Understanding the functions of plant disease resistance proteins.
By G. Martin, Adam J. Bogdanove, G. Sessa. Annual Review of Plant Biology, 2003
977 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/d13ae39cb145330cbac51cc097571efa4e7d6981
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In Plant Science
- Xiangzong Meng
- Zuyu Zheng
- Shuqun Zhang
- Yidong Liu
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Citations in the corpus
- Caipirini: using gene sets to rank literature (2012, background): “The criteria used included explicit mention of either disease-resistance proteins [28], of signaling hormones or other chemicals involved in disease resistance processes [29], or of processes or pathways involved in the hypersensitive response in plants [30].”
- RNA virus interference via CRISPR/Cas13a system in plants (2017, background): “In addition, introduction of plant antiviral genes, such as R genes, into crop plants has gained prominence as an effective approach to engineer transgenic plants resistant to virus infection [23-26].”
- Genetics and breeding for clubroot resistance in Canadian spring canola (Brassica napus L.) (2014, background): “The Toll/interleukin-1 receptor (TIR)- nucleotide binding site (NBS)–Leucine-rich repeat (NBS-LRR) class is the largest among the five wellcharacterized classes of R genes (Pto; TIR-NBS-LRR; Coiled-Coil-NBS-NRR; Cf; Xa21 (Martin et al. 2003; Bernoux et al. 2011).”
- Phosphorylation of a WRKY Transcription Factor by Two Pathogen-Responsive MAPKs Drives Phytoalexin Biosynthesis in Arabidopsis[C][W] (2011, background): “Plant recognition of pathogen-associated molecular patterns (PAMPs) or pathogen-derived effector proteins triggers massive changes in gene expression, cellular metabolism, and eventually induced resistance (Staskawicz et al., 1995; Dangl and Jones, 2001; Nürnberger and Scheel, 2001; Martin et al., 2”
- The molecular bases of plant resistance and defense responses to aphid feeding: current status (2007, background): “2 is a member of the nucleotide-binding site and leucine-rich region (NBS-LRR) Class II family of disease and nematode resistance genes (Rossi et al., 1998; Martin et al., 2003).”
- A Novel Role for the TIR Domain in Association with Pathogen-Derived Elicitors (2007, background): “One possibility is that detection has been technically challenging, presumably because R proteins are present at relatively low levels in plant cells [25].”
- Proteinaceous necrotrophic effectors in fungal virulence (2010, background): “Paradoxically, these domains are common features of plant disease R genes involved in defence against biotrophic pathogens (Martin et al. 2003).”
- Type III secretion system effector proteins: double agents in bacterial disease and plant defense. (2004, background): “This phenomenon has been the focus of most research on TTSS effectors, as recently reviewed (109, 115).”
- The hypersensitive response; the centenary is upon us but how much do we know? (2008, background): “Subsequently , a large number of R genes have been cloned and can be broadly classified into five classes (Martin et al., 2003).”
- The Receptor for the Fungal Elicitor Ethylene-Inducing Xylanase Is a Member of a Resistance-Like Gene Family in Tomato (2004, background): “These R-genes are effective against bacterial, viral, nematode, and fungal pathogens (Jones et al., 1994;Bent, 1996; Baker et al., 1997; Martin et al., 2003).”