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Ss‐Rhs1, a secretory Rhs repeat‐containing protein, is required for the virulence of Sclerotinia sclerotiorum

https://doi.org/10.1111/mpp.12459
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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/jmbi.2000.4315openalex-snapshot
Predicting transmembrane protein topology with a hidden markov model: application to complete genomes11Edited by F. Cohen
inferredcites →https://doi.org/10.1007/bf01977314openalex-snapshot
Infection process of Rhizoctonia solani on Solanum tuberosum and effects of granular nematicides
inferredcites →https://doi.org/10.1007/bf02860868openalex-snapshot
The biology ofSclerotinia sclerotiorum,S. trifoliorum, andS. minor with emphasis on specific nomenclature
inferredcites →https://doi.org/10.1007/bf03356233openalex-snapshot
Ultrastructural and cytochemical studies on the infection process of Sclerotinia sclerotiorum in oilseed rape
inferredcites →https://doi.org/10.1007/s002849900107openalex-snapshot
Purification of endo polygalacturonases from Sclerotinia sclerotiorum: Multiplicity of the complex enzyme system
inferredcites →https://doi.org/10.1016/0022-2836(84)90054-8openalex-snapshot
A repetitive DNA sequence, rhs, responsible for duplications within the Escherichia coli K-12 chromosome
inferredcites →https://doi.org/10.1016/0048-4059(77)90008-xopenalex-snapshot
Penetration of carrot roots by the grey mould fungus Botrytis cinerea Pers. ex Pers
inferredcites →https://doi.org/10.1016/0885-5765(90)90010-uopenalex-snapshot
Use of mutants to demonstrate the role of oxalic acid in pathogenicity of Sclerotinia sclerotiorum on Phaseolus vulgaris
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.fgb.2005.01.002openalex-snapshot
RNA silencing as a tool for exploring gene function in ascomycete fungi
inferredcites →https://doi.org/10.1016/j.fgb.2012.12.002openalex-snapshot
Disruption of heat shock factor 1 reduces the formation of conidia and thermotolerance in the mycoparasitic fungus Coniothyrium minitans
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.pmpp.2004.07.004openalex-snapshot
Characterization and functional analysis of a cAMP-dependent protein kinase A catalytic subunit gene (pka1) in Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1016/j.pmpp.2010.09.001openalex-snapshot
Effect of Mitovirus infection on formation of infection cushions and virulence of Botrytis cinerea
inferredcites →https://doi.org/10.1016/j.pmpp.2015.04.005openalex-snapshot
Ss-Bi1 encodes a putative BAX inhibitor-1 protein that is required for full virulence of Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1016/s0007-1536(84)80105-9openalex-snapshot
Appressorium formation by Sclerotinia sclerotiorum: Scanning electron microscopy
inferredcites →https://doi.org/10.1016/s0378-1097(00)00500-0openalex-snapshot
aspS encoding an unusual aspartyl protease from Sclerotinia sclerotiorum is expressed during phytopathogenesis
inferredcites →https://doi.org/10.1016/s0378-1119(00)00388-7openalex-snapshot
Phylogenetic analysis of teneurin genes and comparison to the rearrangement hot spot elements of E. coli
inferredcites →https://doi.org/10.1016/s0378-1119(97)00330-2openalex-snapshot
A genetic selection for isolating cDNAs encoding secreted proteins
inferredcites →https://doi.org/10.1016/s0953-7562(09)81027-7openalex-snapshot
Developmental biology of sclerotia
inferredcites →https://doi.org/10.1021/bi9908641openalex-snapshot
Identification and Dynamics of a Heparin-Binding Site in Hepatocyte Growth Factor
inferredcites →https://doi.org/10.1038/nature10923openalex-snapshot
Trans-synaptic Teneurin signalling in neuromuscular synapse organization and target choice
inferredcites →https://doi.org/10.1038/nature10926openalex-snapshot
Teneurins instruct synaptic partner matching in an olfactory map
inferredcites →https://doi.org/10.1038/nature12465openalex-snapshot
The BC component of ABC toxins is an RHS-repeat-containing protein encapsulation device
inferredcites →https://doi.org/10.1038/nmeth.1701openalex-snapshot
SignalP 4.0: discriminating signal peptides from transmembrane regions
inferredcites →https://doi.org/10.1073/pnas.1109285109openalex-snapshot
An rhs gene of Pseudomonas aeruginosa encodes a virulence protein that activates the inflammasome
inferredcites →https://doi.org/10.1073/pnas.1300627110openalex-snapshot
Rhs proteins from diverse bacteria mediate intercellular competition
inferredcites →https://doi.org/10.1080/07060669409500766openalex-snapshot
