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Comprehensive characterization and clinical relevance of the SWI/SNF copy number aberrations across human cancers
BACKGROUND: Alterations in genes encoding chromatin regulatory proteins are prevalent in cancers and may confer oncogenic properties and molecular changes linked to therapy resistance. However, the impact of copy number alterations (CNAs) of the SWItch/Sucrose NonFermentable (SWI/SNF) complex on the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487138/ https://www.ncbi.nlm.nih.gov/pubmed/34598711 http://dx.doi.org/10.1186/s41065-021-00203-y |