| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1035667550 |
| P356 | DOI | 10.1038/387049A0 |
| P3181 | OpenCitations bibliographic resource ID | 613439 |
| P698 | PubMed publication ID | 9139821 |
| P2093 | author name string | L. Chin | |
| H. Hou | |||
| L. Alland | |||
| N. Schreiber-Agus | |||
| R. A. DePinho | |||
| J. Potes | |||
| R. Muhle | |||
| P2860 | cites work | Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor | Q24311650 |
| Two human homologues of Saccharomyces cerevisiae SWI2/SNF2 and Drosophila brahma are transcriptional coactivators cooperating with the estrogen receptor and the retinoic acid receptor | Q24317125 | ||
| A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor | Q24317715 | ||
| The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein | Q24318775 | ||
| BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription | Q24319163 | ||
| Mad: a heterodimeric partner for Max that antagonizes Myc transcriptional activity | Q24320236 | ||
| The retinoblastoma protein and BRG1 form a complex and cooperate to induce cell cycle arrest | Q24321861 | ||
| A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A | Q24336667 | ||
| Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3 | Q24648290 | ||
| Mammalian Ras interacts directly with the serine/threonine kinase Raf | Q27860833 | ||
| HDA1 and RPD3 are members of distinct yeast histone deacetylase complexes that regulate silencing and transcription | Q27937238 | ||
| The CBP co-activator is a histone acetyltransferase | Q28131758 | ||
| Mad-Max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3 | Q28236241 | ||
| An amino-terminal domain of Mxi1 mediates anti-Myc oncogenic activity and interacts with a homolog of the yeast transcriptional repressor SIN3 | Q28236250 | ||
| Direct role for Myc in transcription initiation mediated by interactions with TFII-I | Q28262704 | ||
| Histone deacetylase: a regulator of transcription | Q28276231 | ||
| A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p | Q28276243 | ||
| Induction of apoptosis in fibroblasts by c-myc protein | Q29614346 | ||
| Identification of cooperating oncogenes in E mu-myc transgenic mice by provirus tagging | Q29619816 | ||
| Yeast SNF/SWI transcriptional activators and the SPT/SIN chromatin connection | Q29620100 | ||
| Functional interactions between the hBRM/hBRG1 transcriptional activators and the pRB family of proteins | Q36558284 | ||
| Transcriptional repression in Saccharomyces cerevisiae by a SIN3-LexA fusion protein | Q36676648 | ||
| The Saccharomyces cerevisiae SIN3 gene, a negative regulator of HO, contains four paired amphipathic helix motifs | Q36733371 | ||
| RPD1 (SIN3/UME4) is required for maximal activation and repression of diverse yeast genes | Q36744665 | ||
| RPD3 encodes a second factor required to achieve maximum positive and negative transcriptional states in Saccharomyces cerevisiae | Q36744711 | ||
| A link between c-Myc-mediated transcriptional repression and neoplastic transformation | Q37353738 | ||
| Sin3 corepressor function in Myc-induced transcription and transformation | Q37409356 | ||
| myc family oncogenes in the development of normal and neoplastic cells. | Q37511853 | ||
| c-Myc represses transcription in vivo by a novel mechanism dependent on the initiator element and Myc box II | Q37635815 | ||
| Adenovirus E1B oncoprotein tethers a transcriptional repression domain to p53. | Q38312352 | ||
| A nuclear hormone receptor corepressor mediates transcriptional silencing by receptors with distinct repression domains. | Q38352823 | ||
| A role for nucleosome assembly in both silencing and activation of the Xenopus TR beta A gene by the thyroid hormone receptor | Q39471038 | ||
| Mad proteins contain a dominant transcription repression domain. | Q40020073 | ||
| Targeting chromatin disruption: Transcription regulators that acetylate histones | Q40970395 | ||
| Special HATs for special occasions: linking histone acetylation to chromatin assembly and gene activation | Q41044061 | ||
| Cdc25 cell-cycle phosphatase as a target of c-myc | Q41175989 | ||
| Novel zinc finger gene implicated as myc collaborator by retrovirally accelerated lymphomagenesis in E mu-myc transgenic mice. | Q44391026 | ||
| Transcriptional repression directed by the yeast alpha 2 protein in vitro | Q46051755 | ||
| The histone deacetylase RPD3 counteracts genomic silencing in Drosophila and yeast | Q47072158 | ||
| The global transcriptional regulators, SSN6 and TUP1, play distinct roles in the establishment of a repressive chromatin structure. | Q52216137 | ||
| Sequence similarity between the mammalian bmi-1 proto-oncogene and the Drosophila regulatory genes Psc and Su(z)2. | Q52447422 | ||
| Both positive and negative regulators of HO transcription are required for mother-cell-specific mating-type switching in yeast | Q57270194 | ||
| Functional dissection of the yeast Cyc8–Tupl transcriptional co-repressor complex | Q59056491 | ||
| Chromatin structure of the yeast SUC2 promoter in regulatory mutants | Q68062065 | ||
| P433 | issue | 6628 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Histone deacetylase 1 | Q14914426 |
| Nuclear receptor corepressor 1 | Q21425039 | ||
| P304 | page(s) | 49–55 | |
| P577 | publication date | 1997-05-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression | |
| P478 | volume | 387 |
| Q73157313 | A 13-amino acid amphipathic alpha-helix is required for the functional interaction between the transcriptional repressor Mad1 and mSin3A |
| Q35195830 | A CBP/p300 homolog specifies multiple differentiation pathways in Caenorhabditis elegans. |
| Q41653844 | A SAGA of histone acetylation and gene expression |
| Q28141283 | A Smad transcriptional corepressor |
| Q27937262 | A conserved motif common to the histone acetyltransferase Esa1 and the histone deacetylase Rpd3. |
| Q22254089 | A core SMRT corepressor complex containing HDAC3 and TBL1, a WD40-repeat protein linked to deafness |
| Q44285403 | A developmentally regulated splice variant from the complex lola locus encoding multiple different zinc finger domain proteins interacts with the chromosomal kinase JIL-1. |
| Q24598533 | A histone deacetylase corepressor complex regulates the Notch signal transduction pathway |
| Q24522669 | A human RNA polymerase II complex containing factors that modify chromatin structure |
| Q27937976 | A large protein complex containing the yeast Sin3p and Rpd3p transcriptional regulators |
| Q29617070 | A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase |
| Q24292390 | A negative coregulator for the human ER |
| Q28141771 | A new family of human histone deacetylases related to Saccharomyces cerevisiae HDA1p |
| Q33957578 | A new member of the Sin3 family of corepressors is essential for cell viability and required for retroelement propagation in fission yeast |
| Q34366624 | A novel repressive E2F6 complex containing the polycomb group protein, EPC1, that interacts with EZH2 in a proliferation-specific manner |
| Q39447809 | A novel role for helix 12 of retinoid X receptor in regulating repression |
