| scholarly article | Q13442814 |
| P2093 | author name string | C W Wong | |
| M L Privalsky | |||
| P2860 | cites work | Unliganded thyroid hormone receptor alpha can target TATA-binding protein for transcriptional repression | Q24310721 |
| Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor | Q24311650 | ||
| Mad: a heterodimeric partner for Max that antagonizes Myc transcriptional activity | Q24320236 | ||
| Mxi1, a protein that specifically interacts with Max to bind Myc-Max recognition sites | Q24320277 | ||
| Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex | Q24320470 | ||
| Two receptor interaction domains in the corepressor, N-CoR/RIP13, are required for an efficient interaction with Rev-erbA alpha and RVR: physical association is dependent on the E region of the orphan receptors | Q24543959 | ||
| A transferable silencing domain is present in the thyroid hormone receptor, in the v-erbA oncogene product and in the retinoic acid receptor | Q24555696 | ||
| The tau 4 activation domain of the thyroid hormone receptor is required for release of a putative corepressor(s) necessary for transcriptional silencing | Q24646988 | ||
| Cloning and characterization of a corepressor and potential component of the nuclear hormone receptor repression complex | Q24648169 | ||
| Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3 | Q24648290 | ||
| Sodium butyrate inhibits myogenesis by interfering with the transcriptional activation function of MyoD and myogenin | Q41597273 | ||
| Unliganded thyroid hormone receptor inhibits formation of a functional preinitiation complex: implications for active repression | Q42069854 | ||
| Coactivator and corepressor regulation of the agonist/antagonist activity of the mixed antiestrogen, 4-hydroxytamoxifen. | Q42439064 | ||
| Protein encoded by v-erbA functions as a thyroid-hormone receptor antagonist | Q44537287 | ||
| The histone deacetylase RPD3 counteracts genomic silencing in Drosophila and yeast | Q47072158 | ||
| Both positive and negative regulators of HO transcription are required for mother-cell-specific mating-type switching in yeast | Q57270194 | ||
| Repression of transcription mediated at a thyroid hormone response element by the v-erb-A oncogene product | Q59098062 | ||
| Activation of the yeast HO gene by release from multiple negative controls | Q68934076 | ||
| Butyrate and related inhibitors of histone deacetylation block the induction of egg white genes by steroid hormones | Q71432413 | ||
| Stoichiometric and steric principles governing repression by nuclear hormone receptors | Q73231880 | ||
| Gene silencing by chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is mediated by transcriptional corepressors, nuclear receptor-corepressor (N-CoR) and silencing mediator for retinoic acid receptor and thyroid hormone receptor | Q73386741 | ||
| SMRT corepressor interacts with PLZF and with the PML-retinoic acid receptor alpha (RARalpha) and PLZF-RARalpha oncoproteins associated with acute promyelocytic leukemia | Q24653689 | ||
| Repression by Ume6 involves recruitment of a complex containing Sin3 corepressor and Rpd3 histone deacetylase to target promoters | Q27936998 | ||
| HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription | Q27937238 | ||
| Eukaryotic proteins expressed in Escherichia coli: An improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase | Q28131695 | ||
| An amino-terminal domain of Mxi1 mediates anti-Myc oncogenic activity and interacts with a homolog of the yeast transcriptional repressor SIN3 | Q28236250 | ||
| Transcriptional control. Sinful repression | Q28237278 | ||
| What's up and down with histone deacetylation and transcription? | Q28238059 | ||
| Histone deacetylase activity is required for full transcriptional repression by mSin3A | Q28238079 | ||
| Histone deacetylases associated with the mSin3 corepressor mediate mad transcriptional repression | Q28238089 | ||
| The partial agonist activity of antagonist-occupied steroid receptors is controlled by a novel hinge domain-binding coactivator L7/SPA and the corepressors N-CoR or SMRT | Q28239712 | ||
| Role of the histone deacetylase complex in acute promyelocytic leukaemia | Q28263534 | ||
| Rb interacts with histone deacetylase to repress transcription | Q28263985 | ||
