Search results for " LV"

showing 10 items of 85 documents

Genome-wide association scan of attention deficit hyperactivity disorder

2008

Contains fulltext : 70191.pdf (Publisher’s version ) (Closed access) Results of behavioral genetic and molecular genetic studies have converged to suggest that genes substantially contribute to the development of attention deficit/hyperactivity disorder (ADHD), a common disorder with an onset in childhood. Yet, despite numerous linkage and candidate gene studies, strongly consistent and replicable association has eluded detection. To search for ADHD susceptibility genes, we genotyped approximately 600,000 SNPs in 958 ADHD affected family trios. After cleaning the data, we analyzed 438,784 SNPs in 2,803 individuals comprising 909 complete trios using ADHD diagnosis as phenotype. We present t…

Candidate geneLinkage disequilibriumGenetics and epigenetic pathways of disease [NCMLS 6]Medizin2804 Cellular and Molecular NeuroscienceGenome-wide association studyNeuroinformatics [DCN 3]Linkage Disequilibrium2738 Psychiatry and Mental Health0302 clinical medicinePerception and Action [DCN 1]Genetics(clinical)ChildGenetics (clinical)Genetics0303 health sciencesHomozygote10058 Department of Child and Adolescent PsychiatrySNP genotypingPsychiatry and Mental healthChild PreschoolData Interpretation Statistical/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingFunctional Neurogenomics [DCN 2]Algorithms2716 Genetics (clinical)AdolescentSingle-nucleotide polymorphism610 Medicine & healthBiologyMental health [NCEBP 9]Polymorphism Single NucleotideGenetic determinismArticleGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceCognitive neurosciences [UMCN 3.2]SDG 3 - Good Health and Well-beingmedicineSNPAttention deficit hyperactivity disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersAlleles030304 developmental biologyGenome Humanmedicine.diseaseGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with HyperactivityCase-Control Studies030217 neurology & neurosurgeryGenome-Wide Association Study
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Association between DRD2/DRD4 interaction and conduct disorder: a potential developmental pathway to alcohol dependence

2013

1 Department of Genetics, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil 2 King’s College London, Institute of Psychiatry, MRC Social Genetic and Developmental Psychiatry Centre, London, United Kingdom, UK 3 Department of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany 4 Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands 5 Psychology Department, National University of Singapore, Singapore, Singapore 6 Department of Psychiatry, Donders Institute for Brain, Cognition an…

Conduct DisorderMalemedicine.medical_specialty2716 Genetics (clinical)AdolescentMedizin2804 Cellular and Molecular Neuroscience610 Medicine & healthComorbidityGenomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3]03 medical and health sciencesCellular and Molecular Neuroscience2738 Psychiatry and Mental Health0302 clinical medicineChild and adolescent psychiatrymedicineHumansddc:61Psychiatric hospitalddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersSociologyDCN PAC - Perception action and control NCEBP 9 - Mental healthChildGenetics (clinical)030304 developmental biology0303 health sciencesPolymorphism GeneticReceptors Dopamine D2Receptors Dopamine D4Alcohol dependenceEducational psychologyGenomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3]10058 Department of Child and Adolescent PsychiatryPrognosismedicine.diseaseMental healthhumanities3. Good healthAlcoholismPsychiatry and Mental healthClinical neuropsychologyHealth psychologyConduct disorderFamily medicineFemale030217 neurology & neurosurgery
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A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and sibli…

2011

Item does not contain fulltext BACKGROUND: Impulsive drive for immediate reward (IDIR) and delay aversion are dissociable elements of the preference for immediate over delayed rewards seen in attention-deficit/hyperactivity disorder (ADHD). We hypothesized that IDIR would be associated with dopamine regulating genes and delay aversion would be associated with serotonin-regulating genes. METHODS: Impulsive drive for immediate reward and delay aversion were measured in 459 male children and adolescents (328 ADHD and 131 unaffected siblings) with a laboratory choice task. The sample was genotyped for the 5HTT (SLC6A4) promoter serotonin-transporter-linked polymorphic region polymorphism and a …

DEFICIT HYPERACTIVITY DISORDERMedizinSocial Sciencesimpulsivity610 Medicine & healthCHILDRENSingle-nucleotide polymorphismGenomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3]attention-deficit/hyperactivity disorderImpulsivityCOMBINED-TYPE ADHDREACTION-TIME PERFORMANCEDevelopmental psychologyGenomic disorders and inherited multi-system disorders [IGMD 3]DOPAMINE03 medical and health sciences0302 clinical medicineDopaminemedicineAttention deficit hyperactivity disorderddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersAlleleBiological PsychiatrySerotonin transporter030304 developmental biologyDopamine transporterGeneticsMental Health [NCEBP 9]0303 health sciencesDELAY AVERSIONbiologyTRYPTOPHAN DEPLETIONASSOCIATION10058 Department of Child and Adolescent Psychiatrymedicine.diseasePOLYMORPHISM5-HTTLPR (SLC6A4)5-HTTLPRbiology.proteinCRITERION VALIDITYmedicine.symptomDAT1 (SLC6A3)Psychology2803 Biological PsychiatryFunctional Neurogenomics [DCN 2]030217 neurology & neurosurgerymedicine.drugBiological Psychiatry
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On the terminology of voice research

