Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia - Wikidata - wikimedia - TriplyDB

Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

http://www.wikidata.org/entity/Q24658441

about

Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses Structural cerebral variations as useful endophenotypes in schizophrenia: do they help construct "extended endophenotypes"?A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia DISC1: a key lead in studying cortical development and associated brain disorders Markers of vulnerability in schizophrenia DISC1-binding proteins in neural development, signalling and schizophrenia A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia Neuroanatomical and behavioral deficits in mice haploinsufficient for Pericentriolar material 1 (Pcm1).Hook3 interacts with PCM1 to regulate pericentriolar material assembly and the timing of neurogenesis Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases.Cognitive heterogeneity in schizophrenia.Pericentrin in cellular function and disease DISC1 and Huntington's disease--overlapping pathways of vulnerability to neurological disorder?The DISC1 Ser704Cys substitution affects centrosomal localization of its binding partner PCM1 in glia in human brain DISC1 in schizophrenia: genetic mouse models and human genomic imaging.Linking neurodevelopmental and synaptic theories of mental illness through DISC1 Variance decomposition of MRI-based covariance maps using genetically informative samples and structural equation modeling.Neuroplasticity signaling pathways linked to the pathophysiology of schizophrenia.The DAO gene is associated with schizophrenia and interacts with other genes in the Taiwan Han Chinese population.Orbitofrontal volume deficit in schizophrenia and thought disorder.Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.Genetic neuropathology of schizophrenia: new approaches to an old question and new uses for postmortem human brains Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia All in the mind? New molecular insights might bridge the gap between the effects of psychiatric therapy and drugs.Neurodevelopmental mechanisms of schizophrenia: understanding disturbed postnatal brain maturation through neuregulin-1-ErbB4 and DISC1.DISCopathies: brain disorders related to DISC1 dysfunction.A gene expression and systems pathway analysis of the effects of clozapine compared to haloperidol in the mouse brain implicates susceptibility genes for schizophrenia.The X-linked deubiquitinase USP9X is an integral component of centrosome.Microtubule and microtubule associated protein anomalies in psychiatric disease.Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration.DNA methylation signatures of peripheral leukocytes in schizophrenia.Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia.Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects.Linkage and association on 8p21.2-p21.1 in schizophrenia.

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Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

http://www.wikidata.org/entity/Q24658441

description

2006 nî lūn-bûn

@nan

2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի օգոստոսին հրատարակված գիտական հոդված

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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name

Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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Genetic association and brain ...... usceptibility to schizophrenia

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ARCHPSYC.63.8.844

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JAMA Psychiatry

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Genetic association and brain ...... usceptibility to schizophrenia

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Anil K Malhotra

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Catriona D Good

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Digby Quested

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Douglas Blackwood

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Ekaterina Blaveri

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Gursharan Kalsi

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Hugh M D Gurling

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Jacob Lawrence

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Jonathan Pimm

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Khalid Choudhury

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P2860

Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin

The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

Neuregulin 1 and susceptibility to schizophrenia.

Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit

Primer3 on the WWW for general users and for biologist programmers

Voxel-based morphometry--the methods

The human frizzled-3 (FZD3) gene on chromosome 8p21, a receptor gene for Wnt ligands, is associated with the susceptibility to schizophrenia

Thresholding of statistical maps in functional neuroimaging using the false discovery rate

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844-54

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scholarly article

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10.1001/ARCHPSYC.63.8.844

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8

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63

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Richard S. J. Frackowiak

Raymond Joseph Dolan

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Hugo D Critchley

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2006-08-01T00:00:00Z

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