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- W3157686970 startingPage "2211" @default.
- W3157686970 abstract "ATRX gene codifies for a protein member of the SWI-SNF family and was cloned for the first time over 25 years ago as the gene responsible for a rare developmental disorder characterized by α-thalassemia and intellectual disability called Alpha Thalassemia/mental Retardation syndrome X-linked (ATRX) syndrome. Since its discovery as a helicase involved in alpha-globin gene transcriptional regulation, our understanding of the multiple roles played by the ATRX protein increased continuously, leading to the recognition of this multifaceted protein as a central “caretaker” of the human genome involved in cancer suppression. In this review, we report recent advances in the comprehension of the ATRX manifold functions that encompass heterochromatin epigenetic regulation and maintenance, telomere function, replicative stress response, genome stability, and the suppression of endogenous transposable elements and exogenous viral genomes." @default.
- W3157686970 created "2021-05-10" @default.
- W3157686970 creator A5005622956 @default.
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- W3157686970 creator A5014145933 @default.
- W3157686970 creator A5014576319 @default.
- W3157686970 creator A5065760568 @default.
- W3157686970 date "2021-05-05" @default.
- W3157686970 modified "2023-10-13" @default.
- W3157686970 title "The Multiple Facets of ATRX Protein" @default.
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