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1

Hou, Shuguo, Yifei Yang, Daoji Wu, and Chao Zhang. "Plant immunity." Plant Signaling & Behavior 6, no. 6 (June 2011): 794–99. http://dx.doi.org/10.4161/psb.6.6.15143.

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2

Lewis, Jennifer D. "Plant immunity." Seminars in Cell & Developmental Biology 56 (August 2016): 122–23. http://dx.doi.org/10.1016/j.semcdb.2016.07.003.

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3

Nobori, Tatsuya, André C. Velásquez, Jingni Wu, Brian H. Kvitko, James M. Kremer, Yiming Wang, Sheng Yang He, and Kenichi Tsuda. "Transcriptome landscape of a bacterial pathogen under plant immunity." Proceedings of the National Academy of Sciences 115, no. 13 (March 12, 2018): E3055—E3064. http://dx.doi.org/10.1073/pnas.1800529115.

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Plant pathogens can cause serious diseases that impact global agriculture. The plant innate immunity, when fully activated, can halt pathogen growth in plants. Despite extensive studies into the molecular and genetic bases of plant immunity against pathogens, the influence of plant immunity in global pathogen metabolism to restrict pathogen growth is poorly understood. Here, we developed RNA sequencing pipelines for analyzing bacterial transcriptomes in planta and determined high-resolution transcriptome patterns of the foliar bacterial pathogen Pseudomonas syringae in Arabidopsis thaliana with a total of 27 combinations of plant immunity mutants and bacterial strains. Bacterial transcriptomes were analyzed at 6 h post infection to capture early effects of plant immunity on bacterial processes and to avoid secondary effects caused by different bacterial population densities in planta. We identified specific “immune-responsive” bacterial genes and processes, including those that are activated in susceptible plants and suppressed by plant immune activation. Expression patterns of immune-responsive bacterial genes at the early time point were tightly linked to later bacterial growth levels in different host genotypes. Moreover, we found that a bacterial iron acquisition pathway is commonly suppressed by multiple plant immune-signaling pathways. Overexpression of a P. syringae sigma factor gene involved in iron regulation and other processes partially countered bacterial growth restriction during the plant immune response triggered by AvrRpt2. Collectively, this study defines the effects of plant immunity on the transcriptome of a bacterial pathogen and sheds light on the enigmatic mechanisms of bacterial growth inhibition during the plant immune response.
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4

Maksimov, I. V., and R. M. Khairullin. "Plant immunity and plant microbiome." Agrarian science 327, no. 2 (2019): 40–44. http://dx.doi.org/10.32634/0869-8155-2019-326-2-40-44.

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5

Pruitt, Rory N., Andrea A. Gust, and Thorsten Nürnberger. "Plant immunity unified." Nature Plants 7, no. 4 (March 30, 2021): 382–83. http://dx.doi.org/10.1038/s41477-021-00903-3.

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6

Ngou, Bruno Pok Man, Pingtao Ding, and Jonathan D. G. Jones. "Channeling plant immunity." Cell 184, no. 13 (June 2021): 3358–60. http://dx.doi.org/10.1016/j.cell.2021.05.035.

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7

Jamison, Judy. "Boosting plant immunity." Nature Biotechnology 18, no. 7 (July 2000): 703. http://dx.doi.org/10.1038/77240.

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8

Jung, Su-Jin, Hong Gil Lee, and Pil Joon Seo. "Membrane-triggered plant immunity." Plant Signaling & Behavior 9, no. 9 (July 16, 2014): e29729. http://dx.doi.org/10.4161/psb.29729.

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9

Mengiste, Tesfaye. "Plant Immunity to Necrotrophs." Annual Review of Phytopathology 50, no. 1 (September 8, 2012): 267–94. http://dx.doi.org/10.1146/annurev-phyto-081211-172955.

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10

Alderton, Gemma. "Networks in plant immunity." Science 360, no. 6395 (June 21, 2018): 1310.12–1312. http://dx.doi.org/10.1126/science.360.6395.1310-l.

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11

Trujillo, Marco, and Ken Shirasu. "Ubiquitination in plant immunity." Current Opinion in Plant Biology 13, no. 4 (August 1, 2010): 402–8. http://dx.doi.org/10.1016/j.pbi.2010.04.002.

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12

Fehervari, Zoltan. "Turning on plant immunity." Nature Immunology 13, no. 4 (March 19, 2012): 315. http://dx.doi.org/10.1038/ni.2272.

