Academic literature on the topic 'CEHC'

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Journal articles on the topic "CEHC"

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Galli, Piroddi, Iannone, Pagliarani, Tomasi, and Floridi. "A comparison between the antioxidant and peroxynitrite-scavenging functions of the vitamin E metabolites alpha- and gamma-carboxyethyl-6-hydroxychromans." International Journal for Vitamin and Nutrition Research 74, no. 5 (September 1, 2004): 362–73. http://dx.doi.org/10.1024/0300-9831.74.5.362.

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Carboxyethyl-6-hydroxychromans (CEHC) are vitamin E metabolites with proposed in vitro antioxidant function. In this study we compared the antioxidant potency of the two main CEHC metabolites found in biological fluids (i.e., alpha-CEHC and gamma-CEHC) using two different experimental models of lipid oxidation: 1) plasma diluted 1/50 vol/vol in phosphate buffered saline (PBS) exposed to 50 muM Cu2+ ions, and 2) LDL (100 mug of proteins) exposed to different pro-oxidants as 2.5 muM Cu2+, 1 mM of the water soluble peroxyl radical generator 2,2'-Azobis(2-amidinopropane) hydrochloride (AAPH) and human macrophages (4 x 105 cells). Moreover, the two CEHC homologues were assessed for the inhibitory effect on the peroxynitrite (ONOO–)-induced nitration of tyrosine (Tyr). The results showed that in the concentration range 0.015–5 muM the CEHC metabolites and the hydrosoluble analogue Trolox exert similar concentration-dependent inhibition of the Cu2+-induced lipid oxidation of plasma. After in vitro exposure to tert-butyl hydroperoxide/Fe2+, CEHC formed chromanoxyl radicals with electron spin resonance spectra matching exactly those of their parent tocopherols. The LDL oxidation induced by AAPH or Cu2+ was significantly and similarly inhibited by 1 muM of both the CEHC homologues and Trolox. gamma-CEHC showed a slight but significantly higher inhibition of the macrophage-induced low-density lipoprotein (LDL) oxidation than alpha-CEHC. Both the CEHC homologues inhibit Tyr nitration induced by ONOO–. However, gamma-CEHC produced a slightly greater inhibitory effect than alpha-CEHC through the formation of the nitrated congener 5-nitro-gamma-CEHC. In all the systems under investigation, low nanomolar concentrations of CEHC (i.e., the concentration range in the blood of subjects with normal dietary intake of vitamin E) produced feeble antioxidant effects. In conclusion, gamma-CEHC and alpha-CEHC show similar concentration-dependent inhibition of plasma and LDL lipid oxidation. gamma-CEHC has a fairly higher potency than alpha-CEHC as ONOO– scavenger through the formation of 5-nitro-gamma-CEHC. CEHC metabolites show the same in vitro antioxidant chemistry of their parent tocopherols, but the characteristic hydrophilicity of these metabolites could result in different biopotency and roles. Further studies are needed to clarify whether CEHC could contribute to the antioxidant network in biological fluids and tissues.
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Li, Youyou, Leena P. Bharath, Ying Qian, Ting Ruan, Pon Velayutham Anandh Babu, Richard S. Bruno, J. David Symons, and Thunder Jalili. "γ−Carboxyethyl hydroxychroman, a metabolite of γ−tocopherol, preserves nitric oxide bioavailability in endothelial cells challenged with high glucose." Experimental Biology and Medicine 241, no. 18 (July 28, 2016): 2056–62. http://dx.doi.org/10.1177/1535370216661780.

