Literatura académica sobre el tema "IIIT"
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Artículos de revistas sobre el tema "IIIT"
Kaválek, Jaromír, Ulrika Králíková, Vladimír Macháček, Miloš Sedlák y Vojeslav Štěrba. "Kinetics and mechanism of solvolysis of N-aryl sulfuric diamides". Collection of Czechoslovak Chemical Communications 55, n.º 1 (1990): 202–22. http://dx.doi.org/10.1135/cccc19900202.
Texto completoRayaji, A. y A. H. M. Viswanatha Swamy. "IN VIVO AND IN VITRO EVALUATION OF ANTI-CANCER ACTIVITY OF NEWLY SYNTHESIZED COBALT COMPLEX OF COUMARIN SCHIFF BASES". INDIAN DRUGS 54, n.º 04 (28 de abril de 2017): 61–69. http://dx.doi.org/10.53879/id.54.04.10792.
Texto completoAyanwale, Musa Adekunle. "Calibration of Polytomous Response Mathematics Achievement Test Using Generalized Partial Credit Model of Item Response Theory". EDUCATUM Journal Of Science, Mathematics And Technology 8, n.º 1 (4 de junio de 2021): 57–69. http://dx.doi.org/10.37134/ejsmt.vol8.1.7.2021.
Texto completoZykova, S. S., K. V. Namyatova, K. L. Gankova, E. A. Lystsova, T. V. Shavrina y S. N. Shurov. "Antihypoxic Activity of 2,5-diaryl-8,8-dimethyl-3,6,7,8-tetrahydro-2<i>H</i>-pyrido[4,3,2-<i>de</i>]quinnolin-3-ones". Drug development & registration 11, n.º 4 (23 de diciembre de 2022): 22–26. http://dx.doi.org/10.33380/2305-2066-2022-11-4(1)-22-26.
Texto completoSiddiqui, Muhammad y Courtney Dorroll. "IIIT Intellectual Panels". American Journal of Islam and Society 31, n.º 4 (1 de octubre de 2014): 154–58. http://dx.doi.org/10.35632/ajis.v31i4.1084.
Texto completoElaradi, Hadeel. "IIIT Intellectual Panels". American Journal of Islam and Society 34, n.º 2 (1 de abril de 2017): 139–43. http://dx.doi.org/10.35632/ajis.v34i2.875.
Texto completoHützler, Wilhelm Maximilian y Ernst Egert. "N—H...S and N—H...O hydrogen bonds: `pure' and `mixed'R22(8) patterns in the crystal structures of eight 2-thiouracil derivatives". Acta Crystallographica Section C Structural Chemistry 70, n.º 2 (31 de enero de 2014): 241–49. http://dx.doi.org/10.1107/s2053229614001387.
Texto completoSlavík, Jiří, Vladimír Hanuš y Leonora Slavíková. "Alkaloids from Stylophorum lasiocarpum (OLIV.) FEDDE". Collection of Czechoslovak Chemical Communications 56, n.º 5 (1991): 1116–22. http://dx.doi.org/10.1135/cccc19911116.
Texto completoPervez, Saulat. "The International Institute of Islamic Thought Intellectual Panels". American Journal of Islam and Society 33, n.º 3 (1 de julio de 2016): 157–61. http://dx.doi.org/10.35632/ajis.v33i3.933.
Texto completoPervez, Saulat. "IIIT Panels at the 2015 ICNA Convention". American Journal of Islam and Society 32, n.º 3 (1 de julio de 2015): 149–51. http://dx.doi.org/10.35632/ajis.v32i3.1002.
Texto completoTesis sobre el tema "IIIT"
Hüsch, Tanja. "Patienten mit inoperablem, nicht-kleinzelligem Lungenkarzinom im Stadium IIIA oder IIIB nach Induktionschemotherapie". Diss., lmu, 2008. http://nbn-resolving.de/urn:nbn:de:bvb:19-84670.
Texto completoShah, Sheila Marie Alojipan. "Studies on RNA polymerase III transcription : Structural organization of transcription factor IIIb /". Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2001. http://wwwlib.umi.com/cr/ucsd/fullcit?p3025949.
