(Q48110067)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16331412%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

Allele-specific methylation of a functional CTCF binding site upstream of MEG3 in the human imprinted domain of 14q32 (English)

1 reference

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10 January 2020

3

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10 January 2020

author name string

Alberto L Rosa

1

1 reference

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10 January 2020

Yuan-Qing Wu

2

1 reference

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10 January 2020

Karen J Coveler

4

1 reference

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10 January 2020

V Reid Sutton

5

1 reference

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10 January 2020

Lisa G Shaffer

6

1 reference

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10 January 2020

publication date

8 December 2005

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10 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16331412%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

volume

13

1 reference

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10 January 2020

issue

8

1 reference

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10 January 2020

page(s)

809-818

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https://scigraph.springernature.com/pub.10.1007/s10577-005-1015-4

10 January 2020

exact match

0 references

cites work

Mechanisms of Igf2/H19 imprinting: DNA methylation, chromatin and long-distance gene regulation

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10577-005-1015-4

Role of CTCF binding sites in the Igf2/H19 imprinting control region

21 January 2018

1 reference

12 December 2020

Transcriptional control: imprinting insulation

1 reference

12 December 2020

CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus

1 reference

12 December 2020

Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short arms

1 reference

12 December 2020

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

1 reference

12 December 2020

A Pituitary-Derived MEG3 Isoform Functions as a Growth Suppressor in Tumor Cells

1 reference

12 December 2020

Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3.

1 reference

12 December 2020

Poly(ADP-ribosyl)ation regulates CTCF-dependent chromatin insulation.

1 reference

12 December 2020

Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy

1 reference

12 December 2020

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status

1 reference

12 December 2020

Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)

1 reference

12 December 2020

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

1 reference

12 December 2020

Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation

1 reference

12 December 2020

Induction of sequence-specific binding of Drosophila heat shock activator protein without protein synthesis

1 reference

12 December 2020

Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive

1 reference

12 December 2020

CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

1 reference

12 December 2020

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

1 reference

12 December 2020

Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.

1 reference

12 December 2020

Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.

1 reference

12 December 2020

Characterization of the chicken beta-globin insulator

1 reference

12 December 2020

Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region

1 reference

12 December 2020

The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA

1 reference

12 December 2020

Confined placental mosaicism for trisomy 14 and maternal uniparental disomy in association with elevated second trimester maternal serum human chorionic gonadotrophin and third trimester fetal growth restriction

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

Prenatal ultrasound findings in a fetus with paternal uniparental disomy 14q12-qter

1 reference

12 December 2020

A new genetic concept: uniparental disomy and its potential effect, isodisomy

1 reference

12 December 2020

A case of segmental paternal isodisomy of chromosome 14.

1 reference

12 December 2020

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor

1 reference

12 December 2020

Genomic imprinting: CTCF protects the boundaries

1 reference

12 December 2020

Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting.

1 reference

12 December 2020

Alternative splicing and imprinting control of the Meg3/Gtl2-Dlk1 locus in mouse embryos.

1 reference

12 December 2020

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted

1 reference

12 December 2020

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

1 reference

12 December 2020

Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.

1 reference

12 December 2020

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

1 reference

12 December 2020

Gene number, noise reduction and biological complexity

1 reference

12 December 2020

Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion

1 reference

12 December 2020

A 5' element of the chicken beta-globin domain serves as an insulator in human erythroid cells and protects against position effect in Drosophila

1 reference

12 December 2020

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

1 reference

12 December 2020

The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements.

1 reference

12 December 2020

Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8

1 reference

12 December 2020

Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations

1 reference

12 December 2020

Oxidative stress and AP-1 activity in tamoxifen-resistant breast tumors in vivo

1 reference

12 December 2020

10.1007/S10577-005-1015-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16331412%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference