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The EMBO Journal, ISSN 0261-4189, 03/2002, Volume 21, Issue 6, pp. 1427 - 1436
Journal Article
Cell Reports, ISSN 2211-1247, 10/2015, Volume 13, Issue 4, pp. 703 - 711
Journal Article
Molecular Cell, ISSN 1097-2765, 2009, Volume 35, Issue 6, pp. 868 - 880
Journal Article
The EMBO Journal, ISSN 0261-4189, 07/2015, Volume 34, Issue 14, pp. 1905 - 1924
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 4/2004, Volume 165, Issue 1, pp. 31 - 40
Understanding gene expression control requires defining the molecular and cellular basis of mRNA turnover. We have previously shown that the human decapping... 
RNA stability | Yeasts | Messenger RNA | HEK293 cells | RNA | Lymphocytes | Plasmids | Cell lines | Cells | Cytoplasm | FRET | Cell cycle | Green fluorescent protein | Transcriptional and translational inhibitors | cell cycle | DEAD BOX HELICASE | NUCLEAR-PROTEIN | green fluorescent protein | MAMMALIAN-CELLS | SACCHAROMYCES-CEREVISIAE | ENDONUCLEOLYTIC CLEAVAGE | CELL BIOLOGY | transcriptional and translational inhibitors | DECAPPING ENZYME | NONSENSE-MEDIATED DECAY | TERMINATION CODONS | SM-LIKE PROTEINS | Endoribonucleases - genetics | Humans | Phosphoproteins - metabolism | RNA, Messenger - metabolism | Organelles - genetics | Organelles - ultrastructure | RNA Interference | Cytoplasmic Granules - metabolism | Membrane Proteins - metabolism | Protein Biosynthesis - genetics | Receptors, Chemokine - genetics | Proto-Oncogene Proteins - metabolism | Cell Line | DEAD-box RNA Helicases | Endoribonucleases - metabolism | Membrane Proteins - genetics | RNA, Messenger - genetics | Receptors, Chemokine - metabolism | Cell Compartmentation - genetics | Intracellular Signaling Peptides and Proteins | Proto-Oncogene Proteins - genetics | Phosphoproteins - genetics | RNA Nucleotidyltransferases - metabolism | RNA Stability - genetics | Proteins - genetics | Proteins - metabolism | Cytoplasmic Granules - ultrastructure | RNA Nucleotidyltransferases - genetics | Cytoplasmic Granules - genetics | Protein Biosynthesis - drug effects | Receptors, CCR4 | Organelles - metabolism | Research | Proteins | Cellular biology | Ribonucleic acid | Fluorescence | Gene expression | Ribonucleic acid--RNA | Index Medicus | cell cycle; FRET; green fluorescent protein; transcriptional and translational inhibitors; RNA stability
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2019, Volume 116, Issue 12, pp. 5721 - 5726
The Drosophila circadian oscillator relies on a negative transcriptional feedback loop, in which the PERIOD (PER) and TIMELESS (TIM) proteins repress the... 
Circadian rhythms | Clock genes | CCR4–NOT complex | CAF1/POP2 | mRNA poly(A) tail | POSTTRANSCRIPTIONAL REGULATION | MECHANISM | BEHAVIOR | MULTIDISCIPLINARY SCIENCES | circadian rhythms | CCR4-NOT complex | PROTEIN COMPLEX | MESSENGER-RNA DEGRADATION | clock genes | ENTRAINMENT | RHYTHMS | GENE-EXPRESSION | DYNAMICS | Period Circadian Proteins - physiology | ARNTL Transcription Factors - genetics | Phosphorylation | Down-Regulation | Gene Expression Regulation | CLOCK Proteins - genetics | Circadian Clocks - genetics | Circadian Rhythm - physiology | Ribonucleases | Drosophila Proteins - metabolism | RNA, Messenger - metabolism | Drosophila melanogaster - genetics | Drosophila Proteins - physiology | Animals | Period Circadian Proteins - metabolism | Transcription, Genetic | Drosophila Proteins - genetics | Circadian Clocks - physiology | Post-transcription | Poly(A) | Transcription factors | Drosophila | Oscillations | Feedback loops | CLOCK protein | Gene expression | Mutants | Proteins | Insects | Timeless protein | Polyadenylation | Control theory | Inhibition | mRNA stability | Index Medicus | ARNTL Transcription Factors | Drosophila Proteins | Neurons and Cognition | Psychology and behavior | Neurobiology | Circadian Rhythm | Period Circadian Proteins | Life Sciences | CLOCK Proteins | Circadian Clocks | Cognitive Sciences | RNA, Messenger | Drosophila melanogaster
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 11/2017, Volume 232, Issue 11, pp. 2996 - 3005
Gingiva fibroblasts express 12 chemokine receptors. Fourteen chemokines were used to study proliferation (top), migration (middle), and secretion of wound... 