Texto completoCosta, Bruna de Araújo. "Síntese, caracterização e estudo termoanalítico dos tereftalatos de térbio (III), disprósio (III), hólmio(III), érbio (III), túlio (III), ítérbio (III), lutécio (III) e ítrio(III)". Universidade Federal de Goiás, 2015. http://repositorio.bc.ufg.br/tede/handle/tede/4919.
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In this work the synthesis of the heavy lanthanides and yttrium were carried out, using the direct addition of the sodium terephthalate in the respectives metallic chloride solutions. The synthesized compounds were characterized by simultaneous Thermogravimetry and differential scanning calorimetry analysis (TG-DSC), differential scanning calorimetry (DSC), Fourier Transform Infrared Spectroscopy (FTIR), thermogravimetric analyses coupled to Fourier Transform Infrared spectroscopy (TG-FTIR), EDTA complexometry and X ray powder Diffractometry. From the data, it was possible to obtain the general formula of each compound (Ln2(TFta)3.nH2O, where Ln = Tb(III), Dy(III), Ho(III), Er(III), Tm(III), Yb(III), Lu(III) and Y(III), TFta = terephthalate, and n = 4,5 (Tb, Dy and Ho), 4,0 (Er, Tm and Y), 5,0 (Yb) and 6,5 (Lu)), as well as unreported information about the thermal properties, in air atmosphere, thermal stability; molar dehydration enthalpy; main evolved gases from thermal decomposition (H2O, CO2 and CO), the coordination mode between metal and ligand and performing the comparison of the results of X -ray diffraction of the compounds synthesized by the powder method using and the single crystal obtained by hydrothermal synthesis reported in the literature.
A pesquisa na área de compostos de coordenação com ligantes à base de ácidos carboxílicos aromáticos e metais os lantanídeos e ítrio tem sido recorrente devido as suas promissoras aplicabilidades. O presente trabalho tem como objetivo realizar as sínteses dos tereftalatos de lantanídeos pesados e ítrio pelo método direto entre soluções de tereftalato de sódio e os respectivos cloretos metálicos e caracterização dos mesmos por meio das técnicas de análise termogravimétrica e calorimetria exploratória diferencial simultânea (TG-DSC), Calorimetria exploratória diferencial (DSC), Espectroscopia de Infravermelho por Transformada de Fourrier (FTIR), Complexometria por EDTA e Difratometria de raio X pelo método do pó. A partir das informações obtidas desse estudo termoanalítico detalhado, em atmosfera de ar, foi possível obter informações inéditas, como a fórmula geral Ln2(TFta)3.(H2O)2.nH2O, onde Ln corresponde aos Tb(III), Dy(III), Ho(III), Er(III), Tm(III), Yb(III), Lu(III) e Y(III), TFta o tereftalato e n= 2,5 (Tb, Dy e Ho), 2,0 (Er, Tm e Y), 3,0 (Yb) e 4,5 (Lu); estabilidade térmica; grau de hidratação dos compostos; entalpia molar média por molécula de água; indicar os principais produtos gasosos produzidos pela decomposição térmica (H2O, CO2 e CO); sugerir coordenação em ponte entre entre metal e o ligante e realizar a comparação dos resultados de difratometria de raio x dos compostos sintetizados pelo método do pó com os monocristais obtidos por síntese difusão lenta apresentados na literatura.
Nunes, Wilhan Donizete Gonçalves. "Síntese, caracterização e estudo termoanalítico dos isoftalatos de lantânio (III), cério (III), praseodímio (III), neodímio (III), samário (III), európio (III) e gadolínio (III)". Universidade Federal de Goiás, 2015. http://repositorio.bc.ufg.br/tede/handle/tede/4777.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES
In the last years the interest in the chemistry of coordination compounds of polycarboxylic acids and lanthanides or transition metals has substantially increased, due to their interesting characteristics, such as gas storage (Metal-organic frameworks compounds), luminescence and magnetic properties. A literature survey reveals few studies investigating the properties of lighter lanthanide coordination compounds obtained by soft chemistry routes, and mainly the study of their thermal properties in air atmosphere. In this work the reaction between sodium isophthalate and lighter lanthanides solutions (La – Gd) except Pm, led to the formation of two new coordination compounds, and five already reported in the literature, whose thermal behavior and infrared spectra was investigated. The compounds was characterized by simultaneous Thermogravimetric and differential scanning calorimetry analysis (TG-DSC), differential scanning calorimetry (DSC), Fourier Transform Infrared Spectroscopy (FTIR), thermogravimetric analyses coupled to Fourier Transform Infrared spectroscopy (TG-FTIR) and EDTA complexometry. With the TG-DSC and TG-FTIR data was possible to determinate the general formula of compounds (Ln2(L)3.nH2O, where Ln = La – Gd, except Pm, L = isophthalate, n varies from 2 to 13,5), thermal stability and molar dehydration enthalpy per water molecule, as well as the main evolved gases during thermal decomposition (H2O, CO2 and CO). The FTIR spectra suggest that metal-ligand coordination occurs in the bridging bidentate mode.
