References

10.1002/9781118951446

10.1002/9781118951446 · ExternalCitation · doi-reference

10.1002/9781119803041

10.1002/9781119803041 · ExternalCitation · doi-reference

Development and recent progress on ammonia synthesis catalysts for the Haber–Bosch process

10.1002/aesr.202000043 · ExternalCitation · doi-reference

PAMP recognition and the plant–pathogen arms race

10.1002/bies.20457 · ExternalCitation · doi-reference

Microbial modulation of hormone signaling, proteomic dynamics, and metabolomics in plant drought adaptation

10.1002/fes3.513 · ExternalCitation · doi-reference

Climate change impacts on global agricultural water deficit

10.1002/grl.50279 · ExternalCitation · doi-reference

Hydrogen peroxide staining to visualize intracellular bacterial infections of seedling root cells

10.1002/jemt.22375 · ExternalCitation · doi-reference

Root exudation of sugars, amino acids, and organic acids by maize as affected by nitrogen, phosphorus, potassium, and iron deficiency

10.1002/jpln.201000085 · ExternalCitation · doi-reference

10.1007/1-4020-4152-7

10.1007/1-4020-4152-7 · ExternalCitation · doi-reference

10.1007/3-540-27675-0

10.1007/3-540-27675-0 · ExternalCitation · doi-reference

10.1007/978-3-030-66587-6

10.1007/978-3-030-66587-6 · ExternalCitation · doi-reference

10.1007/978-90-481-2666-8

10.1007/978-90-481-2666-8 · ExternalCitation · doi-reference

10.1007/978-94-007-2214-9_3

10.1007/978-94-007-2214-9_3 · ExternalCitation · doi-reference

10.1007/978-94-011-3336-4

10.1007/978-94-011-3336-4 · ExternalCitation · doi-reference

10.1007/978-94-011-5060-6

10.1007/978-94-011-5060-6 · ExternalCitation · doi-reference

10.1007/978-981-10-5589-8

10.1007/978-981-10-5589-8 · ExternalCitation · doi-reference

10.1007/978-981-10-8402-7_11

10.1007/978-981-10-8402-7_11 · ExternalCitation · doi-reference

10.1007/978-981-99-8220-2

10.1007/978-981-99-8220-2 · ExternalCitation · doi-reference

The effects of root-induced pH changes on the depletion of inorganic and organic phosphorus in the rhizosphere

10.1007/bf00007872 · ExternalCitation · doi-reference

Phosphorus efficiency and the forms of soil phosphorus utilized by upland rice cultivars

10.1007/bf00007917 · ExternalCitation · doi-reference

Biological nitrogen fixation for sustainable agriculture: A perspective

10.1007/bf00011307 · ExternalCitation · doi-reference

External hyphal production of vesicular–arbuscular mycorrhizal fungi in pasture and tallgrass prairie communities

10.1007/bf00328420 · ExternalCitation · doi-reference

Nodulation of actinorhizal plants by Frankia strains capable of both root hair infection and intercellular penetration

10.1007/bf01281689 · ExternalCitation · doi-reference

Geosiphon pyriforme, a fungus forming endocytobiosis with Nostoc (cyanobacteria), is an ancestral member of the Glomales: Evidence by SSU rRNA analysis

10.1007/bf02352301 · ExternalCitation · doi-reference

Hopanoid biosynthesis and function in bacteria

10.1007/s001140050592 · ExternalCitation · doi-reference

Salt-tolerant plant growth-promoting bacteria as a versatile tool for combating salt stress in crop plants

10.1007/s00203-024-04071-8 · ExternalCitation · doi-reference

Engineering phosphoribosylpyrophosphate synthetase in Methylobacterium radiotolerans for lettuce growth and quality enhancement

10.1007/s00203-026-04869-8 · ExternalCitation · doi-reference

Mycorrhizae helper bacteria: Unlocking their potential as bioenhancers of plant–arbuscular mycorrhizal fungal associations