1993

Summary This article reviews problems associated with establishment of a scientifically accurate, internationally recognized, multilingual terminology to describe voice. Two strategies for developing terminology are discussed: consensus and dictation. Ontological decisions are considered an integral part of developing terminology. We conclude that terminological problems should be solved by a terminological committee—as yet to be established—as they average from problems in interpreting the literature and the results of voice research. A comprehensive bibliography and audio tape of the multilingual terminology describing voice would help facilitate adaptation and understanding of the terms …

DictationComputer sciencebusiness.industrycomputer.software_genreLPN and LVNLinguisticsTerminologySpeech and HearingOtorhinolaryngologyArtificial intelligenceAudio tapeAdaptation (computer science)businessPsychologyGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)computerNatural language processingJournal of Voice
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Influence of LV neutral grounding on global earthing systems

2015

International Standards define a Global Earthing System as an earthing net created interconnecting local Earthing Systems (generally through the shield of MV cables and/or bare buried conductors). In Italy, the regulatory authority for electricity and gas requires distributors to guarantee the electrical continuity of LV neutral conductor. This requirement has led to the standard practice of realizing “reinforcement groundings” along the LV neutral conductor path and at users’ delivery cabinet. Moreover, in urban high-load scenarios (prime candidates to be part of a Global Earthing System), it is common that LV distribution scheme creates, through neutral conductors, an effective connection…

Engineeringelectrical and electronic engineeringmaxwell subareas method020209 energyEnergy Engineering and Power TechnologyGround and neutralindustrial and manufacturing engineering02 engineering and technologyRegulatory authorityGlobal earthing system (GES) global grounding system (GGS) ground potential LV neutral conductor maxwell subareas method.control and systems engineeringlv neutral conductorShield0202 electrical engineering electronic engineering information engineeringglobal earthing systemmaxwell sub-areas methodGlobal earthing system (GES)Electrical conductorglobal grounding system (GGS)Groundbusiness.industryGES; GGS; global earthing system; global grounding system; ground potential; lv neutral conductor; maxwell sub-areas method; control and systems engineering; industrial and manufacturing engineering; electrical and electronic engineeringElectrical engineeringGlobal Earting SystemGESglobal grounding systemground potentialEarthing systemGGSGlobal earthing system (GES); global grounding system (GGS); ground potential; LV neutral conductor; maxwell subareas method; Control and Systems Engineering; Industrial and Manufacturing Engineering; Electrical and Electronic EngineeringSettore ING-IND/33 - Sistemi Elettrici Per L'EnergiaSettore ING-IND/31 - ElettrotecnicaGlobal Earting System; GES; Global Grounding System; GGS; Ground potential; Maxwell Sub-areas Method; LV neutral conductorHigh loadElectricityGES; GGS; Global earting system; global grounding system; ground potential; lv neutral conductor; maxwell sub-areas method; electrical and electronic engineering; energy engineering and power technologybusiness
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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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Politiskās partijas "KPV LV" priekšvēlēšanu kampaņa 13. Saeimas vēlēšanās - sociālo tīklu analīze

2019

Bakalaura darba tēma ir "Politiskās partijas "KPV LV" priekšvēlēšanu kampaņa 13. Saeimas vēlēšanās - sociālo tīklu analīze". Darba mērķis ir izpētīt, kādus vēstījumus izmanto populistu partija "KPV LV" savā priekšvēlēšanu kampaņā sociālajos tīklos un kā šie vēstījumi ir ietekmējuši vēlēšanu rezultātus. Darba teorētisko pamatu veido jēdziena "populisms" izpēte un teorijas par priekšvēlēšanu kampaņām. Empīriskajā daļā tiek analizēti partiju līderu sociālo tīklu profili, izmantojot kontentanalīzes metodi. Autore secina, ka partijas kandidāti galvenokārt kampaņā ir izmantojuši emocionālus vēstījumus, tomēr nepastāv korelācija starp publicēto emocionālo ierakstu daudzumu skaitu un iegūto balsu s…

KPV LVpopulismspriekšvēlēšanu kampaņasPolitikas zinātnesociālie mediji
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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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