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Endothelial dysfunction occurs when there are imbalances between factors that regulate the synthesis and degradation of nitric oxide (NO•), and has been reported in patients with hyperglycemia and insulin resistance. We reported that supplementation with γ-tocopherol (γ-T) in humans limits impairments in endothelial function otherwise induced by postprandial hyperglycemia. Given the rapid metabolism of γ-T into γ-carboxyethyl hydroxychroman (γ-CEHC), we hypothesized that the vasoprotective activities of γ-T could be attributed to its metabolite γ-CEHC. To test this, human aortic endothelial cells (HAECs) treated with 0 (vehicle control) or 3 µM γ-CEHC for 24 h prior to incubation with normal (5 mM) or high (25 mM) glucose for 48 h. High-glucose increased levels of uncoupled endothelial nitric oxide synthase (eNOS) as evidenced by reduced ( p < 0.05) eNOS dimer:monomer. High glucose also prevented insulin-stimulated increases in p-AktSer473: total Akt, p-eNOSSer1177: total eNOS, and NO• production. These adverse changes were accompanied by increased ( p < 0.05) reactive oxygen species and mRNA expression of inflammatory mediators (VCAM-1, E-selectin, IL-8). However, each deleterious response evoked by high glucose was prevented when HAECs were incubated with γ-CEHC prior to the high glucose challenge. Taken together, our data support the hypothesis that vascular protection provided by γ-T in vivo may be elicited through the bioactivity of its metabolite, γ-CEHC. Furthermore, it is possible that the antioxidant and anti-inflammatory activities of γ-CEHC may mediate this protective activity.
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Lewin, Allison, Allister Crow, Christopher T. C. Hodson, Lars Hederstedt, and Nick E. Le Brun. "Effects of substitutions in the CXXC active-site motif of the extracytoplasmic thioredoxin ResA." Biochemical Journal 414, no. 1 (July 29, 2008): 81–91. http://dx.doi.org/10.1042/bj20080356.

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The thiol–disulfide oxidoreductase ResA from Bacillus subtilis fulfils a reductive role in cytochrome c maturation. The pKa values for the CEPC (one-letter code) active-site cysteine residues of ResA are unusual for thioredoxin-like proteins in that they are both high (>8) and within 0.5 unit of each other. To determine the contribution of the inter-cysteine dipeptide of ResA to its redox and acid–base properties, three variants (CPPC, CEHC and CPHC) were generated representing a stepwise conversion into the active-site sequence of the high-potential DsbA protein from Escherichia coli. The substitutions resulted in large decreases in the pKa values of both the active-site cysteine residues: in CPHC (DsbA-type) ResA, ΔpKa values of −2.5 were measured for both cysteine residues. Increases in midpoint reduction potentials were also observed, although these were comparatively small: CPHC (DsbA-type) ResA exhibited an increase of +40 mV compared with the wild-type protein. Unfolding studies revealed that, despite the observed differences in the properties of the reduced proteins, changes in stability were largely confined to the oxidized state. High-resolution structures of two of the variants (CEHC and CPHC ResA) in their reduced states were determined and are discussed in terms of the observed changes in properties. Finally, the in vivo functional properties of CEHC ResA are shown to be significantly affected compared with those of the wild-type protein.
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Martens, Leon G., Jiao Luo, Fleur L. Meulmeester, Nadia Ashrafi, Esther Winters van Eekelen, Renée de Mutsert, Dennis O. Mook-Kanamori, et al. "Associations between Lifestyle Factors and Vitamin E Metabolites in the General Population." Antioxidants 9, no. 12 (December 15, 2020): 1280. http://dx.doi.org/10.3390/antiox9121280.

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The antioxidant vitamin E (α-tocopherol, α-TOH) protects lipids from oxidation by reactive oxygen species. We hypothesized that lifestyle factors associate with vitamin E metabolism marked by urinary α-tocopheronolactone hydroquinone (α-TLHQ) and α-carboxymethyl-hydroxychroman (α-CEHC levels), as potential reflection of lipid oxidation. We conducted a cross-sectional study in the Netherlands Epidemiology of Obesity Study. Serum α-TOH, and urinary α-TLHQ and α-CEHC were quantified by liquid chromatography coupled with tandem mass spectrometry. Information on the lifestyle factors (sleep, physical activity (PA), smoking and alcohol) were collected through questionnaires. Multivariable linear regression analyses were performed to assess the associations between the lifestyle factors and α-TOH measures. A total of 530 participants (46% men) were included with mean (SD) age of 56 (6) years. Of the examined lifestyle factors, only poor sleep was associated with a higher serum α-TOH (mean difference: 4% (95% CI: 1, 7%)). Current smoking was associated with higher urinary α-CEHC (32%: (14%, 53%)), with evidence of a dose–response relationship with smoking intensity (low pack years, 24% (2, 52%); high pack years, 55% (25, 93%)). Moderate physical activity was associated with a lower α-TLHQ relative to α-CEHC (−17%: (−26, −6%), compared with low PA). Only specific lifestyle factors associate with vitamin E metabolism. Examining serum α-TOH does not provide complete insight in vitamin E antioxidant capacity.
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Traber, Maret G., Scott W. Leonard, Ifechukwude Ebenuwa, Pierre-Christian Violet, Mahtab Niyyati, Sebastian Padayatty, Sheila Smith, Gerd Bobe, and Mark Levine. "Vitamin E catabolism in women, as modulated by food and by fat, studied using 2 deuterium-labeled α-tocopherols in a 3-phase, nonrandomized crossover study." American Journal of Clinical Nutrition 113, no. 1 (November 12, 2020): 92–103. http://dx.doi.org/10.1093/ajcn/nqaa298.

