(Q35884190)

10 August 2017

Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila (English)

1 reference

10 August 2017

0 references

Lyko F

1

1 reference

10 August 2017

Buiting K

series ordinal

2

1 reference

10 August 2017

Horsthemke B

series ordinal

3

1 reference

10 August 2017

Paro R

series ordinal

4

1 reference

10 August 2017

language of work or name

English

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publication date

1 February 1998

1 reference

Proceedings of the National Academy of Sciences of the United States of America

10 August 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

10 August 2017

95

1 reference

10 August 2017

1698-1702

1 reference

10 August 2017

4

1 reference

Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Genomic organization and promoter structure of the human EXT1 gene

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

PcG complexes and chromatin silencing

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

UBE3A/E6-AP mutations cause Angelman syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Parental imprinting and human disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Drosophila Polycomb-group regulated chromatin inhibits the accessibility of a trans-activator to its target DNA.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Gene number, noise reduction and biological complexity

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Transposition of cloned P elements into Drosophila germ line chromosomes.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

CpG islands in vertebrate genomes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Determination of trace amounts of 5-methylcytosine in DNA by reverse-phase high-performance liquid chromatography

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

A stable genomic source of P element transposase in Drosophila melanogaster.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

The Polycomb protein shares a homologous domain with a heterochromatin-associated protein of Drosophila

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

An imprinting element from the mouse H19 locus functions as a silencer in Drosophila.

11 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1698

The absence of detectable methylated bases in Drosophila melanogaster DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1698

Discovering and understanding genes in human DNA sequence using GRAIL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1698

Discrete Polycomb-binding sites in each parasegmental domain of the bithorax complex.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19156

Functional imprinting and epigenetic modification of the human SNRPN gene

24 September 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1698

Imprinting moves to the centre

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1698

21 January 2018

Identifiers

DOI

10.1073/PNAS.95.4.1698

1 reference

10 August 2017

0 references

1 reference

10 August 2017

1 reference