Relevant bibliographies by topics / DCCD

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'DCCD'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "DCCD"

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Matsumura, K., F. J. Lovas, and R. D. Suenram. "Fourier-transform microwave spectroscopy of the deuterated acetylene dimers: The interconversion tunneling motions of (DCCD)2, (DCCH)2, DCCDDCCH, DCCHDCCD, HCCHDCCD, and HCCHDCCH." Journal of Molecular Spectroscopy 150, no. 2 (December 1991): 576–96. http://dx.doi.org/10.1016/0022-2852(91)90250-e.

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MATSUMURA, K., F. J. LOVAS, and R. D. SUENRAM. "ChemInform Abstract: Fourier-Transform Microwave Spectroscopy of the Deuterated Acetylene Dimers: The Interconversion Tunneling Motions of (DCCD)2, (DCCH)2, DCCD-DCCH, DCCH-DCCD, HCCH-DCCD, and HCCH-DCCH." ChemInform 23, no. 9 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199209034.

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Dhyanti, Yustina, Khairul Munadi, and Fitri Arnia. "Penerapan Deskriptor Warna Dominan untuk Temu Kembali Citra Busana pada Peranti Bergerak." Jurnal Rekayasa Elektrika 12, no. 3 (December 15, 2016): 104. http://dx.doi.org/10.17529/jre.v12i3.5701.

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Nowadays, clothes with various designs and color combinations are available for purchasing through an online shop, which is mostly equipped with keyword-based item retrieval. Here, the object in the online database is retrieved based on the keyword inputted by the potential buyers. The keyword-based search may bring potential customers on difficulties to describe the clothes they want to buy. This paper presents a new searching approach, using an image instead of text, as the query into an online shop. This method is known as content-based image retrieval (CBIR). Particularly, we focused on using color as the feature in our Muslimah clothes image retrieval. The dominant color descriptor (DCD) extracts the wardrobe's color. Then, image matching is accomplished by calculating the Euclidean distance between the query and image in the database, and the last step is to evaluate the performance of the DWD by calculating precision and recall. To determine the performance of the DCD in extracting color features, the DCD is compared with another color descriptor, that is dominant color correlogram descriptor (DCCD). The values of precision and recall of DCD ranged from 0.7 to 0.9 while the precision and recall of DCCD ranged from 0.7 to 0.8. These results showed that the DCD produce a superior performance compared to DCCD in retrieving a set of clothing image, either plain or patterned colored clothes.
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Vuokila, P. T., and I. E. Hassinen. "NN′-dicyclohexylcarbodi-imide-sensitivity of bovine heart mitochondrial NADH: ubiquinone oxidoreductase. Inhibition of activity and binding to subunits." Biochemical Journal 249, no. 2 (January 15, 1988): 339–44. http://dx.doi.org/10.1042/bj2490339.

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Dicyclohexylcarbodi-imide (DCCD) inhibition of NADH: ubiquinone oxidoreductase was studied in submitochondrial particles and in the isolated form, together with the binding of the reagent to the enzyme. DCCD inhibited the isolated enzyme in a time- and concentration-dependent manner. Over the concentration range studied, a maximum inhibition of 85% was attained within 60 min. The time course for the binding of DCCD to the enzyme was similar to that of activity inhibition. The NADH:ubiquinone oxidoreductase activity of the submitochondrial particles was also sensitive to DCCD, and the locus of binding of the inhibitor was studied by subsequent resolution of the enzyme into subunit polypeptides. Only two subunits (molecular masses 13.7 and 21.5 kDa) were labelled by [14C]DCCD, whereas, when the enzyme in its isolated form was treated with [14C]DCCD, six subunits (13.7, 16.1, 21.5, 39, 43 and 53 kDa) were labelled. Comparison with the subunit labelling of F1F0-ATPase and ubiquinol:cytochrome c oxidoreductase indicated that the labelling pattern of NADH:ubiquinone oxidoreductase, and enzyme complex with a multitude of subunits, is unique and not due to contamination by other inner-membrane proteins. The correlation between the electron- and proton-transport functions and the DCCD-binding components remains to be established.
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Peerce, B. E. "Molecular mechanism of two noncompetitive inhibitors of Na(+)-glucose cotransporter: comparison of DCCD and PCMB." American Journal of Physiology-Gastrointestinal and Liver Physiology 264, no. 2 (February 1, 1993): G300—G305. http://dx.doi.org/10.1152/ajpgi.1993.264.2.g300.

