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Nature, ISSN 0028-0836, 08/2018, Volume 560, Issue 7719, pp. 504 - 508
Histone H3 lysine 9 methylation (H3K9me) mediates heterochromatic gene silencing and is important for genome stability and the regulation of gene... 
SITE | METHYLATION | JMJC DOMAIN PROTEIN | STRUCTURAL BASIS | MULTIDISCIPLINARY SCIENCES | HETEROCHROMATIN | HISTONE LYSINE METHYLTRANSFERASE | DYNAMICS | INHERITANCE | EXPRESSION | Methyltransferases - chemistry | Schizosaccharomyces pombe Proteins - chemistry | Histones - chemistry | Epigenesis, Genetic | Humans | Methyltransferases - metabolism | Cell Cycle Proteins - metabolism | Gene Silencing | Heterochromatin - chemistry | Cell Cycle Proteins - chemistry | Histone-Lysine N-Methyltransferase - chemistry | Schizosaccharomyces - genetics | Heterochromatin - genetics | Histone Methyltransferases - chemistry | Heterochromatin - metabolism | Histone-Lysine N-Methyltransferase - metabolism | Schizosaccharomyces pombe Proteins - metabolism | Protein Conformation | Schizosaccharomyces - enzymology | Histone Methyltransferases - metabolism | Histones - metabolism | Methylation | Evolution, Molecular | Epigenetic inheritance | Methyltransferases | Analysis | Physiological aspects | Genetic research | Genetic regulation | Phosphorylation | Yeast | Peptides | Methyltransferase | Conservation | Amino acids | Homology | Genomes | Feedback loops | Catalytic activity | Positive feedback | Crystallography | Proteins | Demethylation | Heterochromatin | DNA methylation | Catalysis | Inhibition | Boundary element method | Deoxyribonucleic acid--DNA | Crystal structure | Enzymes | Stability | Gene expression | Substrates | Domains | Gene silencing | Hypotheses | Lysine | Proteomics | Epigenetics | Instability | Software | Scientific imaging | Mutation | Mass spectrometry | Histone H3 | Conformation
Journal Article
IEEE Journal of Selected Topics in Quantum Electronics, ISSN 1077-260X, 09/2010, Volume 16, Issue 5, pp. 1150 - 1157
Journal Article
Journal Article
IEEE journal on selected areas in communications, ISSN 1558-0008, 2018, Volume 36, Issue 12, pp. 2612 - 2620
.... To help network managers and application developers better understand the actual behavior of SDN implementations, we present a hardware/software co-design that enables switch characterization at 40 Gbps and beyond... 
Performance evaluation | Scalability | Random access memory | Switches | Computer architecture | OpenFlow | testing | Software defined networking | switch performances | SOFTWARE-DEFINED NETWORKING | TELECOMMUNICATIONS | ENGINEERING, ELECTRICAL & ELECTRONIC | Freeware | Co-design | Electronic devices | Reproducibility | Hardware | Software | Computer networks
Journal Article
Computer Networks, ISSN 1389-1286, 10/2017, Volume 126, pp. 69 - 80
.... In this article, we design a scalable control mechanism via switch migration locally to maximize control resource utilization, and we define this problem as Switch Migration Problem (SMP... 
Resource utilization | Software-defined networks | Scalability | Switch migrations | COMPUTER SCIENCE, HARDWARE & ARCHITECTURE | COMPUTER SCIENCE, INFORMATION SYSTEMS | TELECOMMUNICATIONS | ENGINEERING, ELECTRICAL & ELECTRONIC | Algorithms | Numerical analysis | Analysis | Switches
Journal Article
Immunity (Cambridge, Mass.), ISSN 1074-7613, 2012, Volume 36, Issue 6, pp. 986 - 1002
.... This potent negative signaling by Ly108 required immunotyrosine switch motifs (ITSMs) and SHP-1 recruitment, resulting in high amounts of SHP-1 at the T... 