Index of plant hosts of Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1094/mpmi-02-12-0049-ropenalex-snapshot
XadM, a Novel Adhesin of Xanthomonas oryzae pv. oryzae, Exhibits Similarity to Rhs Family Proteins and Is Required for Optimum Attachment, Biofilm Formation, and Virulence
inferredcites →https://doi.org/10.1094/mpmi-05-13-0145-ropenalex-snapshot
Novel Secretory Protein Ss-Caf1 of the Plant-Pathogenic Fungus Sclerotinia sclerotiorum Is Required for Host Penetration and Normal Sclerotial Development
inferredcites →https://doi.org/10.1094/mpmi-06-11-0159openalex-snapshot
Sclerotinia sclerotiorumγ-Glutamyl Transpeptidase (Ss-Ggt1) Is Required for Regulating Glutathione Accumulation and Development of Sclerotia and Compound Appressoria
inferredcites →https://doi.org/10.1094/mpmi-18-0849openalex-snapshot
An Endopolygalacturonase from Sclerotinia sclerotiorum Induces Calcium-Mediated Signaling and Programmed Cell Death in Soybean Cells
inferredcites →https://doi.org/10.1094/mpmi-20-8-0944openalex-snapshot
Type 2A Phosphoprotein Phosphatase Is Required for Asexual Development and Pathogenesis of Sclerotinia sclerotiorum
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/mpmi-22-7-0783openalex-snapshot
Gene Disruption of an Arabinofuranosidase/β-Xylosidase Precursor DecreasesSclerotinia sclerotiorumVirulence on Canola Tissue
inferredcites →https://doi.org/10.1094/mpmi.2003.16.9.785openalex-snapshot
The Sclerotinia sclerotiorum pac1 Gene Is Required for Sclerotial Development and Virulence
inferredcites →https://doi.org/10.1094/mpmi.2004.17.12.1402openalex-snapshot
Relationships Among Endo-Polygalacturonase, Oxalate, pH, and Plant Polygalacturonase-Inhibiting Protein (PGIP) in the Interaction Between Sclerotinia sclerotiorum and Soybean
inferredcites →https://doi.org/10.1094/mpmi.2004.17.4.404openalex-snapshot
MAPK Regulation of Sclerotial Development in Sclerotinia sclerotiorum Is Linked with pH and cAMP Sensing
inferredcites →https://doi.org/10.1094/phyto-69-904openalex-snapshot
Control of Plant Diseases Caused bySclerotiniaSpecies
inferredcites →https://doi.org/10.1094/phyto-95-0397openalex-snapshot
Changes in Protein Kinase A Activity Accompany Sclerotial Development inSclerotinia sclerotiorum
inferredcites →https://doi.org/10.1105/tpc.12.11.2191openalex-snapshot
Oxalic Acid, a Pathogenicity Factor for Sclerotinia sclerotiorum, Suppresses the Oxidative Burst of the Host Plant
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb01574.xopenalex-snapshot
Molecular analysis of three major wall‐associated proteins of Bacillus subtilis 168: evidence for processing of the product of a gene encoding a 258 kDa precursor two‐domain ligand‐binding protein
inferredcites →https://doi.org/10.1111/j.1365-2958.1994.tb01074.xopenalex-snapshot
Rhs elements of Escherichia coli: a family of genetic composites each encoding a large mosaic protein
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04390.xopenalex-snapshot
cAMP blocks MAPK activation and sclerotial development via Rap‐1 in a PKA‐independent manner in Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06270.xopenalex-snapshot
The novel Cladosporium fulvum lysin motif effector Ecp6 is a virulence factor with orthologues in other fungal species
inferredcites →https://doi.org/10.1111/j.1365-3059.1995.tb02712.xopenalex-snapshot
Early stages of infection of rapeseed petals and leaves by Sclerotinia sclerotiorum revealed by scanning electron microscopy
inferredcites →https://doi.org/10.1111/mpp.12239openalex-snapshot
Fungal oxalate decarboxylase activity contributes to S clerotinia sclerotiorum early infection by affecting both compound appressoria development and function
inferredcites →https://doi.org/10.1126/science.1190859openalex-snapshot
Conserved Fungal LysM Effector Ecp6 Prevents Chitin-Triggered Immunity in Plants
inferredcites →https://doi.org/10.1128/aem.57.5.1478-1484.1991openalex-snapshot
Production of Cell Wall-Degrading Enzymes by the Phytopathogenic Fungus Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1128/iai.53.3.573-581.1986openalex-snapshot
Cell surface binding site for Clostridium difficile enterotoxin: evidence for a glycoconjugate containing the sequence Gal alpha 1-3Gal beta 1-4GlcNAc
inferredcites →https://doi.org/10.1128/iai.73.3.1735-1743.2005openalex-snapshot
Identification of Enterohemorrhagic Escherichia coli O26:H − Genes Required for Intestinal Colonization in Calves
inferredcites →https://doi.org/10.1128/jb.180.16.4102-4110.1998openalex-snapshot
Rhs Elements Comprise Three Subfamilies Which Diverged Prior to Acquisition by Escherichia coli