| Q39884342 | A role for H3K4 monomethylation in gene repression and partitioning of chromatin readers. |
| Q35207580 | A role for transcriptional repression of p21CIP1 by c-Myc in overcoming transforming growth factor beta -induced cell-cycle arrest |
| Q38712941 | A single allele of Hdac2 but not Hdac1 is sufficient for normal mouse brain development in the absence of its paralog. |
| Q28141695 | Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin |
| Q39576827 | Aberrant recruitment of the nuclear receptor corepressor-histone deacetylase complex by the acute myeloid leukemia fusion partner ETO. |
| Q34334819 | Above and within the genome: epigenetics past and present |
| Q35027641 | Acetylation in hormone signaling and the cell cycle |
| Q34276051 | Acetylation of androgen receptor enhances coactivator binding and promotes prostate cancer cell growth |
| Q41745269 | Acquisition of oncogenic potential by RAR chimeras in acute promyelocytic leukemia through formation of homodimers. |
| Q47754172 | Activation and repression in the nervous system |
| Q27860534 | Activation of p53 sequence-specific DNA binding by acetylation of the p53 C-terminal domain |
| Q42815429 | Activation of the murine dihydrofolate reductase promoter by E2F1. A requirement for CBP recruitment |
| Q31750307 | Activation of the p21WAF1/CIP1 promoter independent of p53 by the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) through the Sp1 sites |
| Q33707816 | Adamantyl-substituted retinoid-related molecules bind small heterodimer partner and modulate the Sin3A repressor. |
| Q24523301 | Adenovirus E1B 55K represses p53 activation in vitro. |
| Q24554508 | Alien, a highly conserved protein with characteristics of a corepressor for members of the nuclear hormone receptor superfamily |
| Q77957413 | Amphibian metamorphosis as a model for studying the developmental actions of thyroid hormone |
| Q77988411 | Amphibian metamorphosis as a model for studying the developmental actions of thyroid hormone |
| Q24535295 | An ERG (ets-related gene)-associated histone methyltransferase interacts with histone deacetylases 1/2 and transcription co-repressors mSin3A/B |
| Q38301863 | An essential role for Mad homology domain 1 in the association of Smad3 with histone deacetylase activity*. |
| Q37406278 | An overview of MYC and its interactome |
| Q77892623 | Analysis of activity and regulation of hGcn5, a human histone acetyltransferase |
| Q34125103 | Androgen receptor acetylation governs trans activation and MEKK1-induced apoptosis without affecting in vitro sumoylation and trans-repression function |
| Q36002801 | Arabidopsis thaliana histone deacetylase 1 (AtHD1) is localized in euchromatic regions and demonstrates histone deacetylase activity in vitro |
| Q39632464 | Autophagy-related intrinsically disordered proteins in intra-nuclear compartments |
| Q34290292 | Avian erythroleukemia: a model for corepressor function in cancer |
| Q22254616 | BCoR, a novel corepressor involved in BCL-6 repression |
| Q38939530 | BRMS1L suppresses breast cancer metastasis by inducing epigenetic silence of FZD10. |
| Q41791631 | Bach1 inhibits oxidative stress-induced cellular senescence by impeding p53 function on chromatin |
| Q42445040 | Binding of the thyroid hormone receptor to a negative element in the basal growth hormone promoter is associated with histone acetylation |
| Q79315264 | Biochemical isolation and analysis of a nuclear receptor corepressor complex |
| Q33959609 | Both TEL and AML-1 contribute repression domains to the t(12;21) fusion protein |
| Q24599788 | Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3 |
| Q34272659 | Breast cancer metastasis suppressor 1 (BRMS1) forms complexes with retinoblastoma-binding protein 1 (RBP1) and the mSin3 histone deacetylase complex and represses transcription |
| Q28116047 | C6orf89 encodes three distinct HDAC enhancers that function in the nucleolus, the golgi and the midbody |
| Q28190788 | CHD1 associates with NCoR and histone deacetylase as well as with RNA splicing proteins |
| Q22008610 | CIR, a corepressor linking the DNA binding factor CBF1 to the histone deacetylase complex |
| Q39445171 | COUP-TF upregulates NGFI-A gene expression through an Sp1 binding site. |
| Q34580151 | COUP-TFs and eye development |
| Q37129336 | Ca2+-operated transcriptional networks: molecular mechanisms and in vivo models. |
| Q28143007 | Cabin1 represses MEF2-dependent Nur77 expression and T cell apoptosis by controlling association of histone deacetylases and acetylases with MEF2 |
| Q42632600 | Catalytic activity of the yeast SWI/SNF complex on reconstituted nucleosome arrays. |
| Q36917061 | Cdk2 and Pin1 negatively regulate the transcriptional corepressor SMRT |
| Q31875497 | Cell type-specific roles of histone deacetylase in TR ligand-independent transcriptional repression |
| Q24670403 | Characterization of a human RPD3 ortholog, HDAC3 |
| Q62644798 | Characterization of two putative histone deacetylase genes from Aspergillus nidulans |
| Q40935773 | Chicken histone deacetylase-2 controls the amount of the IgM H-chain at the steps of both transcription of its gene and alternative processing of its pre-mRNA in the DT40 cell line |
| Q36177291 | Chromatin associated Sin3A is essential for male germ cell lineage in the mouse |
| Q28306534 | Chromatin crosstalk in development and disease: lessons from REST |
| Q34098840 | Chromatin modification and disease |
| Q34366416 | Chromatin modifiers and tumor suppression |
| Q34076836 | Chromatin remodeling and Rb activity |
| Q33703534 | Chromatin remodeling and transcriptional regulation |
| Q41690930 | Chromatin remodeling regulated by steroid and nuclear receptors |
| Q42989713 | Chromatin remodelling of the cardiac beta-myosin heavy chain gene |
| Q80818380 | Chromatin research gathers pace |
| Q34064159 | Chromatin-remodeling complexes involved in gene activation by the glucocorticoid receptor |
| Q34302232 | Chromosomal integration of retinoic acid response elements prevents cooperative transcriptional activation by retinoic acid receptor and retinoid X receptor |
| Q24648169 | Cloning and characterization of a corepressor and potential component of the nuclear hormone receptor repression complex |
| Q22253464 | Cloning and characterization of a novel human class I histone deacetylase that functions as a transcription repressor |
| Q24532118 | Cloning and characterization of a novel human histone deacetylase, HDAC8 |
| Q48014292 | Cloning and characterization of the mouse histone deacetylase-2 gene |
| Q46623959 | Co-activators and co-repressors in the integration of transcriptional responses |
| Q40685198 | Co-repressor release but not ligand binding is a prerequisite for transcription activation by human retinoid acid receptor alpha ligand-binding domain |
| Q22003747 | CoREST: a functional corepressor required for regulation of neural-specific gene expression |
| Q34478884 | Coactivators and corepressors as mediators of nuclear receptor function: an update |
| Q28591431 | Combinatorial roles of the nuclear receptor corepressor in transcription and development |