Nos últimos anos, tem surgido um grande interesse na química dos compostos de coordenação de ácidos dicarboxílicos com metais de transição ou lantanídeos, devido a sua aplicabilidade em compostos de estrutura molecular porosa (Metal-organic frameworks) e interessantes propriedades luminescentes. Uma revisão na literatura revela a falta de trabalhos estudando de forma sistemática as propriedades térmicas de compostos de coordenação de lantanídeos leves com o ligante isoftalato em atmosfera de ar, principalmente obtidos por meio de vias sintéticas classificadas como brandas. Neste trabalho, foi realizada a síntese dois novos compostos de coordenação, e cinco já reportados pela literatura em diferentes trabalhos, utilizando a metodologia de reação direta entre soluções de ácido isoftálico (ácido 1,3- benzenodicarboxílico) e de lantanídeos (La – Gd) exceto Pm. Os compostos sintetizados foram caracterizados e estudados através das técnicas de análise termogravimétrica e calorimetria exploratória diferencial simultânea (TG-DSC), Calorimetria exploratória diferencial (DSC) e Espectroscopia de Infravermelho por Transformada de Fourrier (FTIR) e Complexometria por EDTA. A partir das curvas TG-DSC e TG-FTIR foi possível a determinar a estequiometria dos compostos, com fórmula geral Ln2(L)3.nH2O (Ln = La a Gd, exceto Pm, L = isoftalato) n variando de 2 a 13,5, bem como estabilidade térmica, grau de hidratação dos compostos e os principais produtos gasosos formados pela decomposição térmica (H2O, CO2 e CO). Através das análises de FTIR pode-se sugerir que o tipo de coordenação entre metal e o ligante é bidentado em ponte.
Eckhart, Eric Ashton. "A search for charmless baryonic B meson decays at CLEO". Columbus, OH : Ohio State University, 2003. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1054568796.
Texto completoTitle from first page of PDF file. Document formatted into pages; contains xv, 133 p.: ill. Includes abstract and vita. Advisor: Richard D. Kass, Dept. of Physics. Includes bibliographical references (p. 132-133).
Sultan, Ahmad. "Tell Kashkashok III (Syrie du Nord) et la question de l'urbanisation de la Jazireh syrienne (Ve - IIIe millénaire av. n. è.)". Thesis, Strasbourg, 2019. http://www.theses.fr/2019STRAG046.
Texto completoThe purpose of this research is to provide readers new data from one of the very few sites in the syrian Jazireh namely Tell Kashkashok III which contains a long and continuous sequence of occupation spanning three thousand years, extending from the 5th until the third millenniumB.C. The site documents several periods of the history of Northern Mesopotamia (Obeid, Late Chalcolithic and Archaic Jazireh), each of which is a milestone in the process that led to the emergence of cities in Northern Syria. These archaeological data provide new insights into the nature of development of an urban society in northern Syria. The urban planning elements brought by Kashkashok III reside indeed in the diversity of the monumental architectural remains that the site has produced. They allow to feed the scientific researches on the evolution of settlements in Mesopotamia of the North since the beginning of the 5th millennium B.C
Hüsch, Tanja. "Patienten mit inoperablem, nicht-kleinzelligem Lungenkarzinom im Stadium IIIA oder IIIB nach Induktionschemotherapie : ein Vergleich der Lebensqualitaet anhand alleiniger Radiotherapie versus simultaner Radio- und Chemotherapie". kostenfrei, 2008. http://edoc.ub.uni-muenchen.de/8467/.
