DNA double-strand breaks (DSBs) disrupt the structural integrity of chromosomes. Proper DSB repair pathway choice is critical to avoid the type of gross chromosomal rearrangements that characterize cancer cells. Recent findings reveal S-fatty acylation and membrane anchorage of Rap1-interacting factor 1 (Rif1) as a mechanism providing spatial control over DSB repair pathway choice
DNA damages that cause double-strand breaks (DSBs) to the chromosome are most harmful. Subsequent ch...
SummarySister-chromatid disjunction in anaphase requires the resolution of DNA catenanes by topoisom...
To safeguard genome integrity in response to DNA double-strand breaks (DSBs), mammalian cells mobili...
DNA double-strand breaks (DSBs) disrupt the structural integrity of chromosomes. Proper DSB repair p...
International audienceRif1 is involved in telomere homeostasis, DNA replication timing, and DNA doub...
AbstractDNA double strand breaks (DSBs) are highly toxic to the cells and accumulation of DSBs resul...
DNA double-strand breaks (DSBs) represent a threat to the genome because they can lead to the loss o...
Replication timing (RT) is a cellular program to coordinate initiation of DNA replication in all ori...
The appropriate execution of DNA double-strand break (DSB) repair is critical for genome stability a...
Cells have evolved conserved mechanisms to protect DNA ends, such as those at the termini of linear ...
Timely and accurate genome duplication is essential to maintain genome integrity and cell survival. ...
DNA double-strand break (DSB) repair pathway choice is governed by the opposing activities of 53BP1 ...
Diverse roles in DNA metabolism have been envisaged for budding yeast and mammalian Rif1. In particu...
RIF1 is a multifunctional protein that plays key roles in the regulation of DNA processing. During r...
Sister-chromatid disjunction in anaphase requires the resolution of DNA catenanes by topoisomerase I...
DNA damages that cause double-strand breaks (DSBs) to the chromosome are most harmful. Subsequent ch...
SummarySister-chromatid disjunction in anaphase requires the resolution of DNA catenanes by topoisom...
To safeguard genome integrity in response to DNA double-strand breaks (DSBs), mammalian cells mobili...
DNA double-strand breaks (DSBs) disrupt the structural integrity of chromosomes. Proper DSB repair p...
International audienceRif1 is involved in telomere homeostasis, DNA replication timing, and DNA doub...
AbstractDNA double strand breaks (DSBs) are highly toxic to the cells and accumulation of DSBs resul...
DNA double-strand breaks (DSBs) represent a threat to the genome because they can lead to the loss o...
Replication timing (RT) is a cellular program to coordinate initiation of DNA replication in all ori...
The appropriate execution of DNA double-strand break (DSB) repair is critical for genome stability a...
Cells have evolved conserved mechanisms to protect DNA ends, such as those at the termini of linear ...
Timely and accurate genome duplication is essential to maintain genome integrity and cell survival. ...
DNA double-strand break (DSB) repair pathway choice is governed by the opposing activities of 53BP1 ...
Diverse roles in DNA metabolism have been envisaged for budding yeast and mammalian Rif1. In particu...
RIF1 is a multifunctional protein that plays key roles in the regulation of DNA processing. During r...
Sister-chromatid disjunction in anaphase requires the resolution of DNA catenanes by topoisomerase I...
DNA damages that cause double-strand breaks (DSBs) to the chromosome are most harmful. Subsequent ch...
SummarySister-chromatid disjunction in anaphase requires the resolution of DNA catenanes by topoisom...
To safeguard genome integrity in response to DNA double-strand breaks (DSBs), mammalian cells mobili...