GATA3 cooperates with PARP1 to regulate CCND1 transcription through modulating histone H1 incorporation (Q34817460)

4 August 2017

GATA3 cooperates with PARP1 to regulate CCND1 transcription through modulating histone H1 incorporation (English)

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4 August 2017

L Shan

1

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4 August 2017

X Li

2

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4 August 2017

L Liu

3

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4 August 2017

X Ding

4

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4 August 2017

Q Wang

5

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4 August 2017

Y Zheng

6

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4 August 2017

Y Duan

7

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4 August 2017

C Xuan

8

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4 August 2017

Y Wang

9

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4 August 2017

F Yang

10

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4 August 2017

Y Shang

11

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4 August 2017

L Shi

12

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4 August 2017

language of work or name

English

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publication date

15 July 2013

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4 August 2017

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4 August 2017

33

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4 August 2017

3205-3216

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4 August 2017

24

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https://scigraph.springernature.com/pub.10.1038/onc.2013.270

4 August 2017

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Transcription factor GATA-3 is required for development of the T-cell lineage

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GATA3 inhibits breast cancer metastasis through the reversal of epithelial-mesenchymal transition

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BRCA1 and GATA3 corepress FOXC1 to inhibit the pathogenesis of basal-like breast cancers

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Positive cross-regulatory loop ties GATA-3 to estrogen receptor alpha expression in breast cancer

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NAD+-dependent modulation of chromatin structure and transcription by nucleosome binding properties of PARP-1.

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SIRT6 promotes DNA repair under stress by activating PARP1

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PARP-1, a determinant of cell survival in response to DNA damage

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PARP-1, PARP-2 and ATM in the DNA damage response: functional synergy in mouse development

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The PARP side of the nucleus: molecular actions, physiological outcomes, and clinical targets

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PARP-1 regulates chromatin structure and transcription through a KDM5B-dependent pathway

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PARP-1 attenuates Smad-mediated transcription

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LSD1 is a subunit of the NuRD complex and targets the metastasis programs in breast cancer

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Reciprocal binding of PARP-1 and histone H1 at promoters specifies transcriptional outcomes

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The transcription factor GATA-3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells

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GATA-3 is expressed in association with estrogen receptor in breast cancer

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Re-evaluating PARP1 inhibitor in cancer

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Identifiers

DOI

10.1038/ONC.2013.270

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Dimensions Publication ID

4 August 2017

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