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                <text>&lt;strong&gt;Differentiation of industrial wine yeast strains using microsatellite markers.&lt;/strong&gt;</text>
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                <text>&lt;p&gt;Aims:&amp;ensp;To differentiate nine industrial wine strains of Saccharomyces cerevisiae using microsatellite (simple sequence repeats, SSR) markers.&lt;/p&gt;&#13;
&lt;p&gt;Methods and Results:&amp;ensp;Six of the strains were indigenous yeasts currently used as high-density starter monocultures by the Uruguayan wine industry. Unequivocal differentiation of these six native strains and three commercial S. cerevisiae wine strains was achieved by PCR amplification and polymorphism analysis of loci containing microsatellite markers.&lt;/p&gt;&#13;
&lt;p&gt;Conclusions:&amp;ensp;We recommend the use of this reproducible and simple molecular method to routinely discriminate wine yeast strains. Significance and Impact of the Study:&amp;ensp; Microsatellites are superior to other methods for typing yeasts because the results can be exchanged as quantitative data. Knowledge of the frequencies of the alleles for different SSR markers will eventually lead to an accurate typing method to identify industrial wine yeast strains.&lt;/p&gt;</text>
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                <text>Letters in Applied Microbiology v. 33, no. 1, 2001. -- p. 71-75</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI: 10.1046/j.1472-765X.2001.00946.x</text>
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                <text>&lt;strong&gt;Diffusion and Reptation Quantum Monte Carlo Study of the NaK Molecule&lt;/strong&gt;</text>
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                <text>ALEACIONES</text>
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                <text>Diffusion Monte Carlo (DMC) and Reptation Monte Carlo (RMC) methods, have been applied to study some properties of the NaK molecule. Hartree-Fock (HF), Density Functional (DFT) and single and double configuration interaction (SDCI) wavefunctions with a valence quadruple zeta atomic natural orbital (VQZ/ANO) basis set were used as trial wavefunctions. Values for the potential energy curve, dissociation energy and dipole moment were calculated for all methods and compared with experimental results and previous theoretical derivations. Quantum Monte Carlo (QMC) calculations were shown to be useful methods to recover correlation in NaK, essential to obtain a reasonable description of the molecule. The equilibrium distance&amp;mdash;interpolated from the potential energy curves&amp;mdash;yield a value of 3.5 &amp;Aring;, in agreement with the experimental value. The dissociation energy, however, is not as good. In this case, a conventional CCSD(T) calculation with an extended aug-pc-4 basis set gives a much better agreement to experiment. On the contrary, the CCSD(T), other MO and DFT methods are not able to reproduce correctly the large dipole moment of this molecule. Even DMC methods with a simple HF trial wavefunction are able to give a better agreement to experiment. RMC methods are even better, and the value obtained with a B3LYP trial wavefunction is very close to the experimental one.</text>
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                <text>&lt;strong&gt;Segovia, Marc E&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://www.google.com/url?sa=t&amp;amp;rct=j&amp;amp;q=&amp;amp;esrc=s&amp;amp;source=web&amp;amp;cd=1&amp;amp;ved=2ahUKEwjO5a_q6r_mAhX1IbkGHWsNAxYQFjAAegQIBBAH&amp;amp;url=https%3A%2F%2Fexportcvuy.anii.org.uy%2FCvEstatico%2F%3FurlId%3Da7868d1a46654e7a04ba7167141502086fa0cfad8b13463f75d90af715685994bc8f3eafaad6f6d2f6647277c9782143df93695c8a7d8e14295323ca2e2847d3%26formato%3Dpdf%26convocatoria%3D21&amp;amp;usg=AOvVaw3DgPJlf--GOsjsu4KZ-hpA" target="_self"&gt;&lt;strong&gt;Ventura, Oscar N.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>Molecular Physics v. 117, no. 6, 2019.