Relevant bibliographies by topics / Sulfate recognition

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Sulfate recognition'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Sulfate recognition"

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Kanyo, Z. F., and D. W. Christianson. "Biological recognition of phosphate and sulfate." Journal of Biological Chemistry 266, no. 7 (1991): 4264–68. http://dx.doi.org/10.1016/s0021-9258(20)64316-2.

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Ravikumar, I., and Pradyut Ghosh. "Recognition and separation of sulfate anions." Chemical Society Reviews 41, no. 8 (2012): 3077. http://dx.doi.org/10.1039/c2cs15293b.

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Carruthers, Vern B., Sebastian Håkansson, Olivia K. Giddings, and L. David Sibley. "Toxoplasma gondii Uses Sulfated Proteoglycans for Substrate and Host Cell Attachment." Infection and Immunity 68, no. 7 (2000): 4005–11. http://dx.doi.org/10.1128/iai.68.7.4005-4011.2000.

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ABSTRACT Toxoplasma gondii is an obligate intracellular parasite that actively invades a wide variety of vertebrate cells, although the basis of this pervasive cell recognition is not understood. We demonstrate here that binding to the substratum and to host cells is partially mediated by interaction with sulfated glycosaminoglycans (GAGs). Addition of excess soluble GAGs blocked parasite attachment to serum-coated glass, thereby preventing gliding motility of extracellular parasites. Similarly, excess soluble GAGs decreased the attachment of parasites to human host cells from a variety of lin
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Baydemir, Gözde. "Molecularly imprinted cryogels for chondroitin sulfate recognition." Artificial Cells, Nanomedicine, and Biotechnology 44, no. 2 (2014): 610–17. http://dx.doi.org/10.3109/21691401.2014.975236.

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Mateus, Pedro, Rita Delgado, Vânia André, and M. Teresa Duarte. "Sulfate recognition by a hexaaza cryptand receptor." Organic & Biomolecular Chemistry 13, no. 3 (2015): 834–42. http://dx.doi.org/10.1039/c4ob02027h.

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Shishkanova, Tatiana V, David Sykora, Hana Vinšová, Vladimír Král, Iulia Mihai, and Natalia P Gospodinova. "A Novel Way to Improve Sulfate Recognition." Electroanalysis 21, no. 17-18 (2009): 2010–13. http://dx.doi.org/10.1002/elan.200904632.

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OLIVEIRA, F. O. R., C. R. ALVES, F. SOUZA-SILVA, et al. "Trypanosoma cruzi heparin-binding proteins mediate the adherence of epimastigotes to the midgut epithelial cells of Rhodnius prolixus." Parasitology 139, no. 6 (2012): 735–43. http://dx.doi.org/10.1017/s0031182011002344.

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SUMMARYHeparin-binding proteins (HBPs) have been demonstrated in both infective forms of Trypanosoma cruzi and are involved in the recognition and invasion of mammalian cells. In this study, we evaluated the potential biological function of these proteins during the parasite-vector interaction. HBPs, with molecular masses of 65·8 kDa and 59 kDa, were isolated from epimastigotes by heparin affinity chromatography and identified by biotin-conjugated sulfated glycosaminoglycans (GAGs). Surface plasmon resonance biosensor analysis demonstrated stable receptor-ligand binding based on the associatio
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Lee, Haeri, Dongwon Kim, Hyejin Oh, and Ok-Sang Jung. "Molecular balloon, Pd6L8 cages: recognition of alkyl sulfate surfactants." Chemical Communications 56, no. 19 (2020): 2841–44. http://dx.doi.org/10.1039/c9cc09742b.

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Significant structural contraction and expansion of flexible Pd<sub>6</sub>L<sub>8</sub> cages by encapsulation of alkyl sulfate were demonstrated. The contact angles on the fine-ground microcrystal layers shift according to the chain length of the alkyl sulfate.
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Ravikumar, I., and Pradyut Ghosh. "ChemInform Abstract: Recognition and Separation of Sulfate Anions." ChemInform 43, no. 29 (2012): no. http://dx.doi.org/10.1002/chin.201229279.

