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                <text>Dietary PUFAs (polyunsaturated fatty acids) co-ordinately suppress transcription of a group of hepatic genes encoding glycolytic and lipogenic enzymes. Suppression of Fasn (fatty acid synthase) transcription involves two PUFA-responsive regions, but the majority of PUFA sensitivity maps to a region within the proximal promoter containing binding sites for NF-Y (nuclear factor-Y), Sp1 (stimulatory protein 1), SREBP (sterol-regulatory-elementbinding protein), and USF (upstream stimulatory factor). Promoter activation assays indicate that altered NF-Y is the key component in regulation of Fasn promoter activity by PUFA. Using electrophoretic mobility-shift assay and chromatin immunoprecipitation analysis, we demonstrate for the first time that PUFAs decrease in vivo binding of NF-Y and SREBP-1c to the proximal promoter of the hepatic Fasn gene and the promoters of three additional genes, spot 14, stearoyl-CoA desaturase and farnesyl diphosphate synthase that are also down-regulated by PUFA. The comparable 50% decrease in NF-Y and SREBP-1c binding to the promoters of the respective PUFA-sensitive genes occurred despite no change in nuclear NF-Y content and a 4-fold decrease in SREBP-1c. Together, these findings support a mechanism whereby PUFA reciprocally regulates the binding of NF-Y and SREBP-1c to a subset of genes which share similar contiguous arrangements of sterol regulatory elements and NF-Y response elements within their promoters. PUFA-dependent regulation of SREBP-1c and NF-Y binding to this unique configuration of response elements may represent a nutrient-sensitive motif through which PUFA selectively and co-ordinately targets subsets of hepatic genes involved in lipid metabolism. Key words: fatty acid synthase (FASN), nuclear factor-Y (NF-Y), stimulatory protein 1 (Sp1), sterol-regulatory-element binding-protein (SREBP), polyunsaturated fatty acids (PUFA), liver.</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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&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;&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;Centellograf&amp;iacute;a en el Desarrollo Farmac&amp;eacute;utico : estudios In Vitro e In Vivo de Comprimidos de Ranitidina&lt;/strong&gt;</text>
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                <text>El presente trabajo tiene como objetivo evaluar la utilidad de los estudios centellogra&amp;iacute;ficos in viao e in vivo en el desarrob de una formulaci&amp;oacute;n farmac&amp;eacute;utica. Se eligi&amp;oacute; como trazador del proceso el radiofa&amp;iacute;rmaco 99mTc-a&amp;iacute;cido dietilentriaminopentaac&amp;eacute;tico, que se incorpor&amp;oacute; a 4 formulaciones (Fi a F4) de comprimidos de ranitidina. Se llevaron a cabo estudios de estabilidad del radiofa&amp;iacute;rmaco en polvos, granulados y comprimidos. Las formulaciones en las cuales se verific&amp;oacute; su estabilidad durante 24 h (F2 y F4) fueron utilizadas para ensayos in v i h de disoluci&amp;oacute;n y desintegraci&amp;oacute;n y estudios en 6 voluntarios sanos. La desintegraci&amp;oacute;n in vibo e in vivo fue monitoreada por centellogra&amp;ntilde;a gamma. El radiof4rmaco present&amp;oacute; diferentes cin&amp;eacute;ticas de disoluci&amp;oacute;n a partir de F2 y P4, siendo las respectivas constantes del mismo orden que para la ranitidina en cada formulaci&amp;oacute;n en estudio. La centellograf&amp;iacute;a posibilit&amp;oacute; establecer una correlaci&amp;oacute;n entre las constantes de desintegraci&amp;oacute;n in v i h e in vivo. Esto permitirla predecir el comportamiento en el tracto gastro-intestinal de cada formulaci&amp;oacute;n a partir de la desintegraci&amp;oacute;n in viao. Los estudias centellogra&amp;iacute;-' ricos brindan informaci&amp;oacute;n relevante con economla de tiempo en etapas de desarrollo. SUMMARY."Scintigraphy in Pharmaceutical Development Stage / In vitro 1 In vivo Studies of Ranitidine Tablets". Scintigraphic studies in vitro and in vivo were carried out to evaluate their utility in the development of pharmaceutical forms. A radiopharmaceutical (99mTc-dietilentr&amp;iacute;aminepentacetic acid) was incorporated as the tracer in four tablet formulations (Fi to F4) of ranitidine. Stability of the radiopharmaceuticai with the excipients, granulates and tablets was assesed. Those formulations where the tracer verified stability during 24 hours (F2 and F4) were tested through dissolution and desintegration studies. Scintigraphic images were acquired in gamma camera after administration of ranitidine tablets to 6 healthy volunteers. The radiopharmaceutical showed different dissolution profiles from F2 and F4, The dissolution constants for ranitidine and the radiopharmaceutical had similar vaiues in each formulation. A correlation between in vitrolin vivo disintegration was established. This would enable to predict gastro-intestinal transit ftom in vitro disintegration data. Scintigraphjc studies give relevant information in short time dunng development stages of a pharmaceutical dosage.</text>
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                <text>&lt;strong&gt;Paolino, Andrea&lt;/strong&gt;</text>
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                <text>Acta Farmace&amp;uacute;tica Bonaerense v. 19, no. 3, 2000. -- p. 217-224</text>
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                <text>Colegio de Farmac&amp;eacute;uticos de la Provincia de Buenos Aires</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>ISSN: 0326-2383</text>
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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>Departamento de Documentación y Biblioteca</text>
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                <text>&lt;strong&gt;Cu (II) complexation with his-gly and his-ala. X-ray structure of [Cu(his-gly) (2) center dot]6H (2) O&lt;/strong&gt;</text>
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                <text>Two novel Cu(II)�/dipeptide complexes containing L-histidyl�/L-glycine and L-histidyl�/L-alanine as ligands were prepared and characterised by infrared and electronic spectroscopies. EPR measurements were also made in solution and in the solid state. Cyclic voltammetric studies were carried out on aqueous solution. The crystalline structure of the [Cu(L-histidyl�/L-glycine)2(H2O)2] �/6H2O was determined by X-ray diffractometry. It crystallises in the space group C2. The Cu(II) is in a tetragonally distorted octahedral coordination, where the basal plane is occupied by N-atoms belonging to the histidine portion. The apical positions are occupied by two molecules of water.</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=5df591c19cc13f11564074d135cd4838" target="_blank"&gt;&lt;strong&gt;Facchin, Gianella&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Bar&amp;aacute;n, Enrique J.&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=330eeda61de9937431a7182c44a5ee24" target="_blank"&gt;&lt;strong&gt;Pardo, Helena&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Araujo, M.P.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Batista, A.A.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Costa, A.J.&lt;/strong&gt;</text>
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                <text>Inorganica Chimica Acta v. 355, , 2003. -- p.408-413</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>A simple and fast ultrasound-assisted procedure for the determination of iron and zinc in infant formulas is presented. The analytical determinations were carried out by flame atomic absorption spectrometry. Multivariate experiments were performed for optimization; in addition, a comparative study was carried out using two ultrasonic devices. A method using an ultrasonic bath was selected because several samples can be prepared simultaneously, and there is less contamination risk. Analytical precision (sr(%)) was 3.3% and 4.1% for iron and zinc, respectively. Trueness was assessed using a reference material and by comparison of the results obtained analyzing commercial samples using a reference method. The results were statistically equivalent to the certified values and in good agreement with those obtained using the reference method. The proposed method can be easily implemented in laboratories for routine analysis with the advantage of being rapid and in agreement with green chemistry.</text>
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                <text>&lt;p&gt;The presence of Stone&amp;ndash;Wales, single and double vacancy defect sites in bilayer graphene was studied by means of dispersion corrected density functional theory. Based on the analysis of the formation energies computed for monolayer and bilayer graphene, monovacancies are expected to be equally frequent in both materials. In the case of the single vacancy, the formation energy is barely affected by the second layer and so does the interlayer interaction energy. However, Stone&amp;ndash;Wales and double vacancies may be expected to be more frequent in single layer graphene because their formation energies are expected to be lower as compared to bilayer graphene. Calculations employing very large unit cells would be interesting to reduce the effect of the incommensurability of the unit cells of perfect and defective graphene, and thus confirm the latter statement. The single and double vacancies have the similar formation energy in bilayer graphene but for monolayer graphene, the 5-8-5 divacancy is more stable by at least 0.7 eV, in contrast with recent results. The electronic properties of defective bilayer graphene are similar to those corresponding to monolayer graphene. Finally, we have shown that the magnetic moment of monolayer graphene with a monovacancy is smaller than that of bilayer graphene bearing the same defect, when the unit cell is optimized. Yet, if the unit cells are fixed, different outcomes can be obtained. If the unit cell of perfect graphene is employed the magnetic moment of bilayer graphene with a single vacancy is larger, but if the unit cell of monolayer graphene with a single vacancy is to be employed the magnetic moment of defective bilayer graphene becomes smaller than that of monolayer graphene with a monovacancy&lt;/p&gt;</text>
