| P2093 | author name string | Lei Wang | |
| | Chih-Cheng Tsai | |
| P2860 | cites work | CoREST: a functional corepressor required for regulation of neural-specific gene expression | Q22003747 |
| | Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicity | Q22009069 |
| | Translating the Histone Code | Q22065840 |
| | Evidence for regulation of the PTEN tumor suppressor by a membrane-localized multi-PDZ domain containing scaffold protein MAGI-2 | Q22253866 |
| | A core SMRT corepressor complex containing HDAC3 and TBL1, a WD40-repeat protein linked to deafness | Q22254089 |
| | Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine | Q22254109 |
| | Regulation of chromatin structure by site-specific histone H3 methyltransferases | Q24290115 |
| | Atrophin-1, the dentato-rubral and pallido-luysian atrophy gene product, interacts with ETO/MTG8 in the nuclear matrix and represses transcription | Q24290194 |
| | The human SWI/SNF-B chromatin-remodeling complex is related to yeast rsc and localizes at kinetochores of mitotic chromosomes | Q24290517 |
| | Atrophin recruits HDAC1/2 and G9a to modify histone H3K9 and to determine cell fates | Q24309059 |
| | Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins | Q24310521 |
| | Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor | Q24311650 |
| | Functional architecture of atrophins | Q24323171 |
| | Human MI-ER1 alpha and beta function as transcriptional repressors by recruitment of histone deacetylase 1 to their conserved ELM2 domain | Q24336890 |
| | ETO, a target of t(8;21) in acute leukemia, interacts with the N-CoR and mSin3 corepressors | Q24522848 |
| | Nuclear receptor corepressors | Q24540376 |
| | Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors | Q24541357 |
| | The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript | Q24564573 |
| | Orphan nuclear receptor TLX recruits histone deacetylases to repress transcription and regulate neural stem cell proliferation | Q24564760 |
| | Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3 | Q24599788 |
| | Isolation of a novel histone deacetylase reveals that class I and class II deacetylases promote SMRT-mediated repression | Q24610596 |
| | Nuclear receptor corepressors partner with class II histone deacetylases in a Sin3-independent repression pathway | Q24610640 |
| | ETO, fusion partner in t(8;21) acute myeloid leukemia, represses transcription by interaction with the human N-CoR/mSin3/HDAC1 complex | Q24653699 |
| | Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS | Q24671945 |
| | Osa associates with the Brahma chromatin remodeling complex and promotes the activation of some target genes | Q40911651 |
| | SMRTER, a Drosophila nuclear receptor coregulator, reveals that EcR-mediated repression is critical for development. | Q40928736 |
| | Genomic instability in 1p and human malignancies | Q41170258 |
| | The SANT domain: a putative DNA-binding domain in the SWI-SNF and ADA complexes, the transcriptional co-repressor N-CoR and TFIIIB. | Q41178324 |
| | Molecular and genetic studies on the region of translocation and duplication in the neuroblastoma cell line NGP at the 1p36.13-p36.32 chromosomal site. | Q41198214 |
| | Transcriptional repression by COUP-TF II is dependent on the C-terminal domain and involves the N-CoR variant, RIP13delta1. | Q42450537 |
| | The Drosophila gene tailless is expressed at the embryonic termini and is a member of the steroid receptor superfamily | Q43983015 |
| | Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy | Q44854729 |
| | Krüppel requirement for knirps enhancement reflects overlapping gap gene activities in the Drosophila embryo | Q45757474 |
| | Control of early neurogenesis of the Drosophila brain by the head gap genes tll, otd, ems, and btd. | Q46124022 |
| | Sodium butyrate ameliorates histone hypoacetylation and neurodegenerative phenotypes in a mouse model for DRPLA. | Q46890244 |
| | The Caenorhabditis elegans genes egl-27 and egr-1 are similar to MTA1, a member of a chromatin regulatory complex, and are redundantly required for embryonic patterning | Q47069443 |
| | NURD-complex genes antagonise Ras-induced vulval development in Caenorhabditis elegans | Q47069468 |
| | EGL-27 is similar to a metastasis-associated factor and controls cell polarity and cell migration in C. elegans | Q47069521 |
| | The trithorax group gene osa encodes an ARID-domain protein that genetically interacts with the brahma chromatin-remodeling factor to regulate transcription. | Q47070833 |
| | Grunge, related to human Atrophin-like proteins, has multiple functions in Drosophila development. | Q47071140 |
| | Drosophila atrophin homolog functions as a transcriptional corepressor in multiple developmental processes | Q47071704 |
| | Atrophin contributes to the negative regulation of epidermal growth factor receptor signaling in Drosophila | Q47071965 |
| | The tumor-suppressor and cell adhesion molecule Fat controls planar polarity via physical interactions with Atrophin, a transcriptional co-repressor. | Q47072307 |
| | REREa/Atrophin-2 interacts with histone deacetylase and Fgf8 signaling to regulate multiple processes of zebrafish development | Q47073728 |
| | Molecular cloning of polybromo, a nuclear protein containing multiple domains including five bromodomains, a truncated HMG-box, and two repeats of a novel domain | Q48059078 |
| | Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi disease | Q48209189 |
| | Expression and distribution of the dentatorubral-pallidoluysian atrophy gene product (atrophin-1/drplap) in neuronal and non-neuronal tissues | Q48795581 |
| | Competition for overlapping sites in the regulatory region of the Drosophila gene Krüppel. | Q52231848 |
| | Spatial control of the gap gene knirps in the Drosophila embryo by posterior morphogen system | Q52443475 |
| | The zygotic segmentation mutant tailless alters the blastoderm fate map of the Drosophila embryo. | Q52463412 |
| | A temporal switch in DER signaling controls the specification and differentiation of veins and interveins in the Drosophila wing | Q58380305 |
| | 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 |
| | Role of the conserved Sir3-BAH domain in nucleosome binding and silent chromatin assembly | Q80407843 |
| | Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity | Q95721056 |
| | G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis | Q24673923 |
| | Crystal structure and functional analysis of a nucleosome recognition module of the remodeling factor ISWI | Q27642328 |
| | The language of covalent histone modifications | Q27860931 |
| | Essential role for the SANT domain in the functioning of multiple chromatin remodeling enzymes | Q27933003 |
| | Structure and function of the Saccharomyces cerevisiae Sir3 BAH domain | Q27935710 |
| | Role of interactions between the origin recognition complex and SIR1 in transcriptional silencing | Q27937028 |
| | Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate | Q28144273 |
| | Transcriptionally active chimeric gene derived from the fusion of the AML1 gene and a novel gene on chromosome 8 in t(8;21) leukemic cells | Q28201192 |
| | Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails | Q28216534 |
| | Mi-2/NuRD: multiple complexes for many purposes | Q28250321 |
| | Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) | Q28250990 |
| | The conserved microRNA miR-8 tunes atrophin levels to prevent neurodegeneration in Drosophila | Q28252549 |
| | Atrophin-1-interacting protein 4/human Itch is a ubiquitin E3 ligase for human enhancer of filamentation 1 in transforming growth factor-beta signaling pathways | Q28253459 |
| | Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms | Q28260268 |
| | Junctions of the AML1/MTG8(ETO) fusion are constant in t(8;21) acute myeloid leukemia detected by reverse transcription polymerase chain reaction | Q28261560 |
| | Regulation of LSD1 histone demethylase activity by its associated factors | Q28270391 |
| | Protein aggregation and neurodegenerative disease | Q28273600 |
| | The dermatomyositis-specific autoantigen Mi2 is a component of a complex containing histone deacetylase and nucleosome remodeling activities | Q28286772 |
| | A transcriptional co-repressor that interacts with nuclear hormone receptors | Q28289864 |
| | Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA) | Q28306588 |
| | Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis | Q28505117 |
| | Dentatorubral-pallidoluysian atrophy protein is phosphorylated by c-Jun NH2-terminal kinase | Q28581934 |
| | Loss of the tailless gene affects forebrain development and emotional behavior | Q28585346 |
| | Tlx, an orphan nuclear receptor, regulates cell numbers and astrocyte development in the developing retina | Q28586084 |
| | Expression and function of orphan nuclear receptor TLX in adult neural stem cells | Q28586702 |
| | Nuclear receptor TLX prevents retinal dystrophy and recruits the corepressor atrophin1 | Q28587617 |
| | Nuclear localization of a non-caspase truncation product of atrophin-1, with an expanded polyglutamine repeat, increases cellular toxicity | Q28593520 |