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The effects of noncompetitive inhibitors of Na(+)-dependent glucose uptake, p-chloromercuribenzoate N,N'-dicyclohexylcarbodiimide (DCCD), on substrate-induced cotransporter conformational changes were examined using fluorescein isothiocyanate (FITC) and tryptophan fluorescence. p-chloromercuribenzoate (PCMB) inhibited both substrate-induced conformational changes with similar concentration required for 50% quenching/enhancement of tryptophan or FITC fluorescence. In contrast, DCCD inhibited the Na(+)-induced conformational change with an apparent concentration resulting in 50% inhibition (K0.5) of 18 microM and the glucose-induced conformational change with an apparent K0.5 of 5 microM. DCCD slightly increased the apparent K0.5 for the Na+ concentration required for Na(+)-induced conformational change. DCCD and PCMB altered tryptophan accessibility to quench reagents in all three conformations. Tryptophan residues on the PCMB-treated cotransporter were more Cs+ than I- sensitive in contrast to the unlabeled cotransporter. The PCMB-treated cotransporter had a reduced response to Na+, suggesting that the mode of PCMB inactivation of cotransporter activity resulted from conformational changes in the substrate-free cotransporter. DCCD had a smaller effect on cotransporter tryptophan quench reagent susceptibility. However, DCCD-labeled cotransporter was equally accessible to I- and Cs+, and the DCCD-labeled cotransporter did not respond to substrates. Loss of charge distribution around cotransporter tryptophans correlated with loss of substrate-induced conformational changes.
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Müller, Tina A., Steven M. Byrde, Christoph Werlen, Jan Roelof van der Meer, and Hans-Peter E. Kohler. "Genetic Analysis of Phenoxyalkanoic Acid Degradation in Sphingomonas herbicidovorans MH." Applied and Environmental Microbiology 70, no. 10 (October 2004): 6066–75. http://dx.doi.org/10.1128/aem.70.10.6066-6075.2004.

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ABSTRACT Phenoxyalkanoic acid degradation is well studied in Beta- and Gammaproteobacteria, but the genetic background has not been elucidated so far in Alphaproteobacteria. We report the isolation of several genes involved in dichlor- and mecoprop degradation from the alphaproteobacterium Sphingomonas herbicidovorans MH and propose that the degradation proceeds analogously to that previously reported for 2,4-dichlorophenoxyacetic acid (2,4-D). Two genes for α-ketoglutarate-dependent dioxygenases, sdpA MH and rdpA MH, were found, both of which were adjacent to sequences with potential insertion elements. Furthermore, a gene for a dichlorophenol hydroxylase (tfdB), a putative regulatory gene (cadR), two genes for dichlorocatechol 1,2-dioxygenases (dccA I/II), two for dienelactone hydrolases (dccD I/II), part of a gene for maleylacetate reductase (dccE), and one gene for a potential phenoxyalkanoic acid permease were isolated. In contrast to other 2,4-D degraders, the sdp, rdp, and dcc genes were scattered over the genome and their expression was not tightly regulated. No coherent pattern was derived on the possible origin of the sdp, rdp, and dcc pathway genes. rdpA MH was 99% identical to rdpA MC1, an (R)-dichlorprop/α-ketoglutarate dioxygenase from Delftia acidovorans MC1, which is evidence for a recent gene exchange between Alpha- and Betaproteobacteria. Conversely, DccAI and DccAII did not group within the known chlorocatechol 1,2-dioxygenases, but formed a separate branch in clustering analysis. This suggests a different reservoir and reduced transfer for the genes of the modified ortho-cleavage pathway in Alphaproteobacteria compared with the ones in Beta- and Gammaproteobacteria.
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YANG, Su J., Shih S. JIANG, Soong Y. KUO, Shu H. HUNG, Ming F. TAM, and Rong L. PAN. "Localization of a carboxylic residue possibly involved in the inhibition of vacuolar H+-pyrophosphatase by N,N′-dicyclohexylcarbodi-imide." Biochemical Journal 342, no. 3 (September 5, 1999): 641–46. http://dx.doi.org/10.1042/bj3420641.