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Liu, Yang, Arthur J. Chirino, Ziva Misulovin, et al. "Crystal Structure of the Cysteine-Rich Domain of Mannose Receptor Complexed with a Sulfated Carbohydrate Ligand." Journal of Experimental Medicine 191, no. 7 (2000): 1105–16. http://dx.doi.org/10.1084/jem.191.7.1105.

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The macrophage and epithelial cell mannose receptor (MR) binds carbohydrates on foreign and host molecules. Two portions of MR recognize carbohydrates: tandemly arranged C-type lectin domains facilitate carbohydrate-dependent macrophage uptake of infectious organisms, and the NH2-terminal cysteine-rich domain (Cys-MR) binds to sulfated glycoproteins including pituitary hormones. To elucidate the mechanism of sulfated carbohydrate recognition, we determined crystal structures of Cys-MR alone and complexed with 4-sulfated-N-acetylgalactosamine at 1.7 and 2.2 Å resolution, respectively. Cys-MR fo
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Dissertations / Theses on the topic "Sulfate recognition"

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Genua, Maria. "Combinatorial surface-based electronic tongue development : Analytical applications and conception of 2D and 3D biomimetic surfaces." Thesis, Grenoble, 2013. http://www.theses.fr/2013GRENI044/document.

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L'objectif de cette thèse est le développement d'une langue électronique avec une méthode simplifiée d'obtention de récepteurs à réactivité croisée. Ces récepteurs sont préparés par une approche combinatoire novatrice qui consiste au mélange et à l'auto-assemblage de deux disaccharides. Le couplage de ces récepteurs avec un système de détection d'imagerie par résonance des plasmons de surface nous a permis de réaliser une langue électronique capable de différencier des échantillons de différentes complexités, y compris des protéines pures et des mélanges complexes. Cela se fait grâce aux profi
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Song, Wei. "Structural basis for sulfatide recognition by Disabled-2." Diss., Virginia Tech, 2021. http://hdl.handle.net/10919/101866.

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Disabled-2 (Dab2) is an adaptor protein that plays critical roles in various biological processes, including protein endocytosis, platelet activation and aggregation, tumor growth, and development. In platelets, Dab2 associates with membrane sulfatide at the platelet surface, modulating platelet inside-out and outside-in signaling pathways. A Dab2-derived peptide, named the sulfatide-binding peptide (SBP), is the minimal unit of Dab2 to exert its function as a negative regulator of platelet activation and aggregation. The work of this thesis refines the model of Dab2 SBP binding to sulfatide a
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Singabraya, Dominique. "L’impression moléculaire pour la reconnaissance spécifique des glycannes sulfatés d’intérêt biologique." Thesis, Paris Est, 2010. http://www.theses.fr/2010PEST0049.

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Les glycosaminoglycannes (GAGs) sont des molécules polysaccharidiques polysulfatées intervenant dans des processus aussi variés que la prolifération, différenciation ou migration cellulaire, la coagulation sanguine ou l‟infection virale. Il est généralement admis qu‟une séquence particulière de GAG doit être associée à une fonction biologique spécifique. Les structures chimiques globales des GAGs sont connues. Cependant, contrairement au séquençage des gènes ou des protéines, la détermination de la séquence saccharidique exacte impliquée dans une fonction biologique particulière n‟est encore p
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Santos, Figueroa Luis Enrique. "New approaches for the development of chromo-fluorogenic sensors for chemical species of biological, industrial and environmental interest." Doctoral thesis, Universitat Politècnica de València, 2015. http://hdl.handle.net/10251/43216.

