appropriate to handle, at the same time, both measure conceptions. To do that, we study the underlying metric interrelationships between the above mentioned theories, obtaining six postulates that allow us to consider such kind of spaces in a unique category. As a result, the natural way in which metric spaces can be embedded in both classes leads to a commutative categorical scheme. Each postulate is interpreted in the context of the study of the evolution of fuzzy systems. First properties of fuzzy approach spaces are introduced, including a topology. Finally, we describe a fixed point theorem in the setting of fuzzy approach spaces that can be particularized to the previous existing measure spaces.

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Background Ubiquitination is known to regulate physiological neuronal functions as well as to be involved in a number of neuronal diseases. Several ubiquitin proteomic approaches have been developed during the last decade but, as they have been mostly applied to non-neuronal cell culture, very little is yet known about neuronal ubiquitination pathways in vivo. Methodology/Principal Findings Using an in vivo biotinylation strategy we have isolated and identified the ubiquitinated proteome in neurons both for the developing embryonic brain and for the adult eye of Drosophila melanogaster. Bioinformatic comparison of both datasets indicates a significant difference on the ubiquitin substrates, which logically correlates with the processes that are most active at each of the developmental stages. Detection within the isolated material of two ubiquitin E3 ligases, Parkin and Ube3a, indicates their ubiquitinating activity on the studied tissues. Further identification of the proteins that do accumulate upon interference with the proteasomal degradative pathway provides an indication of the proteins that are targeted for clearance in neurons. Last, we report the proof-of-principle validation of two lysine residues required for nSyb ubiquitination. Conclusions/Significance These data cast light on the differential and common ubiquitination pathways between the embryonic and adult neurons, and hence will contribute to the understanding of the mechanisms by which neuronal function is regulated. The in vivo biotinylation methodology described here complements other approaches for ubiquitome study and offers unique advantages, and is poised to provide further insight into disease mechanisms related to the ubiquitin proteasome system.