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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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2016
2016
IMPRINTING STATUS OF H19 AND SNRPN IN CLONED BOVINE PLACENTAS
2012
2012
Reorganization of Cajal bodies and nucleolar targeting of coilin in motor neurons of type I spinal muscular atrophy
Type I spinal muscular atrophy (SMA) is an autosomal recessive disorder caused by loss or mutations of the survival motor neuron… 
2009
2009
Analysis of pre-mRNA splicing in cell lines derived from patients with retinitis pigmentosa and dominant mutations in pre-mRNA splicing factor genes PRPF 31 , PRPF 8 and PRPF 3
s of oral presentations (in order of the program) 5 Analysis of pre-mRNA splicing in cell lines derived from patients with… 
Review
2008
Review
2008
The Evolution of Genomic Imprinting and X Chromosome Inactivation in Mammals
Genomic imprinting is responsible for monoallelic gene expression that depends on the sex of the parent from which the alleles… 
2007
2007
Expression of imprinted gene SNRPN in human oocytes and preimplantation embryos.
Objective To investigate expression of imprinted gene SNRPN in human oocytes and preimplantation embryos and the effect of SNRPN… 
2003
2003
Identifizierung und Expressionsanalyse der SNURF-SNRPN Sense – UBE3A Antisense Transkriptionseinheit in der Prader-Willi-/Angelman-Syndrom-Region auf Chromosom 15
Die Region 15q11-q13 enthalt zwei unterschiedlich gepragte Gencluster, die der koordinierten Kontrolle eines Imprinting-Centers… 
2000
2000
Methylation imprinting of H19 and SNRPN genes in human benign ovarian teratomas
1996
1996
Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN.
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct clinical disorders resulting from deficiency of paternal (PWS… 
1994
1994
Expression and DNA methylation analysis of SNRPN in Prader-Willi patients
The human SNRPN gene is one of a gene family that encode proteins involved in pre-mRNA splicing and maps to the Prader-Willi… 
1994
1994
Imprinting mutations in Angelman syndrome detected by Southern blotting using a probe containing exon {alpha} of SNRPN
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are associated with paternal and maternal deficiencies respectively, of…