Cargando…

Population-Specific Haplotype Association of the Postsynaptic Density Gene DLG4 with Schizophrenia, in Family-Based Association Studies

The post-synaptic density (PSD) of glutamatergic synapses harbors a multitude of proteins critical for maintaining synaptic dynamics. Alteration of protein expression levels in this matrix is a marked phenomenon of neuropsychiatric disorders including schizophrenia, where cognitive functions are imp...

Descripción completa

Detalles Bibliográficos
Autores principales:	Balan, Shabeesh, Yamada, Kazuo, Hattori, Eiji, Iwayama, Yoshimi, Toyota, Tomoko, Ohnishi, Tetsuo, Maekawa, Motoko, Toyoshima, Manabu, Iwata, Yasuhide, Suzuki, Katsuaki, Kikuchi, Mitsuru, Yoshikawa, Takeo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723755/ https://www.ncbi.nlm.nih.gov/pubmed/23936182 http://dx.doi.org/10.1371/journal.pone.0070302

Ejemplares similares

Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects
por: Balan, Shabeesh, et al.
Publicado: (2014)

Lipid Pathology of the Corpus Callosum in Schizophrenia and the Potential Role of Abnormal Gene Regulatory Networks with Reduced Microglial Marker Expression
por: Shimamoto-Mitsuyama, Chie, et al.
Publicado: (2020)

Genome-Wide Association Study of Schizophrenia in Japanese Population
por: Yamada, Kazuo, et al.
Publicado: (2011)

Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population
por: Yamada, Kazuo, et al.
Publicado: (2011)

Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism
por: Maekawa, Motoko, et al.
Publicado: (2016)

Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism
por: Maekawa, Motoko, et al.
Publicado: (2015)

Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia
por: Balan, Shabeesh, et al.
Publicado: (2021)

Peroxisome proliferator-activated receptor α as a novel therapeutic target for schizophrenia
por: Wada, Yuina, et al.
Publicado: (2020)

A potential role of fatty acid binding protein 4 in the pathophysiology of autism spectrum disorder
por: Maekawa, Motoko, et al.
Publicado: (2020)

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies
por: Shimamoto, Chie, et al.
Publicado: (2015)

Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies
por: Shimamoto, Chie, et al.
Publicado: (2014)

Giant Subependymoma Developed in a Patient with Aniridia: Analyses of PAX6 and Tumor‐relevant Genes
por: Maekawa, Motoko, et al.
Publicado: (2010)

Enhanced carbonyl stress induces irreversible multimerization of CRMP2 in schizophrenia pathogenesis
por: Toyoshima, Manabu, et al.
Publicado: (2019)

Glyoxalase I disruption and external carbonyl stress impair mitochondrial function in human induced pluripotent stem cells and derived neurons
por: Hara, Tomonori, et al.
Publicado: (2021)

Evidence for Altered Metabolism of Sphingosine-1-Phosphate in the Corpus Callosum of Patients with Schizophrenia
por: Esaki, Kayoko, et al.
Publicado: (2020)

Ablation of Mrds1/Ofcc1 Induces Hyper-γ-Glutamyl Transpeptidasemia without Abnormal Head Development and Schizophrenia-Relevant Behaviors in Mice
por: Ohnishi, Tetsuo, et al.
Publicado: (2011)

Association and synergistic interaction between promoter variants of the DRD4 gene in Japanese schizophrenics
por: Nakajima, Mizuho, et al.
Publicado: (2006)

Investigation of betaine as a novel psychotherapeutic for schizophrenia
por: Ohnishi, Tetsuo, et al.
Publicado: (2019)

Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population
por: Kobayashi, Momoko, et al.
Publicado: (2018)

Association of Transcription Factor Gene LMX1B with Autism
por: Thanseem, Ismail, et al.
Publicado: (2011)

Cooperation of LIM domain‐binding 2 (LDB2) with EGR in the pathogenesis of schizophrenia
por: Ohnishi, Tetsuo, et al.
Publicado: (2021)

Fabp7 Maps to a Quantitative Trait Locus for a Schizophrenia Endophenotype
por: Watanabe, Akiko, et al.
Publicado: (2007)

LDB2 locus disruption on 4p16.1 as a risk factor for schizophrenia and bipolar disorder
por: Horiuchi, Yasue, et al.
Publicado: (2020)

VLDL-specific increases of fatty acids in autism spectrum disorder correlate with social interaction
por: Usui, Noriyoshi, et al.
Publicado: (2020)

Genetic Variants on 3q21 and in the Sp8 Transcription Factor Gene (SP8) as Susceptibility Loci for Psychotic Disorders: A Genetic Association Study
por: Kondo, Kenji, et al.
Publicado: (2013)

Discs-large (DLG) is clustered by presynaptic innervation and regulates postsynaptic glutamate receptor subunit composition in Drosophila
por: Chen, Kaiyun, et al.
Publicado: (2005)

Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology
por: Ide, Masayuki, et al.
Publicado: (2019)

Brain region-specific altered expression and association of mitochondria-related genes in autism
por: Anitha, Ayyappan, et al.
Publicado: (2012)

Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
por: Matsuura, Akiko, et al.
Publicado: (2018)

Analysis of induced pluripotent stem cells carrying 22q11.2 deletion
por: Toyoshima, M, et al.
Publicado: (2016)

Age-Dependent Effects of Catechol-O-Methyltransferase (COMT) Gene Val(158)Met Polymorphism on Language Function in Developing Children
por: Sugiura, Lisa, et al.
Publicado: (2017)

Reduced cortical expression of a newly identified splicing variant of the DLG1 gene in patients with early-onset schizophrenia
por: Uezato, A, et al.
Publicado: (2015)

Polyunsaturated fatty acid deficiency during neurodevelopment in mice models the prodromal state of schizophrenia through epigenetic changes in nuclear receptor genes
por: Maekawa, M, et al.
Publicado: (2017)

Zic2 hypomorphic mutant mice as a schizophrenia model and ZIC2 mutations identified in schizophrenia patients
por: Hatayama, Minoru, et al.
Publicado: (2011)

Characterizing the Binding Sites for GK Domain of DLG1 and DLG4 via Molecular Dynamics Simulation
por: Li, Hongwei, et al.
Publicado: (2020)

DLG2 variants in patients with pubertal disorders
por: Jee, Youn Hee, et al.
Publicado: (2020)

A closer look at the synapse: dlg1[4K] enables cell-specific visualization of PSD-95/DLG1
por: Hendricks, Emily L., et al.
Publicado: (2023)

Autism-like behaviours and enhanced memory formation and synaptic plasticity in Lrfn2/SALM1-deficient mice
por: Morimura, Naoko, et al.
Publicado: (2017)

Discs large (Dlg1) complexes in lymphocyte activation
por: Xavier, Ramnik, et al.
Publicado: (2004)

DLG5 in Cell Polarity Maintenance and Cancer Development
por: Liu, Jie, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_uuf00v51dssfl00ajtrg953rm2