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Novel findings on the role of signal exchange in arbuscular and ectomycorrhizal symbioses
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbic.200800477openalex-snapshot
Cooperative Biosynthesis of Trisporoids by the (+) and (−) Mating Types of the Zygomycete Blakeslea trispora
inferredcites →https://doi.org/10.1006/fgbi.1999.1138openalex-snapshot
Cell Wall Proteins of the Ectomycorrhizal Basidiomycete Pisolithus tinctorius: Identification, Function, and Expression in Symbiosis
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Mycorrhizal Development and Cytoskeleton
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Cloning and expression analysis of a new hydrophobin cDNA from the ectomycorrhizal basidiomycete Pisolithus
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Expression profiles of a phosphate transporter gene (GmosPT) from the endomycorrhizal fungus Glomus mosseae
inferredcites →https://doi.org/10.1007/s00572-007-0131-8openalex-snapshot
Flavonoids induce germination of basidiospores of the ectomycorrhizal fungus Suillus bovinus
inferredcites →https://doi.org/10.1007/s00572-011-0424-9openalex-snapshot
Modulation of ethanol stress tolerance by aldehyde dehydrogenase in the mycorrhizal fungus Tricholoma vaccinum
inferredcites →https://doi.org/10.1016/0378-1119(95)00725-3openalex-snapshot
Cloning and characterization of hydrophobins-encoding cDNAs from the ectomycorrhizal Basidiomycete Pisolithus tinctorius
inferredcites →https://doi.org/10.1016/b978-0-12-370526-6.x5001-6openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/j.chom.2012.09.003openalex-snapshot
Phytopathogen Effectors Subverting Host Immunity: Different Foes, Similar Battleground
inferredcites →https://doi.org/10.1016/j.cub.2011.05.033openalex-snapshot
A Secreted Effector Protein of Laccaria bicolor Is Required for Symbiosis Development
inferredcites →https://doi.org/10.1016/j.cub.2011.06.044openalex-snapshot
A Secreted Fungal Effector of Glomus intraradices Promotes Symbiotic Biotrophy
inferredcites →https://doi.org/10.1016/j.cub.2012.08.007openalex-snapshot
DAD2 Is an α/β Hydrolase Likely to Be Involved in the Perception of the Plant Branching Hormone, Strigolactone
inferredcites →https://doi.org/10.1016/j.cub.2012.09.043openalex-snapshot
A Common Signaling Process that Promotes Mycorrhizal and Oomycete Colonization of Plants
inferredcites →https://doi.org/10.1016/j.fgb.2012.01.002openalex-snapshot
Phylogenetic, genomic organization and expression analysis of hydrophobin genes in the ectomycorrhizal basidiomycete Laccaria bicolor
inferredcites →https://doi.org/10.1016/j.pbi.2012.04.004openalex-snapshot
Exploiting an ancient signalling machinery to enjoy a nitrogen fixing symbiosis
inferredcites →https://doi.org/10.1016/j.pbi.2012.08.010openalex-snapshot
Cellular programs for arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1016/j.pbi.2012.11.007openalex-snapshot
Symbiosis and the social network of higher plants
inferredcites →https://doi.org/10.1016/j.phytochem.2005.04.022openalex-snapshot
Biological activity of trisporoids and trisporoid analogues in Mucor mucedo (−)
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.014openalex-snapshot
Carotene derivatives in sexual communication of zygomycete fungi
inferredcites →https://doi.org/10.1016/j.tplants.2009.04.003openalex-snapshot
Strigolactones: discovery of the elusive shoot branching hormone
inferredcites →https://doi.org/10.1016/j.tplants.2012.10.003openalex-snapshot
The biology of strigolactones
inferredcites →https://doi.org/10.1016/s0065-2911(08)60154-xopenalex-snapshot
Hydrophobins: Proteins that Change the Nature of the Fungal Surface
inferredcites →https://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
inferredcites →https://doi.org/10.1038/2231178a0openalex-snapshot
Trisporic Acids: Sexual Hormones from Mucor mucedo and Blakeslea trispora
inferredcites →https://doi.org/10.1038/378626a0openalex-snapshot
A phosphate transporter from the mycorrhizal fungus Glomus versiforme
inferredcites →https://doi.org/10.1038/nature03608openalex-snapshot
Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1038/nature05248openalex-snapshot
Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis
inferredcites →https://doi.org/10.1038/nature06556openalex-snapshot
The genome of Laccaria bicolor provides insights into mycorrhizal symbiosis
inferredcites →https://doi.org/10.1038/nature09622openalex-snapshot
Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza
inferredcites →https://doi.org/10.1038/nature10454openalex-snapshot
Metabolic priming by a secreted fungal effector
inferredcites →https://doi.org/10.1038/nature10625openalex-snapshot
The Medicago genome provides insight into the evolution of rhizobial symbioses
inferredcites →https://doi.org/10.1038/nature10873openalex-snapshot
A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching
inferredcites →https://doi.org/10.1038/ncomms1046openalex-snapshot
Mechanisms underlying beneficial plant–fungus interactions in mycorrhizal symbiosis
inferredcites →https://doi.org/10.1038/ncomms1072openalex-snapshot
Breeding latitude drives individual schedules in a trans-hemispheric migrant bird
inferredcites →https://doi.org/10.1038/nrmicro1705openalex-snapshot
How rhizobial symbionts invade plants: the Sinorhizobium–Medicago model
inferredcites →https://doi.org/10.1038/nrmicro1987openalex-snapshot
Arbuscular mycorrhiza: the mother of plant root endosymbioses
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01848.xopenalex-snapshot
SC3 and SC4 hydrophobins have distinct roles in formation of aerial structures in dikaryons of Schizophyllum commune
inferredcites →https://doi.org/10.1073/pnas.0603228103openalex-snapshot
Legume genome evolution viewed through the Medicago truncatula and Lotus japonicus genomes
inferredcites →https://doi.org/10.1073/pnas.1313452110openalex-snapshot
Genome of an arbuscular mycorrhizal fungus provides insight into the oldest plant symbiosis
inferredcites →https://doi.org/10.1093/aob/mcl063openalex-snapshot
Strigolactones: Chemical Signals for Fungal Symbionts and Parasitic Weeds in Plant Roots
inferredcites →https://doi.org/10.1093/treephys/18.2.103openalex-snapshot
In vitro effects of Laccaria bicolor S238 N and Pseudomonas fluorescens strain BBc6 on rooting of de-rooted shoot hypocotyls of Norway spruce
inferredcites →https://doi.org/10.1094/mpmi-8-0252openalex-snapshot
Flavonoids Are Not Necessary Plant Signal Compounds in Arbuscular Mycorrhizal Symbioses
inferredcites →https://doi.org/10.1094/mpmi.2000.13.6.693openalex-snapshot
The Pre-Symbiotic Growth of Arbuscular Mycorrhizal Fungi Is Induced by a Branching Factor Partially Purified from Plant Root Exudates
inferredcites →https://doi.org/10.1094/mpmi.2001.14.10.1140openalex-snapshot
A Phosphate Transporter Gene from the Extra-Radical Mycelium of an Arbuscular Mycorrhizal Fungus Glomus intraradices Is Regulated in Response to Phosphate in the Environment
inferredcites →https://doi.org/10.1094/mpmi.2001.14.2.135openalex-snapshot
Characterization of Small GTPases Cdc42 and Rac and the Relationship Between Cdc42 and Actin Cytoskeleton in Vegetative and Ectomycorrhizal Hyphae of Suillus bovinus
inferredcites →https://doi.org/10.1104/pp.011882openalex-snapshot
A Diffusible Factor from Arbuscular Mycorrhizal Fungi Induces Symbiosis-Specific MtENOD11 Expression in Roots ofMedicago truncatula
inferredcites →https://doi.org/10.1104/pp.104.057034openalex-snapshot
Sequencing the Genespaces of Medicago truncatula and Lotus japonicus
inferredcites →https://doi.org/10.1104/pp.108.121400openalex-snapshot
GR24, a Synthetic Analog of Strigolactones, Stimulates the Mitosis and Growth of the Arbuscular Mycorrhizal FungusGigaspora roseaby Boosting Its Energy Metabolism
inferredcites →https://doi.org/10.1104/pp.109.141325openalex-snapshot
Truffles Regulate Plant Root Morphogenesis via the Production of Auxin and Ethylene
inferredcites →https://doi.org/10.1104/pp.109.147231openalex-snapshot
The Ectomycorrhizal FungusLaccaria bicolorStimulates Lateral Root Formation in Poplar and Arabidopsis through Auxin Transport and Signaling
inferredcites →https://doi.org/10.1104/pp.110.163774openalex-snapshot
Manipulating Broad-Spectrum Disease Resistance by Suppressing Pathogen-Induced Auxin Accumulation in Rice
inferredcites →https://doi.org/10.1104/pp.112.195990openalex-snapshot
