(Q35020593)

5 August 2017

title

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

1 reference

5 August 2017

A H Huq

1

1 reference

5 August 2017

J S Sutcliffe

2

1 reference

5 August 2017

M Nakao

3

1 reference

5 August 2017

Y Shen

4

1 reference

5 August 2017

R A Gibbs

5

1 reference

5 August 2017

A L Beaudet

6

1 reference

5 August 2017

language of work or name

1 reference

1 June 1997

1 reference

5 August 2017

1 reference

5 August 2017

volume

7

1 reference

5 August 2017

issue

6

1 reference

5 August 2017

page(s)

642-648

1 reference

Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

CENSOR--a program for identification and elimination of repetitive elements from DNA sequences

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

The minimal self-sufficient element in a murine G+C-rich promoter is a large element with imperfect dyad symmetry

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

New insights reveal complex mechanisms involved in 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=310659

Adaptor-based uracil DNA glycosylase cloning simplifies shotgun library construction for large-scale sequencing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

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=310659

Identification of a novel paternally expressed gene in the Prader-Willi syndrome 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=310659

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

Disruption of imprinting caused by deletion of the H19 gene region 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=310659

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi 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=310659

Hypermethylation of human DNA sequences in embryonal carcinoma cells and somatic tissues but not in sperm

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

Primary structure of a human small nuclear ribonucleoprotein polypeptide as deduced by cDNA analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

Transcriptional activation by Sp1 as directed through TATA or initiator: specific requirement for mammalian transcription factor IID

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

DNA methylation and gene expression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

The gene encoding the small nuclear ribonucleoprotein-associated protein N is expressed at high levels in 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=310659

The essentials of DNA methylation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=310659

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1101%2FGR.7.6.642

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1101%2FGR.7.6.642

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1101%2FGR.7.6.642

DNA methylation inhibits transcription indirectly via a methyl-CpG binding protein

21 January 2018

1 reference

12 December 2020

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

12 December 2020

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

12 December 2020

Characteristics of imprinted genes

1 reference

12 December 2020

Identifiers

DOI

10.1101/GR.7.6.642

1 reference

5 August 2017

1 reference

5 August 2017

1 reference