(Q34387306)

1 August 2017

Imprinted expression of SNRPN in human preimplantation embryos (English)

1 reference

1 August 2017

Huntriss J

1

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1 August 2017

Daniels R

series ordinal

2

1 reference

1 August 2017

Bolton V

series ordinal

3

1 reference

1 August 2017

Monk M

series ordinal

4

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1 August 2017

language of work or name

English

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publication date

1 October 1998

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American Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

63

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1 August 2017

4

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1 August 2017

1009-1014

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

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

Paternal repression of the imprinted mouse Igf2r locus occurs during implantation and is stable in all tissues of the post-implantation mouse embryo.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypeptide N.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

IGF2 is parentally imprinted in human preimplantation embryos.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377472

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

27 October 2018

1 reference

12 December 2020

Single nucleotide dimorphism in the transcribed region of the SNRPN gene at 15q12

1 reference

12 December 2020

Stage-specific induction and regulation by genomic imprinting of the mouse U2afbp-rs gene during preimplantation development

1 reference

12 December 2020

Diagnostic test for the Prader-Willi syndrome by SNRPN expression in blood

1 reference

12 December 2020

Identifiers

DOI

10.1086/302039

1 reference

1 August 2017

1 reference

1 August 2017

1 reference