Texto completoBoget, Sophie. "L'implication de certains fibroblast growth factors (Basic FGF, KGF et FGF10) et de leurs récepteurs (FGFR1, FGFR2-IIIb, FGFR2-IIIc et FGFR3) dans l'hypertrophie prostatique bénigne". Lyon 1, 2001. http://www.theses.fr/2001LYO1T197.
Texto completoMuñoz, Muñoz Juan Pablo. "Separación de lantano (III), cerio (III), praseodimio (III) y neodimio (III) mediante extracción por solventes utilizando extractantes organofosforados". Tesis, Universidad de Chile, 2011. http://www.repositorio.uchile.cl/handle/2250/115867.
Texto completoEn esta Memoria de Título se estudió la extracción y separación de lantano (III), cerio (III), praseodimio (III) y neodimio (III) mediante extracción por solventes utilizando como agentes transportadores los extractantes comerciales D2EHPA, PC88A, LIX 272 y CYANEX 301. El análisis de las curvas de especiación química de los elementos tierras raras (ETR) en fase acuosa en función del pH permiten establecer que en el rango de pH de trabajo los iones de La, Ce y Pr se encuentran principalmente como iones complejados con nitrato. Sin embargo, entre pH 1 y 2 se presenta una competencia con la especie ETR-sulfato. Debido a que el ión nitrato presenta un poder ligante muy débil, en la práctica es posible considerar que los iones ETR se encuentran como especies libres cuando se presenta una competencia frente a un ligante más fuerte, tal como sería en el caso de los extractantes organofosforados, mientras que, la especie ETR-sulfato sería la única especie que podría interferir en la extracción de los iones de ETR. Los experimentos de extracción por solventes realizados entre cada uno de los iones metálicos de ETR con cada uno de los extractantes propuestos, se llevaron a cabo considerando las siguientes variables que afectan al proceso: la concentración de cada uno de los extractantes en la fase orgánica, de cada ión metálico presente en la fase acuosa y el pH de la solución acuosa de alimentación. Un análisis de los resultados obtenidos para la variación en la concentración de extractante indicó que, los valores más altos de extracción se logran cuando se utilizan 40 mM. Los resultados varían dependiendo del ión metálico observándose siempre las mayores extracciones para Pr, y en menor grado consecutivo Nd, Ce y La. Los resultados obtenidos para la variación de pH inicial indicaron que, en general, el porcentaje de extracción se incrementa con el aumento del pH inicial de la solución acuosa de alimentación en todos los experimentos realizados. En el caso de los extractantes D2EHPA y PC88A se alcanzaron extracciones sin una distinción práctica entre cada uno de los iones ETR. Mientras que, en el caso de los extractantes LIX 272 y CYANEX 301 se observó que hay diferenciación clara en el grado de extracción para los distintos ETR. Los resultados obtenidos para la variación en la concentración de ión metálico inicial permitieron aseverar que, en general, el grado de extracción disminuye con el incremento de la concentración de ión metálico en la solución de alimentación inicial para los cuatro extractantes estudiados. Los experimentos de retroextracción de los iones metálicos de ETR presentaron una tendencia moderada a la disminución con el incremento de la concentración de H2SO4 en la fase acuosa para los todos los complejos ETR-extractante estudiados. Sólo se observó que en el caso de los complejos ETR-LIX 272 se lograron porcentajes de retroextracción intermedios que podían ser utilizados en una ruta de separación de los iones ETR. El análisis de los estudios de equilibrio permitió apreciar claramente que la extracción de Pr es la más favorecida en todos los casos, y en menor grado consecutivo Nd, Ce y La. Adicionalmente, se pudo observar que desde el punto de vista de los extractantes el D2EHPA es el que más favorece la reacción de extracción y en menor grado consecutivo PC88A, LIX 272 y CYANEX 301. A partir de un análisis de todos los datos obtenidos se pudo deducir que el extractante LIX 272 cumplió de mejor manera con el requisito de extraer preferentemente alguno de los iones de ETR en ciertas condiciones y, de este modo, poder plantear de esa manera alguna posible ruta de separación. Los estudios cinéticos de extracción indicaron que en general es el Pr el que reacciona más rápidamente, y el La el que reacciona más lentamente, con todos los extractantes. Del mismo modo, se observa que el extractante que