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13

Campos, Marcelo L., Jin-Ho Kang, and Gregg A. Howe. "Jasmonate-Triggered Plant Immunity." Journal of Chemical Ecology 40, no. 7 (June 28, 2014): 657–75. http://dx.doi.org/10.1007/s10886-014-0468-3.

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14

Zheng, Xiyin, Yiqing Li, and Yule Liu. "Plant Immunity against Tobamoviruses." Viruses 16, no. 4 (March 29, 2024): 530. http://dx.doi.org/10.3390/v16040530.

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Tobamoviruses are a group of plant viruses that pose a significant threat to agricultural crops worldwide. In this review, we focus on plant immunity against tobamoviruses, including pattern-triggered immunity (PTI), effector-triggered immunity (ETI), the RNA-targeting pathway, phytohormones, reactive oxygen species (ROS), and autophagy. Further, we highlight the genetic resources for resistance against tobamoviruses in plant breeding and discuss future directions on plant protection against tobamoviruses.
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15

Bjornson, Marta, and Cyril Zipfel. "Plant immunity: Crosstalk between plant immune receptors." Current Biology 31, no. 12 (June 2021): R796—R798. http://dx.doi.org/10.1016/j.cub.2021.04.080.

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16

van Wersch, Solveig, Lei Tian, Ryan Hoy, and Xin Li. "Plant NLRs: The Whistleblowers of Plant Immunity." Plant Communications 1, no. 1 (January 2020): 100016. http://dx.doi.org/10.1016/j.xplc.2019.100016.

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17

van Wersch, Solveig, Lei Tian, Ryan Hoy, and Xin Li. "Plant NLRs: The Whistleblowers of Plant Immunity." Plant Communications 1, no. 4 (July 2020): 100090. http://dx.doi.org/10.1016/j.xplc.2020.100090.

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18

Song, Handa, Borong Lin, Qiuling Huang, Longhua Sun, Jiansong Chen, Lili Hu, Kan Zhuo, and Jinling Liao. "The Meloidogyne graminicola effector MgMO289 targets a novel copper metallochaperone to suppress immunity in rice." Journal of Experimental Botany 72, no. 15 (May 11, 2021): 5638–55. http://dx.doi.org/10.1093/jxb/erab208.

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Abstract Recent studies have reported that plant-parasitic nematodes facilitate their infection by suppressing plant immunity via effectors, but the inhibitory mechanisms remain poorly understood. This study found that a novel effector MgMO289 is exclusively expressed in the dorsal esophageal gland of Meloidogyne graminicola and is up-regulated at parasitic third-/fourth-stage juveniles. In planta silencing of MgMO289 substantially increased plant resistance to M. graminicola. Moreover, we found that MgMO289 interacts with a new rice copper metallochaperone heavy metal-associated plant protein 04 (OsHPP04), and that rice cytosolic COPPER/ZINC -SUPEROXIDE DISMUTASE 2 (cCu/Zn-SOD2) is the target of OsHPP04. Rice plants overexpressing OsHPP04 or MgMO289 exhibited an increased susceptibility to M. graminicola and a higher Cu/Zn-SOD activity, but lower O2•− content, when compared with wild-type plants. Meanwhile, immune response assays showed that MgMO289 could suppress host innate immunity. These findings reveal a novel pathway for a plant pathogen effector that utilizes the host O2•−-scavenging system to eliminate O2•− and suppress plant immunity.
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19

Laflamme, Bradley, Maggie Middleton, Timothy Lo, Darrell Desveaux, and David S. Guttman. "Image-Based Quantification of Plant Immunity and Disease." Molecular Plant-Microbe Interactions® 29, no. 12 (December 2016): 919–24. http://dx.doi.org/10.1094/mpmi-07-16-0129-ta.

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Measuring the extent and severity of disease is a critical component of plant pathology research and crop breeding. Unfortunately, existing visual scoring systems are qualitative, subjective, and the results are difficult to transfer between research groups, while existing quantitative methods can be quite laborious. Here, we present plant immunity and disease image-based quantification (PIDIQ), a quantitative, semi-automated system to rapidly and objectively measure disease symptoms in a biologically relevant context. PIDIQ applies an ImageJ-based macro to plant photos in order to distinguish healthy tissue from tissue that has yellowed due to disease. It can process a directory of images in an automated manner and report the relative ratios of healthy to diseased leaf area, thereby providing a quantitative measure of plant health that can be statistically compared with appropriate controls. We used the Arabidopsis thaliana–Pseudomonas syringae model system to show that PIDIQ is able to identify both enhanced plant health associated with effector-triggered immunity as well as elevated disease symptoms associated with effector-triggered susceptibility. Finally, we show that the quantitative results provided by PIDIQ correspond to those obtained via traditional in planta pathogen growth assays. PIDIQ provides a simple and effective means to nondestructively quantify disease from whole plants and we believe it will be equally effective for monitoring disease on excised leaves and stems.
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20