-- p. 813-822</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>With the aim to develop compounds able to target multiple metabolic pathways and, thus, to lower the chances of drug resistance, we investigated the anti-trypanosomal activity and selectivity of a series of symmetric diglycosyl diselenides and disulfides. Of 18 compounds tested the fully acetylated forms of di-&amp;beta;-D-glucopyranosyl and di-&amp;beta;-D-galactopyranosyl diselenides (13 and 15, respectively) displayed strong growth inhibition against the bloodstream stage of African trypanosomes (EC50 0.54 &amp;mu;M for 13 and 1.49 &amp;mu;M for 15) although with rather low selectivity (SI &amp;lt; 10 assayed with murine macrophages). Nonacetylated versions of the same sugar diselenides proved to be, however, much less efficient or completely inactive to suppress trypanosome growth. Significantly, the galactosyl (15), and to a minor extent the glucosyl (13), derivative inhibited glucose catabolism but not its uptake. Both compounds induced redox unbalance in the pathogen. In vitro NMR analysis indicated that diglycosyl diselenides react with glutathione, under physiological conditions, via formation of selenenylsulfide bonds. Our results suggest that non-specific cellular targets as well as actors of the glucose and the redox metabolism of the parasite may be affected. These molecules are therefore promising leads for the development of novel multitarget antitrypanosomal agents.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Digoxina en suero (monitoreo de drogas) : an&amp;aacute;lisis por diferentes m&amp;eacute;todos instrumentales HPLC, GLC, TLC, espectrofotom&amp;eacute;tricos&lt;/strong&gt;</text>
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                <text>In this work, several immobilization strategies for Gluconobacter oxydans NBRC 14819 (Gox) were tested in the bioconversion of crude glycerol to dihydroxyacetone (DHA). Agar, agarose and polyacrylamide were evaluated as immobilization matrixes. Glutaraldehyde crosslinked versions of the agar and agarose preparations were also&lt;br /&gt;tested. Agar immobilized Gox proved to be the best heterogeneous biocatalyst in the bioconversion of crude glycerol reaching a quantitative production of 50 g/L glycerol into DHA solely in water. Immobilization allowed&lt;br /&gt;reutilization for at least eight cycles, reaching four times more DHA than the amount obtained by a single batch of free cells which cannot be reutilized. An increase in scale of 34 times had no impact on DHA productivity. The results obtained herein constitute a contribution to the microbiological production of DHA as they not only attain&lt;br /&gt;unprecedented productivities for the reaction with immobilized biocatalysts but also proved that it is feasible to do it in a clean background of solely water that alleviates the cost of downstream processing.</text>
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                <text>&lt;strong&gt;Trelles, Jorge A.&lt;/strong&gt;</text>
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                <text>Journal of Biotechnology, v. 340, 2021. -- pp. 102-109.</text>
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                <text>&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;br /&gt; &lt;br /&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;br /&gt; &lt;br /&gt; &lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;br /&gt; &lt;br /&gt; (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;br /&gt; &lt;br /&gt; &lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                <text>&lt;strong&gt;Diminished amyloid-M burden in Tg2576 Mice following a prophylactic oral immunization with a salmonella-based amyloid-M derivative vaccine&lt;/strong&gt;</text>
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                <text>Immunotherapy holds great promise for Alzheimer's disease (AD) and other conformational disorders but certain adverse reactions need to be overcome. Prior to the side effects in the first Elan/ Wyeth AD vaccine trial, we proposed using amyloid-&amp;beta; (A&amp;beta;) derivatives as a safer approach. The route of administration may also affect vaccine safety. To assess the feasibility of oral immunization that promotes mucosal immunity, Tg2576 AD model mice were treated prophylactically three times over 6 weeks starting at 3&amp;minus;5 months of age with a Salmonella vaccine expressing K6A&amp;beta;1&amp;minus;30. At 22 &amp;minus;24 months of age, cortical A&amp;beta; plaque burden and total A&amp;beta;40/42 levels were reduced by 48&amp;minus;75% in the immunized mice compared to controls, which received unmodified Salmonella. Plaque clearance was not associated with increased microglial activation which may be explained by the long treatment period. Furthermore, cerebral microhemorrhages were not increased in the treated mice in contrast to several passive A&amp;beta; antibody studies. These results further support our findings with this immunogen delivered subcutaneously, and demonstrate its efficacy when given orally which may provide added benefits for human use. Keywords</text>
