Relevant bibliographies by topics / DMEs

Contents

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

Academic literature on the topic 'DMEs'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "DMEs"

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Yin, Jiayi, Fengcheng Li, Ying Zhou, Minjie Mou, Yinjing Lu, Kangli Chen, Jia Xue, et al. "INTEDE: interactome of drug-metabolizing enzymes." Nucleic Acids Research 49, no. D1 (October 12, 2020): D1233—D1243. http://dx.doi.org/10.1093/nar/gkaa755.

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Abstract Drug-metabolizing enzymes (DMEs) are critical determinant of drug safety and efficacy, and the interactome of DMEs has attracted extensive attention. There are 3 major interaction types in an interactome: microbiome–DME interaction (MICBIO), xenobiotics–DME interaction (XEOTIC) and host protein–DME interaction (HOSPPI). The interaction data of each type are essential for drug metabolism, and the collective consideration of multiple types has implication for the future practice of precision medicine. However, no database was designed to systematically provide the data of all types of DME interactions. Here, a database of the Interactome of Drug-Metabolizing Enzymes (INTEDE) was therefore constructed to offer these interaction data. First, 1047 unique DMEs (448 host and 599 microbial) were confirmed, for the first time, using their metabolizing drugs. Second, for these newly confirmed DMEs, all types of their interactions (3359 MICBIOs between 225 microbial species and 185 DMEs; 47 778 XEOTICs between 4150 xenobiotics and 501 DMEs; 7849 HOSPPIs between 565 human proteins and 566 DMEs) were comprehensively collected and then provided, which enabled the crosstalk analysis among multiple types. Because of the huge amount of accumulated data, the INTEDE made it possible to generalize key features for revealing disease etiology and optimizing clinical treatment. INTEDE is freely accessible at: https://idrblab.org/intede/
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Feng, Siqi, Anqi Li, Yi-Chao Zheng, and Hong-Min Liu. "Role of Drug-metabolizing Enzymes in Cancer and Cancer Therapy." Current Drug Metabolism 21, no. 1 (May 14, 2020): 67–76. http://dx.doi.org/10.2174/1389200221666200103111053.

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Background: Cancer is one of the most serious diseases threatening human health with high morbidity and mortality in the world. For the treatment of cancer, chemotherapy is one of the most widely used strategies, for almost all kinds of tumors and diverse stages of tumor development. The efficacy of chemotherapy not only depends on the activity of the drug administrated but also on whether the compound could reach the effective therapeutic concentration in tumor cells. Therefore, expression and activity of drug-metabolizing enzymes (DMEs) in tumor tissues and metabolic organs of cancer patients are important for the dispositional behavior of anticancer drugs as well as the clinical response of chemotherapy. Methods: This review summarizes the recent advancement of the DMEs expression and activity in various cancers, as well as the potential regulatory mechanisms of major DMEs in cancer and cancer therapy. Results: Compared to normal tissues, expression and activity of major DMEs are significantly dysregulated in patients by various factors including epigenetic modification, ligand-activated transcriptional regulation and signaling pathways. Additionally, DMEs play an important role in anticancer drug efficacy, chemoresistance as well as the activation of prodrugs. Conclusion: This review reinforces a more comprehensive understanding of DMEs in cancer and cancer therapy, and provides more opportunities for cancer therapy.
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Leal, Giselle Mirtes Amaral, Mafra Raiele Torres Oliveira, Vivianne Camila de Souza Bastos, Maria De Fátima Alcântara Barros, Antônio Geraldo Cidrão De Carvalho, Shirley Lima Campos, Marcelo Renato Guerino, Kátia Karina Do Monte-Silva, Angélica Da Silva Tenório, and Maria Das Graças Rodrigues De Araújo. "Study of musculoskeletal disorders in physical therapists: correlation with routine work." Manual Therapy, Posturology & Rehabilitation Journal 12 (September 8, 2014): 191. http://dx.doi.org/10.17784/mtprehabjournal.2014.12.191.

