| P50 | author | David Baulcombe | Q1173676 |
| | Clifford Harris | Q85372511 |
| | Erik J Slootweg | Q55364098 |
| P2093 | author name string | Aska Goverse | |
| P2860 | cites work | The rate and molecular spectrum of spontaneous mutations in Arabidopsis thaliana | Q24622979 |
| | Coiled-coil domain-dependent homodimerization of intracellular barley immune receptors defines a minimal functional module for triggering cell death | Q27666973 |
| | Structural and Functional Analysis of a Plant Resistance Protein TIR Domain Reveals Interfaces for Self-Association, Signaling, and Autoregulation | Q27667269 |
| | The plant immune system | Q28131801 |
| | Hypersensitive response-related death | Q28200993 |
| | STAND, a class of P-loop NTPases including animal and plant regulators of programmed cell death: multiple, complex domain architectures, unusual phyletic patterns, and evolution by horizontal gene transfer | Q28283391 |
| | Hybrid necrosis: autoimmunity as a potential gene-flow barrier in plant species | Q28296228 |
| | A novel role for the TIR domain in association with pathogen-derived elicitors | Q28469160 |
| | AAA+ proteins: have engine, will work | Q29617410 |
| | The domains of death: evolution of the apoptosis machinery | Q30658082 |
| | Genetic and molecular characterization of the I locus of Phaseolus vulgaris | Q33228331 |
| | An NB-LRR protein required for HR signalling mediated by both extra- and intracellular resistance proteins | Q79902387 |
| | A simple and general method for transferring genes into plants | Q80958729 |
| | Arms race co-evolution of Magnaporthe oryzae AVR-Pik and rice Pik genes driven by their physical interactions | Q84581021 |
| | Intragenic allele pyramiding combines different specificities of wheat Pm3 resistance alleles | Q84967003 |
| | Evolutionary dynamics of plant R-genes | Q33952866 |
| | Fitness costs of R-gene-mediated resistance in Arabidopsis thaliana. | Q34193742 |
| | Molecular determinants of resistance activation and suppression by Phytophthora infestans effector IPI-O | Q34205912 |
| | Transgenic resistance confers effective field level control of bacterial spot disease in tomato | Q34369233 |
| | Interfamily transfer of dual NB-LRR genes confers resistance to multiple pathogens | Q34598316 |
| | Artificial evolution extends the spectrum of viruses that are targeted by a disease-resistance gene from potato | Q35214812 |
| | Expanded functions for a family of plant intracellular immune receptors beyond specific recognition of pathogen effectors | Q35239735 |
| | Understanding the functions of plant disease resistance proteins | Q35540278 |
| | Indirect activation of a plant nucleotide binding site-leucine-rich repeat protein by a bacterial protease | Q35623244 |
| | Resistance proteins: molecular switches of plant defence. | Q36483748 |
| | STANDing strong, resistance proteins instigators of plant defence | Q37460302 |
| | Arabidopsis TTR1 causes LRR-dependent lethal systemic necrosis, rather than systemic acquired resistance, to Tobacco ringspot virus | Q37461385 |
| | NB-LRRs work a "bait and switch" on pathogens. | Q37589915 |
| | Improving immunity in crops: new tactics in an old game | Q37870498 |
| | A RanGAP protein physically interacts with the NB-LRR protein Rx, and is required for Rx-mediated viral resistance. | Q38299710 |
| | Interaction between domains of a plant NBS-LRR protein in disease resistance-related cell death. | Q39647973 |
| | Plant disease resistance genes encode members of an ancient and diverse protein family within the nucleotide-binding superfamily | Q41703915 |
| | Natural allelic variation underlying a major fitness trade-off in Arabidopsis thaliana. | Q41859184 |
| | Cell death mediated by the N-terminal domains of a unique and highly conserved class of NB-LRR protein. | Q42486906 |
| | Mutations in the NB-ARC domain of I-2 that impair ATP hydrolysis cause autoactivation. | Q42680832 |
| | RanGAP2 mediates nucleocytoplasmic partitioning of the NB-LRR immune receptor Rx in the Solanaceae, thereby dictating Rx function | Q42776038 |
| | Activation of an Arabidopsis resistance protein is specified by the in planta association of its leucine-rich repeat domain with the cognate oomycete effector | Q42986713 |
| | Structure-function analysis of the coiled-coil and leucine-rich repeat domains of the RPS5 disease resistance protein | Q43413036 |
| | Constitutive gain-of-function mutants in a nucleotide binding site-leucine rich repeat protein encoded at the Rx locus of potato | Q43792709 |
| | An EDS1 orthologue is required for N-mediated resistance against tobacco mosaic virus | Q43902978 |
| | The tomato R gene products I-2 and MI-1 are functional ATP binding proteins with ATPase activity. | Q44205952 |
| | Physical association of the NB-LRR resistance protein Rx with a Ran GTPase-activating protein is required for extreme resistance to Potato virus X. | Q44809238 |
| | An autoactive mutant of the M flax rust resistance protein has a preference for binding ATP, whereas wild-type M protein binds ADP. | Q45302581 |
| | Direct interaction between the tobacco mosaic virus helicase domain and the ATP-bound resistance protein, N factor during the hypersensitive response in tobacco plants | Q45415509 |
| | The Rx gene from potato controls separate virus resistance and cell death responses | Q45749405 |
| | A feature of the coat protein of potato virus X affects both induced virus resistance in potato and viral fitness | Q45778028 |
| | Distinct domains in the ARC region of the potato resistance protein Rx mediate LRR binding and inhibition of activation | Q48086025 |
| | Recognition specificity and RAR1/SGT1 dependence in barley Mla disease resistance genes to the powdery mildew fungus | Q48257288 |
| | Chlorophyll breakdown in senescent Arabidopsis leaves. Characterization of chlorophyll catabolites and of chlorophyll catabolic enzymes involved in the degreening reaction. | Q50757535 |
| | Structural determinants at the interface of the ARC2 and leucine-rich repeat domains control the activation of the plant immune receptors Rx1 and Gpa2. | Q51006190 |
| | Nucleocytoplasmic distribution is required for activation of resistance by the potato NB-LRR receptor Rx1 and is balanced by its functional domains. | Q52606191 |
| | Viral-induced systemic necrosis in plants involves both programmed cell death and the inhibition of viral multiplication, which are regulated by independent pathways. | Q54443765 |
| | The coiled-coil and nucleotide binding domains of the Potato Rx disease resistance protein function in pathogen recognition and signaling. | Q54541984 |
| | From Guard to Decoy: a new model for perception of plant pathogen effectors | Q57441458 |
| | Further analysis of gene-for-gene disease resistance specificity in flax | Q62711907 |
| P433 | issue | 52 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 21189-21194 | |
| P577 | publication date | 2013-12-09 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Stepwise artificial evolution of a plant disease resistance gene | |
| P478 | volume | 110 | |