Frequent silence of chromosome 9p, homozygous DOCK8, DMRT1 and DMRT3 deletion at 9p24.3 in squamous cell carcinoma of the lung
Frequent silence of chromosome 9p, homozygous DOCK8, DMRT1 and DMRT3 deletion at 9p24.3 in squamous cell carcinoma of the lung
复制标题
DOI:
10.3892/ijo_00000681
复制
发表时间:
2010-08-01
影响因子:
5.2
通讯作者:
Park, Jong Woo
中科院分区:
文献类型:
--
作者:
Kang, Ji Un;Koo, Sun Hoe;Park, Jong Woo
Chromosomal alterations are a major genomic force contributing to the development of lung cancer. We subjected 22 cases of squamous cell carcinoma of the lung (SCC) to whole-genome microarray-CGH (resolution, 1 Mb) to identify critical genetic landmarks that might be important mediators in the formation or progression of SCC. On a genome-wide profile, copy number losses (log(2) ratio