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snRNP Biogenesis

The 4 major small nuclear ribonucleoprotein particles (snRNPs), U1, U2, U4/U6, and U5, share 8 proteins which form the snRNP structural core: SNRPB… 
National Institutes of Health

Papers overview

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2015
2015
We validated the RAP-MS approach by defining the proteins that interact with two wellcharacterized non-coding RNAs: (i) U1 small… 
2015
2015
Proximal spinal muscular atrophy (SMA) is an autosomal recessive disorder characterized by degeneration of the second motor… 
2012
2012
Type I spinal muscular atrophy (SMA) is an autosomal recessive disorder caused by loss or mutations of the survival motor neuron… 
2011
2011
Aar2p is an essential yeast protein involved in pre-mRNA splicing and component of a U5 snRNP precursor form. It has been… 
2010
2010
Spinal muscular atrophy (SMA) is a leading genetic cause of childhood mortality, caused by reduced levels of survival motor… 
2006
2006
The survival of motor neurons protein (SMN) is part of a large complex that contains six other proteins, Gemins2–7. The SMN… 
2000
2000
Spinal muscular atrophy (SMA) is a neurodegenerative disease caused by homozygous mutations of the survival motor neuron gene 1… 
1998
1998
ABSTRACT The U1 snRNP functions to nucleate spliceosome assembly on newly transcribed pre-mRNA. Saccharomyces cerevisiae is…