Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2002-2-12
pubmed:abstractText
Because retinoid cascades are involved in the regulation and development of the central nervous system, including dopaminergic neurons, retinoic acid signaling defects may contribute to schizophrenia and substances dependence. Retinoid X receptors (RXRs) form heterodimer complexes with nuclear-related receptor 1 (NURR1) or with peroxisome proliferator-activated receptors (PPARs). We examined 48 Japanese patients with schizophrenia and 32 patients with alcohol dependence to detect mutations in the retinoid X receptor beta gene (RXRB) on chromosome 6p21.3, the NURR1 gene (NR4A2) on chromosome 2q22-q23, and the PPAR alpha gene (PPARA) on chromosome 22q12.2-13.1. A Val95Ala polymorphism of the RXRB gene, a Val227Ala polymorphism in the PPARA gene, and two synonymous single-nucleotide and CA repeat polymorphisms in the 5' region and 3' untranslated region of the NR4A2 gene were identified. Extended case control samples did not suggest an association between the diseases and the RXRB or PPARA polymorphisms. However, they revealed a significant association between the NR4A2 gene haplotype and alcohol dependence, indicating that 2q22-q23 including the NR4A2 gene locus is a possible genomic region contributing to genetic susceptibility to alcohol dependence.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0148-7299
pubmed:author
pubmed:copyrightInfo
Copyright 2001 Wiley-Liss, Inc.
pubmed:issnType
Print
pubmed:day
8
pubmed:volume
114
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
15-23
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11840500-Adolescent, pubmed-meshheading:11840500-Adult, pubmed-meshheading:11840500-Aged, pubmed-meshheading:11840500-Aged, 80 and over, pubmed-meshheading:11840500-Alcoholism, pubmed-meshheading:11840500-Child, pubmed-meshheading:11840500-DNA-Binding Proteins, pubmed-meshheading:11840500-Female, pubmed-meshheading:11840500-Genetic Predisposition to Disease, pubmed-meshheading:11840500-Haplotypes, pubmed-meshheading:11840500-Humans, pubmed-meshheading:11840500-Japan, pubmed-meshheading:11840500-Male, pubmed-meshheading:11840500-Middle Aged, pubmed-meshheading:11840500-Mutation, pubmed-meshheading:11840500-Mutation, Missense, pubmed-meshheading:11840500-Nuclear Receptor Subfamily 4, Group A, Member 2, pubmed-meshheading:11840500-Polymorphism, Genetic, pubmed-meshheading:11840500-Receptors, Cytoplasmic and Nuclear, pubmed-meshheading:11840500-Receptors, Retinoic Acid, pubmed-meshheading:11840500-Retinoid X Receptors, pubmed-meshheading:11840500-Schizophrenia, pubmed-meshheading:11840500-Transcription Factors
pubmed:year
2002
pubmed:articleTitle
Mutation analysis of the retinoid X receptor beta, nuclear-related receptor 1, and peroxisome proliferator-activated receptor alpha genes in schizophrenia and alcohol dependence: possible haplotype association of nuclear-related receptor 1 gene to alcohol dependence.
pubmed:affiliation
Department of Medical Genetics, Institute of Basic Medical Science, University of Tsukuba, Ibaraki, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't