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El presente proyecto de investigación está enfocado al desarrollo de sensores químicos fluoro-cromogénicos, para la detección y determinación de especies químicas de interés biológico, industrial y medioambiental de forma selectiva y con alta sensibilidad. En forma general, se busca el diseñar nuevos sistemas sensores basados en compuestos (receptores) formados por dos unidades: una unidad coordinante que interacciona con el anión a determinar y una unidad generadora de señal que alerta del reconocimiento molecular efectuado. Durante este estudio se están preparando diversas moléculas rece
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El, Sayed Shehata Nasr Sameh. "Supramolecular Chemistry: New chemodosimeters and hybrid materials for the chromo-fluorogenic detection of anions and neutral molecules." Doctoral thesis, Universitat Politècnica de València, 2015. http://hdl.handle.net/10251/52598.

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[EN] Abstract The present PhD thesis entitled "Supramolecular Chemistry: New chemodosimeters and hybrid materials for the chromo-fluorogenic detection of anions and neutral molecules" is based on the application of supramolecular chemistry and material science principles for the development of optical chemosensors for anions and neutral molecules detection. The second chapter of this PhD thesis is devoted to the preparation of chemodosimeters for the chromo-fluorogenic detection of fluoride, diisopropyl fluorophosphates (DFP) and hydrogen sulfide. The optical detection of fluoride anion
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Shumilova, Tatiana A. "New synthetic hosts for sulfate and nucleoside triphosphates: understanding non-covalent interactions." 2017. https://monarch.qucosa.de/id/qucosa%3A20879.

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The present work describes new aspects of organic and supramolecular chemistry. The scientific contribution consists of two parts, which focus on the development of receptors for the sulfate anion and quantitative assessment of stacking interactions between an anthracene dye and nucleobases in an aqueous solution. In Chapter 1, basic concepts concerning supramolecular chemistry and recognition of cations and anions are discussed, as well as modern methods for the determination of binding constants. Particular attention is paid to fluorescence sensing of ions and underlying mechanisms of bindi
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Liu, Yang. "Molecular mechanism of sulfated carbohydrate recognition: structural and biochemical studies of the cysteine-rich domain of mannose receptor." Thesis, 2001. https://thesis.library.caltech.edu/8119/1/Liu%202001.pdf.

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<p>Mannose receptor (MR) is widely expressed on macrophages, immature dendritic cells, and a variety of epithelial and endothelial cells. It is a 180 kD type I transmembrane receptor whose extracellular region consists of three parts: the amino-terminal cysteine-rich domain (Cys-MR); a fibronectin type II-like domain; and a series of eight tandem C-type lectin carbohydrate recognition domains (CRDs). Two portions of MR have distinct carbohydrate recognition properties: Cys-MR recognizes sulfated carbohydrates and the tandem CRD region binds terminal mannose, fucose, and N-acetyl-glucosam
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Book chapters on the topic "Sulfate recognition"

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Tchertanov, Luba, and Claudine Pascard. "Molecular Recognition of Anionic Species: Hydrogenbonding Properties of Sulfate Andthiocyanate." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_99.

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Habermann, B., T. Krüger, H. Stephan, K. Hollmann, and K. Gloe. "Novel Bis(phenoxyalkyl)sulfane Podands — Synthesis and Complex Formation with Thiophilic Metals Ions." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_55.

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Coombe, Deirdre R., and Christopher R. Parish. "Sulfated Polysaccharide-Mediated Sponge Cell Aggregation: The Clue to Invertebrate Self/Nonself-Recognition?" In Invertebrate Historecognition. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1053-2_3.

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Bačuvčík, Michal, Pavel Martauz, Ivan Janotka, and Branislav Cvopa. "The Resistance of New Kind of High-Strength Cement after 5 Years Exposure to Sulfate Solution." In Cement Industry [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.95240.