| Q28284917 | Components of the SMRT corepressor complex exhibit distinctive interactions with the POZ domain oncoproteins PLZF, PLZF-RARalpha, and BCL-6 |
| Q47721327 | Control of cell proliferation by Myc. |
| Q39445547 | Cooperation between phosphorylation and acetylation processes in transcriptional control |
| Q78017200 | Coregulatory proteins in nuclear hormone receptor action |
| Q39445508 | Corepressor required for adenovirus E1B 55,000-molecular-weight protein repression of basal transcription |
| Q31078289 | Corepressor requirement and thyroid hormone receptor function during Xenopus development |
| Q35096766 | Corepressors, nuclear receptors, and epigenetic factors on DNA: a tail of repression |
| Q48018634 | Covalent modifications of histones: expression from chromatin templates |
| Q35193069 | Critical residues for histone acetylation by Gcn5, functioning in Ada and SAGA complexes, are also required for transcriptional function in vivo |
| Q42478309 | DNA binding and interaction with the nuclear receptor corepressor of thyroid hormone receptor are required for ligand-independent stimulation of the mouse preprothyrotropin-releasing hormone gene |
| Q42807402 | DNA binding of USF is required for specific E-box dependent gene activation in vivo |
| Q41536284 | DNA helicases in inherited human disorders |
| Q33632335 | DNA methylation and chromatin modification. |
| Q24655211 | DNA-binding and -bending activities of SAP30L and SAP30 are mediated by a zinc-dependent module and monophosphoinositides |
| Q35850349 | Deciphering the molecular machinery of stem cells: a look at the neoblast gene expression profile |
| Q37677559 | Deconstructing repression: evolving models of co-repressor action |
| Q35910908 | Detection of activity centers in cellular pathways using transcript profiling |
| Q28577247 | Determinants of coactivator LXXLL motif specificity in nuclear receptor transcriptional activation |
| Q40094550 | Differential effects of Mxi1-SRalpha and Mxi1-SRbeta in Myc antagonism |
| Q28145136 | Differential mechanisms of nuclear receptor regulation by receptor-associated coactivator 3 |
| Q40595558 | Differential modulation of androgen receptor transcriptional activity by the nuclear receptor co-repressor (N-CoR). |
| Q33940612 | Direct acetylation of the estrogen receptor alpha hinge region by p300 regulates transactivation and hormone sensitivity |
| Q33775383 | Disruption of higher-order folding by core histone acetylation dramatically enhances transcription of nucleosomal arrays by RNA polymerase III |
| Q89135132 | Dissection of Enhancer Function Using Multiplex CRISPR-based Enhancer Interference in Cell Lines |
| Q54147247 | Distinct interactions of PML-RARalpha and PLZF-RARalpha with co-repressors determine differential responses to RA in APL. |
| Q33888108 | Distinct requirements for chromatin assembly in transcriptional repression by thyroid hormone receptor and histone deacetylase. |
| Q35974510 | Diverse signaling pathways modulate nuclear receptor recruitment of N-CoR and SMRT complexes |
| Q39987780 | Down-regulation of Notch-dependent transcription by Akt in vitro |
| Q28212240 | Dynamic in vivo interactions among Myc network members |
| Q24685706 | E2F mediates cell cycle-dependent transcriptional repression in vivo by recruitment of an HDAC1/mSin3B corepressor complex |
| Q24522848 | ETO, a target of t(8;21) in acute leukemia, interacts with the N-CoR and mSin3 corepressors |
| Q24653699 | ETO, fusion partner in t(8;21) acute myeloid leukemia, represses transcription by interaction with the human N-CoR/mSin3/HDAC1 complex |
| Q39393565 | Effect of histone deacetylase inhibitors on heat shock protein gene expression during Xenopus development |
| Q34310404 | Embedding the Future of Regenerative Medicine into the Open Epigenomic Landscape of Pluripotent Human Embryonic Stem Cells |
| Q34421775 | Emerging roles for chromatin remodeling in cancer biology |
| Q38107626 | Epigenetic control of cytokine gene expression: regulation of the TNF/LT locus and T helper cell differentiation |
| Q42831677 | Epigenetic control of mouse Oct-4 gene expression in embryonic stem cells and trophoblast stem cells |
| Q34462208 | Epigenetic organization of brain sex differences and juvenile social play behavior |
| Q27015084 | Epigenetics of the depressed brain: role of histone acetylation and methylation |
| Q39594681 | Epstein-Barr virus nuclear antigen 3C interacts with histone deacetylase to repress transcription |
| Q33884209 | Erythroid cell-specific alpha-globin gene regulation by the CP2 transcription factor family |
| Q36481113 | Essential Nonredundant Function of the Catalytic Activity of Histone Deacetylase 2 in Mouse Development |
| Q28140995 | Estrogen receptor interaction with co-activators and co-repressors |
| Q44044525 | Estrogen receptor-mediated effects of tamoxifen on human endometrial cancer cells |
| Q41030520 | Estrogen response elements can mediate agonist activity of anti-estrogens in human endometrial Ishikawa cells |
| Q28144968 | Expression of MXI1, a Myc antagonist, is regulated by Sp1 and AP2 |
| Q24670176 | Expression of histone deacetylase 8, a class I histone deacetylase, is restricted to cells showing smooth muscle differentiation in normal human tissues |
| Q31016083 | Expression of novel ING variants is regulated by thyroid hormone in the Xenopus laevis tadpole |
| Q37461105 | FVE, an Arabidopsis homologue of the retinoblastoma-associated protein that regulates flowering time and cold response, binds to chromatin as a large multiprotein complex |
| Q34504786 | FoxOs enforce a progression checkpoint to constrain mTORC1-activated renal tumorigenesis |
| Q28533949 | From bench to bedside: lessons learned in translating preclinical studies in cancer drug development |
| Q28203389 | Full Activation of Estrogen Receptor α Activation Function-1 Induces Proliferation of Breast Cancer Cells |
| Q28198743 | Function and regulation of the transcription factors of the Myc/Max/Mad network |
| Q37431717 | Function of histone deacetylase 6 as a cofactor of nuclear receptor coregulator LCoR. |
| Q47807661 | Functional analysis of a RPD3 histone deacetylase homologue in Arabidopsis thaliana |
| Q40578066 | Functional analysis of the Mad1-mSin3A repressor-corepressor interaction reveals determinants of specificity, affinity, and transcriptional response |
| Q33959046 | Functional analysis of the SIN3-histone deacetylase RPD3-RbAp48-histone H4 connection in the Xenopus oocyte |
| Q40885992 | Functional interactions between the estrogen receptor and DRIP205, a subunit of the heteromeric DRIP coactivator complex |
| Q44470158 | Fusion protein of retinoic acid receptor alpha with promyelocytic leukemia protein or promyelocytic leukemia zinc finger protein recruits N-CoR-TBLR1 corepressor complex to repress transcription in vivo |
| Q37479355 | G protein pathway suppressor 2 (GPS2) is a transcriptional corepressor important for estrogen receptor alpha-mediated transcriptional regulation |
| Q35802800 | Gene silencing by nuclear orphan receptors |
| Q34349653 | Genetic lesions and perturbation of chromatin architecture: a road to cell transformation |
