319 related articles for article (PubMed ID: 23360532)
21. Roles for SKN7 response regulator in stress resistance, conidiation and virulence in the citrus pathogen Alternaria alternata.
Chen LH; Lin CH; Chung KR
Fungal Genet Biol; 2012 Oct; 49(10):802-13. PubMed ID: 22902811
[TBL] [Abstract][Full Text] [Related]
22. Cellular responses required for oxidative stress tolerance, colonization, and lesion formation by the necrotrophic fungus Alternaria alternata in citrus.
Lin CH; Yang SL; Chung KR
Curr Microbiol; 2011 Mar; 62(3):807-15. PubMed ID: 20978890
[TBL] [Abstract][Full Text] [Related]
23. Ethylene signaling pathway and MAPK cascades are required for AAL toxin-induced programmed cell death.
Mase K; Mizuno T; Ishihama N; Fujii T; Mori H; Kodama M; Yoshioka H
Mol Plant Microbe Interact; 2012 Aug; 25(8):1015-25. PubMed ID: 22512379
[TBL] [Abstract][Full Text] [Related]
24. Epidermal chloroplasts are defense-related motile organelles equipped with plant immune components.
Irieda H; Takano Y
Nat Commun; 2021 May; 12(1):2739. PubMed ID: 34016974
[TBL] [Abstract][Full Text] [Related]
25. UDP-glucosyltransferase UGT84A2/BRT1 is required for Arabidopsis nonhost resistance to the Asian soybean rust pathogen Phakopsora pachyrhizi.
Langenbach C; Campe R; Schaffrath U; Goellner K; Conrath U
New Phytol; 2013 Apr; 198(2):536-545. PubMed ID: 23356583
[TBL] [Abstract][Full Text] [Related]
26. Cytological and molecular analyses of non-host resistance of Arabidopsis thaliana to Alternaria alternata.
Narusaka Y; Narusaka M; Seki M; Ishida J; Shinozaki K; Nan Y; Park P; Shiraishi T; Kobayashi M
Mol Plant Pathol; 2005 Nov; 6(6):615-27. PubMed ID: 20565684
[TBL] [Abstract][Full Text] [Related]
27. [Molecular mechanisms of non-host resistance].
Takano Y
Tanpakushitsu Kakusan Koso; 2007 May; 52(6 Suppl):705-10. PubMed ID: 17566378
[No Abstract] [Full Text] [Related]
28. CCA1 and LHY contribute to nonhost resistance to
Yamaura S; Yamauchi Y; Makihara M; Yamashino T; Ishikawa A
Biosci Biotechnol Biochem; 2020 Jan; 84(1):76-84. PubMed ID: 31478783
[TBL] [Abstract][Full Text] [Related]
29. Identification of candidate genes responsible for the susceptibility of apple (Malus × domestica Borkh.) to Alternaria blotch.
Moriya S; Terakami S; Okada K; Shimizu T; Adachi Y; Katayose Y; Fujisawa H; Wu J; Kanamori H; Yamamoto T; Abe K
BMC Plant Biol; 2019 Apr; 19(1):132. PubMed ID: 30961541
[TBL] [Abstract][Full Text] [Related]
30. Metabolite profiling of Arabidopsis inoculated with Alternaria brassicicola reveals that ascorbate reduces disease severity.
Botanga CJ; Bethke G; Chen Z; Gallie DR; Fiehn O; Glazebrook J
Mol Plant Microbe Interact; 2012 Dec; 25(12):1628-38. PubMed ID: 23134520
[TBL] [Abstract][Full Text] [Related]
31. EDS1 contributes to nonhost resistance of Arabidopsis thaliana against Erwinia amylovora.
Moreau M; Degrave A; Vedel R; Bitton F; Patrit O; Renou JP; Barny MA; Fagard M
Mol Plant Microbe Interact; 2012 Mar; 25(3):421-30. PubMed ID: 22316300
[TBL] [Abstract][Full Text] [Related]
32. Glutathione and tryptophan metabolism are required for Arabidopsis immunity during the hypersensitive response to hemibiotrophs.
Hiruma K; Fukunaga S; Bednarek P; Pislewska-Bednarek M; Watanabe S; Narusaka Y; Shirasu K; Takano Y
Proc Natl Acad Sci U S A; 2013 Jun; 110(23):9589-94. PubMed ID: 23696664
[TBL] [Abstract][Full Text] [Related]
33. Zinc triggers signaling mechanisms and defense responses promoting resistance to Alternaria brassicicola in Arabidopsis thaliana.
Martos S; Gallego B; Cabot C; Llugany M; Barceló J; Poschenrieder C
Plant Sci; 2016 Aug; 249():13-24. PubMed ID: 27297986
[TBL] [Abstract][Full Text] [Related]
34. AGB1 and PMR5 contribute to PEN2-mediated preinvasion resistance to Magnaporthe oryzae in Arabidopsis thaliana.
Maeda K; Houjyou Y; Komatsu T; Hori H; Kodaira T; Ishikawa A
Mol Plant Microbe Interact; 2009 Nov; 22(11):1331-40. PubMed ID: 19810803
[TBL] [Abstract][Full Text] [Related]
35. Most AAL toxin-sensitive Nicotiana species are resistant to the tomato fungal pathogen Alternaria alternata f. sp. lycopersici.
Brandwagt BF; Kneppers TJ; Van der Weerden GM; Nijkamp HJ; Hille J
Mol Plant Microbe Interact; 2001 Apr; 14(4):460-70. PubMed ID: 11310733
[TBL] [Abstract][Full Text] [Related]
36. The basal transcription factor II H subunit Tfb5 is required for stress response and pathogenicity in the tangerine pathotype of Alternaria alternata.
Fu H; Chung KR; Gai Y; Mao L; Li H
Mol Plant Pathol; 2020 Oct; 21(10):1337-1352. PubMed ID: 32776683
[TBL] [Abstract][Full Text] [Related]
37. Inheritance and genetic mapping of resistance to Alternaria alternata f. sp. lycopersici in Lycopersicon pennellii.
van der Biezen EA; Glagotskaya T; Overduin B; Nijkamp HJ; Hille J
Mol Gen Genet; 1995 May; 247(4):453-61. PubMed ID: 7770053
[TBL] [Abstract][Full Text] [Related]
38. Glutathione and tryptophan metabolites are key players in Arabidopsis nonhost resistance against Colletotrichum gloeosporioides.
Hiruma K; Fukunaga S; Bednarek P; Takano Y
Plant Signal Behav; 2013 Sep; 8(9):. PubMed ID: 23838955
[TBL] [Abstract][Full Text] [Related]
39. The membrane-anchored BOTRYTIS-INDUCED KINASE1 plays distinct roles in Arabidopsis resistance to necrotrophic and biotrophic pathogens.
Veronese P; Nakagami H; Bluhm B; Abuqamar S; Chen X; Salmeron J; Dietrich RA; Hirt H; Mengiste T
Plant Cell; 2006 Jan; 18(1):257-73. PubMed ID: 16339855
[TBL] [Abstract][Full Text] [Related]
40. The FUS3 MAPK signaling pathway of the citrus pathogen Alternaria alternata functions independently or cooperatively with the fungal redox-responsive AP1 regulator for diverse developmental, physiological and pathogenic processes.
Lin CH; Yang SL; Wang NY; Chung KR
Fungal Genet Biol; 2010 Apr; 47(4):381-91. PubMed ID: 20036749
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