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ABSTRACT Background Human vitamin E (α-tocopherol) catabolism is a mechanism for regulating whole-body α-tocopherol. Objectives To determine the roles of the intestine and liver on α-tocopherol catabolism as affected by fat or fasting, 2 deuterium-labeled (intravenous d6- and oral d3-) forms of α-tocopherol were used. Methods Healthy women received intravenous d6-α-tocopherol and consumed d3-α-tocopherol with a 600-kcal defined liquid meal (DLM; 40% or 0% fat, n = 10) followed by controlled meals; or the 0% fat DLM (n = 7) followed by a 12-h fast (0% fat-fast), then controlled meals ≤72 h. The order of the 3-phase crossover design was not randomized and there was no blinding. Samples were analyzed by LC/MS to determine the α-tocopherol catabolites and α-carboxyethyl hydroxychromanol (α-CEHC) in urine, feces, and plasma that were catabolized from administered oral d3- and intravenous d6-α-tocopherols. Results Urinary and plasma d3- and d6-α-CEHC concentrations varied differently with the interventions. Mean ± SEM cumulative urinary d6-α-CEHC derived from the intravenous dose excreted over 72 h during the 40% fat (2.50 ± 0.37 μmol/g creatinine) and 0% fat (2.37 ± 0.37 μmol/g creatinine) interventions were similar, but a ∼50% decrease was observed during the 0% fat-fast (1.05 ± 0.39 μmol/g creatinine) intervention (compared with 0% fat, P = 0.0005). Cumulative urinary d3-α-CEHC excretion was not significantly changed by any intervention. Total urinary and fecal excretion of catabolites accounted for &lt;5% of each of the administered doses. Conclusions Differential catabolism of the intravenous d6-α-tocopherol and oral d3-α-tocopherol doses shows both liver and intestine have roles in α-tocopherol catabolism. During the 40% fat intervention, &gt;90% of urinary d3-α-CEHC excretion was estimated to be liver-derived, whereas during fasting &lt;50% was from the liver with the remainder from the intestine, suggesting that there was increased intestinal α-tocopherol catabolism while d3-α-tocopherol was retained in the intestine in the absence of adequate fat/food for α-tocopherol absorption. This trial was registered at clinicaltrials.gov as NCT00862433.
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Li, Yi-Jen, Sheng-Ching Luo, Yi-Jing Lee, Fu-Jung Lin, Chi-Cheng Cheng, Yung-Shung Wein, Yueh-Hsiung Kuo, and Ching-jang Huang. "Isolation and Identification of α-CEHC Sulfate in Rat Urine and an Improved Method for the Determination of Conjugated α-CEHC." Journal of Agricultural and Food Chemistry 56, no. 23 (December 10, 2008): 11105–13. http://dx.doi.org/10.1021/jf802459d.

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Fais, Antonella, Enrico Cacace, Luigi Atzori, Benedetta Era, and Valeria Ruggiero. "Plasma phospholipase, γ-CEHC and antioxidant capacity in fibromyalgia." International Journal of Rheumatic Diseases 20, no. 5 (November 20, 2015): 550–54. http://dx.doi.org/10.1111/1756-185x.12787.

