The complexity of disease signaling in Arabidopsis.
By Bart P. H. J. Thomma, I. Penninckx, W. Broekaert, B. P. Cammue. Current Opinion in Immunology, 2001
703 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/2ce4e23f8df245414d8a9dda44cb4fdc3290359c
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In Plant Science
- C. Pieterse
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- Saskia C. M. Van Wees
- Jonathan D. G. Jones
- M. Bolton
- Kemal Kazan
- R. Solano
Citations in the corpus
- Class III peroxidases in plant defence reactions. (2009, background): “, 2000), whereas the SA-dependent response is triggered by biotrophic pathogens (Thomma et al., 2001).”
- Cellular Response of Pea Plants to Cadmium Toxicity: Cross Talk between Reactive Oxygen Species, Nitric Oxide, and Calcium1[W][OA] (2009, background): “The up-regulation of genes involved in protein folding in response to Cd treatment has been observed in Arabidopsis plants (Suzuki et al., 2001), which demonstrates that Cd toxicity is in part due to the induction of protein denaturation, probably by oxidative modifications (Romero-Puertas et al., 2”
- Plant pathogenesis-related (PR) proteins: a focus on PR peptides. (2008, background): “Table 1 Main properties of classified families of PR proteins Family Type member Typical size (kDa) Properties Proposed microbial target Original reference PR-1 Tobacco PR-1a 15 Antifungal Unknown [3] PR-2 Tobacco PR-2 30 b-1,3-Glucanase b-1,3-Glucan [3] PR-3 Tobacco P, Q 25–30 Chitinase (class I,II”
- Abscisic Acid and Callose: Team Players in Defence Against Pathogens? (2005, background): “…parasitica and Erysiphe orontii or the hemibiotroph Pseudomonas syringae in Arabidopsis, the latter one is implicated when plants are challenged by necrotrophic organisms such as Botrytis cinerea, Alternaria brassicicola or Erwinia carotovora (Rojo et al., 1999; Thomma et al., 2001).”
- JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis (2004, background): “Thus, whereas it has often been shown that JA is necessary and sufficient for resistance to necrotrophic pathogens (Thomma et al., 2001; Turner et al., 2002; Farmer et al., 2003; Rojo et al., 2003), jin1 alleles exhibit a significant increase in their resistance to pathogens of this type, such as…”
- Antagonistic Interaction between Abscisic Acid and Jasmonate-Ethylene Signaling Pathways Modulates Defense Gene Expression and Disease Resistance in Arabidopsis (2004, background): “By contrast, the SA signaling pathway is believed to mediate the resistance to biotrophic pathogens, such as Erysiphe orontii, Peronospora parasitica, and Pseudomonas syringae (Thomma et al., 2001; Rojo et al., 2003).”