References
- Proc Natl Acad Sci USA v.95 Different requirements for the EDS1 and NDR1 by disease resistance genes define at least two R gene-mediated signaling pathways in Arabidopsis Aarts N;Metz M;Holub E;Staskawicz BJ;Daniels MJ;Parker JE
- Proc Natl Acad Sci U S A v.95 Defense activation and enhanced pathogen tolerance induced by H202 in transgenic tobacco Chamnongpol S;Willekens H;Moeder W;Langebartels C;Sandermann H Jr;Van Montagu M;Inze D;Van Camp W https://doi.org/10.1073/pnas.95.10.5818
- Mol Plant Microbe Interact v.13 The Pseudomonas syringae avrRpt2 gene product promotes pathogen virulence from inside plant cells Chen Z;Kloek AP;Boch J;Katagiri F;Krnkel BN https://doi.org/10.1094/MPMI.2000.13.12.1312
- Proc Natl Acad Sci U S A 2001 v.98 Signal interactions between nitric oxide and reactive oxygen intermediates in the plant hypersensitive disease resistance response Delledonne M;Zeier J;Marocco A;Lamb C https://doi.org/10.1073/pnas.231178298
- Proc Natl Acad Sci USA v.98 Abrogation of disease development in plants expressing animal antiapoptotic genes Dickman MB;Par YK;Oltersdorf T;Li W;Clement T;French R https://doi.org/10.1073/pnas.091108998
- Physiol Plant Pathol v.23 Involvement of superoxide anion generation in the hypersensitive response of potato-tuber tissues to infection with an incompatible race of Phytophthora infestans and to the hyphal wall components Doke N https://doi.org/10.1016/0048-4059(83)90019-X
- Plant Physiology v.109 An Arabidopsis thaliana thionin gene is inducible via a signal transduction pathway different from that for pathogenesis-rilated proteins Epple P;Apel K;Bohlmann H https://doi.org/10.1104/pp.109.3.813
- Mol Cell v.5 FLS2: An LRR receptor kinase involved in the perception of bacterial flagellin in Arabidopsis Gomez-Gomez L.;Boller T https://doi.org/10.1016/S1097-2765(00)80265-8
- Curr Biol v.10 The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea Govrin EM;Levine A https://doi.org/10.1016/S0960-9822(00)00560-1
- Plant Physiol v.124 Role of reactive oxygen intermediates and cognate redox signaling in disease resistance Grant JJ;Loake GJ https://doi.org/10.1104/pp.124.1.21
- Plant Journal v.24 Oxidative burst and cognate redox signalling reported by luciferase imaging:Identification of a signal network that functions independently of ethylene, SA and Me-JA but is dependent on MAPKK activity Grant JJ;Yun BW;Loake GJ https://doi.org/10.1046/j.1365-313x.2000.00902.x
- Annu Rev Plant Physiol Plant Mol Biol v.48 Programmed cell death in plant: pathogen interactions Greenberg JT https://doi.org/10.1146/annurev.arplant.48.1.525
- J Immunol v.165 Contribution of cyclopentenone prostaglandins to the resolution of inflammation through the potentiation of apoptosis in activated macrophages Hortelano S;Castrillo A;Alvarez AM;Bosca L https://doi.org/10.1146/annurev.arplant.48.1.525
- Plant Cell v.12 Evidence for a role of the N terminus and leucine-rich repeat region of the Mi gene product in regulation of localised cell death Hwang CF;Bhakta AV;Truesdell GM;Pudlo WM;Williamson VM https://doi.org/10.1105/tpc.12.8.1319
- J Biol Chem v.276 Human Nod1 confers responsiveness to lipopolysaccharides Inohara N;Ogura Y;Chen F;Nunez G https://doi.org/10.1074/jbc.M009728200
- Plant Cell 2001 v.13 The DEFECTIVE IN ANTHER DEHISCIENCE gene encodes a novel phospholipase A1 catalyzing the initial step of jasmonic acid biosynthesis, which synchronizes pollen maturation, anther dehiscence, and flower opening in Arabidopsis Ishiguro S;Kawai-Oda A;Ueda J;Nishida I;Okada K https://doi.org/10.1105/tpc.13.10.2191
- Science v.273 Initiation of runnaway cell death in an Arabidodpis mutant by extracellular superoxide Jabs T;Dietrich RA;Dangl JL https://doi.org/10.1126/science.273.5283.1853
- Curr Opin Plant Biol v.4 Putting knowledge of plant disease resistance genes to work Jones J https://doi.org/10.1016/S1369-5266(00)00174-6
- J Mol Biol v.277 Structural diversity of leucine-rich repeat proteins Kajava AV https://doi.org/10.1006/jmbi.1998.1643
- Nature v.346 Widespread distribution and fitness contribution of Xanthomonas campestris avirulence gene avrBs2 Kearney B;Staskawicz BJ https://doi.org/10.1038/346385a0
- Plant Cell v.11 Pathogen-induced elicitin production in transgenic tobacco generates a hypersensitive response and nonspecific disease resistance Keller H;Pamboukdjian N;Ponchet M;Poupet A;Delon R;Verrier JL;Roby D;Ricci P https://doi.org/10.1105/tpc.11.2.223
- Molecular Plant-Microbe Interactions v.12 Systemic resistance in Arabidopsis induced by rhizo bacteria requires ethylene-dependent signaling at the site of application Knoester M;Pieterse CMJ;Bol JF;Van Loon LC https://doi.org/10.1094/MPMI.1999.12.8.720
- Curr Biol v.6 Calcium-mediated apoptosis in plant hypersensitive disease resistance response Levine A;Pennell RI;Alvarez ME;Palmer R;Lamb C https://doi.org/10.1016/S0960-9822(02)00510-9
- Current Biology v.11 Plant cell death: Unmasking the gatekeepers Loake GJ https://doi.org/10.1016/S0960-9822(01)00262-7
- Encyclopedia of applied plant science Role of jasmonates in plant development and defence Loake GJ;Thomas B(ed.);Murphy D(ed.);Murray B(ed.)