| A transcriptional co-repressor that interacts with nuclear hormone receptors | Q28289864 | ||
| Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression | Q28513708 | ||
| A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression | Q28578229 | ||
| Two receptor interacting domains in the nuclear hormone receptor corepressor RIP13/N-CoR | Q28586882 | ||
| Nuclear receptor repression mediated by a complex containing SMRT, mSin3A, and histone deacetylase | Q29547913 | ||
| Fusion proteins of the retinoic acid receptor-alpha recruit histone deacetylase in promyelocytic leukaemia | Q29616211 | ||
| Epistasis analysis of suppressor mutations that allow HO expression in the absence of the yeast SW15 transcriptional activator | Q33962612 | ||
| Suppressors of defective silencing in yeast: effects on transcriptional repression at the HMR locus, cell growth and telomere structure. | Q33966150 | ||
| Identification of TRACs (T3 receptor-associating cofactors), a family of cofactors that associate with, and modulate the activity of, nuclear hormone receptors | Q34398024 | ||
| The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70. | Q34669136 | ||
| Interaction of human thyroid hormone receptor beta with transcription factor TFIIB may mediate target gene derepression and activation by thyroid hormone | Q36556508 | ||
| Corepressor SMRT binds the BTB/POZ repressing domain of the LAZ3/BCL6 oncoprotein | Q36594782 | ||
| Functional evidence for ligand-dependent dissociation of thyroid hormone and retinoic acid receptors from an inhibitory cellular factor | Q36664756 | ||
| Transcriptional repression in Saccharomyces cerevisiae by a SIN3-LexA fusion protein | Q36676648 | ||
| RPD3 encodes a second factor required to achieve maximum positive and negative transcriptional states in Saccharomyces cerevisiae | Q36744711 | ||
| SMRT isoforms mediate repression and anti-repression of nuclear receptor heterodimers | Q36813375 | ||
| The erbA oncogene represses the actions of both retinoid X and retinoid A receptors but does so by distinct mechanisms | Q36822461 | ||
| The centromere and promoter factor, 1, CPF1, of Saccharomyces cerevisiae modulates gene activity through a family of factors including SPT21, RPD1 (SIN3), RPD3 and CCR4. | Q38316201 | ||
| A nuclear hormone receptor corepressor mediates transcriptional silencing by receptors with distinct repression domains. | Q38352823 | ||
| Differential recognition of liganded and unliganded thyroid hormone receptor by retinoid X receptor regulates transcriptional repression | Q40023991 | ||
| Trichostatin A and trapoxin: novel chemical probes for the role of histone acetylation in chromatin structure and function | Q40547910 | ||
| Chromatin unfolds | Q41021102 | ||
| Characterization of receptor interaction and transcriptional repression by the corepressor SMRT. | Q41066584 | ||
| Retinoid X and retinoic acid receptors interact with transcription factor II-B by distinct mechanisms | Q41115072 | ||
| Polarity-specific activities of retinoic acid receptors determined by a co-repressor. | Q41284148 | ||
| Nuclear receptor coactivators and corepressors | Q41447637 | ||
| Histone acetylation: chromatin in action | Q41468916 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 5500-5510 | |
| P577 | publication date | 1998-09-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB. | |
| P478 | volume | 18 |
| Q33598783 | A conserved lysine in the thyroid hormone receptor-alpha1 DNA-binding domain, mutated in hepatocellular carcinoma, serves as a sensor for transcriptional regulation |
| Q22254089 | A core SMRT corepressor complex containing HDAC3 and TBL1, a WD40-repeat protein linked to deafness |
| Q28141676 | A mechanism of repression by acute myeloid leukemia-1, the target of multiple chromosomal translocations in acute leukemia |
| Q34144764 | A novel mechanism involving coordinated regulation of nuclear levels and acetylation of NF-YA and Bcl6 activates RGS4 transcription. |
| Q46617735 | AML1B transcriptional repressor function is impaired by the Flt3-internal tandem duplication |
| Q39576827 | Aberrant recruitment of the nuclear receptor corepressor-histone deacetylase complex by the acute myeloid leukemia fusion partner ETO. |
| Q35639785 | Alternative mRNA splicing of corepressors generates variants that play opposing roles in adipocyte differentiation. |
