Search results for "Asian People"

showing 10 items of 59 documents

The neural mechanisms of word order processing revisited: electrophysiological evidence from Japanese.

2008

We present two ERP studies on the processing of word order variations in Japanese, a language that is suited to shedding further light on the implications of word order freedom for neurocognitive approaches to sentence comprehension. Experiment 1 used auditory presentation and revealed that initial accusative objects elicit increased processing costs in comparison to initial subjects (in the form of a transient negativity) only when followed by a prosodic boundary. A similar effect was observed using visual presentation in Experiment 2, however only for accusative but not for dative objects. These results support a relational account of word order processing, in which the costs of comprehen…

AdultMaleLinguistics and LanguagePhraseCognitive NeuroscienceDative caseExperimental and Cognitive PsychologylinearizationLanguage and LinguisticsSpeech and HearingAsian PeopleSubject (grammar)P600HumansN400Argument (linguistics)Evoked PotentialsLanguageInformation processingBrainElectroencephalographyLinguisticsElectrophysiologyJapaneseSpeech PerceptionVisual PerceptionFemalePsychologySentenceWord orderCognitive psychologyInitial and terminal objectsBrain and language
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Reversibility in Chinese word formation influences target identification.

2011

We recorded event-related brain potentials during the processing of visually presented compound words in Mandarin Chinese. We capitalized on a particular characteristic of Chinese word formation, where two constituents can be combined in two different orders (A+B or B+A), yielding distinct meanings-so-called "reversible words". By investigating the impact of structural reversibility on the processing of compounds in Chinese during a lexical decision task, the present study revealed a pronounced difference between reversible and non-reversible words. Analyses revealed a more enhanced negativity (N400) for reversible words, reflecting demands during semantic processing, followed by a P300-lik…

AdultMaleMandarin ChineseYoung AdultCognitionAsian PeopleLexical decision taskSemantic memoryHumansChinese wordLanguageCommunicationbusiness.industryVerbal BehaviorGeneral NeuroscienceCognitionNegativity effectlanguage.human_languageN400Pattern Recognition VisualReadingCompoundlanguageEvoked Potentials VisualFemalebusinessPsychologyCognitive psychologyNeuroscience letters
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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error

2013

Refractive errors are common eye disorders of public health importance worldwide. Ocular axial length (AL) is the major determinant of refraction and thus of myopia and hyperopia. We conducted a meta-analysis of genome-wide association studies for AL, combining 12,531 Europeans and 8,216 Asians. We identified eight genome-wide significant loci for AL (RSPO1, C3orf26, LAMA2, GJD2, ZNRF3, CD55, MIP, and ALPPL2) and confirmed one previously reported AL locus (ZC3H11B). Of the nine loci, five (LAMA2, GJD2, CD55, ALPPL2, and ZC3H11B) were associated with refraction in 18 independent cohorts (n = 23,591). Differential gene expression was observed for these loci in minus-lens-induced myopia mouse …

AdultMaleRefractive errorAdolescentGene ExpressionLocus (genetics)Genome-wide association studyBiologyOcular Axial LengthPolymorphism Single NucleotideWhite PeopleArticle03 medical and health sciences0302 clinical medicineAsian PeopleSDG 3 - Good Health and Well-beingmedicineGeneticsHumansGWASGenetic Predisposition to DiseaseGenetics(clinical)RSPO1Eye ProteinsGeneGenetics (clinical)030304 developmental biologyGenetic associationAgedGenetics0303 health sciencesta1184HeritabilityMiddle Agedta3121medicine.diseaseRefractive ErrorsAxial Length EyeGenetic Loci030221 ophthalmology & optometryEye disorderFemaleGenome-Wide Association StudySignal Transduction
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Venous thromboembolism after oral and maxillofacial oncologic surgery: Report and analysis of 14 cases in Chinese population.

