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The pathogenic development of Sclerotinia sclerotiorum in soybean requires specific host NADPH oxidases
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/978-1-62703-278-0_11openalex-snapshot
Virus-Induced Gene Silencing in Soybean and Common Bean
inferredcites →https://doi.org/10.1016/j.bbamcr.2011.09.011openalex-snapshot
Protein phosphorylation is a prerequisite for the Ca2+-dependent activation of Arabidopsis NADPH oxidases and may function as a trigger for the positive feedback regulation of Ca2+ and reactive oxygen species
inferredcites →https://doi.org/10.1016/j.fbr.2007.10.001openalex-snapshot
Sclerotial development in Sclerotinia sclerotiorum: awakening molecular analysis of a “Dormant” structure
inferredcites →https://doi.org/10.1016/j.molcel.2014.02.021openalex-snapshot
Direct Regulation of the NADPH Oxidase RBOHD by the PRR-Associated Kinase BIK1 during Plant Immunity
inferredcites →https://doi.org/10.1016/j.pbi.2005.05.014openalex-snapshot
Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development
inferredcites →https://doi.org/10.1016/j.plantsci.2014.12.018openalex-snapshot
Pathogenic attributes of Sclerotinia sclerotiorum : Switching from a biotrophic to necrotrophic lifestyle
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot
ROS signaling: the new wave?
inferredcites →https://doi.org/10.1016/j.tplants.2011.10.001openalex-snapshot
A burst of plant NADPH oxidases
inferredcites →https://doi.org/10.1016/s0960-9822(00)00560-1openalex-snapshot
The hypersensitive response facilitates plant infection by the necrotrophic pathogen Botrytis cinerea
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth
inferredcites →https://doi.org/10.1038/nature08670openalex-snapshot
Genome sequence of the palaeopolyploid soybean
inferredcites →https://doi.org/10.1038/nri1312openalex-snapshot
NOX enzymes and the biology of reactive oxygen
inferredcites →https://doi.org/10.1042/bst20130242openalex-snapshot
Glyoxalases and stress tolerance in plants
inferredcites →https://doi.org/10.1046/j.1365-3040.2001.00778.xopenalex-snapshot
The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01342.xopenalex-snapshot
The plasma membrane oxidase NtrbohD is responsible for AOS production in elicited tobacco cells
inferredcites →https://doi.org/10.1073/pnas.012452499openalex-snapshot
Arabidopsis gp91 phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response
inferredcites →https://doi.org/10.1073/pnas.1221294110openalex-snapshot
Calcium-dependent protein kinase/NADPH oxidase activation circuit is required for rapid defense signal propagation
inferredcites →https://doi.org/10.1074/jbc.m109.058909openalex-snapshot
Structure of the N-terminal Regulatory Domain of a Plant NADPH Oxidase and Its Functional Implications
inferredcites →https://doi.org/10.1093/emboj/cdg277openalex-snapshot
NADPH oxidase AtrbohD and AtrbohF genes function in ROS‐dependent ABA signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/ert375openalex-snapshot
ROS as key players in plant stress signalling
inferredcites →https://doi.org/10.1093/nar/gkn180openalex-snapshot
Phylogeny.fr: robust phylogenetic analysis for the non-specialist
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SMART: recent updates, new developments and status in 2015
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The Pfam protein families database: towards a more sustainable future
inferredcites →https://doi.org/10.1093/pcp/pcv063openalex-snapshot
Regulation of the NADPH Oxidase RBOHD During Plant Immunity
inferredcites →https://doi.org/10.1094/mpmi-01-13-0014-ropenalex-snapshot
Characterization of the LOV1 -Mediated, Victorin-Induced, Cell-Death Response with Virus-Induced Gene Silencing
inferredcites →https://doi.org/10.1094/mpmi-21-5-0605openalex-snapshot
Oxalic Acid Is an Elicitor of Plant Programmed Cell Death during Sclerotinia sclerotiorum Disease Development
inferredcites →https://doi.org/10.1094/pdis-93-2-0149openalex-snapshot
Soybean Stem Lignin Concentration Relates to Resistance to Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1094/pdis.2002.86.9.971openalex-snapshot
Selected Soybean Plant Introductions with Partial Resistance to Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1104/pp.106.078089openalex-snapshot
Production of Reactive Oxygen Species by Plant NADPH Oxidases
inferredcites →https://doi.org/10.1104/pp.109.141994openalex-snapshot
Dual Roles of Reactive Oxygen Species and NADPH Oxidase RBOHD in an Arabidopsis- Alternaria Pathosystem
inferredcites →https://doi.org/10.1104/pp.109.151639openalex-snapshot
The Development of an Efficient Multipurpose Bean Pod Mottle Virus Viral Vector Set for Foreign Gene Expression and RNA Silencing
inferredcites →https://doi.org/10.1104/pp.111.185686openalex-snapshot
Soybean Homologs of MPK4 Negatively Regulate Defense Responses and Positively Regulate Growth and Development
inferredcites →https://doi.org/10.1104/pp.126.3.1281openalex-snapshot
Superoxide Production by Plant Homologues of the gp91phox NADPH Oxidase. Modulation of Activity by Calcium and by Tobacco Mosaic Virus Infection
inferredcites →https://doi.org/10.1105/tpc.106.048884openalex-snapshot
Calcium-Dependent Protein Kinases Regulate the Production of Reactive Oxygen Species by Potato NADPH Oxidase
inferredcites →https://doi.org/10.1105/tpc.107.055624openalex-snapshot
Regulation of Rice NADPH Oxidase by Binding of Rac GTPase to Its N-Terminal Extension
inferredcites →https://doi.org/10.1105/tpc.113.120642openalex-snapshot
Ca2+-Activated Reactive Oxygen Species Production by Arabidopsis RbohH and RbohJ Is Essential for Proper Pollen Tube Tip Growth
inferredcites →https://doi.org/10.1111/1462-2920.12818openalex-snapshot