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A vacuolar H+-pyrophosphatase (EC 3.6.1.1) that catalyses PPi hydrolysis and the electrogenic translocation of protons from the cytosol to the vacuole lumen, was purified from etiolated hypocotyls of mung bean seedlings (Vigna radiata L.). Group-specific modification was used to identify a carboxylic residue involved in the inhibition of vacuolar H+-pyrophosphatase. Carbodi-imides, such as N,N′-dicyclohexylcarbodi-imide (DCCD) and 1-ethyl-3-(3-dimethylamino-propyl)carbodi-imide, and Woodward's reagent K caused a progressive decline in the enzymic activity of vacuolar H+-pyrophosphatase in a time- and concentration-dependent manner. The stoichiometry of labelling of the vacuolar H+-pyrophosphatase by [14C]DCCD determined that DCCD modifies one carboxylic residue per subunit of the enzyme. Protection studies suggest that the DCCD-reactive carboxylic residue resides at or near the substrate-binding site. Furthermore, peptide mapping analysis reveals that Asp283, located in the putative loop V of a tentative topological model of vacuolar H+-pyrophosphatase on the cytosolic side, was labelled by radioactive [14C]DCCD. Cytosolic loop V contains both DCCD-sensitive Asp283 and a conserved motif sequence, rendering it a candidate for the catalytic site of vacuolar H+-pyrophosphatase. A topological picture of the active domain of vacuolar H+-pyrophosphatase is tentatively proposed.
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Lauzin, Clément, N. Moazzen-Ahmadi, and A. R. W. McKellar. "Infrared spectra of acetylene dimers and acetylene–nitrogen: (DCCD)2, H-bonded DCCD–HCCH, and DCCD–NN in the 4.1μm region." Journal of Molecular Spectroscopy 269, no. 1 (September 2011): 124–28. http://dx.doi.org/10.1016/j.jms.2011.05.010.

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Vgenopoulou, Irini, Anja C. Gemperli, and Julia Steuber. "Specific Modification of a Na+ Binding Site in NADH:Quinone Oxidoreductase from Klebsiella pneumoniae with Dicyclohexylcarbodiimide." Journal of Bacteriology 188, no. 9 (May 1, 2006): 3264–72. http://dx.doi.org/10.1128/jb.188.9.3264-3272.2006.

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ABSTRACT The respiratory NADH:quinone oxidoreductase (complex I) (NDH-1) is a multisubunit enzyme that translocates protons (or in some cases Na+) across energy-conserving membranes from bacteria or mitochondria. We studied the reaction of the Na+-translocating complex I from the enterobacterium Klebsiella pneumoniae with N,N′-dicyclohexylcarbodiimide (DCCD), with the aim of identifying a subunit critical for Na+ binding. At low Na+ concentrations (0.6 mM), DCCD inhibited both quinone reduction and Na+ transport by NDH-1 concurrent with the covalent modification of a 30-kDa polypeptide. In the presence of 50 mM Na+, NDH-1 was protected from inhibition by DCCD, and the modification of the 30-kDa polypeptide with [14C]DCCD was prevented, indicating that Na+ and DCCD competed for the binding to a critical carboxyl group in NDH-1. The 30-kDa polypeptide was assigned to NuoH, the homologue of the ND1 subunit from mitochondrial complex I. It is proposed that Na+ binds to the NuoH subunit during NADH-driven Na+ transport by NDH-1.
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Kisnierienë, Vilma, and Vidmantas Sakalauskas. "The effect of aluminium on bioelectrical activity of the Nitellopsis obtusa cell membrane after H+-ATPase inhibition." Open Life Sciences 2, no. 2 (June 1, 2007): 222–32. http://dx.doi.org/10.2478/s11535-007-0009-y.

