(Q38357990)

2 September 2017

title

Characterization of the human Snrpn minimal promoter and cis elements within it. (English)

1 reference

2 September 2017

Yael Green Finberg

1

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2 September 2017

Boris Kantor

series ordinal

2

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2 September 2017

Alon Y Hershko

series ordinal

3

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2 September 2017

Aharon Razin

series ordinal

4

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2 September 2017

language of work or name

English

0 references

publication date

1 January 2003

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2 September 2017

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2 September 2017

volume

304

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2 September 2017

page(s)

201-206

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

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

A small-scale procedure for preparation of nuclear extracts that support efficient transcription and pre-mRNA splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

Imprinting in Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

Imprinting-mutation mechanisms in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

The imprinting mechanism of the Prader-Willi/Angelman regional control center

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

Cloning, characterization, and expression in Escherichia coli of the gene coding for the CpG DNA methylase from Spiroplasma sp. strain MQ1(M.SssI).

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

The imprinting box of the Prader-Willi/Angelman syndrome domain

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2901212-X

7 January 2021

10.1016/S0378-1119(02)01212-X

Identifiers

DOI

1 reference

2 September 2017

1 reference