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This article deals with the determination of technically important properties, the recognition of microstructure and pore structure, and the mortar resistance of a new cement kind NONRIVAL CEM I 52.5 N containing 7.94% wt. of C3A to 5% sodium sulfate solution. Both reference types of cement were industrially manufactured: 1) ordinary Portland cement CEM I 42.5 R and 2) Portland cement CEM I 42.5 R – SR 0, declared as sulfate resistant because of C3A = 0%. The research was carried out at standardized mortars. The used sodium sulfate solution, which contained 33802.8 mg of aggressive SO4 2− per liter, exceeded approximately 5 to 10 times the concentration of the third degree of aggressiveness of the XA chemical environment according to STN EN 206 + A1. The reference medium was drinking water. The 5-year results of non-destructive and destructive physical-mechanical tests as well as the formed microstructure and pore structure in both liquid media were evaluated. The cause of the NONRIVAL CEM I 52.5 N sulfate resistance was explained, despite the manufacturer’s declared C3A content of up to 8% by weight. Sulfate resistance of NONRIVAL CEM I 52.5 N is found comparable to that of sulfate resistant CEM I 42.5 R – SR 0.
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Honke, Koichi, Naoki Ikeda, and Naoyuki Taniguchi. "Differences in Recognition of Sulfated and Sialylated Carbohydrate Chains." In Recognition of Carbohydrates in Biological Systems, Part B: Specific Applications. Elsevier, 2003. http://dx.doi.org/10.1016/s0076-6879(03)01054-1.

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Hepbildikler, Stefan T., Michaela Wendeler, Roger Sandhoff, and Konrad Sandhoff. "Interaction of the GM2 Activator Protein with Sulfated and Sialylated Glycosphingolipids." In Recognition of Carbohydrates in Biological Systems, Part B: Specific Applications. Elsevier, 2003. http://dx.doi.org/10.1016/s0076-6879(03)01053-x.

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Tossell, John A., and David J. Vaughan. "Applications To Geochemical Problems." In Theoretical Geochemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/oso/9780195044034.003.0010.

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In this, the last major chapter of the book, we turn our attention to the applications of modern electronic structure models and concepts to more general geochemical problems; namely, those described by Goldschmidt as being concerned with the “distribution of elements in the geochemical spheres and the laws governing the distribution of the elements” (see Preface). The majority of minerals and rocks originally formed by crystallization from melts, and so the first section of this chapter is devoted to considering the nature of melts (and glasses), structure and bonding in melts, and the partitioning of elements (particularly transition elements) between the melt and crystallizing solid phases. The classic work of Bowen (1928) led to the recognition of particular sequences of crystallization and crystal-melt reaction relationships in the silicate melts from which major rock types form, as enshrined in the “Bowen Reaction Series.” Attempts were also made to explain the incorporation of particular elements into particular mineral structures using simple crystal chemical arguments, notably as laid down in “Goldschmidt’s Rules” (Goldschmidt, 1937). Such concepts are reappraised in the light of modern electronic structure theories. The other major realm of formation of minerals and rocks, and the most important medium of transport and redistribution of the chemical elements at the Earth’s surface, is the aqueous solution. The molecular and electronic structures of aqueous solutions, their behavior at elevated temperatures, formation and stabilities of complexes in solution, and the mechanisms of reactions in solution are all considered in the second section of this chapter. The surfaces of minerals (or other crystalline solids) differ from the bulk material in terms of both crystal structure and electronic structure. A great variety of spectroscopic, diffraction, scanning, and other techniques are now available to study the nature of solid surfaces, and models are being developed to interpret and explain the experimental data. These approaches are discussed with reference to a few examples of oxide and sulfide minerals. Although relatively few studies have been undertaken specifically of the surfaces of minerals, many of the reaction phenomena that occur in natural systems take place at mineral surfaces, so that such surface studies represent an important area of future research.
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Conference papers on the topic "Sulfate recognition"

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Newbound, T. D., A. N. Al-Nasser, M. P. Sang, and W. J. Carrigan. "Recognition and Prevention of Distillate Fuel Emulsions." In ASME Turbo Expo 2006: Power for Land, Sea, and Air. ASMEDC, 2006. http://dx.doi.org/10.1115/gt2006-90030.

