Search results for "termini"

showing 10 items of 365 documents

Zvaigžņotā Debess: 2013/14, Ziema (222)

2013

Latvijas Universitāte

Linards Reiziņš1952. gada diplomandi LVU astronomijas:NATURAL SCIENCES::Physics::Astronomy and astrophysics::Astronomy [Research Subject Categories]Stendera “Augstas gudrības grāmata” – astronomijas terminiMarss – ūdens meklējumiPlutona pavadoņiLU Astronomijas institūts 2012.gadāAstronomiskās parādības 2014Starptautiskās Astronomijas Savienības XXVIII Ģenerālā Asambleja PekināPlanētu redzamības kompleksā diagramma 2014Kuģa Ķīļa miglājs – ALMA’s panorāmaKazimirs Lapuška (1936-2013)Vulkāns Cerbers StiksaVerners Heizenbergs – par humanitāro izglītību un dabaszinātnēmBumeranga MiglājsLatvijas 63. matemātikas olimpiāde – uzdevumu atrisinājumiDebess spīdekļi – 2013/14. gada ziemaAstronomijas studijas ārzemēsZvaigžņu tēma mākslā – dzeja un zīmējumiBora atommodelisALMA – pēdējā antenaLatvijas 38. atklātā fizikas olimpiādeKaķa Ķepas miglājs – uzņēmums ar ESO APEX teleskopu un ArTeMiS kameruTitāns – Saturna pavadonisRiekstu kalna apkaimeEiropas žurnālistikas balva astronomijā 2013Jurijs FrancmanisBetlēmes zvaigzneSaules pulksteņi Mārsnēnos un Ķegumā
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Génétique des textes et système chaotique

2016

Textual genetics and chaotic system Although we share Louis Hay's idea that it is impossible to homologate and systematize the operations which can be observed in manuscripts, it is however possible to interpret whatever creation process in terms of the passage from entropy to order. The possibility of an analogy between text and chaotic system had been advanced by Noëlle Batt according to whom each work actually satisfies the principles of the chaotic system. It is starting from such principles that we will try to show the analogy between chaotic system and textual genetics: 1. The fact that we are dealing with an evolving system (with variables and permanent features) endowed with a tempo…

Linguistics and LanguageHistorylcsh:French literature - Italian literature - Spanish literature - Portuguese literatureLiterature and Literary Theorymanuscritsattracteur étrangeSystème chaotique génétique des textes manuscrits attracteur étrange déterminisme imprévisibilité.Language and Linguisticsimprévisibilité.lcsh:PQ1-3999chaotic system Textual Genetics manuscripts Strange attractor determinism unpredictability.Settore L-LIN/03 - Letteratura Francesegénétique des textessystème chaotiquedéterminisme
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The Myth of Eros in Michael Field’s Sapphic Project: from a New Materialism to a Tragic Determinism

2020

espanolEl objetivo de este articulo consiste en examinar como Katharine Bradley y su sobrina Edith Cooper reinterpretan la figura de Safo en conexion directa con el mito de Eros en Long Ago (1889), el primer poemario que compusieron bajo el pseudonimo de Michael Field. Con este proposito en mente, seleccionamos una serie de poemas dirigidos a la deidad griega del amor, realizamos un analisis detallado de los mismos y demostramos que las Fields componen una mitografia dramatica que explora la identidad paradojica del dios y, al mismo tiempo, revela toda una verdad intemporal inherente al propio mito de Eros: el amor constituye un fenomeno ambivalente que crea, inspira y eleva tanto como dest…

Linguistics and Languageparadoxmichael fieldLiterature and Literary TheoryPoetryField (Bourdieu)PhilosophyP1-1091MythologymythLyricsDeterminismLanguage and LinguisticsNephew and niecelong agoerosMaterialismPhilology. LinguisticsHumanitiessapphoAnuario de Estudios Filológicos
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Soliloquia de humani arbitrii libertate ar potestate / [Constantius Applanus

1496

Sign.: a12, b-z4, &4, t/4, R/4, A-C4, D-K8, L12. - Data completa, 4 octubre, 1496 L. rom. - 2 mides. - 28 lín. - Min. p. inic. - Postil·les marginals. - Filigr.: balança encerclada. - Errors de fol.