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Flisiak, Robert. "Meeting of Initiative Group for Central European Hepatologic Collaboration (CEHC)." Clinical and Experimental Hepatology 1 (2016): 1. http://dx.doi.org/10.5114/ceh.2016.58848.

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Mazzini, Francesco, Francesco Galli, and Piero Salvadori. "Vitamin E Metabolites: Synthesis of [D2]- and [D3]-γ-CEHC." European Journal of Organic Chemistry 2006, no. 24 (December 2006): 5588–93. http://dx.doi.org/10.1002/ejoc.200600652.

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Otter, Don, Mingshu Cao, Hui-Ming Lin, Karl Fraser, Shelley Edmunds, Geoff Lane, and Daryl Rowan. "Identification of Urinary Biomarkers of Colon Inflammation in IL10-/-Mice Using Short-Column LCMS Metabolomics." Journal of Biomedicine and Biotechnology 2011 (2011): 1–12. http://dx.doi.org/10.1155/2011/974701.

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The interleukin-10-deficient (IL10-/-) mouse develops colon inflammation in response to normal intestinal microflora and has been used as a model of Crohn's disease. Short-Column LCMS metabolite profiling of urine from IL10-/-and wild-type (WT) mice was used, in two independent experiments, to identify mass spectral ions differing in intensity between these two genotypes. Three differential metabolites were identified as xanthurenic acid and as the glucuronides of xanthurenic acid and of α-CEHC (2,5,7,8-tetramethyl-2-(2′-carboxyethyl)-6-hydroxychroman). The significance of several differential metabolites as potential biomarkers of colon inflammation was evaluated in an experiment which compared metabolite concentrations in IL10-/-and WT mice housed, either under conventional conditions and dosed with intestinal microflora, or maintained under specific pathogen-free (SPF) conditions. Concentrations of xanthurenic acid, α-CEHC glucuronide, and an unidentified metabolitem/z495-/497+were associated with the degree of inflammation in IL10-/-mice and may prove useful as biomarkers of colon inflammation.
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Dissertations / Theses on the topic "CEHC"

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Lecea, Romera Mercedes. "Stereoselective synthesis of the natural metabolite of tocopherol, (S)-y-CEHC, and monofluorinated trisubstituted olefins." Phd thesis, Université de Strasbourg, 2012. http://tel.archives-ouvertes.fr/tel-01064056.

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This PhD work has been focused in two different subjects : - The stereoselective synthesis of 2,2-disubstituted chroman moiety assisted by sulfoxides as only source of chirality has been realized with good yields and good diastereoselectivities. The total synthesis of the natural metabolite of tocopherol, (S)-γ-CEHC, has been realized in ten steps and in 18.4% of overall yield using as key step the formation of ally sulfinyl chroman by reaction with allyl trimethyl silane in the presence of a Lewis acid. - The stereoselective synthesis of monofluorinated trisusbtituted olefins has been realized in moderated yields and excellents selectivities in some cases (95 :5) from readily available 3,3,3-trifluoropropionates.The Diels-Alder reaction using fluorinated dienophiles and cyclopentadiene led to unexpected complex structures.
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Pfluger, Paul Thomas. "Der Metabolismus der Tocopherole und Tocotrienole." Phd thesis, kostenfrei, 2007. http://opus.kobv.de/ubp/volltexte/2008/1601/.

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Letelier, Valle José Francisco. "CEAC: centro de apoyo cultural." Tesis, Universidad de Chile, 2012. http://www.repositorio.uchile.cl/handle/2250/111197.

