SF3B4 gene

Known as: SPLICEOSOME-ASSOCIATED PROTEIN, 49-KD, SAP49, SF3b49 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2018
024619962018

Papers overview

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2016
2016
Mandibulofacial dysostosis (MFD) is a human developmental disorder characterized by defects of the facial bones. It is the second… (More)
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2016
2016
BACKGROUND/AIM Defects in alternative splicing contribute to carcinogenesis, cancer progression and chemoresistance. The… (More)
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2014
2014
Nager syndrome belongs to the group of acrofacial dysostosis, which are characterized by the association of craniofacial and limb… (More)
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2014
2014
Nager syndrome, or acrofacial dysostosis type 1 (AFD1), is a rare multiple malformation syndrome characterized by hypoplasia of… (More)
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2013
2013
Nager syndrome (MIM #154400) is the best-known preaxial acrofacial dysostosis, mainly characterized by craniofacial and preaxial… (More)
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2012
2012
Nager syndrome, first described more than 60 years ago, is the archetype of a class of disorders called the acrofacial dysostoses… (More)
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2009
2009
The 5'-ends of all Kinetoplastid mRNAs consist of a short sequence added by trans splicing. In contrast to cis splicing in… (More)
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1998
1998
Retroviruses display a unique form of alternative splicing in which both spliced and unspliced RNAs accumulate in the cytoplasm… (More)
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1997
1997
Splicing of mRNA precursors (pre-mRNAs) occurs in a multimolecular complex, termed spliceosome, which is comprised of pre-mRNA… (More)
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1997
1997
We have isolated the mouse homologue of human spliceosome-associated protein SAP49, mSAP49. mSAP49 contains two RNA recognition… (More)
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