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Introduction: Work-Related Musculoskeletal Disorders (MSDs) affect health professionals by frequent exposure to physical and mental overloads during the workday. Physiotherapy aims to promote functional health of the individual, however ergonomic conditions in their workplace are often precarious and that along with the activities and repetitive movements resisted overload the musculoskeletal system inducing damage to your physical condition. Objective: Identify the occurrence of Musculoskeletal Disorders (DMEs) in physical therapists working in public and private health services in Recife-Pernambuco, recording determinants and establishing relationship with clinical practice and the workload of the tests. Method: Observational study of physiotherapists of both genders. Peres administered questionnaire collected personal information, professional performance and DMEs Results: 41 physiotherapists; 85.4% reported DMEs, females (80.5%); 41.4% between 24-30 years; places of work, hospitals (70.7%) and clinical (63.4%); predominance of lesions in the spine and upper limbs; 65.7% changed work habits due to the occurrence of DMEs. Significant correlation between age and gender prevalence in females; since the occurrence of DMEs was not significantly correlated with time of practice, with workload, with the number of daily visits nor to rest at work. Conclusion: The volunteers showed high percentage of involvement by DMEs, especially in the spine, which seems to be related to the age and gender of the therapist. The study indicates that physical therapists are an exposed to risk for developing occupational musculoskeletal disorders profession, requiring awareness of students and professionals about proper use of the body itself, the risks of the profession in order to prevent future physical limitations.
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Liu, Chunxiao, Hui Li, Jing Lin, Ying Wang, Xiaoyang Xu, Zong-Ming (Max) Cheng, and Yonghong Chang. "Genome-Wide Characterization of DNA Demethylase Genes and Their Association with Salt Response in Pyrus." Genes 9, no. 8 (August 6, 2018): 398. http://dx.doi.org/10.3390/genes9080398.

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DNA methylation plays important roles in genome protection and the regulation of gene expression and it is associated with plants’ responses to environments. DNA demethylases are very important proteins in DNA methylation regulation. In this study, we performed genome-wide and deep analysis of putative demethylases (DMEs) in pear. Seven DME genes were found in the pear genome and were defined as PbDME1–7 based on their domain organization. Results were supported by the gene structural characteristics and phylogenetic analysis. The gene structure of the DME genes were relatively complex and the DME7 proteins didn’t contain the Perm_CXXC domain. The DME genes experienced a whole genome duplication event (WGD) that occurred in the ancestor genome of pear and apple before their divergence based on the Ks values. Expression results showed that high salinity stress could influence the expression level of DMEs and salt-responsive genes in Pyrus betulaefolia. Furthermore, the methylation levels of salt-responsive genes changed under salt stress treatment. Results suggested important roles of PbDME genes in response to salt stress and are useful for better understanding the complex functions of this DME genes, which will facilitate epigenetic studies in pear trees salt tolerance.
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Li, Xiaoyan, Yiyan Lu, Xiaojun Ou, Sijing Zeng, Ying Wang, Xiaoxiao Qi, Lijun Zhu, and Zhongqiu Liu. "Changes and sex- and age-related differences in the expression of drug metabolizing enzymes in a KRAS-mutant mouse model of lung cancer." PeerJ 8 (November 18, 2020): e10182. http://dx.doi.org/10.7717/peerj.10182.

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Background This study aimed to systematically profile the alterations and sex- and age-related differences in the drug metabolizing enzymes (DMEs) in a KRAS-mutant mouse model of lung cancer (KRAS mice). Methodology In this study, the LC-MS/MS approach and a probe substrate method were used to detect the alterations in 21 isoforms of DMEs, as well as the enzymatic activities of five isoforms, respectively. Western blotting was applied to study the protein expression of four related receptors. Results The proteins contents of CYP2C29 and CYP3A11, were significantly downregulated in the livers of male KRAS mice at 26 weeks (3.7- and 4.4-fold, respectively, p < 0.05). SULT1A1 and SULT1D1 were upregulated by 1.8- to 7.0- fold at 20 (p = 0.015 and 0.017, respectively) and 26 weeks (p = 0.055 and 0.031, respectively). There were positive correlations between protein expression and enzyme activity for CYP2E1, UGT1A9, SULT1A1 and SULT1D1 (r2 ≥ 0.5, p < 0.001). Western blotting analysis revealed the downregulation of AHR, FXR and PPARα protein expression in male KRAS mice at 26 weeks. For sex-related differences, CYP2E1 was male-predominant and UGT1A2 was female-predominant in the kidney. UGT1A1 and UGT1A5 expression was female-predominant, whereas UGT2B1 exhibited male-predominant expression in liver tissue. For the tissue distribution of DMEs, 21 subtypes of DMEs were all expressed in liver tissue. In the intestine, the expression levels of CYP2C29, CYP27A1, UGT1A2, 1A5, 1A6a, 1A9, 2B1, 2B5 and 2B36 were under the limitation of quantification. The subtypes of CYP7A1, 1B1, 2E1 and UGT1A1, 2A3, 2B34 were detected in kidney tissue. Conclusions This study, for the first time, unveils the variations and sex- and age-related differences in DMEs in C57 BL/6 (WT) mice and KRAS mice.
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Qi, Shixiong, Xiuli Wang, Xue Li, Tao Qian, and Qiwen Zhang. "Enhancing Integrated Energy Distribution System Resilience through a Hierarchical Management Strategy in District Multi-Energy Systems." Sustainability 11, no. 15 (July 26, 2019): 4048. http://dx.doi.org/10.3390/su11154048.

