Search results for " Variation"

showing 10 items of 1712 documents

Validation of lung densitometry threshold at CT for the distinction between senile lung and emphysema in elderly subjects

2015

Background and Aims. An ageing lung is characterised by distal airspace enlargement without alveolar wall destruction: therefore the anatomical distinction between senile lung and emphysema is clear-cut. In clinical settings the definition of precise boundaries between normalcy and pathology is more difficult with the risk of overdiagnosis. CT is an important diagnostic advancement in the field of COPD. Most methods for the evaluation of emphysema are based on the detection and measurement of areas characterised by a density level below a threshold assumed to characterize parenchymal destruction. Methods. Our retrospective study included 47 healthy subjects (65-91 years), 36 never smokers a…

MalePulmonary and Respiratory MedicineAgingmedicine.medical_specialtyCoefficient of variationlcsh:MedicineRespiratory physiologySettore MED/10 - Malattie Dell'Apparato RespiratorioAbsorptiometry PhotonLung densitometry CTsenile lung emphysemaImage Processing Computer-AssistedmedicineHumansSenile lungOverdiagnosisLungAgedAged 80 and overEmphysemaCOPDLungbusiness.industrylcsh:RRetrospective cohort studymedicine.diseaseSurgeryrespiratory tract diseasesAgeingmedicine.anatomical_structurePulmonary EmphysemaDensity distributionRadiologyCardiology and Cardiovascular MedicinebusinessDensitometryTomography Spiral ComputedAlgorithmsCTDensitometryMonaldi Archives for Chest Disease
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Tracking Five Millennia of Horse Management with Extensive Ancient Genome Time Series

2019

Summary Horse domestication revolutionized warfare and accelerated travel, trade, and the geographic expansion of languages. Here, we present the largest DNA time series for a non-human organism to date, including genome-scale data from 149 ancient animals and 129 ancient genomes (≥1-fold coverage), 87 of which are new. This extensive dataset allows us to assess the modern legacy of past equestrian civilizations. We find that two extinct horse lineages existed during early domestication, one at the far western (Iberia) and the other at the far eastern range (Siberia) of Eurasia. None of these contributed significantly to modern diversity. We show that the influence of Persian-related horse …

MaleRange (biology)BiologíaBreeding horsesBreedingGenomeDomestication0302 clinical medicinePaleobiologíaComputingMilieux_MISCELLANEOUSHistory AncientPhylogenyhorses0303 health sciencesDiversityGenomeAncient DNAanimal breedingBiological EvolutionmuleshumanitiesManagementEuropeDomestication animalEquestrian civilizationsEthnologyFemalemanagementequestrian civilizationsExtinct lineagesAsia[SHS.ARCHEO]Humanities and Social Sciences/Archaeology and PrehistoryselectionMultiple allelesCaballosBiologyMulesArticleGeneral Biochemistry Genetics and Molecular Biologydiversity03 medical and health sciencesdomesticationCaballo de Przewalskiddc:570[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]AnimalsGenetic variationHorsesDNA AncientDomesticationSelectionancient DNAInstitut für Biochemie und Biologie030304 developmental biologyAnimal breedingSeries (stratigraphy)Genetic diversityGenetic VariationEquidaeGenéticaextinct lineagesAncient DNAdomestication ; selection ; equestrian civilizations ; horses ; ancient DNA ; mules ; animal breeding ; extinct lineages ; management ; diversityAnálisisancient DNA ; domestication ; animal breeding ; horses ; mules ; extinct lineages ; selection ; diversity ; management ; equestrian civilizations030217 neurology & neurosurgery
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BENEFITS OF MULTI-DOMAIN FEATURE OF MISMATCH NEGATIVITY EXTRACTED BY NON-NEGATIVE TENSOR FACTORIZATION FROM EEG COLLECTED BY LOW-DENSITY ARRAY

2012

Through exploiting temporal, spectral, time-frequency representations, and spatial properties of mismatch negativity (MMN) simultaneously, this study extracts a multi-domain feature of MMN mainly using non-negative tensor factorization. In our experiment, the peak amplitude of MMN between children with reading disability and children with attention deficit was not significantly different, whereas the new feature of MMN significantly discriminated the two groups of children. This is because the feature was derived from multi-domain information with significant reduction of the heterogeneous effect of datasets.

MaleReading disabilityAdolescentComputer Networks and CommunicationsSpeech recognitionMismatch negativityContingent Negative VariationElectroencephalographybehavioral disciplines and activitiesDyslexiaReduction (complexity)Event-related potentialmedicineHumansChildMathematicsModels StatisticalTensor factorizationmedicine.diagnostic_testbusiness.industryElectroencephalographyPattern recognitionGeneral MedicineBrain WavesAmplitudeAcoustic StimulationAttention Deficit Disorder with HyperactivityFeature (computer vision)Case-Control StudiesAuditory PerceptionEvoked Potentials AuditoryFemaleArtificial intelligencebusinesspsychological phenomena and processesInternational Journal of Neural Systems
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Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes

2014

Rare copy number variants (CNVs) disrupting ASTN2 or both ASTN2 and TRIM32 have been reported at 9q33.1 by genome-wide studies in a few individuals with neurodevelopmental disorders (NDDs). The vertebrate-specific astrotactins, ASTN2 and its paralog ASTN1, have key roles in glial-guided neuronal migration during brain development. To determine the prevalence of astrotactin mutations and delineate their associated phenotypic spectrum, we screened ASTN2/TRIM32 and ASTN1 (1q25.2) for exonic CNVs in clinical microarray data from 89 985 individuals across 10 sites, including 64 114 NDD subjects. In this clinical dataset, we identified 46 deletions and 12 duplications affecting ASTN2. Deletions o…

MaleReceptors Cell Surface/geneticsAutismChild Development Disorders Pervasive/geneticsGene ExpressionGenome-wide association studyMedical and Health SciencesTripartite Motif ProteinsRisk FactorsReceptors2.1 Biological and endogenous factorsProtein IsoformsNerve Tissue Proteins/geneticsCopy-number variationAetiologyChildGenetics (clinical)Sequence DeletionPediatricGenetics & HeredityGeneticseducation.field_of_studySingle NucleotideArticlesGeneral MedicineExonsBiological SciencesMental HealthPhenotypeAutism spectrum disorderOrgan SpecificityCerebellar cortexChild PreschoolCell SurfaceSpeech delayFemalemedicine.symptomTranscription Initiation SiteAttention Deficit Disorder with Hyperactivity/geneticsChromosomes Human Pair 9HumanPair 9AdultPediatric Research InitiativeChild Development DisordersAdolescentDNA Copy Number VariationsIntellectual and Developmental Disabilities (IDD)Ubiquitin-Protein LigasesPopulationTranscription Factors/geneticsNerve Tissue ProteinsReceptors Cell SurfaceBiologyPolymorphism Single NucleotideChromosomesYoung AdultClinical ResearchProtein Isoforms/geneticsBehavioral and Social ScienceGeneticsmedicineAttention deficit hyperactivity disorderHumansGenetic Predisposition to DiseasePolymorphismPreschooleducationMolecular BiologyGenetic Association StudiesPervasiveGlycoproteinsHuman GenomeNeurosciencesInfant NewbornGlycoproteins/geneticsInfantNewbornmedicine.diseaseBrain DisordersAttention Deficit Disorder with HyperactivityChild Development Disorders PervasiveCase-Control StudiesAutismTranscription Factors
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Genetic variation in neuromuscular performance.

1973

Using a simple cumulative model of heredity plus environment, based on intrapair differences observed in monozygous (MZ) and dizygous (DZ) twins, the relative contribution of heredity to the interindividual variance in several neuromuscular parameters was determined with 15 pairs of male (8 MZ and 7 DZ) and 14 pairs of female (7 MZ and 7 DZ) twins ranging in age from 10 to 14 years. The data disclosed that in boys the variability in maximal mechanical (anaerobic) power was 99.2% genetically determined under the environmental conditions of the study. The corresponding heritability estimate values for the patellar reflex time and reaction time were 97.5% and 85.7%, respectively. In girls the …

MaleReflex StretchAdolescentPhysiologyPhysical ExertionNeuromuscular JunctionTwinsPhysiologyBiologymedicine.disease_causePregnancyPhysiology (medical)Genetic variationHereditymedicineReaction TimeHumansOrthopedics and Sports MedicineGenetic variabilityChildGeneticsmedicine.diagnostic_testBody WeightPublic Health Environmental and Occupational HealthPatellar reflexGeneral MedicineHuman physiologyPatellaHeritabilityBody HeightGenetic TechniquesGenetic CodeFemaleInternationale Zeitschrift fur angewandte Physiologie, einschliesslich Arbeitsphysiologie
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XRCC5 as a Risk Gene for Alcohol Dependence : Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans

2015

Genetic factors play as large a role as environmental factors in the etiology of alcohol dependence. Although genome-wide association studies (GWAS) enable systematic searches for loci not hitherto implicated in the etiology of alcohol dependence, many true findings may be missed due to correction for multiple testing. The aim of the present study was to circumvent this limitation by searching for biological system-level differences, and then following up these findings in humans and animals. Gene-set based analysis of GWAS data from 1333 cases and 2168 controls identified 19 significantly associated gene-sets of which five could be replicated in an independent sample. Clustered in these ge…

MaleRiskAdolescentMedizinGenome-wide association studyBiologyPolymorphism Single NucleotideWhite PeopleAnimals Genetically ModifiedRNA interferenceGermanyGenetic variationAnimalsHumansGene silencingGenetic Predisposition to DiseaseKu AutoantigenGeneGenetic associationPharmacologyGeneticsEthanolAlcohol dependenceDNA HelicasesCentral Nervous System DepressantsPhenotypeAlcoholismPsychiatry and Mental healthDrosophila melanogasterFemaleOriginal ArticleFollow-Up StudiesGenome-Wide Association Study
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Concordance of assays designed for the quantification of JAK2V617F: a multicenter study

