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                <text>&lt;strong&gt;Susceptibility and resistance to Echinococcus granulosus infection : Associations between mouse strains and early peritoneal immuneresponses&lt;/strong&gt;</text>
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                <text>In helminth infections, there are no easy associations between host susceptibility and immune responses.Interestingly, immunity to cestodes &amp;ndash; unlike most helminths &amp;ndash; seems to require Th1-type effectors. Inthis sense, we reported recently that Balb/c and C57Bl/6 mice are high and low susceptible strains,respectively, to experimental infection by Echinococcus granulosus. However, the role of the early cel-lular peritoneal response in such differential susceptibility is unknown. Here, we analyzed the kineticsof cytokines expression and cellular phenotypes in peritoneal cells from infected Balb/c and C57Bl/6mice. Additionally, Principal Components Analysis (PCA) were conducted to highlight the most rele-vant differences between strains. Finally, the anti-parasite activities of peritoneal cells were assessedthrough in vitro systems. PCAs clustered C57Bl/6 mice by their early mixed IL-5/TNF-� responses andless intense expression of Th2-type cytokines. Moreover, they exhibited lower counts of eosinophils andhigher numbers of macrophages and B cells. Functional studies showed that peritoneal cells from infectedC57Bl/6 mice displayed greater anti-parasite activities, in accordance with higher rates of NO productionand more efficient ADCC responses. In conclusion, mild Th2-responses and active cellular mechanismsare key determinants in murine resistance to E. granulosus infection, supporting the cestode immuneexception among helminth parasites.</text>
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                <text>&lt;strong&gt;Mourglia Ettlin, Gustavo Daniel&lt;/strong&gt;</text>
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                <text>Immunobiology v. 221, 2016. -- p. 418-426</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;</text>
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                <text>&lt;strong&gt;Sustainable food choices as an impression management strategy&lt;/strong&gt;</text>
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                <text>Although living standards in certain parts of the world have improved significantly in recent decades, these improvements have often been accompanied by environmental degradation that poses health risks to millions of people. Sustainable food choices play a critical role in addressing these environmental challenges. The current review summarizes how sustainable food choices are used as an impression management action aimed at projecting a desirable image of oneself to others. We show how three distinct factors &amp;mdash; status striving, group cooperation, and the desire to attract a partner &amp;mdash; influence the use of sustainable food as an impression management tactic. The review concludes by highlighting several future research directions based on recent research on related topics.</text>
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                <text>&lt;strong&gt;Folwarczny, Michał&lt;/strong&gt;</text>
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                <text>Current Opinion in Food Science v.49, 2023. -- e100969</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;&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>&lt;strong&gt;Synthesis : characterization and biological evaluation of a novel "3 + 1 " mixed ligand 99mTc complex having an aliphatic thiol as coligand.&lt;/strong&gt;</text>
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                <text>A novel &amp;ldquo;3 + 1&amp;rdquo; mixed ligand 99mTc complex with N,N-bis(2-mercaptoethyl)-N&amp;prime;N&amp;prime;-diethyl-ethilenediamine as ligand and 1-octanethiol as coligand was prepared and evaluated as potential brain radiopharmaceutical. Preparation at tracer level was accomplished by substitution, using 99mTc-glucoheptonate as precursor and a coligand/ligand ratio of 5. Under these conditions the labeling yield was over 80% and a major product with radiochemical purity &amp;gt;80% was isolated by HPLC methods and used for biological evaluation. Chemical characterization at carrier level was developed using the corresponding rhenium and 99gTc complexes. Results were consistent with the expected &amp;ldquo;3 + 1&amp;rdquo; structure and X-ray diffraction study demonstrated that the complex adopted a distorted trigonal bipyramidal geometry. All sulphur atoms underwent ionization leading to the formation of a neutral compound. Biodistribution in mice demonstrated early brain uptake, fast blood clearance and excretion through hepatobiliary system. Although brain/blood ratio increased significantly with time, this novel 99mTc complex did not exhibit ideal properties as brain perfusion radiopharmaceutical since brain uptake was too low.