Chromosome rearrangements in B lymphocytes can be initiated by AID-associated double strand breaks (DSBs), with others arising by unclear mechanisms. A recent study by Barlow and colleagues in Cell reports on genomic regions, termed early replicating fragile sites, that may explain many AID-independent DSBs and creates a compelling link between replication stress, transcription, and chromosome rearrangements
Recurrent chromosomal translocations can drive oncogenesis, but how they form has remained elusive. ...
SummaryCancer genomes exhibit numerous deletions, some of which inactivate tumor suppressor genes an...
Gene rearrangements such as chromosomal translocations have been shown to contribute to cancer devel...
SummaryDNA double-strand breaks (DSBs) in B lymphocytes arise stochastically during replication or a...
SummaryWhereas chromosomal translocations are common pathogenetic events in cancer, mechanisms that ...
DNA double-strand breaks (DSBs) are a significant threat to the viability of a normal cell, since th...
Summary: Analysis of translocation breakpoints in human B cell malignancies reveals that DNA double-...
Chromosomal translocations involving antigen receptor loci are common in lymphoid malignancies. Tran...
Although it is known that replication stress causes genetic instability, the underlying mechanisms a...
DNA DSBs (double-strand breaks) are a significant threat to the viability of a normal cell, since th...
SummaryChromosomal rearrangements, including translocations, require formation and joining of DNA do...
Chromosomal translocations that juxtapose antigen receptor genes and oncogenes are frequently associ...
Common fragile sites (CFSs) are conserved genomic regions that preferentially form gaps and breaks o...
Recent developments in sequencing the cancer genome have provided the first in-depth mapping of stru...
Chromosomal translocations between antigen receptor loci and oncogenes are a hallmark of lymphoid ca...
Recurrent chromosomal translocations can drive oncogenesis, but how they form has remained elusive. ...
SummaryCancer genomes exhibit numerous deletions, some of which inactivate tumor suppressor genes an...
Gene rearrangements such as chromosomal translocations have been shown to contribute to cancer devel...
SummaryDNA double-strand breaks (DSBs) in B lymphocytes arise stochastically during replication or a...
SummaryWhereas chromosomal translocations are common pathogenetic events in cancer, mechanisms that ...
DNA double-strand breaks (DSBs) are a significant threat to the viability of a normal cell, since th...
Summary: Analysis of translocation breakpoints in human B cell malignancies reveals that DNA double-...
Chromosomal translocations involving antigen receptor loci are common in lymphoid malignancies. Tran...
Although it is known that replication stress causes genetic instability, the underlying mechanisms a...
DNA DSBs (double-strand breaks) are a significant threat to the viability of a normal cell, since th...
SummaryChromosomal rearrangements, including translocations, require formation and joining of DNA do...
Chromosomal translocations that juxtapose antigen receptor genes and oncogenes are frequently associ...
Common fragile sites (CFSs) are conserved genomic regions that preferentially form gaps and breaks o...
Recent developments in sequencing the cancer genome have provided the first in-depth mapping of stru...
Chromosomal translocations between antigen receptor loci and oncogenes are a hallmark of lymphoid ca...
Recurrent chromosomal translocations can drive oncogenesis, but how they form has remained elusive. ...
SummaryCancer genomes exhibit numerous deletions, some of which inactivate tumor suppressor genes an...
Gene rearrangements such as chromosomal translocations have been shown to contribute to cancer devel...