Characterization of DNA polymerase β splicing variants in gastric cancer: The most frequent exon 2-deleted isoform is a non-coding RNA

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 670, Issue 1-2, 2009, Pages 79-87

  Simonelli, Valeria ^a   D'Errico, Mariarosaria ^a   Palli, Domenico ^b   Prasad, Rajendra ^c   Wilson, Samuel H ^c   Dogliotti, Eugenia ^a  

^a ISTITUTO SUPERIORE DI SANITÀ   (Italy)

^b CANCER RESEARCH AND PREVENTION INSTITUTE ISPO   (Italy)

^c NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES   (United States)

Author keywords

DNA polymerase beta; DNA repair; Gastric cancer; ncRNA; Splicing variants

Indexed keywords

DNA DIRECTED DNA POLYMERASE BETA; MESSENGER RNA;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; DNA REPAIR; FIBROBLAST; GENE MUTATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOFLUORESCENCE; MOUSE; MUTANT; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA SPLICING; STOMACH CANCER; WESTERN BLOTTING; WILD TYPE;

ALTERNATIVE SPLICING; ANIMALS; CASE-CONTROL STUDIES; CELL LINE; CELL LINE, TUMOR; DNA POLYMERASE BETA; DNA REPAIR; EXONS; HUMANS; MICE; PROTEIN ISOFORMS; RNA SPLICING; RNA, UNTRANSLATED; STOMACH; STOMACH NEOPLASMS; TRANSFECTION;

MURINAE;

EID: 70350007192     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2009.07.007     Document Type: Article

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