Search results for " Variation"

showing 10 items of 1712 documents

Aproximación al léxico del turismo activo: codificación lexicográfica, formación y variación denominativa

2015

En el presente artículo se describe el léxico que conforma el llamado turismo activo del español europeo y se analiza desde tres puntos de vista: su codificación lexicográfica, contrastando el diccionario de la Real Academia Española con diccionarios descriptivos; la formación de sus unidades, que abarca el fenómeno del préstamo y los distintos mecanismos de creación de palabras; y, en tercer lugar, la variación formal y denominativa que caracteriza este vocabulario. El corpus de voces y de muestras de uso ha sido extraído de Internet, en concreto de determinadas fuentes legislativas disponibles en la red y de diferentes páginas web promocionales. Igualmente, se han tomado como referencia d…

Linguistics and LanguageInternetencoding in dictionariesPhilosophyturismo activo ; léxico ; Internet ; codificación lexicográfica ; formación ; variación active tourism ; lexicon ; Internet ; encoding in dictionaries ; word formation ; lexical variation Artículoturismo activo:SOCIOLOGÍA::Cambio y desarrollo social [UNESCO]léxicocodificación lexicográficaLanguage and Linguisticsvariación active tourismword formationformaciónlexiconlexical variation ArtículoUNESCO::SOCIOLOGÍA::Cambio y desarrollo socialHumanities
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The Polysemy of the verbs «pegar», «apegar» and «empegar» in Catalan : a synchronic manifestation of semantic change

2015

In this paper we study the polysemy that the verbs pegar ('hit/stick'), apegar ('stick') and empegar ('stick') possess today in the Catalan language. First of all, we perform a thorough description of the meanings that each of these verbs have acquired not only in the standard but also in the colloquial language. Each of the meanings has been differentiated from the others by analysing the most prominent dictionaries currently available and a corpus of written texts. Additionally, a number of surveys on the spoken language have also been taken into account. Our research has shown that in the different Catalan dialects they do not always have the same meanings or the same verb forms. To be a…

Linguistics and LanguageP1-1091semantic changePolisèmiaLanguage and Linguisticslinguistic variationCatalanCatalàSemantic changePolysemyPhilology. LinguisticsCanvi semànticMetonymypolysemyPhilosophyCatalà Termes i locucionsLinguisticslanguage.human_languageMetonymyLingüística cognitivaLinguistic variationlanguageCognitive linguisticsCatalancognitive linguisticsmetonymyMetonímiaVariació lingüísticaPolysemySemantic change
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Idiomatic intonation and forensic phonetics: sociolinguistic and dialectal information from intonation in Spanish

2015

Las investigaciones de carácter geoprosódico realizadas sobre el español y sus variedades ponen en evidencia que la entonación puede reportar importantes beneficios a la fonética forense, ya que esta lleva asociada información de carácter dialectal y sociolingüístico de especial relevancia sobre el individuo –grupo sociocultural al que pertenece, origen geográfico, medio social en el que se inserta–, además de otros rasgos, cualidades o circunstancias como la edad, el sexo, o incluso su temperamento, carácter o estado de ánimo. Para ello se hace necesario no solo saber qué parámetros acústicos suprasegmentales son relevantes para la identificación del hablante, sino también analizar la vari…

Linguistics and Languagefonética forenseFilologíassociolingüísticavariación lingüísticaProsodyPhorensic PhoneticsLanguage and Linguisticslinguistic variationintonationentonaciónfonética perceptivaUNESCO::LINGÜÏSTICAAcoustic Phoneticsreconocimiento de locutordialectologíaspeaker identificationPhilosophy:LINGÜÏSTICA [UNESCO]geolingüísticaFilologías hispánicasSociolinguisticsProsodiaSpeaker identificationHumanitiesfonética acústica
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Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity.

2008

Contains fulltext : 69953.pdf (Publisher’s version ) (Closed access) Multiple studies have reported an association between attention deficit hyperactivity disorder (ADHD) and the 10-repeat allele of a variable number tandem repeat (VNTR) polymorphism in the 3'-untranslated region (3'UTR) of the dopamine transporter gene (DAT1). Yet, recent meta-analyses of available data find little or no evidence for this association; although there is strong evidence for heterogeneity between datasets. This pattern of findings could arise for several reasons including the presence of relatively rare risk alleles on common haplotype backgrounds or the functional interaction of two or more loci within the g…