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La presente memoria posee como finalidad interiorizar en el desarrollo y comprensión del proyecto de Arquitectura llevado a cabo durante el proceso de Titulación, en base a la problemática sobre los efectos urbanos de la edificación en altura en la ciudad. De tal manera, se elabora un proyecto trendsetter que explore dichas problemáticas y genere una nueva tipología de hacer ciudad vertical. Teniendo como objetivo que el barrio adquiera un nuevo valor y potencie tanto su dinámica como su propia identidad. La resolución del proyecto se origina a partir de la comprensión de los trendsetters como elementos que generan tendencia en lugares y barrios que se desean activar como polos de actividades, de manera que el sector pase de un estado neutro a un estado de prosperidad. El barrio seleccionado para su análisis e intervención es el Barrio El Golf, por ser el principal escenario influenciado por desarrollos de mercado y su edificación en altura, modificando su configuración urbana residencial hacia un polo de actividad financiera; Se define un emplazamiento especifico a intervenir, por ser un punto estratégico de entrada al barrio por metro, por su conexión con plaza Perú y su posicionamiento sobre la calle principal Isidora Goyenechea. Finalmente, tras un exhaustivo análisis de las carencias y necesidades del sector, surge un mix programático constituido por la integración de actividades de formación, información, recreación y trabajo. Todos juntos dan origen al CENTRO DE APOYO CULTURAL _ CEAC proporcionando ser un lugar de encuentro en el barrio y un apoyo para la biblioteca comunal de Las Condes, que busca permanecer en el tiempo, generando nuevas tendencias y usos en el sector.
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Fortune, Tyler John. "CHRONIC LOW-LEVEL LEAD EXPOSURE AFFECTS THE MONOAMINERGIC SYSTEM IN THE MOUSE SUPERIOR OLIVARY COMPLEX." The University of Montana, 2008. http://etd.lib.umt.edu/theses/available/etd-12172007-145904/.

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Low-level lead (Pb) exposure is associated with behavioral and cognitive dysfunction. It is not clear how Pb produces these behavioral changes but low-level Pb exposure and learning disabilities have been associated with altered auditory temporal processing in both humans and animals. Temporal processing is used to decode complex sounds and to detect a signal within a noise background, and it is thought that neurons of the superior olivary complex (SOC) in the brainstem play a role in sound detection in noisy environments and in selective auditory attention. The SOC receives a catecholaminergic and a serotonergic innervation from the locus coeruleus and the dorsal raphe respectively. While the physiological role of the noradrenergic input has yet to be defined, serotonin is involved in auditory temporal processing. Because Pb exposure modulates auditory temporal processing, the serotonergic system is a potential target for Pb. The current study was undertaken to determine whether developmental Pb exposure preferentially changes the expression of serotonin within the SOC. Pb-treated mice were exposed to no Pb, 0.01 mM (very low) or 0.1 mM (Low) Pb acetate throughout gestation and through 21 days postnatally. Brainstem sections from control and Pb-exposed mice were immunostained for the vesicular monoamine transporter 2 (VMAT2), serotonin, and dopamine beta hydroxylase (DβH, a marker for norepinephrine) in order to elucidate the effect of Pb on monoaminergic input into the SOC. In addition, sections were immunolabeled with antibodies to VGLUT1, VGAT and VAChT in order to determine whether Pb exposure alters the glutaminergic, gaba-ergic, or cholinergic systems. Pb exposure caused a significant decrease in VMAT2, 5HT, and DβH expression while VGLUT1, VGAT and VAChT showed no change. These results provide evidence that Pb exposure during development alters normal monoaminergic expression in the auditory brainstem.
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Forestier, François. "Plaquette et CEC. : Atteinte plaquettaire en chirurgie cardiaque avec CEC : aspects physiopathologiques, prévention, détection et traitement." Bordeaux 2, 1998. http://www.theses.fr/1998BOR23017.

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Boughtflower, Robert J. "Operating parameters for capillary electrochromatography (CEC)." Thesis, University of Edinburgh, 2000. http://hdl.handle.net/1842/12403.