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                <text>&lt;strong&gt;Boutajangout, A.,&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Go&amp;ntilde;i, Fernando&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Knudsen, E&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Schreiber, F&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Asuni, A&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Quartermain, D&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Frangione, B.,&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Chabalgoity, Alejandro&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Wisniewski, T&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Sigurdsson, E.M.&lt;/strong&gt;</text>
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                <text>Journal of Alzheimer's Disease v. 18, no. 4, 2009. -- p. 961-972</text>
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                <text>IOS Press</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt; La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Din&amp;aacute;mica de los residuos de pesticidas empelados en la cadena citr&amp;iacute;cola&lt;/strong&gt;</text>
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                <text>La agricultura posee un rol preponderante en el desarrollo humano, resultando de importancia sustancial la investigaci&amp;oacute;n que promueva su desarrollo y comprenda en su campo de acci&amp;oacute;n el control de enfermedades que puedan afectar su rendimento y productividad o amenazar la salud humana como por ejemplo, la contaminaci&amp;oacute;n microbiana o la presencia de micotoxinas. En este sentido, la industria citr&amp;iacute;cola cumple con estrictas pr&amp;aacute;cticas de sanitizaci&amp;oacute;n durante el cultivo y packing de las frutas frescas de forma de prevenir y controlar la contaminaci&amp;oacute;n microbiana que puede causar el deterioro de la fruta. Sumado al deteriodo de la calidad de los frutos que son afectados por pestes en el campo, las p&amp;eacute;rdidas durante el almacenamiento y transporte de los frutos c&amp;iacute;tricos, provocadas directamente por ataques de hongos pat&amp;oacute;genos en postcosecha, han sido estimadas en un 90 %, en aquellos casos en que no se aplican fungicidas. Es por ello, que los productos qu&amp;iacute;micos utilizados en la producci&amp;oacute;n se han convertido en una herramienta que permite la obtenci&amp;oacute;n de niveles de rendimiento y calidad. El estudio de la din&amp;aacute;mica de los residuos de pesticidas resultantes en las distintas etapas de la cadena productiva, su distribuci&amp;oacute;n en los productos procesados y en los compartimentos ambientales es cr&amp;iacute;tica para comprobar el cumplimiento de las buenas pr&amp;aacute;cticas agr&amp;iacute;colas, la sustentabilidad del sistema productivo global y la inocuidad de los alimentos y sub-productos que resulten. Para realizar este estudio, la instrumentaci&amp;oacute;n de alta sensibilidad junto a modernos tratamientos de muestra, permiten trabajar con metodolog&amp;iacute;as anal&amp;iacute;ticas con l&amp;iacute;mites de cuantificaci&amp;oacute;n a nivel de trazas. El objetivo de esta tesis fue estudiar la din&amp;aacute;mica de los residuos de pesticidas en la cadena citr&amp;iacute;cola. Los objetivos espec&amp;iacute;ficos, contemplando la cadena globalmente fueron: 1) Desarrollo de metodolog&amp;iacute;as anal&amp;iacute;ticas y estudio de los factores que influyen en la eficiencia de las determinaciones como ser el Efecto Matriz; 2) Estudio de la disipaci&amp;oacute;n de pesticidas de precosecha en el campo; 3) Adecuaci&amp;oacute;n de los tratamientos de pre y poscosecha en las condiciones de producci&amp;oacute;n para cumplir con las disposiciones vigentes y asegurar la inocuidad de los productos; 4) Estudio de la eficacia de nuevas alternativas para la disminuci&amp;oacute;n del uso de RESUMEN 19 fungicidas de poscosecha; 5) Caracterizaci&amp;oacute;n de los niveles de residuos de pesticidas en los efluentes de los packings nacionales y estudio de posibles v&amp;iacute;as