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The requirement for energy sustainability drives the development of integrated energy distribution systems (IEDSs). In this paper, considering the coordination of district multi-energy systems (DMESs), a hierarchical management strategy is proposed to enhance IEDS resilience. The proposed strategy is divided into three modes: the normal operation mode, the preventive operation mode and the resilient operation mode. In the normal operation mode, the objective of DEMSs is to minimize the operation costs. In the preventive operation mode, the objective of DEMSs is to maximize the stored energy for mitigating outage. The resilient operation mode consists of two stages. DMESs schedule their available resources and broadcast excess generation capacities or unserved loads to neighboring DMESs through the cyber communication network in the first stage. In the second stage, DMESs interchange electricity and natural gas with each other through the physical common bus for global optimization. A consensus algorithm was applied to determine the allocated proportions of exported or imported electricity and natural gas for each DMES in a distributed way. An IEDS including five DMESs was used as a test system. The results of the case studies demonstrate the effectiveness of the proposed hierarchical management strategy and algorithm.
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Šadibolová, Michaela, Tomáš Zárybnický, Tomáš Smutný, Petr Pávek, Zdeněk Šubrt, Petra Matoušková, Lenka Skálová, and Iva Boušová. "Sesquiterpenes Are Agonists of the Pregnane X Receptor but Do Not Induce the Expression of Phase I Drug-Metabolizing Enzymes in the Human Liver." International Journal of Molecular Sciences 20, no. 18 (September 14, 2019): 4562. http://dx.doi.org/10.3390/ijms20184562.

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Sesquiterpenes, the main components of plant essential oils, are bioactive compounds with numerous health-beneficial activities. Sesquiterpenes can interact with concomitantly administered drugs due to the modulation of drug-metabolizing enzymes (DMEs). The aim of this study was to evaluate the modulatory effects of six sesquiterpenes (farnesol, cis-nerolidol, trans-nerolidol, α-humulene, β-caryophyllene, and caryophyllene oxide) on the expression of four phase I DMEs (cytochrome P450 3A4 and 2C, carbonyl reductase 1, and aldo-keto reductase 1C) at both the mRNA and protein levels. For this purpose, human precision-cut liver slices (PCLS) prepared from 10 patients and transfected HepG2 cells were used. Western blotting, quantitative real-time PCR and reporter gene assays were employed in the analyses. In the reporter gene assays, all sesquiterpenes significantly induced cytochrome P450 3A4 expression via pregnane X receptor interaction. However in PCLS, their effects on the expression of all the tested DMEs at the mRNA and protein levels were mild or none. High inter-individual variabilities in the basal levels as well as in modulatory efficacy of the tested sesquiterpenes were observed, indicating a high probability of marked differences in the effects of these compounds among the general population. Nevertheless, it seems unlikely that the studied sesquiterpenes would remarkably influence the bioavailability and efficacy of concomitantly administered drugs.
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Slámka, M. "Real Time Dispatch Training Simulator based on TRIS/DMES ELEKTROSYSTEM." IFAC-PapersOnLine 49, no. 27 (2016): 201–6. http://dx.doi.org/10.1016/j.ifacol.2016.10.683.

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Shao, Yun-yun, Jing Huang, Yan-rong Ma, Miao Han, Kang Ma, Hong-yan Qin, Zhi Rao, and Xin-an Wu. "Serum serotonin reduced the expression of hepatic transporter Mrp2 and P-gp via regulating nuclear receptor CAR in PI-IBS rats." Canadian Journal of Physiology and Pharmacology 93, no. 8 (August 2015): 633–39. http://dx.doi.org/10.1139/cjpp-2015-0039.

