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1. Full Text Translational repression by deadenylases
by Cooke, Amy and Prigge, Andrew and Wickens, Marvin
The Journal of biological chemistry, ISSN 0021-9258, 09/2010, Volume 285, Issue 37, pp. 28506 - 28513
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | RNA-Binding Proteins - genetics | Exoribonucleases - genetics | Xenopus Proteins - genetics | Oocytes - metabolism | Humans | Xenopus laevis | Protein Biosynthesis - physiology | RNA Caps - metabolism | Oocytes - cytology | Animals | Xenopus Proteins - metabolism | Mice | Drosophila melanogaster | Exoribonucleases - metabolism | RNA Caps - genetics | RNA-Binding Proteins - metabolism | Schizosaccharomyces | Index Medicus | Xenopus | Repressor Protein | Poly(A) | MicroRNA | RNA | POP2 | CAF1 | Deadenylases | mRNA Decay | Translational Repression | Developmental Biology | Translation Control
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2. Full Text Carbon catabolite repression in Pseudomonas: optimizing metabolic versatility and interactions with the environment
by Rojo, Fernando
FEMS microbiology reviews, ISSN 0168-6445, 09/2010, Volume 34, Issue 5, pp. 658 - 684
translational control | Pseudomonas | gene expression | catabolite repression control | global regulation | Life Sciences & Biomedicine | Microbiology | Science & Technology | Virulence | Bacterial Proteins - genetics | Pseudomonas - pathogenicity | Bacillus subtilis - genetics | Catabolite Repression | Escherichia coli - genetics | Biotransformation | Escherichia coli - metabolism | Bacterial Proteins - metabolism | Environment | Gene Expression Regulation, Bacterial | Pseudomonas - genetics | Bacillus subtilis - metabolism | Pseudomonas - metabolism | Gene expression | Mathematical optimization | Bioremediation | Catabolite repression | Genes | Metabolism | Environmental impact | Carbon | Optimization | Molecular modelling | Virulence factors | Regulatory mechanisms (biology) | Bacteria | Nutrients | Carbon sources | Index Medicus
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3. Full Text EAR motif-mediated transcriptional repression in plants
: An underlying mechanism for epigenetic regulation of gene expression
by Kagale, Sateesh and Rozwadowski, Kevin
Epigenetics, ISSN 1559-2294, 02/2011, Volume 6, Issue 2, pp. 141 - 146
Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | Post-translational modification | TPL | Phosphorylation | Repressome | Co-repressors | EAR motif | SAP18 | Epigenetic regulation | HDA19 | Histone deacetylation | Chromatin modification | Transcriptional repression | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Epigenomics | Plants, Genetically Modified - genetics | Repressor Proteins - genetics | Co-Repressor Proteins - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Co-Repressor Proteins - genetics | Amino Acid Motifs | Arabidopsis - genetics | DNA-Binding Proteins - metabolism | Plant Proteins - genetics | Plants - genetics | Gene Expression Regulation, Plant | Plant Proteins - metabolism | Repressor Proteins - metabolism | Evolution, Molecular | Index Medicus | chromatin modification | co-repressors | post-translational modification | epigenetic regulation | Point-of-View | transcriptional repression | repressome | histone deacetylation | phosphorylation
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4. Full Text PUF proteins: repression, activation and mRNA localization
by Quenault, Tara and Lithgow, Trevor and Traven, Ana
Trends in cell biology, ISSN 0962-8924, 2010, Volume 21, Issue 2, pp. 104 - 112
Pathology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Protein Biosynthesis | Animals | Humans | RNA-Binding Proteins - chemistry | Mitochondria - metabolism | Protein Processing, Post-Translational | RNA, Messenger - metabolism | RNA-Binding Proteins - metabolism | Yeasts - metabolism | Index Medicus
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5. Full Text A postprandial FGF19‐SHP‐LSD1 regulatory axis mediates epigenetic repression of hepatic autophagy
by Byun, Sangwon and Kim, Young‐Chae and Zhang, Yang and Kong, Bo and Guo, Grace and Sadoshima, Junichi and Ma, Jian and Kemper, Byron and Kemper, Jongsook Kim
The EMBO journal, ISSN 0261-4189, 06/2017, Volume 36, Issue 12, pp. 1755 - 1769