Lliure albir i determinisme Obres anteriors a 1800DIG-BH
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Soliloquia de humani arbitrii libertate ar potestate

1496

Sign.: a12, b-z4, &4, t/4, R/4, A-C4, D-K8, L12. - Data completa, 4 octubre, 1496 L. rom. - 2 mides. - 28 lín. - Min. p. inic. - Postil·les marginals. - Filigr.: balança encerclada. - Errors de fol

Lliure albir i determinisme Obres anteriors al 1800
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Rumination for innovation? : analyzing the longitudinal effects of work-related rumination on creativity at work and off-job recovery

2017

ABSTRACTWork-related rumination is not a single construct, but consists of a dimension associated with negative emotions or affect (affective rumination), and a dimension associated with reflective thinking and applying strategies to solve problems (problem-solving pondering). In this three-wave longitudinal study across two years (N = 630) we investigated whether the relationships between work-related rumination, off-job recovery, and creativity at work varied along the two dimensions of work-related rumination. In addition, we tested whether the relationships followed normal, reversed, or reciprocal causation. The results showed, first, that in a one-year perspective affective rumination,…

Longitudinal studymedia_common.quotation_subject050109 social psychologyponderingAffect (psychology)Work relatedDevelopmental psychologyrecoverystress0502 economics and businessmedicine0501 psychology and cognitive sciencesMeasurement invarianceApplied Psychologyta515media_commonPsykologia - Psychology05 social sciencesPerspective (graphical)ruminationReciprocal determinismCreativityinnovationRuminationmedicine.symptomPsychology050203 business & management
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A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.

2010

International audience; To identify genetic susceptibility factors conferring increased risk of venous thrombosis (VT), we conducted a multistage study, following results of a previously published GWAS that failed to detect loci for developing VT. Using a collection of 5862 cases with VT and 7112 healthy controls, we identified the HIVEP1 locus on chromosome 6p24.1 as a susceptibility locus for VT. Indeed, the HIVEP1 rs169713C allele was associated with an increased risk for VT, with an odds ratio of 1.20 (95% confidence interval 1.13-1.27, p = 2.86 x 10(-9)). HIVEP1 codes for a protein that participates in the transcriptional regulation of inflammatory target genes by binding specific DNA …

MESH : Transcription Factors[SDV]Life Sciences [q-bio]Genome-wide association study030204 cardiovascular system & hematologyMESH : Chromosomes Human Pair 60302 clinical medicineGenetics(clinical)Genetics (clinical)GeneticsVenous Thrombosis0303 health sciencesMESH: Polymorphism Single NucleotideMESH : Polymorphism Single NucleotideMESH: Genetic Predisposition to DiseaseMESH: Follow-Up StudiesMESH: Transcription FactorsMESH : Venous ThrombosisMESH: Case-Control StudiesDNA-Binding ProteinsChromosomes Human Pair 6MESH : DNA-Binding ProteinsErratumMESH : Genome-Wide Association StudyMESH : Case-Control StudiesMESH: Chromosomes Human Pair 6Locus (genetics)BiologyPolymorphism Single NucleotideGenetic determinism03 medical and health sciencesReportGenetic predispositionGeneticsHumansGenetic Predisposition to DiseaseAlleleGene030304 developmental biologyMESH: Humans[ SDV ] Life Sciences [q-bio]MESH : Humanslinking inflammation protein atherothrombosis sequence riskCase-control studyChromosomeMESH : Follow-Up StudiesCase-Control StudiesMESH: Genome-Wide Association StudyMESH: Venous ThrombosisMESH : Genetic Predisposition to Disease030217 neurology & neurosurgeryMESH: DNA-Binding ProteinsFollow-Up StudiesGenome-Wide Association StudyTranscription Factors
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Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate…

2008

Contains fulltext : 70192.pdf (Publisher’s version ) (Closed access) Attention deficit hyperactivity disorder (ADHD) is a complex condition with environmental and genetic etiologies. Up to this point, research has identified genetic associations with candidate genes from known biological pathways. In order to identify novel ADHD susceptibility genes, 600,000 SNPs were genotyped in 958 ADHD proband-parent trios. After applying data cleaning procedures we examined 429,981 autosomal SNPs in 909 family trios. We generated six quantitative phenotypes from 18 ADHD symptoms to be used in genome-wide association analyses. With the PBAT screening algorithm, we identified 2 SNPs, rs6565113 and rs5526…