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                <text>Cycloaddition reactions onto graphene were studied by means of first-principle calculations. We found that for all reactions studied there is a cooperative behavior responsible for dramatically increasing the reaction energies. This result explains the reason why the 1,3 dipolar cycloaddition of azomethine ylides is both feasible and slow. The cooperative effect decreases in the following order: [2 + 2]-addition of benzynes &amp;gt;1,3-dipolar cycloaddition &amp;gt;[2 + 1]-cycloaddition of NH. This cooperative behavior can open new avenues to fine-tune the physical and chemical properties of graphene. Our results indicate that it is possible to fine tune the band gap of graphene from 0 to 2 eV by varying the number of azomethine groups attached.</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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&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;
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                <text>The C60H28 buckycatcher (BC) is an excellent host for fullerenes. This receptor features two corannulene pincers which trap C60/C70 via &amp;pi; stacking interactions. Although, the formation of C60@C60H28 complexes is readily observed, the dimerization of C60H28 is not a competitive process, even at high concentrations. By means of first principle calculations, we have studied the thermodynamics of the polymerization of BCs and the formation of fullerene complexes. The results obtained with the M06-2X, B97-D, B3LYP-D3BJ, PBE-D2, and PBE-D3 functionals indicated that the interaction energy of (C60H28)2 is larger than the one computed for C60@C60H28, by 8&amp;ndash;10 kcal/mol. Because of the greater number of atoms, and due to the presence of more hydrogens, the inclusion of free energy corrections lowers the energetic separation between (C60H28)2 and C60@C60H28, even though the dimer maintains its position as being slightly more bound than that of the C60@C60H28. Our calculations indicated that up to the C60H28 trimer could be formed with a free energy change larger than that corresponding to the dimerization and fullerene complexation processes. Finally, we found that the inversion of the corannulene pincers attached to the cyclooctatetraene core is 2&amp;ndash;3 kcal/mol lower than that corresponding to free corannulene. We expect that this work can motivate new investigations that may lead to the observation of C60H28 polymers. &amp;copy; 2015 Wiley Periodicals, Inc.</text>
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                <text>For glutathione reductase (GR), amammalian reduced nicotinamide adenine dinucleotide phosphate dependent &amp;macr;avoenzyme participating in free-radical detoxi&amp;reg;cation pathways, we present a quantum chemical study addressing aspects of its electronic mechanism. The system is known to sustain both ping-pong and sequentially ordered mechanisms depending upon par- ticular conditions. Isoalloxazine and nicotinamide- N-protonated rings are taken as a minimum model. The AM1 method and the AMSOL program are used throughout. Starting from a transition-state structure, docked at GRs active site, and successively including molecular elements of the active site relevant to the redox processes, geometry-optimized binary and tertiary complexes are characterized suggesting a plausible description for the sequentially ordered mechanism. The ping-pong mechanism relates to an electron-transfer (ET) mechanism. An ET binary complex between nicotinamide and the isoalloxazine ring was character- ized. Its electronic structure is controlled by the proto- nation state of the proton relay found at this active site. The excess proton in the relay comes from the previous hydride-transfer step. The experimental stereoselectivity is then ful&amp;reg;lled. The state of charge (standard Mulliken population analysis) shows an excess of two electrons on the isoalloxazine ring and almost one on the nicotin- amide ring. The overall results suggest that both mechanisms can be controlled by the same hydride- transfer structure, the dierence between them being determined by changes in the oxidized coenzyme binding strength to the protein and/or the strength of the protein&amp;plusmn;substrate interactio</text>
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                <text>Theoretical Chemistry Accounts v. 103, no. 6, 2000. -- p. 451-462</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;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 ethanolic extract of ripe fruits of Melia azedarach (Meliaceae) and its subfractions were tested against four insect species, portraying important agricultural pests. Five limonoids were isolated: two tirucallane type triterpenoids never isolated before from this species (21</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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                <text>Various cutaneous glands have been identified as sources of chemical signals that mediate many social interactions in deer. The pampas deer, a species considered near threatened, inhabits grasslands of South America. In this work, the chemical compositions from preorbital, tarsal, and digital gland secretions of semi-captive males were characterized by gas chromatography&amp;ndash;mass spectrometry. The composition of these secretions showed a great complexity, with 143 compounds detected. Hierarchical cluster and principal component analyses show no relation to age or secretion type. Five compound classes (esters, fatty alcohols, lactones, sterols, and sulphuretted) differed with glands. The chemical complexity of the secretions, the individual differences in the whole compounds composition, and the absence of clustering by age lead to the hypothesis that these secretions may encode at once for individual information and for social status information.