SLAM FAMILY RECEPTORS | NATURAL-KILLER-CELLS | HUMORAL IMMUNITY | IMMUNOLOGY | CHRONIC VIRAL-INFECTION | MOLECULE-ASSOCIATED PROTEIN | LINKED LYMPHOPROLIFERATIVE-DISEASE | PROTEIN-TYROSINE-PHOSPHATASE | GERMINAL-CENTER | GENE-PRODUCT | CUTTING EDGE | Phosphorylation | Germinal Center - immunology | Antigens, Ly - genetics | Inositol Polyphosphate 5-Phosphatases | CD4-Positive T-Lymphocytes - immunology | Intracellular Signaling Peptides and Proteins - deficiency | Lymphopoiesis - physiology | Phosphotyrosine - physiology | Antigens, Ly - physiology | Immunologic Deficiency Syndromes - immunology | Intracellular Signaling Peptides and Proteins - genetics | Mice, Inbred C57BL | Natural Killer T-Cells - cytology | Mice, Transgenic | Phosphoric Monoester Hydrolases - physiology | Amino Acid Motifs | Mice, Knockout | Animals | B-Lymphocytes - immunology | Signaling Lymphocytic Activation Molecule Associated Protein | Immunological Synapses - immunology | Immunologic Deficiency Syndromes - genetics | Mice | Protein Processing, Post-Translational | Intracellular Signaling Peptides and Proteins - physiology | Lymphocyte Cooperation - physiology | Computer software industry | T cells | Genetic disorders | Proteins | Confidence intervals | Biomedical research | Lymphocytes | Rodents | Viral infections | Immune system | Cell adhesion & migration
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2009, Volume 284, Issue 16, pp. 10296 - 10300
DEXD/H-box RNA helicases couple ATP hydrolysis to RNA remodeling by an unknown mechanism. We used x-ray crystallography and biochemical analysis of the human... 
MESSENGER-RNA | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN DBP5 | EXPORT | EXON JUNCTION COMPLEX | SOFTWARE
Journal Article
EMBO molecular medicine, ISSN 1757-4684, 2019, Volume 11, Issue 8, pp. e10409 - n/a
Mitophagy can selectively remove damaged toxic mitochondria, protecting a cell from apoptosis. The molecular spatial–temporal mechanisms governing... 
apoptosis | mitophagy | diabetes mellitus | methionine sulfoxide reductase | platelets | MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | PROTEIN | MITOFUSIN 2 | UBIQUITIN | AUTOPHAGY | CELL-DEATH | MOUSE MODEL | RESISTANCE | MELANOCYTES | Blood Platelets - pathology | Diabetes Mellitus - blood | Diabetes Mellitus - pathology | Mitochondria - enzymology | Oxidative Stress | Diabetes Mellitus - genetics | Humans | Microfilament Proteins - blood | Blood Platelets - enzymology | Methionine Sulfoxide Reductases - genetics | Mitophagy | Ubiquitination | Female | Methionine Sulfoxide Reductases - blood | Microfilament Proteins - genetics | Cell Line | Microtubule-Associated Proteins - blood | Mitochondrial Membrane Transport Proteins - metabolism | Parkinson Disease - pathology | Microfilament Proteins - deficiency | Ubiquitin-Protein Ligases - blood | Oxidation-Reduction | Signal Transduction | Mice, Inbred C57BL | Mitochondria - pathology | Parkinson Disease - genetics | Mice, Knockout | Animals | Mutation | Parkinson Disease - blood | Methionine Sulfoxide Reductases - deficiency | Ubiquitin-Protein Ligases - genetics | Circuit components | Ubiquitin | Enzymes | Amino acids | Genetic transcription | Diabetes | Heart | Oxidative stress | Reactive oxygen species | Data analysis | Parkinson's disease | Transcription | Neurodegenerative diseases | Gene regulation | Diabetes mellitus | Methionine | Autophagy | Insulin | Experiments | Proteins | Mitochondria | Microscopy | Software | Parkin protein | Matrix protein | Platelets | Movement disorders | Apoptosis | Neuroscience | Metabolism
Journal Article