283 related articles for article (PubMed ID: 22187939)
1. The major volatile organic compound emitted from Arabidopsis thaliana flowers, the sesquiterpene (E)-β-caryophyllene, is a defense against a bacterial pathogen.
Huang M; Sanchez-Moreiras AM; Abel C; Sohrabi R; Lee S; Gershenzon J; Tholl D
New Phytol; 2012 Mar; 193(4):997-1008. PubMed ID: 22187939
[TBL] [Abstract][Full Text] [Related]
2. Floral and insect-induced volatile formation in Arabidopsis lyrata ssp. petraea, a perennial, outcrossing relative of A. thaliana.
Abel C; Clauss M; Schaub A; Gershenzon J; Tholl D
Planta; 2009 Jun; 230(1):1-11. PubMed ID: 19322583
[TBL] [Abstract][Full Text] [Related]
3. Two sesquiterpene synthases are responsible for the complex mixture of sesquiterpenes emitted from Arabidopsis flowers.
Tholl D; Chen F; Petri J; Gershenzon J; Pichersky E
Plant J; 2005 Jun; 42(5):757-71. PubMed ID: 15918888
[TBL] [Abstract][Full Text] [Related]
4. Isoprene and β-caryophyllene confer plant resistance via different plant internal signalling pathways.
Frank L; Wenig M; Ghirardo A; van der Krol A; Vlot AC; Schnitzler JP; Rosenkranz M
Plant Cell Environ; 2021 Apr; 44(4):1151-1164. PubMed ID: 33522606
[TBL] [Abstract][Full Text] [Related]
5. IDL6-HAE/HSL2 impacts pectin degradation and resistance to Pseudomonas syringae pv tomato DC3000 in Arabidopsis leaves.
Wang X; Hou S; Wu Q; Lin M; Acharya BR; Wu D; Zhang W
Plant J; 2017 Jan; 89(2):250-263. PubMed ID: 27618493
[TBL] [Abstract][Full Text] [Related]
6. Diverse mechanisms of resistance to Pseudomonas syringae in a thousand natural accessions of Arabidopsis thaliana.
Velásquez AC; Oney M; Huot B; Xu S; He SY
New Phytol; 2017 Jun; 214(4):1673-1687. PubMed ID: 28295393
[TBL] [Abstract][Full Text] [Related]
7. The Polycomb-Group Repressor MEDEA Attenuates Pathogen Defense.
Roy S; Gupta P; Rajabhoj MP; Maruthachalam R; Nandi AK
Plant Physiol; 2018 Aug; 177(4):1728-1742. PubMed ID: 29954867
[TBL] [Abstract][Full Text] [Related]
8. Proteomics and functional analyses of Arabidopsis nitrilases involved in the defense response to microbial pathogens.
Choi du S; Lim CW; Hwang BK
Planta; 2016 Aug; 244(2):449-65. PubMed ID: 27095107
[TBL] [Abstract][Full Text] [Related]
9. The Arabidopsis ATAF1, a NAC transcription factor, is a negative regulator of defense responses against necrotrophic fungal and bacterial pathogens.
Wang X; Basnayake BM; Zhang H; Li G; Li W; Virk N; Mengiste T; Song F
Mol Plant Microbe Interact; 2009 Oct; 22(10):1227-38. PubMed ID: 19737096
[TBL] [Abstract][Full Text] [Related]
10. Pseudomonas syringae elicits emission of the terpenoid (E,E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene in Arabidopsis leaves via jasmonate signaling and expression of the terpene synthase TPS4.
Attaran E; Rostás M; Zeier J
Mol Plant Microbe Interact; 2008 Nov; 21(11):1482-97. PubMed ID: 18842097
[TBL] [Abstract][Full Text] [Related]
11. Glycan-binding F-box protein from Arabidopsis thaliana protects plants from Pseudomonas syringae infection.
Stefanowicz K; Lannoo N; Zhao Y; Eggermont L; Van Hove J; Al Atalah B; Van Damme EJ
BMC Plant Biol; 2016 Oct; 16(1):213. PubMed ID: 27716048
[TBL] [Abstract][Full Text] [Related]
12. Engineering storage capacity for volatile sesquiterpenes in Nicotiana benthamiana leaves.
Delatte TL; Scaiola G; Molenaar J; de Sousa Farias K; Alves Gomes Albertti L; Busscher J; Verstappen F; Carollo C; Bouwmeester H; Beekwilder J
Plant Biotechnol J; 2018 Dec; 16(12):1997-2006. PubMed ID: 29682901
[TBL] [Abstract][Full Text] [Related]
13. Safe sex in plants.
Stephenson AG
New Phytol; 2012 Mar; 193(4):827-829. PubMed ID: 22300518
[No Abstract] [Full Text] [Related]
14. 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]
15. Phytohormones mediate volatile emissions during the interaction of compatible and incompatible pathogens: the role of ethylene in Pseudomonas syringae infected tobacco.
Huang J; Schmelz EA; Alborn H; Engelberth J; Tumlinson JH
J Chem Ecol; 2005 Mar; 31(3):439-59. PubMed ID: 15898494
[TBL] [Abstract][Full Text] [Related]
16. Homologous and heterologous expression of grapevine E-(β)-caryophyllene synthase (VvGwECar2).
Salvagnin U; Carlin S; Angeli S; Vrhovsek U; Anfora G; Malnoy M; Martens S
Phytochemistry; 2016 Nov; 131():76-83. PubMed ID: 27561253
[TBL] [Abstract][Full Text] [Related]
17. MicroRNA400-guided cleavage of Pentatricopeptide repeat protein mRNAs Renders Arabidopsis thaliana more susceptible to pathogenic bacteria and fungi.
Park YJ; Lee HJ; Kwak KJ; Lee K; Hong SW; Kang H
Plant Cell Physiol; 2014 Sep; 55(9):1660-8. PubMed ID: 25008976
[TBL] [Abstract][Full Text] [Related]
18. Regulation of miR163 and its targets in defense against Pseudomonas syringae in Arabidopsis thaliana.
Chow HT; Ng DW
Sci Rep; 2017 Apr; 7():46433. PubMed ID: 28401908
[TBL] [Abstract][Full Text] [Related]
19. The influence of intact-plant and excised-leaf bioassay designs on volicitin- and jasmonic acid-induced sesquiterpene volatile release in Zea mays.
Schmelz EA; Alborn HT; Tumlinson JH
Planta; 2001 Dec; 214(2):171-9. PubMed ID: 11800380
[TBL] [Abstract][Full Text] [Related]
20. Differential volatile emissions and salicylic acid levels from tobacco plants in response to different strains of Pseudomonas syringae.
Huang J; Cardoza YJ; Schmelz EA; Raina R; Engelberth J; Tumlinson JH
Planta; 2003 Sep; 217(5):767-75. PubMed ID: 12712338
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