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AbstractAluminium induced membrane potential (Em) changes and potential changes during repolarization phase of the action potential (AP) in the internodal cells of Nitellopsis obtusa after blocking H+-ATPase activity by DCCD were investigated. Micromolar concentrations of DCCD are sufficient to give complete and irreversible inhibition of proton pumping. The membrane potential was measured by conventional glass-microelectrode technique. We found that the half-amplitude pulse duration differs significantly between standard conditions, after DCCD application, and after H+-ATPase blocking and subsequent Al3+ treatment: 4.9, 7.7 and 17.2 seconds, respectively. We propose that in the short term (2 hours) treatment of Al3+, the decrease in membrane potential was compensated for by H+-ATPase activity. Blocking H+-ATPase activity by DCCD can enhance the influence of Al3+ on the bioelectrical activity of cell membranes.
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Dissertations / Theses on the topic "DCCD"

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AlShammeri, Mohammed. "Dynamic Committees for Handling Concept Drift in Databases (DCCD)." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23498.

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Concept drift refers to a problem that is caused by a change in the data distribution in data mining. This leads to reduction in the accuracy of the current model that is used to examine the underlying data distribution of the concept to be discovered. A number of techniques have been introduced to address this issue, in a supervised learning (or classification) setting. In a classification setting, the target concept (or class) to be learned is known. One of these techniques is called “Ensemble learning”, which refers to using multiple trained classifiers in order to get better predictions by using some voting scheme. In a traditional ensemble, the underlying base classifiers are all of the same type. Recent research extends the idea of ensemble learning to the idea of using committees, where a committee consists of diverse classifiers. This is the main difference between the regular ensemble classifiers and the committee learning algorithms. Committees are able to use diverse learning methods simultaneously and dynamically take advantage of the most accurate classifiers as the data change. In addition, some committees are able to replace their members when they perform poorly. This thesis presents two new algorithms that address concept drifts. The first algorithm has been designed to systematically introduce gradual and sudden concept drift scenarios into datasets. In order to save time and avoid memory consumption, the Concept Drift Introducer (CDI) algorithm divides the number of drift scenarios into phases. The main advantage of using phases is that it allows us to produce a highly scalable concept drift detector that evaluates each phase, instead of evaluating each individual drift scenario. We further designed a novel algorithm to handle concept drift. Our Dynamic Committee for Concept Drift (DCCD) algorithm uses a voted committee of hypotheses that vote on the best base classifier, based on its predictive accuracy. The novelty of DCCD lies in the fact that we employ diverse heterogeneous classifiers in one committee in an attempt to maximize diversity. DCCD detects concept drifts by using the accuracy and by weighing the committee members by adding one point to the most accurate member. The total loss in accuracy for each member is calculated at the end of each point of measurement, or phase. The performance of the committee members are evaluated to decide whether a member needs to be replaced or not. Moreover, DCCD detects the worst member in the committee and then eliminates this member by using a weighting mechanism. Our experimental evaluation centers on evaluating the performance of DCCD on various datasets of different sizes, with different levels of gradual and sudden concept drift. We further compare our algorithm to another state-of-the-art algorithm, namely the MultiScheme approach. The experiments indicate the effectiveness of our DCCD method under a number of diverse circumstances. The DCCD algorithm generally generates high performance results, especially when the number of concept drifts is large in a dataset. For the size of the datasets used, our results showed that DCCD produced a steady improvement in performance when applied to small datasets. Further, in large and medium datasets, our DCCD method has a comparable, and often slightly higher, performance than the MultiScheme technique. The experimental results also show that the DCCD algorithm limits the loss in accuracy over time, regardless of the size of the dataset.
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Omolewu, Rachel. "Characterization of Three Mutations in Conserved Domain of Subunit III of Cytochrome c Oxidase from Rhodobacter sphaeroides." Wright State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=wright1292612174.

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Moffat, Jeffrey C. "Properties of Conductance and Inhibition of Proton Channels: M2 from Influenza A Virus and Fo from Escherichia coli ATP Synthase." BYU ScholarsArchive, 2006. https://scholarsarchive.byu.edu/etd/479.

