Cloning of a retinoic acid-induced gene, GT1, in the embryonal carcinoma cell line P19: neuron-specific expression in the mouse brain.
about
The nuclear factor SPBP contains different functional domains and stimulates the activity of various transcriptional activatorsThe ePHD protein SPBP interacts with TopBP1 and together they co-operate to stimulate Ets1-mediated transcriptionGenes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mousePenetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alikeInteraction between the transcription factor SPBP and the positive cofactor RNF4. An interplay between protein binding zinc fingersFunctional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis SyndromeMouse gene trap approach: identification of novel genes and characterization of their biological functions.Rai1 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 BehaviorIntegrated module and gene-specific regulatory inference implicates upstream signaling networksExpression 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.Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brainFailure of neuronal homeostasis results in common neuropsychiatric phenotypes.Smith-Magenis syndrome: haploinsufficiency of RAI1 results in altered gene regulation in neurological and metabolic pathways.Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions.Modeling human craniofacial disorders in Xenopus.A functional role for structural variation in metabolism.How much is too much? Phenotypic consequences of Rai1 overexpression in mice.RAI1 gene mutations: mechanisms of Smith-Magenis syndrome.Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.
P2860
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P2860
Cloning of a retinoic acid-induced gene, GT1, in the embryonal carcinoma cell line P19: neuron-specific expression in the mouse brain.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@ast
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@en
type
label
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@ast
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@en
prefLabel
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@ast
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@en
P2093
P1476
Cloning of a retinoic acid-ind ...... expression in the mouse brain.
@en
P2093
P356
10.1016/0169-328X(95)00020-S
P577
1995-07-01T00:00:00Z