Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.11889/4171
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dc.contributor.authorQutob, Nouar-
dc.contributor.authorSamuels, Yardena-
dc.contributor.authorElnitski, Laura-
dc.contributor.authorGartner, Jared J.-
dc.date.accessioned2017-01-30T08:45:09Z-
dc.date.available2017-01-30T08:45:09Z-
dc.date.issued2015-
dc.identifier.urihttp://hdl.handle.net/20.500.11889/4171-
dc.description.abstractRecent technological advances in sequencing have flooded the field of cancer research with knowledge about somatic mutations for many different cancer types. Most cancer genomics studies focus on mutations that alter the amino acid sequence, ignoring the potential impact of synonymous mutations. However, accumulating experimental evidence has demonstrated clear consequences for gene function, leading to a widespread recognition of the functional role of synonymous mutations and their causal connection to various diseases. Here, we review the evidence supporting the direct impact of synonymous mutations on gene function via gene splicing; mRNA stability, folding, and translation; protein folding; and miRNA-based regulation of expression. These results highlight the functional contribution of synonymous mutations to oncogenesis and the need to further investigate their detection and prioritization for experimental assessment.en_US
dc.language.isoen_USen_US
dc.subjectCancer - Molecular diagnosisen_US
dc.subjectMelanoma - Molecular diagnosisen_US
dc.titleThe functional relevance of somatic synonymous mutations in melanoma and other cancersen_US
dc.typeArticleen_US
newfileds.departmentEngineering and TechnologyEngineering and Technologyen_US
newfileds.item-access-typeopen_accessen_US
newfileds.thesis-prognoneen_US
newfileds.general-subjectnoneen_US
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.languageiso639-1other-
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