YOSHIHISA, Ayaka, Keita SHIMADA, Satomi YOSHIMURA, Koji YAMAGUCHI, and Tsutomu KAWASAKI. "Frontier Of Plant Immune Research: Activation of Plant Immunity and Inhibitory Mechanism of Plant Immunity by Pathogens." KAGAKU TO SEIBUTSU 58, no. 7 (July 1, 2020): 396–403. http://dx.doi.org/10.1271/kagakutoseibutsu.58.396.

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21

Yamaguchi, Koji, and Tsutomu Kawasaki. "Pathogen- and plant-derived peptides trigger plant immunity." Peptides 144 (October 2021): 170611. http://dx.doi.org/10.1016/j.peptides.2021.170611.

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22

Huang, Min, Zilin Wu, Jingxin Li, Yuyu Ding, Shilin Chen, and Xiangyang Li. "Plant Protection against Viruses: An Integrated Review of Plant Immunity Agents." International Journal of Molecular Sciences 24, no. 5 (February 23, 2023): 4453. http://dx.doi.org/10.3390/ijms24054453.

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Plant viruses are an important class of pathogens that seriously affect plant growth and harm crop production. Viruses are simple in structure but complex in mutation and have thus always posed a continuous threat to agricultural development. Low resistance and eco-friendliness are important features of green pesticides. Plant immunity agents can enhance the resilience of the immune system by activating plants to regulate their metabolism. Therefore, plant immune agents are of great importance in pesticide science. In this paper, we review plant immunity agents, such as ningnanmycin, vanisulfane, dufulin, cytosinpeptidemycin, and oligosaccharins, and their antiviral molecular mechanisms and discuss the antiviral applications and development of plant immunity agents. Plant immunity agents can trigger defense responses and confer disease resistance to plants, and the development trends and application prospects of plant immunity agents in plant protection are analyzed in depth.
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23

S, Ghosh. "Immune Modulation in Goats by Plant Derived Melatonin: A Review." Journal of Natural & Ayurvedic Medicine 6, no. 3 (July 5, 2022): 1–8. http://dx.doi.org/10.23880/jonam-16000357.

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The basic structure of melatonin is evolutionarily conserved. Hence, it was speculated that melatonin may be present in different animals (from unicellular to multi-cellular) and even in plants. Melatonin in plans is generally regarded as phytomelatonin. Like the role of melatonin in animals, phyto-melatonin can perform a number of functions like attenuation of apoptosis, prevention of free radical generation, protection against UV irradiation etc. But, unlike phyto-estrogen, the role of phyto-melatonin in animals is totally an unexplored area. Hence, aim of the present study was to note the role of phytomelatonin in maintenance of general health and immunity of goats. To fulfil the aim, we supplemented the goats with phytomelatonin rich diet i.e. corn (Zea mays) which is having 1.4 ng/gm of dry weight of tissue and they are also edible to goats. We noted significantly high level of body weight, hematological (AST, ALT level, total RBC count and %Hb), immunological (TLC, %LC, %SR of PBMCs), metabolic (plasma glucose, cholesterol, HDL, LDL, protein levels and HDL: LDL ration), free radical (SOD, catalase, GPx levels), hormonal (estrogen, melatonin), cytokine (IL-6 and TNF-α) levels and significantly low level of MDA. However, plasma testosterone was unaffected upon phyto-melatonin treatment. Thus, for the first time role of phytomelatonin as a protective molecule with improving effect on the health and immunity of Indian goat Capra hircusis being proposed, as the effect of phyto-melatonin supplementation can be brought back to normal and this dietary supplement might be utilizing the similar pathway as commercial melatonin. There are so many less expensive and readily available sources of phyto-melatonin that requires the proper knowledge of exploitation of these sources for extreme benefit for animals as well as for the human beings in near or far future.
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24

Yang, Shengming, Fang Tang, and Hongyan Zhu. "Alternative Splicing in Plant Immunity." International Journal of Molecular Sciences 15, no. 6 (June 10, 2014): 10424–45. http://dx.doi.org/10.3390/ijms150610424.