2016

Background Venous thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE) is a leading cause of death in cancer patients. The aim of this study was to explore the potential risk factor of VTE in oral and maxillofacial oncological surgery. Material and Methods The data of patients who received operation in our institution were gathered in this retrospective study. A diagnosis of VTE was screened and confirmed by computer tomography angiography (CTA) of pulmonary artery or ultrasonography examination of lower extremity. Medical history and all perioperative details were analyzed. Results 14 patients were diagnosed as VTE, including 6 cases of PE, 7 cases of DVT,…

AdultMalemedicine.medical_specialtyDeep vein03 medical and health sciences0302 clinical medicinePostoperative ComplicationsAsian PeopleRisk FactorsMedicineHumansMedical historycardiovascular diseasesGeneral DentistryCause of deathAgedRetrospective StudiesMaxillary Neoplasmsbusiness.industryResearchRetrospective cohort study030206 dentistryPerioperativeVenous ThromboembolismMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseThrombosisSurgeryPulmonary embolismmedicine.anatomical_structure030228 respiratory systemOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASOral and maxillofacial surgerySurgeryFemaleMouth NeoplasmsRadiologyFacial NeoplasmsOral SurgerybusinessMedicina oral, patologia oral y cirugia bucal
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Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

2015

Primary open-angle glaucoma is the most common optic neuropathy and an important cause of irreversible blindness worldwide. The optic nerve head or optic disc is divided in two parts: a central cup (without nerve fibers) surrounded by the neuroretinal rim (containing axons of the retinal ganglion cells). The International Glaucoma Genetics Consortium conducted a meta-analysis of genome-wide association studies consisting of 17,248 individuals of European ancestry and 6,841 individuals of Asian ancestry. The outcomes of the genome-wide association studies were disc area and cup area. These specific measurements describe optic nerve morphology in another way than the vertical cup-disc ratio, …

Aginggenetic structuresEpidemiologyOptic diskGlaucomaGenome-wide association studyNeurodegenerativeEyeOptic neuropathyOptic Nerve DiseasesNERVEGWASGenetics (clinical)GeneticsNEIGHBORHOOD ConsortiumATOH7Asiansmedicine.anatomical_structurecup areaOptic nervePublic Health and Health ServicesOPEN-ANGLE GLAUCOMATRAITSOptic discAsian Continental Ancestry Groupmedicine.medical_specialtyOpen angle glaucomaEuropean Continental Ancestry GroupOptic DiskQuantitative Trait LociBiologyOCULAR-TISSUESRetinal ganglionArticleWhite PeopleAsian PeopleOphthalmologymedicineGeneticsHumansdisc areaEye Disease and Disorders of VisionWhitesHuman GenomeNeurosciencesGlaucomaGENOTYPESmedicine.diseaseGENEeye diseasesSIZEglaucomasense organsGenome-Wide Association Study
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‘Early Neolithic’ graves of the Carpathian Basin are in fact 6000 years younger—Appeal for real interdisciplinarity between archaeology and ancient D…

2012

‘Early Neolithic’ graves of the Carpathian Basin are in fact 6000 years younger—Appeal for real interdisciplinarity between archaeology and ancient DNA research

Ancient DNAHistoryAsian PeopleHaplotypesPannonian basinGeneticsAppealHumansDNA MitochondrialPolymorphism Single NucleotideArchaeologyGenetics (clinical)Journal of Human Genetics
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The mitochondrial‐derived peptide MOTS ‐c: a player in exceptional longevity?

2015

Mitochondrial-derived peptides (MDP) are encoded by functional short open reading frames in the mitochondrial DNA (mtDNA). These include humanin, and the recently discovered mitochondrial open reading frame of the 12S rRNA-c (MOTS-c). Although more research is needed, we suggest that the m.1382A>C polymorphism located in the MOTS-c encoding mtDNA, which is specific for the Northeast Asian population, may be among the putative biological mechanisms explaining the high longevity of Japanese people. 5.760 JCR (2015) Q1, 36/187 Cell biology, 3/49 Geriatrics & gerontology UEM