| Q36173644 | Glucose mediates the translocation of NeuroD1 by O-linked glycosylation |
| Q35196294 | Groucho acts as a corepressor for a subset of negative regulators, including Hairy and Engrailed |
| Q64241000 | HDA9-PWR-HOS15 Is a Core Histone Deacetylase Complex Regulating Transcription and Development |
| Q64910381 | HDAC1-mediated repression of the retinoic acid-responsive gene ripply3 promotes second heart field development. |
| Q36908411 | HDAC3: taking the SMRT-N-CoRrect road to repression |
| Q24291533 | HERP, a novel heterodimer partner of HES/E(spl) in Notch signaling |
| Q40817108 | Heat shock factor-4 (HSF-4a) represses basal transcription through interaction with TFIIF. |
| Q24554353 | Helix-loop-helix proteins: regulators of transcription in eucaryotic organisms |
| Q35635550 | Hematopoiesis and retinoids: development and disease |
| Q43785646 | High Oct-ane fuel powers the stem cell |
| Q40997382 | Histone H4 acetylation during interleukin-2 stimulation of mouse T cells. |
| Q33540069 | Histone acetylases and deacetylases in cell proliferation |
| Q33632377 | Histone acetylation and cancer |
| Q28131749 | Histone acetylation in chromatin structure and transcription |
| Q52166627 | Histone acetylation is a checkpoint in FGF-stimulated mesoderm induction. |
| Q34956099 | Histone acetyltransferases and deacetylases in the control of cell proliferation and differentiation |
| Q33958899 | Histone deacetylase 1 can repress transcription by binding to Sp1. |
| Q27934206 | Histone deacetylase activity of Rpd3 is important for transcriptional repression in vivo |
| Q33671506 | Histone deacetylase directs the dominant silencing of transcription in chromatin: association with MeCP2 and the Mi-2 chromodomain SWI/SNF ATPase |
| Q57143889 | Histone deacetylase function in CD4 T cells |
| Q40563094 | Histone deacetylase inhibitors activate INK4d gene through Sp1 site in its promoter |
| Q40450785 | Histone deacetylase inhibitors differentially stabilize acetylated p53 and induce cell cycle arrest or apoptosis in prostate cancer cells. |
| Q33860585 | Histone deacetylase inhibitors down-regulate bcl-2 expression and induce apoptosis in t(14;18) lymphomas |
| Q24671020 | Histone deacetylase inhibitors induce remission in transgenic models of therapy-resistant acute promyelocytic leukemia |
| Q35011880 | Histone deacetylase inhibitors: from target to clinical trials |
| Q40381640 | Histone deacetylase-1 represses transcription by interacting with zinc-fingers and interfering with the DNA binding activity of Sp1. |
| Q33926323 | Histone deacetylases, transcriptional control, and cancer |
| Q33632987 | Histone deacetylases: transcriptional repression with SINers and NuRDs |
| Q34322087 | Histone modification enzymes: novel targets for cancer drugs |
| Q36551230 | Holocarboxylase synthetase interacts physically with nuclear receptor co-repressor, histone deacetylase 1 and a novel splicing variant of histone deacetylase 1 to repress repeats |
| Q41653866 | How does DNA methylation repress transcription? |
| Q28214548 | Human class I histone deacetylase complexes show enhanced catalytic activity in the presence of ATP and co-immunoprecipitate with the ATP-dependent chaperone protein Hsp70 |
| Q36978826 | Human cytomegalovirus pUL97 regulates the viral major immediate early promoter by phosphorylation-mediated disruption of histone deacetylase 1 binding |
| Q35901931 | Hypoxia-induced and stress-specific changes in chromatin structure and function |
| Q24302754 | Identification and characterization of SAP25, a novel component of the mSin3 corepressor complex |
| Q24300908 | Identification and characterization of three new components of the mSin3A corepressor complex |
| Q28116129 | Identification of a novel testicular orphan receptor-4 (TR4)-associated protein as repressor for the selective suppression of TR4-mediated transactivation |
| Q34158629 | Identification of common genetic modifiers of neurodegenerative diseases from an integrative analysis of diverse genetic screens in model organisms |
| Q24292515 | Identification of mammalian Sds3 as an integral component of the Sin3/histone deacetylase corepressor complex |
| Q37211310 | Identification of protein O-GlcNAcylation sites using electron transfer dissociation mass spectrometry on native peptides |
| Q35615116 | In vivo transcription factor recruitment during thyroid hormone receptor-mediated activation |
| Q43831000 | Increased expression of unmethylated CDKN2D by 5-aza-2'-deoxycytidine in human lung cancer cells |
| Q28592881 | Increased susceptibility to tumorigenesis of ski-deficient heterozygous mice |
| Q42445503 | Inhibition of MMTV transcription by HDAC inhibitors occurs independent of changes in chromatin remodeling and increased histone acetylation |
| Q39602340 | Inhibition of histone deacetylation induces constitutive derepression of the beta interferon promoter and confers antiviral activity |
| Q39686347 | Inhibition of polyomavirus ori-dependent DNA replication by mSin3B |
| Q36002405 | Integrative genomic analysis in K562 chronic myelogenous leukemia cells reveals that proximal NCOR1 binding positively regulates genes that govern erythroid differentiation and Imatinib sensitivity. |
| Q39758389 | Interaction among Rb/p16, Rb/E2F1 and HDAC1 proteins in gallbladder carcinoma |
| Q47759812 | Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions |
| Q78036268 | Interactions in the transcriptional regulation exerted by Stat5 and by members of the steroid hormone receptor family |
| Q36447432 | Interplay of nuclear factor-kappaB and B-myb in the negative regulation of androgen receptor expression by tumor necrosis factor alpha |
| Q24650557 | Involvement of the histone deacetylase SIRT1 in chicken ovalbumin upstream promoter transcription factor (COUP-TF)-interacting protein 2-mediated transcriptional repression |
| Q24291980 | Isolation and characterization of a novel class II histone deacetylase, HDAC10 |
| Q28594682 | Isolation and characterization of mammalian HDAC10, a novel histone deacetylase |
| Q24610596 | Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression |
| Q37262437 | Keeping things quiet: roles of NuRD and Sin3 co-repressor complexes during mammalian development |
| Q78169779 | Leukemia: the sophisticated subversion of hematopoiesis by nuclear receptor oncoproteins |
| Q42663412 | Leukemic transformation by the v-ErbA oncoprotein entails constitutive binding to and repression of an erythroid enhancer in vivo. |
| Q47926688 | Life with nucleosomes: chromatin remodelling in gene regulation |
| Q34171522 | Ligand-dependent nuclear receptor corepressor LCoR functions by histone deacetylase-dependent and -independent mechanisms |
| Q24541489 | Ligand-specific allosteric regulation of coactivator functions of androgen receptor in prostate cancer cells |
| Q59076671 | Local or global? |
| Q33963925 | Mad1 function is regulated through elements within the carboxy terminus |
| Q42776387 | Max is acetylated by p300 at several nuclear localization residues |
