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small nuclear ribonucleoprotein-associated protein N

Known as: Small Nuclear Ribonucleoprotein Associated Protein N, Sm Protein N, Tissue-Specific-Splicing Protein 
Small nuclear ribonucleoprotein-associated protein N (240 aa, ~25 kDa) is a nucleotide metabolism protein that is encoded by the human SNRPN gene and… 
National Institutes of Health

Related topics

Related topics

4 relations
Genes, RegulatorRNA SplicingSNRPN gene

Broader (1)

snRNP Core Proteins

Papers overview

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Highly Cited
2008
Highly Cited
2008
Superovulation alters the expression of imprinted genes in the midgestation mouse placenta.
Imprinted genes play important roles in embryonic growth and development as well as in placental function. Many imprinted genes… 
Highly Cited
2004
Highly Cited
2004
Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease, characterized by degeneration of the anterior horn… 
Highly Cited
2004
Highly Cited
2004
Timing of establishment of paternal methylation imprints in the mouse.
Highly Cited
2001
Highly Cited
2001
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A.
The imprinted domain on human chromosome 15 consists of two oppositely imprinted gene clusters, which are under the coordinated… 
Highly Cited
2001
Highly Cited
2001
Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein.
Spinal muscular atrophy (SMA) is a genetic disorder caused by mutations in the human survival of motor neuron 1 gene, SMN1. SMN… 
Highly Cited
1999
Highly Cited
1999
An imprinted, mammalian bicistronic transcript encodes two independent proteins.
Polycistronic transcripts are common in prokaryotes but rare in eukaryotes. Phylogenetic analysis of the SNRPN (SmN) mRNA in five… 
Highly Cited
1997
Highly Cited
1997
Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy
Spinal muscular atrophy (SMA) is a motor neuron disease characterized by degeneration of the anterior horn cells of the spinal… 
Highly Cited
1994
Highly Cited
1994
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
To determine the molecular basis of Prader-Willi syndrome (PWS) and Angelman syndrome (AS), we have isolated new transcripts from… 
Highly Cited
1994
Highly Cited
1994
Maternal imprinting of human SNRPN, a gene deleted in Prader–Willi syndrome
Prader–Willi syndrome (PWS), a human neuroendocrine disorder, is associated with deficiencies of paternal chromosome 15q12. Small… 
Highly Cited
1992
Highly Cited
1992
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region
Prader–Willi syndrome (PWS) is associated with paternal gene deficiencies in human chromosome 15q11–13, suggesting that PWS is… 
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