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- W2162561014 endingPage "192" @default.
- W2162561014 startingPage "169" @default.
- W2162561014 abstract "Chromosomal fragile sites are specific loci that preferentially exhibit gaps and breaks on metaphase chromosomes following partial inhibition of DNA synthesis. Their discovery has led to novel findings spanning a number of areas of genetics. Rare fragile sites are seen in a small proportion of individuals and are inherited in a Mendelian manner. Some, such as FRAXA in the FMR1 gene, are associated with human genetic disorders, and their study led to the identification of nucleotide-repeat expansion as a frequent mutational mechanism in humans. In contrast, common fragile sites are present in all individuals and represent the largest class of fragile sites. Long considered an intriguing component of chromosome structure, common fragile sites have taken on novel significance as regions of the genome that are particularly sensitive to replication stress and that are frequently rearranged in tumor cells. In recent years, much progress has been made toward understanding the genomic features of common fragile sites and the cellular processes that monitor and influence their stability. Their study has merged with that of cell cycle checkpoints and DNA repair, and common fragile sites have provided insight into understanding the consequences of replication stress on DNA damage and genome instability in cancer cells." @default.
- W2162561014 created "2016-06-24" @default.
- W2162561014 creator A5002683233 @default.
- W2162561014 creator A5015832310 @default.
- W2162561014 date "2007-12-01" @default.
- W2162561014 modified "2023-10-10" @default.
- W2162561014 title "Chromosome Fragile Sites" @default.
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