Search results for " array"

showing 10 items of 895 documents

FLUMO: FLexible Underwater MOdem

2019

The last years have seen a growing interest in underwater acoustic communications because of its applications in marine research, oceanography, marine commercial operations, the offshore oil industry and defense. High-speed communication in the underwater acoustic channel has been challenging because of limited bandwidth, extended multipath, refractive properties of the medium, severe fading, rapid time variation and large Doppler shifts. In this paper, we show an implementation of a flexible Software-Defined Acoustic (SDA) underwater modem, where modulation parameters are completely tunable to optimize performance. In particular, we develop the system architecture following two key ideas. …

extended multipathSDAOrthogonal frequency-division multiplexingComputer sciencemarine commercial operationsUnderwater; acoustic ; software defined ; modem; JANUS; SDA; FSK; RedPitaya; WatermarkSettore ING-INF/01 - ElettronicaacousticFSKmodulate signalsDemodulationcontrolled testbedsUnderwaterunderwater acoustic channelOFDMFrequency-shift keyingFLUMOunderwater acoustic communicationsBandwidth (signal processing)Frequency shift keyingflexible Software-Definedoffshore oil industrysoftware definedRedPitayaflexible underwater MOdemmodulated signalsmodulation parameterstunable systemrefractive propertiesMultipath propagationStandardssystem architectureDoppler shiftsunderwater acoustic communicationhigh-speed communicationflexible systemElectronic engineeringDoppler shiftFadingoceanographymodemSettore ING-INF/03 - Telecomunicazionirapid time variationField programmable gate arraysmarine researchmodemsJANUSWatermarkSystems architectureUnderwater
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Construction and validation of cDNA-based Mt6k-RIT macro- and microarrays to explore root endosymbioses in the model legume Medicago truncatula

2004

To construct macro- and microarray tools suitable for expression profiling in root endosymbioses of the model legume Medicago truncatula, we PCR-amplified a total of 6048 cDNA probes representing genes expressed in uninfected roots, mycorrhizal roots and young root nodules [Nucleic Acids Res. 30 (2002) 5579]. Including additional probes for either tissue-specific or constitutively expressed control genes, 5651 successfully amplified gene-specific probes were used to grid macro- and to spot microarrays designated Mt6k-RIT (M. truncatula 6k root interaction transcriptome). Subsequent to a technical validation of microarray printing, we performed two pilot expression profiling experiments usin…

0106 biological sciencesRoot nodule[SDV]Life Sciences [q-bio]Plant Roots01 natural sciencesApplied Microbiology and BiotechnologyTranscriptomeADNCGene Expression Regulation PlantGene Expression Regulation FungalMycorrhizaeMedicagoPCR-basedComputingMilieux_MISCELLANEOUSOligonucleotide Array Sequence AnalysisPlant ProteinsExpressed Sequence Tags2. Zero hunger0303 health sciencesnodulin genesroot nodule symbiosisarbuscular mycorrhizafood and beveragesEquipment DesignGeneral MedicineMedicago truncatulaArbuscular mycorrhiza[SDV] Life Sciences [q-bio]expression profilingDNA microarrayBiotechnologyBioengineeringComputational biologyBiologySensitivity and Specificity03 medical and health sciencesComplementary DNABotanySymbiosisLeghemoglobin030304 developmental biologyGene Expression ProfilingfungiReproducibility of Resultsbiology.organism_classificationEquipment Failure AnalysisGene expression profilingphosphate transportercDNA array010606 plant biology & botany
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Different sample treatment approaches for the analysis of T-2 and HT-2 toxins from oats-based media.

2010

A LC-DAD method is proposed for the determination of the T-2 and HT-2 toxins in cultures of Fusarium langsethiae in oat-based and other in vitro media. Test media consisted of freshly prepared milled oats to which T-2 and HT-2 toxin stock solutions were added. Different mixtures of extraction solvent (acetonitrile:water and methanol water), extraction times (30', 60' or 90') and drying methods were investigated. Results showed that extraction with methanol: water (80:20, v/v) for 90 min, drying with N-2 and subsequent analysis by LC-DAD was the fastest and most user friendly method for detecting HT-2 and T-2 toxins production by F. langsethiae strains grown on oat-based media at levels of 0…

