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Molecular Cell, ISSN 1097-2765, 2011, Volume 42, Issue 3, pp. 330 - 341
Journal Article
Genes and Development, ISSN 0890-9369, 04/2011, Volume 25, Issue 8, pp. 801 - 813
In the absence of growth signals, cells exit the cell cycle and enter into G0 or quiescence. Alternatively, cells enter senescence in response to inappropriate... 
Phosphorylation | Down syndrome | Growth arrest | Retinoblastoma-like protein p130 | Cell cycle | Cellular senescence | cell cycle | DEVELOPMENTAL BIOLOGY | CELL-CYCLE CONTROL | DROSOPHILA | CELL BIOLOGY | REPRESSOR COMPLEX | cellular senescence | CAENORHABDITIS-ELEGANS | DOWN-SYNDROME | IN-VIVO | GENETICS & HEREDITY | growth arrest | IDENTIFICATION TECHNOLOGY | E2F | TUMOR-SUPPRESSOR | B-MYB | phosphorylation | retinoblastoma-like protein p130 | Cell Cycle - genetics | NIH 3T3 Cells | Cell Proliferation | Transcription Factor DP1 - metabolism | Protein-Tyrosine Kinases - metabolism | Humans | Retinoblastoma-Binding Protein 4 - genetics | Transcription Factor DP1 - genetics | Protein-Tyrosine Kinases - genetics | Retinoblastoma-Like Protein p130 - metabolism | Tumor Suppressor Proteins - genetics | Trans-Activators - genetics | Nuclear Proteins - genetics | E2F4 Transcription Factor - metabolism | Protein-Serine-Threonine Kinases - metabolism | Retinoblastoma-Binding Protein 4 - metabolism | Cell Line | Cellular Senescence - genetics | Tumor Suppressor Proteins - metabolism | Cells, Cultured | Protein-Serine-Threonine Kinases - genetics | Cellular Senescence - physiology | Nuclear Proteins - metabolism | E2F4 Transcription Factor - genetics | Animals | Cell Cycle - physiology | Cell Line, Tumor | Trans-Activators - metabolism | Mice | Retinoblastoma-Like Protein p130 - genetics | Ras genes | Analysis | Aging | Physiological aspects | Genetic aspects | Research | Index Medicus | Research Paper
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2014, Volume 289, Issue 32, pp. 21844 - 21855
The nucleosome remodeling and deacetylase (NuRD) complex is a widely conserved transcriptional co-regulator that harbors both nucleosome remodeling and histone... 
SOMATIC-CELLS | PROTEIN | DNA METHYLATION | STRUCTURAL BASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | HISTONE DEACETYLASE COMPLEX | ZINC-FINGER | TRANSCRIPTIONAL REPRESSION | MI-2/NURD COMPLEX | BINDING | DOMAINS | Transcription Factors - chemistry | Retinoblastoma-Binding Protein 7 - chemistry | Humans | Molecular Sequence Data | Retinoblastoma-Binding Protein 4 - genetics | Crystallography, X-Ray | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Mi-2 Nucleosome Remodeling and Deacetylase Complex - metabolism | Retinoblastoma-Binding Protein 7 - metabolism | Conserved Sequence | Protein Interaction Domains and Motifs | Nuclear Proteins - genetics | Retinoblastoma-Binding Protein 4 - chemistry | Repressor Proteins - metabolism | Retinoblastoma-Binding Protein 4 - metabolism | Amino Acid Sequence | Repressor Proteins - chemistry | Histone Deacetylases - genetics | Histone Deacetylases - chemistry | Chromatin Assembly and Disassembly | Models, Molecular | Nucleosomes - metabolism | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Nuclear Proteins - metabolism | Transcription Factors - genetics | Nuclear Proteins - chemistry | Sequence Homology, Amino Acid | Transcription Factors - metabolism | Retinoblastoma-Binding Protein 7 - genetics | Animals | Mi-2 Nucleosome Remodeling and Deacetylase Complex - chemistry | Histones - metabolism | Index Medicus | Gene Regulation | Chromatin | RbAp48 | MTA1 | RBBP4 | Chromatin Structure | NuRD Complex | Protein Structure | Protein Assembly
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2829 - 16
Recent studies suggest the emerging roles of armadillo (ARM) family proteins in tumor progression. However, the functions and underlying mechanisms of ARM... 