para su remediaci&amp;oacute;n empleando procesos de oxidaci&amp;oacute;n avanzada. Durante todo el per&amp;iacute;odo de trabajo en estos estudios de posgrado 1. Se desarrollaron y validaron metodolog&amp;iacute;as anal&amp;iacute;ticas para la determinaci&amp;oacute;n de residuos de pesticidas en fruta fresca (naranja, mandarina y lim&amp;oacute;n), en aceites esenciales y en jugo concentrado de lim&amp;oacute;n. Estas metodolog&amp;iacute;as permiten determinar la mayor&amp;iacute;a de los pesticidas seleccionados a niveles adecuados para cada matriz estudiada, logr&amp;aacute;ndose en todos los casos, l&amp;iacute;mites de cuantificaci&amp;oacute;n menores que los l&amp;iacute;mites m&amp;aacute;ximos de residuos establecidos para cada matriz. Las metodolog&amp;iacute;as desarrolladas se emplearon para el an&amp;aacute;lisis de muestras reales as&amp;iacute; como tambi&amp;eacute;n para determinar el residuo remanente sobre muestras de ensayos realizados a campo y en poscosecha. 2. Se desarroll&amp;oacute; una base de datos de alta resoluci&amp;oacute;n para el monitoreo de residuos de pesticidas en naranja con un sistema instrumental de alta resoluci&amp;oacute;n GC-ToF. Por otro lado, uno de los aspectos que influyen en la determinaci&amp;oacute;n anal&amp;iacute;tica de residuos de pesticidas con espectrometr&amp;iacute;a de masas utilizando ionizaci&amp;oacute;n por electospray es el Efecto Matriz, esto es la influencia de los coextractivos de la matriz en estudio sobre la determinaci&amp;oacute;n. El Efecto Matriz se estudi&amp;oacute; durante el an&amp;aacute;lisis de pesticidas utilizando una metodolog&amp;iacute;a acetato de etilo desarrollada (que fuera previamente validada) y trabajando con un sistema instrumental de alta resoluci&amp;oacute;n LC-ToF. Los resultados obtenidos indican que para una correcta cantificaci&amp;oacute;n de residuos de pesticidas, es necesario trabajar con curvas de calibraci&amp;oacute;n preparadas en la misma matriz que la muestra o en su defecto, utilizando una variedad de la misma especie. Se pudo determinar que la coelucion de analitos y metabolitos coextra&amp;iacute;dos de la matriz, es una de las causas m&amp;aacute;s importantes del Efecto Matriz y que este efecto de la coeluci&amp;oacute;n puede minimizarse al trabajar con masas exactas de alta resoluci&amp;oacute;n. 2. Se desarrollaron experimentos a campo sobre variedades de mandarinas y naranja para establecer las curvas de disipaci&amp;oacute;n de 5 pesticidas utilizados habitualmente en instancias de precosecha y para los mismos se establecieron los tiempos de vida media bajo las condiciones del estudio. Los resultados mostraron que abamectina, spinosad, piraclostrobina, difenoconazol e imidacloprid se disipan en las condiciones de la producci&amp;oacute;n nacional, alcanzando concentraciones menores que sus respectivos LMR al RESUMEN 20 momento de la cosecha. Se evalu&amp;oacute; tambi&amp;eacute;n c&amp;oacute;mo influye el almacenamiento en fr&amp;iacute;o de la fruta durante la poscosecha de mandarinas Clementinas, sobre el nivel de residuos de pesticidas que fueron aplicados a nivel de campo. El nivel de residuo luego de 30 d&amp;iacute;as de almacenamiento en fr&amp;iacute;o no fue significativamente diferente para los activos estudiados en dicha variedad. 4. Se evalu&amp;oacute; la utilizaci&amp;oacute;n de NaHCO3 conjuntamente con imazalil como tratamiento de poscosecha en la l&amp;iacute;nea de empaque buscando disminuir la carga de pesticida a ser utilizado y de esta forma influir sobre la generaci&amp;oacute;n de resistencia y disminuci&amp;oacute;n de su impacto ambiental. La incorporaci&amp;oacute;n de la sal no mostr&amp;oacute; diferencias significativas entre los tratamientos ni en el nivel de residuo de imazalil obtenido sobre la fruta. 