Linkage disequilibriumGenetics and epigenetic pathways of disease [NCMLS 6]Medizin2804 Cellular and Molecular NeuroscienceNeuroinformatics [DCN 3]Linkage Disequilibrium2738 Psychiatry and Mental Health0302 clinical medicineGene FrequencyRisk FactorsPerception and Action [DCN 1]Genetics(clinical)Promoter Regions GeneticGenetics (clinical)Genetics0303 health sciences10058 Department of Child and Adolescent PsychiatryEuropeVariable number tandem repeatPsychiatry and Mental health/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingAllelic heterogeneityFunctional Neurogenomics [DCN 2]Genetic Markers2716 Genetics (clinical)Single-nucleotide polymorphism610 Medicine & healthBiologyPolymorphism Single NucleotideMental health [NCEBP 9]White PeopleGenomic disorders and inherited multi-system disorders [IGMD 3]Genetic Heterogeneity03 medical and health sciencesCellular and Molecular NeuroscienceSDG 3 - Good Health and Well-beingCognitive neurosciences [UMCN 3.2]Humansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersAlleleAllele frequencyAlleles030304 developmental biologyDopamine Plasma Membrane Transport ProteinsGenetic heterogeneityHaplotypeGenetic VariationHaplotypesGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivity5' Untranslated Regions030217 neurology & neurosurgeryMicrosatellite Repeats
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Genetic signature consistent with selection against the CYP3A4*1B allele in non-African populations.

2005

Cytochrome P450 3A enzymes (CYP3A) play a major role in the metabolism of steroid hormones, drugs and other chemicals, including many carcinogens. The individually variable CYP3A expression, which remains mostly unexplained, has been suggested to affect clinical phenotypes. We investigated the CYP3A locus in five ethnic groups. The degree of linkage disequilibrium (LD) differed among ethnic groups, but the most common alleles of the conserved LD regions were remarkably similar. Non-African haplotypes are few; for example, only four haplotypes account for 80% of common European Caucasian alleles. Large LD blocks of high frequencies were suggestive of selection. Accordingly, European Caucasia…

Linkage disequilibriumPopulationBlack PeopleSingle-nucleotide polymorphismLocus (genetics)BiologyLinkage DisequilibriumWhite PeopleAsian PeopleCytochrome P-450 Enzyme SystemGeneticsCytochrome P-450 CYP3AHumansGeneral Pharmacology Toxicology and PharmaceuticsAlleleSelection GeneticeducationCYP3A5Molecular BiologyGenetics (clinical)AllelesGeneticseducation.field_of_studyHaplotypeGenetic VariationHaplotypesLiverMolecular MedicinePharmacogeneticsPharmacogenetics and genomics
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Phylogeography of lions (Panthera leossp.) reveals three distinct taxa and a late Pleistocene reduction in genetic diversity

2009

Lions were the most widespread carnivores in the late Pleistocene, ranging from southern Africa to the southern USA, but little is known about the evolutionary relationships among these Pleistocene populations or the dynamics that led to their extinction. Using ancient DNA techniques, we obtained mitochondrial sequences from 52 individuals sampled across the present and former range of lions. Phylogenetic analysis revealed three distinct clusters: (i) modern lions, Panthera leo; (ii) extinct Pleistocene cave lions, which formed a homogeneous population extending from Europe across Beringia (Siberia, Alaska and western Canada); and (iii) extinct American lions, which formed a separate popula…

LionsPleistocenePopulationcave lionDNA MitochondrialBeringiaEvolution MolecularmegafaunaSpecies SpecificityMegafaunaAmerican lionbiology.animalGeneticsAnimalseducationancient DNAPhylogenyEcology Evolution Behavior and SystematicsPanthera leo spelaeaeducation.field_of_studyBeringiaGeographybiologyextinctionFossilsEcologyGenetic VariationSequence Analysis DNAsocial sciencesbiology.organism_classificationhumanitiesAmerican lionPhylogeographyGenetics PopulationPantheraMolecular Ecology
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La incorporación de la regla variable en la enseñanza de E/LE

2017

Resumen: Desde hace algunos anos se viene insitiendo en la conveniencia de incorporar la informacion sociolinguistica en la didactica de una lengua. En el ambito anglosajon ya se habla en ocasiones de la «gramatica sociolinguistica», y existen algunos intentos de enriquecer la informacion gramatical con datos variacionistas. Sin embargo, en el caso del espanol pocas veces se atiende a esa informacion, mas alla de la necesidad de atender a las diferencias de registro a la hora de ensenar espanol a los alumnos extranjeros. Presentamos una propuesta de incorporacion de la variable sociolinguistica a la ensenanza de ELE, retomando la diferencia de Bernstein entre codigo restringido y codigo ela…