| Q34290292 | Avian erythroleukemia: a model for corepressor function in cancer |
| Q31875497 | Cell type-specific roles of histone deacetylase in TR ligand-independent transcriptional repression |
| Q34678559 | Chromosomal localization links the SIN3-RPD3 complex to the regulation of chromatin condensation, histone acetylation and gene expression |
| Q39681319 | Competitive cofactor recruitment by orphan receptor hepatocyte nuclear factor 4alpha1: modulation by the F domain |
| Q28284917 | Components of the SMRT corepressor complex exhibit distinctive interactions with the POZ domain oncoproteins PLZF, PLZF-RARalpha, and BCL-6 |
| Q31078289 | Corepressor requirement and thyroid hormone receptor function during Xenopus development |
| Q33632335 | DNA methylation and chromatin modification. |
| Q35130222 | Direct interaction of NRSF with TBP: chromatin reorganization and core promoter repression for neuron-specific gene transcription |
| Q24514479 | Domain structure of the NRIF3 family of coregulators suggests potential dual roles in transcriptional regulation |
| Q36832163 | Emerging roles of the corepressors NCoR1 and SMRT in homeostasis |
| Q39092838 | Epigenetic targets in hepatocellular carcinoma cells: identification of chaperone protein complexes with histone deacetylases |
| Q52580083 | Estrogen-induced and TAFII30-mediated gene repression by direct recruitment of the estrogen receptor and co-repressors to the core promoter and its reversal by tamoxifen. |
| Q34722386 | FMR1 silencing and the signals to chromatin: a unified model of transcriptional regulation |
| Q34813109 | Gene silencing |
| Q28505345 | Glucocorticoid receptor (GR)-associated SMRT binding to C/EBPbeta TAD and Nrf2 Neh4/5: role of SMRT recruited to GR in GSTA2 gene repression |
| Q22253934 | Histone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2. |
| Q33632987 | Histone deacetylases: transcriptional repression with SINers and NuRDs |
| Q38298930 | Identification of a neurorestrictive suppressor element (NRSE) in the human mu-opioid receptor gene |
| Q39436081 | Identification of nuclear orphan receptors as regulators of expression of a neurotransmitter receptor gene |
| Q28141911 | Ikaros interactions with CtBP reveal a repression mechanism that is independent of histone deacetylase activity |
| Q28215092 | Ikaros-CtIP interactions do not require C-terminal binding protein and participate in a deacetylase-independent mode of repression |
| Q39686347 | Inhibition of polyomavirus ori-dependent DNA replication by mSin3B |
| Q30453299 | Involvement of histone methylation and phosphorylation in regulation of transcription by thyroid hormone receptor |
| Q34889102 | Isotype-restricted corepressor recruitment: a constitutively closed helix 12 conformation in retinoic acid receptors beta and gamma interferes with corepressor recruitment and prevents transcriptional repression |
| Q33630360 | MeCP2 driven transcriptional repression in vitro: selectivity for methylated DNA, action at a distance and contacts with the basal transcription machinery |
| Q36902922 | Molecular antagonism between X-chromosome and autosome signals determines nematode sex. |
| Q24532232 | Msx3 protein recruits histone deacetylase to down-regulate the Msx1 promoter |
| Q40811024 | Negative regulation of bcl-2 expression by p53 in hematopoietic cells |
| Q24644926 | Neural restrictive silencer factor recruits mSin3 and histone deacetylase complex to repress neuron-specific target genes |
| Q34621596 | Nuclear receptor-dependent transcription with chromatin. Is it all about enzymes? |
| Q24290950 | PSF is a novel corepressor that mediates its effect through Sin3A and the DNA binding domain of nuclear hormone receptors |
| Q35802815 | Pharmacology of nuclear receptor-coregulator recognition. |
| Q34324051 | Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation |
| Q24302865 | Recruitment of O-GlcNAc transferase to promoters by corepressor mSin3A: coupling protein O-GlcNAcylation to transcriptional repression |
| Q24657661 | Recruitment of SMRT/N-CoR-mSin3A-HDAC-repressing complexes is not a general mechanism for BTB/POZ transcriptional repressors: the case of HIC-1 and gammaFBP-B |