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25

Li, Lei. "My journey studying plant immunity." Cell Host & Microbe 30, no. 4 (April 2022): 463–65. http://dx.doi.org/10.1016/j.chom.2022.03.009.

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26

Han, Xiaowei, and Kenichi Tsuda. "Evolutionary footprint of plant immunity." Current Opinion in Plant Biology 67 (June 2022): 102209. http://dx.doi.org/10.1016/j.pbi.2022.102209.

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27

Zhichkin, K. A., V. V. Nosov, and L. N. Zhichkina. "Plant immunity and crop insurance." Economy of agricultural and processing enterprises, no. 5 (2021): 38–42. http://dx.doi.org/10.31442/0235-2494-2021-0-5-38-42.

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Agricultural insurance with state support (in crop production) creates conditions for stable and effective activity in the cultivation of basic agricultural crops, which is especially important in conditions of uncertain weather factors typical for the risky agriculture zone, which includes the Samara region. Dry summers, frosty winters with a minimum of precipitation make agricultural production largely dependent on natural and climatic factors. The study purpose is to substantiate the need to take into account the characteristics of individual varieties when insuring agricultural crops with state support. It is necessary to solve the following tasks: - to formulate the biological characteristics of individual varieties of agricultural crops; - to classify all emergencies according to the type of impact on plants; - substantiate (using the spring barley example) the need to correct the existing approach when signing agricultural insurance contracts with state support in crop production. When developing an insurance algorithm, it is necessary to take into account the breeding potential of both agricultural crops and individual varieties associated with their genetic characteristics. The widespread use of the achievements of genetics, realized in the form of the formation of plant immunity, makes it possible to achieve a significant degree of resistance to abiotic and biotic factors that have a compensated and uncompensated nature. As can be seen from the presented calculation, it cannot be said that the presence of a variety in the State Register of Breeding Achievements is a prerequisite for its successful cultivation. Therefore, it is necessary for each agricultural crop to identify a number of features, the presence of which makes this variety resistant to the totality of all factors of the given microregion.
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28

Macho, Alberto P., and Carmen R. Beuzón. "Insights into plant immunity signaling." Plant Signaling & Behavior 5, no. 12 (December 2010): 1590–93. http://dx.doi.org/10.4161/psb.5.12.13843.

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29

Kozyrovska, N. O. "Mechanisms of plant innate immunity." Biopolymers and Cell 22, no. 2 (March 20, 2006): 91–101. http://dx.doi.org/10.7124/bc.000721.

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30

Bolouri Moghaddam, M. R., and W. Van den Ende. "Sugars and plant innate immunity." Journal of Experimental Botany 63, no. 11 (May 2, 2012): 3989–98. http://dx.doi.org/10.1093/jxb/ers129.

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31

Shamrai, S. N. "Plant immune system: Basal immunity." Cytology and Genetics 48, no. 4 (July 2014): 258–71. http://dx.doi.org/10.3103/s0095452714040057.

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32

Kangasjärvi, Saijaliisa. "Pic1, counteracting plant immunity signalling." Biochemical Journal 476, no. 16 (August 28, 2019): 2347–50. http://dx.doi.org/10.1042/bcj20190369.

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Abstract Plants are equipped with versatile pattern recognition receptors (PRRs), which monitor their external environment and elicit defensive measures upon detection of potential risk for disease. Inside the cell, receptor-like cytoplasmic kinases (RLCKs) are key components of PRR signalling, but their molecular functions and regulatory interactions are not yet fully understood. In tomato, two RLCKs, Pti1a and Pti1b, are important signalling components that relay early defence signals elicited by bacterial flagellin, a conserved pattern common to various pathogenic and non-pathogenic microbes. An important question to resolve is how plant immune reactions are regulated to prevent unnecessary defensive measures. A recent paper published in the Biochemical Journal by Giska and Martin [Biochem. J. (2019) 476, 1621–1635] reports the identification and biochemical characterization of a new tomato (Solanum lycopersicum) protein phosphatase that negatively controls early defence signalling. The phosphatase, termed pattern-triggered immunity inhibiting PP2C 1 (Pic1), negatively controls the signalling function of Pti1b and therefore holds a central position in the defence signalling network. The Pti1b–Pic1 kinase–phosphatase interaction provides mechanistic insights that forward our understanding of protein phosphatases and their importance in plant immunity.
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33

TADAMURA, Kazuki, and Kenji NAKAHARA. "Plant Innate Immunity against Viruses." KAGAKU TO SEIBUTSU 52, no. 12 (2014): 805–13. http://dx.doi.org/10.1271/kagakutoseibutsu.52.805.