inferredcites →https://doi.org/10.1146/annurev.py.13.090175.001125openalex-snapshot
Sclerotial Morphogenesis in Fungi
inferredcites →https://doi.org/10.1186/1471-2164-15-336openalex-snapshot
Secretome analysis reveals effector candidates associated with broad host range necrotrophy in the fungal plant pathogen Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1186/1471-2229-11-110openalex-snapshot
Fusarium graminearum forms mycotoxin producing infection structures on wheat
inferredcites →https://doi.org/10.1371/journal.pone.0027217openalex-snapshot
Rust Secreted Protein Ps87 Is Conserved in Diverse Fungal Pathogens and Contains a RXLR-like Motif Sufficient for Translocation into Plant Cells
inferredcites →https://doi.org/10.1371/journal.pone.0034962openalex-snapshot
Ss-Sl2, a Novel Cell Wall Protein with PAN Modules, Is Essential for Sclerotial Development and Cellular Integrity of Sclerotinia sclerotiorum
inferredcites →https://doi.org/10.1371/journal.pone.0053901openalex-snapshot
A Secretory Protein of Necrotrophic Fungus Sclerotinia sclerotiorum That Suppresses Host Resistance
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/10.1534/genetics.107.076182openalex-snapshot
Triple Mutants Uncover Three New Genes Required for Social Motility inMyxococcus xanthus

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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A GDSL-lipase,SsGLIP1, is involved in regulating the sclerotia formation and virulence of Sclerotinia sclerotiorum
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The complexity of the Sclerotinia sclerotiorum pathosystem in soybean: virulence factors, resistance mechanisms, and their exploitation to control Sclerotinia stem rot
inferred← citeshttps://doi.org/10.1007/s40858-023-00571-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111732openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cj.2024.01.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fgb.2024.103896openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.funbio.2021.09.004openalex-snapshot
The cAMP-dependent protein kinase A pathway perturbs autophagy and plays important roles in development and virulence of Sclerotinia sclerotiorum
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The glycoside hydrolase 7 member VdGH7a regulates Verticillium dahliae pathogenicity and induces host defenses by interacting with GhOLP1
inferred← citeshttps://doi.org/10.1016/j.jia.2025.02.014openalex-snapshot
SsBMR1 as a putative ABC transporter is required for pathogenesis by promoting antioxidant export and antifungal resistance in Sclerotinia sclerotiorum
inferred← citeshttps://doi.org/10.1016/j.micres.2022.126981openalex-snapshot
Host-induced gene silencing reveals the role of Sclerotinia sclerotiorum oxaloacetate acetylhydrolase gene in fungal oxalic acid accumulation and virulence
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100046openalex-snapshot
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Biocontrol potential of Penicillium manginii SWU-P6 against Sclerotinia rot of cabbage and its complete genome sequence analysis
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c07351openalex-snapshot
Sclerotinia Stem Rot Resistance in Rapeseed: Recent Progress and Future Prospects
inferred← citeshttps://doi.org/10.1038/s41467-021-27388-0openalex-snapshot
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Simultaneous Transcriptome Analysis of Host and Pathogen Highlights the Interaction Between Brassica oleracea and Sclerotinia sclerotiorum
inferred← citeshttps://doi.org/10.1101/2020.01.09.900217openalex-snapshot
Sclerotinia sclerotiorum hijacks copper from its host for infection
inferred← citeshttps://doi.org/10.1111/jipb.70175openalex-snapshot
OsPDCB1 mediates plasmodesmal callose defense and is targeted by a conserved planthopper effector
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Survival factor 1 contributes to the oxidative stress response and is required for full virulence of Sclerotinia sclerotiorum
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Sclerotinia sclerotiorum Thioredoxin1 (SsTrx1) is required for pathogenicity and oxidative stress tolerance
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Host-Induced Gene Silencing of a Multifunction Gene Sscnd1 Enhances Plant Resistance Against Sclerotinia sclerotiorum
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Genome scale analysis of Arabidopsis thaliana quantitative disease resistance to the generalist fungal pathogen Sclerotinia sclerotiorum
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