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Proton channels are essential for many of the processes of life. The influenza A viral protein M2 is responsible for sensing the conditions necessary for viral RNA release. The proton-translocating FoF1 ATPase (ATP synthase) uses a proton gradient to drive adenosine triphosphate (ATP) synthesis. We have directly measured proton uptake in vesicles containing reconstituted M2 or FO by monitoring external pH after addition of valinomycin to vesicles with 100-fold diluted external [K+]. This proton flux assay was utilized to quantify proton flux through single M2 and Fo channels. Contrary to previous reports, proton uptake by M2 was not significantly altered by acidification of the extravesicular pH. We conclude that pH only weakly affects proton flux through M2 in the pH range of 5.4 - 7.0. Theoretical analysis utilized for such vesicle uptake assays illuminates the appropriate time scale of the initial slope and an important limitation that must be placed on inferences about channel ion selectivity. The rise in pH over 10 seconds after ionophore addition yielded time-averaged single channel conductances of 0.35±0.2 aS and 0.72±0.4 aS at pH 5.4 and 7.0 respectively. Such a low time-average conductance implies that M2 is only conductive 10^-6 to 10^-4 of the time. M2 selectivity for hydrogen over potassium is ~10^7. Fo translocates protons across membranes, converting electrochemical energy to rotational inertia. Previous experiments have been partially confounded by a contaminating channel, CL, which co-purifies with Fo and leaks cations. CL activity is shown to not decrease following deletion of the previously uncharacterized yraM open reading frame of E. coli. Fo purified from a deletion strain lacking yraM is just as active as Fo purified from the wild-type strain. Using Fo from the deletion strain, the single-hit hypothesis of DCCD inhibition of passive proton flux through Fo was examined. A DCCD-induced reduction in ATP synthase activity correlates with a reduction in the total initial slope, the number of functional Fo per µg protein, and the single channel proton flux. At least 2 DCCD per Fo are required to totally inactivate passive proton flux. M2 and Fo have similar single channel conductances but different open probabilities.
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Jonnalagadda, Sneha R. "Molecular Modulation of a-Subunit VISIT-DG Sequence Residue Asp-350 in the Catalytic sites of Escherichia coli ATP Synthase." Digital Commons @ East Tennessee State University, 2011. https://dc.etsu.edu/etd/1296.

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ATP Synthase is the fundamental means of cellular energy production in animals, plants, and almost all microorganisms. In order to understand the mechanism of ATP catalysis, critical amino acid residues involved in Pi binding have to be identified. The αVISIT-DG sequence at the interface of α/β subunits that contains residues from 345-351 is highly conserved and αAsp-350 has been chosen because of its negative charge side chain and its close proximity (~2.8 Å) to the known phosphate binding residue αArg-376. The mutant's αD350R, αD350Q, αD350A, αR376A/D, and αG351R/A/D were generated by site directed mutagenesis and several biochemical assays were performed on them to understand the role played by the amino acid residues in Pi binding. Biochemical results suggest that αD350 may be involved in catalysis of ATP synthase and play an important role in Pi binding, whereas αG351 may be involved only in the structural integrity.
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Barbagallo, Mariano. "HV Interleaved Multiphase DcDc Buck-Boost Converter." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2017.

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in electric vehicle (ev) systems, bi-directional dc-dc converters are used to interface the rechargeable energy storage system (ress) such as the battery bank with the high voltage dc-link of the inverter. currently multi-cell batteries used in automotive systems, such as ev or hev, are subject to a higher failure rate than single cell batteries. the more cells are used in series, the greater the opportunities to fail and the worse the reliability. when a cell has failed the entire string or even worse the battery must be replaced, which is extremely costly [1]. so, to have less cells in series increases the reliability of the system, which also leads to a lower voltage of the dc link. for this reason and many others, in a hybrid or electric vehicle powertrain, a boost dc-dc converter enables optimization of the battery system. this work aims to investigate all the benefits that come with interleaving technique in dc-dc converters for automotive systems. indeed, these kind of converters for use in high-performance and high-power applications have received increasing interest in recent years. in particular this research work, done with sevcon ltd focuses on the theory behind bi-directional multiphase interleaved (imc) converter and how it could be used to interface a rechargeable energy storage system (ress) to the powertrain of a hybrid or electric vehicle. more specifically, it was investigated if it is possible to use (after appropriate hardware and software amendments) a standard three phase ac motor inverter as a multiphase interleaved converter. for this purpose two motor controller, produced by sevcon have been analysed. both the gen4 size 10 and the hvlp inverters were considered for use as a dc-dc converter. the voltage can step up or down based on the power flow direction. each phase is indeed a bi-directional buck or boost converter, which is composed of a bridge of power switches and inductor.
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Poliszuk, Shirley. "Kinetics of DCOD consumption by bacterial suspensions." ScholarWorks@UNO, 2004. http://louisdl.louislibraries.org/u?/NOD,169.