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This paper describes a case study involving chronic plugging of 5μm particulate filters in a gas turbine diesel fuel system in a Red Sea refinery. Rapid plugging of the filters was caused by water-in-diesel emulsions generated in diesel fuel supply tanks. Sludge with a wax-like appearance recovered from the 5 μm filters was, in fact, found to be composed of up to 50 percent water with no significant wax content. X-ray studies of the filter catch solids revealed a variety of iron oxide phases, sodium chloride, and high concentrations of sodium sulfate. Microbial cultures inoculated from storage
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Tomaslni, B. R., and D. F. Mosher. "PREFERENTIAL RECOGNITION OF VITRONECTIN (S-PR0TEIN) BY A MONOCLONAL ANTIBODY UPON INTERACTION WITH THROMBIN, ANTITHROMBIN AND GLYCOSAMINOGLYCANS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643634.

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V1tronect1n/S-Prote1n (VN/SP) is a glycoprotein present at a concentration of 200-400 ug/ml 1n plasma and serum. It has been shown to promote cel 1-substratum adhesion and to act as an Inhibitor of the membrane attack complex of complement and of the inactivation of thrombin by antithrombin III in the presence of low levels of heparin. We have previously shown that VN/SP binds more avidly to heparln-agarose and to a monoclonal antibody (MaVN/SP)-Sepharose column when present 1n serum rather than 1n plasma. In order to examine the possibility of a serum-induced conformational change, we utilize
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Vermeer, C., BA M. Soute, and MM W. Ulrich. "IN VITRO CARBOXYLATION OF EXOGENOUS PROTEIN SUBSTRATES BY VITAMIN K-DEPENDENT CARBOXYLASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643994.

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In vivo treatment of experimental animals with vitamin K-antagonists induces the accumulation of non-carboxylated coagulation factor precursors in the liver, where they are tightly bound to vitamin K-dependent carboxylase. If hepatic carboxylase is isolated from warfarin-treated animals, it is obtained therefore almost exclusively in the form of an enzyme/substrate complex. If carboxylase is prepared from non-treated animals, on the other hand, the resulting enzyme is predominantly substrate-free. Small substrates like F L E E L or decarboxylated osteocalcinare carboxylated equally well by bot
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Cao, Huai-xiang, Chun-mao Wang, and Xing-qi Qiu. "Study on the Cause and Nondestructive Test of Backside Cracks in Stainless Steel Linings." In ASME 2012 Pressure Vessels and Piping Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/pvp2012-78410.

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In this paper, the cause and nondestructive test technology of backside cracks were studied. On the one hand, failure analysis revealed that, the backside cracks, which were found universally in the stainless steel inner linings of urea reactors in recent years, were caused by the interaction of wet hydrogen sulfide (H2S) and chloride ions (Cl−) stress corrosion cracking (SCC), and the source of the H2S and Cl− was the leak detection steam. On the other hand, the use of Lamb wave inspection was studied because of the inapplicability of other inspection methods. The dispersion curves of phase a
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Chen, Kok Hao, and Jong Hyun Choi. "Nanoparticle-Aptamer: An Effective Growth Inhibitor for Human Cancer Cells." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11966.

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Semiconductor nanocrystals have unique optical properties due to quantum confinement effects, and a variety of promising approaches have been devised to interface the nanomaterials with biomolecules for bioimaging and therapeutic applications. Such bio-interface can be facilitated via a DNA template for nanoparticles as oligonucleotides can mediate the aqueous-phase nucleation and capping of semiconductor nanocrystals.[1,2] Here, we report a novel scheme of synthesizing fluorescent nanocrystal quantum dots (NQDs) using DNA aptamers and the use of this biotic/abiotic nanoparticle system for gro
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