Literaturebusiness.industrymedia_common.quotation_subjectContext (language use)ArtLexical variationlcsh:Philology. Linguisticslcsh:P1-1091:PEDAGOGÍA [UNESCO]businesslcsh:LUNESCO::PEDAGOGÍAHumanitiesmedia_commonlcsh:EducationForo de profesores de E/LE
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Association between MICA Gene Variants and the Risk of Hepatitis C Virus-Induced Hepatocellular Cancer in a Sicilian Population Sample

2018

There are currently no biomarkers that predict hepatocellular carcinoma (HCC) risk in patients with hepatitis C virus (HCV)-related cirrhosis. We investigated the relationships among major histocompatibility complex (MHC) class I chain-related gene A (MICA) polymorphisms, plasma levels of soluble MICA (sMICA), and HCC risk in patients with HCV-related HCC. One hundred fifty-four HCV-related HCC patients, 93 HCV-related liver cirrhosis (LC) cases, and 244 healthy controls, all sampled from the native Sicilian population, were genotyped using the KASP™ single-nucleotide polymorphism genotyping method. The MICA rs2596542 polymorphism showed that the G/G genotype was significantly more frequent…

Liver CirrhosisMale0301 basic medicineGenetic LinkageHepacivirusHepacivirusmedicine.disease_causeGastroenterologyBiochemistryLinkage DisequilibriumMiceLiver disease0302 clinical medicineGenotypeOdds RatioAged 80 and overeducation.field_of_studybiologyHepatitis Chepatocellular carcinomaMiddle AgedHepatitis CItalyPopulation Surveillance030220 oncology & carcinogenesisHepatocellular carcinomagenetic association studyHCVMolecular MedicineFemaleDisease SusceptibilityCell-Free Nucleic AcidsBiotechnologymedicine.medical_specialtyCarcinoma HepatocellularGenotypeHepatitis C virusPopulation03 medical and health sciencesInternal medicinemedicineGeneticsAnimalsHumanseducationMolecular BiologyAllelesAgedbusiness.industryliver cirrhosiDecision TreesHistocompatibility Antigens Class IGenetic VariationOdds ratiomedicine.diseasebiology.organism_classificationdigestive system diseases030104 developmental biologyMICAbusinessBiomarkers
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Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease.

2020

Metabolic associated fatty liver disease (MAFLD) is the most prevalent liver disease in Western nations, with high heritability. A recent study of Japanese patients with the disease suggested that TLL1 rs17047200 is associated with fibrosis; whether a similar association is observed in Caucasian patients with MAFLD is unknown. We investigated the association of the TLL1 rs17047200 polymorphism with liver fibrosis in a cohort of Caucasian patients with MAFLD (n = 728). We also investigated whether TLL1 expression is altered during liver injury in humans, in murine models of fibrosis, and in in-vitro. While TLL1 expression is upregulated in the liver of humans with MAFLD and in mice, the rs17…

Liver CirrhosisMaleSteatosisGene ExpressionDiseasePathology and Laboratory MedicineInbred C57BLGastroenterologyPathogenesisCytopathologyCohort StudiesLiver diseaseMice0302 clinical medicineFibrosisMedicine and Health SciencesLiver injury0303 health sciencesMultidisciplinaryLiver DiseasesQFatty liverRTLL1Single NucleotideMiddle Aged3. Good healthUp-RegulationAdult; Animals; Cohort Studies; Fatty Liver; Female; Genetic Variation; Humans; Liver Cirrhosis; Male; Mice; Mice Inbred C57BL; Middle Aged; Tolloid-Like Metalloproteinases; Up-Regulation; Polymorphism Single NucleotideMedicineLiver Fibrosis030211 gastroenterology & hepatologyFemaleAnatomyResearch ArticleAdultmedicine.medical_specialtyHistologyTolloid-Like MetalloproteinasesSettore MED/12 - GASTROENTEROLOGIAScienceGastroenterology and HepatologyPolymorphism Single Nucleotide03 medical and health sciencesInternal medicinemedicineGeneticsAnimalsHumansPolymorphism030304 developmental biologyNutritionbusiness.industryAdult Animals Cohort Studies Fatty Liver Female Genetic Variation Humans Liver Cirrhosis Male Mice Mice Inbred C57BL Middle Aged Tolloid-Like Metalloproteinases Up-Regulation Polymorphism Single NucleotideBiology and Life SciencesGenetic Variationmedicine.diseaseFibrosisDietFatty LiverMice Inbred C57BLn/aAnatomical PathologySteatosisbusinessDevelopmental Biology
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Variational measures related to local systems and the Ward propery of P-adic path bases

2006

Some properties of absolutely continuous variational measures associated with local systems of sets are established. The classes of functions generating such measures are described. It is shown by constructing an example that there exists a P-adic path system that defines a differentiation basis which does not possess Ward property.

Local system P-adic system differentiation basis variational measure Ward property.
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