Search results for "FAK"

showing 10 items of 843 documents

Éléments d'analyse économique des faux diplômes

2007

Despite the fact that fake degrees have been used since the creation of legitimate diplomas, the fake degrees business is reaching epidemic proportions, notably because of globalization, new information and communication technologies and “diploma race”. We define the concept of fake degrees and distinguish different kinds of fakes. We also indicate the main functions of diplomas in the economic literature. We identify the supply and demand sides of the market of fake degrees and also consider other affected parties. We show that this growing business generates several negative spillovers that harm, among others, non traditional education institutions such as distance learning institutions a…

Faux diplômeFake degreeUniversities[SHS.EDU]Humanities and Social Sciences/Education[SHS.EDU] Humanities and Social Sciences/Educationfake degree diploma mills universities05 social sciences[ SHS.EDU ] Humanities and Social Sciences/EducationComputingMilieux_LEGALASPECTSOFCOMPUTING[SHS.ECO]Humanities and Social Sciences/Economics and Finance0502 economics and business[ SHS.ECO ] Humanities and Social Sciences/Economies and financesDiploma millsUniversités050207 economicsBusiness and International Management[SHS.ECO] Humanities and Social Sciences/Economics and FinanceUsines à diplômesLawGeneral Economics Econometrics and Finance050205 econometrics Revue internationale de droit économique
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Pēc sešiem mirkļiem 100 gadi : izstādes plakāti

2013

Izstāde, kas veltīta Latvijas Universitātes 94. gadadienai, atspoguļo informāciju par 18 LU Kultūras, Mākslas un Izglītības jaunrades biedrības "Juventus" mākslinieciskās pašdarbības kolektīviem.

Fizikas un matemātikas fakultātes jauktais koris "Aura"Bioloģijas fakultātes jauktais koris «DeCoro»Senās mūzikas ansamblis "Canto"LU Pūtēju orķestrisLU KamerorķestrisJauktais koris "Dziesmuvara"Vokālais ansamblis "Dancis"Deju kolektīvs «Dancītis»Jauktais koris "Juventus"Sieviešu koris «Latve»Tautas lietišķās mākslas studija «Vāpe»Folkloras deju kopa «Dandari»Sieviešu koris "Minjona"Vīru koris "Dziedonis"Prezidiju konventa vīru korisTautas deju ansamblis "Dancis"LU Studentu teātrisAbsolventu jauktais koris "Jubilate"
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Suomalaismiesten kognitiivisen kykyprofiilin muutokset 1988-2001 : Flynnin efektiä suomalaisessa aineistossa?

2007

Flynnin efektimiehetsuomalaisetkognitiivinen kykyprofiilig-faktori
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Attēlu fona modelēšanas algoritmi

2019

Datorredzes izpētes laukā ir sastopami dažādi izacinājumi, kas atstāj iespaidu uz fona modelēšanas algoritmu darbību. Piemēram, apgaismojuma maiņas, dinamisks fons un ēnas. Pie fona modelēšanas izaicinājumiem var pieskaītīt arī ar video filmēšanas tehniskajām grūtībām radītios izaicinājumus, pie kuriem pieder arī kompresijas artefakti. Taču, ir jāatzīmē, ka kompresijas artefaktu atstātāis efekts uz fona modelēšanas algoritmiem ir maz pētīts. Šī darba ietvaros tika pētīta kompresijas artefaktu atstātā ietekme uz dažiem fona modelēšanas algoritmiem. Izpētei tika izvēlēti divi algoritmi Mixture of Gaussians (MOG) un K-Nearest Neighbours (KNN), kas tika darbināti uz CDNET video datu kopas ar un…

Fona modelēšanas algoritmiDatorzinātneKompresijas artefaktiKNNMOGDatorredze
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LU Filoloģijas un filozofijas fakultātes bibliotēkas krājuma veidošanās pirmskara periodā

2017

The faculties of the humanities of the newly established University of Latvia had to create their libraries from the ground up, as opposed to the technical libraries who had partly preserved the stocks from the departments of the predecessor, the RPI. Books for the library of the Faculty of Philology and Philosophy were obtained through governmental allocations, purchases, and donations, and so it grew from 350 books in 1919 to more than 40 thousand in 1939. This article explores the first years of the formation of library holdings.