Transcriptional Responses toward Diffusible Signals from Symbiotic Microbes Reveal MtNFP- and MtDMI3-Dependent Reprogramming of Host Gene Expression by Arbuscular Mycorrhizal Fungal Lipochitooligosaccharides
inferredcites →https://doi.org/10.1105/tpc.105.035410openalex-snapshot
Arbuscular Mycorrhizal Fungi Elicit a Novel Intracellular Apparatus in Medicago truncatula Root Epidermal Cells before Infection[W]
inferredcites →https://doi.org/10.1111/1758-2229.12029openalex-snapshot
LbNrt RNA silencing in the mycorrhizal symbiont L accaria bicolor reveals a nitrate‐independent regulatory role for a eukaryotic NRT2 ‐type nitrate transporter
inferredcites →https://doi.org/10.1111/j.1364-3703.2008.00470.xopenalex-snapshot
Indole‐3‐acetic acid (IAA) biosynthesis in the smut fungus Ustilago maydis and its relevance for increased IAA levels in infected tissue and host tumour formation
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07728.xopenalex-snapshot
Two linked genes encoding a secreted effector and a membrane protein are essential for Ustilago maydis‐induced tumour formation
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02522.xopenalex-snapshot
Nod factors and a diffusible factor from arbuscular mycorrhizal fungi stimulate lateral root formation in Medicago truncatula via the DMI1/DMI2 signalling pathway
inferredcites →https://doi.org/10.1111/j.1462-2920.2009.01912.xopenalex-snapshot
RNA silencing in the model mycorrhizal fungus Laccaria bicolor : gene knock‐down of nitrate reductase results in inhibition of symbiosis with Populus
inferredcites →https://doi.org/10.1111/j.1469-8137.1996.tb04342.xopenalex-snapshot
Analysis of factors involved in fungal recognition responses to host‐derived signals by arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02102.xopenalex-snapshot
Cloning of Pinus sylvestris SCARECROW gene and its expression pattern in the pine root system, mycorrhiza and NPA‐treated short roots
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03948.xopenalex-snapshot
The transcriptome of the arbuscular mycorrhizal fungus Glomus intraradices (DAOM 197198) reveals functional tradeoffs in an obligate symbiont
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04209.xopenalex-snapshot
Origin of strigolactones in the green lineage
inferredcites →https://doi.org/10.1111/nph.12120openalex-snapshot
Hydrogen peroxide‐regulated genes in the Medicago truncatula–Sinorhizobium meliloti symbiosis
inferredcites →https://doi.org/10.1111/nph.12146openalex-snapshot
Short‐chain chitin oligomers from arbuscular mycorrhizal fungi trigger nuclear C a 2+ spiking in M edicago truncatula roots and their production is enhanced by strigolactone
inferredcites →https://doi.org/10.1111/nph.12234openalex-snapshot
Combined phosphate and nitrogen limitation generates a nutrient stress transcriptome favorable for arbuscular mycorrhizal symbiosis in M edicago truncatula
inferredcites →https://doi.org/10.1111/pce.12036openalex-snapshot
Involvement of auxin pathways in modulating root architecture during beneficial plant–microorganism interactions
inferredcites →https://doi.org/10.1126/science.1128691openalex-snapshot
The Genome of Black Cottonwood, Populus trichocarpa (Torr. & Gray)
inferredcites →https://doi.org/10.1126/science.1205411openalex-snapshot
The Plant Cell Wall–Decomposing Machinery Underlies the Functional Diversity of Forest Fungi
inferredcites →https://doi.org/10.1128/aem.68.3.1408-1413.2002openalex-snapshot
Identification of a Hydrophobin Gene That is Developmentally Regulated in the Ectomycorrhizal Fungus Tricholoma terreum
inferredcites →https://doi.org/10.1146/annurev-phyto-073009-114447openalex-snapshot
Hormone Crosstalk in Plant Disease and Defense: More Than Just JASMONATE-SALICYLATE Antagonism
inferredcites →https://doi.org/10.1146/annurev.micro.58.030603.123749openalex-snapshot
SIGNALING IN THE ARBUSCULAR MYCORRHIZAL SYMBIOSIS
inferredcites →https://doi.org/10.1371/journal.pone.0044742openalex-snapshot
Heart of Endosymbioses: Transcriptomics Reveals a Conserved Genetic Program among Arbuscular Mycorrhizal, Actinorhizal and Legume-Rhizobial Symbioses
inferredcites →https://doi.org/10.1371/journal.ppat.1003177openalex-snapshot