| Q28594917 | Mechanism for nucleocytoplasmic shuttling of histone deacetylase 7 |
| Q35210560 | Mechanism of corepressor binding and release from nuclear hormone receptors. |
| Q28362793 | Metabolic and cellular analysis of alopecia in vitamin D receptor knockout mice |
| Q35019557 | Methylation of adjacent CpG sites affects Sp1/Sp3 binding and activity in the p21(Cip1) promoter |
| Q37106839 | Minireview: the PGC-1 coactivator networks: chromatin-remodeling and mitochondrial energy metabolism |
| Q22254702 | Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? |
| Q43649376 | Mmip-2/Rnf-17 enhances c-Myc function and regulates some target genes in common with glucocorticoid hormones |
| Q34091001 | Modifying histones to tame cancer: clinical development of sodium phenylbutyrate and other histone deacetylase inhibitors |
| Q43864423 | Modulation of HMG-N2 binding to chromatin by butyrate-induced acetylation in human colon adenocarcinoma cells |
| Q36389311 | Modulation of cellular radiation responses by histone deacetylase inhibitors |
| Q37143831 | Modulation of transcription parameters in glucocorticoid receptor-mediated repression. |
| Q34491450 | Molecular action of androgen in the normal and neoplastic prostate |
| Q30733405 | Molecular cloning and characterization of a steroid receptor-binding regulator of G-protein signaling protein cDNA. |
| Q30838844 | Molecular cloning and characterization of the mouse histone deacetylase 1 gene: integration of a retrovirus in 129SV mice |
| Q47871313 | Molecular determinants of the interaction of Mad with the PAH2 domain of mSin3. |
| Q33633027 | Molecular genetics of acute promyelocytic leukemia. |
| Q29620260 | Molecular genetics of the RNA polymerase II general transcriptional machinery |
| Q50335765 | Multimeric Coactivator Complexes for Steroid/Nuclear Receptors. |
| Q50717551 | Multiple N-CoR complexes contain distinct histone deacetylases. |
| Q47665602 | Multiplex Enhancer Interference Reveals Collaborative Control of Gene Regulation by Estrogen Receptor α-Bound Enhancers |
| Q34608754 | Mutational analysis of a histone deacetylase in Drosophila melanogaster: missense mutations suppress gene silencing associated with position effect variegation |
| Q35150661 | Mxi1 and mxi1-0 antagonize N-myc function and independently mediate apoptosis in neuroblastoma |
| Q24643042 | Mxi1 inhibits the proliferation of U87 glioma cells through down-regulation of cyclin B1 gene expression |
| Q38311476 | Mxi1 is a potential cellular target of carcinogens and frequently mutated in experimental rat tumors and tumor cell lines |
| Q38329998 | Mxi1 is a repressor of the c-Myc promoter and reverses activation by USF. |
| Q33233066 | Mxi1 is essential for neurogenesis in Xenopus and acts by bridging the pan-neural and proneural genes |
| Q28188728 | Mxi1, a Myc antagonist, suppresses proliferation of DU145 human prostate cells |
| Q41831140 | Mxi1-0, an alternatively transcribed Mxi1 isoform, is overexpressed in glioblastomas. |
| Q28286396 | Mxi1-SRalpha: a novel Mxi1 isoform with enhanced transcriptional repression potential |
| Q28592882 | Myt1 family recruits histone deacetylase to regulate neural transcription |
| Q37448077 | N-Myc differentially regulates expression of MXI1 isoforms in neuroblastoma |
| Q40889482 | N-terminal region, C-terminal region, nuclear export signal, and deacetylation activity of histone deacetylase-3 are essential for the viability of the DT40 chicken B cell line |
| Q24292362 | NAPP2, a peroxisomal membrane protein, is also a transcriptional corepressor |
| Q33826645 | NCoR1 mediates papillomavirus E8;E2C transcriptional repression |
| Q40698580 | NF-kappaB inhibits transcription of the H(+)-K(+)-ATPase alpha(2)-subunit gene: role of histone deacetylases |
| Q29615750 | NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities |
| Q41833592 | Negative autoregulation of BMP dependent transcription by SIN3B splicing reveals a role for RBM39. |
| Q24534166 | Net, a negative Ras-switchable TCF, contains a second inhibition domain, the CID, that mediates repression through interactions with CtBP and de-acetylation |
| Q24644926 | Neural restrictive silencer factor recruits mSin3 and histone deacetylase complex to repress neuron-specific target genes |
| Q37184168 | New insights into the functions and regulation of the transcriptional corepressors SMRT and N-CoR |
| Q47830017 | Nuclear histone acetylases and deacetylases and transcriptional regulation: HATs off to HDACs. |
| Q33786584 | Nuclear receptor DAX-1 recruits nuclear receptor corepressor N-CoR to steroidogenic factor 1 |
| Q28287280 | Nuclear receptor binding factor-1 (NRBF-1), a protein interacting with a wide spectrum of nuclear hormone receptors |
| Q28566321 | Nuclear receptor binding factor-2 (NRBF-2), a possible gene activator protein interacting with nuclear hormone receptors |
| Q33694883 | Nuclear receptor coactivators: multiple enzymes, multiple complexes, multiple functions. |
| Q33745092 | Nuclear receptor cofactors as chromatin remodelers |
| Q34448240 | Nuclear receptor corepressor complexes in cancer: mechanism, function and regulation |
| Q34443197 | Nuclear receptor corepressor recruitment by unliganded thyroid hormone receptor in gene repression during Xenopus laevis development |
| Q24610640 | Nuclear receptor corepressors partner with class II histone deacetylases in a Sin3-independent repression pathway |
| Q35802810 | Nuclear receptor recruitment of histone-modifying enzymes to target gene promoters |
| Q37726333 | Nuclear receptor repression: regulatory mechanisms and physiological implications. |
| Q40168015 | Oct-1 is involved in the transcriptional repression of the p15(INK4b) gene |
| Q24550754 | Oligomerization of ETO is obligatory for corepressor interaction |
| Q45130667 | Oncogenic activation of c-Myb correlates with a loss of negative regulation by TIF1beta and Ski. |
| Q34792710 | Ordered recruitment: gene-specific mechanism of transcription activation |
| Q24564760 | Orphan nuclear receptor TLX recruits histone deacetylases to repress transcription and regulate neural stem cell proliferation |
| Q40777160 | PML-RARalpha alleviates the transcriptional repression mediated by tumor suppressor Rb. |
| Q42811126 | Pag, a putative tumor suppressor, interacts with the Myc Box II domain of c-Myc and selectively alters its biological function and target gene expression |
| Q39449291 | Pbx-Hox heterodimers recruit coactivator-corepressor complexes in an isoform-specific manner |
| Q31998516 | Persistent interactions of core histone tails with nucleosomal DNA following acetylation and transcription factor binding |
| Q24291300 | Pf1, a novel PHD zinc finger protein that links the TLE corepressor to the mSin3A-histone deacetylase complex |
| Q42667452 | Phenobarbital alters protein binding to the CYP2B1/2 phenobarbital-responsive unit in native chromatin |
| Q43578157 | Pho23 is associated with the Rpd3 histone deacetylase and is required for its normal function in regulation of gene expression and silencing in Saccharomyces cerevisiae |
| Q52193003 | Photoreceptor cell differentiation requires regulated proteolysis of the transcriptional repressor Tramtrack. |