pH dependency of sclerotial development and pathogenicity revealed by using genetically defined oxalate‐minus mutants of S clerotinia sclerotiorum
inferredcites →https://doi.org/10.1111/j.1364-3703.2005.00316.xopenalex-snapshot
Sclerotinia sclerotiorum (Lib.) de Bary: biology and molecular traits of a cosmopolitan pathogen
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04816.xopenalex-snapshot
AtRbohF is a crucial modulator of defence‐associated metabolism and a key actor in the interplay between intracellular oxidative stress and pathogenesis responses in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.1997.tb04778.xopenalex-snapshot
Reactive oxygen species and antioxidants: Relationships in green cells
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01787.xopenalex-snapshot
Seed dormancy and the control of germination
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03005.xopenalex-snapshot
The NADPH‐oxidase AtrbohB plays a role in Arabidopsis seed after‐ripening
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03509.xopenalex-snapshot
A Medicago truncatula NADPH oxidase is involved in symbiotic nodule functioning
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00808.xopenalex-snapshot
Alternative Splicing and Differential Expression of Two Transcripts of Nicotine Adenine Dinucleotide Phosphate Oxidase B Gene from Zea mays
inferredcites →https://doi.org/10.1111/mpp.12211openalex-snapshot
Oxaloacetate acetylhydrolase gene mutants of S clerotinia sclerotiorum do not accumulate oxalic acid, but do produce limited lesions on host plants
inferredcites →https://doi.org/10.1111/nph.12714openalex-snapshot
RbohB, a Phaseolus vulgaris NADPH oxidase gene, enhances symbiosome number, bacteroid size, and nitrogen fixation in nodules and impairs mycorrhizal colonization
inferredcites →https://doi.org/10.1111/ppl.12389openalex-snapshot
The plasma membrane NADPH oxidase OsRbohA plays a crucial role in developmental regulation and drought‐stress response in rice
inferredcites →https://doi.org/10.1111/tpj.12452openalex-snapshot
Pollen tube NAD (P)H oxidases act as a speed control to dampen growth rate oscillations during polarized cell growth
inferredcites →https://doi.org/10.1126/scisignal.2000448openalex-snapshot
The Plant NADPH Oxidase RBOHD Mediates Rapid Systemic Signaling in Response to Diverse Stimuli
inferredcites →https://doi.org/10.1134/s0003683810050017openalex-snapshot
Structural and functional characteristics of plant NADPH oxidase: A review
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141701openalex-snapshot
REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction
inferredcites →https://doi.org/10.1155/2012/217037openalex-snapshot
Reactive Oxygen Species, Oxidative Damage, and Antioxidative Defense Mechanism in Plants under Stressful Conditions
inferredcites →https://doi.org/10.1186/1471-2148-10-1openalex-snapshot
Genome size differentiates co-occurring populations of the planktonic diatom Ditylum brightwellii(Bacillariophyta)
inferredcites →https://doi.org/10.1186/1471-2148-10-8openalex-snapshot
BLAST-EXPLORER helps you building datasets for phylogenetic analysis
inferredcites →https://doi.org/10.1186/1756-0500-6-255openalex-snapshot
A virus-induced gene silencing method to study soybean cyst nematode parasitism in Glycine max
inferredcites →https://doi.org/10.1271/bbb.130092openalex-snapshot
AtRbohF Contributes to Non-Host Resistance toMagnaporthe oryzaein Arabidopsis
inferredcites →https://doi.org/10.1271/bbb.70216openalex-snapshot
Improved Gateway Binary Vectors: High-Performance Vectors for Creation of Fusion Constructs in Transgenic Analysis of Plants
inferredcites →https://doi.org/10.1371/journal.pgen.1002230openalex-snapshot
Genomic Analysis of the Necrotrophic Fungal Pathogens Sclerotinia sclerotiorum and Botrytis cinerea
inferredcites →https://doi.org/10.1371/journal.ppat.1002107openalex-snapshot
Tipping the Balance: Sclerotinia sclerotiorum Secreted Oxalic Acid Suppresses Host Defenses by Manipulating the Host Redox Environment
inferredcites →https://doi.org/10.1371/journal.ppat.1003287openalex-snapshot
Cell Death Control: The Interplay of Apoptosis and Autophagy in the Pathogenicity of Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1603/ipm11033openalex-snapshot
Biology, Yield loss and Control of Sclerotinia Stem Rot of Soybean
inferredcites →https://doi.org/10.3389/fpls.2015.00463openalex-snapshot
Tomato SlRbohB, a member of the NADPH oxidase family, is required for disease resistance against Botrytis cinerea and tolerance to drought stress
inferredcites →https://doi.org/10.3390/ijms14059440openalex-snapshot
Characterization of Rice NADPH Oxidase Genes and Their Expression under Various Environmental Conditions
inferredcites →https://doi.org/10.3390/ijms141224169openalex-snapshot
Genome-Wide Analysis of Respiratory Burst Oxidase Homologs in Grape (Vitis vinifera L.)
inferredcites →https://doi.org/10.3835/plantgenome2008.02.0091openalex-snapshot
Identification of Four Soybean Reference Genes for Gene Expression Normalization
inferredcites →https://doi.org/10.4161/psb.22455openalex-snapshot
Reactive oxygen species generation and signaling in plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Sclerotinia stem rot in tomato: a review on biology, pathogenicity, disease management and future research priorities
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SsCat2 encodes a catalase that is critical for the antioxidant response, QoI fungicide sensitivity, and pathogenicity of Sclerotinia sclerotiorum
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Antagonism of Plant Pathogens by Calotropis procera
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