10.1007/s00248-021-01831-7 · ExternalCitation · doi-reference

Cytokinin-producing, plant growth-promoting rhizobacteria that confer resistance to drought stress in Platycladus orientalis container seedlings

10.1007/s00253-013-5193-2 · ExternalCitation · doi-reference

Investigation of endophytic bacterial community in supposedly axenic cultures of pineapple and orchids with evidence of abundant intracellular bacteria

10.1007/s00284-016-1163-0 · ExternalCitation · doi-reference

Arthrobacter sp. inoculation improves cactus pear growth, fruit quality, and the nutraceutical properties of cladodes

10.1007/s00284-023-03368-z · ExternalCitation · doi-reference

Dual PGPR-AMF inoculation offsets salinity stress impact on the fodder halophyte Sulla carnosa by concomitantly modulating plant ABA content and leaf antioxidant response

10.1007/s00344-024-11438-0 · ExternalCitation · doi-reference

Alleviation of drought stress effects in sunflower seedlings by the exopolysaccharide-producing Pseudomonas putida strain GAP-P45

10.1007/s00374-009-0401-z · ExternalCitation · doi-reference

Microbial interactions in the rhizosphere: Beneficial influences of plant growth-promoting rhizobacteria on nutrient acquisition processes—A review

10.1007/s00374-015-0996-1 · ExternalCitation · doi-reference

Bacteria associated with spores of arbuscular mycorrhizal fungi: A review

10.1007/s00374-026-01998-6 · ExternalCitation · doi-reference

Paraglomus and Glomus arbuscular mycorrhizal fungi induce the green tea catechin quality index and phosphorus bioavailability in tropical soils

10.1007/s00572-025-01185-9 · ExternalCitation · doi-reference

Intricate phytohormonal orchestration mediates mycorrhizal symbiosis and stress tolerance

10.1007/s00572-025-01189-5 · ExternalCitation · doi-reference

Hyphosphere interactions: P-solubilizing fungi modulate AMF phosphatase activity and mycorrhizal symbiosis via exudate-mediated communication

10.1007/s00572-025-01242-3 · ExternalCitation · doi-reference

MAPK signaling pathway and rhizosphere modulation: Mechanisms of arbuscular mycorrhizal symbiosis in enhancing Phragmites communis tolerance to triclocarban stress

10.1007/s00572-026-01291-2 · ExternalCitation · doi-reference

Recent advances in research on phosphate starvation signaling in plants

10.1007/s10265-024-01545-0 · ExternalCitation · doi-reference

Beneficial bacteria of agricultural importance

10.1007/s10529-010-0347-0 · ExternalCitation · doi-reference

A search for glomuferrin: A potential siderophore of arbuscular mycorrhizal fungi of the genus Glomus

10.1007/s10534-017-0026-x · ExternalCitation · doi-reference

Induction of defence responses in cacao against Phytophthora palmivora by Pseudomonas chlororaphis CP07

10.1007/s10658-024-02982-2 · ExternalCitation · doi-reference

Elucidating multifaceted urease-producing marine Pseudomonas aeruginosa BG as a cogent PGPR and biocontrol agent

10.1007/s10725-014-9949-1 · ExternalCitation · doi-reference

Enhancing soil health and crop productivity: The role of zinc-solubilizing bacteria in sustainable agriculture

10.1007/s10725-025-01294-7 · ExternalCitation · doi-reference

The significant effects of strigolactones on plant growth and microbe interactions: A review

10.1007/s10725-025-01325-3 · ExternalCitation · doi-reference

Rhizosphere: Biophysics, biogeochemistry, and ecological relevance

10.1007/s11104-008-9885-9 · ExternalCitation · doi-reference

Carbon flow in the rhizosphere: Carbon trading at the soil–root interface

10.1007/s11104-009-9925-0 · ExternalCitation · doi-reference

Endophytic colonization of Arabidopsis thaliana by Gluconacetobacter diazotrophicus and its effect on plant growth promotion, plant physiology, and activation of plant defense

10.1007/s11104-015-2672-5 · ExternalCitation · doi-reference

In situ observation of localized, sub-millimeter-scale changes in phosphorus biogeochemistry in the rhizosphere

10.1007/s11104-017-3542-0 · ExternalCitation · doi-reference

Exploring the secrets of the hyphosphere of arbuscular mycorrhizal fungi: Processes and ecological functions

10.1007/s11104-022-05621-z · ExternalCitation · doi-reference

Arbuscular mycorrhiza: Advances and retreats in our understanding of the ecological functioning of the mother of all root symbioses

10.1007/s11104-023-06045-z · ExternalCitation · doi-reference

Arbuscular mycorrhizal fungi affect root morphology locally but not systemically through altering nutrient- and phytohormone-related gene expression at low soil P levels

10.1007/s11104-024-07150-3 · ExternalCitation · doi-reference

Endophytic interaction of the plant growth-promoting strain Pantoea dispersa UYSB45 and sweet sorghum (Sorghum bicolor) plants

10.1007/s11104-025-07598-x · ExternalCitation · doi-reference

Arbuscular mycorrhizal fungi-mediated hormonal interplay under drought stress conditions: Current insights and future directions

10.1007/s11104-025-07972-9 · ExternalCitation · doi-reference

Effects of co-inoculation of plant growth-promoting bacteria and Rhizoglomus clarum on growth, nutrition, and the root microbiome of first-season maize

10.1007/s11104-026-08546-z · ExternalCitation · doi-reference

Common mycorrhizal networks regulate nutrient-and hormone-related gene expression in tomato under a tomato–potato–onion intercropping system

10.1007/s11104-026-08661-x · ExternalCitation · doi-reference

Bacteriosomes in axenic plants: Endophytes as stable endosymbionts

10.1007/s11274-009-0073-8 · ExternalCitation · doi-reference

The role of protons excreted by Advenella kashmirensis DF12 during ammonium assimilation in phosphate solubilization

10.1007/s11274-024-04087-8 · ExternalCitation · doi-reference

Assessing the impact of arsenic on symbiotic and free-living PGPB: Plant growth-promoting traits, bacterial compatibility, and adhesion on soybean seed

10.1007/s11274-024-04233-2 · ExternalCitation · doi-reference

Effect of salinity stress on plants and its tolerance strategies: A review

10.1007/s11356-014-3739-1 · ExternalCitation · doi-reference

Forms of nitrogen uptake, translocation, and transfer via arbuscular mycorrhizal fungi: A review

10.1007/s11427-012-4330-y · ExternalCitation · doi-reference

Microbial biofortification of iron in Solanum tuberosum L. through siderophore-producing rhizobacteria along with L-tryptophan and iron sulfate supply

10.1007/s11540-024-09785-2 · ExternalCitation · doi-reference

Arbuscular mycorrhiza symbiosis—From molecular dialogues to biotechnological applications

10.1007/s11557-025-02084-1 · ExternalCitation · doi-reference

Diversity and plant growth properties of rhizospheric bacteria associated with medicinal plants

10.1007/s12088-024-01275-w · ExternalCitation · doi-reference

Plant growth-promoting bacteria induce antioxidant tolerance against salinity stress through biochemical and physiological mechanisms

10.1007/s12298-022-01128-0 · ExternalCitation · doi-reference

Efficiency of arbuscular mycorrhizal fungi for the growth promotion of sugarcane under pot conditions

10.1007/s12355-022-01129-z · ExternalCitation · doi-reference

Plant–mycorrhiza communication and mycorrhizae in inter-plant communication

10.1007/s13199-022-00837-0 · ExternalCitation · doi-reference

Streptomyces consortia-mediated plant growth promotion and yield performance in chickpea

10.1007/s13205-022-03389-8 · ExternalCitation · doi-reference

Effects of Rhizobium inoculum compared with mineral nitrogen fertilizer on nodulation and seed yield of common bean: A meta-analysis

10.1007/s13593-022-00784-6 · ExternalCitation · doi-reference

Arbuscular mycorrhizal and dark septate endophytic fungal symbioses in three different citrus species from hillside orchards of north-eastern India

10.1007/s40003-025-00870-7 · ExternalCitation · doi-reference

Drought and its impacts on plants: A short review

10.1007/s40011-025-01715-7 · ExternalCitation · doi-reference

Strategies for managing fungicide resistance in the Brazilian tropical agroecosystem: Safeguarding food safety, health, and environmental quality

10.1007/s40858-023-00632-2 · ExternalCitation · doi-reference

Phosphate-solubilizing microorganisms: Mechanisms and their role in phosphate solubilization and uptake

10.1007/s42729-020-00342-7 · ExternalCitation · doi-reference

The mode of integration between Azotobacter and Rhizobium affects plant growth, yield, and physiological responses of pea (Pisum sativum L.)

10.1007/s42729-021-00727-2 · ExternalCitation · doi-reference

Phosphorus-solubilizing rhizobacteria improve P availability to mung bean via enhanced soil phosphatase activity and promote its growth

10.1007/s42729-023-01473-3 · ExternalCitation · doi-reference

Harnessing the efficacy of a Rhizobium strain in individual and consortium modes to promote sustainable lentil production and biofortification under diverse soil conditions

10.1007/s42729-024-01900-z · ExternalCitation · doi-reference

Revealing the mechanisms behind high potassium efficiency in vegetable soybean through rhizospheric microbial community recruitment and potassium activation

10.1007/s42832-026-0488-2 · ExternalCitation · doi-reference

Enacting partner specificity in legume–rhizobia symbioses

10.1007/s42994-024-00193-1 · ExternalCitation · doi-reference

Influence of sugar metabolism on the dialogue between arbuscular mycorrhizal fungi and plants

10.1007/s44281-023-00001-8 · ExternalCitation · doi-reference

Beneficial networking between AMF and plants leads to improved stress tolerance

10.1007/s44372-026-00494-3 · ExternalCitation · doi-reference

Soil fertility improvement using Paenibacillus spp. as biofertiliser in the Paloh Jenang oil palm plantation

10.1007/s44447-026-00137-9 · ExternalCitation · doi-reference

Adaptation in bacterial chemotaxis: CheB-dependent modification permits additional methylations of sensory transducer proteins

10.1016/0092-8674(82)90438-x · ExternalCitation · doi-reference

Demonstration of abscisic acid in spores and hyphae of the arbuscular-mycorrhizal fungus Glomus and in the N2-fixing cyanobacterium Anabaena variabilis

10.1016/0168-9452(94)90115-5 · ExternalCitation · doi-reference

10.1016/b978-0-12-805251-8.00002-8

10.1016/b978-0-12-805251-8.00002-8 · ExternalCitation · doi-reference

10.1016/b978-0-12-819773-8.00003-4

10.1016/b978-0-12-819773-8.00003-4 · ExternalCitation · doi-reference

A critical review of soil phosphorus dynamics and biogeochemical processes for unlocking soil phosphorus reserves

10.1016/bs.agron.2024.02.004 · ExternalCitation · doi-reference

Veh1 modulates Ca2+ dynamics through VdMid1 and VdMcu1 to control hyphopodium-mediated infection in Verticillium dahliae

10.1016/j.abiote.2026.100076 · ExternalCitation · doi-reference

Relationship between phosphorus uptake via indigenous arbuscular mycorrhizal fungi and crop response: A 32P-labeling study

10.1016/j.apsoil.2022.104624 · ExternalCitation · doi-reference

Regulation of the chemotaxis histidine kinase CheA: A structural perspective

10.1016/j.bbamem.2019.183030 · ExternalCitation · doi-reference

Synergistic effects of arbuscular mycorrhizal fungi associated with plant growth-promoting rhizobacteria in the suppression of soil-borne Fusarium wilt of date palm

10.1016/j.bcab.2023.102753 · ExternalCitation · doi-reference

Unlocking plant defenses: Harnessing the power of beneficial microorganisms for induced systemic resistance in vegetables—A systematic review

10.1016/j.biocontrol.2023.105428 · ExternalCitation · doi-reference

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10.1016/j.cell.2024.03.045 · ExternalCitation · doi-reference