5. Se ajust&amp;oacute; la determinaci&amp;oacute;n de pesticidas de poscosecha en efluentes de packings y se analizaron muestras reales. En base a los compuestos detectados, se evalu&amp;oacute; a escala de laboratorio la utilizaci&amp;oacute;n de fotocat&amp;aacute;lisis heterogena utilizando TiO2 como catalizador como herramienta para remediar efluentes. Los resultados obtenidos muestran una degradaci&amp;oacute;n de m&amp;aacute;s del 97 % de cada pesticida trabajando con el est&amp;aacute;ndar puro a una concentraci&amp;oacute;n de 10 mg L-1. Los aportes de este trabajo sirven, por un lado para comprender mejor aspectos de la din&amp;aacute;mica de pesticidas en el marco de las actividades productivas y tecnolog&amp;iacute;as que la industria citrica realiza, que llevan a obtener los niveles de residuos observados. Se corrobora en estas condiciones, el cumplimiento de los l&amp;iacute;mites m&amp;aacute;ximos de residuos y por lo tanto, la inocuidad de la fruta producida. Por otro lado, se plantean estrategias de remediaci&amp;oacute;n de los residuos de pesticidas generados en los packing c&amp;iacute;tricos para disminuir el impacto ambiental de la producci&amp;oacute;n citr&amp;iacute;cola sobre el ambiente acuatico</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;p&gt;A new crystal structure for complex [Cu2Cl2(bipy)2(&amp;mu;-Cl)(&amp;mu;-CH3O)] was obtained. X-ray diffraction data showed dinuclear complexes with metal-ions seated on two symmetrically related pentacoordinated environment, in which, a trigonal bipyramidal&lt;br /&gt;(TBPY-5) coordination polyhedra was observed. While chloride was detected as monodentate and as a bridging-ligand,&lt;br /&gt;the diimine unit and a bridging oxygen from methoxide occupied the remaining positions. The crystal structure accounted for dinuclear complexes interacting to each other via H-bonds involving C&amp;ndash;H groups of bipy and monodentate chloride anions of an adjacent molecule. Theoretical studies were conducted by DFT methods employing B3LYP in combination with 6-31G(d). Larger basis sets (6-311G(d) and cc-pVDZ) were taken into account to assess the performance of B3LYP/6-31G(d) in dealing with equilibrium geometry and population analysis. This standard methodology showed to be a reasonable performer to reproduce geometric parameters keeping the computational cost very low.&lt;/p&gt;</text>
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                <text>The reaction of K2ReCl6 with 1,2-bis(2,3-dimercaptobenzamido)ethane (H4-1), and 1,2-bis(2,3-dimercaptobenzamido) benzene (H4-2) in the presence of Na2CO3 in methanol affords dinuclear complexes of ReV. Experimental evidence supports the presence of self-assembled complexes with two {Re(S2C6H3)3} units connected in a triple-stranded fashion. Density Functional Theory (DFT) studies on geometry and electronic properties were conducted employing the hybrid B3LYP and PBE1PBE functionals. The helical (DD and KK) and meso-helical (DK) isomers were considered. For the helicate complexes included in this study, differences in the stability of the isomers were observed originating in different steric and strain interactions between the three ligand strands. The geometries at the minimum exhibit a distorted trigonal-prismatic coordination environment at the metal centers. Natural bond orbitals (NBO) analysis indicates the presence of Re&amp;ndash;S bonds which are strongly polarized toward the non-metal. Time-Dependent DFT (TD-DFT) calculations were performed for a further understanding of the optical spectra. The calculations show the occupied 5d orbitals of the rhenium lying beneath occupied sulfur-based MOs. The general features of the electronic spectra in the visible region are reasonably reproduced by the calculations. The analysis of molecular orbitals also allows the assignment of the origin for all experimentally detected absorption bands. In the high-energy region of the spectrum the absorptions are attributed to ligand-to-metal&amp;ndash;ligand charge transfer (LMLCT), in which sulfur-based orbitals and unoccupied orbitals at the rhenium atom and the benzene-o-dithiolato groups are involved. Also in the blue region, shoulders originating from LMLCT are observed</text>
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                <text>The kinetic isotope effects, KIEs, for hydrogen abstraction from the isotopologs CH4, 13CH4, CH3D, and CD4 by chlorine atoms have been studied by the dual-level direct dynamics approach with the MORATE computer program. Low-level calculations of the potential energy surface were carried out at the NDDO-SRP level (in particular the AM1-SRP level), using two different sets of specific reaction parameters labeled SRP4 and SRP13. High-level structural and energetic properties of the reactants, saddle point, and products were obtained at the MP2-SAC and MP2 levels using the 6-311G(2d,d,p) basis set and were used to interpolate corrections to the low-level calculations. The dual-level calculations were carried out using the ICL-Eckart improved interpolated