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Journal Article
Nature, ISSN 0028-0836, 02/2011, Volume 470, Issue 7334, pp. 404 - 408
Activating AMPK or inactivating calcineurin slows ageing in Caenorhabditis elegans(1,2) and both have been implicated as therapeutic targets for age-related... 
COACTIVATOR CRTC2 | TORC2 | UNFOLDED PROTEIN RESPONSE | CAENORHABDITIS-ELEGANS | PATHWAY | INSULIN-RESISTANCE | ER STRESS | MULTIDISCIPLINARY SCIENCES | KINASE | GENE-REGULATION | C-ELEGANS | AMP-Activated Protein Kinases - metabolism | Phosphorylation | Caenorhabditis elegans Proteins - chemistry | Humans | Caenorhabditis elegans Proteins - metabolism | Trans-Activators - chemistry | Gene Knockdown Techniques | Caenorhabditis elegans - physiology | Calcineurin Inhibitors | HEK293 Cells | Trans-Activators - genetics | Transcription, Genetic | Protein-Serine-Threonine Kinases - metabolism | Cyclic AMP Response Element-Binding Protein - biosynthesis | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Down-Regulation | Transcription Factors - biosynthesis | Longevity - genetics | Transcription Factors - metabolism | Animals | Trans-Activators - deficiency | Aging - physiology | Energy Metabolism | Cyclic AMP Response Element-Binding Protein - metabolism | Trans-Activators - metabolism | Enzyme Activation | Caenorhabditis elegans Proteins - genetics | Longevity - physiology | Caenorhabditis elegans - enzymology | Calcineurin - metabolism | Aging - metabolism | Caenorhabditis elegans Proteins - biosynthesis | Physiological aspects | Chemical properties | Protein kinases | Calcineurin | Proteins | Homeostasis | Mutation | Kinases | DNA repair | Metabolic disorders | Binding sites
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 12, p. e52493
Numerous studies have shown that resistance to oxidative stress is crucial to stay healthy and to reduce the adverse effects of aging. Accordingly, nutritional... 
BIFIDOBACTERIUM-LONGUM | AGING PROCESS | LONGEVITY | INFLAMMATORY-BOWEL-DISEASE | PROBE LEVEL | MULTIDISCIPLINARY SCIENCES | LACTIC-ACID BACTERIA | RECEPTOR NHR-49 | INDUCED COLITIS | C.-ELEGANS | FREE-RADICALS | Caenorhabditis elegans - microbiology | Reactive Oxygen Species - metabolism | Species Specificity | Humans | Caenorhabditis elegans Proteins - metabolism | Gene Expression Profiling | Caenorhabditis elegans - physiology | Trinitrobenzenesulfonic Acid - adverse effects | Inflammation - metabolism | Colitis - chemically induced | Female | Inflammation - microbiology | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Longevity | Probiotics - pharmacology | HT29 Cells | Transcription Factors - metabolism | Insulin - metabolism | Animals | Colitis - microbiology | Signal Transduction - drug effects | Colitis - metabolism | Receptor, Insulin - metabolism | Lactobacillus - physiology | Mice | Oxidative Stress - drug effects | Forkhead Transcription Factors | Antioxidants | Oxidative stress | Caenorhabditis elegans | Anti-inflammatory drugs | Bacteria | Research | Nematoda | Food | Slopes | Salmonella | Cell culture | Biotechnology | Lactic acid bacteria | Animal models | Hydrogen peroxide | Disease | Biology | Lipopolysaccharides | Oxidation resistance | Rodents | Quality | Older people | Aging | Strains (organisms) | Worms | Cytokines | Food production | Inflammation | Metabolism | Insulin | Fatty acids | Quality of life | Probiotics | Screening | Life span | Insects | Nematodes | Lactic acid | Colitis | Diabetes | Laboratory animals | Viability | Geriatrics | Caenorhabditis elegans Proteins | Reactive Oxygen Species | Oxidative Stress | Signal Transduction | Trinitrobenzenesulfonic Acid | Life Sciences | Receptor, Insulin | Transcription Factors | Lactobacillus
Journal Article
PLoS pathogens, ISSN 1553-7374, 2014, Volume 10, Issue 6, p. e1004200
Microsporidia comprise a phylum of over 1400 species of obligate intracellular pathogens that can infect almost all animals, but little is known about the host... 
