about
Comparative, topographically-based evaluation of behavioural phenotype and specification of D(1)-like:D(2) interactions in a line of incipient congenic mice with D(2) dopamine receptor 'knockout'Phenotypic resolution of spontaneous and D1-like agonist-induced orofacial movement topographies in congenic dopamine D1A receptor 'knockout' miceGenetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers.Chronic adolescent exposure to Δ-9-tetrahydrocannabinol in COMT mutant mice: impact on psychosis-related and other phenotypes.Dysregulation of Specialized Delay/Interference-Dependent Working Memory Following Loss of Dysbindin-1A in Schizophrenia-Related Phenotypes.Phenotypic effects of maternal immune activation and early postnatal milieu in mice mutant for the schizophrenia risk gene neuregulin-1.Phenotypic effects of repeated psychosocial stress during adolescence in mice mutant for the schizophrenia risk gene neuregulin-1: a putative model of gene × environment interaction.Disruption of thermal nociceptive behaviour in mice mutant for the schizophrenia-associated genes NRG1, COMT and DISC1.Schizophrenia-related endophenotypes in heterozygous neuregulin-1 'knockout' mice.Physiological and behavioural responsivity to stress and anxiogenic stimuli in COMT-deficient mice.Phenotypic, ethologically based resolution of spontaneous and D(2)-like vs D(1)-like agonist-induced behavioural topography in mice with congenic D(3) dopamine receptor "knockout".Congenic D1A dopamine receptor mutants: ethologically based resolution of behavioural topography indicates genetic background as a determinant of knockout phenotype.Genetic diversity within the R408W phenylketonuria mutation lineages in Europe.Comparative phenotypic resolution of spontaneous, D2-like and D1-like agonist-induced orofacial movement topographies in congenic mutants with dopamine D2 vs. D3 receptor "knockout".Ethological resolution of behavioural topography and D1-like versus D2-like agonist responses in congenic D5 dopamine receptor mutants: identification of D5:D2-like interactions.Phenotype of spontaneous orofacial dyskinesia in neuregulin-1 'knockout' mice.Ethological resolution of behavioral topography and D2-like vs. D1-like agonist responses in congenic D4 dopamine receptor "knockouts": identification of D4:D1-like interactions.Altered cytokine profile, pain sensitivity, and stress responsivity in mice with co-disruption of the developmental genes Neuregulin-1×DISC1.Conservation of behavioural topography to dopamine D1-like receptor agonists in mutant mice lacking the D1A receptor implicates a D1-like receptor not coupled to adenylyl cyclase.Exploratory and habituation phenotype of heterozygous and homozygous COMT knockout mice.Phenotypic characterization of spatial cognition and social behavior in mice with 'knockout' of the schizophrenia risk gene neuregulin 1.Sexually dimorphic changes in the exploratory and habituation profiles of heterozygous neuregulin-1 knockout mice.Epistatic and Independent Effects on Schizophrenia-Related Phenotypes Following Co-disruption of the Risk Factors Neuregulin-1 × DISC1.Genetic vs. pharmacological inactivation of COMT influences cannabinoid-induced expression of schizophrenia-related phenotypes.Topographical evaluation of the phenotype of spontaneous behaviour in mice with targeted gene deletion of the D1A dopamine receptor: paradoxical elevation of grooming syntax.Confirmation That the Renin Gene Distal Enhancer Polymorphism REN -5312C/T Is Associated With Increased Blood PressureNational scientific medical meeting 1997 abstractsSeventeenth sir peter freyer memorial lecture and surgical symposiumIrish society of gastroenterology. Proceedings of meeting heldEthologically Based Resolution of D2-Like Dopamine Receptor Agonist-versus Antagonist-Induced Behavioral Topography in Dopamine- and Adenosine 3',5'-Monophosphate-Regulated Phosphoprotein of 32 kDa "Knockout" Mutants Congenic on the C57BL/6 Genetic BFrequency distribution of the Los Angeles and Duarte galactose-1-phosphate uridyltransferase variant alleles in the Irish populationIdentification of sequence variation in the galactose-1-phosphate uridyl transferase gene by dHPLCHypercholesterolaemia: simvastatin and pravastatin alter cholesterol metabolism by different mechanisms
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description
hulumtuese
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wetenschapper
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հետազոտող
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Orna Tighe
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Orna Tighe
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Orna Tighe
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Orna Tighe
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Orna Tighe
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type
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Orna Tighe
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Orna Tighe
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Orna Tighe
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Orna Tighe
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Orna Tighe
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P106
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0000-0003-0931-1254
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2000-01-01T00:00:00Z