corrections algorithm. Tunneling was included by the microcanonical optimized multidimensional tunneling (&amp;mu;OMT) method, and we find that large-curvature tunneling paths usually provide the dominant contribution, with significant participation of excited vibrational states. Both rectilinear and curvilinear coordinates were applied to the unsubstituted reaction. The 12C/13C KIEs calculated at the MP2-SAC///SRP4 level using MP2 frequencies are in very close agreement with the experimental ones, with values of 1.07 and 1.06 at 243 and 297 K, respectively, as compared to experimental values of 1.07 at both temperatures. For the reaction CH3D + Cl, the calculated H/D KIEs are equal to 1.55 and 1.45 at 223 and 296 K, while the measured values are equal to 1.59 and 1.50, respectively. The H/D KIE for the reaction CD4 + Cl is calculated to decrease from 11 to 4.7 as the temperature increases from 300 K to 450 K, whereas the experimental value decreases from 12 to 3.9. We also make comparison with previous results for the unsubstituted reaction CH4 + Cl.</text>
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                <text>The symbiosis of the Fourier transform spectrometer with the computer permits the development of novel procedures for handling spectroscopic data. Two such procedures are here described. The first one produces directly the spectrum of the intermolecular interaction perturbation in solutions, while the second obtains the spectrum of pressure broadening coefficients of a gas sample. The interpretation of these techniques are discussed in the light of experimental results and shown to be critically dependent on a constant, well defined slit function and on nearly perfect spectral and intensity registration.&lt;br /&gt;&lt;br /&gt;</text>
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                <text>&lt;p&gt;Almost all human cancers display dysregulated expression and/or function of one or more receptor tyrosine kinases (RTKs). The strong causative association between altered RTK function and cancer progression has been translated into novel therapeutic strategies that target these cell surface receptors in cancer. Yet, the full spectrum of RTKs that may alter the oncogenic process is not completely understood. Accumulating evidence suggests that a unique set of RTKs known as the discoidin domain receptors (DDRs) play a key role in cancer progression by regulating the interactions of tumor cells with their surrounding collagen matrix. The DDRs are the only RTKs that specifically bind to and are activated by collagen. DDRs control cell and tissue homeostasis by acting as collagen sensors, transducing signals that regulate cell polarity, tissue morphogenesis, and cell differentiation. In cancer, DDRs are hijacked by tumor cells to disrupt normal cell&amp;ndash;matrix communication and initiate pro-migratory and pro-invasive programs. Importantly, several cancer types exhibit DDR mutations, which are thought to alter receptor function and contribute to cancer progression. Other evidence suggests that the actions of DDRs in cancer are complex, either promoting or suppressing tumor cell behavior in a DDR type/isoform specific- and context-dependent manner. Thus, there is still a considerable gap in our knowledge of DDR actions in cancer tissues. This review summarizes and discusses the current knowledge on DDR expression and function in cancer. It is hoped that this effort will encourage more research into these poorly understood but unique RTKs, which have the potential of becoming novel therapeutic targets in cancer.&lt;/p&gt;</text>
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                <text>Conceptual 2D group III nitrides and oxides (e.g., 2D InN and 2D InO) in heterostructures with graphene have been realized by metal&amp;ndash;organic chemical vapor deposition (MOCVD). MOCVD is expected to bring forth the same impact in the advancement of 2D semiconductor materials as in the fabrication of estab lished semiconductor materials and device heterostructures. MOCVD employs metal&amp;ndash;organic precursors such as trimethyl-indium, -gallium, and -aluminum, with (strong) metal&amp;ndash;carbon bonds. Mechanisms that regulate MOCVD processes at the atomic scale are largely unknown. Here, we employ density functional molecular dynamics &amp;ndash; accounting for van der Waals interactions &amp;ndash; to identify the reaction pathways responsible for dissociation of the trimethylindium (TMIn) precursor in the gas phase as well as on top-layer and zero-layer graphene. The simulations reveal how collisions with hydrogen molecules, intramolecular or surface-mediated proton transfer, and direct TMIn/graphene reactions assist TMIn transformations, which ultimately enables delivery of In monomers or InH and CH3In admolecules, on graphene. This work provides knowledge for understanding the nucleation and intercalation mechanisms at the atomic scale and for carrying out epitaxial growth of 2D materials and graphene heterostructures.</text>
