Search results for "ethnic"

showing 10 items of 497 documents

Predicting who fails to meet the physical activity guideline in pregnancy: a prospective study of objectively recorded physical activity in a populat…

2016

Background A low physical activity (PA) level in pregnancy is associated with several adverse health outcomes. Early identification of pregnant women at risk of physical inactivity could inform strategies to promote PA, but no studies so far have presented attempts to develop prognostic models for low PA in pregnancy. Based on moderate-to-vigorous intensity PA (MVPA) objectively recorded in mid/late pregnancy, our objectives were to describe MVPA levels and compliance with the PA guideline (≥150 MVPA minutes/week), and to develop a prognostic model for non-compliance with the PA guideline. Methods From a multi-ethnic population-based cohort, we analysed data from 555 women with MVPA recorde…

Friends:Medisinske Fag: 700::Klinisk medisinske fag: 750::Gynekologi og obstetrikk: 756 [VDP]Logistic regressionBody fat percentage0302 clinical medicinePregnancyObstetrics and GynaecologyAccelerometryMedicineProspective Studies030212 general & internal medicineProspective cohort studyAdiposityeducation.field_of_studyObstetrics and GynecologyGalvanic Skin ResponseMiddle AgedEuropeParityCohortFemalePsychosocialResearch ArticleAdultmedicine.medical_specialtyAsiaPregnancy Trimester ThirdPhysical ExertionPopulationGuidelines as TopicMulti-ethnicMiddle EastYoung Adult03 medical and health sciencesHumansOccupationseducationExercisePregnancybusiness.industryPhysical activity030229 sport sciencesGuidelinemedicine.diseaseVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Gynekologi og obstetrikk: 756North AmericaPhysical therapyPatient ComplianceEnergy MetabolismSkin TemperaturePredictionbusinessForecastingDemography
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Cinematic images of nation-ness: Space, time and gender inYoung Eagles(Estonia) andLāčplēsis(Latvia)

2012

ABSTRACTIn this article, I analyse cinematic time and space and their interaction, in which nation-ness is articulated as a unifying identity in the epic films Lācplēsis/Bear-Slayer (Latvia, Aleksandrs Rusteiķis, 1930) and Noored Kotkad/Young Eagles (Estonia, Theodor Luts, 1927, digitally remastered in 2008). In discussing the timespace organization of nation-ness in these films, I address representations of the political ‘birth of a nation’ and modern national identity. I discuss the ways in which the narratives in Young Eagles and Lācplēsis re-claim a traditional gender binary, predicated on a splitting and differentiating relationship with Otherness, embodied in the sexual threat of male…

Gender binaryPoliticsVisual Arts and Performing ArtsEmbodied cognitionCommunicationNational identityEthnic groupIdentity (social science)NarrativeGender studiesSociologyAdversaryStudies in Eastern European Cinema
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Track Descriptions: Track 1 - Gender, Ethnicity and Diversity in Planning

2008

Gender Ethnicity and Diversity in Planning Planning theorySettore ICAR/21 - Urbanistica
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Linguistic, geographic and genetic isolation: a collaborative study of Italian populations

2014

Summary - The animal and plant biodiversity of the Italian territory is known to be one of the richest in the Mediterranean basin and Europe as a whole, but does the genetic diversity of extant human populations show a comparable pattern? According to a number of studies, the genetic structure of Italian populations retains the signatures of complex peopling processes which took place from the Paleolithic to modern era. Although the observed patterns highlight a remarkable degree of genetic heterogeneity, they do not, however, take into account an important source of variation. In fact, Italy is home to numerous ethnolinguistic minorities which have yet to be studied systematically. Due to …

Gene FlowChromosomes Human YReproductive IsolationMinority languagesLinguistic diversitySettore BIO/08 - ANTROPOLOGIAGenetic structure Linguistic diversity Minority languages Linguistic islands.LinguisticsSettore BIO/08LinguisticIsolatesMinority languageDNA MitochondrialWhite PeopleGenetics PopulationItalyAnthropologyGenetic structure Linguistic diversity Minority languages Linguistic islandsEthnicityLinguistic islandsHumansGenetic structure Linguistic diversity Minority languagesLinguistic islandsGenetic structurelinguistic islands; minority languages; linguistic diversity; genetic structure
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Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families

2005

We have screened 143 Sicilian (Italian) families with one autistic child to verify, by a linkage disequilibrium approach, the involvement of the 2q31.1 region in the cause of the disease in these families. Our study design includes the use of intrafamilial association to prevent a population stratification bias and ethnic homogeneity of the sample. The results of our analysis provided suggestive evidence of the occurrence of transmission disequilibrium between autism and the D2S2188 polymorphism in Sicilian TRIO families, a finding which provides further and independent support to the hypothesis of the existence of a susceptibility gene (or genes) for autism on chromosome 2q.

Genetic MarkersLinkage disequilibriumDisequilibriumEthnic groupautism ds2188 pcrDiseaseBiologyPopulation stratificationSettore BIO/13 - Biologia ApplicataPolymorphism (computer science)GeneticsmedicineHumansFamilyAutistic DisorderSicilyBiological PsychiatryGenetics (clinical)GeneticsPolymorphism GeneticChromosome Mappingmedicine.diseaselanguage.human_languagePsychiatry and Mental healthChromosomes Human Pair 2languageAutismmedicine.symptomSicilianPsychiatric Genetics
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The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula

2008

12 páginas, 6 figuras.-- et al.