Formation of library holdingsIzdevumu ieguves avotiBook acquisitionFiloloģijas un filozofijas fakultātes bibliotēkaHistory of the University of LatviaLatvijas UniversitāteLibrary of the Faculty of Philology and PhilosophyBibliotēkas krājuma veidošanāsLatvijas Universitātes vēsture:SOCIAL SCIENCES::Other social sciences::Library and information science [Research Subject Categories]University of Latvia
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Information disorder. Learning to recognize fake news

2022

The advent of the internet and digital platforms has revolutionised the way information is produced and disseminated. The aim of this paper was to examine whether it is possible to draw from Article 21 of the Italian Constitution that there is a right to good information, as an expression of the rights to be informed and to receive information. It also looked at what form of regulation is possible for the dissemination of information on the Web in order to ensure that it is true, objective, and unbiased and whether public- only regulation, private- only regulation or a form of co- regulation, which seems to be model chosen in the EU’s draft Regulation, the so- called Digital Services Act, i…

Freedom of speech fake news digital platform regulationSettore IUS/08 - Diritto Costituzionale
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Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics stud…

2008

Contains fulltext : 71374.pdf (Publisher’s version ) (Closed access) Attention-deficit/hyperactivity disorder (ADHD) is typically characterized by inattention, excessive motor activity, impulsivity, and distractibility. Individuals with ADHD have significant impairment in family and peer relations, academic functioning, and show high co-morbidity with a wide range of psychiatric disorders including oppositional defiant disorder (ODD), conduct disorder (CD), anxiety disorder, depression, substance abuse, and pervasive developmental disorder (PDD). Family studies suggest that ADHD + CD represents a specific subtype of the ADHD disorder with familial risk factors only partly overlapping with t…

Genetics and epigenetic pathways of disease [NCMLS 6]2804 Cellular and Molecular NeuroscienceMedizinPoison controlComorbidityNeuroinformatics [DCN 3]Linkage DisequilibriumCohort Studies2738 Psychiatry and Mental Health0302 clinical medicinePerception and Action [DCN 1]Genetics(clinical)ChildGenetics (clinical)Oligonucleotide Array Sequence Analysis0303 health sciencesAntisocial Personality Disorder10058 Department of Child and Adolescent Psychiatry3. Good healthPedigreeEuropePsychiatry and Mental healthConduct disorderAttention Deficit and Disruptive Behavior DisordersADHD -- conduct disorder -- genome wide association study -- genetic association information networkmedicine.symptomPsychologyFunctional Neurogenomics [DCN 2]Anxiety disorderAlgorithmsClinical psychologyConduct DisorderGenetic Markers2716 Genetics (clinical)Quantitative Trait LociContext (language use)610 Medicine & healthChild Behavior DisordersImpulsivityPolymorphism Single NucleotideMental health [NCEBP 9]behavioral disciplines and activitiesGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceCognitive neurosciences [UMCN 3.2]mental disordersmedicinePervasive developmental disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und Jugendalters030304 developmental biologyPsychiatric Status Rating ScalesGenome HumanAntisocial personality disordermedicine.diseaseComorbidityGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivity030217 neurology & neurosurgeryGenome-Wide Association Study
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Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

2008

Contains fulltext : 69243.pdf (Publisher’s version ) (Closed access) Genetic contribution to the development of attention deficit hyperactivity disorder (ADHD) is well established. Seven independent genome-wide linkage scans have been performed to map loci that increase the risk for ADHD. Although significant linkage signals were identified in some of the studies, there has been limited replications between the various independent datasets. The current study gathered the results from all seven of the ADHD linkage scans and performed a Genome Scan Meta Analysis (GSMA) to identify the genomic region with most consistent linkage evidence across the studies. Genome-wide significant linkage (P(S…

Genetics and epigenetic pathways of disease [NCMLS 6]Genetic LinkageEuropean Continental Ancestry GroupMedizinGenome ScanBiologyNeuroinformatics [DCN 3]Mental health [NCEBP 9]Genetic determinismWhite PeopleArticleChromosomesGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineGene mappingCognitive neurosciences [UMCN 3.2]Genetic linkageGenetic predispositionmedicinePerception and Action [DCN 1]Attention deficit hyperactivity disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersGenetics (clinical)030304 developmental biologyProbabilityLinkage (software)Genetics0303 health sciencesGenomeGenome HumanPair 16Chromosome Mappingmedicine.diseasePsychiatry and Mental healthGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityMeta-analysisLod ScoreFunctional Neurogenomics [DCN 2]030217 neurology & neurosurgeryChromosomes Human Pair 16HumanAmerican Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
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No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.

