Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome (Q35200175)

7 August 2017

title

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome (English)

1 reference

7 August 2017

Makiko Meguro-Horike

1

1 reference

7 August 2017

Dag H Yasui

2

1 reference

7 August 2017

Weston Powell

3

1 reference

7 August 2017

Diane I Schroeder

4

1 reference

7 August 2017

Mitsuo Oshimura

5

1 reference

7 August 2017

Janine M Lasalle

6

1 reference

7 August 2017

Shin-ichi Horike

7

1 reference

7 August 2017

publication date

1 July 2011

1 reference

7 August 2017

published in

Human Molecular Genetics

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7 August 2017

volume

20

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7 August 2017

issue

19

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7 August 2017

page(s)

3798-3810

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Nicotinamide adenine dinucleotide (NAD)-regulated DNA methylation alters CCCTC-binding factor (CTCF)/cohesin binding and transcription at the BDNF locus

7 August 2017

cites work

1 reference

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28 July 2018

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Functional impact of global rare copy number variation in autism spectrum disorders

28 July 2018

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The clinical context of copy number variation in the human genome

28 July 2018

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CTCF shapes chromatin by multiple mechanisms: the impact of 20 years of CTCF research on understanding the workings of chromatin

28 July 2018

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Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

28 July 2018

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Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

28 July 2018

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Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

28 July 2018

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The pluripotency factor Oct4 interacts with Ctcf and also controls X-chromosome pairing and counting

28 July 2018

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Enhanced apoptosis during early neuronal differentiation in mouse ES cells with autosomal imbalance

28 July 2018

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Copy-number variations associated with neuropsychiatric conditions

28 July 2018

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Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

28 July 2018

1 reference

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Cohesin mediates transcriptional insulation by CCCTC-binding factor

28 July 2018

1 reference

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Maintenance of imprinting and nuclear architecture in cycling cells

28 July 2018

1 reference

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15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

28 July 2018

1 reference

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

28 July 2018

1 reference

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CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2

28 July 2018

1 reference

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Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples

28 July 2018

1 reference

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

28 July 2018

1 reference

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Autism as a paradigmatic complex genetic disorder

28 July 2018

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A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

28 July 2018

1 reference

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High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage

28 July 2018

1 reference

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Epidemiological surveys of autism and other pervasive developmental disorders: an update

28 July 2018

1 reference

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Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32

28 July 2018

1 reference

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Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Association between a GABRB3 polymorphism and autism.

28 July 2018

1 reference

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Genetics of austim: complex aetiology for a heterogeneous disorder

28 July 2018

1 reference

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Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6.

28 July 2018

1 reference

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Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein

28 July 2018

1 reference

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Genomic imprinting: parental influence on the genome

28 July 2018

1 reference

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Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

28 July 2018

1 reference

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

28 July 2018

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Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting

28 July 2018

1 reference

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LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

28 July 2018

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Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

28 July 2018

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A mouse model for Prader-Willi syndrome imprinting-centre mutations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

UBE3A/E6-AP mutations cause Angelman syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Differentiation and survival influences of growth factors in human neuroblastoma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Construction of mouse A9 clones containing a single human chromosome tagged with neomycin-resistance gene via microcell fusion

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

The role of CTCF in regulating nuclear organization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Epigenetics of autism spectrum disorders

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Autism and maternally derived aberrations of chromosome 15q.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

COBRA: a sensitive and quantitative DNA methylation assay

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3168289

A corrected karyotype for the SH-SY5Y human neuroblastoma cell line

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21725066

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Homologous association of oppositely imprinted chromosomal domains

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21725066

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDR298

1 reference

7 August 2017

1 reference

7 August 2017

1 reference