| The G protein-coupled receptor FSHR-1 is required for the Caenorhabditis elegans innate immune response. Powell J.R., Kim D.H., Ausubel F.M.
Proc. Natl. Acad. Sci. U.S.A. 106:2782-2787(2009) · Mapped (1) |
| Temporal global expression data reveal known and novel salicylate-impacted processes and regulators mediating powdery mildew growth and reproduction on Arabidopsis. Chandran D., Tai Y.C., Hather G., Dewdney J., Denoux C., Burgess D.G., Ausubel F.M., Speed T.P., Wildermuth M.C.
Plant Physiol. 149:1435-1451(2009) · Mapped (4) |
| Glucosinolate metabolites required for an Arabidopsis innate immune response. Clay N.K., Adio A.M., Denoux C., Jander G., Ausubel F.M.
Science 323:95-101(2009) · UniProtKB (1) · Mapped (15) |
| Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans. Troemel E.R., Felix M.A., Whiteman N.K., Barriere A., Ausubel F.M.
PLoS Biol. 6:2736-2752(2008) · Mapped (5) |
| Role for beta-catenin and HOX transcription factors in Caenorhabditis elegans and mammalian host epithelial-pathogen interactions. Irazoqui J.E., Ng A., Xavier R.J., Ausubel F.M.
Proc. Natl. Acad. Sci. U.S.A. 105:17469-17474(2008) · Mapped (30) |
| The AtrbohD-mediated oxidative burst elicited by oligogalacturonides in Arabidopsis is dispensable for the activation of defense responses effective against Botrytis cinerea. Galletti R., Denoux C., Gambetta S., Dewdney J., Ausubel F.M., De Lorenzo G., Ferrari S.
Plant Physiol. 148:1695-1706(2008) · Mapped (3) |
| DAF-16-dependent suppression of immunity during reproduction in Caenorhabditis elegans. Miyata S., Begun J., Troemel E.R., Ausubel F.M.
Genetics 178:903-918(2008) · UniProtKB (1) · Mapped (13) |
| Staphylococcal biofilm exopolysaccharide protects against Caenorhabditis elegans immune defenses. Begun J., Gaiani J.M., Rohde H., Mack D., Calderwood S.B., Ausubel F.M., Sifri C.D.
PLoS Pathog. 3:e57-e57(2007) · Mapped (7) |
| Resistance to Botrytis cinerea induced in Arabidopsis by elicitors is independent of salicylic acid, ethylene, or jasmonate signaling but requires PHYTOALEXIN DEFICIENT3. Ferrari S., Galletti R., Denoux C., De Lorenzo G., Ausubel F.M., Dewdney J.
Plant Physiol. 144:367-379(2007) · Mapped (18) |
| Antifungal chemical compounds identified using a C. elegans pathogenicity assay. Breger J., Fuchs B.B., Aperis G., Moy T.I., Ausubel F.M., Mylonakis E.
PLoS Pathog. 3:e18-e18(2007) · Mapped (1) |
| p38 MAPK regulates expression of immune response genes and contributes to longevity in C. elegans. Troemel E.R., Chu S.W., Reinke V., Lee S.S., Ausubel F.M., Kim D.H.
PLoS Genet. 2:E183-E183(2006) · UniProtKB (1) · Mapped (52) |
| Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial. Lee D.G., Urbach J.M., Wu G., Liberati N.T., Feinbaum R.L., Miyata S., Diggins L.T., He J., Saucier M., Deziel E. et al.
Genome Biol. 7:R90.1-R90.14(2006) · UniProtKB (5,886) |
| Peroxidase-dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistance. Bindschedler L.V., Dewdney J., Blee K.A., Stone J.M., Asai T., Plotnikov J., Denoux C., Hayes T., Gerrish C., Davies D.R. et al.
Plant J. 47:851-863(2006) · Mapped (5) |
| RESISTANCE TO FUSARIUM OXYSPORUM 1, a dominant Arabidopsis disease-resistance gene, is not race specific. Diener A.C., Ausubel F.M.
Genetics 171:305-321(2005) · UniProtKB (1) · Mapped (5) |
| A high-throughput, near-saturating screen for type III effector genes from Pseudomonas syringae. Chang J.H., Urbach J.M., Law T.F., Arnold L.W., Hu A., Gombar S., Grant S.R., Ausubel F.M., Dangl J.L.
Proc. Natl. Acad. Sci. U.S.A. 102:2549-2554(2005) · UniProtKB (6) · Mapped (1) |
| Staphylococcus aureus virulence factors identified by using a high-throughput Caenorhabditis elegans-killing model. Begun J., Sifri C.D., Goldman S., Calderwood S.B., Ausubel F.M.
Infect. Immun. 73:872-877(2005) · UniProtKB (2) |
| Cytotoxicity of hydrogen peroxide produced by Enterococcus faecium. Moy T.I., Mylonakis E., Calderwood S.B., Ausubel F.M.
Infect. Immun. 72:4512-4520(2004) · UniProtKB (3) · Mapped (2) |
| Integration of Caenorhabditis elegans MAPK pathways mediating immunity and stress resistance by MEK-1 MAPK kinase and VHP-1 MAPK phosphatase. Kim D.H., Liberati N.T., Mizuno T., Inoue H., Hisamoto N., Matsumoto K., Ausubel F.M.
Proc. Natl. Acad. Sci. U.S.A. 101:10990-10994(2004) · Mapped (8) |
| Caenorhabditis elegans-based screen identifies Salmonella virulence factors required for conserved host-pathogen interactions. Tenor J.L., McCormick B.A., Ausubel F.M., Aballay A.
Curr. Biol. 14:1018-1024(2004) · Mapped (3) |
| Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response. Liberati N.T., Fitzgerald K.A., Kim D.H., Feinbaum R., Golenbock D.T., Ausubel F.M.
Proc. Natl. Acad. Sci. U.S.A. 101:6593-6598(2004) · UniProtKB (2) · Mapped (3) |
| The Caenorhabditis elegans MAPK phosphatase VHP-1 mediates a novel JNK-like signaling pathway in stress response. Mizuno T., Hisamoto N., Terada T., Kondo T., Adachi M., Nishida E., Kim D.H., Ausubel F.M., Matsumoto K.
EMBO J. 23:2226-2234(2004) · UniProtKB (1) · Mapped (8) |
| Arabidopsis local resistance to Botrytis cinerea involves salicylic acid and camalexin and requires EDS4 and PAD2, but not SID2, EDS5 or PAD4. Ferrari S., Plotnikova J.M., De Lorenzo G., Ausubel F.M.
Plant J. 35:193-205(2003) · UniProtKB (1) · Mapped (6) |
| Long-lived C. elegans daf-2 mutants are resistant to bacterial pathogens. Garsin D.A., Villanueva J.M., Begun J., Kim D.H., Sifri C.D., Calderwood S.B., Ruvkun G., Ausubel F.M.
Science 300:1921-1921(2003) · Mapped (3) |
| Caenorhabditis elegans as a model host for Staphylococcus aureus pathogenesis. Sifri C.D., Begun J., Ausubel F.M., Calderwood S.B.
Infect. Immun. 71:2208-2217(2003) · Mapped (2) |
| Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis. Alonso J.M., Stepanova A.N., Solano R., Wisman E., Ferrari S., Ausubel F.M., Ecker J.R.
Proc. Natl. Acad. Sci. U.S.A. 100:2992-2997(2003) · UniProtKB (3) · Mapped (5) |
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