BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

358 related articles for article (PubMed ID: 16838789)

  • 21. NTRC and chloroplast-generated reactive oxygen species regulate Pseudomonas syringae pv. tomato disease development in tomato and Arabidopsis.
    Ishiga Y; Ishiga T; Wangdi T; Mysore KS; Uppalapati SR
    Mol Plant Microbe Interact; 2012 Mar; 25(3):294-306. PubMed ID: 22112219
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Virulence systems of Pseudomonas syringae pv. tomato promote bacterial speck disease in tomato by targeting the jasmonate signaling pathway.
    Zhao Y; Thilmony R; Bender CL; Schaller A; He SY; Howe GA
    Plant J; 2003 Nov; 36(4):485-99. PubMed ID: 14617079
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Erwinia amylovora avrRpt2EA gene contributes to virulence on pear and AvrRpt2EA is recognized by Arabidopsis RPS2 when expressed in pseudomonas syringae.
    Zhao Y; He SY; Sundin GW
    Mol Plant Microbe Interact; 2006 Jun; 19(6):644-54. PubMed ID: 16776298
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Pseudomonas syringae pv. tomato avrE1/hopM1 mutant is severely reduced in growth and lesion formation in tomato.
    Badel JL; Shimizu R; Oh HS; Collmer A
    Mol Plant Microbe Interact; 2006 Feb; 19(2):99-111. PubMed ID: 16529372
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins.
    Schechter LM; Vencato M; Jordan KL; Schneider SE; Schneider DJ; Collmer A
    Mol Plant Microbe Interact; 2006 Nov; 19(11):1180-92. PubMed ID: 17073301
    [TBL] [Abstract][Full Text] [Related]  

  • 26. AlgR functions in algC expression and virulence in Pseudomonas syringae pv. syringae.
    Peñaloza-Vázquez A; Fakhr MK; Bailey AM; Bender CL
    Microbiology (Reading); 2004 Aug; 150(Pt 8):2727-2737. PubMed ID: 15289569
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pseudomonas syringae lytic transglycosylases coregulated with the type III secretion system contribute to the translocation of effector proteins into plant cells.
    Oh HS; Kvitko BH; Morello JE; Collmer A
    J Bacteriol; 2007 Nov; 189(22):8277-89. PubMed ID: 17827286
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A virus-induced gene silencing screen identifies a role for Thylakoid Formation1 in Pseudomonas syringae pv tomato symptom development in tomato and Arabidopsis.
    Wangdi T; Uppalapati SR; Nagaraj S; Ryu CM; Bender CL; Mysore KS
    Plant Physiol; 2010 Jan; 152(1):281-92. PubMed ID: 19915014
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Regulatory interactions between the Hrp type III protein secretion system and coronatine biosynthesis in Pseudomonas syringae pv. tomato DC3000.
    Peñaloza-Vázquez A; Preston GM; Collmer A; Bender CL
    Microbiology (Reading); 2000 Oct; 146 ( Pt 10)():2447-2456. PubMed ID: 11021921
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pseudomonas syringae pv. tomato DC3000 HopPtoM (CEL ORF3) is important for lesion formation but not growth in tomato and is secreted and translocated by the Hrp type III secretion system in a chaperone-dependent manner.
    Badel JL; Nomura K; Bandyopadhyay S; Shimizu R; Collmer A; He SY
    Mol Microbiol; 2003 Sep; 49(5):1239-51. PubMed ID: 12940984
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Negative Autogenous Control of the Master Type III Secretion System Regulator HrpL in Pseudomonas syringae.
    Waite C; Schumacher J; Jovanovic M; Bennett M; Buck M
    mBio; 2017 Jan; 8(1):. PubMed ID: 28119474
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A translocated protein tyrosine phosphatase of Pseudomonas syringae pv. tomato DC3000 modulates plant defence response to infection.
    Bretz JR; Mock NM; Charity JC; Zeyad S; Baker CJ; Hutcheson SW
    Mol Microbiol; 2003 Jul; 49(2):389-400. PubMed ID: 12828637
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A pseudomonas syringae pv. tomato DC3000 Hrp (Type III secretion) deletion mutant expressing the Hrp system of bean pathogen P. syringae pv. syringae 61 retains normal host specificity for tomato.
    Fouts DE; Badel JL; Ramos AR; Rapp RA; Collmer A
    Mol Plant Microbe Interact; 2003 Jan; 16(1):43-52. PubMed ID: 12580281
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of the hrpC and hrpRS operons of Pseudomonas syringae pathovars syringae, tomato, and glycinea and analysis of the ability of hrpF, hrpG, hrcC, hrpT, and hrpV mutants to elicit the hypersensitive response and disease in plants.
    Deng WL; Preston G; Collmer A; Chang CJ; Huang HC
    J Bacteriol; 1998 Sep; 180(17):4523-31. PubMed ID: 9721291
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Jasmonate ZIM-domain (JAZ) protein regulates host and nonhost pathogen-induced cell death in tomato and Nicotiana benthamiana.
    Ishiga Y; Ishiga T; Uppalapati SR; Mysore KS
    PLoS One; 2013; 8(9):e75728. PubMed ID: 24086622
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Simple and rapid capillary zone electrophoresis method for the detection of coronamic acid, a precursor to the Pseudomonas syringae phytotoxin coronatine.
    Sreedharan A; Penaloza-Vazquez A; Escober MC; Bender CL; Rayas-Duarte P
    J Agric Food Chem; 2009 Nov; 57(22):10518-23. PubMed ID: 19886659
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Stringent Response Mediated by (p)ppGpp Is Required for Virulence of Pseudomonas syringae pv. tomato and Its Survival on Tomato.
    Chatnaparat T; Li Z; Korban SS; Zhao Y
    Mol Plant Microbe Interact; 2015 Jul; 28(7):776-89. PubMed ID: 25675257
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pseudomonas syringae pv. tomato OxyR Is Required for Virulence in Tomato and Arabidopsis.
    Ishiga Y; Ichinose Y
    Mol Plant Microbe Interact; 2016 Feb; 29(2):119-31. PubMed ID: 26554736
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A gene in the Pseudomonas syringae pv. tomato Hrp pathogenicity island conserved effector locus, hopPtoA1, contributes to efficient formation of bacterial colonies in planta and is duplicated elsewhere in the genome.
    Badel JL; Charkowski AO; Deng WL; Collmer A
    Mol Plant Microbe Interact; 2002 Oct; 15(10):1014-24. PubMed ID: 12437299
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Variable suites of non-effector genes are co-regulated in the type III secretion virulence regulon across the Pseudomonas syringae phylogeny.
    Mucyn TS; Yourstone S; Lind AL; Biswas S; Nishimura MT; Baltrus DA; Cumbie JS; Chang JH; Jones CD; Dangl JL; Grant SR
    PLoS Pathog; 2014 Jan; 10(1):e1003807. PubMed ID: 24391493
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.