Genetic MarkersMalemedia_common.quotation_subjectPopulationIslamHaplogroupArticleChristianityReligious intoleranceGenetic driftPopulation GroupsReligious conversionPeninsulaGeneticsEthnicityHumansGenetics(clinical)educationGenetics (clinical)Phylogenymedia_commonDemographyGeneticsgeographyeducation.field_of_studyGenetic diversitygeography.geographical_feature_categoryChromosomes Human YPortugalEmigration and ImmigrationGenealogyhumanitiesHaplotypesSpainJewsDiversity (politics)
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Founder mutations in BRCA1 and BRCA2 genes

2007

BRCA1 and BRCA2 germline mutations contribute to a significant number of familial and hereditary breast and/or ovarian cancers. The proportion of high-risk families with breast and/or ovarian cancer cases due to mutations in these tumor suppressor genes varies widely among populations. In some population, a wide spectrum of different mutations in both genes are present, whereas in other groups specific mutations in BRCA1 and BRCA2 have been reported with high frequency. Most of these mutations are prevalent in restricted populations as consequence of a founder effect. The comparison of haplotypes between families with the same mutation can distinguish whether high-frequency alleles derive f…

Genetic counselingPopulationBiologymedicine.disease_causeGermline mutationEthnicitymedicineHumansGenetic TestingeducationGenetic testingBRCA2 ProteinGeneticseducation.field_of_studyMutationmedicine.diagnostic_testBRCA1 ProteinHaplotypeHematologyPenetranceFounder EffectOncologyMutationApoptosis Regulatory ProteinsBRCA1 BRCA2 founder mutationFounder effect
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Factors associated with first- versus second-generation long-acting antipsychotics prescribed under ordinary clinical practice in Italy

2018

Background For many years, long-acting intramuscular (LAI) antipsychotics have been prescribed predominantly to chronic and severe patients, as a last resort when other treatments failed. Recently, a broader and earlier use of LAIs, particularly second-generation LAIs, has been emphasized. To date, few studies attempted to frame how this change in prescribing took place in real-world practice. Therefore, this study aimed to describe the clinical features of patients prescribed with LAIs, and to explore possible prescribing differences between first- and second-generations LAIs under ordinary clinical practice in Italy. Methods The STAR Network "Depot" Study is an observational, longitudinal…

Genetics and Molecular Biology (all)MalePediatricsEuropean PeopleBipolar DisorderCross-sectional studyEconomicsEpidemiologymedicine.medical_treatmentassessmentviruseslcsh:MedicineSocial SciencesLongitudinal StudieBiochemistryPrescriptionGeographical locations0302 clinical medicineMathematical and Statistical TechniquesBiochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)immune system diseasesEpidemiologyMedicine and Health Scienceslong-acting intramuscular (LAI) antipsychotics; clinical practice; assessment; second-generation antipsychotic (SGA) LAIsAntipsychoticsEthnicitiesLongitudinal Studieslcsh:ScienceMultidisciplinaryvirus diseasesDrugsMiddle Agedclinical practiceItalian PeopleEuropePrescriptionsItalyPhysical SciencesAripiprazoleFemaleBivariate AnalysisStatistics (Mathematics)medicine.drugHumanResearch ArticleAntipsychotic AgentsEmploymentAdultmedicine.medical_specialtyAdolescentResearch and Analysis Methods03 medical and health sciencesMental Health and PsychiatrymedicineHumansPaliperidoneBipolar disorderEuropean UnionStatistical MethodsAntipsychoticCross-Sectional StudiePharmacologyRisperidoneBiochemistry Genetics and Molecular Biology (all)business.industryMood Disorderslcsh:Rmedicine.disease030227 psychiatryAntipsychotic AgentCross-Sectional StudiesAgricultural and Biological Sciences (all)Labor EconomicsMultivariate AnalysisSchizophreniaObservational studylcsh:QPopulation Groupingslong-acting intramuscular (LAI) antipsychoticsPeople and placesbusiness030217 neurology & neurosurgerysecond-generation antipsychotic (SGA) LAIsMathematicsPLoS ONE
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Frequencies of pseudocholinesterase variants in Icelanders, Greeks and Pakistanis.

1968

THE formation of the human pseudocholinesterase variants is controlled by at least four alleles at one autosomal locus termed E1 (ref. 1). The four alleles are , , and (refs. 2–5). The heterozygotes have been found in remarkably uniform frequencies, about 3 to 6 per cent, in Caucasians from Europe and North America3,8–11, and also in Australian aborigines12 and Mexican Indians13, but are relatively rare among Negroes11 and Mongoloids10,11,14.

GeneticsMultidisciplinaryGreececommonDibucaineIcelandLocus (genetics)BiologyIsoenzymesPhenotypeGene FrequencySpectrophotometrycommon.groupGermanyIcelandersEthnicityCholinesterasesHumansPakistanCholinesterase InhibitorsAlleleGreeksMolecular BiologyAllelesNature
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A study of the polymorphism and ethnic distribution differences of human serum paraoxonase

1983

The enzyme serum paraoxonase shows a polymorphism in Europeans which is governed by two alleles. The first allele has a gene frequency plow of 0.716–0.777, and is manifested as a low activity group in homozygotes. More than 50% of all European test subjects can be included in this group. A second allele with a gene frequency qhigh of 0.223–0.284 was found in typical European distributions and is manifested in both the form of a second heterozygotic and a third homozygotic group with high activities. The Hardy-Weinberg rule for a two-allele model is valid for the distribution. The gene frequency plow of the first allele decreases as one moves from Europe in the direction of Africa and Asia. …

Geneticseducation.field_of_studyPolymorphism GeneticModels GeneticbiologyAryldialkylphosphatasePopulationParaoxonaseMongoloidPhosphoric Monoester HydrolasesGene FrequencyPolymorphism (computer science)AnthropologyEthnicitybiology.proteinHumansAnatomyAlleleSerum paraoxonaseeducationAllele frequencyAllelesNegroidAmerican Journal of Physical Anthropology
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