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Thesis (M.S.)--University of New Orleans, 2004.
Title from electronic submission form. "A thesis ... in partial fulfillment of the requirements for the degree of Master of Science in Environmental Engineering."--Thesis t.p. Vita. Includes bibliographical references.
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Rodríguez, González Hortencia Naizzara. "Apuestas literarias en el Caribe colombiano: Luis Carlos López, Oscar Delgado y Jorge Artel. Poesía y periodismo en contrapunteo con el provincianismo nacional (1990-1948)." Thesis, Universidad de las Américas Puebla, 2012. http://catarina.udlap.mx/u_dl_a/tales/documentos/dctd/rodriguez_g_hn/.

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Kurjenoja, Lounassaari Anne Kristiina. "Arquitectura con visión femenina: el cuerpo como nueva centralidad sensible." Thesis, Universidad de las Américas Puebla, 2010. http://catarina.udlap.mx/u_dl_a/tales/documentos/dctd/kurjenoja_l_ak/.

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Childs, Edward William. "The roles of the locust DCMD in collision detection." Thesis, University of Newcastle Upon Tyne, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300191.

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Pereira, Villarroel Sergio Alejandro. "Portal de Proyectos Externos del DCC." Tesis, Universidad de Chile, 2010. http://www.repositorio.uchile.cl/handle/2250/103723.

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El objetivo general del presente trabajo de título es desarrollar un portal de Proyectos Externos que permita al Departamento de Ciencias de la Computación (DCC) mejorar: (1) el vínculo con las Empresas y (2) la gestión interna del área. Se espera que éste pueda dar a conocer a la industria los proyectos realizados dentro del Departamento, promover la realización de nuevos proyectos, y, también, permitir una mejor toma de decisiones en futuras gestiones dentro del área. El DCC realiza constantemente diversos proyectos de extensión relacionados con Empresas externas. En la actualidad, no existe ningún lugar donde quede registro de éstos proyectos, sino que simplemente son los profesores encargados quienes mantienen esta información. Frente a lo cual, se torna complejo el proceso de obtención de aquella información. Es por esta razón, que se propone el “Portal de Proyectos Externos del DCC”. Es decir, una aplicación web que permita el manejo de la información en un lugar centralizado, lo cual facilitará el acceso para quienes busquen conocer los proyectos que el Departamento realiza. En este portal, se da solución a los problemas planteados mediante una aplicación a la que se accede vía web, en la cual Alumnos, Empresas y Profesores son partícipes en el debido proceso de publicaciones y postulaciones a proyectos. Más aún, se dispone de información suficiente como para poder tener conocimiento de lo que el Departamento está realizando. De la misma forma, la aplicación se integra a módulos estadísticos que permiten obtener reportes inmediatos para un Administrador, a quién se le facilita la gestión y toma de decisiones para futuros proyectos. El resultado final ha sido satisfactorio e interesante al mismo tiempo, puesto que han surgido mayores interesados que los que se esperaban, permitiendo dar aún mayores soluciones que las propuestas y generando expectativas para posibles trabajos futuros a realizar, tomando como base lo hecho hasta ahora. Asimismo, los usuarios de este portal se hacen partícipes de éste, logrando en una primera instancia acercamientos que previo a la realización de este trabajo no se tenían. Se concluye que el portal permitirá un mayor acercamiento con la industria, comportándose como una vitrina frente al mundo exterior. Por otro lado, se podrá llevar a cabo una mayor gestión interna dentro del DCC, obteniéndose estadísticas de cantidad y desempeño de proyectos a lo largo del tiempo.
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Books on the topic "DCCD"

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Polsgrove, Mike. DCC projects & applications. Waukesha, Wisconsin: Kalmbach Books, 2015.

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The DCC guide. Waukesha, Wisconsin: Kalmbach Books, 2014.

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Renz, Peter, and Bernhard Wicht. Integrated Hybrid Resonant DCDC Converters. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63944-0.

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Data, Compression Conference (3rd 1993 Snowbird Utah). DCC '93: Data Compression Conference. Los Alamitos, Calif: IEEE Computer Society Press, 1993.

