The synthesized 2-(2-fluorophenyl)-6,7-methylenedioxyquinolin-4-one (CHM-1) promoted G2/M arrest through inhibition of CDK1 and induced apoptosis through the mitochondrial-dependent pathway in CT-26 murine colorectal adenocarcinoma cells.
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P2860
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P2860
The synthesized 2-(2-fluorophenyl)-6,7-methylenedioxyquinolin-4-one (CHM-1) promoted G2/M arrest through inhibition of CDK1 and induced apoptosis through the mitochondrial-dependent pathway in CT-26 murine colorectal adenocarcinoma cells.
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2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
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2009年學術文章
@zh-hant
name
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@en
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@nl
type
label
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@en
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@nl
prefLabel
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@en
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@nl
P2093
P50
P1476
The synthesized 2-(2-fluorophe ...... lorectal adenocarcinoma cells.
@en
P2093
Hsi-Chin Wu
Jo-Hua Chiang
Kuan-Tin Chen
Li-Chen Chou
Li-Jiau Huang
Sheng-Chu Kuo
P304
P356
10.1007/S00535-009-0111-1
P577
2009-08-14T00:00:00Z