2008

Contains fulltext : 71091.pdf (Publisher’s version ) (Closed access) Several independent studies have reported association between serotonin transporter gene (SLC6A4) polymorphisms and attention deficit hyperactivity disorder (ADHD). Five studies found evidence for association between the long-allele of a 44-bp insertion/deletion polymorphism (5-HTTLPR) and ADHD. Another two studies corroborated this finding while a further six studies did not find such an association. For a second polymorphism within the gene, a variable number tandem repeat (VNTR) within intron 2, one study demonstrated that the 12/12 genotype was significantly less frequent in ADHD cases compared to controls, while a sec…

Genetics and epigenetic pathways of disease [NCMLS 6]MedizinNeuroinformatics [DCN 3]0302 clinical medicinePolymorphism (computer science)GenotypePerception and Action [DCN 1]Childhealth care economics and organizationsSerotonin transporterGenetics (clinical)GeneticsSerotonin Plasma Membrane Transport Proteins0303 health sciencesDepression030305 genetics & heredityTransmission disequilibrium testhumanitiesVariable number tandem repeatPsychiatry and Mental healthChild Preschool/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingFunctional Neurogenomics [DCN 2]medicine.medical_specialtyAdolescenteducationBiologybehavioral disciplines and activitiesMental health [NCEBP 9]Genomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceSDG 3 - Good Health and Well-beingCognitive neurosciences [UMCN 3.2]Internal medicinemental disordersmedicineAttention deficit hyperactivity disorderHumansGenetic Predisposition to Diseaseddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersAssociation (psychology)Gene030304 developmental biologyFamily HealthPolymorphism Geneticbusiness.industryMood Disordersmedicine.diseaseMoodEndocrinologyMood disordersGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivitybiology.proteinbusiness030217 neurology & neurosurgery
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Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.

2014

Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with breast cancer risk. To clarify the role of CASP8 in breast cancer susceptibility, we carried out dense genotyping of this region in the Breast Cancer Association Consortium (BCAC). Single-nucleotide polymorphisms (SNPs) spanning a 1 Mb region around CASP8 were genotyped in 46 450 breast cancer cases and 42 600 controls of European origin from 41 studies participating in the BCAC as part of a custom genotyping array experiment (iCOGS). Missing genotypes and SNPs were imputed and, after quality exclusions, 501 typed and 1232 imputed SNPs were included in logistic regressionmodels adjusting for stud…

Genotyping TechniquesResearch Support U.S. Gov't P.H.S.CASP8 and FADD-Like Apoptosis Regulating ProteinGenome-wide association studyP.H.S.Medical and Health SciencesBreast and Ovarian Cancer Susceptibility (BOCS) StudyMedizinische FakultätGenetics(clinical)Non-U.S. Gov'tGenetics (clinical)GeneticsGenetics & HeredityvariantsCaspase 8Research Support Non-U.S. Gov'tAssociation Studies ArticlesGeneral MedicineBiological Sciencesddc:Chromosomes Human Pair 2kConFab InvestigatorsFemaleGENICA NetworkAustralian Ovarian Cancer Study GroupEuropean Continental Ancestry GroupNon-P.H.S.Single-nucleotide polymorphismBreast Neoplasms-BiologyResearch SupportPolymorphism Single NucleotideWhite PeopleN.I.H.Breast cancerResearch Support N.I.H. ExtramuralSDG 3 - Good Health and Well-beingmedicineGeneticsJournal ArticleHumansGenetic Predisposition to Diseaseddc:610geneGenotyping TechniquesGenotypingMolecular BiologyGenetic associationdiseaseExtramuralProteinsOdds ratiomedicine.diseasesusceptibility lociMinor allele frequencyCase-Control Studiesgenome-wide associationenhancersU.S. Gov'tcasp8Research Support U.S. Gov't Non-P.H.S.Genome-Wide Association Study
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