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Miniaturisation of chromatographic systems is becoming increasingly desirable. Future developments will demand the analysis of smaller samples, at faster rates, with increasingly complex separations required. These demands are already starting to exceed the capabilities of conventional HPLC systems. Systems will require more column efficiency, operation at higher flow rates and detection of the undiluted eluent in the most sensitive detectors available. CEC offers the opportunity to achieve these goals. The main obstacles to using CEC reliably are the relatively unstable nature of purely electrically driven flows in packed beds, the lack of good quality CEC columns and the lack of dedicated instruments to perform CEC analysis. Also, CEC shares some of the same problems with HPLC of miniaturising the separation system without incurring dispersion related losses. The work detailed in this thesis contributes considerable advancements in most of these areas. Novel methods to produce high quality columns are described. The work demonstrates effective methods for coupling CEC to MS that make allowance for control of dispersion. The thermal limits of operation are discussed and demonstrated. Pressure-assisted CEC, demonstrating the practicality of performing CEC based analysis that is as reliable as current HPLC systems is shown. Proper optimisation of these type of uses will ultimately deliver CEC in a reliable format which will encourage a whole new audience of users to reap the benefits available.
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Martinot, Stéphane. "Comportement oxymétrique et hémodynamique du foetus ovin in utero sous CEC pulsatile : comparaison avec la CEC continue." Lyon 1, 1995. http://www.theses.fr/1995LYO1T128.

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Adams, Peter. "Algebraic topics in the Stone-Cech compactification of discrete semigroups." Thesis, University of Hull, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.395633.

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Norton, Dean Stephen. "Capillary Electrochromatography-Mass Spectrometry (CEC-MS) of Surfactants." Digital Archive @ GSU, 2007. http://digitalarchive.gsu.edu/chemistry_diss/13.

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This research presents advancements in the coupling of capillary electrochromatography (CEC) to mass spectrometry (MS) for the analysis of different chemical classes of surfactants. Chapter 1 provides a brief introduction that summarizes the mechanics and fundamentals of CEC, including instrumentation and applications for CEC-MS. Chapter 2 describes the on-line hyphenation of a packed CEC column with an internally tapered tip coupled to electrospray ionization-mass spectrometry (ESI-MS) and atmospheric pressure chemical ionization-mass spectrometry (APCI-MS) for the analysis of betaine-type amphoteric or zwitterionic surfactants (Zwittergent®). The interesting aspects include CEC-MS column manufacture and charaterization, as well as a comparison between the CEC-ACPI-MS and CEC-ESI-MS ionization pattern of zwittergents. In Chapter 3, the CEC-MS of alkyltrimethyl-ammonium ions (ATMA+) with chain length ranging from C1-C18 is optimized using an internally tapered CEC-MS column packed with mixed mode C6/strong cation exchange stationary phase and coupled to an ESI source. In addition, the optimized CEC-ESI-MS protocol is applied for the challenging analysis of commercial sample Arquad S-50 ATMA+ containing cis-trans unsaturated and saturated soyabean fatty acid derivatives. In Chapter 4, a novel CEC-UV method for separation of the various Triton X-100 oligomers is presented. A systematic mobile phase tuning and comparison of monomeric vs. polymeric stationary phases was conducted. In Chapter 5, we present the first application of CEC coupled to MS for analysis of Triton X (TX-) series surfactants. A characterization from the viewpoint of the ion and adduct formation for TX-series nonionic surfactants with a variable number of ethoxy units (n=1.5-16) in the scan mode are first discussed. Next, utilizing the TX-series as model alkylphenolpolyethoxylates (APEOs), a detailed investigation of the chromatographic separation and MS detection are performed followed by analysis of very long chain TX series with n=30-70. In Chapter 6, CEC-MS utilizing full scan positive ion mode of ESI was employed to study the effect of fragmentor voltage on the in-source collision induced dissociation (IS-CID) of several APEO nonionic surfactants. Finally, in Chapter 7, the preparation and characterization of a novel liquid crystalline stationary phase suitable for separation of neutral and charged compounds in packed column CEC is evaluated.
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Salinas, David. "Reconstruction en grandes dimensions." Phd thesis, Université de Grenoble, 2013. http://tel.archives-ouvertes.fr/tel-00947303.

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Dans cette thèse, nous cherchons à reconstruire une approximation d'une variété connue seulement à partir d'un nuage de points de grande dimension l'échantillonnant. Nous nous efforçons de trouver des méthodes de reconstructions efficaces et produisant des approximations ayant la même topologie que la variété échantillonnée. Une attention particulière est consacrée aux flag-complexes et particulièrement aux complexes de Rips. Nous montrons que le complexe de Rips capture la topologie d'une variété échantillonnée en supposant de bonnes conditions d'échantillonnage. En tirant avantage de la compacité des flags-complexes qui peuvent être représentés de manière compacte avec un graphe, nous présentons une structure de données appelée squelette/bloqueurs pour complexes simpliciaux. Nous étudions ensuite deux opérations de simplifications, la contraction d'arête et le collapse simplicial, qui s'avèrent utiles pour réduire un complexe simplicial sans en changer sa topologie.
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Books on the topic "CEHC"

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Anglada, Maria Angels. Cerc ados. Barcelona: Ediciones Destino, 1998.

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Kupka, J. S. Cech jako poleno. Praha: Knizni klub, 1997.

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Goma, Paul. În cerc: Roman. București: Editura Eminescu, 1995.

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Perpar-Prokić, Nada. Ceh: Roman. Beograd: Žagor, 2009.

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Perpar-Prokić, Nada. Ceh: Roman. Beograd: Žagor, 2009.

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Rudzroga, A. Cehu-Latviesu V Vardnica. Riga: Avots, 1986.

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Atwood, Margaret Eleanor. L' assassí cec. Barcelona: Punt de Lectura, 2003.

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Dictionnaire CEC jeunesse. 3rd ed. [Montréal]: CEC, 1992.

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Dictionnaire mathématique CEC. Anjou, Québec: Éditions CEC, 2011.

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Oriyano, Sean-Philip. CEH™v9. Indianapolis, Indiana: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119419303.

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Book chapters on the topic "CEHC"

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Auer, Stefan, and Thomas Stiegler. "CEEC–China." In China's Relations with Central and Eastern Europe, 83–99. Abingdon, Oxon ; New York, NY : Routledge, 2018. | Series: Routledge contemporary China series ; 172: Routledge, 2017. http://dx.doi.org/10.4324/9781315226644-6.

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Smith, David W. "“Working with the CECC System”." In Mikroelektronik in Österreich, 113–17. Vienna: Springer Vienna, 1985. http://dx.doi.org/10.1007/978-3-7091-8821-7_19.

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Schmid, Michael C., and Judith A. Varner. "Circulating Endothelial Progenitor Cells (CEPC)." In Methods in Molecular Biology, 139–55. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-241-0_8.

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Mennink, Bart. "The Relation Between CENC and NEMO." In Cryptology and Network Security, 177–89. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-00434-7_9.

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Hammami, B., M. I. Miladi, and Y. Rouxeville. "Le CEC d’auriculothérapie à Sfax." In Abrégé de physiologie à l’usage des acupuncteurs et des réflexothérapeutes, 11–14. Paris: Springer Paris, 2013. http://dx.doi.org/10.1007/978-2-8178-0361-6_2.

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Ratnayake, Chitra, and Michael Henry. "Cec." In Encyclopedia of Chromatography, Third Edition (Print Version). CRC Press, 2009. http://dx.doi.org/10.1201/noe1420084597.ch69.

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"Introduction." In Civil Engineering Heritage Ireland, 1–9. Thomas Telford Publishing, 1998. http://dx.doi.org/10.1680/cehi.26278.0001.

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"I. Dublin City and District." In Civil Engineering Heritage Ireland, 11–55. Thomas Telford Publishing, 1998. http://dx.doi.org/10.1680/cehi.26278.0002.

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"2. North Leinster (except Dublin City and District)." In Civil Engineering Heritage Ireland, 56–89. Thomas Telford Publishing, 1998. http://dx.doi.org/10.1680/cehi.26278.0003.

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"3. SOUTH LEINSTER (EXCEPT DUBLIN CITY AND DISTRICT)." In Civil Engineering Heritage Ireland, 90–129. Thomas Telford Publishing, 1998. http://dx.doi.org/10.1680/cehi.26278.0004.

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Conference papers on the topic "CEHC"

1

Gadkari, Ambar A., S. Ramesh, and Rubin A. Parekhji. "CESC." In Proceedins of the 14th ACM Great Lakes symposium. New York, New York, USA: ACM Press, 2004. http://dx.doi.org/10.1145/988952.989038.

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"CEEC 2018 TOC." In 2018 10th Computer Science and Electronic Engineering (CEEC). IEEE, 2018. http://dx.doi.org/10.1109/ceec.2018.8674205.