TRIGGERED IMMUNITY | IMMUNE-RESPONSE | LIFE-SPAN | MICROBIOLOGY | CELL-PROLIFERATION | LARGE GENE LISTS | TRANSLATIONAL INHIBITION | CAENORHABDITIS-ELEGANS | VIROLOGY | INTRACELLULAR BACTERIA | TRANSCRIPTION FACTOR | PARASITOLOGY | INNATE IMMUNITY | Caenorhabditis elegans Proteins - immunology | SKP Cullin F-Box Protein Ligases - genetics | Ubiquitin - metabolism | Caenorhabditis elegans Proteins - metabolism | Microsporidia - immunology | Autophagy - immunology | RNA Interference | Base Sequence | Caenorhabditis elegans - parasitology | Autophagy - genetics | Caenorhabditis elegans - virology | SKP Cullin F-Box Protein Ligases - metabolism | SKP Cullin F-Box Protein Ligases - antagonists & inhibitors | Caenorhabditis elegans - immunology | Microsporidia - pathogenicity | Host-Pathogen Interactions | Animals | Sequence Analysis, RNA | Caenorhabditis elegans Proteins - antagonists & inhibitors | RNA, Small Interfering | Cullin Proteins - immunology | Transcription, Genetic - genetics | Caenorhabditis elegans Proteins - genetics | Ubiquitination - genetics | Caenorhabditis elegans Proteins - biosynthesis | Cullin Proteins - biosynthesis | Ubiquitin | Distribution | Genetic aspects | Research | Gene expression | Health aspects | Microsporidia | Medical research | Nematodes | Infections | Experiments | Autophagy | Viral infections | Worms
Journal Article
Nature (London), ISSN 1476-4687, 2012, Volume 489, Issue 7415, pp. 263 - 268
Journal Article
The Journal of cell biology, ISSN 1540-8140, 2006, Volume 173, Issue 6, pp. 949 - 961
Polarized intracellular trafficking in epithelia is critical in development, immunity, and physiology to deliver morphogens, defensins, or ion pumps to the... 
Larvae | Phenotypes | Secretion | Epithelial cells | Animal cuticle | Canals | Epidermis | Cell membranes | Exosomes | Genetic mutation | MDCK CELLS | RECYCLING ENDOSOMES | STEROL-SENSING DOMAIN | TRANS-GOLGI-NETWORK | YEAST V-ATPASE | C-ELEGANS | EXTRACELLULAR-MATRIX | ANCHORED PROTEINS | POLARIZED EPITHELIAL-CELLS | PLASMA-MEMBRANE | CELL BIOLOGY | Protein Structure, Tertiary | Amino Acid Sequence | Vacuolar Proton-Translocating ATPases - genetics | Mutagenesis, Site-Directed | Caenorhabditis elegans - growth & development | Secretory Vesicles - ultrastructure | Caenorhabditis elegans Proteins - chemistry | Caenorhabditis elegans Proteins - metabolism | Molecular Sequence Data | Protein Transport - physiology | Hedgehog Proteins | Phenotype | Sequence Alignment | Animals | Caenorhabditis elegans - cytology | Models, Biological | Vacuolar Proton-Translocating ATPases - chemistry | Vacuolar Proton-Translocating ATPases - physiology | Secretory Vesicles - physiology | Trans-Activators - metabolism | Caenorhabditis elegans Proteins - physiology | Caenorhabditis elegans Proteins - genetics | Caenorhabditis elegans - enzymology | Physiological aspects | Caenorhabditis elegans | Research | Adenosine triphosphatase | Caenorhabditis elegans Proteins | Trans-Activators | Biochemistry, Molecular Biology | Secretory Vesicles | Protein Transport | Life Sciences | Molecular biology | Vacuolar Proton-Translocating ATPases
Journal Article
Nature, ISSN 0028-0836, 09/2011, Volume 477, Issue 7365, pp. 482 - 485
Journal Article
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Journal Article