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Hepatic transporters and drug metabolizing enzymes (DMEs) play important roles in the pharmacological effects and (or) side-effects of many drugs, and are regulated by several mediators, including neurotransmitters. This work aimed to investigate whether serum levels of 5-hydroxytryptamine (5-HT) affected the expression of hepatic transporters or DMEs. The expression of hepatic transporters was assessed using the Western-blot technique in a 2,4,6-trinitrobenzenesulfonic-acid-induced rat model of post-infectious irritable bowel syndrome (PI-IBS), in which serum levels of 5-HT were significantly elevated. To further clarify the underlying mechanism, the 5-HT precursor 5-hydroxytryptophan (5-HTP) and the 5-HT depleting agent parachlorophenylalanine (pCPA) were applied to adjust serum levels of 5-HT. Serum levels of 5-HT were measured using LC-MS/MS; the expression of hepatic transporters, DMEs, and nuclear receptors were examined by Western-blot technique. Our results showed that in PI-IBS rats the expression of multidrug resistance protein 2 (Mrp2) was significantly decreased, while colonic enterochromaffin cell density and serum levels of 5-HT were all significantly increased. Moreover, 5-HTP treatment significantly increased serum levels of 5-HT and decreased the expression of Mrp2 and glycoprotein P (P-gp), whereas treatment with pCPA markedly decreased serum levels of 5-HT and increased the expression of Mrp2 and P-gp. Our results indicated that serum 5-HT regulates the expression of Mrp2 and P-gp, and the underlying mechanism may be related to the altered expression of the nuclear receptor constitutive androstane receptor (CAR).
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Prasad, Bhagwat. "Quantitative analysis of hepatic transporters and DMEs during growth and development." Drug Metabolism and Pharmacokinetics 32, no. 1 (January 2017): S12. http://dx.doi.org/10.1016/j.dmpk.2016.10.060.

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Dissertations / Theses on the topic "DMEs"

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Delgoda, Rupika. "A study of arylamine N-acetyltransferase from Salmonella typhimurium." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302221.

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Lhoumaud, Priscillia. "Rôle de l'histone méthyl-transférase dMes-4 dans l'expression des gènes, la pause et l'épissage." Toulouse 3, 2014. http://www.theses.fr/2014TOU30096.

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Les protéines qui se fixent aux séquences dites 'insulatrices' sont appelées les 'IBPs' (pour 'Insulator Binding Proteins'). Ces facteurs réguleraient de nombreux gènes via leur rôle dans l'organisation de la chromatine. Une hypothèse de travail est que cette fonction des IBPs reposerait sur leur capacité à ouvrir la chromatine localement, favorisant ainsi le recrutement de facteurs impliqués dans la régulation des gènes. Lors de mon travail de thèse, j'ai tout d'abord identifié l'enzyme de méthylation d'histones (HMT), dMes4, comme un partenaire structural et fonctionnel important des protéines insulatrices BEAF-32/dCTCF. Ainsi, mes résultats ont montré que déplétion de dMes4 récapitulait les défauts d'expression obtenus après déplétions des IBPs, démontrant son rôle prépondérant en tant que co-facteur des IBPs. DMes-4 est la seule enzyme capable de di-méthyler l'histone H3 sur la lysine 36 (H3K36me2) chez la Drosophile, une modification d'histone qui jouerait un rôle déterminant dans le recrutement des complexes d'acétylation des histones (HATs) qui permettent l'ouverture de la chromatine. Mes recherches ont par ailleurs souligné le rôle prépondérant des IBPs dans le recrutement de cette HMT, permettant ainsi l'ouverture de la chromatine aux promoteurs de gènes. De plus, j'ai montré que ce mécanisme dMes-4 dépendant était requis pour le recrutement de l'activateur transcriptionnel DREF, un facteur clé dans la régulation des oncogènes. DREF active l'élongation de la transcription par l'ARN polymérase II qui est couplée à la tri-méthylation H3K36me3 par l'enzyme dHypB. De façon intéressante, la tri-méthylation est requise dans le recrutement des facteurs d'épissage et mes résultats ont montré que la marque H3K36me2 servirait dans ce contexte à prédéfinir un état chromatinien 'compétent' pour que l'activation transcriptionnelle soit couplée à la bonne maturation des ARNs. Un deuxième volet de mes travaux a permis de caractériser la fonction de dMes-4 et de dHypB dans la transition entre les étapes de " pause " et d'élongation de l'ARN polymérase II, via le recrutement du complexe P-TEFb, qui est nécessaire à la bonne maturation de l'ARN polymérase II et à la dissociation concomitante du facteur de pause appelé NELF. Mes résultats montrent que NELF servirait de point de contrôle permettant de coupler l'élongation à l'épissage et la maturation des transcrits. Aussi, ce couplage dépendrait notamment de la fonction dMes-4-dépendante dans le recrutement de P-TEFb et de celle de NELF dans le contrôle de la 'maturation' de l'ARN polymérase II. Mes résultats suggèrent que ces défauts de maturation seraient dus à l'incapacité de la forme immature à recruter dHypB, entraînant ainsi des défauts d'épissage dépendants de H3K36me3. Mes travaux permettent ainsi de mieux comprendre le rôle de la pause dans la maturation des ARNs, via les HMTs dMes-4/dHypB
The Drosophila insulator-binding proteins (IBPs) Beaf32/dCTCF regulate gene expression, through mechanisms that may involve their role in chromatin organization. One hypothesis is that chromatin insulators may lead to open chromatin locally, thereby recruiting factors involved in transcriptional activation. During my PhD, I have identified a key histone modifier, dMes-4, as a novel co-factor of IBPs involved in chromatin accessibility, which specifically co-regulates hundreds of genes flanked by Beaf32/dCTCF. DMes-4, the only H3K36me2 histone methyltransferase in Drosophila, may play a key role in the recruitment of Histone acetyltransferases (HATs) leading to a chromatin opening. Our results show that dMes-4 is recruited at gene promoters through IBPs, thereby opening chromatin locally for the recruitment of the transcriptional activator DREF. Such transcriptional activation is involved in oncogene activation. Our results show that DREF triggers RNAPII elongation concomitantly with the trimethylation of H3K36 (H3K36me3) by dHypB, thereby allowing H3K36me3-dependent RNA splicing. Our work highlights a key role of IBPs/dMes-4 in presetting chromatin for transcriptional activation and proper RNA splicing. A second part of my Ph. D. Work was to characterize the respective roles of dMes-4 and dHypB in the "switch" from RNAPII pausing to transcription elongation, through the recruitment of the complex P-TEFb. We show that P-TEFb is required for the maturation of RNAPII, which is under the control of the paused factor NELF. My data show that NELF may serve as a "checkpoint" coupling RNAPII maturation with RNA splicing. This checkpoint may involve both dMes-4 in recruiting P-TEFb, and of NELF in preventing the release of RNAPII before its "maturation". Our data further show that NELF depletion leads to splicing defects due to the impaired recruitment of dHypB on such immature RNAPII, leading to defects in H3K36me3 deposition. As such, my work highlights a key function of the HMTs dMes-4/dHypB and of NELF-mediated RNAPII pausing in RNA maturation
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Deml, Christoph. "Analyse und Modellierung des DMOS-Transistors." [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=969618816.

