Published in
Springer Verlag, Journal of Gastroenterology, 3(52), p. 327-340
DOI: 10.1007/s00535-016-1222-0
Links
Tools
Aberrant BLM cytoplasmic expression associates with DNA damage stress and hypersensitivity to DNA-damaging agents in colorectal cancer
Journal article published in 2016 by
Carolina Votino,
Carmelo Laudanna,
Pietro Parcesepe,
Guido Giordano,
Andrea Remo,
Erminia Manfrin 
,
Massimo Pancione
,
Massimo Pancione
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 
Abstract
Bloom syndrome is a rare and recessive disorder characterized by loss-of-function mutations of the BLM gene, which encodes a RecQ 3'-5' DNA helicase. Despite its putative tumor suppressor function, the contribution of BLM to human sporadic colorectal cancer (CRC) remains poorly understood.