cytokine | migration | chemokine | gingiva | proliferation | PERIODONTAL-DISEASES | PHYSIOLOGY | PHENOTYPIC DIFFERENCES | KERATINOCYTES | MESENCHYMAL STEM-CELLS | CELL BIOLOGY | HUMAN GINGIVAL FIBROBLASTS | GROWTH-FACTOR | ACCUMULATION | EXPRESSION | SKIN INFLAMMATION | Fibroblasts - secretion | Hepatocyte Growth Factor - secretion | Humans | Dose-Response Relationship, Drug | Receptors, CCR4 - metabolism | Tissue Inhibitor of Metalloproteinase-1 - metabolism | Gingiva - metabolism | Gingiva - pathology | Gingiva - drug effects | Gingiva - secretion | Interleukin-6 - metabolism | Wound Healing - drug effects | Fibroblasts - metabolism | Chemokines, CC - pharmacology | Fibroblasts - pathology | Interleukin-6 - secretion | Receptors, CCR4 - agonists | Hepatocyte Growth Factor - metabolism | Cell Movement - drug effects | Receptors, CCR3 - metabolism | Signal Transduction - drug effects | Fibroblasts - drug effects | Ligands | Cell Proliferation - drug effects | Tissue Inhibitor of Metalloproteinase-1 - secretion | Receptors, CCR3 - agonists | Cell Line, Transformed | Wound healing | Flow cytometry | CXCL12 protein | Leukocyte migration | Mucosa | CXCL13 protein | CX3CR1 protein | Stimulation | Tissue inhibitor of metalloproteinase 1 | Interleukin 6 | CCL22 protein | Receptors | CXCR5 protein | Fibroblasts | CCL20 protein | Activation analysis | Secretion | CXCR2 protein | Chemokine receptors | CXCR4 protein | CCR6 protein | Cytometry | Healing | CXCL11 protein | Gingiva | CCR9 protein | Chemokines | Cell migration | Index Medicus | Original | Original s
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 12/2001, Volume 314, Issue 4, pp. 683 - 694
The CCR4-NOT complex is an evolutionarily conserved, transcriptional regulatory complex that is involved in controlling mRNA initiation, elongation and... 
mRNA degradation | transcription | elongation | CCR4-NOT complex | yeast | Yeast | Transcription | Elongation | DIFFERENTIALLY AFFECTS | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SACCHAROMYCES-CEREVISIAE | MASS-SPECTROMETRY | REGULATOR | PROMOTERS | GENE-EXPRESSION | DOMAINS | Fungal Proteins - chemistry | Molecular Weight | Transcription Factors - chemistry | Saccharomyces cerevisiae - genetics | Humans | Cell Cycle Proteins - chemistry | Proteins | Sequence Homology | Gene Deletion | Mass Spectrometry | Cell Cycle Proteins - genetics | Saccharomyces cerevisiae Proteins - isolation & purification | Fungal Proteins - isolation & purification | Binding Sites | Cell Cycle Proteins - isolation & purification | Cell Cycle Proteins - metabolism | Ribonucleases | Fungal Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Transcription Factors - genetics | Blotting, Western | Precipitin Tests | Saccharomyces cerevisiae - chemistry | Macromolecular Substances | Transcription Factors - metabolism | Two-Hybrid System Techniques | Phenotype | Models, Biological | Saccharomyces cerevisiae Proteins - metabolism | Protein Binding | Transcription Factors - isolation & purification | Chromatography, Gel | Evolution, Molecular | Fungal Proteins - metabolism | Saccharomyces cerevisiae Proteins - chemistry | NOT1 protein | caf130 gene | CAF130 protein | CCR4 protein | NOT2 protein | NOT4 protein | NOT3 protein | caf40 gene | CAF40 protein | Index Medicus
Journal Article