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Deml, Christoph Hoffmann Kurt. "Analyse und Modellierung des DMOS-Transistors." Neubiberg Universitätsbibliothek der Universität der Bundeswehr, 2008. http://d-nb.info/998614890/34.

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Faigle, Christopher Tyler. "DMS-Splines and radiosity." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624727.

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Zupac, Dragan. "Radiation-induced mobility degradation in DMOS transistors." Diss., The University of Arizona, 1993. http://hdl.handle.net/10150/186456.

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Effects of radiation-induced interface-trapped charge and oxide-trapped charge on the inversion-layer carrier mobility in double-diffused metal-oxide-semiconductor (DMOS) power transistors are investigated. Interface-trapped charge is more effective in scattering inversion-layer carriers than oxide-trapped charge. However, the effects of oxide-trapped charge must be taken into account in order to properly describe the mobility behavior. An effective approach to detecting effects of oxide-trapped charge and separating these effects from effects of interface-trapped charge is demonstrated. Detection is based on analyzing mobility data sets which have different functional relationships between the two trapped charge components. These relationships may be linear or nonlinear. Separation of effects of oxide-trapped charge and interface-trapped charge is possible only if these two trapped charge components are not linearly dependent. A significant contribution of oxide-trapped charge to mobility degradation is demonstrated and quantified. Effects of oxide-trapped charge may be dominant in non-hardened DMOS transistors irradiated at relatively high dose rates. In addition, DMOS devices have been irradiated at room temperature and mobility measurements performed at room temperature and at 77 K to analyze mobility degradation due to the same density of radiation-induced defects at these two different temperatures. Radiation-induced mobility degradation is more pronounced at 77 K than at room temperature, due to increased relative importance of Coulomb scattering from trapped charge when phonon scattering is significantly reduced. Effects of oxide-trapped charge on mobility are more pronounced at cryogenic temperatures than at room temperature.
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Hung, Merit Y. (Merit Yi). "Double diffused (DMOS) FETs for analog applications." Thesis, Massachusetts Institute of Technology, 1990. http://hdl.handle.net/1721.1/13698.

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Angel, Mattias, and Albert Berggren. "Regionala DMOs marknadsföring och sociala mediers påverkan." Thesis, Mittuniversitetet, Institutionen för ekonomi, geografi, juridik och turism, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:miun:diva-39247.