| Q34444363 | Regulation of SMRT corepressor dimerization and composition by MAP kinase phosphorylation |
| Q40898485 | Resistance to thyroid hormone (RTH) syndrome reveals novel determinants regulating interaction of T3 receptor with corepressor |
| Q37175201 | Response of SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) and N-CoR (nuclear receptor corepressor) corepressors to mitogen-activated protein kinase kinase kinase cascades is determined by alternative mRNA splicing |
| Q37241518 | Retinoid isomers differ in the ability to induce release of SMRT corepressor from retinoic acid receptor-alpha |
| Q30440069 | SMRT and N-CoR corepressors are regulated by distinct kinase signaling pathways |
| Q40652029 | Signal-dependent N-CoR Requirement for Repression by the Ski Oncoprotein |
| Q41013482 | Signaling by tyrosine kinases negatively regulates the interaction between transcription factors and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) corepressor |
| Q28254928 | Structure-function analysis of the estrogen receptor alpha corepressor scaffold attachment factor-B1: identification of a potent transcriptional repression domain |
| Q38318863 | Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene. |
| Q21284161 | TBLR1 regulates the expression of nuclear hormone receptor co-repressors |
| Q42827376 | TEL contacts multiple co-repressors and specifically associates with histone deacetylase-3. |
| Q37284561 | Targeted chromatin binding and histone acetylation in vivo by thyroid hormone receptor during amphibian development |
| Q34732688 | Targeting of N-CoR and histone deacetylase 3 by the oncoprotein v-erbA yields a chromatin infrastructure-dependent transcriptional repression pathway |
| Q24292959 | The ErbB3 binding protein Ebp1 interacts with Sin3A to repress E2F1 and AR-mediated transcription |
| Q34441108 | The SIN3/RPD3 deacetylase complex is essential for G(2) phase cell cycle progression and regulation of SMRTER corepressor levels |
| Q28343797 | The SMRT corepressor is a target of phosphorylation by protein kinase CK2 (casein kinase II) |
| Q39455172 | The SMRT corepressor is regulated by a MEK-1 kinase pathway: inhibition of corepressor function is associated with SMRT phosphorylation and nuclear export |
| Q22253389 | The adenovirus E1A binding protein BS69 is a corepressor of transcription through recruitment of N-CoR |
| Q30888959 | The adenovirus-2 E1B-55K protein interacts with a mSin3A/histone deacetylase 1 complex |
| Q34313320 | The biology of human lymphoid malignancies revealed by gene expression profiling. |
| Q22253387 | The co-repressor mSin3A is a functional component of the REST-CoREST repressor complex |
| Q40549870 | The highly conserved region of the co-repressor Sin3A functionally interacts with the co-repressor Alien |
| Q28144226 | The minimal repression domain of MBD2b overlaps with the methyl-CpG-binding domain and binds directly to Sin3A |
| Q24550992 | The neuron-restrictive silencer element-neuron-restrictive silencer factor system regulates basal and endothelin 1-inducible atrial natriuretic peptide gene expression in ventricular myocytes |
| Q34141139 | The silencing mediator of retinoic acid and thyroid hormone receptors can interact with the aryl hydrocarbon (Ah) receptor but fails to repress Ah receptor-dependent gene expression |
| Q35089956 | The thyroid hormone receptor and the insulator protein CTCF: two different factors with overlapping functions |
| Q34493334 | Towards understanding the epigenetics of transcription by chromatin structure and the nuclear matrix |
| Q37241513 | Transcriptional anti-repression. Thyroid hormone receptor beta-2 recruits SMRT corepressor but interferes with subsequent assembly of a functional corepressor complex |
| Q39451978 | Transcriptional repression by blimp-1 (PRDI-BF1) involves recruitment of histone deacetylase |
| Q33826663 | Transcriptional repression by nuclear hormone receptors |
| Q40816966 | Transcriptional repression by thyroid hormone receptors. A role for receptor homodimers in the recruitment of SMRT corepressor |
| Q34698342 | Tzfp represses the androgen receptor in mouse testis |
| Q24524018 | mSin3A regulates murine erythroleukemia cell differentiation through association with the TAL1 (or SCL) transcription factor |
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