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"CEEC 2019 Index." In 2019 11th Computer Science and Electronic Engineering (CEEC). IEEE, 2019. http://dx.doi.org/10.1109/ceec47804.2019.8974326.

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Deutch, Daniel, and Nave Frost. "CEC." In CIKM '18: The 27th ACM International Conference on Information and Knowledge Management. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3269206.3269214.

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"CEEC 2018 Copyright Page." In 2018 10th Computer Science and Electronic Engineering (CEEC). IEEE, 2018. http://dx.doi.org/10.1109/ceec.2018.8674184.

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"CEEC 2018 Author Index." In 2018 10th Computer Science and Electronic Engineering (CEEC). IEEE, 2018. http://dx.doi.org/10.1109/ceec.2018.8674226.

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"Welcome to CEFC 2018." In 2016 IEEE Conference on Electromagnetic Field Computation (CEFC). IEEE, 2016. http://dx.doi.org/10.1109/cefc.2016.7816429.

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Liang, Zhijun. "Electroweak Physics at CEPC." In 38th International Conference on High Energy Physics. Trieste, Italy: Sissa Medialab, 2017. http://dx.doi.org/10.22323/1.282.0692.

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Li, Gang. "Detector optimization at CEPC." In 38th International Conference on High Energy Physics. Trieste, Italy: Sissa Medialab, 2017. http://dx.doi.org/10.22323/1.282.1164.

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Gao, Jie. "CEPC Accelerator Towards TDR." In 40th International Conference on High Energy physics. Trieste, Italy: Sissa Medialab, 2021. http://dx.doi.org/10.22323/1.390.0686.

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Reports on the topic "CEHC"

1

Marchetto, William, and Ed Carr. CENC PSN VOID FY20 Report. Office of Scientific and Technical Information (OSTI), October 2020. http://dx.doi.org/10.2172/1672109.

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Reason, Joseph. Cooperative Engagement Capability (CEC). Fort Belvoir, VA: Defense Technical Information Center, November 2015. http://dx.doi.org/10.21236/ad1019001.

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Villwock, Robert D. 2015 CEC Annual Workshop on Electrochemistry. Fort Belvoir, VA: Defense Technical Information Center, November 2015. http://dx.doi.org/10.21236/ad1008815.

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Malby, Jeffrey A., and George F. Turk. The Coastal Engineering Research Center, Volume CERC-97-4. Fort Belvoir, VA: Defense Technical Information Center, October 1997. http://dx.doi.org/10.21236/ada334922.

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Pinayev, I. Requirements for CEC POP Machine Protection System. Office of Scientific and Technical Information (OSTI), February 2015. http://dx.doi.org/10.2172/1172093.

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Huang, Zhenyu, B. Lesieutre, Steve Yang, A. Ellis, A. Meklin, B. Wong, A. Gaikwad, et al. Load Monitoring CEC/LMTF Load Research Program. Office of Scientific and Technical Information (OSTI), November 2007. http://dx.doi.org/10.2172/937047.

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Yoon, Roe-Hoan, and C. I. Basilio. Development of the chemical and electrochemical coal cleaning (CECC) process. Office of Scientific and Technical Information (OSTI), May 1992. http://dx.doi.org/10.2172/6985055.

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Williams, Gregory L., and Kris Visser. The CERCular (Coastal Engineering Research Center), Vol. CERC-98-2. Fort Belvoir, VA: Defense Technical Information Center, July 1998. http://dx.doi.org/10.21236/ada351444.

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Mueller, C., C. Caruthers, W. Cowell, W. Ellingson, T. Ewing, F. Moszur, R. Harrison, et al. The CERC (Center for Energy Research Computation) report: Results of the CERC Project with recommendations for ANL (Argonne National Laboratory) institutional strategies in advanced scientific computing. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/7159492.

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Yoon, Roe-Hoan, and C. I. Basilio. Development of the chemical and electrochemical coal cleaning (CECC) process. Final report. Office of Scientific and Technical Information (OSTI), May 1992. http://dx.doi.org/10.2172/10175171.

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