(Q40765263)

23 September 2017

title

The mouse Snrpn minimal promoter and its human orthologue: activity and imprinting (English)

1 reference

23 September 2017

Hershko AY

1

1 reference

23 September 2017

Finberg Y

2

1 reference

23 September 2017

Kantor B

3

1 reference

23 September 2017

Shemer R

4

1 reference

23 September 2017

Razin A

5

1 reference

23 September 2017

publication date

1 November 2001

1 reference

23 September 2017

1 reference

23 September 2017

volume

6

1 reference

23 September 2017

issue

11

1 reference

23 September 2017

page(s)

967-975

1 reference

Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

Imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

Imprinting-mutation mechanisms in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2001.00474.X

10.1046/J.1365-2443.2001.00474.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference