Nonhost resistance and nonspecific plant defenses.

By M. C. Heath. Current opinion in plant biology, 2000

628 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/2da9e43dbd2c8700f28ce569faa90c59b75b3909

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Citations in the corpus

Advances in Pectin and Pectinase Research (2003, background): “M. (1993) Structural models of prirnary cell walls in flowering plants: consistency of molecular structure with the physical properties of the walls during growth.”
Fungal Pathogens: The Battle for Plant Infection (2006, background): “Recognition of multiple signals derived from each pathogen may result in finer tuned response or may induce redundant recognition systems that act as independent back-up systems (Heath, 2000; Kamoun, 2001; Thordal-Christensen, 2003).”
Programmed cell death, mitochondria and the plant hypersensitive response (2001, background): “In plants, this phenomenon forms part of the hypersensitive response (HR) and its classification is based mainly on morphological criteria of the resultant cell-death lesions as well as the functional suppression of pathogen growt”
Resistance genes to Leptosphaeria maculans in Brassica napus (2006, background): “Briefly, these include the concept of host–pathogen specificity and the gene-for-gene hypothesis (Flor 1971), the boom-and-bust cycle of racespecific resistance and the effects of resistance on population biology of pathogens as pioneered by van der Plank (1963), the concepts of nonhost resistance (”
Plant Phenolics – Secondary Metabolites with Diverse Functions (2009, background): “Other defense genes encode these regulatory proteins, important for defense-signal transduction, and this form of induced defense response is referred to as systemic acquired resistance (SAR) (Lattanzio & Palmieri, 1994; Lattanzio et al., 1994; Heath, 2000; Huitema et al., 2003; Mysore & Ryu, 2004; ”
Coping with Stresses: Roles of Calcium- and Calcium/Calmodulin-Regulated Gene Expression[W][OA] (2011, background): “Heath, M.C. (2000). Nonhost resistance and nonspecific plant defenses.”
Coffee resistance to the main diseases: leaf rust and coffee berry disease (2006, background): “…(Grant and Mansfield 1999; Guest et al., 1999; Heath, 2000a, Dangl and Jones, 2001; Peck, 2003), involvement of plasma-membrane-bound NADPH oxidases, cell-wall-bound peroxidases, amino oxidases in the apoplast and phosphoproteins (Bestwick et al., 1997; Heath, 2000a, Laloi et al., 2004).”
Innate immunity in plants and animals: striking similarities and obvious differences (2004, background): “Infrequent changes in the host range of phytopathogens are indicative of the stability of species immunity (16).”
Arabidopsis PEN3/PDR8, an ATP Binding Cassette Transporter, Contributes to Nonhost Resistance to Inappropriate Pathogens That Enter by Direct Penetration[W][OA] (2006, result): “This is consistent with an early model of nonhost resistance in which it was proposed that this form of resistance consists of several barriers operating in parallel to limit pathogen colonization (Heath, 2000).”
Understanding the functions of plant disease resistance proteins. (2003, background): “Plants resist pathogen attacks both with preformed defenses such as antimicrobial secondary compounds and by inducing defense responses (72, 74).”