In: Journal of Chemical Ecology, 2005, vol. 31, no. 9, p. 1985-2002
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In: Euphytica, 2002, vol. 124, no. 2, p. 237-243
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In: Annals of Botany, 2006, vol. 97, no. 5, p. 779-784
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In: Journal Of Experimental Botany, 2015, vol. 66, no. 17, p. 5327-5336
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In: Annals of Botany, 2012, vol. 110, no. 7, p. 1423-1428
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In: Journal Of Experimental Botany, 2015, vol. 66, no. 9, p. 2527-2534
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In: Journal of Tropical Ecology, 2010, vol. 26, no. 5, p. 555-557
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In: The Plant Journal, 2011, vol. 68, no. 3, p. 507–519
Botrytis cinerea is a major pre- and post-harvest necrotrophic pathogen with a broad host range that causes substantial crop losses. The plant hormone jasmonic acid (JA) is involved in the basal resistance against this fungus. Despite basal resistance, virulent strains of B. cinerea can cause disease on Arabidopsis thaliana and virulent pathogens can interfere with the metabolism of the host in a...
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In: The Plant Journal, 2010, vol. 62, no. 5, p. 876 - 885
Plants activate direct and indirect defences in response to insect egg deposition. However, whether eggs can manipulate plant defence is unknown. In Arabidopsis thaliana, oviposition by the butterfly Pieris brassicae triggers cellular and molecular changes that are similar to the changes caused by biotrophic pathogens. In the present study, we found that the plant defence signal salicylic acid...
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In: Molecular Plant-Microbe Interactions, 2006, vol. 19, no. 10, p. 1062–1071
Infection of plants by necrotizing pathogens or colonization of plant roots with certain beneficial microbes causes the induction of a unique physiological state called “priming.” The primed state can also be induced by treatment of plants with various natural and synthetic compounds. Primed plants display either faster, stronger, or both activation of the various cellular defense responses...
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