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SNRPN gene
Known as:
small nuclear ribonucleoprotein N
, tissue-specific splicing protein
, SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE N
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This gene plays a role in splicing of mRNA.
National Institutes of Health
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Related topics
Related topics
3 relations
RNA Splicing
SNRPD3 gene
small nuclear ribonucleoprotein-associated protein N
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Deletion of SNURF/SNRPN U1B and U1B* upstream exons in a child with developmental delay and excessive weight
C. Koufaris
,
Angelos Alexandrou
,
Ioannis Papaevripidou
,
Ioanna Alexandrou
,
Violetta Christophidou-Anastasiadou
,
C. Sismani
Journal Genetika
2016
Corpus ID: 255487111
Prader–Willi syndrome is a rare syndrome characterized by hypotonia, developmental delay and excessive appetite. This syndrome is…
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2011
2011
Genes Primer sequences H 19 Forward : gtattgtgggaggggttagtatag Reverse : actttattctctaatccaaaatccttatat SLC 22 A 18 Forward : tggttgaggtattatttttttgaga Reverse : ataaaaccctaacacccctaaactt SNRPN…
E. Jung
,
H. Son
,
Min Kwon Jeung
,
Chang-Kyu Lee
,
S. Hyun
,
E. Jeung
2011
Corpus ID: 207909709
Some human embryonic stem cell lines have shown genomic instabilities over long-term culture. To study the controversial origin…
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Review
2008
Review
2008
The Evolution of Genomic Imprinting and X Chromosome Inactivation in Mammals
T. Hore
2008
Corpus ID: 36551847
Genomic imprinting is responsible for monoallelic gene expression that depends on the sex of the parent from which the alleles…
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2008
2008
Two active X Chromosomes and methylation of the imprinted gene in human parthenogenetic embryonic stem cell line
Xiaofang Sun
,
Shaorong Gao
,
+9 authors
Guohong Xiao
Cell Research
2008
Corpus ID: 44258141
Two active X Chromosomes and methylation of the imprinted gene in human parthenogenetic embryonic stem cell line
2007
2007
Molecular diagnosis of Prader-Willi Syndrome and relative study
2007
Corpus ID: 55548997
Prader-Willi syndrome (PWS) is associated with distinct phenotypes which include mental retardation and caused by loss of…
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2006
2006
Histone acetylation and expression of SMN, the spinal muscular atrophy gene.
L. Kernochan
2006
Corpus ID: 52356956
Spinal Muscular Atrophy (SMA) is an inherited neuromuscular disorder caused by mutation of the Survival Motor Neuron (SMN1) gene…
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Review
2001
Review
2001
Phenotype and genotype correlation in childhood spinal muscular atrophy.
I. Hausmanowa-Petrusewicz
Neurologia i Neurochirurgia Polska
2001
Corpus ID: 23040210
In the period 1998-2000 almost all new cases of childhood spinal muscular atrophy (SMA) in addition to those from our database…
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2001
2001
Studies on Replication Manner of Chromosome 22q11 Region and Control of Expression of Imprinted SNRPN Gene in Human Genome
香田 淳
2001
Corpus ID: 87850219
1998
1998
Potential pitfall in Prader-Willi syndrome and Angelman syndrome molecular diagnosis.
Marc Delpech
American journal of medical genetics
1998
Corpus ID: 19018926
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct neurodevelopmental disorders [Holm et al., 1993; Williams et…
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1997
1997
Identification of novel exons 3' to the human SNRPN gene.
K. Buiting
,
B. Dittrich
,
Sabine U. Endele
,
Bernhard Horsthemke
Genomics
1997
Corpus ID: 43075903
The gene for the small nuclear ribonucleoprotein N (SNRPN) maps to human chromosome 15 and has 10 exons. Using cDNA cloning…
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