reacciona de manera más rápida con los iones metálicos es el D2EHPA y en menor grado consecutivo PC88A, LIX 272 y CYANEX 301. Por otro lado, los experimentos cinéticos de retroextracción indicaron que los complejos ETR-D2EHPA y ETR-PC88A son los que más rápidamente liberan los iones de ETR. Asimismo, el complejo ETR-CYANEX 301 es el que los libera más lentamente. La ruta de separación de iones metálicos en dos etapas propuesta en este estudio utilizando como extractante el LIX 272 cumple en cierta medida con el objetivo planteado. En la primera etapa de extracción se logró incrementar la pureza del La en la fase acuosa hasta un 40%, aproximadamente. Una proyección de este resultado en 8 contactos permitiría obtener un refino constituido exclusivamente por La, alcanzando a aislar cerca del 70% del La inicial. En la segunda etapa de la ruta de separación, que considera la retroextracción de los complejos ETR-LIX 272, se logró aislar cerca del 74% del Ce inicial con una pureza superior al 98%. Una proyección de 3 contactos para esta etapa permitiría obtener una fase acuosa final con un 99,97% de pureza de Ce y con un rendimiento global del proceso de un 54,8%. Esta ruta de separación por equilibrios deja el problema de separación relegado solamente a la dupla Pr y Nd. Por otro lado, la diferencia en un orden de magnitud de las constantes cinéticas de retroextracción para los complejos Pr-LIX 272 y Nd-LIX 272 permitiría proyectar una separación de ambos iones en el tiempo
The extraction and separation of lanthanum (III), cerium (III), praseodymium (III), and neodymium (III) was studied by means of solvent extraction using D2EHPA, PC88A, LIX 272, and CYANEX 301 as extractant. The analysis of the chemical speciation curves of rare earth elements (REE) in aqueous phase as a function of pH allow to establish that in the working pH range the lanthanum, cerium, and praseodymium ions are complexed mainly with nitrate. However, between pH 1 and 2 a competition with REE-sulfate species is observed. Due to the nitrate ion has a very weak binding power, in fact it is possible to consider that REE ions are as free species when there is a competition with a stronger binder, as would be the case of organophosphorus extractants, while REE-sulfate species would be the only species that could interfere in the extraction of REE ions. The solvent extraction experiments, performed between each of the metal ions of REE with each of the proposed extractants, were carried out considering the following variables that affect the process: the concentration of each of the extractants in the organic phase, the concentration of each metal ion present in the aqueous phase and the pH of the aqueous feed solution. An analysis of the obtained results for the variation in the extractant concentration indicated that the highest values of extraction are achieved when using 40 mM. Results vary depending on the metal ion, always showing a preference for the praseodymium and in less consecutive degree for neodymium, cerium, and lanthanum. The obtained results for the variation of initial pH indicated that, in general, the extraction percentage increases with rising initial pH of the aqueous feed solution in all experiments. While in the case of extractants D2EHPA and PC88A no practical distinction between each of the REE ions were achieved, in the case of extractants LIX 272 and CYANEX 301 it was noted that there was clear difference in the degree of extraction for different REE. The results obtained for the variation in initial metal ion concentration allowed to assert that, in general, the extraction degree decreases while increasing metal ion concentration in the initial feed solution for the four extractants studied. Stripping experiments of REE metal ions showed a moderate tendency to decrease with increasing H2SO4 concentration in the aqueous phase for all REE-extractant complexes studied. It was observed that only in the case of REE-LIX 272 complex intermediate stripping percentages were achieved that could be used in a route of the separation of REE ions. The analysis of the equilibrium studies allowed to appreciate clearly that the extraction of praseodymium is the most favored in all cases, and less consecutive neodymium, cerium and lanthanum. Additionally, it was noted that from the point of view of the extractants, D2EHPA is which most favors the extraction reaction and in less