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Molecular Systems Biology, ISSN 1744-4292, 2011, Volume 7, Issue 1, pp. 521 - n/a
Synthetic biology aims to systematically design and construct novel biological systems that address energy, environment, and health issues. Herein, we describe... 
synthetic biology | Pseudomonas aeruginosa | pyocin | quorum sensing | genetic circuits | CELLS | BACTERIA | PROTEIN | SENSITIVE METHOD | SPECIFICITY | EFFICACY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLASMID | OTITIS | PERACETIC-ACID | BINDING | Recombinant Fusion Proteins - pharmacology | Humans | Pseudomonas aeruginosa - growth & development | Biofilms - growth & development | Escherichia coli - pathogenicity | Escherichia coli - metabolism | Homoserine - pharmacology | Homoserine - analogs & derivatives | Organisms, Genetically Modified - genetics | Genes, Reporter | Biofilms - drug effects | Recombinant Fusion Proteins - biosynthesis | Green Fluorescent Proteins - analysis | Quorum Sensing - drug effects | Pseudomonas Infections - drug therapy | 4-Butyrolactone - pharmacology | Pyocins - biosynthesis | Pseudomonas aeruginosa - drug effects | Escherichia coli - chemistry | Pseudomonas Infections - microbiology | Gene Expression Regulation, Bacterial - drug effects | Bacterial Proteins - pharmacology | Pyocins - pharmacology | Escherichia coli - genetics | Green Fluorescent Proteins - biosynthesis | Plasmids | Synthetic Biology - methods | Biosensing Techniques - methods | Anti-Bacterial Agents - biosynthesis | Anti-Bacterial Agents - pharmacology | Bacterial Proteins - biosynthesis | 4-Butyrolactone - analogs & derivatives | Antibiosis - genetics | Chassis | Water-borne diseases | Cell culture | Mixed culture | Escherichia coli | Fluorescence | Confocal microscopy | Infections | Biology | E7 protein | Devices | Matrix methods | Antiinfectives and antibacterials | Proteins | Engineering | Microorganisms | Microbiota | Biological weapons | E coli | Helicobacter pylori | Mathematical analysis | Bacteria | Synthetic biology | Inhibition | Public health | Killing | Pathogens | Escherichia | Damage assessment | Empirical equations | Transfer functions | Data processing | Membrane proteins | Biofilms | Infectious diseases | Antibiotics | Microscopy | Lysis | Green fluorescent protein | Strategy | Cholera | Detection | Index Medicus
Journal Article
American Journal of Physiology - Gastrointestinal and Liver Physiology, ISSN 0193-1857, 04/2008, Volume 294, Issue 4, pp. G1060 - G1069
Probiotics promote intestinal epithelial integrity and reduce infection and diarrhea. We evaluated the effect of Lactobacillus rhamnosus GG-produced soluble... 
Protein kinase C | Zonula occludens-1 | Intestine | Lactobacillus rhamnosus GG | Mucosal protection | Occludin | zonula occludens-1 | mucosal protection | OXIDATIVE STRESS | PHYSIOLOGY | intestine | DIARRHEA | PERMEABILITY | CYTOSKELETON | CACO-2 CELL MONOLAYER | LACTOBACILLUS GG | TIGHT JUNCTIONS | occludin | IN-VIVO | GROWTH | INTESTINAL BARRIER | GASTROENTEROLOGY & HEPATOLOGY | protein kinase C | Protein Kinase C beta | Intestinal Mucosa - metabolism | Cadherins - metabolism | Nitriles - pharmacology | Humans | Tight Junctions - enzymology | Phosphoproteins - metabolism | Intestinal Mucosa - drug effects | Dose-Response Relationship, Drug | Lactobacillus rhamnosus - chemistry | Time Factors | Protein Kinase C - metabolism | Intestinal Mucosa - enzymology | Indoles - pharmacology | Membrane Proteins - metabolism | Tight Junctions - drug effects | Caco-2 Cells | Hydrogen Peroxide - toxicity | Tight Junctions - metabolism | Butadienes - pharmacology | Protein Kinase C - antagonists & inhibitors | Electric Impedance | Permeability | Probiotics - pharmacology | beta Catenin - metabolism | Probiotics - isolation & purification | Protein Transport | HT29 Cells | Bacterial Proteins - pharmacology | Pyrroles - pharmacology | Zonula Occludens-1 Protein | Mitogen-Activated Protein Kinase 3 - metabolism | Mitogen-Activated Protein Kinases - antagonists & inhibitors | Protein Kinase C-epsilon - metabolism | Inulin - metabolism | Protein Kinase Inhibitors - pharmacology | Bacterial Proteins - isolation & purification | Mitogen-Activated Protein Kinase 1 - metabolism | Mitogen-Activated Protein Kinases - metabolism | Studies | Bacteria | Kinases | Bacterial proteins | Digestive system | Cells | Index Medicus
Journal Article
Immunity, ISSN 1074-7613, 2006, Volume 25, Issue 4, pp. 607 - 617
Journal Article
Neuron, ISSN 0896-6273, 11/2012, Volume 76, Issue 4, pp. 735 - 749
Axons must switch responsiveness to guidance cues during development for correct pathfinding. Sonic Hedgehog (Shh) attracts spinal cord commissural axons... 