&lt;br /&gt;&lt;br /&gt;Varias gl&amp;aacute;ndulas cut&amp;aacute;neas han sido identificadas como productoras de se&amp;ntilde;ales qu&amp;iacute;micas que median interacciones sociales en losciervos. El venado de las pampas es una especie considerada casi amenazada que habita los pastizales de Sudam&amp;eacute;rica. En este trabajo se caracteriz&amp;oacute; la composici&amp;oacute;n qu&amp;iacute;mica de las secreciones de las gl&amp;aacute;ndulas preorbital, tarsal e interdigital de machos por cromatograf&amp;iacute;a de gases-espectrometr&amp;iacute;a de masas. Estas secreciones mostraron una gran complejidad en su composici&amp;oacute;n, con 143 compuestos detectados. No se observ&amp;oacute; ninguna agrupaci&amp;oacute;n de compuestos relacionada con la edad o el tipo de secreci&amp;oacute;n. Cinco clases de compuestos (&amp;eacute;steres, alcoholes grasos, lactonas, esteroles, y compuestos azufrados) difirieron de acuerdo al origen glandular. La complejidad qu&amp;iacute;mica de las secreciones, las diferencias individuales en dicha composici&amp;oacute;n, y la ausencia de agrupamiento por edad, llevan a postular la hip&amp;oacute;tesis de que estas secreciones pueden codificar a la vez tanto informaci&amp;oacute;n individual como del estado social.&lt;br /&gt;&lt;br /&gt;</text>
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                <text>Journal of Mammalogy v. 97, no. 1, 2016.-- p. 167-168</text>
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                <text>&lt;p class="western" style="margin-bottom: 0cm; line-height: 100%;"&gt;&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.&lt;/p&gt;</text>
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                <text>ISSN: 1510-3870</text>
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              <name>Description</name>
              <description>An account of the resource</description>
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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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          <element elementId="50">
            <name>Title</name>
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                <text>Determinaci&amp;oacute;n del pH &amp;oacute;ptimo para la hidr&amp;oacute;lisis enzim&amp;aacute;tica de un aceite</text>
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                <text>ACEITES</text>
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                <text>CINETICA QUIMICA</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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              <elementText elementTextId="361046">
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          <element elementId="87">
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                <text>Esta pr&amp;aacute;ctica est&amp;aacute; dise&amp;ntilde;ada para un curso universitario de nivel introductorio en Fisicoqu&amp;iacute;mica o en Bioqu&amp;iacute;mica. Ejemplifica simult&amp;aacute;neamente varios conceptos que se vinculan con la cin&amp;eacute;tica qu&amp;iacute;mica y la cat&amp;aacute;lisis con la qu&amp;iacute;mica de los l&amp;iacute;pidos y su metabolismo. Se estudia la cantidad de &amp;aacute;cidos grasos producidos al hacer reaccionar durante 1hora a 37 grC una cantidad constante de aceite de girasol con una cantidad constante de lipasa pancre&amp;aacute;tica de cerdo |b a diferentes pH. Se determina as&amp;iacute; el pH &amp;oacute;ptimo de trabajo de la mencionada lipasa.</text>
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            <name>Creator</name>
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                <text>&lt;strong&gt;Pazo, Gabriela&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Fern&amp;aacute;ndez, M&lt;/strong&gt;</text>
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              <elementText elementTextId="361051">
                <text>&lt;strong&gt;Minetti, A.&lt;/strong&gt;</text>
              </elementText>
              <elementText elementTextId="361052">
                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=6586904caf76687142b8c1917494e201" target="_blank"&gt;&lt;strong&gt;Grompone, Ma. Antonia&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>Anuario Latinoamericano de Educaci&amp;oacute;n Qu&amp;iacute;mica. v. 4, no. 4, 1991. -- p. 21-26</text>
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              <elementText elementTextId="361054">
                <text>Universidad Nacional de San Luis</text>
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                <text>&lt;p&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/p&gt;&#13;
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