Found: 29
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Pathogenicity of enterotoxigenic Escherichia coli in Caenorhabditis elegans as an alternative model host.
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- Bioscience, Biotechnology & Biochemistry, 2024, v. 88, n. 4, p. 453, doi. 10.1093/bbb/zbad185
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Avoidance behavior and experience-dependent tolerance in response to bitter compounds in Caenorhabditis elegans.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 3, p. 314, doi. 10.1093/bbb/zbac200
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- Article
The defense response of Caenorhabditis elegans to Cutibacterium acnes SK137 via the TIR-1-p38 MAPK signaling pathway.
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- Bioscience, Biotechnology & Biochemistry, 2022, v. 86, n. 3, p. 374, doi. 10.1093/bbb/zbab218
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Caenorhabditis elegans homologue of Prox1/Prospero is expressed in the glia and is required for sensory behavior and cold tolerance.
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- Genes to Cells, 2016, v. 21, n. 9, p. 936, doi. 10.1111/gtc.12394
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Depletion of mboa-7, an enzyme that incorporates polyunsaturated fatty acids into phosphatidylinositol ( PI), impairs PI 3-phosphate signaling in Caenorhabditis elegans.
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- Genes to Cells, 2012, v. 17, n. 9, p. 748, doi. 10.1111/j.1365-2443.2012.01624.x
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Improvement of Locomotion Caused by Lactococcus lactis subsp. lactis in the Model Organism Caenorhabditis elegans.
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- Nutrients, 2023, v. 15, n. 20, p. 4482, doi. 10.3390/nu15204482
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Clostridium butyricum MIYAIRI 588 Increases the Lifespan and Multiple-Stress Resistance of Caenorhabditis elegans.
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- Nutrients, 2018, v. 10, n. 12, p. 1921, doi. 10.3390/nu10121921
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Imbalanced Expression of Tau and Tubulin Induces Neuronal Dysfunction in <italic>C. elegans</italic> Models of Tauopathy.
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- Frontiers in Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnins.2018.00415
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Single/low-copy integration of transgenes in Caenorhabditis elegans using an ultraviolet trimethylpsoralen method.
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- BMC Biotechnology, 2012, v. 12, n. 1, p. 1, doi. 10.1186/1472-6750-12-1
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Impacts of Endocrine Disruptor di-n-Butyl Phthalate Ester on Microalga Chlorella vulgaris Verified by Approaches of Proteomics and Gene Ontology.
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- Molecules, 2020, v. 25, n. 18, p. 4304, doi. 10.3390/molecules25184304
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The small GTPase ARF-1.2 is a regulator of unicellular tube formation in Caenorhabditis elegans.
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- Journal of Physiological Sciences, 2019, v. 69, n. 1, p. 47, doi. 10.1007/s12576-018-0617-5
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Seroepidemiological survey on pigs and cattle for novel K88 (F4)-like colonisation factor detected in human enterotoxigenic Escherichia coli.
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- Epidemiology & Infection, 2022, v. 150, p. 1, doi. 10.1017/S0950268821002697
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The Tumor Suppressor BCL7B Functions in the Wnt Signaling Pathway.
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- PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004921
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Ceramide glucosyltransferase of the nematode Caenorhabditis elegans is involved in oocyte formation and in early embryonic cell division.
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- Glycobiology, 2011, v. 21, n. 6, p. 834, doi. 10.1093/glycob/cwr019
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- Article
Sesamin extends lifespan through pathways related to dietary restriction in <italic>Caenorhabditis elegans</italic>.
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- European Journal of Nutrition, 2018, v. 57, n. 3, p. 1137, doi. 10.1007/s00394-017-1396-0
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Impacts of Bacillus subtilis var. natto on the lifespan and stress resistance of Caenorhabditis elegans.
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- Journal of Applied Microbiology, 2023, v. 134, n. 4, p. 1, doi. 10.1093/jambio/lxad082
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Distinct roles of the two VPS33 proteins in the endolysosomal system in Caenorhabditis elegans.
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- Traffic, 2016, v. 17, n. 11, p. 1197, doi. 10.1111/tra.12430
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A Conditional Knockout Toolkit for Caenorhabditis elegans Based on the Cre/loxP Recombination.
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- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0114680
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The Homologous Carboxyl-Terminal Domains of Microtubule-Associated Protein 2 and TAU Induce Neuronal Dysfunction and Have Differential Fates in the Evolution of Neurofibrillary Tangles.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0089796
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NRFL-1, the C. elegans NHERF Orthologue, Interacts with Amino Acid Transporter 6 (AAT-6) for Age-Dependent Maintenance of AAT-6 on the Membrane.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043050
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Magnesium Excretion in C. elegans Requires the Activity of the GTL-2 TRPM Channel.
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- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009589
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Two Very Long Chain Fatty Acid Acyl-CoA Synthetase Genes, acs-20 and acs-22, Have Roles in the Cuticle Surface Barrier in Caenorhabditis elegans.
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- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008857
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The Roles and Acting Mechanism of Caenorhabditis elegans DNase II Genes in Apoptotic DNA Degradation and Development.
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- PLoS ONE, 2009, v. 4, n. 10, p. 1, doi. 10.1371/journal.pone.0007348
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Endomembrane-associated RSD-3 is important for RNAi induced by extracellular silencing RNA in both somatic and germ cells of Caenorhabditis elegans.
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- Scientific Reports, 2016, p. 28198, doi. 10.1038/srep28198
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Caenorhabditis elegans transthyretin-like protein TTR-52 mediates recognition of apoptotic cells by the CED-1 phagocyte receptor.
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- Nature Cell Biology, 2010, v. 12, n. 7, p. 655, doi. 10.1038/ncb2068
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Metolazone upregulates mitochondrial chaperones and extends lifespan in Caenorhabditis elegans.
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- Biogerontology, 2021, v. 22, n. 1, p. 119, doi. 10.1007/s10522-020-09907-6
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A trophic role for Wnt-Ror kinase signaling during developmental pruning in Caenorhabditis elegans.
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- Nature Neuroscience, 2009, v. 12, n. 8, p. 981, doi. 10.1038/nn.2347
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Influence of oral supplementation with sesamin on longevity of Caenorhabditis elegans and the host defense.
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- European Journal of Nutrition, 2014, v. 53, n. 8, p. 1659, doi. 10.1007/s00394-014-0671-6
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Mitochondria-type GPAT is required for mitochondrial fusion.
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- EMBO Journal, 2013, v. 32, n. 9, p. 1265, doi. 10.1038/emboj.2013.77
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