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SNRPN gene

Known as: small nuclear ribonucleoprotein N, tissue-specific splicing protein, SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE N 
This gene plays a role in splicing of mRNA.
National Institutes of Health

Papers overview

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Highly Cited
2002
Highly Cited
2002
DNA methylation differences between maternal and paternal alleles of many imprinted genes are inherited from the male and female… Expand
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Highly Cited
2002
Highly Cited
2002
Dnmt3L is required for the establishment of maternal methylation imprints at imprinting centers (ICs). Dnmt3L, however, lacks the… Expand
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Highly Cited
2001
Highly Cited
2001
In mice and humans, the locus encoding the gene for small nuclear ribonucleoprotein N (SNRPN/Snrpn), as well as other loci in the… Expand
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Highly Cited
1997
Highly Cited
1997
The analysis of allelic methylation differences in 15q11-q13 has been established as a valid test for the Angelman and Prader… Expand
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Highly Cited
1997
Highly Cited
1997
The mouse Snrpn gene encodes the Smn protein, which is involved in RNA splicing. The gene maps to a region in the central part of… Expand
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Highly Cited
1996
Highly Cited
1996
Imprinting on human chromosome 15 is regulated by an imprinting centre, which has been mapped to a 100–kb region including exon 1… Expand
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Highly Cited
1996
Highly Cited
1996
The human SNRPN (small nuclear ribonucleoprotein polypeptide N) gene is one of a gene family that encode proteins involved in pre… Expand
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Highly Cited
1995
Highly Cited
1995
A subset of patients with Angelman and Prader–Willi syndrome have apparently normal chromosomes of biparental origin, but… Expand
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Highly Cited
1993
Highly Cited
1993
The SNRPN gene encodes a small nuclear ribonucleoprotein subunit, SmN, thought to be involved in splicing of pre-mRNA. A closely… Expand
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Highly Cited
1992
Highly Cited
1992
Prader–Willi syndrome (PWS) is associated with paternally derived chromosomal deletions in region 15q11–13 or with maternal… Expand
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