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Article

<i>CDKN1A-RAB44</i> transcript fusion and activation in cancers

2017-03-02

Abstract excerpt

Splicing contributes to gene regulation and protein diversity, while abnormal splicing underlies both hereditary diseases and cancers. Various mutations that disrupt splicing factors, exonic or intronic splicing enhancers or silencers, as well as splice sites, could be responsible for abnormal splicing. Characterization of abnormal splicing events is not only helpful for understanding the molecular processes linki...

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Identifiers and source

Literature Corpus work
ddacd20c-e008-5d29-9bb1-6aa1f8184816
DOI
10.1101/111856
Open publication

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<i>CDKN1A-RAB44</i> transcript fusion and activation in cancersDOI 10.1101/111856
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