(Q39381116)

11 September 2017

MiR-520h-mediated FOXC2 regulation is critical for inhibition of lung cancer progression by resveratrol (English)

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11 September 2017

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M Hsiao

9

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author name string

Y-H Yu

1

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11 September 2017

H-A Chen

2

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11 September 2017

P-S Chen

3

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11 September 2017

Y-J Cheng

4

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11 September 2017

W-H Hsu

5

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11 September 2017

Y-W Chang

6

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11 September 2017

Y-H Chen

7

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11 September 2017

Y Jan

8

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11 September 2017

T-Y Chang

10

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11 September 2017

Y-H Liu

11

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11 September 2017

Y-M Jeng

12

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11 September 2017

C-H Wu

13

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11 September 2017

M-T Huang

14

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11 September 2017

Y-H Su

15

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11 September 2017

M-C Hung

16

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11 September 2017

M-H Chien

17

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11 September 2017

C-Y Chen

18

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11 September 2017

M-L Kuo

19

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11 September 2017

J-L Su

20

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11 September 2017

language of work or name

English

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publication date

12 March 2012

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11 September 2017

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11 September 2017

32

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4

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11 September 2017

431-443

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https://scigraph.springernature.com/pub.10.1038/onc.2012.74

11 September 2017

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Resveratrol-caused apoptosis of human prostate carcinoma LNCaP cells is mediated via modulation of phosphatidylinositol 3'-kinase/Akt pathway and Bcl-2 family proteins

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Foxc transcription factors directly regulate Dll4 and Hey2 expression by interacting with the VEGF-Notch signaling pathways in endothelial cells

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A new role of protein phosphatase 2a in adenoviral E1A protein-mediated sensitization to anticancer drug-induced apoptosis in human breast cancer cells

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Activation of NF-kappaB by Akt upregulates Snail expression and induces epithelium mesenchyme transition

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Resveratrol decreases the levels of miR-155 by upregulating miR-663, a microRNA targeting JunB and JunD

21 January 2018

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21 January 2018

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The microRNAs miR-373 and miR-520c promote tumour invasion and metastasis

21 January 2018

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21 January 2018

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21 January 2018

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The AKT/I kappa B kinase pathway promotes angiogenic/metastatic gene expression in colorectal cancer by activating nuclear factor-kappa B and beta-catenin

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31 March 2020

Identifiers

DOI

10.1038/ONC.2012.74

1 reference

11 September 2017

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