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34

Wu, Chih-Hang, Lida Derevnina, and Sophien Kamoun. "Receptor networks underpin plant immunity." Science 360, no. 6395 (June 21, 2018): 1300–1301. http://dx.doi.org/10.1126/science.aat2623.

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35

ALVAREZ, MARÍA E., FLORENCIA NOTA, and DAMIÁN A. CAMBIAGNO. "Epigenetic control of plant immunity." Molecular Plant Pathology 11, no. 4 (June 1, 2010): 563–76. http://dx.doi.org/10.1111/j.1364-3703.2010.00621.x.

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36

Pitsili, Eugenia, Ujjal J. Phukan, and Nuria S. Coll. "Cell Death in Plant Immunity." Cold Spring Harbor Perspectives in Biology 12, no. 6 (October 15, 2019): a036483. http://dx.doi.org/10.1101/cshperspect.a036483.

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37

Pieterse, Corné M. J., Dieuwertje Van der Does, Christos Zamioudis, Antonio Leon-Reyes, and Saskia C. M. Van Wees. "Hormonal Modulation of Plant Immunity." Annual Review of Cell and Developmental Biology 28, no. 1 (November 10, 2012): 489–521. http://dx.doi.org/10.1146/annurev-cellbio-092910-154055.

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38

Moore, John W., Gary J. Loake, and Steven H. Spoel. "Transcription Dynamics in Plant Immunity." Plant Cell 23, no. 8 (August 2011): 2809–20. http://dx.doi.org/10.1105/tpc.111.087346.

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39

Tsuda, Kenichi, and Imre E. Somssich. "Transcriptional networks in plant immunity." New Phytologist 206, no. 3 (January 26, 2015): 932–47. http://dx.doi.org/10.1111/nph.13286.

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40

Howe, Gregg A., and Georg Jander. "Plant Immunity to Insect Herbivores." Annual Review of Plant Biology 59, no. 1 (June 2008): 41–66. http://dx.doi.org/10.1146/annurev.arplant.59.032607.092825.

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41

Hausladen, A., and J. S. Stamler. "Nitric oxide in plant immunity." Proceedings of the National Academy of Sciences 95, no. 18 (September 1, 1998): 10345–47. http://dx.doi.org/10.1073/pnas.95.18.10345.

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42

Gu, Yangnan, Raul Zavaliev, and Xinnian Dong. "Membrane Trafficking in Plant Immunity." Molecular Plant 10, no. 8 (August 2017): 1026–34. http://dx.doi.org/10.1016/j.molp.2017.07.001.

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43

Schneider, David S. "Plant Immunity and Film Noir." Cell 109, no. 5 (May 2002): 537–40. http://dx.doi.org/10.1016/s0092-8674(02)00764-x.

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44

Shirasu, Ken, Richard A. Dixon, and Chris Lamb. "Signal transduction in plant immunity." Current Opinion in Immunology 8, no. 1 (February 1996): 3–7. http://dx.doi.org/10.1016/s0952-7915(96)80097-5.

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45

Yun, Hye Sup, and Chian Kwon. "Vesicle trafficking in plant immunity." Current Opinion in Plant Biology 40 (December 2017): 34–42. http://dx.doi.org/10.1016/j.pbi.2017.07.001.

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46

Seay, Montrell, Shalaka Patel, and Savithramma P. Dinesh-Kumar. "Autophagy and plant innate immunity." Cellular Microbiology 8, no. 6 (June 2006): 899–906. http://dx.doi.org/10.1111/j.1462-5822.2006.00715.x.

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47

Egorov, Ts A., and T. I. Odintsova. "Defense peptides of plant immunity." Russian Journal of Bioorganic Chemistry 38, no. 1 (January 2012): 1–9. http://dx.doi.org/10.1134/s1068162012010062.

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48

James, Andrew. "Plant immunity. Methods and protocols." Annals of Botany 111, no. 1 (January 2013): viii. http://dx.doi.org/10.1093/aob/mcs272.

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49

Jung, Ho Won, Timothy J. Tschaplinski, Lin Wang, Jane Glazebrook, and Jean T. Greenberg. "Priming in Systemic Plant Immunity." Science 324, no. 5923 (April 3, 2009): 89–91. http://dx.doi.org/10.1126/science.1170025.

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50

Schroeder, Frank C. "How bacteria subvert plant immunity." Science 388, no. 6744 (April 18, 2025): 252–53. https://doi.org/10.1126/science.adx0288.

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