Search results for " mes"

showing 10 items of 3765 documents

Estimating Applicability of New Mobile Content Formats to Organizational Use

2003

Innovations on information and communication technology reshape organizational communication. Our ability to estimate applicability of new technologies and content formats to organizational use has been limited to generic quantitative methods at the level of technologies and industries and elaborate qualitative methods targeting specific phenomena at the organizational level. In this paper we estimate quantitatively the applicability of MMS, SMS, XHTML, and XML to organizational use based on an analysis of all communication of an organization unit. We enumerate over 700 communication genres using a genre-based information systems planning method, categorise them with taxonomy of communicati…

3G mobile communicationmobile computingmultimedia communicationelectronic data interchangeelectronic messaging
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Genomic organization and promoter characterization of the gene encoding a putative endoplasmic reticulum chaperone, ERp29

2002

Abstract ERp29 is a soluble protein localized in the endoplasmic reticulum (ER) of eukaryotic cells, which is conserved in all mammalian species. The N-terminal domain of ERp29 displays sequence and structural similarity to the protein disulfide isomerase despite the lack of the characteristic double cysteine motif. Although the exact function of ERp29 is not yet known, it was hypothesized that it may facilitate folding and/or export of secretory proteins in/from the ER. ERp29 is induced by ER stress, i.e. accumulation of unfolded proteins in the ER. To gain an insight into the mechanisms regulating ERp29 expression we have cloned and characterized the rat ERp29 gene and studied in details …

5' Flanking RegionRecombinant Fusion ProteinsMolecular Sequence DataCHO CellsBiologyCell LineMiceCricetinaeSequence Homology Nucleic AcidGene expressionTumor Cells CulturedGeneticsAnimalsHumansRNA MessengerLuciferasesPromoter Regions GeneticProtein disulfide-isomeraseGeneHeat-Shock ProteinsPhylogenyBase SequenceGene Expression ProfilingEndoplasmic reticulumPromoter3T3 CellsDNAExonsSequence Analysis DNAGeneral MedicineMolecular biologyIntronsRatsHousekeeping geneSecretory proteinGenesUnfolded protein responseFemaleTranscription Initiation SiteSequence AlignmentHeLa CellsGene
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"Table 1.4" of "Probing the effects of strong electromagnetic fields with charge-dependent directed flow in Pb-Pb collisions at the LHC"

2020

Directed flow D0 meson 10-40%

5023.0High Energy Physics::LatticeHigh Energy Physics::PhenomenologyNuclear TheoryHigh Energy Physics::ExperimentD0 mesonDirected flowNuclear Experiment
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"Table 1.5" of "Probing the effects of strong electromagnetic fields with charge-dependent directed flow in Pb-Pb collisions at the LHC"

2020

Directed flow D0-bar meson 10-40%

5023.0High Energy Physics::LatticeNuclear TheoryHigh Energy Physics::PhenomenologyD0-bar mesonHigh Energy Physics::ExperimentDirected flowNuclear Experiment
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A Universal Length-Dependent Vibrational Mode in Graphene Nanoribbons

2019

Graphene nanoribbons (GNRs) have attracted considerable interest as their atomically tunable structure makes them promising candidates for future electronic devices. However, obtaining detailed information about the length of GNRs has been challenging and typically relies on low-temperature scanning tunneling microscopy. Such methods are ill-suited for practical device application and characterization. In contrast, Raman spectroscopy is a sensitive method for the characterization of GNRs, in particular for investigating their width and structure. Here, we report on a length-dependent, Raman active low-energy vibrational mode that is present in atomically precise, bottom-up synthesized armch…

