Mnt transcriptional repressor is functionally regulated during cell cycle progression (Q28508199)

24 January 2017

title

Mnt transcriptional repressor is functionally regulated during cell cycle progression (English)

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Transcriptional regulator, SIN3B (yeast)

24 January 2017

main subject

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Max binding protein

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Transcriptional regulator, SIN3A (yeast)

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Histone deacetylase 1

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Nikita Popov

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24 January 2017

Therese Wahlström

series ordinal

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24 January 2017

Peter J. Hurlin

series ordinal

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24 January 2017

Marie Henriksson

series ordinal

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24 January 2017

language of work or name

English

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publication date

15 December 2005

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24 January 2017

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24 January 2017

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24 January 2017

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24 January 2017

page(s)

8326–8337

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Mad-Max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3

24 January 2017

cites work

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https://api.crossref.org/works/10.1038/SJ.ONC.1208961

Signaling disrupts mSin3A binding to the Mad1-like Sin3-interacting domain of TIEG2, an Sp1-like repressor

21 April 2017

1 reference

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Genomic targets of the human c-Myc protein

21 April 2017

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The Myc/Max/Mad network and the transcriptional control of cell behavior

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/SJ.ONC.1208961

Histone deacetylase activity is required for full transcriptional repression by mSin3A

21 April 2017

1 reference

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Mga, a dual-specificity transcription factor that interacts with Max and contains a T-domain DNA-binding motif

21 April 2017

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Deletion of Mnt leads to disrupted cell cycle control and tumorigenesis

21 April 2017

1 reference

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Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression

21 April 2017

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The novel ATM-related protein TRRAP is an essential cofactor for the c-Myc and E2F oncoproteins

21 April 2017

1 reference

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Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor.

21 April 2017

1 reference

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The human ROX gene: genomic structure and mutation analysis in human breast tumors

21 April 2017

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Acute mutation of retinoblastoma gene function is sufficient for cell cycle re-entry

21 April 2017

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An amino-terminal domain of Mxi1 mediates anti-Myc oncogenic activity and interacts with a homolog of the yeast transcriptional repressor SIN3

21 April 2017

1 reference

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Repression of p15INK4b expression by Myc through association with Miz-1

21 April 2017

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Transcriptional control. Sinful repression

21 April 2017

1 reference

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Mxi1, a protein that specifically interacts with Max to bind Myc-Max recognition sites

21 April 2017

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Cofactor dynamics and sufficiency in estrogen receptor-regulated transcription

21 April 2017

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Inhibition of cell growth and apoptosis by inducible expression of the transcriptional repressor Mad1.

21 April 2017

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Direct examination of histone acetylation on Myc target genes using chromatin immunoprecipitation

21 January 2018

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A large scale genetic analysis of c-Myc-regulated gene expression patterns

21 January 2018

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The myc oncogene: MarvelouslY Complex

21 January 2018

1 reference

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Mnt-Max to Myc-Max complex switching regulates cell cycle entry

21 January 2018

1 reference

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Switch from Myc/Max to Mad1/Max binding and decrease in histone acetylation at the telomerase reverse transcriptase promoter during differentiation of HL60 cells.

21 January 2018

1 reference

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Transcriptional activation by the human c-Myc oncoprotein in yeast requires interaction with Max.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208961

7 January 2021

Mnt, a novel Max-interacting protein is coexpressed with Myc in proliferating cells and mediates repression at Myc binding sites

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208961

7 January 2021

Mnt: a novel Max-interacting protein and Myc antagonist

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208961

7 January 2021

Myc and Max proteins possess distinct transcriptional activities

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208961

7 January 2021

Sequential expression of the MAD family of transcriptional repressors during differentiation and development.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1208961

7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/SJ.ONC.1208961

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1032861573

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