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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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2016
2016
Prader–Willi syndrome is a rare syndrome characterized by hypotonia, developmental delay and excessive appetite. This syndrome is… 
2011
2011
Some human embryonic stem cell lines have shown genomic instabilities over long-term culture. To study the controversial origin… 
Review
2008
Review
2008
Genomic imprinting is responsible for monoallelic gene expression that depends on the sex of the parent from which the alleles… 
2008
2008
Two active X Chromosomes and methylation of the imprinted gene in human parthenogenetic embryonic stem cell line 
2007
2007
  • 2007
  • Corpus ID: 55548997
Prader-Willi syndrome (PWS) is associated with distinct phenotypes which include mental retardation and caused by loss of… 
2006
2006
Spinal Muscular Atrophy (SMA) is an inherited neuromuscular disorder caused by mutation of the Survival Motor Neuron (SMN1) gene… 
Review
2001
Review
2001
In the period 1998-2000 almost all new cases of childhood spinal muscular atrophy (SMA) in addition to those from our database… 
1998
1998
  • Marc Delpech
  • 1998
  • Corpus ID: 19018926
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct neurodevelopmental disorders [Holm et al., 1993; Williams et… 
1997
1997
The gene for the small nuclear ribonucleoprotein N (SNRPN) maps to human chromosome 15 and has 10 exons. Using cDNA cloning…