food.ingredientTime FactorsWater activityAvenaClinical BiochemistryTrichotheceneBiochemistryAnalytical Chemistrychemistry.chemical_compoundfoodFusariumAnalysis Type A trichothecenes Diode array Cereals performance liquid-chromatography diode-array detection gas-chromatography mass-spectrometry immunoaffinity cleanup fluorescence detection fusarium-langsethiae retention indexes b-trichothecene cerealsGlycerolAgarSample preparationDesiccationChromatographybiologyAnalytic Sample Preparation MethodsCell BiologyGeneral MedicineReference Standardsbiology.organism_classificationCulture MediaFusarium langsethiaeT-2 ToxinAvenachemistrySolventsMethanolChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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A fully-digital realtime SoC FPGA based phase noise analyzer with cross-correlation

2017

We report on a fully-digital and realtime operation of a phase noise analyzer using modern digital techniques with cross-correlation. With the advent of system on chip field-programmable gate arrays (SoC FPGAs) embedding hard core central processing unit, coprocessor and FPGA onto a single integrated circuit, the building of sensitive analysis devices for Time & Frequency research is made accessible at virtually no cost and benefits from reconfigurability. Used with high-speed digitizers we have successfully implemented a four-channel system whose preliminary results at 10 MHz shows a residual white noise floor < −185 dBrad2/Hz up to 5 MHz off the carrier, and flicker < −127 dBrad2/Hz using…

010302 applied physicsEngineeringSpectrum analyzerNoise measurementbusiness.industryReconfigurabilityIntegrated circuitWhite noise01 natural scienceslaw.inventionlaw0103 physical sciencesPhase noiseElectronic engineeringSystem on a chipField-programmable gate arraybusiness010301 acoustics2017 Joint Conference of the European Frequency and Time Forum and IEEE International Frequency Control Symposium (EFTF/IFC)
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Global Functional Analyses of Cellular Responses to Pore-Forming Toxins

2011

Here we present the first global functional analysis of cellular responses to pore-forming toxins (PFTs). PFTs are uniquely important bacterial virulence factors, comprising the single largest class of bacterial protein toxins and being important for the pathogenesis in humans of many Gram positive and Gram negative bacteria. Their mode of action is deceptively simple, poking holes in the plasma membrane of cells. The scattered studies to date of PFT-host cell interactions indicate a handful of genes are involved in cellular defenses to PFTs. How many genes are involved in cellular defenses against PFTs and how cellular defenses are coordinated are unknown. To address these questions, we pe…

MAPK/ERK pathwayTranscription GeneticImmunology/Innate ImmunityMessengerInteractomeInfectious Diseases/Bacterial InfectionsRNA interference2.1 Biological and endogenous factorsAetiologyBiology (General)Genes HelminthCaenorhabditis elegansOligonucleotide Array Sequence AnalysisGenetics0303 health sciencesGenomebiologyReverse Transcriptase Polymerase Chain ReactionGenetics and Genomics/Functional Genomics030302 biochemistry & molecular biologyrespiratory systemCell biologyInfectious DiseasesMedical MicrobiologyRNA InterferenceSignal transductionDNA microarrayTranscriptionBiotechnologyResearch ArticleSignal TransductionPore Forming Cytotoxic ProteinsQH301-705.5Virulence FactorsMAP Kinase Signaling System1.1 Normal biological development and functioningBacterial ToxinsImmunologyMicrobiologyDNA-binding proteinCell Line03 medical and health sciencesBacterial ProteinsGeneticUnderpinning researchVirologyEscherichia coliHelminthGeneticsAnimalsHumansRNA MessengerCaenorhabditis elegansCaenorhabditis elegans ProteinsMolecular BiologyGene030304 developmental biologyGenome HelminthCell MembraneGenetics and GenomicsRC581-607biology.organism_classificationrespiratory tract diseasesTranscription Factor AP-1Emerging Infectious DiseasesGenesRNAParasitologyGeneric health relevanceRNA HelminthImmunologic diseases. AllergyPLoS Pathogens
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Obtaining dynamic Norton parameters of a solar panel from manufacturer data

2016

Photovoltaic arrays have been shown to possess significant influence on the dynamic performance of coupled source-converter-load system while its dynamic resistance is the most important parameter, contributing to the overall system dynamics. In this paper, a method of deriving the parameters of linearized photovoltaic equivalent circuit from manufacturer data is proposed. The approach allows predicting the range of dynamic Norton parameters for the expected irradiation and temperature operation conditions thus defining clear bounds required for robust design of the system controller.

