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Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotypingMapping the new frontier: complex genetic disorders.Kynurenine 3-monooxygenase polymorphisms: relevance for kynurenic acid synthesis in patients with schizophrenia and healthy controlsCircuit-based framework for understanding neurotransmitter and risk gene interactions in schizophreniaAssociation of Huntington's disease and schizophrenia-like psychosis in a Huntington's disease pedigree.Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome.Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes.Association analyses of the interaction between the ADSS and ATM genes with schizophrenia in a Chinese population.In vivo magnetic resonance studies reveal neuroanatomical and neurochemical abnormalities in the serine racemase knockout mouse model of schizophrenia.The myelin-pathogenesis puzzle in schizophrenia: a literature review.Genomic convergence analysis of schizophrenia: mRNA sequencing reveals altered synaptic vesicular transport in post-mortem cerebellum.Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients.A MicroRNA gene is hosted in an intron of a schizophrenia-susceptibility gene.Mean diffusivity and fractional anisotropy as indicators of disease and genetic liability to schizophreniaInfluence of CYP2D6 polymorphisms on symptomatology and side-effects of patients with schizophrenia in MalaysiaC677T Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphism in Schizophrenia and Bipolar Disorder: An Association Study in Iranian PopulationClinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular eraAn association study of ADSS gene polymorphisms with schizophrenia.Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia.SNAP-25 in neuropsychiatric disorders.Toward dissecting the etiology of schizophrenia: HDAC1 and DAXX regulate GAD67 expression in an in vitro hippocampal GABA neuron model.Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophreniaAccept or refuse? A pilot study of patients' perspective on participating as imaginary research subjects in schizophrenia.A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.A brief review on recent developments in animal models of schizophreniaAn environmental analysis of genes associated with schizophrenia: hypoxia and vascular factors as interacting elements in the neurodevelopmental model.The peroxisome: an update on mysteries.Improving myelin/oligodendrocyte-related dysfunction: a new mechanism of antipsychotics in the treatment of schizophrenia?Evidence of aberrant DNA damage response signalling but normal rates of DNA repair in dividing lymphoblasts from patients with schizophrenia.Association between upstream purine complexes of human caveolin-1 gene and schizophrenia in qazvin province of iran.Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia.Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality.Functional -141C Ins/Del polymorphism in the dopamine D2 receptor gene promoter and schizophrenia in a Chinese Han population.Relationships between exploratory eye movement dysfunction and clinical symptoms in schizophrenia.Psychiatric endophenotypes and the development of valid animal models.Volume, neuron density and total neuron number in five subcortical regions in schizophrenia.Impairment of exploratory eye movement in schizophrenia patients and their siblings.Association study of H2AFZ with schizophrenia in a Japanese case-control sample.Association study between BDNF C-281A polymorphism and paranoid schizophrenia in Polish population.Case history and genome-wide scans for copy number variants in a family with patient having 15q11.1-q11.2 duplication and 22q11.2 deletion, and schizophrenia.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
name
Finding schizophrenia genes.
@ast
Finding schizophrenia genes.
@en
type
label
Finding schizophrenia genes.
@ast
Finding schizophrenia genes.
@en
prefLabel
Finding schizophrenia genes.
@ast
Finding schizophrenia genes.
@en
P2860
P356
P1476
Finding schizophrenia genes.
@en
P2093
Michael J Owen
P2860
P304
P356
10.1172/JCI24759
P407
P577
2005-06-01T00:00:00Z