DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Molecular Biology
Link
http://www.nature.com/articles/onc2009502.pdf
Reference51 articles.
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3. Bongarzone I, Butti MG, Fugazzola L, Pacini F, Pinchera A, Vorontsova TV et al. (1997). Comparison of the breakpoint regions of ELE1 and RET genes involved in the generation of RET/PTC3 oncogene in sporadic and in radiation-associated papillary thyroid carcinomas. Genomics 42: 252–259.
4. Burrow AA, Williams LE, Pierce LC, Wang YH . (2009). Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites. BMC Genomics 10: 59.
5. Casper AM, Durkin SG, Arlt MF, Glover TW . (2004). Chromosomal instability at common fragile sites in Seckel syndrome. Am J Hum Genet 75: 654–660.
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