consecutive degree for PC88A, LIX 272, and CYANEX 301. From an analysis of all the obtained data it is allowed to conclude that extractant LIX 272 is which better complies with the requirement for removing any REE ions preferably under certain conditions and, thus, can propound some possible separation route. Extraction kinetic studies indicated that in general praseodymium will react faster with all the extractants and also in general, lanthanum reacts more slowly. In the same way, it is noted that the extractant that react faster with the metal ions is D2EHPA and in less consecutive degree for PC88A, LIX 272, and CYANEX 301. Furthermore, stripping kinetic experiments indicated that REE-D2EHPA, and REE-PC88A complexes are the fastest in releasing REE ions. Likewise, REE-CYANEX 301 complex is that which release them more slowly. The separation route of metal ions in two stages proposed in this study using the LIX 272 extractant fulfill in some extent with the stated objective. In the first extraction step it was able to increase the purity of lanthanum in the aqueous phase up to 40%, approximately. A projection of this result for 8 contacts would obtain a refine constituted exclusively of lanthanum, reaching out to isolate about 70% of the original lanthanum. In the second stage of the separation route, that considers the stripping of REE-LIX 272 complexes, about 74% of the initial cerium was isolated with a purity exceeding 98%. A projection of 3 contacts for this stage would provide a final aqueous phase with a purity of 99.97% for cerium and an overall process yield of 54.8%. This equilibrium separation route leaves the separation problem relegated only to the couple praseodymium and neodymium. On the other hand, the difference in an order of magnitude of the stripping kinetic constants for Pr-LIX 272, and Nd-LIX 272 complexes would allow to project a separation of both ions at time
Meinel, Gotthard y Ulrich Schumacher. "Flächennutzungsmonitoring III". Rhombos-Verl, 2011. https://slub.qucosa.de/id/qucosa%3A4658.
Texto completoLibros sobre el tema "IIIT"
1948-, Ahmad Imad-ad-Dean, ed. Proceedings of IIIT Lunar Calendar Conference held at the International Institute of Islamic Thought, Herndon, VA., 9-10 Shawwal, 1407 A H., 6-7 June, 1987 A.C. Herndon, VA: International Institute of Islamic Thought, 1988.
Buscar texto completoOrganisation for economic co-operation and development. SET: National Accounts of OECD Countries 2009, Volume IIIa, Volume IIIb. Paris: OECD Publishing, 2010.
Buscar texto completoNowicki, Krzysztof. Defensible sites in Crete c. 1200-800 B.C: LM IIIB/IIIC through early geometric. Liège, Belgium: Université de Liège, Histoire de l'art et archéologie de la Grèce antique, 2000.
Buscar texto completoKrzysztof, Nowicki. Defensible sites in Crete, c. 1200-800 B.C.: LM IIIB/IIIC through Early Geometric. Liège, Belgique: Université de Liège, Histoire de l'art et archéologie de la Grèce antique, 2000.
Buscar texto completoEdward, Jones. Using dBase III. Berkeley, Calif: Osborne/McGraw-Hill, 1985.
Buscar texto completoGorham, Kenneth D. Personal productivity with dBase III. Dubuque, Iowa: Wm. C. Brown Publishers, 1987.
Buscar texto completoTownsend, Carl. Mastering dBASE III: A structured approach. Berkeley: SYBEX, 1985.
Buscar texto completoGarrison, Catherine. dBase III: A ready reference manual. Reading, Mass: Addison-Wesley, 1987.
Buscar texto completoOlympia, P. L. dBas e power: Building and using programming tools. Torrance, Calif: Ashton-Tate, 1988.
Buscar texto completoBernardo Frey Pinto de Almeida. III + III olhares, Rivoli. [Porto]: Rivoli Teatro Municipal, 1997.
Buscar texto completoCapítulos de libros sobre el tema "IIIT"
Mishra, Ashutosh, Shyam Nandan Rai, Anand Mishra y C. V. Jawahar. "IIIT-CFW: A Benchmark Database of Cartoon Faces in the Wild". En Lecture Notes in Computer Science, 35–47. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-46604-0_3.
Texto completoGongidi, Santhoshini y C. V. Jawahar. "iiit-indic-hw-words: A Dataset for Indic Handwritten Text Recognition". En Document Analysis and Recognition – ICDAR 2021, 444–59. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-86337-1_30.
Texto completoMondal, Ajoy, Peter Lipps y C. V. Jawahar. "IIIT-AR-13K: A New Dataset for Graphical Object Detection in Documents". En Document Analysis Systems, 216–30. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-57058-3_16.
