Search results for "frequ"

showing 10 items of 2272 documents

Stability of charge-pump phase-locked loops : the hold-in and pull-in ranges

2020

The problem of design and analysis of synchronization control circuits is a challenging task for many applications: satellite navigation, digital communication, wireless networks, and others. In this article the Charge-Pump Phase-Locked Loop (CP-PLL) electronic circuit, which is used for frequency synthesis and clock generation in computer architectures, is studied. Analysis of CP-PLL is not trivial: full mathematical model, rigorous definitions, and analysis still remain open issues in many respects. This article is devoted to development of a mathematical model, taking into account engineering aspects of the circuit, interpretation of core engineering problems, definition in relation to m…

CP-PLLPFDcontrol of phase synchronizationsäätöteoriaphase-frequency detectorcharge-pumpsäätötekniikkaphase-locked loopselektroniset piiritnonlinear analysispull-in rangematemaattiset mallithold-in range
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Assessing sediment connectivity in dendritic and parallel calanchi systems

2019

Abstract Calanchi, a type of Italian badlands created by a combination of water erosion processes and environmental constraints controlling their development, is a striking example of long-term landscape evolution. Sediment connectivity can be defined as the degree to which a system facilitates the fluxes of sediments through itself. The goal of this research is testing the use of simple morphometric variables for assessing sediment connectivity of calanchi landforms distinguishing between dendritic and parallel systems. For detecting the morphological characteristics controlling the sediment connectivity of calanchi basins, literature data (146 calanchi basins) and measurements carried out…

Calanchigeographygeography.geographical_feature_category010504 meteorology & atmospheric sciencesLandformDrainage basinSedimentHack's law04 agricultural and veterinary sciencesStructural basinMelton's law01 natural sciencesSystem aCumulative frequency distribution040103 agronomy & agricultureSettore AGR/08 - Idraulica Agraria E Sistemazioni Idraulico-Forestali0401 agriculture forestry and fisheriesSediment transportBasin scaleGeomorphologyGeologySediment connectivity0105 earth and related environmental sciencesEarth-Surface ProcessesCATENA
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PO-002 Angiotensin II-induced hypertension increases the mutation frequency in the rat kidney

2018

Introduction Epidemiological studies revealed an increased risk for kidney cancer in hypertensive patients. In many of these patients, the blood pressure regulating renin angiotensin aldosterone system (RAAS) is activated. A stimulated RAAS can lead to oxidative stress and DNA damage, as we have shown both in vitro and in animal models of hypertension. Here, we used a rat model to quantify mutations generated by 20 weeks of angiotensin II-infusion. Material and methods BigBlue+/- rats, which carry a transgenic lacI gene for mutation analysis, were treated with 0.4 mg angiotensin II/kg/day with the help of osmotic minipumps. Urinary samples were collected in week 15 by placing the rats into …

Cancer ResearchKidneymedicine.medical_specialtyDNA damagebusiness.industryUrinary systemmedicine.disease_causeAngiotensin IImedicine.anatomical_structureEndocrinologyOncologyInternal medicineRenal physiologyRenin–angiotensin systemmedicineMutation frequencybusinessOxidative stressESMO Open
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Epidemiological, clinical and molecular characterization of Lynch‐like syndrome: A population‐based study

2019

Colorectal carcinomas that are mismatch repair (MMR)‐deficient in the absence of MLH1 promoter methylation or germline mutations represent Lynch‐like syndrome (LLS). Double somatic events inactivating MMR genes are involved in the etiology of LLS tumors. Our purpose was to define the clinical and broader molecular hallmarks of LLS tumors and the population incidence of LLS, which remain poorly characterized. We investigated 762 consecutive colorectal carcinomas operated in Central Finland in 2000–2010. LLS cases were identified by a stepwise protocol based on MMR protein expression, MLH1 methylation and MMR gene mutation status. LLS tumors were profiled for CpG Island Methylator Phenotype (…

Cancer ResearchMICROSATELLITE INSTABILITYDNA mismatch repairMISMATCH-REPAIR DEFICIENCYGene mutationmedicine.disease_cause0302 clinical medicinelynch syndromeFinlandMolecular Epidemiologyeducation.field_of_studyMutationISLAND METHYLATOR PHENOTYPENONPOLYPOSIS COLORECTAL-CANCERlynch-like syndromeTUMORSLynch syndrome3. Good healthOncology030220 oncology & carcinogenesissyöpätauditColorectal NeoplasmsMutL Protein Homolog 1Lynch-like syndromeAdult3122 CancersPopulationsuolistosyövätCpG island methylator phenotypeBiologyta3111FREQUENCYMLH103 medical and health sciencesGermline mutationcolorectal carcinomaBRAF MUTATIONCOLONmedicineHumansLynchin oireyhtymäeducationneoplasmsMSIAgedRetrospective StudiesCpG Island Methylator PhenotypeMicrosatellite instabilityDNASOMATIC MUTATIONSta3122CpG Island Methylator phenotypemedicine.diseaseColorectal Neoplasms Hereditary Nonpolyposisdigestive system diseasesCOPY NUMBERMutationCancer researchInternational Journal of Cancer
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High frequency of a non-functional TAP1/LMP2 promoter polymorphism in human tumors

2002

The Tap1 and Tap2 genes encoding for a heterodimeric peptide transporter play a key role in antigen processing and presentation. The TAP complex mediates the transport of peptides generated by the IFN-gamma-inducible proteasome subunits LMP2, 7 and 10 from the cytosol into the endoplasmic reticulum (ER), where they bind to MHC class I molecules. In contrast to the frequent polymorphisms within the rat Tap genes which exert functional differences, polymorphic regions within the human Tap genes have been demonstrated, but not systematically analyzed in terms of their functional significance. Both the Tap1 and Lmp2 genes are transcribed from a bidirectional intergenic promoter which is regulat…

Cancer ResearchTransfectionViral Matrix ProteinsIntergenic regionGene FrequencyGenotypeMHC class ITumor Cells CulturedAnimalsHumansRNA MessengerATP Binding Cassette Transporter Subfamily B Member 2Promoter Regions GeneticCarcinoma Renal CellMelanomaGeneGeneticsPolymorphism GeneticbiologyReverse Transcriptase Polymerase Chain ReactionAntigen processingEndoplasmic reticulumMolecular biologyGene Expression Regulation NeoplasticOncologyCOS Cellsbiology.proteinTAP2ATP-Binding Cassette TransportersTAP1International Journal of Oncology
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REsect: Blinded assessment of amenability to potentially curative treatment of previously unresectable colorectal cancer liver metastases (CRC LM) af…

2017

3532 Background: Secondary resection and radiofrequency ablation (RFA) of primarily unresectable LM from CRC can prolong survival and cure some patients (pts). Effective downsizing treatments are needed but their impact on secondary amenability to surgery/RFA is difficult to evaluate objectively. The added value of SIRT is not well established. Methods: Baseline (BL) and follow-up (FU) imaging at best response for CRC pts treated with FOLFOX chemotherapy±bevacizumab (bev) (CT) vs. CT+SIRT in the phase III SIRFLOX RCT were reviewed by 3−5 expert HPB surgeons (from a panel of 15) for resectability of LM. Reviewers were blinded to each other and to all clinical information incl. time of imagi…

Cancer Researchmedicine.medical_specialtyChemotherapyRadiofrequency ablationbusiness.industryColorectal cancermedicine.medical_treatmentmedicine.diseaselaw.inventionResection03 medical and health sciences0302 clinical medicineOncologyRandomized controlled trialFOLFOXlawCurative treatment030220 oncology & carcinogenesisClinical informationmedicine030211 gastroenterology & hepatologyRadiologybusinessmedicine.drugJournal of Clinical Oncology
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The association between extremely low-frequency electromagnetic fields and childhood leukaemia in epidemiology: enough is enough?

2010

Background: Previous pooled analyses have reported an association between magnetic fields and childhood leukaemia. We present a pooled analysis based on primary data from studies on residential magnetic fields and childhood leukaemia published after 2000. Methods: Seven studies with a total of 10 865 cases and 12 853 controls were included. The main analysis focused on 24-h magnetic field measurements or calculated fields in residences. Results: In the combined results, risk increased with increase in exposure, but the estimates were imprecise. The odds ratios for exposure categories of 0.1–0.2 μT, 0.2–0.3 μT and ⩾0.3 μT, compared with <0.1 μT, were 1.07 (95% CI 0.81–1.41), 1.16 (0.69–1.93)…

Cancer Researchmedicine.medical_specialtyLeukemiaNeoplasms Radiation-Inducedbusiness.industryEpidemiologyExtremely low frequency electromagnetic fieldsChildhood cancerOdds ratiomagnetic fieldsConfidence intervalUnited KingdomChildhood leukaemiameta-analysisIncreased riskExposure groupElectromagnetic FieldsOncologychildhood leukaemiaEpidemiologymedicineHumanspooled analysisbusinessDemographyBritish journal of cancer
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

2013

Elevated serum urate concentrations can cause gout, a prevalent and painful inflammatory arthritis. By combining data from &gt;140,000 individuals of European ancestry within the Global Urate Genetics Consortium (GUGC), we identified and replicated 28 genome-wide significant loci in association with serum urate concentrations (18 new regions in or near TRIM46, INHBB, SFMBT1, TMEM171, VEGFA, BAZ1B, PRKAG2, STC1, HNF4G, A1CF, ATXN2, UBE2Q2, IGF1R, NFAT5, MAF, HLF, ACVR1B-ACVRL1 and B3GNT4). Associations for many of the loci were of similar magnitude in individuals of non-European ancestry. We further characterized these loci for associations with gout, transcript expression and the fractional…

