Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
about
Analysis of four DLX homeobox genes in autistic probandsTranscriptional repression and DNA hypermethylation of a small set of ES cell marker genes in male germline stem cellsCTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardationA family of human zinc finger proteins that bind methylated DNA and repress transcriptionSpecific binding of the methyl binding domain protein 2 at the BRCA1-NBR2 locus.The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivatorRegulatory long non-coding RNAs and neuronal disordersMedicine. Activating a repressorBalanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitryCharacterization of conserved and nonconserved imprinted genes in swineReciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autismIntegrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genesThe odyssey of MeCP2 and parental imprintingDLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disordersComputational and experimental identification of novel human imprinted genesInhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndromeTpk3 and Snf1 protein kinases regulate Rgt1 association with Saccharomyces cerevisiae HXK2 promoterEpigenetic Effect of Environmental Factors on Autism Spectrum DisordersUnderstanding Spatial Genome Organization: Methods and InsightsRett Syndrome: Crossing the Threshold to Clinical TranslationMECP2 disorders: from the clinic to mice and backDNA modifications: function and applications in normal and disease StatesCytosine modifications in neurodevelopment and diseasesThe complex transcription regulatory landscape of our genome: control in three dimensionsFunctional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis DeformationBeta-globin LCR and intron elements cooperate and direct spatial reorganization for gene therapyDosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathiesMice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsySAFB1 mediates repression of immune regulators and apoptotic genes in breast cancer cellsImmunologic and neurodevelopmental susceptibilities of autismAssociation of modified cytosines and the methylated DNA-binding protein MeCP2 with distinctive structural domains of lampbrush chromatinMeet the neighbours: tools to dissect nuclear structure and functionAlzheimer's disease and environmental exposure to lead: the epidemiologic evidence and potential role of epigeneticsInteraction of MAGED1 with nuclear receptors affects circadian clock functionRett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressorAnalysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivoMetabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome modelGene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome
P2860
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P2860
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
description
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artikull shkencor
@sq
artículu científicu espublizáu en 2005
@ast
im Januar 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2005
@uk
مقالة علمية (نشرت عام 2005)
@ar
name
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@ast
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@en
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@nl
type
label
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@ast
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@en
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@nl
prefLabel
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@ast
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@en
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@nl
P2093
P2860
P921
P3181
P356
P1433
P1476
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
@en
P2093
Jan-Fang Cheng
Masaru Miyano
Shutao Cai
Terumi Kohwi-Shigematsu
P2860
P2888
P3181
P356
10.1038/NG1491
P407
P577
2005-01-01T00:00:00Z
P5875
P6179
1021284694