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Destination management organizations (DMOs) är organisationer som ofta är uppbyggda av två eller flera medlemsorganisationer. En huvudsaklig uppgift som DMOs har är att marknadsföra destinationen. Sociala medier är något som förändrat sättet många organisationer bedriver sin marknadsföring på. Kommunikationen har gått från statisk envägs, alltså från den som producerar budskap till den som konsumerar, till mer dynamisk tvåvägskommunikation där relationer, samarbete och kommunikation mellan de två parterna kommit att bli allt viktigare. Vi undersöker i den här uppsatsen hur svenska regionala DMOs använder sig av sociala medier i sitt marknadsföringsarbete. Empirin har samlats in genom kvalitativa, semistrukturerade intervjuer med personer som arbetar med marknadsföring vid fyra svenska regionala DMOs. Detta har kombinerats med en analys av berörda DMOs respektive sidor på de sociala medierna Facebook och Instagram. Resultaten visar att de olika organisationerna har både likheter och skillnader i hur de operativt och strategiskt använder sig av sociala medier i marknadsföringssyfte.
Destination management organizations (DMOs) are usually structured by two or more member-organizations. One of the main tasks for a DMO is to market the destination. Social medias have changed the way a lot of organizations manages their marketing. Communication has gone from a static one directional, from the producer to the consumer, to a more dynamic two-way communication where the interaction between the two parts has become more important. In this paper we examine how swedish regional DMOs use social medias in their marketing. The empirical data has been gathered by qualitative semi-structured interviews with persons who work with marketing at four different swedish regional DMOs. This has been combined with analysis of the concerned DMOs social media pages on Facebook and Instagram. The results show that the different organizations have both similarities and differences in their strategic and operative use of social media in marketing efforts.

2020-06-08

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Ito, H., D. Suzuki, Y. Yokochi, S. Kuroda, M. Umemiya, H. Miyasaka, K.-I. Sugiura, M. Yamashita, and H. Tajima. "Quasi-one-dimensional electronic structure of (DMET)_2CuCl_2." The American Physical Society, 2005. http://hdl.handle.net/2237/7127.

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Schepp, Oliver. "Simulations- und Meßmethoden zur Bestimmung der Temperatur von LeistungsMOSFETs /." Düsseldorf : VDI-Verl, 1998. http://www.gbv.de/dms/bs/toc/251116484.pdf.

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Books on the topic "DMEs"

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Marsden, C. J. DMUs. London: Ian Allan, 1986.

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McCully, Emily Arnold. Gran dmas trick-or-treat. New York: HarperCollins Publishers, 2001.

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Supertex. Databook: [integrated circuits and DMOS transistors]. Sunnyvale, Calif: Supertex Inc., 1991.

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Thomas, John. Corneal endothelial transplant: (DSAEK, DMEK & DLEK). New Delhi: Jaypee-Highlights Medical Pub., 2010.

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Robinson, Jennifer. DMS SuperNode system description. [Ottawa, Ont.?]: BNR, Software Development Technology, 1988.

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Gosselin, Mark S. DMS: Diagnostic Modeling System. Vicksburg, Miss: U.S. Army Corps of Engineers, Engineer Research and Development Center, 1999.

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Brillet, Jean Louis. Le modèle Micro-DMS. Paris: République française, Institut national de la statistiques et des études économiques, Direction générale, 1994.

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United States. General Accounting Office. RCED. VOR/DME and LORAN expansion. Washington, D.C: The Office, 1993.

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RCED, United States General Accounting Office. VOR/DME and LORAN expansion. Washington, D.C: The Office, 1993.

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Stajda, Eric. Document management with SAP DMS. 2nd ed. Bonn: Galileo Press, 2013.

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Book chapters on the topic "DMEs"

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Li, Yeting, Chunmei Dong, Xinyu Chu, and Haiming Chen. "Learning DMEs from Positive and Negative Examples." In Database Systems for Advanced Applications, 434–38. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-18590-9_61.

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Lukas, Thomas J., Daniela V. Rosa, Luiz Alexandre V. Magno, Bruno R. Souza, Marco A. Romano-Silva, Hisao Masai, Kazuhisa Kohda, et al. "Dmel." In Encyclopedia of Signaling Molecules, 526. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100355.

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Simola, Nicola, Micaela Morelli, Tooru Mizuno, Suzanne H. Mitchell, Harriet de Wit, H. Valerie Curran, Celia J. A. Morgan, et al. "DMTS." In Encyclopedia of Psychopharmacology, 416. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4207.