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Data Compression Conference (2nd 1992 Snowbird, Utah). DCC '92: Data Compression Conference. Los Alamitos, Calif: IEEE Computer Society Press, 1992.

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Data Compression Conference (1st 1991 Snowbird, Utah). DCC '91: Data Compression Conference. Los Alamitos, Calif: IEEE Computer Society Press, 1991.

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Affairs, Illinois Dept of Commerce and Community. Teltape information system: 800-835-3222 (TEL-DCCA). [Springfield, Ill.]: Illinois Department of Commerce and Community Affairs, 1985.

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Data Compression Conference (4th 1994 Snowbird, Utah). DCC '94, Data Compression Conference: Proceedings. Los Alamitos, Calif: IEEE Computer Society Press, 1994.

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Tournier, Jean-Nicolas. Le Vivant dcod (Quelle nouvelle dfinition donner la vie). Les Ulis: EDP Sciences, 2005.

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Polsgrove, Mike. Basic DCC wiring for your model railroad. Waukesha, Wis: Kalmbach Books, 2011.

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Book chapters on the topic "DCCD"

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Walters, Robin G., and Peter Horton. "DCCD Binds to Lumen-Exposed Glutamate Residues in LHCIIc." In Photosynthesis: from Light to Biosphere, 299–302. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_70.

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Rabon, Edd C., and Kent Smillie. "DCCD Inhibition of Cation Binding in the Gastric H,K-ATPase." In Molecular and Cellular Mechanisms of H+ Transport, 79–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-79301-1_9.

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Palmer, D. N., I. M. Fearnley, S. M. Medd, J. E. Walker, R. D. Martinus, S. L. Bayliss, N. A. Hall, B. D. Lake, L. S. Wolfe, and R. D. Jolly. "Lysosomal Storage of the DCCD Reactive Proteolipid Subunit of Mitochondrial ATP Synthase in Human and Ovine Ceroid Lipofuscinoses." In Lipofuscin and Ceroid Pigments, 211–23. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-5339-1_15.

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Evron, Yoav. "The CF0 Energy-Transfer Inhibitors DCCD and Venturicidin Greatly Vary in their Effect on Proton Flux Across the Thylakoid Membrane." In Photosynthesis: Mechanisms and Effects, 1683–86. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-3953-3_393.

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Heyde, Sandra, and Peter Jahns. "The Influence of N,N’-Dicyclohexylcarbodiimide (DCCD) on the Kinetics and pH-Dependence of Zeaxanthin Formation in Isolated Pea (Pisum sativum) Thylakoids." In Photosynthesis: Mechanisms and Effects, 2285–88. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-3953-3_535.

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Jahns, Peter, and Wolfgang Junge. "The shortcircuit by DCCD of the proton pumping activity of Photosystem II is a common feature of all redox transitions of the water oxidase." In Current Research in Photosynthesis, 881–84. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_204.

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Kolff, Willem J., Belding H. Scribner, Thomas Starzl, and Eli A. Friedman. "DCCT - Bad or Good." In Strength and Compassion in Kidney Failure, 62–67. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5296-9_12.

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Macedonio, Francesca. "Direct Contact Membrane Distillation (DCMD)." In Encyclopedia of Membranes, 559–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_185.

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Macedonio, Francesca. "Direct Contact Membrane Distillation (DCMD)." In Encyclopedia of Membranes, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_185-1.

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Cao, Guangxi, Ling-Yun He, and Jie Cao. "Asymmetric DCCA Cross-Correlation Coefficient." In Multifractal Detrended Analysis Method and Its Application in Financial Markets, 129–53. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-7916-0_7.

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Conference papers on the topic "DCCD"

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Akram, Junaid, Zhendong Shi, Majid Mumtaz, and Ping Luo. "DCCD: An Efficient and Scalable Distributed Code Clone Detection Technique for Big Code." In The 30th International Conference on Software Engineering and Knowledge Engineering. KSI Research Inc. and Knowledge Systems Institute Graduate School, 2018. http://dx.doi.org/10.18293/seke2018-117.

