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- W4238328529 abstract "The histone H2A variant, H2AX, is a core component of chromatin that is phosphorylated in chromatin flanking DNA double strand breaks (DSBs). Here, we summarize H2AX functions and outline a specific anchoring model, that can explain the translocation prone phenotype of H2AX-deficient and H2AX/p53-deficient mice. We also discuss how this model of H2AX function could account for some aspects of the genomic instability and cancer prone human phenotypes associated with Ataxia Telangiectasia (AT), Nijmegen Breakage Syndrome (NBS), Ataxia Telangiectasia Like Disorder (ATLD), and Bloom's Syndrome (BS)." @default.
- W4238328529 created "2022-05-12" @default.
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- W4238328529 date "2004-02-01" @default.
- W4238328529 modified "2023-10-14" @default.
- W4238328529 title "H2AX May Function as an Anchor to Hold Broken Chromosomal DNA Ends in Close Proximity" @default.
- W4238328529 doi "https://doi.org/10.4161/cc.3.2.684" @default.
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