SLIT | RESPONSIVENESS | KINASE-A | CHEMOATTRACTANT | GROWTH-CONE ATTRACTION | NETRIN-1 | SPINAL-CORD | GUIDANCE | SPECIFICATION | NEUROSCIENCES | INTERNEURONS | RNA, Small Interfering - genetics | Wnt1 Protein - genetics | Hedgehog Proteins - pharmacology | Embryo, Mammalian | Zinc Finger Protein Gli2 | Hedgehog Proteins - metabolism | Axons - physiology | Green Fluorescent Proteins - genetics | Spinal Cord Injuries - pathology | Basic Helix-Loop-Helix Transcription Factors - metabolism | Time Factors | Neurons - metabolism | Cyclic AMP - metabolism | 14-3-3 Proteins - genetics | Gene Expression Regulation, Developmental - physiology | Basic Helix-Loop-Helix Transcription Factors - genetics | Simplexvirus - genetics | Enzyme Inhibitors - pharmacology | Gene Expression Regulation, Developmental - drug effects | Rats | Mice, Transgenic | Piperazines - pharmacology | Rats, Sprague-Dawley | 14-3-3 Proteins - metabolism | Analysis of Variance | Signal Transduction - drug effects | Chickens | Luminescent Proteins - genetics | Mice | beta-Galactosidase - genetics | Carbazoles - pharmacology | Kruppel-Like Transcription Factors - genetics | RNA, Small Interfering - metabolism | Gene Expression Regulation, Developmental - genetics | Neurons - cytology | Wnt1 Protein - metabolism | DNA-Binding Proteins - metabolism | Neurons - classification | Protein Isoforms - metabolism | Hedgehog Proteins - genetics | Kruppel-Like Transcription Factors - metabolism | beta-Galactosidase - metabolism | Female | Pyrazoles - pharmacology | Cyclic AMP-Dependent Protein Kinases - metabolism | Bacterial Proteins - genetics | Cells, Cultured | Axons - drug effects | Electroporation | DNA-Binding Proteins - genetics | Chemotaxis | Amino Acids | Pregnancy | Pyrroles - pharmacology | Animals | Protein Isoforms - genetics | Proteins | Neurons | Medical research | Spinal cord | Rodents | Migration | Mammals | Index Medicus
Journal Article
PLoS Pathogens, ISSN 1553-7366, 05/2011, Volume 7, Issue 5, pp. e1002042 - e1002042
Over the last decade a significant number of studies have highlighted the central role of host antimicrobial (or defence) peptides in modulating the response... 
IMMUNE-RESPONSE | PROTEIN SECONDARY STRUCTURE | ENTERIC NEMATODE | PATHOGEN FASCIOLA-HEPATICA | MICROBIOLOGY | DEFENSE PEPTIDES | SIZE-DISTRIBUTION ANALYSIS | CIRCULAR-DICHROISM SPECTRA | ALTERNATIVELY ACTIVATED MACROPHAGES | VIROLOGY | CATHELICIDIN FAMILY | LIPOPOLYSACCHARIDE-BINDING | PARASITOLOGY | Helminth Proteins - pharmacology | Membrane Glycoproteins - metabolism | Anti-Infective Agents - metabolism | Humans | Helminth Proteins - chemistry | Lipopolysaccharides - metabolism | Molecular Sequence Data | Antimicrobial Cationic Peptides - metabolism | Anti-Infective Agents - immunology | Inflammation - metabolism | Molecular Mimicry | Fasciola hepatica - chemistry | Fascioliasis - parasitology | Sepsis - metabolism | Carrier Proteins - pharmacology | Endotoxemia - immunology | Toll-Like Receptors - metabolism | Helminth Proteins - metabolism | Fasciola hepatica - metabolism | Recombinant Proteins - metabolism | Amino Acid Sequence | Sepsis - immunology | Acute-Phase Proteins - metabolism | Antimicrobial Cationic Peptides - chemistry | Membrane Glycoproteins - pharmacology | Toll-Like Receptors - immunology | Antimicrobial Cationic Peptides - pharmacology | Helminth Proteins - genetics | Inflammation - immunology | Recombinant Proteins - genetics | Recombinant Proteins - pharmacology | Immunity, Innate | Fasciola hepatica - immunology | Animals | Carrier Proteins - metabolism | Fascioliasis - immunology | Lipopolysaccharides - pharmacology | Mice | Mice, Inbred BALB C | Endotoxemia - metabolism | Acute-Phase Proteins - pharmacology | Proteolysis | Antimicrobial peptides | Worms, Intestinal and parasitic | Physiological aspects | Research | Health aspects | Helminths | Medical research | Peptides | Cytokines | Rodents | Immune system | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 07/2016, Volume 535, Issue 7610, pp. 153 - 158
Inflammatory caspases (caspases 1, 4, 5 and 11) are activated in response to microbial infection and danger signals. When activated, they cleave mouse and... 