Texto completoLi, Tatsien y Bopeng Rao. "Preliminaries on Problem (III) and (III0)". En Progress in Nonlinear Differential Equations and Their Applications, 231–38. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-32849-8_19.
Texto completoLeung, Alexander K. C., William Lane M. Robson, Carsten Büning, Johann Ockenga, Janine Büttner, Hartmut Schmidt, Antonio V. Delgado-Escueta et al. "Lattice Corneal Dystrophy III and IIIa". En Encyclopedia of Molecular Mechanisms of Disease, 1145. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_7899.
Texto completoBensard, Denis D., Kathryn M. Beauchamp, Ryan T. Hurt, Stephen A. McClave, Angela M. Mills, Esther H. Chen, J. P. J. Wester et al. "Gustilo-Anderson Type IIIB or IIIC Open Fracture". En Encyclopedia of Intensive Care Medicine, 1003. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-00418-6_1660.
Texto completoPierre, Ulwyn L. J. "The Methodology". En The Myth of Black Corporate Mobility, 55–84. New York: Routledge, 2021. http://dx.doi.org/10.4324/9781003250036-iii.
Texto completoZwillinger, Daniel y Vladimir Dobrushkin. "Approximate Analytical Methods". En Handbook of Differential Equations, 371–476. 4a ed. Boca Raton: Chapman and Hall/CRC, 2021. http://dx.doi.org/10.1201/9780429286834-iii.
Texto completoShengyu, Fan. "“Comes to Life on the Page”". En The Translator's Mirror for the Romantic, 59–107. London: Routledge, 2022. http://dx.doi.org/10.4324/9781003240990-iii.
Texto completo"IIIT Publications". En Outlines of a Cultural Strategy, 16–29. International Institute of Islamic Thought, 1995. http://dx.doi.org/10.2307/j.ctvk8w294.5.
Texto completoActas de conferencias sobre el tema "IIIT"
Yashaswi, P., Yarrabelly Navya y Veera Raghavendra Chikka. "Regular and unusual data visualization IIIT-H". En 2014 IEEE Conference on Visual Analytics Science and Technology (VAST). IEEE, 2014. http://dx.doi.org/10.1109/vast.2014.7042570.
Texto completoRallabandi, Sai Sirisha, Sai Krishna Rallabandi y Suryakanth V. Gangashetty. "IIIT Hyderabad's entry to Blizzard Challenge 2016". En The Blizzard Challenge 2016. ISCA: ISCA, 2016. http://dx.doi.org/10.21437/blizzard.2016-5.
Texto completoSingh, Vishwanath Pratap, J. M. S. Rohith, Yash Mittal y V. K. Mittal. "IIIT-S CSSD: A Cough Speech Sounds Database". En 2016 Twenty Second National Conference on Communication (NCC). IEEE, 2016. http://dx.doi.org/10.1109/ncc.2016.7561190.
Texto completoMukherjee, Ananya y Manish Shrivastava. "IIIT HYD’s Submission for WMT23 Test-suite Task". En Proceedings of the Eighth Conference on Machine Translation. Stroudsburg, PA, USA: Association for Computational Linguistics, 2023. http://dx.doi.org/10.18653/v1/2023.wmt-1.24.
Texto completoRallabandi, Sai Krishna, Anandaswarup Vadapalli, Sivanand Achanta y Suryakanth V. Gangashetty. "IIIT Hyderabad's submission to the Blizzard Challenge 2015". En The Blizzard Challenge 2015. ISCA: ISCA, 2015. http://dx.doi.org/10.21437/blizzard.2015-8.
Texto completoGoyal, Vikrant y Dipti Misra Sharma. "The IIIT-H Gujarati-English Machine Translation System for WMT19". En Proceedings of the Fourth Conference on Machine Translation (Volume 2: Shared Task Papers, Day 1). Stroudsburg, PA, USA: Association for Computational Linguistics, 2019. http://dx.doi.org/10.18653/v1/w19-5316.