DELTA-CATENIN | BREAST-CANCER CELLS | INVASION | GASTRIC-CANCER | MULTIDISCIPLINARY SCIENCES | HISTONE DEACETYLASE COMPLEX | IN-VIVO | GENE-EXPRESSION | TUMOR-SUPPRESSOR | CERVICAL-CANCER | BETA-CATENIN | Neurons - pathology | Polycomb Repressive Complex 2 - genetics | Prognosis | Humans | Retinoblastoma-Binding Protein 4 - genetics | Neuroblastoma - mortality | Armadillo Domain Proteins - genetics | Carcinogenesis - metabolism | Brain Neoplasms - metabolism | Cell-Penetrating Peptides - pharmacology | Retinoblastoma-Binding Protein 4 - antagonists & inhibitors | HEK293 Cells | Armadillo Domain Proteins - antagonists & inhibitors | Female | Antineoplastic Agents - pharmacology | Neurons - metabolism | Brain Neoplasms - mortality | Neurons - drug effects | Retinoblastoma-Binding Protein 4 - metabolism | Enhancer of Zeste Homolog 2 Protein - genetics | Enhancer of Zeste Homolog 2 Protein - metabolism | Neuroblastoma - genetics | Carcinogenesis - genetics | Brain Neoplasms - genetics | Brain Neoplasms - drug therapy | Disease Progression | Carcinogenesis - pathology | Xenograft Model Antitumor Assays | Animals | Mice, Nude | Neuroblastoma - drug therapy | Armadillo Domain Proteins - metabolism | Survival Analysis | Cell Line, Tumor | Protein Binding | Mice | Neuroblastoma - metabolism | Polycomb Repressive Complex 2 - metabolism | Proteins | Gene silencing | Polycomb group proteins | Aggressive behavior | Cell lines | Tumorigenesis | Neuroblastoma | Gene expression | Retinoblastoma | Tumors | Index Medicus
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2011, Volume 286, Issue 2, pp. 1196 - 1203
Chromatin-modifying complexes such as the NuRD complex are recruited to particular genomic sites by gene-specific nuclear factors. Overall, however, little is... 
Transcription Factors - chemistry | Histones - chemistry | Protein Interaction Domains and Motifs - physiology | Molecular Sequence Data | Retinoblastoma-Binding Protein 4 - genetics | Crystallography, X-Ray | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Mi-2 Nucleosome Remodeling and Deacetylase Complex - metabolism | Spodoptera | Binding Sites - physiology | Conserved Sequence | Microfilament Proteins - metabolism | Nuclear Proteins - genetics | Retinoblastoma-Binding Protein 4 - chemistry | Repressor Proteins - metabolism | Retinoblastoma-Binding Protein 4 - metabolism | Protein Structure, Tertiary | Recombinant Proteins - metabolism | Amino Acid Sequence | Microfilament Proteins - chemistry | Repressor Proteins - chemistry | Histone Deacetylases - genetics | Cells, Cultured | Histone Deacetylases - chemistry | Recombinant Proteins - chemistry | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Nuclear Proteins - metabolism | Recombinant Proteins - genetics | Transcription Factors - genetics | Nuclear Proteins - chemistry | Transcription Factors - metabolism | Transcription, Genetic - physiology | Animals | Histones - genetics | Mi-2 Nucleosome Remodeling and Deacetylase Complex - chemistry | Histones - metabolism | Index Medicus | Gene Regulation | Transcription Regulation | RbAp48 | X-ray Crystallography | NuRD Complex | GATA-1 | Transcription Factors | FOG-1 | Protein-Protein Interactions
Journal Article
Journal Article
Protein Science, ISSN 0961-8368, 08/2016, Volume 25, Issue 8, pp. 1472 - 1482
The nucleosome remodeling and deacetylase (NuRD) complex remodels the genome in the context of both gene transcription and DNA damage repair. It is essential... 
