Fragile site orthologs FHIT/FRA3B and Fhit/Fra14A2: Evolutionarily conserved but highly recombinogenic
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference48 articles.
1. DNA polymerase ? inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
2. Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
3. FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis
4. Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat
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1. Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes;Nature;2022-10-05
2. New Era of Mapping and Understanding Common Fragile Sites: An Updated Review on Origin of Chromosome Fragility;Frontiers in Genetics;2022-05-20
3. Genome-wide high-resolution mapping of mitotic DNA synthesis sites and common fragile sites by direct sequencing;Cell Research;2020-06-19
4. The epicenter of chromosomal fragility of Fra14A2, the mouse ortholog of human FRA3B common fragile site, is largely attached to the nuclear matrix in lymphocytes but not in other cell types that do not express such a fragility;Journal of Cellular Biochemistry;2019-10-23
5. Fhit–Fdxr interaction in the mitochondria: modulation of reactive oxygen species generation and apoptosis in cancer cells;Cell Death & Disease;2019-02-15
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