| Q42537499 | Pocket protein complexes are recruited to distinct targets in quiescent and proliferating cells |
| Q35696363 | Prognostic classification of pediatric medulloblastoma based on chromosome 17p loss, expression of MYCC and MYCN, and Wnt pathway activation |
| Q33888436 | Prolonged glucocorticoid exposure dephosphorylates histone H1 and inactivates the MMTV promoter |
| Q35202493 | Proteasomal regulation of nuclear receptor corepressor-mediated repression |
| Q34271581 | Protein modules that manipulate histone tails for chromatin regulation |
| Q24290894 | Purification and characterization of mSin3A-containing Brg1 and hBrm chromatin remodeling complexes |
| Q36627675 | Purified histone acetyltransferase complexes stimulate HIV-1 transcription from preassembled nucleosomal arrays |
| Q28272098 | RAP46 is a negative regulator of glucocorticoid receptor action and hormone-induced apoptosis |
| Q22008019 | RMP, a novel RNA polymerase II subunit 5-interacting protein, counteracts transactivation by hepatitis B virus X protein |
| Q33411313 | RTA promoter demethylation and histone acetylation regulation of murine gammaherpesvirus 68 reactivation |
| Q33900128 | Rb function in cell-cycle regulation and apoptosis |
| Q28263985 | Rb interacts with histone deacetylase to repress transcription |
| Q37277846 | Recruitment of N-CoR/SMRT-TBLR1 corepressor complex by unliganded thyroid hormone receptor for gene repression during frog development |
| 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 |
| Q35874448 | Regulated clearance of histone deacetylase 3 protects independent formation of nuclear receptor corepressor complexes. |
| Q38854079 | Regulation of PXR and CAR by protein-protein interaction and signaling crosstalk |
| Q35080744 | Regulation of cyclin D2 gene expression by the Myc/Max/Mad network: Myc-dependent TRRAP recruitment and histone acetylation at the cyclin D2 promoter. |
| Q44547321 | Regulation of glucose-6-phosphatase gene expression in cultured hepatocytes and H4IIE cells by short-chain fatty acids: role of hepatic nuclear factor-4alpha |
| Q34325666 | Regulation of histone deacetylase 4 expression by the SP family of transcription factors |
| Q28585055 | Regulation of mammalian epithelial differentiation and intestine development by class I histone deacetylases |
| Q24323211 | Regulation of nuclear receptor transcriptional activity by a novel DEAD box RNA helicase (DP97) |
| Q24289242 | Regulatory factor for X-box family proteins differentially interact with histone deacetylases to repress collagen alpha2(I) gene (COL1A2) expression |
| Q36835168 | Regulatory polymorphism in vitamin K epoxide reductase complex subunit 1 (VKORC1) affects gene expression and warfarin dose requirement |
| Q33539516 | Repression and activation of muscarinic receptor genes |
| Q24534154 | Repression by Ikaros and Aiolos is mediated through histone deacetylase complexes |
| Q40753304 | Repression of in vivo growth of Myc/Ras transformed tumor cells by Mad1. |
| Q38023496 | Reprogramming chromatin |
| Q24310350 | Requirement of the co-repressor homeodomain-interacting protein kinase 2 for ski-mediated inhibition of bone morphogenetic protein-induced transcriptional activation |
| Q28262144 | Retinoblastoma protein recruits histone deacetylase to repress transcription |
| Q28262155 | Retinoblastoma protein represses transcription by recruiting a histone deacetylase |
| Q34153888 | Retinoblastoma tumor suppressor and genome stability |
| Q47804022 | Retinoids and related signals in early development of the vertebrate central nervous system. |
| Q34498098 | Retinoids and their receptors in cancer development and chemoprevention |
| Q34348792 | Reversible histone acetylation and deacetylation mediate genome-wide, promoter-dependent and locus-specific changes in gene expression during plant development |
| Q24291380 | Role of PML and PML-RARalpha in Mad-mediated transcriptional repression |
| Q39478322 | Role of an Arabidopsis AP2/EREBP-type transcriptional repressor in abscisic acid and drought stress responses |
| Q24537037 | Role of the Sin3-histone deacetylase complex in growth regulation by the candidate tumor suppressor p33(ING1). |
| Q28263534 | Role of the histone deacetylase complex in acute promyelocytic leukaemia |
| Q34608860 | Roles for the Saccharomyces cerevisiae SDS3, CBK1 and HYM1 genes in transcriptional repression by SIN3. |
| Q28279441 | SAP30, a component of the mSin3 corepressor complex involved in N-CoR-mediated repression by specific transcription factors |
| Q24311791 | SAP30, a novel protein conserved between human and yeast, is a component of a histone deacetylase complex |
| Q22253329 | SKIP, a CBF1-associated protein, interacts with the ankyrin repeat domain of NotchIC To facilitate NotchIC function |
| Q43576559 | SMRTE inhibits MEF2C transcriptional activation by targeting HDAC4 and 5 to nuclear domains |
| Q40928736 | SMRTER, a Drosophila nuclear receptor coregulator, reveals that EcR-mediated repression is critical for development. |
| Q22009109 | SMRTe, a silencing mediator for retinoid and thyroid hormone receptors-extended isoform that is more related to the nuclear receptor corepressor |
| Q55280429 | Same agent, different messages: insight into transcriptional regulation by SIN3 isoforms. |
| Q27932143 | Sds3 (suppressor of defective silencing 3) is an integral component of the yeast Sin3[middle dot]Rpd3 histone deacetylase complex and is required for histone deacetylase activity. |
| Q22253162 | Sequestration and inhibition of Daxx-mediated transcriptional repression by PML |
| Q35159032 | Sex differences in epigenetic mechanisms may underlie risk and resilience for mental health disorders |
| Q73215842 | Sex steroids modulate the synthesis and phosphorylation of proteins in the brain cortex of aging mice |
| Q24601805 | Sharp, an inducible cofactor that integrates nuclear receptor repression and activation |
| Q40652029 | Signal-dependent N-CoR Requirement for Repression by the Ski Oncoprotein |
| Q41006466 | Signal-specific co-activator domain requirements for Pit-1 activation |
| Q47824763 | Silencing and activation of embryonic globin gene expression. |
| Q35964130 | Sin3: a flexible regulator of global gene expression and genome stability. |
| Q37511108 | Sin3: master scaffold and transcriptional corepressor |
| Q39298013 | Sin3a acts through a multi-gene module to regulate invasion in Drosophila and human tumors |
| Q24299671 | Sin3b interacts with Myc and decreases Myc levels |
| Q24317645 | Ski co-repressor complexes maintain the basal repressed state of the TGF-beta target gene, SMAD7, via HDAC3 and PRMT5 |
| Q22008813 | Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor |
| Q24312160 | Ski-interacting protein, a bifunctional nuclear receptor coregulator that interacts with N-CoR/SMRT and p300 |
| Q34550834 | Snail mediates E-cadherin repression by the recruitment of the Sin3A/histone deacetylase 1 (HDAC1)/HDAC2 complex |
| Q27628842 | Solution structure of the interacting domains of the Mad-Sin3 complex: implications for recruitment of a chromatin-modifying complex |