LISTERIA-MONOCYTOGENES | INTERLEUKIN-1-BETA | MULTIDISCIPLINARY SCIENCES | MIXED LINEAGE KINASE | PERFORIN | NLRP3 INFLAMMASOME | INTRACELLULAR BACTERIA | GRANZYMES | CASPASE-1 ACTIVATION | GRANULYSIN | CELL-DEATH | Conserved Sequence - genetics | Inflammasomes - metabolism | Phosphatidylinositol Phosphates - metabolism | Pyroptosis - drug effects | Escherichia coli - drug effects | Humans | Molecular Sequence Data | Neoplasm Proteins - pharmacology | Escherichia coli - cytology | Neoplasm Proteins - metabolism | Escherichia coli - metabolism | Protein Multimerization - genetics | Listeria monocytogenes - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Listeria monocytogenes - cytology | Porosity - drug effects | Neoplasm Proteins - genetics | Cell Membrane - drug effects | Staphylococcus aureus - metabolism | Amino Acid Sequence | Cell Line | Microbial Viability - drug effects | Membrane Proteins - genetics | Mice, Inbred C57BL | Phosphatidylserines - metabolism | Neoplasm Proteins - chemistry | Cardiolipins - metabolism | Cell Membrane - ultrastructure | Protein Structure, Tertiary - genetics | Microscopy, Electron | Pyroptosis - genetics | Protein Transport | Liposomes - chemistry | Animals | Membrane Proteins - chemistry | Cell Membrane Permeability - drug effects | Staphylococcus aureus - cytology | Liposomes - metabolism | Mice | Mutation | Staphylococcus aureus - drug effects | Listeria monocytogenes - drug effects | Observations | Apoptosis | Proteins | Membranes | Bacterial infections | Immunology | Plasmids | Bacteria | Infections | Cells | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2010, Volume 107, Issue 30, pp. 13473 - 13478
Staphylococcus aureus α-hemolysin (Hla), a potent cytotoxin, plays an important role in the pathogenesis of staphylococcal diseases, including those caused by... 
Receptors | Epithelial cells | Cell lines | Erythrocytes | Small interfering RNA | Cytotoxicity | Toxins | Cell membranes | Focal adhesions | Staphylococcus aureus | Cellular receptor | Pore-forming cytotoxin | CELLS | INFECTIONS | TYROSINE PHOSPHORYLATION | PROTECTION | pore-forming cytotoxin | TOXIN | MULTIDISCIPLINARY SCIENCES | P130(CAS) | MURINE MODEL | ERYTHROCYTES | PORE | BINDING | cellular receptor | Amyloid Precursor Protein Secretases - genetics | Epithelial Cells - metabolism | Hemolysin Proteins - pharmacology | Staphylococcus aureus - physiology | Hemolysin Proteins - genetics | Humans | Focal Adhesions | Molecular Sequence Data | Immunoblotting | RNA Interference | Membrane Proteins - metabolism | Staphylococcus aureus - metabolism | Staphylococcus aureus - genetics | Amino Acid Sequence | Cell Line | Cell Survival - drug effects | Rabbits | Membrane Proteins - genetics | Electrophoresis, Polyacrylamide Gel | Bacterial Proteins - genetics | ADAM10 Protein | Epithelial Cells - pathology | Host-Pathogen Interactions | Integrin beta1 - metabolism | ADAM Proteins - metabolism | Amyloid Precursor Protein Secretases - metabolism | Bacterial Proteins - pharmacology | Animals | Epithelial Cells - microbiology | Erythrocytes - metabolism | Cell Line, Tumor | Protein Binding | Bacterial Proteins - metabolism | Mutation | ADAM Proteins - genetics | Integrin beta1 - genetics | Hemolysin Proteins - metabolism | Index Medicus | Biological Sciences
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2015, Volume 11, Issue 4, pp. e1005124 - e1005124
Journal Article