EngineeringSettore ING-IND/11 - Fisica Tecnica Ambientalebusiness.industryPhotovoltaic systemPhotovoltaic arraysControl engineeringstabilitySystem dynamicsDynamic resistanceRobust designRange (statistics)Solar energy generatorEquivalent circuitbusinessdynamic resistanceSystem controller
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Luminometric Sub-nanoliter Droplet-to-droplet Arrays (LUMDA-chip) for Drug Screening on Phase I Metabolism Enzymes

2013

Here we show the fabrication of the Luminometric Sub-nanoliter Droplet-to-droplet Array (LUMDA chip) by inkjet printing. The chip is easy to be implemented and allows for amultiplexed multi-step biochemical assay in sub-nanoliter liquid spots. This concept is here applied to the integral membrane enzyme CYP3A4, i.e. themost relevant enzymatic target for phase I drug metabolism, and to some structurally-related inhibitors.

Ink-Jet printing biochip biosensors array
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Flavonoid determination in onion, chili and leek by hard cap espresso extraction and liquid chromatography with diode array detection

2018

Abstract A low cost extraction procedure, based on the use of a hard cap espresso machine, has been developed for the extraction of myricetin, quercetin, luteolin and kaempferol from vegetables by using 50 mL of ethanol in water (80% v/v) in

0301 basic medicinechemistry.chemical_classification030109 nutrition & dieteticsChromatography010401 analytical chemistryExtraction (chemistry)Flavonoid01 natural sciencesDiode array0104 chemical sciencesAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundEspressochemistryMyricetinQuercetinKaempferolLuteolinSpectroscopyMicrochemical Journal
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A Logical Framework for Augmented Simulations of Wireless Sensor Networks

2006

This paper describes a framework for practical and efficient monitoring of a wireless sensor network. The architecture proposed exploits the dynamic reasoning capabilities of the situation calculus in order to assess the sensor network behavior before actually deploying all the nodes. Designing a wireless sensor network for a specific application typically involves a preliminary phase of simulations that rely on specialized software, whose behavior does not necessarily reproduce what will be experienced by an actual network. On the other hand, delaying the test phase until deployment may not be advisable due to unreasonable costs. This paper suggests the adoption of a hybrid approach that i…

Network architectureWi-Fi arrayVisual sensor networkbusiness.industryService setWireless networkComputer scienceWireless ad hoc networkDistributed computingWSNSensor webNetwork simulationIntelligent computer networkKey distribution in wireless sensor networksWireless site surveyMobile wireless sensor networkbusinessWireless sensor networkNetwork management stationHeterogeneous networkComputer network
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Meox2/Tcf15 Heterodimers Program the Heart Capillary Endothelium for Cardiac Fatty Acid Uptake

2015

Background— Microvascular endothelium in different organs is specialized to fulfill the particular needs of parenchymal cells. However, specific information about heart capillary endothelial cells (ECs) is lacking. Methods and Results— Using microarray profiling on freshly isolated ECs from heart, brain, and liver, we revealed a genetic signature for microvascular heart ECs and identified Meox2/Tcf15 heterodimers as novel transcriptional determinants. This signature was largely shared with skeletal muscle and adipose tissue endothelium and was enriched in genes encoding fatty acid (FA) transport–related proteins. Using gain- and loss-of-function approaches, we showed that Meox2/Tcf15 media…

CD36 AntigensHeterozygoteEndotheliumCD36Cardiac Output LowAdipose tissueLipoproteins VLDLBiologyFatty Acid-Binding ProteinsMicePhysiology (medical)Protein Interaction MappingBasic Helix-Loop-Helix Transcription FactorsmedicineAnimalsHumansRNA Small InterferingTranscription factorCells CulturedHomeodomain Proteinschemistry.chemical_classificationLipoprotein lipaseMyocardiumFatty AcidsEndothelial CellsFatty acidSkeletal muscleMetabolismCoronary VesselsCell biologyMice Inbred C57BLLipoprotein LipaseGlucosemedicine.anatomical_structureAdipose TissuechemistryBiochemistryTissue Array Analysisbiology.proteinTranscriptomeCardiology and Cardiovascular MedicineCirculation
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