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                <text>Physical Chemistry Chemical Physics v.25, 2023. -- pp. 829-837</text>
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&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt;&amp;nbsp;de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt;&amp;nbsp;La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>In this study, we report a strategy using dynamic combinatorial chemistry for targeting the thioredoxin (Trx)-reductase catalytic site on Trx glutathione reductase (TGR), a pyridine nucleotide thiol-disulfide oxido-reductase. We chose Echinococcus granulosus TGR since it is a bottleneck enzyme of platyhelminth parasites and a validated pharmacological target. A dynamic combinatorial library (DCL) was constructed based on thiol-disulfide reversible exchange. We demonstrate the use of 5-thio-2-nitrobenzoic acid (TNB) as a non-covalent anchor fragment in a DCL templated by E. granulosus TGR. The heterodimer of TNB and bisthiazolidine (2af) was identified, upon library analysis by HPLC (IC[Formula: see text] = 24 [Formula: see text]M). Furthermore, 14 analogs were synthetically prepared and evaluated against TGR. This allowed the study of a structure-activity relationship and the identification of a disulfide TNB-tricyclic bisthiazolidine (2aj) as the best enzyme inhibitor in these series, with an IC[Formula: see text] = 14 [Formula: see text]M. Thus, our results validate the use of DCL for targeting thiol-disulfide oxido-reductases.</text>
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                <text>&lt;strong&gt;Saiz, Cecilia&lt;/strong&gt;</text>
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                <text>Molecular Diversity v. 18, 2014. -- p. 1-12</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora. &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp; &amp;nbsp;&amp;nbsp;&lt;/p&gt;</text>
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                <text>The parasitic kinetoplastid diseases Leishmaniasis, Chagas disease and Human African Trypanosomiasis constitute serious threats for populations throughout the (sub-)tropics. Most available drugs to treat these diseases possess inadequate properties and candidates to fill the drug pipeline are urgently needed. Paullone-N5 -acetamides inhibit trypanothione synthe tase (TryS), an essential kinetoplastid enzyme, and exhibit antiparasitic activity in the low micromolar range, but lack the desired selectivity against mammalian cells (selectivity index (SI):&amp;lt;10). With the aim to identify the paullones&amp;rsquo; moieties responsible for TryS inhibition and bioactivity, we applied molecular simplification and ring disconnection approaches. The new indolylacetamides lost activity against the expected molecular target (TryS) compared to the reference paullone MOL2008 (Leishmania infantum TryS IC50 :150 nM; Trypanosoma brucei bloodstream form EC50: 4.3 &amp;mu;M and SI: 2.4). However, several of them retained potency (T. b. brucei EC50: 2.4&amp;ndash;12.0 &amp;mu;M) and improved selectivity (SI: 5 to &amp;gt;25).</text>
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                <text>&lt;strong&gt;Lindhof, Jens C.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Ihnatenko, Irina&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;M&amp;uuml;ller, Marco J.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Ort&amp;iacute;z, Cecilia&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Ben&amp;iacute;tez, Diego&lt;/strong&gt;</text>
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                <text>&lt;a href="https://export.cvuy.uy/cv/?c50accd8ba8f87507bd244c82c8bef107eb8797238ec50e53b84c3687045a6048ff50bdd01c2c969dd60452410cde98caf41164262cccd9e688bda88809eab3c" target="_blank"&gt;&lt;strong&gt;Dibello, Estefan&amp;iacute;a&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Seidl, Leonardo&amp;nbsp;L.&amp;nbsp;&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Comini, Marcelo A.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Kunick, Conrad&lt;/strong&gt;</text>