</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&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>Two cationic complexes containing a ReV(O)2 + core have been prepared by substitution on the precursor [Re(O)2(PPh3)2I]. Careful control of reaction conditions allowed the synthesis of [Re(O)2L2]I (L=bis(1,2-diphenylylphosphino)ethane (dppe), bis(1,3-diphenylphosphino)propane (dppp)) compounds in high yield. Complexes were characterized by UV&amp;ndash;Vis and IR spectrophotometry, elemental analyses, FAB, 1H, 13C{1H} and 31P{1H} NMR spectra and high-performance liquid chromatography. Four compounds have also been characterized by single-crystal X-ray analyses. Cations consist of a six-coordinated rhenium atom bonded to two trans-oxo groups. The phosphines lie on the equatorial plane, almost perpendicular to the ReV(O)2 + core. The average value for the ReO bond is 1.77 &amp;Aring;, similar to that in other Re(V) dioxo complexes. Diphosphine ligands form five- and six-membered rings in which &amp;lambda;&amp;delta; conformation is adopted. The unexpected [Re(O)(OCH3)(dppp)(Cl)2]&amp;middot;CH3OH has been additionally characterized from X-ray data. It is also an octahedral complex with a methoxy ligand trans to an oxo group. Species are very stable towards redox processes and can be protonated in acidic media (70:30 dioxane:water, v/v) to yield [Re(OH)2L2]3+. The protonation constants of the diphosphine ligands are also obtained for the first time.</text>
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                <text>A new rhenium(III) complex, [Re(SC(NH2)2)6]3+, has been prepared by reduction of perrhenate with tin chloride in strongly acidic solution in the presence of thiurea. The complex has been characterized in solution and the solid state by elemental and thermal analyses, electronic and IR spectroscopy, conductimetric measurements, EPR spectra and cyclic voltammetry. Stability in aqueous solution was tested spectrophotometrically. The molecular structure of the complex in the [Re(tu-S)6]Cl3&amp;middot;4H2O salt was determined by X-ray diffraction. The compound is isomorphous to [Tc(tu-S)6]Cl3&amp;middot;4H2O. The rhenium ion, sited at an inversion center, is quasi-octahedrally coordinated by six thiourea sulfur atoms [d(ReS) vary from 2.412(2) to 2.429(2) &amp;Aring;]. Average thiourea bond distances are similar to those observed for the Tc analog Full-size image (&amp;lt;1 K).</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;&#13;
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                <text>&lt;strong&gt;Synthesis : Characterization and Potentiometric Studies of Trans-Dioxorhenium(V) Complexes-X-Ray Crystal-Structure of (Reo2(TN)(2))I-Center-Dot-H2O.&lt;/strong&gt;</text>
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                <text>[ReO2(PPh3)2I] has been used as starting material to prepare [RevO2(tn)2]I (tn = trimethylenediamine) in high yield. The complex was characterized by elemental analysis and spectroscopic methods. The complex [ReO2(en)2]I (en = 1,2-diaminoethane) was prepared analogously for comparison. The crystal structure of [ReO2(tn)2]I&amp;middot;H2O was determined from X-ray data. It consists of a six-coordinate rhenium atom bonded to two trans-oxo groups. The amines lie in the equatorial plane, almost perpendicular to the ReO2 core. The average value for the ReO bond is 1.76 &amp;Aring;, similar to that in other Re(V) dioxo complexes. The successive protonations of the oxo groups were determined for both complexes.</text>
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                <text>In this work, we report the synthesis, characterization and potentiometric studies of new Re(V) complexes of general formula [ReO2(amine)2]+ (amine = 1,2-diaminopropane, 1,4-diaminobutane, N,N&amp;prime;-diethylethylenediamine, diethylenetriamine, triethylenetetramine and N-tris(2-aminoethyl)amine). Compounds were prepared starting from [ReO2I(PPh3)2] and characterized by several techniques. The presence of different substituent groups in the diamines (including alkyl and amine groups) allows the presence of pendant arms. When these groups are free amino groups, they can react with acids such as H+ and M2+ cations and studied by potentiometry. The formation of very stable binuclear species was demonstrated.</text>
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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;
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                <text>&lt;strong&gt;Synthesis : crystal structure and magnetic properties of tetraphenylarsonium tetrachloro(oxalato)rhenate (IV) and bis (2,2'-bipyridine)tetrachloro (mu-oxalato)copper (II) rhenium (IV)&lt;br /&gt;&lt;/strong&gt;</text>