| | The COUP-TF nuclear receptors regulate cell migration in the mammalian basal forebrain | Q28594806 |
| | The SMRT and N-CoR corepressors are activating cofactors for histone deacetylase 3 | Q28609763 |
| | Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains | Q28609779 |
| | Biological roles and mechanistic actions of co-repressor complexes | Q28640957 |
| | NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities | Q29615750 |
| | Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila | Q29616737 |
| | Mutation of the atrophin2 gene in the zebrafish disrupts signaling by fibroblast growth factor during development of the inner ear. | Q30499440 |
| | Identification and characterization of novel genes located at the t(1;15)(p36.2;q24) translocation breakpoint in the neuroblastoma cell line NGP. | Q30849521 |
| | Reversal of H3K9me2 by a small-molecule inhibitor for the G9a histone methyltransferase | Q33272939 |
| | Drosophila brakeless interacts with atrophin and is required for tailless-mediated transcriptional repression in early embryos | Q33284704 |
| | Polyglutamine neurodegenerative diseases and regulation of transcription: assembling the puzzle | Q33343058 |
| | Dentatorubral-pallidoluysian atrophy (DRPLA): clinical features and molecular genetics. | Q33748372 |
| | The BAH (bromo-adjacent homology) domain: a link between DNA methylation, replication and transcriptional regulation | Q33856691 |
| | The CoRNR motif controls the recruitment of corepressors by nuclear hormone receptors | Q33881484 |
| | Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA. | Q33890266 |
| | Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription | Q33916580 |
| | Glutamine repeats and neurodegeneration | Q33938576 |
| | Human RERE is localized to nuclear promyelocytic leukemia oncogenic domains and enhances apoptosis | Q33944948 |
| | Histone deacetylase inhibitors reduce polyglutamine toxicity | Q33953013 |
| | Genomic organization of the human mi-er1 gene and characterization of alternatively spliced isoforms: regulated use of a facultative intron determines subcellular localization | Q33961469 |
| | The SANT domain of human MI-ER1 interacts with Sp1 to interfere with GC box recognition and repress transcription from its own promoter | Q33977927 |
| | Regulation of SMRT and N-CoR corepressor function | Q34145996 |
| | The BAH domain, polybromo and the RSC chromatin remodelling complex | Q34258291 |
| | Molecular mechanism of chicken ovalbumin upstream promoter-transcription factor (COUP-TF) actions | Q34267857 |
| | Emerging roles of MTA family members in human cancers | Q34276177 |
| | The SANT domain: a unique histone-tail-binding module? | Q34308307 |
| | Relationship between Drosophila gap gene tailless and a vertebrate nuclear receptor Tlx. | Q34331321 |
| | Histone deacetylase inhibitors as new cancer drugs | Q34416846 |
| | The tailless nuclear receptor acts as a dedicated repressor in the early Drosophila embryo | Q34564826 |
| | EODJEMORE | Q34567156 |
| | A role for adult TLX-positive neural stem cells in learning and behaviour | Q34743630 |
| | Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease | Q34763178 |
| | Genetic interactions among scribbler, Atrophin and groucho in Drosophila uncover links in transcriptional repression | Q34895744 |
| | Osa-containing Brahma chromatin remodeling complexes are required for the repression of wingless target genes | Q35209119 |
| | Nuclear receptor recruitment of histone-modifying enzymes to target gene promoters | Q35802810 |
| | Do protein motifs read the histone code? | Q36017986 |
| | Histone deacetylase inhibitors: gathering pace | Q36509550 |
| | MTA family of coregulators in nuclear receptor biology and pathology | Q37050256 |
| | A SANT motif in the SMRT corepressor interprets the histone code and promotes histone deacetylation | Q38353000 |
| | Aberrant recruitment of the nuclear receptor corepressor-histone deacetylase complex by the acute myeloid leukemia fusion partner ETO. | Q39576827 |
| P921 | main subject | intracellular receptor | Q117980 |
| | transcription factor | Q407384 |
| | regulation of gene expression | Q411391 |
| | transport protein | Q2111029 |
| | DNA-binding protein | Q2252764 |
| | nerve tissue protein | Q6996861 |
| | arthropod proteins | Q75832127 |
| P304 | page(s) | e009 | |
| P577 | publication date | 2008-10-31 | |
| P1433 | published in | Nuclear Receptor Signaling | Q15766610 |
| P1476 | title | Atrophin proteins: an overview of a new class of nuclear receptor corepressors | |
| P478 | volume | 6 | |