Plant-pathogen arms races at the molecular level.

[1]  J G Bishop,et al.  Rapid evolution in plant chitinases: molecular targets of selection in plant-pathogen coevolution. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[2]  J. Labavitch,et al.  Identification of target amino acids that affect interactions of fungal polygalacturonases and their plant inhibitors , 2000 .

[3]  A. Verkleij,et al.  The cell wall architecture of Candida albicans wild‐type cells and cell wall‐defective mutants , 2000, Molecular microbiology.

[4]  B. Staskawicz,et al.  Expression of the Bs2 pepper gene confers resistance to bacterial spot disease in tomato. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[5]  E. A. van der Biezen,et al.  Pronounced Intraspecific Haplotype Divergence at the RPP5 Complex Disease Resistance Locus of Arabidopsis , 1999, Plant Cell.

[6]  D. Gabriel.  COMMENTARY Why do pathogens carry avirulence genes , 1999 .

[7]  E. Stahl,et al.  Dynamics of disease resistance polymorphism at the Rpm1 locus of Arabidopsis , 1999, Nature.

[8]  E. Nevo,et al.  Molecular diversity at the major cluster of disease resistance genes in cultivated and wild Lactuca spp. , 1999, Theoretical and Applied Genetics.

[9]  J. Delcour,et al.  Triticum aestivum xylanase inhibitor (TAXI), a new class of enzyme inhibitor affecting breadmaking performance , 1999 .

[10]  E. Brodie,et al.  Predator-Prey Arms Races Asymmetrical selection on predators and prey may be reduced when prey are dangerous , 1999 .

[11]  Jonathan D. G. Jones,et al.  Recombination between diverged clusters of the tomato Cf-9 plant disease resistance gene family. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[12]  A. Hemmings,et al.  The specificity of polygalacturonase‐inhibiting protein (PGIP): a single amino acid substitution in the solvent‐exposed β‐strand/β‐turn region of the leucine‐rich repeats (LRRs) confers a new recognition capability , 1999, The EMBO journal.

[13]  T. Boller,et al.  Plants have a sensitive perception system for the most conserved domain of bacterial flagellin. , 1999, The Plant journal : for cell and molecular biology.

[14]  T. Boller,et al.  A single locus determines sensitivity to bacterial flagellin in Arabidopsis thaliana. , 1999, The Plant journal : for cell and molecular biology.

[15]  J. Thompson,et al.  Specific Hypotheses on the Geographic Mosaic of Coevolution , 1999, The American Naturalist.

[16]  A. Henk,et al.  A new Ac-like transposon of Arabidopsis is associated with a deletion of the RPS5 disease resistance gene. , 1999, Genetics.

[17]  J. Luck,et al.  Identification of Regions in Alleles of the Flax Rust Resistance Gene L That Determine Differences in Gene-for-Gene Specificity , 1999, Plant Cell.

[18]  G. Williamson,et al.  A novel class of protein from wheat which inhibits xylanases. , 1999, The Biochemical journal.

[19]  P. Kareiva.  Coevolutionary arms races: is victory possible? , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[20]  B. Kunkel,et al.  Diversity and molecular evolution of the RPS2 resistance gene in Arabidopsis thaliana. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[21]  P. De Wit,et al.  THE TOMATO-CLADOSPORIUM FULVUM INTERACTION: A Versatile Experimental System to Study Plant-Pathogen Interactions. , 1999, Annual review of phytopathology.

[22]  B C Meyers,et al.  Plant disease resistance genes encode members of an ancient and diverse protein family within the nucleotide-binding superfamily. , 1999, The Plant journal : for cell and molecular biology.

[23]  M. Grant,et al.  Independent deletions of a pathogen-resistance gene in Brassica and Arabidopsis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[24]  E. Kondorosi,et al.  Plant chitinase/lysozyme isoforms show distinct substrate specificity and cleavage site preference towards lipochitooligosaccharide Nod signals , 1998 .