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                <text>Two new rhenium(IV) compounds of formula (AsPh4)(2)[ReCl4(ox)] (1) and [ReCl4(mu-ox)Cu(bipy)(2)] (2) (AsPh4 = tetraphenylarsonium cation, ox = oxalate anion, and bipy = 2,2'-bipyridine) have been synthesized and their crystal structures determined by single-crystal X-ray diffraction. 1 and 2 crystallize in the monoclinic system, space groups P2(1)/c and P2(1)/n, respectively, with a = 22.250(5) Angstrom, b = 11.245(3) Angstrom, c = 19.089(4) Angstrom, beta = 96.59(2)degrees, and Z = 4 for 1 and a = 9.421(2) Angstrom, b= 16.909(4) Angstrom, c = 16.179(4) Angstrom, beta = 93.97(2)degrees, and Z = 4 for 2. The structure of 1 is made up of [ReCl4(ox)](2-) anions and AsPh4+ cations held united by electrostatic forces. Rhenium(IV) is hexacoordinate, with two oxygens of a chelating ox and four chlorine atoms building adistorted octahedron around the metal atom. There is no contact between the [ReCl4(ox)](2-) anions, the shortest Re ... Re and Cl ... Cl distances being 10.345 and 7.209 Angstrom, respectively. This anionic complex is coordinated to a [Cu(bipy)(2)](2+) cation in 2, through one oxalate-oxygen, giving a neutral heterometallic dinuclear unit. The Cu(II) ion shows a very distorted five-coordinated geometry, four bipy-nitrogens occuping the equatorial positions and the oxygen atom the apical one. The basal plane geometry isdistorted toward the tetrahedron, the dihedral angle between the mean planes of the two bipy ligands is 37.6(2)degrees. These [ReCl4(mu-ox)Cu(bipy)(2)] units are arranged in such a way that a chlorine atom of one of them points toward the copper atom of the neighboring one, forming helicoid chains. The intrachain Re Cu distances through chloro and oxalato bridges are 4.658 and 4.798 Angstrom, respectively. The magnetic behavior of 1 and 2 has been investigated over the temperature range 1.8-300 K. 1 is a magnetically diluted Re(IV) complex, the great value of zero-field splitting of the ground level (D = 60 cm(-1)) accounting for the variation of chi(M)T with T in the low-temperature range. 2 behaves as a ferrimagnetic chain, with weak antiferromagnetic interactions between Re(IV) and Cu(II) through oxalato and single chloro bridges.</text>
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                <text>Inorganic Chemistry v. 38, no. 21, 1999. -- p. 4745-4752</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&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.&lt;/p&gt;</text>
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                <text>The preparation of the sodium salt of dicyano-acetic acid methyl ester (NaCH3OC(O)C(CN)2) (NaL) is reported. The structure of this anion is related to the structure of the dicyanamide, whose chelating capability has been used to develop 2D networks. Two new complexes of formula [M(L)2(H2O)2] (M=Mn2+ (1) and Cu2+ (2)) have been synthesized and their crystal structures determined by single-crystal X-ray diffraction. The coordination geometry of Mn atom in 1 is approximately octahedral, and the Mn atoms are &amp;mu;2-bridged by two pairs of L&amp;minus; resulting in an infinite one-dimensional chain. Two types of hydrogen bonds link the chains within a 3-dimensional infinite lattice. The coordination geometry of copper in 2 is tetragonal bipyramidal, showing considerable Jahn&amp;ndash;Teller distortion. Each copper atom is connected by four ligands to four different neighboring copper atoms, resulting in sheets of an infinite two-dimensional network. The large separation between the paramagnetic centers in both compounds produces a weak antiferromagnetic interaction.</text>
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                <text>Inorganica Chimica Acta v. 314, no. 1-2, 2001. -- p. 83-90</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.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Synthesis :&amp;nbsp; characterization and some reactions of trans-[co(nh2ch3)br]2+ and trans-[Co(NH3)4(NH2CH3)(NO3)]2+ complexes&lt;/strong&gt;</text>
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                <text>The preparation of trans-[Co(NH3)4(CH3NH2)Br]2+ and trans-[Co(NH3)4(CH3NH2)-(NO3)]2+ complexes is described. The UV-VIS spectra of the complexes indicate a decrease of the ligand field compared to the parent pentaammines. Infrared spectra match with the pattern of the corresponding pentaammines. The catalyzed (by Hg2+) aquation of the trans-bromomethylamine complex go under retention of the stereochemical configuration. The base hydrolysis (studied at 25&amp;deg;C) products show trans to cis rearrangement for both complexes. 1H NMR spectroscopy is used for identification of the stereochemical configuration of the compounds.</text>
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                <text>&lt;strong&gt;Sienra, Beatriz&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Massaferro, A.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Piriz, Clara.&lt;/strong&gt;</text>
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                <text>Zeitschrift fur Anorganische and Allgemeine Chemie&amp;nbsp; v. 590, , 1990. -- p. 222-228</text>
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                <text>&lt;p&gt;Wiley&lt;/p&gt;</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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