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Picutti, Barbara, Guido Franzoni, Paolo Vergani, Fabio Brignoli, Lucrezia Del Gesso, and Francesca Rabino. "DCCD™ - A New Dual Column Cryogenic Distillation Technology for Natural Gas Sweetening: The Operations of a Laboratory Scale Pilot Plant." In Abu Dhabi International Petroleum Exhibition & Conference. Society of Petroleum Engineers, 2018. http://dx.doi.org/10.2118/193230-ms.

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Barnat, Jiří, Nikola Beneš, Ivana Černá, and Zuzana Petruchová. "DCCL." In the 16th International ACM Sigsoft symposium. New York, New York, USA: ACM Press, 2013. http://dx.doi.org/10.1145/2465449.2465453.

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"DCCS Reviewers." In 2005 International Conference on Dependable Systems and Networks (DSN'05). IEEE, 2005. http://dx.doi.org/10.1109/dsn.2005.35.

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"DCCS reviewers." In 2004 International Conference on Dependable Systems and Networks. IEEE, 2004. http://dx.doi.org/10.1109/dsn.2004.1311864.

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Kohler, Eddie, Mark Handley, and Sally Floyd. "Designing DCCP." In the 2006 conference. New York, New York, USA: ACM Press, 2006. http://dx.doi.org/10.1145/1159913.1159918.

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"DCCS reviewers." In 2008 IEEE International Conference on Dependable Systems and Networks With FTCS and DCC (DSN). IEEE, 2008. http://dx.doi.org/10.1109/dsn.2008.4630058.

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"DCCS Program Committee." In 2005 International Conference on Dependable Systems and Networks (DSN'05). IEEE, 2005. http://dx.doi.org/10.1109/dsn.2005.34.

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"DCCS Program Committee." In 2006 International Conference on Dependable Systems and Networks. IEEE, 2006. http://dx.doi.org/10.1109/dsn.2006.24.

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"DCCS Program Committee." In 37th Annual IEEE/IFIP International Conference on Dependable Systems and Networks (DSN'07). IEEE, 2007. http://dx.doi.org/10.1109/dsn.2007.30.

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Reports on the topic "DCCD"

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Kohler, E., M. Handley, and S. Floyd. Datagram Congestion Control Protocol (DCCP). RFC Editor, March 2006. http://dx.doi.org/10.17487/rfc4340.

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Balenson, David M., Peter Dismore, Michael Heyman, Peter S. Kruus, and Caroline Scace. Dynamic Cryptographic Context Management (DCCM). Fort Belvoir, VA: Defense Technical Information Center, December 2000. http://dx.doi.org/10.21236/ada386812.

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Fairhurst, G. The Datagram Congestion Control Protocol (DCCP) Service Codes. RFC Editor, September 2009. http://dx.doi.org/10.17487/rfc5595.

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Perkins, C. RTP and the Datagram Congestion Control Protocol (DCCP). RFC Editor, April 2010. http://dx.doi.org/10.17487/rfc5762.

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Fairhurst, G., and A. Sathiaseelan. Quick-Start for the Datagram Congestion Control Protocol (DCCP). RFC Editor, August 2009. http://dx.doi.org/10.17487/rfc5634.

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Floyd, S., M. Handley, and E. Kohler. Problem Statement for the Datagram Congestion Control Protocol (DCCP). RFC Editor, March 2006. http://dx.doi.org/10.17487/rfc4336.

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Renker, G., and G. Fairhurst. Sender RTT Estimate Option for the Datagram Congestion Control Protocol (DCCP). RFC Editor, July 2011. http://dx.doi.org/10.17487/rfc6323.

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Phelan, T. Datagram Transport Layer Security (DTLS) over the Datagram Congestion Control Protocol (DCCP). RFC Editor, May 2008. http://dx.doi.org/10.17487/rfc5238.

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Phelan, T., G. Fairhurst, and C. Perkins. DCCP-UDP: A Datagram Congestion Control Protocol UDP Encapsulation for NAT Traversal. RFC Editor, November 2012. http://dx.doi.org/10.17487/rfc6773.

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Fairhurst, G. Datagram Congestion Control Protocol (DCCP) Simultaneous-Open Technique to Facilitate NAT/Middlebox Traversal. RFC Editor, September 2009. http://dx.doi.org/10.17487/rfc5596.

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