- Science v.262 Map-based cloning of a protein kinase gene conferring disease resistance in tomato Martin GB;Brommonschenkel SH;Chunwongse J;Frary A;Ganal MW;Spivey R;Wu T;Earle ED;Tanksley SD https://doi.org/10.1126/science.7902614
- Molecular Plant-Microbe Interactions v.13 Interacting signal pathways control defense gene expression in Arabidopsis in response to cell wall-degrading enzymes from Erwinia carotovora Norman-Setterblad C;Vidal S;Palva ET https://doi.org/10.1094/MPMI.2000.13.4.430
- Plant Cell v.8 Pathogen-induced systemic activation of a plant defensin gene in Arabidopsis follows a salicylic acid-independent pathway Penninckx I;Eggermont K;Terras FRG;Thomma B;DeSamblanx GW;Buchala A;Metraux JP;Manners JM;Broekaert WF https://doi.org/10.1105/tpc.8.12.2309
- Plant Cell v.10 Concomitant activation of jasmonate and ethylene response pathways is required for induction of a plant defensin gene in Arabidopsis Penninckx I;Thomma B;Buchala A;Metraux JP;Broekaert WF https://doi.org/10.1105/tpc.10.12.2103
- Plant Cell v.10 A novel signaling pathway controlling induced systemic resistance in Arabidopsis Pieterse CMJ;van Wees SCM;van Pelt JA;Knoester M;Laan R;Gerrits N;Weisbeek PJ;van Loon LC https://doi.org/10.1105/tpc.10.9.1571
- Eur J Biochem v.183 Structure and activity of proteins from pathogenic fungi Phytophthora eliciting necrosis and acquired resistance in tobacco Ricci P;Bonnet P;Huet JC;Sallantin M;Beauvais-Cante F;Bruneteau M;Billard V;Michel G;Pernollet JC https://doi.org/10.1111/j.1432-1033.1989.tb21084.x
- Plant Mol Biol v.47 The promoter of a basic PR1-like gene, AtPRB1, from Arabidopsis establishes an organ-specific expression pattern and responsiveness to ethylene and methy1 jasmonate Santamaria M;Thomson CJ;Read ND;Loake GJ https://doi.org/10.1023/A:1012410009930
- Proc Natl Acad Sci USA v.98 Jasmonic acid carboxyl methyltransferase: A key enzyme for jasmonate-regulated plant responses Seo HS;Song JT;Cheong JJ;Lee YH;Lee YW;Hwang I;Lee JS;Choi YD
- Plant Journal v.15 Jasmonate signaling mutants of Arabidopsis are susceptible to the soil fungus Pythium irregulare Staswick PE;Yuen GY;Lehman CC https://doi.org/10.1046/j.1365-313X.1998.00265.x
- Proc Natl Acad Sci USA v.95 Separate jasmonate-dependent and salicylate-dependent defense-response pathways in Arabidopsis are essential for resistance to distinct microbial pathogens Thomma B;Eggermont K;Penninckx I;Mauch-Mani B;Vogelsang R;Cammue BPA;Broekaert, WF
- Plant Physiology and Biochemistry v.38 Disease development of several fungi on Arabidopsis can be reduced by treatment with methyl jasmonate Thomma B;Eggermont K;Broekaert WF;Cammue BPA https://doi.org/10.1016/S0981-9428(00)00756-7
- Proc Natl Acad Sci USA v.97 Predicting durability of a disease resistance gene based on an assessment of the fitness loss and epidemiological consequences of avirulence gene mutation Vera Cruz CM;Bai J;Ona I;Leung H;Nelson RJ;Mew TW;Leach JE
- Plant Cell v.8 Apoptosis:a functional paradigm for programmed cell death induced by a host-selective phytotoxin and invoked during development Wang H;Li J;Bostock RM;Gilchrist DG https://doi.org/10.1105/tpc.8.3.375
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Plant Cell
v.7
Disease resistance conferred by expression of a gene encoding
$H_2O_2$ -generating glucose oxidase in transgenic potato plants Wu G;Shortt B;Lawrence EB;Levine EB;Fitzsimmons KC;Shah DM https://doi.org/10.1105/tpc.7.9.1357 - Science v.291 Broad-spectrum mildew resistance in Arabidopsis thaliana mediated by RPW8 Xiao S;Ellwood S;Calis O;Patrick E;Li T;Coleman M;Turner, JG https://doi.org/10.1126/science.291.5501.118
- Mol Plant Microbe Interact v.13 Identification of Arabidopsis mutants exhibiting an altered hypersensitive response in gene-for-gene disease resistance Yu I;Fengler KA;Clough SJ;Bent AF https://doi.org/10.1094/MPMI.2000.13.3.277
- Plant Cell v.13 Cell-autonomous expression of barley Mla1 confers race-specific resistance to the powdery mildew fungus via a Rar1-independent signaling pathway Zhou F;Kurth J;Wei F;Elliott C;Val G;Yahiaoui N;Keller B;Somerville S;Wise R;Schulze-Lefert P https://doi.org/10.1105/tpc.13.2.337
- Nature v.406 Genetic diversity and disease control in rice Zhu Y;Chen H;Fan J;Wang Y;Li Y;Chen J;Fan J;Yang S;Hu L;Leung H;Mew TW;Teng PS;Wang Z;Mundt CC https://doi.org/10.1038/35021046