Texto completoBhat, Irshad Ahmad, Vandan Mujadia, Aniruddha Tammewar, Riyaz Ahmad Bhat y Manish Shrivastava. "IIIT-H System Submission for FIRE2014 Shared Task on Transliterated Search". En the Forum for Information Retrieval Evaluation. New York, New York, USA: ACM Press, 2015. http://dx.doi.org/10.1145/2824864.2824872.
Texto completoMukherjee, Ananya y Manish Shrivastava. "MEE4 and XLsim : IIIT HYD’s Submissions’ for WMT23 Metrics Shared Task". En Proceedings of the Eighth Conference on Machine Translation. Stroudsburg, PA, USA: Association for Computational Linguistics, 2023. http://dx.doi.org/10.18653/v1/2023.wmt-1.66.
Texto completoPalakurthi, Ashish y Radhika Mamidi. "IIIT at SemEval-2016 Task 11: Complex Word Identification using Nearest Centroid Classification". En Proceedings of the 10th International Workshop on Semantic Evaluation (SemEval-2016). Stroudsburg, PA, USA: Association for Computational Linguistics, 2016. http://dx.doi.org/10.18653/v1/s16-1158.
Texto completoAlluri, K. N. R. K. Raju y Anil Kumar Vuppala. "IIIT-H Spoofing Countermeasures for Automatic Speaker Verification Spoofing and Countermeasures Challenge 2019". En Interspeech 2019. ISCA: ISCA, 2019. http://dx.doi.org/10.21437/interspeech.2019-1623.
Texto completoInformes sobre el tema "IIIT"
Unknown. DEVELOPMENT OF A NATURAL GAS SYSTEMS ANALYSIS MODEL (GSAM) VOLUME I - SUMMARY REPORT VOLUME II - USER'S GUIDE VOLUME IIIA - RP PROGRAMMER'S GUIDE VOLUME IIIB - SRPM PROGRAMMER'S GUIDE VOLUME IIIC - E&P PROGRAMMER'S GUIDE VOLUME IIID - D&I PROGRAMMER'S GUIDE. Office of Scientific and Technical Information (OSTI), febrero de 2001. http://dx.doi.org/10.2172/810376.
Texto completoWiersma, B. DETERMINATION OF CORROSION INHIBITOR CRITERIA FOR TYPE III IIIA TANKS DURING SALT DISSOLUTION OPERATIONS. Office of Scientific and Technical Information (OSTI), enero de 2008. http://dx.doi.org/10.2172/927594.
Texto completoCounts, K., B. Bruce Wiersma y J. John Mickalonis. DETERMINATION OF CORROSION INHIBITOR CRITERIA FOR TYPE III/IIIA TANKS DURING SALT DISSOLUTION OPERATIONS INTERIM REPORT. Office of Scientific and Technical Information (OSTI), diciembre de 2007. http://dx.doi.org/10.2172/925849.
Texto completoMickalonis, J., B. Wiersma y B. Garcia-Diaz. DETERMINATION OF CORROSION INHIBITOR CRITERIA FOR TYPE III/IIIA TANKS DURING SALT DISSOLUTION OPERATIONS SUMMARY DOCUMENT. Office of Scientific and Technical Information (OSTI), octubre de 2009. http://dx.doi.org/10.2172/969283.
Texto completoAnderson, K. E. Recovery of valuable chlorosilane intermediates by a novel waste conversion process. Technical report for phase IIIA (final) and phase IIIB (progress). Office of Scientific and Technical Information (OSTI), octubre de 1998. http://dx.doi.org/10.2172/362599.
Texto completoCooley, William. Global Positioning System III (GPS III). Fort Belvoir, VA: Defense Technical Information Center, diciembre de 2013. http://dx.doi.org/10.21236/ada613478.
Texto completoCarey, J. TERMIUM III. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/298206.
Texto completoCarey, J. TERMIUM III. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1986. http://dx.doi.org/10.4095/298215.
Texto completoMadsen, M. M., J. M. Taylor, R. M. Ostmeyer y P. C. Reardon. RADTRAN III. Office of Scientific and Technical Information (OSTI), febrero de 1986. http://dx.doi.org/10.2172/6008168.
Texto completoCheok, Geralding S. y Marek Franaszek. Phase III :. Gaithersburg, MD: National Institute of Standards and Technology, 2009. http://dx.doi.org/10.6028/nist.ir.7659.
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