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|Conserved C-terminal motifs required for avirulence and suppression of cell death by Phytophthora sojae effector Avr1b|
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The Plant Cell 20 (4), 1118-1133, 2008
|Transcriptional programming and functional interactions within the Phytophthora sojae RXLR effector repertoire|
Q Wang, C Han, AO Ferreira, X Yu, W Ye, S Tripathy, SD Kale, B Gu, ...
The Plant Cell 23 (6), 2064-2086, 2011
|The bZIP transcription factor MoAP1 mediates the oxidative stress response and is critical for pathogenicity of the rice blast fungus Magnaporthe oryzae|
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PLoS pathog 7 (2), e1001302, 2011
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Y Qiao, L Liu, Q Xiong, C Flores, J Wong, J Shi, X Wang, X Liu, Q Xiang, ...
Nature genetics 45 (3), 330-333, 2013
|Molecular detection of Fusarium oxysporum f. sp. niveum and Mycosphaerella melonis in infected plant tissues and soil|
Z Zhang, J Zhang, Y Wang, X Zheng
FEMS Microbiology Letters 249 (1), 39-47, 2005
|Phytophthora sojae avirulence effector Avr3b is a secreted NADH and ADP-ribose pyrophosphorylase that modulates plant immunity|
S Dong, W Yin, G Kong, X Yang, D Qutob, Q Chen, SD Kale, Y Sui, ...
PLoS Pathog 7 (11), e1002353, 2011
|Copy number variation and transcriptional polymorphisms of Phytophthora sojae RXLR effector genes Avr1a and Avr3a|
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PloS one 4 (4), e5066, 2009
|A Phytophthora sojae glycoside hydrolase 12 protein is a major virulence factor during soybean infection and is recognized as a PAMP|
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The Plant Cell 27 (7), 2057-2072, 2015
|Two host cytoplasmic effectors are required for pathogenesis of Phytophthora sojae by suppression of host defenses|
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Plant physiology 155 (1), 490-501, 2011
|Development of a loop-mediated isothermal amplification assay for detection of Phytophthora sojae|
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FEMS microbiology letters 334 (1), 27-34, 2012
|MgCRZ1, a transcription factor of Magnaporthe grisea, controls growth, development and is involved in full virulence|
H Zhang, Q Zhao, K Liu, Z Zhang, Y Wang, X Zheng
FEMS microbiology letters 293 (2), 160-169, 2009
|The role of vacuolar processing enzyme (VPE) from Nicotiana benthamiana in the elicitor-triggered hypersensitive response and stomatal closure|
H Zhang, S Dong, M Wang, W Wang, W Song, X Dou, X Zheng, Z Zhang
Journal of experimental botany 61 (13), 3799-3812, 2010
|The RxLR effector Avh241 from Phytophthora sojae requires plasma membrane localization to induce plant cell death|
X Yu, J Tang, Q Wang, W Ye, K Tao, S Duan, C Lu, X Yang, S Dong, ...
New Phytologist 196 (1), 247-260, 2012
|A paralogous decoy protects Phytophthora sojae apoplastic effector PsXEG1 from a host inhibitor|
Z Ma, L Zhu, T Song, Y Wang, Q Zhang, Y Xia, M Qiu, Y Lin, H Li, L Kong, ...
Science 355 (6326), 710-714, 2017
|Roles of small RNAs in soybean defense against Phytophthora sojae infection|
J Wong, L Gao, Y Yang, J Zhai, S Arikit, Y Yu, S Duan, V Chan, Q Xiong, ...
The Plant Journal 79 (6), 928-940, 2014
|Digital Gene Expression Profiling of the Phytophthora sojae Transcriptome|
W Ye, X Wang, K Tao, Y Lu, T Dai, S Dong, D Dou, M Gijzen, Y Wang
Molecular plant-microbe interactions 24 (12), 1530-1539, 2011
|Global genome and transcriptome analyses of Magnaporthe oryzae epidemic isolate 98-06 uncover novel effectors and pathogenicity-related genes, revealing gene gain and lose …|
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PLoS Pathog 11 (4), e1004801, 2015
|The role of respiratory burst oxidase homologues in elicitor-induced stomatal closure and hypersensitive response in Nicotiana benthamiana|
H Zhang, Q Fang, Z Zhang, Y Wang, X Zheng
Journal of experimental botany 60 (11), 3109-3122, 2009
|The NLP Toxin Family in Phytophthora sojae Includes Rapidly Evolving Groups That Lack Necrosis-Inducing Activity|
S Dong, G Kong, D Qutob, X Yu, J Tang, J Kang, T Dai, H Wang, M Gijzen, ...
Molecular plant-microbe interactions 25 (7), 896-909, 2012