protein structure | transcription regulation | MTA1 | RBBP4 | chromatin | NuRD complex | Chromatin | Protein structure | Transcription regulation | CHROMATIN REMODELER | RECOGNITION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CRYO-EM | PLURIPOTENCY | MASS-SPECTROMETRY | FACTOR ISWI | SEQUENCE | ARCHITECTURE | PROTEIN COMPLEXES | PROTEOMICS | Nucleosomes - chemistry | Retinoblastoma-Binding Protein 7 - chemistry | Humans | Protein Multimerization | Retinoblastoma-Binding Protein 4 - genetics | Protein Subunits - metabolism | Thermodynamics | Retinoblastoma-Binding Protein 7 - metabolism | Cloning, Molecular | HEK293 Cells | Conserved Sequence | Transcription, Genetic | Protein Interaction Domains and Motifs | Retinoblastoma-Binding Protein 4 - chemistry | Repressor Proteins - metabolism | Retinoblastoma-Binding Protein 4 - metabolism | Protein Subunits - genetics | Recombinant Proteins - metabolism | Amino Acid Sequence | Gene Expression | Repressor Proteins - chemistry | Cross-Linking Reagents - chemistry | Histone Deacetylases - genetics | Protein Structure, Secondary | Histone Deacetylases - chemistry | Models, Molecular | Nucleosomes - metabolism | Recombinant Proteins - chemistry | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Recombinant Proteins - genetics | Retinoblastoma-Binding Protein 7 - genetics | Sequence Alignment | Animals | Protein Subunits - chemistry | Kinetics | Mutation | Crosslinked polymers | Analysis | Genomics | Genetic transcription | Metastasis | Nematoda | Protein binding | Index Medicus
Journal Article
Journal Article
PLoS Pathogens, ISSN 1553-7366, 06/2010, Volume 6, Issue 6, pp. e1000965 - e1000965
Histone deacetylation plays a pivotal role in regulating human cytomegalovirus gene expression. In this report, we have identified candidate HDAC1-interacting... 
INDUCED CELL-DEATH | TRANSCRIPTIONAL ACTIVATION | FUNCTIONAL INTERACTION | HISTONE DEACETYLASE INHIBITION | MICROBIOLOGY | MI-2/NURD COMPLEX | EARLY PROMOTER/ENHANCER | VIRAL REPLICATION | VIROLOGY | CHROMATIN-REMODELING COMPLEX | LENTIVIRAL VECTOR | GENE-EXPRESSION | PARASITOLOGY | Autoantigens - metabolism | Immunoprecipitation | Luciferases - metabolism | Humans | Retinoblastoma-Binding Protein 4 - genetics | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Mi-2 Nucleosome Remodeling and Deacetylase Complex - metabolism | Cytomegalovirus Infections - metabolism | Cytomegalovirus Infections - genetics | Autoantigens - genetics | Viral Proteins - metabolism | Mi-2 Nucleosome Remodeling and Deacetylase Complex - antagonists & inhibitors | RNA, Viral - genetics | Chromatin Immunoprecipitation | Cytomegalovirus Infections - virology | Histone Deacetylase 1 - antagonists & inhibitors | Histone Deacetylase 1 - genetics | Hydroxamic Acids - pharmacology | Repressor Proteins - metabolism | Retinoblastoma-Binding Protein 4 - metabolism | Fibroblasts - metabolism | Cytomegalovirus - pathogenicity | Promoter Regions, Genetic | Histone Deacetylases - genetics | RNA, Messenger - genetics | Cells, Cultured | Repressor Proteins - genetics | Viral Proteins - genetics | Histone Deacetylases - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Immediate-Early Proteins - genetics | Virus Replication | Fibroblasts - drug effects | Fluorescent Antibody Technique | Histone Deacetylase Inhibitors - pharmacology | Fibroblasts - cytology | Histone Deacetylase 1 - metabolism | RNA | Viral proteins | Cytomegaloviruses | Physiological aspects | Genetic aspects | Research | Health aspects | Index Medicus | Enzymes | Histone deacetylase | Pathogens | proteomics | NuRD protein | Mass spectroscopy | Gene expression | Histone acetyltransferase | Promoters | Host-pathogen interactions | Infection | HDAC1 protein | Deacetylation | DNA | Persistent infection | Histones | Nucleosomes | Replication | Trichostatin A | Acetylation | Differentiation | Cancer | Proteins | Cytomegalovirus | Chromatin | Microbiology | Peptides | Genetics | Genomes | Mass spectrometry | Molecular weight
Journal Article