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                <text>ChemMedChem, 2023.</text>
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            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="673274">
                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt;&amp;nbsp;de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt;&amp;nbsp;La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>10.1002/cmdc.202300036</text>
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        <name>Trypanosoma brucei</name>
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                  <text>Bibliografía Nacional Química</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                <text>&lt;strong&gt;Discovery of new orally effective analgesic and anti-inflammatory hybrid furoxanyl N-acylhydrazone derivatives&lt;/strong&gt;</text>
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            <name>Subject</name>
            <description>The topic of the resource</description>
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                <text>ANTIINFLAMATORIOS</text>
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                <text>ANALGESICOS Y ANTIPIRETICOS</text>
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                <text>INTERLEUQUINA 8</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>2012</text>
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          <element elementId="87">
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                <text>&lt;p&gt;We report the design, the synthesis and the biological evaluation of the analgesic and anti-inflammatory activities of furoxanyl N-acylhydrazones (furoxanyl-NAH) by applying molecular hybridization approach. Hybrid compounds with IL-8-release inhibition capabilities were identified. Among them, furoxanyl- NAH, 17, and benzofuroxanyl-derivative, 24, together with furoxanyl-NAH derivative, 31, without IL-8 inhibition displayed both orally analgesic and anti-inflammatory activities. These hybrid derivatives do not have additional LOX- or COX-inhibition activities. For instance, LOX-inhibition by furoxanyl-NAH derivative, 42, emerged as a structural lead to develop new inhibitors. The lack of mutagenicity of the active derivatives 17, 31, and 42, allow us to propose them as candidates for further clinical studies. These results confirmed the success in the exploitation of hybridization strategy for identification of novel N-acylhydrazones (NAH) with optimized activities&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Hernandez, Paola&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Cabrera, Mauricio&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Lavaggi, Mar&amp;igrave;a Laura&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Celano Jorc&amp;iacute;n, Laura Teresita&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Tiscornia, In&amp;eacute;s&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Rodrigues da Costa, Tiago&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Thomson, Leonor&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Bollati-Fogolin, Mariela&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Miranda, Ana Luisa P.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Lima, Lidia M.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Barreiro, Eliezer J.&lt;/strong&gt;</text>
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                <text>Bioorganic and Medicinal Chemistry v. 20, no. 6, 2012. -- p. 2158-2171</text>
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                <text>Elsevier</text>
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                <text>&lt;p align="LEFT"&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;/p&gt;&#13;
&lt;p&gt;(LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p style="margin-bottom: 0cm;"&gt;&lt;strong&gt;ADVERTENCIA&lt;/strong&gt; - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;&#13;
&lt;p&gt;&lt;br /&gt;&lt;br /&gt;&lt;/p&gt;&#13;
&lt;p style="margin-bottom: 0cm;"&gt;&amp;nbsp;&lt;/p&gt;</text>
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