Asian Continental Ancestry GroupAgingMitochondrial DNAMitochondrial-Derived Peptide MOTS-cBiologíamedia_common.quotation_subjectLongevityMolecular biology of agingmitochondrial DNAGenética humanaMitochondrionBiologyDNA MitochondrialPolymorphism Single Nucleotidelongevity geneOpen Reading FramesAsian PeopleJapanCentenariansHumansmolecular biology of agingBiología humanaHumaninmedia_commonGeneticsBiología molecularGenMitochondrial DNA abnormalitiesLongevityCell Biologylongevity regulationLongevity geneMitochondrial DNAmitochondrial DNA abnormalitiesMitochondriaLongevity regulationOpen reading frameRNA RibosomalCommentaryAsian populationcentenariansPeptidesAging Cell
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The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

2015

Summary Over the past few years, studies of DNA isolated from human fossils and archaeological remains have generated considerable novel insight into the history of our species. Several landmark papers have described the genomes of ancient humans across West Eurasia, demonstrating the presence of large-scale, dynamic population movements over the last 10,000 years, such that ancestry across present-day populations is likely to be a mixture of several ancient groups [1, 2, 3, 4, 5, 6, 7]. While these efforts are bringing the details of West Eurasian prehistory into increasing focus, studies aimed at understanding the processes behind the generation of the current West Eurasian genetic landsc…

Asian Continental Ancestry GroupGene FlowGenetics and Molecular Biology (all)genetics and molecular biologyEvolutionHuman MigrationEuropean Continental Ancestry GroupPopulationSettore BIO/08 - ANTROPOLOGIABiologyDNA MitochondrialBiochemistryArticleWhite PeopleGeneral Biochemistry Genetics and Molecular BiologyEvolution MolecularArcheology Eurasia.Henomics AdmixtureAsian PeopleSettore BIO/13 - Biologia ApplicataReportGeneticsHumansComputer Simulationagricultural and biological sciencesPhylogenyAgricultural and Biological Sciences(all)Biochemistry Genetics and Molecular Biology(all)FossilsGenetic VariationMolecularDNAGenomicsMitochondrialAsian Continental Ancestry Group; Computer Simulation; DNA Mitochondrial; European Continental Ancestry Group; Fossils; Genetic Variation; Genetics Population; Genomics; Haplotypes; Humans; Phylogeny; Evolution Molecular; Gene Flow; Human Migration; Biochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)Genetics PopulationHaplotypesAgricultural and Biological Sciences (all)Evolutionary biologyadmixtureCurrent (fluid)agricultural and biological sciences; biochemistry; genetics and molecular biologyGeneral Agricultural and Biological ScienceseuropeCurrent Biology
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[Cardiovascular health in Asian immigrants to Italy: risk factors, pathogenesis and pharmacological treatment].

2021

In the last decades a significant increase of the migratory phenomenon from South Asian countries to the western world has occurred due to several factors, such as economic crisis, political instabilities, persecutions and wars. It is well established that South Asians (SA) have a higher prevalence of coronary artery disease (CAD) and premature onset of myocardial infarction episodes than other populations. This higher predisposition might be caused by genetic factors, common in both SA residing in their birth country and in those residing abroad, but it may also be due to the new spatial environment in which they live. We have found a higher prevalence of traditional cardiovascular risk fa…

Asian PeopleRisk FactorsPrevalenceEmigrants and ImmigrantsHumansAsian immigrantCoronary Artery DiseaseObesityCardiovascular healthCardiovascular risk factorsGiornale italiano di cardiologia (2006)
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Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families.

2011

Asian originMaleNerve Tissue ProteinsBiologyDentatorubral-pallidoluysian atrophyPolymorphism Single NucleotideGeneticAsian PeoplePolymorphism (computer science)medicineHumansGenetic Association StudiesFamily healthGeneticsFamily HealthDentatorubral-pallidoluysian atrophyHaplotypemedicine.diseaseMyoclonic Epilepsies ProgressiveItalian familiesNeurologyHaplotypesItalySettore MED/26 - NeurologiaFemaleNeurology (clinical)Microsatellite RepeatsMovement disorders : official journal of the Movement Disorder Society
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