Candidate geneInhibins/geneticsGenome-wide association studyGENETIC-LOCIchemistry.chemical_compound0302 clinical medicineserum urateGene FrequencyGout/bloodassociation analysis serum urateGlucose/metabolismSettore MED/14 - NEFROLOGIAHyperuricemiaserum; urate; genePOPULATIONMETABOLIC SYNDROMEGenetics0303 health scienceseducation.field_of_studybiologyPolymorphism Single Nucleotide/genetics3. Good healthHYPERURICEMIAGenetic Loci/genetics/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingSLC22A12Single Nucleotide/geneticsSNPsSignal TransductionMOLECULAR PHYSIOLOGYserum urate concentrations gout genome-wide meta-analysisEuropean Continental Ancestry GroupPopulationPolymorphism Single NucleotideWhite PeopleUric Acid/bloodserum urate concentrationsgenome-wide meta-analysis03 medical and health sciencesSDG 3 - Good Health and Well-beinguric acidGeneticsmedicineHumansInhibinsPolymorphismeducation030304 developmental biology030203 arthritis & rheumatologyAnalysis of VarianceGOUTIDENTIFICATIONTRANSPORTERCARDIOVASCULAR-DISEASE RISKta3121medicine.diseaseassociation analysisGoutmeta-analysisGlucosechemistryGenetic Locigenome-wide association studiesbiology.proteinSignal Transduction/geneticsUric acidURIC-ACID LEVELSGenome-Wide Association StudySLC2A9
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Power-Line Communication in Medium-Voltage System: Simulation Model and Onfield Experimental Tests

2012

The aim of this paper is to develop a complete model of a power-line communication (PLC) system operating on a medium-voltage (MV) network. The core-shield configuration was chosen for signal transmission in the power cables. In order to validate the developed model experimental, the medium-voltage network of the Favignana island was used to carry out detailed testing. The transmission was performed between two transformer substations in the presence of mains voltage (i.e., 24 kV). ST7540 FSK power-line transceivers, together with capacitive coupling interfaces, were used for the transmission and the reception of the communication signal. The correlation between the experimental measurement…

Capacitive couplingEngineeringFrequency-shift keyingmedium-voltage (MV) cablebusiness.industrypower-line communication (PLC)Electrical engineeringEnergy Engineering and Power TechnologyCommunications systemlaw.inventionpower system communicationPower-line communicationTransmission (telecommunications)lawElectronic engineeringElectrical and Electronic EngineeringTransceiverCommunication systemTransformerbusinessCommunication System Power System Communication Medium Voltage cable Power line communicationSettore ING-INF/07 - Misure Elettriche E ElettronicheVoltageIEEE Transactions on Power Delivery
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Electrocardiographic Imaging for Atrial Fibrillation: A Perspective From Computer Models and Animal Experiments to Clinical Value

2021

[EN] Electrocardiographic imaging (ECGI) is a technique to reconstruct non-invasively the electrical activity on the heart surface from body-surface potential recordings and geometric information of the torso and the heart. ECGI has shown scientific and clinical value when used to characterize and treat both atrial and ventricular arrhythmias. Regarding atrial fibrillation (AF), the characterization of the electrical propagation and the underlying substrate favoring AF is inherently more challenging than for ventricular arrhythmias, due to the progressive and heterogeneous nature of the disease and its manifestation, the small volume and wall thickness of the atria, and the relatively large…

Cardiac arrhythmiasmedicine.medical_specialtyVOLUME CONDUCTORPhysiologymedicine.medical_treatmentROTORSCatheter ablationReview030204 cardiovascular system & hematologyTECNOLOGIA ELECTRONICA03 medical and health sciencesPERSISTENT0302 clinical medicinePhysiology (medical)Internal medicineMAGNETIC-RESONANCEmedicineQP1-981PULMONARY VEIN ISOLATIONSistema cardiovascularImatges tridimensionals en medicinabusiness.industrySmall volumeECGAF characterizationPerspective (graphical)Electrocardiographic imagingAtrial fibrillationmedicine.diseaseAtrial fibrillationDOMINANT FREQUENCYKey factorsElectrocardiographic imagingClinical valueCardiologyEnginyeria biomèdicaCatheter ablationbusinessWall thicknessTORSO INHOMOGENEITIESINVERSE PROBLEMInverse solutionTreatment guidance030217 neurology & neurosurgery
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