(Q74312289)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

review article

1 reference

title

Mechanisms of genomic imprinting (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

language of work or name

English

0 references

publication date

5 September 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

10 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

67

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

777-787

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

10 November 2019

cites work

1 reference

12 December 2020

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

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12 December 2020

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

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12 December 2020

Role for DNA methylation in genomic imprinting

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12 December 2020

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

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12 December 2020

A new imprinted gene cloned by a methylation-sensitive genome scanning method

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12 December 2020

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

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12 December 2020

Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

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12 December 2020

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia

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12 December 2020

Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene

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12 December 2020

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

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12 December 2020

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

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12 December 2020

An imprinted, mammalian bicistronic transcript encodes two independent proteins

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12 December 2020

DNA methylation and chromatin modification.

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12 December 2020

Mechanisms of genomic imprinting

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12 December 2020

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

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12 December 2020

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

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12 December 2020

The paternal allele of the H19 gene is progressively silenced during early mouse development: the acetylation status of histones may be involved in the generation of variegated expression patterns.

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12 December 2020

Location of enhancers is essential for the imprinting of H19 and Igf2 genes

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12 December 2020

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

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12 December 2020

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

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12 December 2020

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

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12 December 2020

Imprinting in Prader-Willi and Angelman syndromes.

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12 December 2020

Imprinting in Angelman and Prader-Willi syndromes.

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12 December 2020

A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

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12 December 2020

Structure and function correlations at the imprinted mouse Snrpn locus.

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12 December 2020

Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene.

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12 December 2020

Chromatin conformation of the H19 epigenetic mark.

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12 December 2020

A model system to study genomic imprinting of human genes

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12 December 2020

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

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12 December 2020

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation

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12 December 2020

Imprinting-mutation mechanisms in Prader-Willi syndrome

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12 December 2020

Mechanism of imprinting on mouse distal chromosome 7

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12 December 2020

The impact of genomic imprinting for neurobehavioral and developmental disorders

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12 December 2020

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

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12 December 2020

Orientation of DNA replication establishes mating-type switching pattern in S. pombe.

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12 December 2020

The protein CTCF is required for the enhancer blocking activity of vertebrate insulators

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12 December 2020

Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation.

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12 December 2020

Epigenetics: regulation through repression

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12 December 2020

The 87A7 chromomere. Identification of novel chromatin structures flanking the heat shock locus that may define the boundaries of higher order domains

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12 December 2020

Parental origin effects in mice

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12 December 2020

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

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12 December 2020

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

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12 December 2020

Parental imprinting of the mouse insulin-like growth factor II gene.

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12 December 2020

A position-effect assay for boundaries of higher order chromosomal domains

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12 December 2020

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

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12 December 2020

DNA methyltransferases

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12 December 2020

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

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12 December 2020

Beckwith-Wiedemann syndrome

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12 December 2020

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

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12 December 2020

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

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12 December 2020

Disruption of imprinting caused by deletion of the H19 gene region in mice

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12 December 2020

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

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12 December 2020

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

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12 December 2020

An enhancer deletion affects both H19 and Igf2 expression

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12 December 2020

Establishment of functional imprinting of the H19 gene in human developing placentae

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12 December 2020

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization.

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12 December 2020

Gametic imprinting in mammals

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12 December 2020

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

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12 December 2020

Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms

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12 December 2020

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

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12 December 2020

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

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12 December 2020

Homologous association of oppositely imprinted chromosomal domains

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12 December 2020

Creation of genomic methylation patterns

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12 December 2020

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

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12 December 2020

Interchromosomal Transfer of Epigenetic States in Ascobolus: Transfer of DNA Methylation Is Mechanistically Related to Homologous Recombination

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12 December 2020

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

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12 December 2020

The structural H19 gene is required for transgene imprinting

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12 December 2020

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

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12 December 2020

A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprinting

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12 December 2020

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

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12 December 2020

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

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12 December 2020

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

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12 December 2020

Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

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12 December 2020

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

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12 December 2020

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

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12 December 2020

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

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12 December 2020

Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome

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12 December 2020

H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.

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12 December 2020

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

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12 December 2020

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

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12 December 2020

Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function.

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12 December 2020

A transcriptional insulator at the imprinted H19/Igf2 locus

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12 December 2020

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

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12 December 2020

Completion of mouse embryogenesis requires both the maternal and paternal genomes

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12 December 2020

A group of scs elements function as domain boundaries in an enhancer-blocking assay

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12 December 2020

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

12 December 2020

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

1 reference

12 December 2020

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

1 reference

12 December 2020

Parental-origin-specific epigenetic modification of the mouse H19 gene

1 reference

12 December 2020

Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control

1 reference

12 December 2020

Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

1 reference

12 December 2020

DNA methylation, genomic imprinting and cancer.

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12 December 2020

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

1 reference

12 December 2020

The 5' flank of mouse H19 in an unusual chromatin conformation unidirectionally blocks enhancer-promoter communication

1 reference

12 December 2020

Identifiers

DOI

10.1086/303101

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986038%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference