DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency - Test2 - elhamkhani - TriplyDB

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

http://www.wikidata.org/entity/Q24677959

about

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice Balanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitry Characterization of conserved and nonconserved imprinted genes in swine Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes.Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines.Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin looping Split hand/foot malformation due to chromosome 7q aberrations(SHFM1): additional support for functional haploinsufficiency as the causative mechanism.Molecular signatures of cardiac defects in Down syndrome lymphoblastoid cell lines suggest altered ciliome and Hedgehog pathways.Binding of the Rett syndrome protein, MeCP2, to methylated and unmethylated DNA and chromatin.DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex.Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing.MECP2 genomic structure and function: insights from ENCODE The MBD protein family-reading an epigenetic mark?Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.DNA methylation and methyl-CpG binding proteins: developmental requirements and function.Evolving role of MeCP2 in Rett syndrome and autism.Genetic and epigenetic dysregulation of imprinted genes in the brain.Epigenetics and brain evolution.An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain.MECP2, a multi-talented modulator of chromatin architecture.Spatial genome organization and cognition.Functional assessment of MeCP2 in Rett syndrome and cancers of breast, colon, and prostate.Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.MeCP2, A Modulator of Neuronal Chromatin Organization Involved in Rett Syndrome.

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P2860

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

http://www.wikidata.org/entity/Q24677959

description

2007 nî lūn-bûn

@nan

2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@ast

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@en

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@nl

type

label

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@ast

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@en

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@nl

prefLabel

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@ast

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@en

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@nl

P1433

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P1433

American Journal of Human Genetics

P1476

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

@en

P2093

Birgitt Schüle

http://www.w3.org/2001/XMLSchema#string

Carolin Purmann

http://www.w3.org/2001/XMLSchema#string

Claudia Fisch-Kohl

http://www.w3.org/2001/XMLSchema#string

Hong Hua Li

http://www.w3.org/2001/XMLSchema#string

Uta Francke

http://www.w3.org/2001/XMLSchema#string

P2860

Analysis of four DLX homeobox genes in autistic probands

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia

Identification of a direct Dlx homeodomain target in the developing mouse forebrain and retina by optimization of chromatin immunoprecipitation

Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation

The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted

A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21

Developmental functions of the Distal-less/Dlx homeobox genes

P304

492-506

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scholarly article

P356

10.1086/520063

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P433

3

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81

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2007-09-01T00:00:00Z

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6137669

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17701895

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1950824

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