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A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression
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scholarly article
1 reference
stated in
PubMed
PubMed ID
9139820
retrieved
31 January 2017
title
A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression
(English)
1 reference
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PubMed
PubMed ID
9139820
retrieved
31 January 2017
author name string
T. Heinzel
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1
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PubMed
PubMed ID
9139820
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31 January 2017
R. M. Lavinsky
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PubMed
PubMed ID
9139820
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31 January 2017
T. M. Mullen
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PubMed
PubMed ID
9139820
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31 January 2017
M. Söderstrom
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PubMed
PubMed ID
9139820
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31 January 2017
C. D. Laherty
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PubMed
PubMed ID
9139820
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31 January 2017
J. Torchia
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PubMed
PubMed ID
9139820
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31 January 2017
W. M. Yang
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PubMed
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9139820
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G. Brard
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9139820
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S. D. Ngo
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9139820
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J. R. Davie
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9139820
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E. Seto
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PubMed ID
9139820
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31 January 2017
R. N. Eisenman
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PubMed
PubMed ID
9139820
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31 January 2017
D. W. Rose
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PubMed
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9139820
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31 January 2017
C. K. Glass
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PubMed
PubMed ID
9139820
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31 January 2017
M. G. Rosenfeld
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15
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PubMed
PubMed ID
9139820
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31 January 2017
language of work or name
English
0 references
publication date
1 May 1997
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PubMed
PubMed ID
9139820
retrieved
31 January 2017
published in
Nature
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PubMed
PubMed ID
9139820
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31 January 2017
volume
387
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PubMed
PubMed ID
9139820
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31 January 2017
page(s)
43–48
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PubMed
PubMed ID
9139820
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31 January 2017
issue
6628
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PubMed
PubMed ID
9139820
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31 January 2017
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A role for nucleosome assembly in both silencing and activation of the Xenopus TR beta A gene by the thyroid hormone receptor
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The thyroid hormone receptor binds with opposite transcriptional effects to a common sequence motif in thyroid hormone and estrogen response elements
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Interaction of human thyroid hormone receptor beta with transcription factor TFIIB may mediate target gene derepression and activation by thyroid hormone
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7 January 2021
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The tau 4 activation domain of the thyroid hormone receptor is required for release of a putative corepressor(s) necessary for transcriptional silencing
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7 January 2021
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Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor
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Polarity-specific activities of retinoic acid receptors determined by a co-repressor.
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A nuclear hormone receptor corepressor mediates transcriptional silencing by receptors with distinct repression domains.
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7 January 2021
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Mad: a heterodimeric partner for Max that antagonizes Myc transcriptional activity
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A switch from Myc:Max to Mad:Max heterocomplexes accompanies monocyte/macrophage differentiation.
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The Max transcription factor network: involvement of Mad in differentiation and an approach to identification of target genes.
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Mad-Max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3
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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
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Mad proteins contain a dominant transcription repression domain.
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Both positive and negative regulators of HO transcription are required for mother-cell-specific mating-type switching in yeast
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Activation of the yeast HO gene by release from multiple negative controls
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7 January 2021
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The Saccharomyces cerevisiae SIN3 gene, a negative regulator of HO, contains four paired amphipathic helix motifs
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7 January 2021
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RPD1 (SIN3/UME4) is required for maximal activation and repression of diverse yeast genes
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7 January 2021
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RPD3 encodes a second factor required to achieve maximum positive and negative transcriptional states in Saccharomyces cerevisiae
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7 January 2021
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The yeast SIN3 gene product negatively regulates the activity of the human progesterone receptor and positively regulates the activities of GAL4 and the HAP1 activator
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7 January 2021
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A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p
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Trichostatin A and trapoxin: novel chemical probes for the role of histone acetylation in chromatin structure and function
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Crossref
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Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3
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Crossref
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Expression of c-fos and AP-1 activity in senescent human fibroblasts is not sufficient for DNA synthesis
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ERF: an ETS domain protein with strong transcriptional repressor activity, can suppress ets-associated tumorigenesis and is regulated by phosphorylation during cell cycle and mitogenic stimulation
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The activities of two Ets-related transcription factors required for Drosophila eye development are modulated by the Ras/MAPK pathway
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7 January 2021
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A transcriptional co-repressor that interacts with nuclear hormone receptors
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
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HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription
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Crossref
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7 January 2021
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Regulation of gene expression by nucleosomes
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
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inferred from DOI database lookup
Active repression mechanisms of eukaryotic transcription repressors
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Crossref
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7 January 2021
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The price of repression
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
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inferred from DOI database lookup
Multiple SWItches to turn on chromatin?
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Crossref
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7 January 2021
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Histone acetylation and chromatin assembly: a single escort, multiple dances?
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Crossref
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Targeting chromatin disruption: Transcription regulators that acetylate histones
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
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A positive role for histone acetylation in transcription factor access to nucleosomal DNA
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ssn6-Tup1 is a general repressor of transcription in yeast
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Histone acetylation influences both gene expression and development of Xenopus laevis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
based on heuristic
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The transcriptional coactivators p300 and CBP are histone acetyltransferases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
The CBP co-activator is a histone acetyltransferase
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
based on heuristic
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A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
retrieved
7 January 2021
based on heuristic
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Properties of chicken erythrocyte histone deacetylase associated with the nuclear matrix
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
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Sequence and characterization of a coactivator for the steroid hormone receptor superfamily
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
based on heuristic
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A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A
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Crossref
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https://api.crossref.org/works/10.1038%2F387043A0
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7 January 2021
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Identifiers
DOI
10.1038/387043A0
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2918204
Dimensions Publication ID
1027015027
0 references
OpenCitations bibliographic resource ID
2918204
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2918204
PubMed ID
9139820
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2918204
Springer Nature article ID
10.1038/387043a0
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