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Gooch, Jan W. "DMEP." In Encyclopedic Dictionary of Polymers, 238. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3892.

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Baydoun, Lamis, Isabel Dapena, and Gerrit Melles. "Evolution of Posterior Lamellar Keratoplasty: PK – DLEK – DSEK/DSAEK – DMEK – DMET." In Current Treatment Options for Fuchs Endothelial Dystrophy, 73–85. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43021-8_5.

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Berkhout, Marco. "DMOS Technology." In Integrated Audio Amplifiers in BCD Technology, 17–61. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6083-8_2.

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Meißner, D., and T. Arndt. "DMPS(-Test)." In Lexikon der Medizinischen Laboratoriumsdiagnostik, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49054-9_3728-1.

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Nahler, Gerhard. "loi DMOS." In Dictionary of Pharmaceutical Medicine, 107. Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-89836-9_800.

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Meißner, D., and T. Arndt. "DMPS(-Test)." In Springer Reference Medizin, 715–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_3728.

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Kosnett, Michael J. "Unithiol (DMPS)." In Critical Care Toxicology, 1–4. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-20790-2_21-1.

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Conference papers on the topic "DMEs"

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Run-yang Zhong, Qing-yun Dai, Ke Zhou, and Xin-bo Dai. "Design and implementation of DMES based on RFID." In 2008 2nd International Conference on Anti-counterfeiting, Security and Identification. IEEE, 2008. http://dx.doi.org/10.1109/iwasid.2008.4688433.

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Kim, Euiho. "Investigation of APNT optimized DME/DME network using current state-of-the-art DMEs: Ground station network, accuracy, and capacity." In 2012 IEEE/ION Position, Location and Navigation Symposium - PLANS 2012. IEEE, 2012. http://dx.doi.org/10.1109/plans.2012.6236876.

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Hedberg, Thomas, Moneer Helu, and Timothy Sprock. "A Standards and Technology Roadmap for Scalable Distributed Manufacturing Systems." In ASME 2018 13th International Manufacturing Science and Engineering Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/msec2018-6550.

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The increasing decentralization of manufacturing has contributed to the growing interest in scalable distributed manufacturing systems (DMSs). The emerging body of work from smart manufacturing, Industrie 4.0, Industrial Internet of Things (IIoT), and cyber-physical systems can enable the continued development of scalable DMS, particularly through the digital thread. However, significant challenges exist in understanding how to apply the digital thread most appropriately for scalable DMS. This paper describes these major challenges and provides a standards and technology roadmap developed from the digital thread viewpoint and consensus-built industrial standards to realize scalable DMS. The goal of this roadmap is to guide research that enables manufacturers to take advantage of opportunities provided by scalable DMS, including improved agility, flexibility, traceability, dynamic decision making, and utilization of manufacturing resources.
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Borovicka, Michael. "DMIS." In the 6th International Conference. New York, New York, USA: ACM Press, 2008. http://dx.doi.org/10.1145/1497185.1497288.

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Baxter, Ira D. "DMS." In the international workshop. New York, New York, USA: ACM Press, 2002. http://dx.doi.org/10.1145/512035.512047.

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Sezginer, Kaan, Mustafa Gul, Alican Bekoz, Y. Bugra Ozer, and Cosku Kasnakoglu. "DME/DME position and velocity estimation." In 2018 26th Signal Processing and Communications Applications Conference (SIU). IEEE, 2018. http://dx.doi.org/10.1109/siu.2018.8404414.

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Li, Shuyu, Yude Ni, and Na Cai. "Optimal strategy of DME beacon distrbution for DME/DME area navigation." In 2012 11th International Conference on Signal Processing (ICSP 2012). IEEE, 2012. http://dx.doi.org/10.1109/icosp.2012.6491981.

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Hüllmann, Joschka A., Ajith Sivakumar, and Simone Krebber. "Data Management Platforms: An Empirical Taxonomy." In Digital Support from Crisis to Progressive Change. University of Maribor Press, 2021. http://dx.doi.org/10.18690/978-961-286-485-9.10.