530 Physicssubstrate transferSTMFOS: Physical sciencesGeneral Physics and Astronomy02 engineering and technology010402 general chemistryDFT01 natural sciencessymbols.namesakegraphene nanoribbons; Raman spectroscopy; length-dependent mode; STM; substrate transfer; vibrational modes; DFT540 ChemistryMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials Sciencevibrational modesCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicsbusiness.industryGeneral EngineeringMode (statistics)Materials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesMolecular vibrationRaman spectroscopysymbols570 Life sciences; biologyOptoelectronicslength-dependent mode0210 nano-technologybusinessRaman spectroscopyGraphene nanoribbonsgraphene nanoribbons
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Investigation of charge ratio variation in mRNA – DEAE-dextran polyplex delivery systems

2019

Biomaterials 192, 612 - 620 (2019). doi:10.1016/j.biomaterials.2018.10.020

570Static ElectricityBiophysicsBioengineering02 engineering and technologyGene deliveryBiomaterials03 medical and health scienceschemistry.chemical_compoundDrug Delivery SystemsX-Ray DiffractionDynamic light scatteringddc:570Scattering Small AngleHumansRNA MessengerParticle Size030304 developmental biology0303 health sciencesMessenger RNAHeparinSmall-angle X-ray scatteringDEAE-DextranBiological activityDendritic CellsTransfection021001 nanoscience & nanotechnologySmall-angle neutron scatteringDextranchemistryMechanics of MaterialsCeramics and CompositesBiophysics0210 nano-technology
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Post-Transcriptional Regulation of Iron Homeostasis in Saccharomyces cerevisiae

2013

Iron is an essential micronutrient for all eukaryotic organisms because it participates as a redox cofactor in a wide variety of biological processes. Recent studies in Saccharomyces cerevisiae have shown that in response to iron deficiency, an RNA-binding protein denoted Cth2 coordinates a global metabolic rearrangement that aims to optimize iron utilization. The Cth2 protein contains two Cx8Cx5Cx3H tandem zinc fingers (TZFs) that specifically bind to adenosine/uridine-rich elements within the 3' untranslated region of many mRNAs to promote their degradation. The Cth2 protein shuttles between the nucleus and the cytoplasm. Once inside the nucleus, Cth2 binds target mRNAs and stimulate…

572 Biochemistryalternative 3' end processingSaccharomyces cerevisiae ProteinsIronTristetraprolinSaccharomyces cerevisiaeSaccharomyces cerevisiaeReviewyeastCatalysisInorganic Chemistrylcsh:ChemistryCth1TristetraprolinmRNA decayGene Expression Regulation FungalCth2medicineRNA MessengerRnt1Physical and Theoretical Chemistry3' Untranslated RegionsMolecular BiologyTranscription factorlcsh:QH301-705.5SpectroscopyMessenger RNAalternative 3′ end processingbiologyThree prime untranslated regionOrganic ChemistryQR MicrobiologyGeneral MedicineIron deficiencymedicine.diseasebiology.organism_classificationComputer Science ApplicationsDNA-Binding ProteinsRibonucleotide reductaseBiochemistrylcsh:Biology (General)lcsh:QD1-999Cytoplasmalternative 3' end processingTranscription Factorspost-transcriptional regulationInternational Journal of Molecular Sciences
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9-cis-Retinoic acid enhances fatty acid-induced expression of the liver fatty acid-binding protein gene

1997

The role of retinoic acids (RA) on liver fatty acid- binding protein (L-FABP) expression was investigated in the well differentiated FAO rat hepatoma cell line. 9-cis-Retinoic acid (9-ci's-RA) specifically enhanced L-FABP mRNA levels in a time- and dose-dependent manner. The higher induction was found 6 h after addition of 10 -6 M 9-CK-RA in the medium. RA also enhanced further both L-FABP mRNA levels and cytosolic L-FABP protein content induced by oleic acid. The retinoid X receptor (RXR) and the peroxisome proliferator-activated receptor (PPAR), which are known to be activated, respectively, by 9-c/s-RA and long chain fatty acid (LCFA), co-operated to bind specifically the peroxisome prol…

