(Q34956275)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Neuronal chromatin dynamics of imprinting in development and disease (English)

1 reference

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20 January 2020

4

1 reference

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20 January 2020

author name string

Karen N Leung

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Stormy J Chamberlain

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Marc Lalande

series ordinal

3

1 reference

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20 January 2020

publication date

1 February 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

Journal of Cellular Biochemistry

20 January 2020

published in

1 reference

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20 January 2020

volume

112

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

365-373

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes

20 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Digital Genome-Wide ncRNA Expression, Including SnoRNAs, across 11 Human Tissues Using PolyA-Neutral Amplification

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Sex-specific parent-of-origin allelic expression in the mouse brain

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Clone- and gene-specific aberrations of parental imprinting in human induced pluripotent stem cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Copy-number variations associated with neuropsychiatric conditions

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Gender influences monoallelic expression of ATP10A in human brain

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Large recurrent microdeletions associated with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

MeCP2, a key contributor to neurological disease, activates and represses transcription

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Environmental epigenomics and disease susceptibility

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Epigenetics of autism spectrum disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Chromosome territories--a functional nuclear landscape.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

How imprinting centres work

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Autism as a paradigmatic complex genetic disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Angelman syndrome: a review of the clinical and genetic aspects

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Methylation-induced repression--belts, braces, and chromatin

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090268

A genome-wide scan for common alleles affecting risk for autism

8 July 2018

1 reference

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

21 January 2018

1 reference

Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study.

21 January 2018

1 reference

A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced

21 January 2018

1 reference

The X chromosome is organized into a gene-rich outer rim and an internal core containing silenced nongenic sequences

21 January 2018

1 reference

Nongenic transcription, gene regulation and action at a distance

21 January 2018

1 reference

Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation

21 January 2018

1 reference

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

21 January 2018

1 reference

Early loss of Xist RNA expression and inactive X chromosome associated chromatin modification in developing primordial germ cells.

21 January 2018

1 reference

Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation

21 January 2018

1 reference

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

21 January 2018

1 reference

Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals

21 January 2018

1 reference

Molecular biology. Chromatin higher order folding--wrapping up transcription

21 January 2018

1 reference

Antisense transcription occurs at the promoter of a mouse imprinted gene, commd1, on the repressed paternal allele

21 January 2018

1 reference

A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.

21 January 2018

1 reference

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb

21 January 2018

1 reference

On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?

21 January 2018

1 reference

Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression

21 January 2018

1 reference

Biogenesis and intranuclear trafficking of human box C/D and H/ACA RNPs

21 January 2018

1 reference

A chromosomal memory triggered by Xist regulates histone methylation in X inactivation

21 January 2018

1 reference

Gene order and dynamic domains

21 January 2018

1 reference

Evolving role of MeCP2 in Rett syndrome and autism

21 January 2018

1 reference

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

21 January 2018

1 reference

Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component

21 January 2018

1 reference

Indications of centromere movement during interphase and differentiation

21 January 2018

1 reference

Nuclear topology of murine, cerebellar Purkinje neurons: changes as a function of development.

21 January 2018

1 reference

Evidence that the AAA+ proteins TIP48 and TIP49 bridge interactions between 15.5K and the related NOP56 and NOP58 proteins during box C/D snoRNP biogenesis.

21 January 2018

1 reference

A census of mammalian imprinting.

21 January 2018

1 reference

The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin

21 January 2018

1 reference

Crucial role of antisense transcription across the Xist promoter in Tsix-mediated Xist chromatin modification.

21 January 2018

1 reference

The imprinting mechanism of the Prader-Willi/Angelman regional control center

21 January 2018

1 reference

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

21 January 2018

1 reference

Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs

21 January 2018

1 reference

Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus

21 January 2018

1 reference

Non-coding RNAs in imprinted gene clusters

21 January 2018

1 reference

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.

21 January 2018

1 reference

The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing

21 January 2018

1 reference

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

21 January 2018

1 reference

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

21 January 2018

1 reference

A computational screen for C/D box snoRNAs in the human genomic region associated with Prader-Willi and Angelman syndromes

21 January 2018

1 reference

Long noncoding RNA as modular scaffold of histone modification complexes

21 January 2018

1 reference

Long nuclear-retained non-coding RNAs and allele-specific higher-order chromatin organization at imprinted snoRNA gene arrays.

21 January 2018

1 reference

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

21 January 2018

1 reference

A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome

21 January 2018

1 reference

Genomic imprinting effects on brain development and function

21 January 2018

1 reference

Transient homologous chromosome pairing marks the onset of X inactivation

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/JCB.22958

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21268055%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

21268055

1 reference