| Q35005873 | Specific targeting and constitutive association of histone deacetylase complexes during transcriptional repression |
| Q43930898 | Stimulation of the alpha-fetoprotein promoter by unliganded thyroid hormone receptor in association with protein deacetylation |
| Q43239840 | Structural basis for nuclear receptor corepressor recruitment by antagonist-liganded androgen receptor |
| Q92676543 | Structurally Diverse Histone Deacetylase Photoreactive Probes: Design, Synthesis, and Photolabeling Studies in Live Cells and Tissue |
| Q35041364 | Switch from Myc/Max to Mad1/Max binding and decrease in histone acetylation at the telomerase reverse transcriptase promoter during differentiation of HL60 cells. |
| Q42827376 | TEL contacts multiple co-repressors and specifically associates with histone deacetylase-3. |
| Q24535000 | TIS7 interacts with the mammalian SIN3 histone deacetylase complex in epithelial cells. |
| Q33888207 | Targeted disruption of the MYC antagonist MAD1 inhibits cell cycle exit during granulocyte differentiation. |
| Q73731417 | Targeted recruitment of histone acetyltransferase activity to a locus control region |
| Q27938598 | Targeted recruitment of the Sin3-Rpd3 histone deacetylase complex generates a highly localized domain of repressed chromatin in vivo |
| Q33940715 | Telomerase activation by histone deacetylase inhibitor in normal cells |
| Q27931014 | The ADA complex is a distinct histone acetyltransferase complex in Saccharomyces cerevisiae |
| Q28266637 | The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53 |
| Q28216196 | The LIM-only protein DRAL/FHL2 interacts with and is a corepressor for the promyelocytic leukemia zinc finger protein |
| Q40031496 | The MMSET protein is a histone methyltransferase with characteristics of a transcriptional corepressor |
| Q35808823 | The MTG proteins: chromatin repression players with a passion for networking |
| Q33671500 | The Mad protein family links transcriptional repression to cell differentiation |
| Q40762449 | The Mad1 transcription factor is a novel target of activin and TGF-beta action in keratinocytes: possible role of Mad1 in wound repair and psoriasis |
| Q34416302 | The Mammalian Sin3 Proteins Are Required for Muscle Development and Sarcomere Specification |
| Q33967079 | The Max network gone mad. |
| Q39791268 | The N-CoR/histone deacetylase 3 complex is required for repression by thyroid hormone receptor |
| Q34441108 | The SIN3/RPD3 deacetylase complex is essential for G(2) phase cell cycle progression and regulation of SMRTER corepressor levels |
| Q33860695 | The SRC family of nuclear receptor coactivators |
| Q24599753 | The Ski oncoprotein interacts with the Smad proteins to repress TGFbeta signaling |
| Q24291417 | The Ski protein family is required for MeCP2-mediated transcriptional repression |
| Q31140532 | The Use of Phage Display Technique for the Isolation of Androgen Receptor Interacting Peptides with (F/W)XXL(F/W) and FXXLY New Signature Motifs |
| Q39175293 | The actions of thyroid hormone signaling in the nucleus |
| Q22253389 | The adenovirus E1A binding protein BS69 is a corepressor of transcription through recruitment of N-CoR |
| Q35193278 | The androgen receptor: structure, mutations, and antiandrogens |
| Q24533171 | The basic helix-loop-helix transcription factor Mist1 functions as a transcriptional repressor of myoD |
| Q37013896 | The c-myc promoter: still MysterY and challenge |
| Q42832933 | The cancer preventive seed peptide lunasin from rye is bioavailable and bioactive |
| Q28275328 | The carboxy-terminal region of adenovirus E1A activates transcription through targeting of a C-terminal binding protein-histone deacetylase complex |
| Q34566036 | The chromatin signaling pathway: diverse mechanisms of recruitment of histone-modifying enzymes and varied biological outcomes |
| Q35730122 | The cloning and characterization of the histone acetyltransferase human homolog Dmel\TIP60 in Drosophila melanogaster: Dmel\TIP60 is essential for multicellular development |
| Q22253387 | The co-repressor mSin3A is a functional component of the REST-CoREST repressor complex |
| Q46393939 | The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1. |
| Q34669136 | The corepressor N-CoR and its variants RIP13a and RIP13Delta1 directly interact with the basal transcription factors TFIIB, TAFII32 and TAFII70. |
| Q94465154 | The corepressor NCOR1 and OCT4 facilitate early reprogramming by suppressing fibroblast gene expression |
| Q28286772 | The dermatomyositis-specific autoantigen Mi2 is a component of a complex containing histone deacetylase and nucleosome remodeling activities |
| Q57574782 | The emerging role of class II histone deacetylases |
| Q24600925 | The glucocorticoid receptor inhibits NFkappaB by interfering with serine-2 phosphorylation of the RNA polymerase II carboxy-terminal domain |
| Q40394964 | The hTERT and hTERC telomerase gene promoters are activated by the second exon of the adenoviral protein, E1A, identifying the transcriptional corepressor CtBP as a potential repressor of both genes |
| Q24600264 | The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor |
| Q40549870 | The highly conserved region of the co-repressor Sin3A functionally interacts with the co-repressor Alien |
| Q35201383 | The histone acetylase PCAF is a nuclear receptor coactivator. |
| Q24294872 | The histone deacetylase 9 gene encodes multiple protein isoforms |
| Q35160462 | The histone deacetylase inhibitor valproic acid selectively induces proteasomal degradation of HDAC2 |
| Q35155073 | The histone deacetylase-3 complex contains nuclear receptor corepressors |
| Q28609066 | The homeodomain protein NK-3 recruits Groucho and a histone deacetylase complex to repress transcription |
| Q33315477 | The human SIN3B corepressor forms a nucleolar complex with leukemia-associated ETO homologues |
| Q24336423 | The human tumor antigen PRAME is a dominant repressor of retinoic acid receptor signaling |
| Q28203006 | The hunt for huntingtin function: interaction partners tell many different stories |
| Q36485649 | The in vivo role of nuclear receptor corepressors in thyroid hormone action |
| Q24676589 | The localization and interactions of huntingtin |
| Q42176327 | The mSin3A chromatin-modifying complex is essential for embryogenesis and T-cell development |
| Q28191705 | The many roles of the transcriptional regulator CTCF |
| Q34312427 | The mycoestrogen zearalenone induces CYP3A through activation of the pregnane X receptor |
| Q28513974 | The nuclear corepressor, NCoR, regulates thyroid hormone action in vivo |
| Q36067452 | The nuclear receptor corepressor (NCoR) controls thyroid hormone sensitivity and the set point of the hypothalamic-pituitary-thyroid axis |
| Q33735565 | The nuclear receptor corepressor has organizational effects within the developing amygdala on juvenile social play and anxiety-like behavior |
| Q24554243 | The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding |
| Q24548313 | The orphan nuclear receptor, COUP-TF II, inhibits myogenesis by post-transcriptional regulation of MyoD function: COUP-TF II directly interacts with p300 and myoD |
| Q33723609 | The pathogenesis of acute promyelocytic leukaemia: evaluation of the role of molecular diagnosis and monitoring in the management of the disease |
| Q24530668 | The peroxisome proliferator-activated receptor delta, an integrator of transcriptional repression and nuclear receptor signaling |
| Q24293229 | The phosphorylation status of nuclear NF-kappa B determines its association with CBP/p300 or HDAC-1 |
| Q28200929 | The proto-oncogene c-myc in hematopoietic development and leukemogenesis |
| Q33671479 | The regulation of gene activity by histones and the histone deacetylase RPD3. |
| Q28585253 | The sno gene, which encodes a component of the histone deacetylase complex, acts as a tumor suppressor in mice |
| Q35121737 | The t(8;21) fusion protein contacts co-repressors and histone deacetylases to repress the transcription of the p14ARF tumor suppressor |
| Q40781028 | The tamoxifen-responsive estrogen receptor alpha mutant D351Y shows reduced tamoxifen-dependent interaction with corepressor complexes |
| Q24529077 | The thymine DNA glycosylase MBD4 represses transcription and is associated with methylated p16(INK4a) and hMLH1 genes |
| Q35089956 | The thyroid hormone receptor and the insulator protein CTCF: two different factors with overlapping functions |
| Q33634303 | The thyrotropin-releasing hormone gene is regulated by thyroid hormone at the level of transcription in vivo |
| Q33671563 | The transcriptional basis of steroid physiology |
| Q36425877 | The transcriptional corepressor SMRTER influences both Notch and ecdysone signaling during Drosophila development |
| Q36001865 | The transposon-driven evolutionary origin and basis of histone deacetylase functions and limitations in disease prevention |
| Q28505952 | The winged-helix/forkhead protein myocyte nuclear factor beta (MNF-beta) forms a co-repressor complex with mammalian sin3B |
| Q34132635 | Thoughts on tamoxifen resistant breast cancer. Are coregulators the answer or just a red herring? |
| Q34578472 | Thyroid hormone and COUP-TF1 regulate kallikrein-binding protein (KBP) gene expression |
| Q33834152 | Thyroid hormone receptor, v-ErbA, and chromatin. |
| Q28509846 | Thyroid hormone signaling in vivo requires a balance between coactivators and corepressors |
| Q40906060 | Thyroid hormone-independent interaction between the thyroid hormone receptor beta2 amino terminus and coactivators |
| Q28199349 | Tip60 is a nuclear hormone receptor coactivator |
| Q38156341 | Transcription and beyond: the role of mammalian class I lysine deacetylases |
| Q46148904 | Transcription of chromatin: these are complex times |
| Q36053034 | Transcriptional activities of retinoic acid receptors |
| Q37241513 | Transcriptional anti-repression. Thyroid hormone receptor beta-2 recruits SMRT corepressor but interferes with subsequent assembly of a functional corepressor complex |
| Q28237278 | Transcriptional control. Sinful repression |
| Q41565013 | Transcriptional control: calling in histone deacetylase |
| Q34435531 | Transcriptional regulation in acute promyelocytic leukemia. |
| Q33775085 | Transcriptional regulation of the MDR1 gene by histone acetyltransferase and deacetylase is mediated by NF-Y. |
| Q43823894 | Transcriptional regulation of the transforming growth factor beta type II receptor gene by histone acetyltransferase and deacetylase is mediated by NF-Y in human breast cancer cells |
| Q28576708 | Transcriptional repression by REST: recruitment of Sin3A and histone deacetylase to neuronal genes |
| Q27931527 | Transcriptional repression by UME6 involves deacetylation of lysine 5 of histone H4 by RPD3. |
| Q39451978 | Transcriptional repression by blimp-1 (PRDI-BF1) involves recruitment of histone deacetylase |
| Q33826663 | Transcriptional repression by nuclear hormone receptors |
| Q33779119 | Transcriptional repression by the SMRT-mSin3 corepressor: multiple interactions, multiple mechanisms, and a potential role for TFIIB. |
| Q24515375 | Transcriptional repression by the insulator protein CTCF involves histone deacetylases |
| Q24324026 | Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex |
| Q74191064 | Transcriptional repression. The cancer-chromatin connection |
| Q34626885 | Transcriptional repressors, corepressors and chromatin modifying enzymes in T cell development |
| Q34041216 | Transcriptional transgene silencing and chromatin components |
| Q28594081 | Transgenic targeting of a dominant negative corepressor to liver blocks basal repression by thyroid hormone receptor and increases cell proliferation |
| Q36260468 | Trichostatin A causes selective loss of DNA methylation in Neurospora |
| Q39594198 | Trichostatin A up-regulates human papillomavirus type 11 upstream regulatory region-E6 promoter activity in undifferentiated primary human keratinocytes |
| Q47761111 | Tuberous sclerosis gene 2 product modulates transcription mediated by steroid hormone receptor family members |
| Q40606259 | Tumor-specific adenoviral gene therapy: transcriptional repression of gene expression by utilizing p53-signal transduction pathways |
| Q33670203 | Two MAD tails: what the recent knockouts of Mad1 and Mxi1 tell us about the MYC/MAX/MAD network |
| Q24336164 | Two distinct nuclear receptor interaction domains in NSD1, a novel SET protein that exhibits characteristics of both corepressors and coactivators |
| Q24674108 | Unique forms of human and mouse nuclear receptor corepressor SMRT |
| Q28366303 | Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells |
| Q33975839 | Vitamin A and cancer |
| Q35173888 | Vitamin A and infancy. Biochemical, functional, and clinical aspects |
| Q40650789 | Vitamin D-dependent recruitment of DNA-PK to the chromatinized negative vitamin D response element in the PTHrP gene is required for gene repression by vitamin D. |
| Q28238059 | What's up and down with histone deacetylation and transcription? |
| Q37288077 | Who's in charge? Nuclear receptor coactivator and corepressor function in brain and behavior |
| Q38297257 | Widespread collaboration of Isw2 and Sin3-Rpd3 chromatin remodeling complexes in transcriptional repression |
| Q27933513 | Yeast HOS3 forms a novel trichostatin A-insensitive homodimer with intrinsic histone deacetylase activity |
| Q24653823 | ZEB represses transcription through interaction with the corepressor CtBP |
| Q28143677 | c-MYC interacts with INI1/hSNF5 and requires the SWI/SNF complex for transactivation function |
| Q33956988 | c-Myc target genes involved in cell growth, apoptosis, and metabolism |
| Q24524018 | mSin3A regulates murine erythroleukemia cell differentiation through association with the TAL1 (or SCL) transcription factor |
| Q24679145 | mSin3A/histone deacetylase 2- and PRMT5-containing Brg1 complex is involved in transcriptional repression of the Myc target gene cad |
| Q35641322 | p204, a p200 family protein, as a multifunctional regulator of cell proliferation and differentiation |
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