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10.1016/j.cell.2024.12.024 · ExternalCitation · doi-reference

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10.1016/j.celrep.2024.114910 · ExternalCitation · doi-reference

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10.1016/j.chom.2014.01.011 · ExternalCitation · doi-reference

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10.1016/j.copbio.2024.103150 · ExternalCitation · doi-reference

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10.1016/j.cpb.2026.100587 · ExternalCitation · doi-reference

A CCaMK–CYCLOPS–DELLA complex activates transcription of RAM1 to regulate arbuscule branching

10.1016/j.cub.2016.01.069 · ExternalCitation · doi-reference

The genome of Geosiphon pyriformis reveals ancestral traits linked to the emergence of the arbuscular mycorrhizal symbiosis

10.1016/j.cub.2021.01.058 · ExternalCitation · doi-reference

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10.1016/j.cub.2023.05.057 · ExternalCitation · doi-reference

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10.1016/j.cub.2023.06.057 · ExternalCitation · doi-reference

Plant–microbe interactions: Plant-exuded myo-inositol attracts specific bacterial taxa

10.1016/j.cub.2023.06.066 · ExternalCitation · doi-reference

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10.1016/j.cub.2024.03.015 · ExternalCitation · doi-reference

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10.1016/j.ejsobi.2018.12.002 · ExternalCitation · doi-reference

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10.1016/j.envexpbot.2024.106010 · ExternalCitation · doi-reference

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10.1016/j.envres.2022.115200 · ExternalCitation · doi-reference

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10.1016/j.geoderma.2004.12.038 · ExternalCitation · doi-reference

Alkaline phosphatase activity mediates soil organic phosphorus mineralization in a subalpine forest ecosystem

10.1016/j.geoderma.2021.115376 · ExternalCitation · doi-reference

Effect of the strigolactone analogs methyl phenlactonoates on spore germination and root colonization of arbuscular mycorrhizal fungi

10.1016/j.heliyon.2018.e00936 · ExternalCitation · doi-reference

An extensive review on the consequences of chemical pesticides on human health and the environment

10.1016/j.jclepro.2020.124657 · ExternalCitation · doi-reference

Soil salinity under climate change: Challenges for sustainable agriculture and food security

10.1016/j.jenvman.2020.111736 · ExternalCitation · doi-reference

Low-phosphorus stress induces GmSTOP1-3-mediated organic acid exudation to recruit phosphate-solubilizing bacteria for organic phosphorus mineralization in soybean rhizosphere

10.1016/j.jia.2025.08.015 · ExternalCitation · doi-reference

The biofilm regulatory network from Bacillus subtilis: A structure–function analysis

10.1016/j.jmb.2022.167923 · ExternalCitation · doi-reference

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10.1016/j.mib.2024.102526 · ExternalCitation · doi-reference

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10.1016/j.mib.2025.102660 · ExternalCitation · doi-reference

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Growth-promoting bacteria and arbuscular mycorrhizal fungus enhance maize tolerance to saline stress

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Plant growth-promoting microorganisms: New insights and the way forward

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Arbuscular mycorrhizal fungi and their role in plant disease control: A state-of-the-art

10.1016/j.microb.2025.100438 · ExternalCitation · doi-reference

Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications

10.1016/j.molp.2021.12.005 · ExternalCitation · doi-reference

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10.1016/j.pbi.2014.03.001 · ExternalCitation · doi-reference

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Exploiting root exudates to manage soil-borne disease complexes in a changing climate

10.1016/j.tim.2023.07.011 · ExternalCitation · doi-reference

Swimming towards each other: The role of chemotaxis in bacterial interactions

10.1016/j.tim.2023.12.008 · ExternalCitation · doi-reference

Small peptides: Novel targets for modulating plant–rhizosphere microbe interactions

10.1016/j.tim.2024.03.011 · ExternalCitation · doi-reference

A resurrected scenario: Single gain and massive loss of nitrogen-fixing nodulation