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Data management platforms (DMPs) are a widely used means of placing targeted advertising, for example, commercial or political advertisements. However, only a few academic papers shed light on the platforms’ mechanisms. These mechanisms’ opacity makes it hard for consumers to understand what happens with their data, and regulators struggle to implement effective regulations. Hence, we develop a taxonomy to understand and compare different characteristics of DMPs. Following Nickerson’s (2013) method and combining an inductive and deductive approach, eight dimensions emerge that differentiate DMPs. We evaluate the taxonomy’s applicability and test it with a set of nine DMPs, which we select by feasibility, relevance, and popularity. The application shows that the eight dimensions cover the significant features that explain most of the variance in characteristics between DMPs. The evaluation revealed opportunities for further development of the taxonomy
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Anderson, Andrew G., Kenneth A. Markoski, Quan Shi, Stephen L. Coy, Evgeny V. Krylov, and Erkinjon G. Nazarov. "DMS-IMS2, GC-DMS, DMS-MS: DMS hybrid devices combining orthogonal principles of separation for challenging applications." In SPIE Defense and Security Symposium, edited by Augustus Way Fountain III and Patrick J. Gardner. SPIE, 2008. http://dx.doi.org/10.1117/12.782429.

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Mordas, Genrik, Ada Steponavičiūtė, Aušra Selskienė, Jurijus Tretjakovas, and Sergejus Borodinas. "Direct Metal Laser Sintering of stainless steel alloy: microstructure and mechanical properties." In The 13th international scientific conference “Modern Building Materials, Structures and Techniques”. Vilnius Gediminas Technical University, 2019. http://dx.doi.org/10.3846/mbmst.2019.201.

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Additive manufacturing (AM) is a type of manufacturing technologies whereby the material is added a layer upon layer to produce a 3D object. Produced 3D parts are applied in such industry sectors as space, aviation, automotive, building and has excellent future promises. Ourdays, the commercialy promised technique for metal manufacturing is Direct Metal Laser Sintering (DMLS). Our study concentrated on the investigation of the mechanical properties of produced17-4H (stainless steel) parts using DMLS. The effect of the DMLS process parameters (laser power, scanning speed and energy density) on the ultimate strength, yield strength and Young’s modulus was determined. We showed an evolution of the microstructure. The detected defects were classified. This study allowed to determine the optimal regimes of DMLS for SS 17-4H and describe mechanical properties of the produced parts as well as helped to show future possibilities of DMLS development.
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Reports on the topic "DMEs"

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Kramer, Thomas R., Frederick M. Proctor, William G. Rippey, and Harry Scott. The NIST DMIS interpreter. Gaithersburg, MD: National Institute of Standards and Technology, 1997. http://dx.doi.org/10.6028/nist.ir.6012.

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Kramer, Thomas R., and John Horst. Users manual for version 2.1.5 of the NIST DMIS test suite (for DMIS 5.1). Gaithersburg, MD: National Institute of Standards and Technology, 2009. http://dx.doi.org/10.6028/nist.ir.7603.

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Kramer, Thomas R., and John Horst. Maintainers manual for version 2.2.1 of the NIST DMIS test suite (for DMIS 5.2). Gaithersburg, MD: National Institute of Standards and Technology, 2010. http://dx.doi.org/10.6028/nist.ir.7720.

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Kramer, Thomas R., and John Horst. Users manual for version 2.2.1 of the NIST DMIS test suite (for DMIS 5.2). Gaithersburg, MD: National Institute of Standards and Technology, 2010. http://dx.doi.org/10.6028/nist.ir.7735.

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Kramer, Thomas R., and John Horst. System builders manual for version 2.1.5 of the NIST DMIS test suite (for DMIS 5.1). Gaithersburg, MD: National Institute of Standards and Technology, 2009. http://dx.doi.org/10.6028/nist.ir.7610.

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Kramer, Thomas R., and John Horst. System builders manual for version 2.2.1 of the NIST DMIS test suite (for DMIS 5.2). Gaithersburg, MD: National Institute of Standards and Technology, 2010. http://dx.doi.org/10.6028/nist.ir.7715.

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Taylor, Samantha. ProX 200 DMLS Process Space Exploration. Office of Scientific and Technical Information (OSTI), August 2018. http://dx.doi.org/10.2172/1467546.

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Li, Qizhen. FinalReport-DOE BES DMSE-UNR-QLi. Office of Scientific and Technical Information (OSTI), May 2014. http://dx.doi.org/10.2172/1130472.

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Kramer, Thomas R., Frederick M. Proctor, William G. Rippey, and Harry Scott. The NIST DMIS interpreter, version 2. Gaithersburg, MD: National Institute of Standards and Technology, 1998. http://dx.doi.org/10.6028/nist.ir.6252.

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Craig, Kenneth R., Mark S. Gosselin, Daryl S. Cook, and Thad C. Pratt. DMS: Diagnostic Modeling System. Report 3. DMS Data Manager - A User's Guide. Fort Belvoir, VA: Defense Technical Information Center, September 2001. http://dx.doi.org/10.21236/ada397613.

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