FXR | CRTC2 | FGF15 | CREB | bile acid | lipophagy | TFEB | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Microscopy, Electron, Transmission | Epigenetic Repression | Mice, Inbred C57BL | Nerve Tissue Proteins - deficiency | Autophagy | Mice, Knockout | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Fibroblast Growth Factors - metabolism | Histone Demethylases - metabolism | Animals | Hepatocytes - ultrastructure | Liver - cytology | Protein Processing, Post-Translational | Histones - metabolism | Index Medicus | Chromatin, Epigenetics, Genomics & Functional Genomics | Autophagy & Cell Death | Metabolism
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6. Full Text Manganese causes neurotoxic iron accumulation via translational repression of amyloid precursor protein and H‐Ferritin
by Venkataramani, Vivek and Doeppner, Thorsten R and Willkommen, Desiree and Cahill, Catherine M and Xin, Yongjuan and Ye, Guilin and Liu, Yanyan and Southon, Adam and Aron, Allegra and Au‐Yeung, Ho Yu and Huang, Xudong and Lahiri, Debomoy K and Wang, Fudi and Bush, Ashley I and Wulf, Gerald G and Ströbel, Philipp and Michalke, Bernhard and Rogers, Jack T
Journal of neurochemistry, ISSN 0022-3042, 12/2018, Volume 147, Issue 6, pp. 831 - 848
manganese (Mn) | H‐ferritin | reactive oxygen species (ROS) | amyloid precursor protein (APP) | SH‐SY5Y neural‐like cell line | iron responsive element (IRE) | H-ferritin | SH-SY5Y neural-like cell line | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cell Line | Cell Survival - drug effects | Reactive Oxygen Species - metabolism | Oxidative Stress | Humans | Mice, Inbred C57BL | Rats | Iron - metabolism | Rats, Sprague-Dawley | Apoferritins - metabolism | Animals | 5' Untranslated Regions | Amyloid beta-Protein Precursor - metabolism | Apoferritins - antagonists & inhibitors | Mice | Amyloid beta-Protein Precursor - antagonists & inhibitors | Protein Modification, Translational - drug effects | Manganese Poisoning - metabolism | Neuroprotection | Oxidative stress | Reactive oxygen species | Animal models | Parkinson's disease | Transcription | Toxicity | Oxidative metabolism | Ferritin | Homology | Lipids | Iron | Accumulation | Mimicry | Proteins | Neurotoxicity | Precursors | Biocompatibility | Alzheimer's disease | Movement disorders | Translation | Neurodegenerative diseases | Mass spectroscopy | Exposure | Metabolism | Amyloid precursor protein | Inductively coupled plasma | Ferrous ions | Mass spectrometry | Manganese | Index Medicus | Manganese (Mn) | H-Ferritin | neurotoxicity | neuroprotection | iron | Manganism
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7. Full Text Translational repression of Ccl5 and Cxcl10 by 4E‐BP1 and 4E‐BP2 restrains the ability of mouse macrophages to induce migration of activated T cells
by William, Mirtha and Leroux, Louis‐Philippe and Chaparro, Visnu and Graber, Tyson E and Alain, Tommy and Jaramillo, Maritza
European journal of immunology, ISSN 0014-2980, 08/2019, Volume 49, Issue 8, pp. 1200 - 1212
mTOR | 4E‐BP | macrophages | mRNA translation | chemokines | Life Sciences & Biomedicine | Immunology | Science & Technology | Eukaryotic Initiation Factors - genetics | Eukaryotic Initiation Factors - metabolism | Protein Biosynthesis | Epigenetic Repression | Signal Transduction | Lymphocyte Activation | Cell Cycle Proteins - metabolism | Cells, Cultured | Mechanistic Target of Rapamycin Complex 1 - metabolism | Mice, Knockout | Animals | Chemokine CXCL10 - genetics | Adaptor Proteins, Signal Transducing - genetics | Chemokine CCL5 - genetics | Cell Cycle Proteins - genetics | T-Lymphocytes - immunology | Cell Differentiation | Mice | Protein Processing, Post-Translational | Adaptor Proteins, Signal Transducing - metabolism | Macrophages - immunology | Cell Movement | RNA | T cells | Binding proteins | Macrophages | Genetic translation | Protein binding | TOR protein | Chemotactic factors | Translation | Phosphorylation | Leukocyte migration | Lymphocytes T | Rapamycin | Inflammation | Lipopolysaccharides | Proteins | Lymphocytes | CXCL10 protein | Initiation factor eIF-4E | Chemokines | Cell migration | Index Medicus | Life Sciences | Biochemistry, Molecular Biology
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