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

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Topic mentions per year

1992-2018
051019922018

Papers overview

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Highly Cited
2010
Highly Cited
2010
Prader–Willi syndrome (PWS) is a neurobehavioral disorder manifested by infantile hypotonia and feeding difficulties in infancy… (More)
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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… (More)
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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… (More)
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Highly Cited
2000
Highly Cited
2000
Prader-Willi syndrome (PWS) is a neurogenetic disease characterized by infantile hypotonia, gonadal hypoplasia, obsessive… (More)
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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… (More)
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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… (More)
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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… (More)
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1994
1994
Prader–Willi syndrome (PWS), a human neuroendocrine disorder, is associated with deficiencies of paternal chromosome 15q12. Small… (More)
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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… (More)
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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… (More)
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