Compatibility in the Ustilago maydis–Maize Interaction Requires Inhibition of Host Cysteine Proteases by the Fungal Effector Pit2
inferredcites →https://doi.org/10.1556/amicr.55.2008.2.5openalex-snapshot
Sexual attraction: On the role of fungal pheromone/receptor systems (A review)
inferredcites →https://doi.org/10.3389/fpls.2013.00204openalex-snapshot
Multiple control levels of root system remodeling in arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.3390/12071290openalex-snapshot
Flavonoids and Strigolactones in Root Exudates as Signals in Symbiotic and Pathogenic Plant-Fungus Interactions
inferredcites →https://doi.org/10.4161/psb.5.7.11896openalex-snapshot
Lateral root stimulation in the early interaction betweenArabidopsis thalianaand the ectomycorrhizal fungusLaccaria bicolor
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.e142356zenodo-depositor-declared
Suillus bovinus sesquiterpenes stimulate root growth and ramification of host and non-host plants by coordinating plant auxin signaling pathways
inferred← citeshttps://doi.org/10.1002/jobm.201500381openalex-snapshot
Dehydrogenase genes in the ectomycorrhizal fungus Tricholoma vaccinum: A role for Ald1 in mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1007/978-3-031-81904-9_5openalex-snapshot
Ectomycorrhizae for the Rescue: Ectomycorrhizosphere Signaling in Agroforestry and Afforestation
inferred← citeshttps://doi.org/10.1007/978-3-319-29532-9_10openalex-snapshot
10 Mycorrhizal Fungi and the Soil Carbon and Nutrient Cycling
inferred← citeshttps://doi.org/10.1007/978-3-319-71740-1_6openalex-snapshot
Volatiles in Communication of Agaricomycetes
inferred← citeshttps://doi.org/10.1007/978-981-10-6593-4_12openalex-snapshot
Harnessing the Plant Microbiome: A Key Towards Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-13-8487-5_6openalex-snapshot
Ectomycorrhizal Diversity and Tree Sustainability
inferred← citeshttps://doi.org/10.1007/s00572-015-0667-yopenalex-snapshot
The role of pre-symbiotic auxin signaling in ectendomycorrhiza formation between the desert truffle Terfezia boudieri and Helianthemum sessiliflorum
inferred← citeshttps://doi.org/10.1007/s00572-016-0758-4openalex-snapshot
Comparative genomics and expression levels of hydrophobins from eight mycorrhizal genomes
inferred← citeshttps://doi.org/10.1007/s00572-020-01005-2openalex-snapshot
Phytohormones and volatile organic compounds, like geosmin, in the ectomycorrhiza of Tricholoma vaccinum and Norway spruce (Picea abies)
inferred← citeshttps://doi.org/10.1007/s11056-017-9601-9openalex-snapshot
Prior contact of Pinus tabulaeformis with ectomycorrhizal fungi increases plant growth and survival from damping-off
inferred← citeshttps://doi.org/10.1007/s11356-015-4354-5openalex-snapshot
Hartig’ net formation of Tricholoma vaccinum-spruce ectomycorrhiza in hydroponic cultures
inferred← citeshttps://doi.org/10.1016/b978-0-323-91734-6.00001-6openalex-snapshot
Role of phytohormones in modulating plant microbe interaction
inferred← citeshttps://doi.org/10.1016/j.fbr.2023.100309openalex-snapshot
In search of the phytohormone functions in Fungi:Cytokinins
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101068openalex-snapshot
Arbuscular mycorrhizal fungi-mediated abiotic stress tolerance: Emerging roles in nutrient exchange, antioxidant defence, and hormonal crosstalk
inferred← citeshttps://doi.org/10.1039/c7cs00343aopenalex-snapshot
Chemical signaling involved in plant–microbe interactions
inferred← citeshttps://doi.org/10.1080/00275514.2025.2499439openalex-snapshot
The orchestration of ectomycorrhizal symbiosis: a review of fungal-produced symbiotic regulators and their functions
inferred← citeshttps://doi.org/10.1093/femsec/fiv120openalex-snapshot
Tricholoma vaccinumhost communication during ectomycorrhiza formation
inferred← citeshttps://doi.org/10.1093/treephys/tpae094openalex-snapshot
Inter-generational consistency of the ectomycorrhizal fungal community in a mixed pine–cedar post-fire stand
inferred← citeshttps://doi.org/10.1093/treephys/tpag065openalex-snapshot
Integrative omics analyses of ectomycorrhizal fungi modulate root growth and defense for mitigating aluminum toxicity in Pinus massoniana
inferred← citeshttps://doi.org/10.1111/1462-2920.13160openalex-snapshot