MaleCandidate geneGenetics and epigenetic pathways of disease [NCMLS 6]2804 Cellular and Molecular NeuroscienceMedizinGenome-wide association studyNeuroinformatics [DCN 3]Genome2738 Psychiatry and Mental Health0302 clinical medicinePerception and Action [DCN 1]Cluster AnalysisGenetics(clinical)Genetics (clinical)Genetics0303 health sciences10058 Department of Child and Adolescent PsychiatryCadherinsPedigreePsychiatry and Mental healthFemaleFunctional Neurogenomics [DCN 2]CDH13AlgorithmsGenetic Markers2716 Genetics (clinical)GenotypeQuantitative Trait Loci610 Medicine & healthSingle-nucleotide polymorphismBiologyQuantitative trait locusPolymorphism Single NucleotideMental health [NCEBP 9]Genetic determinismGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceCognitive neurosciences [UMCN 3.2]medicineADHDAttention deficit hyperactivity disorderHumansGenetic Predisposition to Diseaseddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersGene030304 developmental biologyProbabilityModels GeneticGenome Humancandidate genefamily-based associationmedicine.diseaseIntronsHaplotypesGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivitygenome-wide association030217 neurology & neurosurgeryGenome-Wide Association StudyAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics
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Structural and functional characterization of a human IgG monoclonal antiphospholipid antibody

2009

Antiphospholipid antibodies (aPL) are likely involved in the pathogenesis of the antiphospholipid syndrome (APS). This study analyzes the structural and functional characteristics of a human monoclonal aPL (HL7G) from the IgG2 subtype with λ light chains generated from a patient with primary APS and recurrent cerebral microemboli. DNA encoding the variable region of heavy and light chains of the antibody was sequenced, analyzed, and compared to HL5B a previously described monoclonal aPL from the same patient. Both antibodies are derived from the same germline genes. HL7G had similar but more extensive somatic mutations in the CDR1 and 2 regions than HL5B, indicating that both antibodies are…

MaleCardiolipinsmedicine.drug_classImmunologySomatic hypermutationComplementarity determining regionMonoclonal antibodyImmunoglobulin light chainThromboplastinAntigenimmune system diseasesAntiphospholipid syndromemedicineHumansImmunology and AllergyneoplasmsCells CulturedMolecular StructurebiologyAntibodies MonoclonalT-Lymphocytes Helper-InducerHematologyMiddle AgedAntiphospholipid Syndromemedicine.diseaseComplementarity Determining RegionsMolecular biologybeta 2-Glycoprotein IImmunoglobulin GImmunologyMonoclonalAntibodies Antiphospholipidbiology.proteinSomatic Hypermutation ImmunoglobulinAntibodyImmunobiology
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Identical T-cell expansions in the colon mucosa and the synovium of a patient with enterogenic spondyloarthropathy.

2000

Abstract Intestinal T lymphocytes activated by antigen are suspected to play a key role in enterogenic spondyloarthropathies (SpA). Therefore, we aimed to identify and functionally characterize T-cell clones that are coexpanded in the intestinal mucosa and the synovium. Colon, peripheral blood, and synovium of a patient with enterogenic SpA were screened for clonal T-cell expansions by TCRB-CDR3 length analysis and sequencing. T-cell clones expanded in vivo were isolated from archived synovial cells by targeted T-cell cloning and characterized for phenotype, cytokine production, and antigen specificity. The synovial TCRBV18 + T-cell repertoire of the patient was dominated by 2 CD8 + T-cell …

MaleColonT cellReceptors Antigen T-Cell alpha-betaT-LymphocytesMolecular Sequence DataCD8-Positive T-LymphocytesPeripheral blood mononuclear cellAntigenIntestinal mucosaMedicineSynovial fluidHumansAmino Acid SequenceIntestinal MucosaHepatologybusiness.industryT-cell receptorSynovial MembraneGastroenterologyInterleukinMiddle AgedComplementarity Determining RegionsClone CellsIntestinal Diseasesmedicine.anatomical_structureImmunologyCytokinesATP-Binding Cassette TransportersSpinal DiseasesbusinessCD8T-Lymphocytes CytotoxicGastroenterology
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