2008

Background Many different techniques have been designed for the quantification of JAK2 V617F allelic burden, sometimes producing discrepant results. Design and Methods JAK2 V617F quantification techniques were compared among 16 centers using 11 assays based on quantitative polymerase chain reaction (with mutation-specific primers or probes, or fluorescent resonance energy transfer/melting curve analysis), allele-specific polymerase chain reaction, conventional sequencing or pyrosequencing. Results A first series of blinded samples (granulocyte DNA, n=29) was analyzed. Seven assays (12 centers) reported values inside the mean±2SD; the mean coefficient of variation was 31%. Sequencing techniq…

MaleSerial dilutionPhenylalanineCoefficient of variationBiologyMelting curve analysislaw.inventionlawhemic and lymphatic diseasesTaqManHumansAllelesPolymerase chain reactionValineOriginal ArticlesHematologyJanus Kinase 2Molecular biologyPedigreePhenotypeReal-time polymerase chain reactionMutationPyrosequencingFemalePrimer (molecular biology)Thrombocythemia EssentialHaematologica
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Personality may confound common measures of mate-choice.

2011

5 pages; International audience; The measurement of female mating preferences is central to the study of the evolution of male ornaments. Although several different methods have been developed to assess sexual preference in some standardized way, the most commonly used procedure consists of recording female spatial association with different males presented simultaneously. Sexual preference is then inferred from time spent in front of each male. However, the extent to which the measurement of female mate-choice is related to exploration tendencies has not been addressed so far. In the present study we assessed the influence of variation in exploration tendencies, a trait closely associated …

MaleSexual SelectionEvolutionary ProcessesAnimal Evolutionmedia_common.quotation_subjectlcsh:MedicineBiologyDevelopmental psychologyBehavioral Ecology[ SDV.EE.IEO ] Life Sciences [q-bio]/Ecology environment/SymbiosisPersonalityAnimalsBig Five personality traitslcsh:ScienceZebra finchBiologymedia_commonEvolutionary Biology[ SDE.BE ] Environmental Sciences/Biodiversity and EcologyMultidisciplinaryAnimal Behaviorlcsh:RMating Preference AnimalExplained variationPreferenceMating preferencesOrganismal EvolutionMate choiceEvolutionary EcologyTraitFemalelcsh:QFinches[SDE.BE]Environmental Sciences/Biodiversity and EcologyResearch ArticlePersonality[SDV.EE.IEO]Life Sciences [q-bio]/Ecology environment/Symbiosis
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Predicting and Measuring Decision Rules for Social Recognition in a Neotropical Frog.

2022

AbstractMany animals use signals, such as vocalizations, to recognize familiar individuals. However, animals risk making recognition mistakes because the signal properties of different individuals often overlap due to within-individual variation in signal production. To understand the relationship between signal variation and decision rules for social recognition, we studied male golden rocket frogs, which recognize the calls of territory neighbors and respond less aggressively to a neighbor’s calls than to the calls of strangers. We quantified patterns of individual variation in acoustic properties of calls and predicted optimal discrimination thresholds using a signal detection theory mod…

MaleSignal variationComputer scienceSpeech recognitionRecognition PsychologyDecision ruleSignalSocial recognitionAggressionVariation (linguistics)Signal productionAnimalsDetection theoryAnuraVocalization AnimalTerritorialityEcology Evolution Behavior and SystematicsSocial categoryThe American naturalist
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Cognitive vs. affective listening modes and judgments of music - An ERP study

2010

The neural correlates of processing deviations from Western music rules are relatively well known. Less is known of the neural dynamics of top-down listening modes and affective liking judgments in relation with judgments of tonal correctness. In this study, subjects determined if tonal chord sequences sounded correct or incorrect, or if they liked them or not, while their electroencephalogram (EEG) was measured. The last chord of the sequences could be congruous with the previous context, ambiguous (unusual but still enjoyable) or harmonically inappropriate. The cognitive vs. affective listening modes were differentiated in the event-related potential (ERP) responses already before the end…

MaleStatistics as TopicEXPECTANCYNeuropsychological TestsElectroencephalographyEvent-related potential (ERP)CognitionProfessional Competence0302 clinical medicineBRAIN-REGIONSJudgment processesmedia_commonBrain Mappingmedicine.diagnostic_testLate positive potential (LPP)General Neuroscience05 social sciencesElectroencephalographyCognitionhumanitiesContingent negative variationNeuropsychology and Physiological PsychologyEMOTIONSAuditory PerceptionEvoked Potentials AuditoryFemaleMusic perceptionPsychologypsychological phenomena and processesSENSORY CONSONANCECognitive psychologyAdultAdolescentmedia_common.quotation_subjectEarly right anterior negativity (ERAN)AestheticsEVENT-RELATED POTENTIALSbehavioral disciplines and activities050105 experimental psychologyBIOELECTRICAL ECHOESJudgmentYoung Adult03 medical and health sciencesEvent-related potentialPerceptionReaction TimemedicineHumans0501 psychology and cognitive sciencesActive listeningCONTINGENT NEGATIVE-VARIATIONAnalysis of VarianceNeural correlates of consciousnessPERCEPTIONMusical preferenceAffectAcoustic StimulationChord (music)LikingMusic030217 neurology & neurosurgeryAUDITORY-CORTEXRESPONSES
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