9-cw-Retinoic acidReceptors Retinoic Acid[SDV]Life Sciences [q-bio]Receptors Cytoplasmic and NuclearPeroxisome proliferator-activated receptorMyelin P2 ProteinMicrobodiesBiochemistry0302 clinical medicineStructural BiologyTumor Cells CulturedAlitretinoinchemistry.chemical_classification0303 health sciencesChemistryFatty AcidsDrug SynergismPeroxisomeNeoplasm Proteins9-cis-Retinoic acidLiverBiochemistryFree fatty acid receptorlipids (amino acids peptides and proteins)Peroxisome proliferator-activated receptor alphaLong chain fatty acidFatty Acid-Binding Protein 7DimerizationPeroxisome proliferator-activated receptor gammaCarcinoma HepatocellularBiophysicsNerve Tissue ProteinsTretinoinRetinoid X receptorFatty Acid-Binding ProteinsLiver fatty acid-binding protein03 medical and health sciencesGeneticsAnimalsRNA MessengerMolecular Biology030304 developmental biologyFAO hepatoma cellFatty acidCell BiologyFatty acidRatsRetinoid X ReceptorsGene Expression RegulationNuclear receptorGene expressionCarrier Proteins[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition030217 neurology & neurosurgeryTranscription FactorsFEBS Letters
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Identificación y caracterización de precursores mesodérmicos con capacidad hematopoyética en el tejido adiposo humano

2013

La fracción vascular estromal (FVE) del tejido adiposo humano contiene precursores mesodérmicos con capacidad de generar in vitro unidades formadoras de colonias hematopoyéticas (CFUs) y colonias mixtas de células hematopoyéticas y endoteliales. El trabajo realizado en esta tesis doctoral ha tenido como objetivo el estudio de estos progenitores hematopoyéticos. Para ello, se aislaron las diferentes subpoblaciones celulares que componen la FVE y tras su caracterización inmunofenotípica, se determinó su capacidad formadora de CFUs y la expresión de los principales factores de transcripción implicados en la hematopoyesis. Para estimar la ontogenia de los progenitores hematopoyéticos contenidos…

:CIENCIAS DE LA VIDA::Biología celular::Cultivo celular [UNESCO]células stem hematpoyéticas HSCcélulas stem mesenquimales MSC:CIENCIAS DE LA VIDA::Inmunología::Inmunoquímica [UNESCO]UNESCO::CIENCIAS DE LA VIDA::Biología celular::Cultivo celularhematopoyesis:CIENCIAS DE LA VIDA::Biología celular::Cultivo de tejidos [UNESCO]tejido adiposoUNESCO::CIENCIAS DE LA VIDA::Inmunología::InmunoquímicaangiogénesisUNESCO::CIENCIAS DE LA VIDA::Biología celular::Cultivo de tejidos
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Modulação gênica em embriões humanos

2018

O recente implemento de moderna tecnologia -CRISPR/Cas9- possibilitou o avanço inquestionável da edição gênica em linhagem germinativa humana, seja por meio da manipulação de células precursoras de gametas, células tronco pluripotentes, gametas ou, até mesmo, de embriões. Mesmo levando em conta os benefícios terapêuticos preventivos demonstrados nas pesquisas básicas e préclínicas em embriões humanos, tais investigações encontram barreiras de aceitação em todo o mundo. Tal situação exige mudança de atitude no sentido de incrementar o debate em torno da aplicabilidade dessas novas tecnologias. Assim, a adequação das atuais regulamentações faz-se necessária e deve incluir a superação dos desa…

:CIENCIAS JURÍDICAS [UNESCO]2386-4567 22661 Actualidad jurídica iberoamericana 502169 2018 9 6653325 Modulação gênica em embriões humanos Trindade Clementeaté mesmoGene editingpesquisas clínicaslinhagem germinativa humanagametas ouUNESCO::CIENCIAS JURÍDICASembriões humanos.human germlineGraziella O recente implemento de moderna tecnologia -CRISPR/Cas9- possibilitou o avanço inquestionável da edição gênica em linhagem germinativa humanaCRISPR/Cas9células tronco pluripotentes
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