[25]  B C Meyers,et al.  Clusters of resistance genes in plants evolve by divergent selection and a birth-and-death process. , 1998, Genome research.

[26]  David A. Jones,et al.  The Tomato Cf-5 Disease Resistance Gene and Six Homologs Show Pronounced Allelic Variation in Leucine-Rich Repeat Copy Number , 1998, Plant Cell.

[27]  P. Rohani,et al.  Receptor-like Genes in the Major Resistance Locus of Lettuce Are Subject to Divergent Selection , 1998, Plant Cell.

[28]  S. Goff,et al.  Intragenic Recombination and Diversifying Selection Contribute to the Evolution of Downy Mildew Resistance at the RPP8 Locus of Arabidopsis , 1998, Plant Cell.

[29]  R. Michelmore,et al.  The Major Resistance Gene Cluster in Lettuce Is Highly Duplicated and Spans Several Megabases , 1998, Plant Cell.

[30]  Jonathan D. G. Jones,et al.  Three Genes of the Arabidopsis RPP1 Complex Resistance Locus Recognize Distinct Peronospora parasitica Avirulence Determinants , 1998, Plant Cell.

[31]  J. Bodeau,et al.  The Root Knot Nematode Resistance Gene Mi from Tomato Is a Member of the Leucine Zipper, Nucleotide Binding, Leucine-Rich Repeat Family of Plant Genes , 1998, Plant Cell.

[32]  P. Goodwin,et al.  Successful search for a resistance gene in tomato targeted against a virulence factor of a fungal pathogen. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Shiping Zhang,et al.  Xa21D Encodes a Receptor-like Molecule with a Leucine-Rich Repeat Domain That Determines Race-Specific Recognition and Is Subject to Adaptive Evolution , 1998, Plant Cell.

[34]  W. Goddard,et al.  The role of enzyme distortion in the single displacement mechanism of family 19 chitinases. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[35]  M. Hahn,et al.  Oligosaccharide Elicitors in Host-Pathogen Interactions , 1998 .

[36]  A. Stintzi,et al.  Substrate specificities of tobacco chitinases. , 1998, The Plant journal : for cell and molecular biology.

[37]  M. Hahn,et al.  Oligosaccharide elicitors in host-pathogen interactions. Generation, perception, and signal transduction. , 1998, Sub-cellular biochemistry.

[38]  Jonathan D. G. Jones,et al.  Novel Disease Resistance Specificities Result from Sequence Exchange between Tandemly Repeated Genes at the Cf-4/9 Locus of Tomato , 1997, Cell.

[39]  A. Vivian,et al.  Avirulence genes in plant-pathogenic bacteria: signals or weapons? , 1997, Microbiology.

[40]  P. Albersheim,et al.  Fungal pathogens secrete an inhibitor protein that distinguishes isoforms of plant pathogenesis-related endo-β-1,3-glucanases , 1997 .

[41]  Jonathan D. G. Jones,et al.  The Role of Leucine-Rich Repeat Proteins in Plant Defences , 1997 .

[42]  R. Leah,et al.  Enhanced quantitative resistance against fungal disease by combinatorial expression of different barley antifungal proteins in transgenic tobacco. , 1995, The Plant journal : for cell and molecular biology.

[43]  J. Dangl,et al.  The avrRpm1 gene of Pseudomonas syringae pv. maculicola is required for virulence on Arabidopsis. , 1995, Molecular plant-microbe interactions : MPMI.

[44]  J. Mikkelsen,et al.  Plant chitinases. , 2008, The Plant journal : for cell and molecular biology.

[45]  M. Sela-Buurlage,et al.  Only Specific Tobacco (Nicotiana tabacum) Chitinases and [beta]-1,3-Glucanases Exhibit Antifungal Activity , 1993, Plant physiology.

[46]  W. Bugbee.  A pectin lyase inhibitor protein from cell walls of sugar beet , 1993 .

[47]  J. Krebs,et al.  Arms races between and within species , 1979, Proceedings of the Royal Society of London. Series B. Biological Sciences.