Influence of zygomycete‐derived D 'orenone on IAA signalling in T richoloma ‐spruce ectomycorrhiza
inferred← citeshttps://doi.org/10.1111/1462-2920.13670openalex-snapshot
The ectomycorrhizal basidiomycete Hebeloma cylindrosporum undergoes early waves of transcriptional reprogramming prior to symbiotic structures differentiation
inferred← citeshttps://doi.org/10.1111/nph.13546openalex-snapshot
Comparative genomics, proteomics and transcriptomics give new insight into the exoproteome of the basidiomycete H ebeloma cylindrosporum and its involvement in ectomycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1111/nph.18066openalex-snapshot
Mycorrhizal symbiosis pathway and edaphic fertility frame root economics space among tree species
inferred← citeshttps://doi.org/10.1111/ppl.13845openalex-snapshot
Unearthing the alteration in plant volatiles induced by mycorrhizal fungi: A shield against plant pathogens
inferred← citeshttps://doi.org/10.1371/journal.pone.0167773openalex-snapshot
Hydrophobins in the Life Cycle of the Ectomycorrhizal Basidiomycete Tricholoma vaccinum
inferred← citeshttps://doi.org/10.1371/journal.pone.0240886openalex-snapshot
Phytohormone production by the arbuscular mycorrhizal fungus Rhizophagus irregularis
inferred← citeshttps://doi.org/10.1590/01047760201723022342openalex-snapshot
Parapiptadenia rigida MYCORRHIZATION WITH SPORES OF Scleroderma citrinum
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3360728/v1openalex-snapshot
Mycorrhizal synthesis and physiological responses of Entoloma clypeatum and Malus robusta
inferred← citeshttps://doi.org/10.26686/wgtn.21974357openalex-snapshot
The interplay between host plants and priority effects in community assembly processes of arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.32604/phyton.2024.056114openalex-snapshot
Mycorrhizal Synthesis and Physiological Responses of Entoloma clypeatum and Three Rosaceae Fruit Trees
inferred← citeshttps://doi.org/10.3389/fevo.2019.00010openalex-snapshot
The Influence of Contrasting Microbial Lifestyles on the Pre-symbiotic Metabolite Responses of Eucalyptus grandis Roots
inferred← citeshttps://doi.org/10.3389/fmicb.2018.01646openalex-snapshot
Role of Phytohormones in Piriformospora indica-Induced Growth Promotion and Stress Tolerance in Plants: More Questions Than Answers
inferred← citeshttps://doi.org/10.3389/fmicb.2018.03015openalex-snapshot
Editorial: Mycorrhizosphere Communication: Mycorrhizal Fungi and Endophytic Fungus-Plant Interactions
inferred← citeshttps://doi.org/10.3389/fmicb.2019.00307openalex-snapshot
The Ectomycorrhizospheric Habitat of Norway Spruce and Tricholoma vaccinum: Promotion of Plant Growth and Fitness by a Rich Microorganismic Community
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1280485openalex-snapshot
Pre-symbiotic response of the compatible host spruce and low-compatibility host pine to the ectomycorrhizal fungus Tricholoma vaccinum
inferred← citeshttps://doi.org/10.3389/fpls.2016.01240openalex-snapshot
How Auxin and Cytokinin Phytohormones Modulate Root Microbe Interactions
inferred← citeshttps://doi.org/10.3389/fpls.2018.00546openalex-snapshot
The Hydrophobin-Like OmSSP1 May Be an Effector in the Ericoid Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.3390/biology13121044openalex-snapshot
Insights into the Biotic Factors Shaping Ectomycorrhizal Associations
inferred← citeshttps://doi.org/10.3844/ojbsci.2021.12.25openalex-snapshot
Arbuscular Mycorrhizae: Under-Tapped Potential Benefits and Perspective on Africa
inferred← citeshttps://doi.org/10.3897/imafungus.16.142356openalex-snapshot
Suillus bovinus sesquiterpenes stimulate root growth and ramification of host and non-host plants by coordinating plant auxin signaling pathways
inferred← citeshttps://doi.org/10.5586/am.1110openalex-snapshot
Strigolactones as mediators between fungi and plants
inferred← citeshttps://doi.org/10.5772/61331openalex-snapshot
Symbiotic Proteomics — State of the Art in Plant–Mycorrhizal Fungi Interactions
inferred← citeshttps://doi.org/10.63369/ijat.2026.22.2.959-976openalex-snapshot
Phytohormone-like activity of Volvariella volvacea (Bull. Ex Fr.) Singer
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