10.1016/j.tplants.2018.10.005 · ExternalCitation · doi-reference

Root exudates impact plant performance under abiotic stress

10.1016/j.tplants.2021.08.003 · ExternalCitation · doi-reference

Arbuscular mycorrhizal fungi conducting the hyphosphere bacterial orchestra

10.1016/j.tplants.2021.10.008 · ExternalCitation · doi-reference

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10.1016/j.xplc.2020.100104 · ExternalCitation · doi-reference

Cellular basis of legume–rhizobium symbiosis

10.1016/j.xplc.2024.101045 · ExternalCitation · doi-reference

ABA promotes fatty acid biosynthesis and transport to boost arbuscular mycorrhizal symbiosis in apple roots

10.1016/j.xplc.2025.101426 · ExternalCitation · doi-reference

Bacteria associated with Glomus clarum spores influence mycorrhizal activity

10.1016/s0038-0717(03)00003-8 · ExternalCitation · doi-reference

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10.1021/acs.estlett.4c00208 · ExternalCitation · doi-reference

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10.1021/acs.jafc.3c08837 · ExternalCitation · doi-reference

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10.1021/acs.jafc.4c07428 · ExternalCitation · doi-reference

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10.1021/acsomega.2c02353 · ExternalCitation · doi-reference

Structural basis of biological nitrogen fixation

10.1021/cr9500545 · ExternalCitation · doi-reference

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10.1073/pnas.1313452110 · ExternalCitation · doi-reference

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10.1073/pnas.2114583119 · ExternalCitation · doi-reference

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10.1073/pnas.2427021122 · ExternalCitation · doi-reference

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10.1073/pnas.90.13.6091 · ExternalCitation · doi-reference

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10.1073/pnas.92.7.2647 · ExternalCitation · doi-reference

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10.1080/12538078.1996.10515364 · ExternalCitation · doi-reference

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10.1093/femsec/fiae004 · ExternalCitation · doi-reference

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10.1093/femsre/fuad066 · ExternalCitation · doi-reference

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10.1093/jxb/ert031 · ExternalCitation · doi-reference

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10.1093/molbev/msh047 · ExternalCitation · doi-reference

10.1093/oso/9780195124927.003.0010

10.1093/oso/9780195124927.003.0010 · ExternalCitation · doi-reference

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10.1093/pcp/pcac113 · ExternalCitation · doi-reference

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10.1093/pcp/pcq058 · ExternalCitation · doi-reference

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10.1093/plphys/kiab280 · ExternalCitation · doi-reference

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10.1093/plphys/kiag483 · ExternalCitation · doi-reference

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10.1094/mpmi-08-11-0204 · ExternalCitation · doi-reference

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10.1094/mpmi-09-14-0251-r · ExternalCitation · doi-reference

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10.1094/phyto-10-22-0370-kd · ExternalCitation · doi-reference

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10.1098/rspb.2021.0675 · ExternalCitation · doi-reference

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10.1098/rstb.2023.0369 · ExternalCitation · doi-reference

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10.1098/rstb.2024.0106 · ExternalCitation · doi-reference

10.1101/2020.06.11.146126

10.1101/2020.06.11.146126 · ExternalCitation · doi-reference

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10.1101/cshperspect.a018093 · ExternalCitation · doi-reference

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10.1104/pp.108.121400 · ExternalCitation · doi-reference

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10.1104/pp.109.141879 · ExternalCitation · doi-reference

Root nutrient foraging

10.1104/pp.114.245225 · ExternalCitation · doi-reference

A H+-ATPase that energizes nutrient uptake during mycorrhizal symbioses in rice and Medicago truncatula

10.1105/tpc.113.120527 · ExternalCitation · doi-reference

Meta-analysis of effects of common mycorrhizal networks formed by arbuscular mycorrhizal fungi on plant and fungal parameters

10.1111/1365-2435.70125 · ExternalCitation · doi-reference

Evolution and biogeography of actinorhizal plants and legumes: A comparison

10.1111/1365-2745.13600 · ExternalCitation · doi-reference

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10.1111/gfs.70042 · ExternalCitation · doi-reference

