Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.
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Epigenomic profiling reveals DNA-methylation changes associated with major psychosisThe ePHD protein SPBP interacts with TopBP1 and together they co-operate to stimulate Ets1-mediated transcriptionActin binding proteins in blood-testis barrier functionPhenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse modelsSmith-Magenis syndromePenetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alikeFunctional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis SyndromeRai1 frees mice from the repression of active wake behaviors by light.Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith-Magenis syndrome without the 17p11.2 deletion.Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic BehaviorRAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome.Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome.A phylogenetic study of SPBP and RAI1: evolutionary conservation of chromatin binding modules.Expression in the human brain of retinoic acid induced 1, a protein associated with neurobehavioural disorders.RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions.Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith-Magenis syndrome.Pharmacogenomics of multigenic diseases: sex-specific differences in disease and treatment outcome.Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).Behavioral disturbance and treatment strategies in Smith-Magenis syndromeEvidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brainRAI14 (retinoic acid induced protein 14) is an F-actin regulator: Lesson from the testis.Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions.Yin-yang actions of histone methylation regulatory complexes in the brain.Increased expression of retinoic acid-induced gene 1 in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation.A chicken ovalbumin upstream promoter transcription factor I (COUP-TFI) complex represses expression of the gene encoding tumor necrosis factor alpha-induced protein 8 (TNFAIP8).Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome.How much is too much? Phenotypic consequences of Rai1 overexpression in mice.RAI1 gene mutations: mechanisms of Smith-Magenis syndrome.Identification of two independent nucleosome-binding domains in the transcriptional co-activator SPBP
P2860
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P2860
Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
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2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Molecular cloning and characte ...... associated with schizophrenia.
@en
Molecular cloning and characte ...... associated with schizophrenia.
@nl
type
label
Molecular cloning and characte ...... associated with schizophrenia.
@en
Molecular cloning and characte ...... associated with schizophrenia.
@nl
prefLabel
Molecular cloning and characte ...... associated with schizophrenia.
@en
Molecular cloning and characte ...... associated with schizophrenia.
@nl
P2093
P1433
P1476
Molecular cloning and characte ...... associated with schizophrenia.
@en
P2093
Daniel Rochefort
Julie Roussel
Ridha Joober
P304
P356
10.1016/S0888-7543(03)00101-0
P577
2003-08-01T00:00:00Z