443 related articles for article (PubMed ID: 25211078)
21. Decreased abundance of type III secretion system-inducing signals in Arabidopsis mkp1 enhances resistance against Pseudomonas syringae.
Anderson JC; Wan Y; Kim YM; Pasa-Tolic L; Metz TO; Peck SC
Proc Natl Acad Sci U S A; 2014 May; 111(18):6846-51. PubMed ID: 24753604
[TBL] [Abstract][Full Text] [Related]
22. RAR1, a central player in plant immunity, is targeted by Pseudomonas syringae effector AvrB.
Shang Y; Li X; Cui H; He P; Thilmony R; Chintamanani S; Zwiesler-Vollick J; Gopalan S; Tang X; Zhou JM
Proc Natl Acad Sci U S A; 2006 Dec; 103(50):19200-5. PubMed ID: 17148606
[TBL] [Abstract][Full Text] [Related]
23. Arabidopsis proteins important for modulating defense responses to Pseudomonas syringae that secrete HopW1-1.
Lee MW; Jelenska J; Greenberg JT
Plant J; 2008 May; 54(3):452-65. PubMed ID: 18266921
[TBL] [Abstract][Full Text] [Related]
24. The pan-genome effector-triggered immunity landscape of a host-pathogen interaction.
Laflamme B; Dillon MM; Martel A; Almeida RND; Desveaux D; Guttman DS
Science; 2020 Feb; 367(6479):763-768. PubMed ID: 32054757
[TBL] [Abstract][Full Text] [Related]
25. Homologous RXLR effectors from Hyaloperonospora arabidopsidis and Phytophthora sojae suppress immunity in distantly related plants.
Anderson RG; Casady MS; Fee RA; Vaughan MM; Deb D; Fedkenheuer K; Huffaker A; Schmelz EA; Tyler BM; McDowell JM
Plant J; 2012 Dec; 72(6):882-93. PubMed ID: 22709376
[TBL] [Abstract][Full Text] [Related]
26. Phytopathogen Effectors Use Multiple Mechanisms to Manipulate Plant Autophagy.
Lal NK; Thanasuwat B; Huang PJ; Cavanaugh KA; Carter A; Michelmore RW; Dinesh-Kumar SP
Cell Host Microbe; 2020 Oct; 28(4):558-571.e6. PubMed ID: 32810441
[TBL] [Abstract][Full Text] [Related]
27. A receptor-like cytoplasmic kinase phosphorylates the host target RIN4, leading to the activation of a plant innate immune receptor.
Liu J; Elmore JM; Lin ZJ; Coaker G
Cell Host Microbe; 2011 Feb; 9(2):137-46. PubMed ID: 21320696
[TBL] [Abstract][Full Text] [Related]
28. The Pseudomonas syringae type III effector AvrRpt2 promotes pathogen virulence via stimulating Arabidopsis auxin/indole acetic acid protein turnover.
Cui F; Wu S; Sun W; Coaker G; Kunkel B; He P; Shan L
Plant Physiol; 2013 Jun; 162(2):1018-29. PubMed ID: 23632856
[TBL] [Abstract][Full Text] [Related]
29. Quantitative Interactor Screening with next-generation Sequencing (QIS-Seq) identifies Arabidopsis thaliana MLO2 as a target of the Pseudomonas syringae type III effector HopZ2.
Lewis JD; Wan J; Ford R; Gong Y; Fung P; Nahal H; Wang PW; Desveaux D; Guttman DS
BMC Genomics; 2012 Jan; 13():8. PubMed ID: 22230763
[TBL] [Abstract][Full Text] [Related]
30. All Roads Lead to Susceptibility: The Many Modes of Action of Fungal and Oomycete Intracellular Effectors.
He Q; McLellan H; Boevink PC; Birch PRJ
Plant Commun; 2020 Jul; 1(4):100050. PubMed ID: 33367246
[TBL] [Abstract][Full Text] [Related]
31. Host-Mediated
Ling T; Bellin D; Vandelle E; Imanifard Z; Delledonne M
Plant Cell; 2017 Nov; 29(11):2871-2881. PubMed ID: 29084872
[TBL] [Abstract][Full Text] [Related]
32. Arabidopsis nonhost resistance gene PSS1 confers immunity against an oomycete and a fungal pathogen but not a bacterial pathogen that cause diseases in soybean.
Sumit R; Sahu BB; Xu M; Sandhu D; Bhattacharyya MK
BMC Plant Biol; 2012 Jun; 12():87. PubMed ID: 22694952
[TBL] [Abstract][Full Text] [Related]
33. Recognition of the Hyaloperonospora parasitica effector ATR13 triggers resistance against oomycete, bacterial, and viral pathogens.
Rentel MC; Leonelli L; Dahlbeck D; Zhao B; Staskawicz BJ
Proc Natl Acad Sci U S A; 2008 Jan; 105(3):1091-6. PubMed ID: 18198274
[TBL] [Abstract][Full Text] [Related]
34. Gene gain and loss during evolution of obligate parasitism in the white rust pathogen of Arabidopsis thaliana.
Kemen E; Gardiner A; Schultz-Larsen T; Kemen AC; Balmuth AL; Robert-Seilaniantz A; Bailey K; Holub E; Studholme DJ; Maclean D; Jones JD
PLoS Biol; 2011 Jul; 9(7):e1001094. PubMed ID: 21750662
[TBL] [Abstract][Full Text] [Related]
35. The long-term maintenance of a resistance polymorphism through diffuse interactions.
Karasov TL; Kniskern JM; Gao L; DeYoung BJ; Ding J; Dubiella U; Lastra RO; Nallu S; Roux F; Innes RW; Barrett LG; Hudson RR; Bergelson J
Nature; 2014 Aug; 512(7515):436-440. PubMed ID: 25043057
[TBL] [Abstract][Full Text] [Related]
36. HopA1 Effector from
Dahale SK; Ghosh D; Ingole KD; Chugani A; Kim SH; Bhattacharjee S
Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299060
[No Abstract] [Full Text] [Related]
37. Downy Mildew effector HaRxL21 interacts with the transcriptional repressor TOPLESS to promote pathogen susceptibility.
Harvey S; Kumari P; Lapin D; Griebel T; Hickman R; Guo W; Zhang R; Parker JE; Beynon J; Denby K; Steinbrenner J
PLoS Pathog; 2020 Aug; 16(8):e1008835. PubMed ID: 32785253
[TBL] [Abstract][Full Text] [Related]
38. Genome-wide transcriptional analysis of the Arabidopsis thaliana interaction with the plant pathogen Pseudomonas syringae pv. tomato DC3000 and the human pathogen Escherichia coli O157:H7.
Thilmony R; Underwood W; He SY
Plant J; 2006 Apr; 46(1):34-53. PubMed ID: 16553894
[TBL] [Abstract][Full Text] [Related]
39. Resistance to the Pseudomonas syringae effector HopA1 is governed by the TIR-NBS-LRR protein RPS6 and is enhanced by mutations in SRFR1.
Kim SH; Kwon SI; Saha D; Anyanwu NC; Gassmann W
Plant Physiol; 2009 Aug; 150(4):1723-32. PubMed ID: 19525323
[TBL] [Abstract][Full Text] [Related]
40. Host-parasite coevolutionary conflict between Arabidopsis and downy mildew.
Allen RL; Bittner-Eddy PD; Grenville-Briggs LJ; Meitz JC; Rehmany AP; Rose LE; Beynon JL
Science; 2004 Dec; 306(5703):1957-60. PubMed ID: 15591208
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]