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Effects of disease in wild plant populations and the evolution of pathogen aggressiveness

10.1111/j.1469-8137.1995.tb04308.x · ExternalCitation · doi-reference

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10.1111/j.1469-8137.2004.01095.x · ExternalCitation · doi-reference

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10.1111/j.1469-8137.2005.01425.x · ExternalCitation · doi-reference

Rhizosphere geometry and heterogeneity arising from root-mediated physical and chemical processes

10.1111/j.1469-8137.2005.01512.x · ExternalCitation · doi-reference

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10.1111/j.1469-8137.2007.02191.x · ExternalCitation · doi-reference

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10.1111/j.1469-8137.2008.02753.x · ExternalCitation · doi-reference

Arbuscular mycorrhizal-like fungi in Carboniferous arborescent lycopsids

10.1111/j.1469-8137.2011.03752.x · ExternalCitation · doi-reference

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10.1111/j.1472-4669.2009.00220.x · ExternalCitation · doi-reference

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10.1111/j.1472-4669.2011.00278.x · ExternalCitation · doi-reference

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10.1111/j.1574-6968.2005.00027.x · ExternalCitation · doi-reference

Indole-3-acetic acid in microbial and microorganism–plant signaling

10.1111/j.1574-6976.2007.00072.x · ExternalCitation · doi-reference

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10.1111/jam.15796 · ExternalCitation · doi-reference

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10.1111/nph.12146 · ExternalCitation · doi-reference

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10.1111/nph.12805 · ExternalCitation · doi-reference

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10.1111/nph.13252 · ExternalCitation · doi-reference

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10.1111/nph.13427 · ExternalCitation · doi-reference

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10.1111/nph.14533 · ExternalCitation · doi-reference

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10.1111/nph.70688 · ExternalCitation · doi-reference

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10.1111/nph.71107 · ExternalCitation · doi-reference

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10.1111/nph.71230 · ExternalCitation · doi-reference

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10.1111/nph.71254 · ExternalCitation · doi-reference

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10.1111/pala.12178 · ExternalCitation · doi-reference

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10.1111/pala.12185 · ExternalCitation · doi-reference

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10.1111/pce.13551 · ExternalCitation · doi-reference

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10.1111/pce.15245 · ExternalCitation · doi-reference

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10.1111/pce.15341 · ExternalCitation · doi-reference

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10.1111/pce.15621 · ExternalCitation · doi-reference

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10.1111/ppl.14495 · ExternalCitation · doi-reference

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10.1111/wre.70011 · ExternalCitation · doi-reference

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10.1126/sciadv.abh4048 · ExternalCitation · doi-reference

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10.1126/science.aad4501 · ExternalCitation · doi-reference

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10.1126/science.aat1743 · ExternalCitation · doi-reference

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10.1126/science.aaz7614 · ExternalCitation · doi-reference

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10.1126/science.aba6605 · ExternalCitation · doi-reference

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10.1128/aem.00241-26 · ExternalCitation · doi-reference

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10.1128/aem.02928-09 · ExternalCitation · doi-reference

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10.1128/mr.57.2.293-319.1993 · ExternalCitation · doi-reference

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10.1128/msystems.00422-24 · ExternalCitation · doi-reference

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10.1128/spectrum.03464-23 · ExternalCitation · doi-reference

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10.1146/annurev.micro.61.080706.093316 · ExternalCitation · doi-reference

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10.1146/annurev.micro.62.081307.162918 · ExternalCitation · doi-reference

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10.1186/s12284-023-00636-1 · ExternalCitation · doi-reference

10.1186/s12866-022-02454-9

10.1186/s12866-022-02454-9 · ExternalCitation · doi-reference

10.1186/s12866-024-03591-z

10.1186/s12866-024-03591-z · ExternalCitation · doi-reference

10.1186/s12870-023-04259-y

10.1186/s12870-023-04259-y · ExternalCitation · doi-reference

10.1186/s12870-023-04403-8

10.1186/s12870-023-04403-8 · ExternalCitation · doi-reference

10.1186/s12870-023-04641-w

10.1186/s12870-023-04641-w · ExternalCitation · doi-reference

10.1186/s12870-024-05638-9

10.1186/s12870-024-05638-9 · ExternalCitation · doi-reference

10.1186/s12870-025-06412-1

10.1186/s12870-025-06412-1 · ExternalCitation · doi-reference

10.1186/s12915-024-02011-y

10.1186/s12915-024-02011-y · ExternalCitation · doi-reference

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10.1371/journal.pbio.3003093 · ExternalCitation · doi-reference

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10.1371/journal.pone.0104201 · ExternalCitation · doi-reference

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10.1371/journal.pone.0173203 · ExternalCitation · doi-reference

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10.17521/cjpe.2018.0089 · ExternalCitation · doi-reference

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10.3389/fagro.2025.1578915 · ExternalCitation · doi-reference

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10.3389/ffgc.2020.00099 · ExternalCitation · doi-reference

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10.3389/fmicb.2013.00201 · ExternalCitation · doi-reference

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10.3389/fmicb.2017.02104 · ExternalCitation · doi-reference

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10.3389/fmicb.2017.02552 · ExternalCitation · doi-reference

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10.3389/fmicb.2020.509919 · ExternalCitation · doi-reference

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10.3389/fmicb.2021.798525 · ExternalCitation · doi-reference

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10.3389/fmicb.2022.1114089 · ExternalCitation · doi-reference

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10.3389/fmicb.2022.945498 · ExternalCitation · doi-reference

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10.3389/fmicb.2024.1470469 · ExternalCitation · doi-reference

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10.3389/fmicb.2025.1568209 · ExternalCitation · doi-reference

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10.3389/fpls.2013.00134 · ExternalCitation · doi-reference

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10.3389/fpls.2014.00237 · ExternalCitation · doi-reference

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10.3389/fpls.2014.00399 · ExternalCitation · doi-reference

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10.3389/fpls.2016.00429 · ExternalCitation · doi-reference

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10.3389/fpls.2016.01711 · ExternalCitation · doi-reference

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10.3389/fpls.2018.01270 · ExternalCitation · doi-reference

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10.3389/fpls.2019.00080 · ExternalCitation · doi-reference

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10.3389/fpls.2020.00386 · ExternalCitation · doi-reference

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10.3389/fpls.2021.661842 · ExternalCitation · doi-reference

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10.3389/fpls.2021.699618 · ExternalCitation · doi-reference

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10.3389/fpls.2022.923880 · ExternalCitation · doi-reference

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10.3389/fpls.2022.928367 · ExternalCitation · doi-reference

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10.3389/fpls.2022.929114 · ExternalCitation · doi-reference

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10.3389/fpls.2022.952397 · ExternalCitation · doi-reference

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10.3389/fpls.2023.1101932 · ExternalCitation · doi-reference

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10.3389/fpls.2023.1114840 · ExternalCitation · doi-reference

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10.3389/fpls.2023.1140467 · ExternalCitation · doi-reference

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10.3389/fpls.2023.1284720 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1377793 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1379562 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1418699 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1431004 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1461893 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1481650 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1482739 · ExternalCitation · doi-reference

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10.3389/fpls.2024.1491495 · ExternalCitation · doi-reference

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10.3389/fpls.2025.1567707 · ExternalCitation · doi-reference

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10.3389/fpls.2025.1692304 · ExternalCitation · doi-reference

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10.3389/fsoil.2022.979246 · ExternalCitation · doi-reference

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10.3389/fsufs.2024.1378436 · ExternalCitation · doi-reference

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10.3389/fsufs.2024.1432599 · ExternalCitation · doi-reference

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10.3390/agriculture14030358 · ExternalCitation · doi-reference

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10.3390/biom15010118 · ExternalCitation · doi-reference

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10.3390/plants15020206 · ExternalCitation · doi-reference

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10.3390/su13031140 · ExternalCitation · doi-reference

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10.3390/su131910986 · ExternalCitation · doi-reference

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