On the public citation graph

Fungal association and utilization of phosphate by plants: success, limitations, and future prospects

0 signed · 266 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

1 of the 129 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1074/jbc.m110.111021 (notice 2021-01-01).

Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4020-8435-5_5openalex-snapshot
Root strategies for phosphorus acquisition
inferredcites →https://doi.org/10.1007/978-3-642-15271-9_5openalex-snapshot
Modelling Phosphorus Dynamics in the Soil–Plant System
inferredcites →https://doi.org/10.1007/978-3-642-68885-0_15openalex-snapshot
Physiology and Metabolism of Phosphate and Its Compounds
inferredcites →https://doi.org/10.1007/978-94-011-0221-6_1openalex-snapshot
Global extent, development and economic impact of acid soils
inferredcites →https://doi.org/10.1007/978-94-015-9783-8_11openalex-snapshot
Plant Responses to Nutritional Stresses
inferredcites →https://doi.org/10.1007/978-94-017-2685-6_19openalex-snapshot
Regulation of Expression of Genes Encoding Phosphate Transporters in Barley Roots
inferredcites →https://doi.org/10.1007/bf00009558openalex-snapshot
Global extent, development and economic impact of acid soils
inferredcites →https://doi.org/10.1007/bf00012037openalex-snapshot
A critical review on the role of mycorrhizal fungi in the uptake of phosphorus by plants
inferredcites →https://doi.org/10.1007/bf00017675openalex-snapshot
Comparison of phosphatase localization in the intraradical hyphae of arbuscular mycorrhizal fungi, Glomus spp. and Gigaspora spp.
inferredcites →https://doi.org/10.1007/bf00193988openalex-snapshot
Phosphate transport across biomembranes and cytosolic phosphate homeostasis in barley leaves
inferredcites →https://doi.org/10.1007/bf00951459openalex-snapshot
Phosphate uptake inLemna gibba G1: energetics and kinetics
inferredcites →https://doi.org/10.1007/bf02197935openalex-snapshot
Effects of liming on phosphate availability in acid soils
inferredcites →https://doi.org/10.1007/s00232-001-0054-9openalex-snapshot
Proton- and Sodium-Coupled Phosphate Transport Systems and Energy Status of Yarrowia lipolytica Cells Grown in Acidic and Alkaline Conditions
inferredcites →https://doi.org/10.1007/s00374-009-0399-2openalex-snapshot
Cell-specific gene expression of phosphate transporters in mycorrhizal tomato roots
inferredcites →https://doi.org/10.1007/s00425-006-0408-8openalex-snapshot
Phosphate starvation responses are mediated by sugar signaling in Arabidopsis
inferredcites →https://doi.org/10.1007/s004250000323openalex-snapshot
Differential activation of H + -ATPase genes by an arbuscular mycorrhizal fungus in root cells of transgenic tobacco
inferredcites →https://doi.org/10.1007/s004250050394openalex-snapshot
Functional analysis and cell-specific expression of a phosphate transporter from tomato
inferredcites →https://doi.org/10.1007/s004380050776openalex-snapshot
Identification, cloning and characterization of a derepressible Na+-coupled phosphate transporter in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/s00442-005-0193-2openalex-snapshot
Piriformospora indica and Sebacina vermifera increase growth performance at the expense of herbivore resistance in Nicotiana attenuata
inferredcites →https://doi.org/10.1007/s00572-005-0006-9openalex-snapshot
Expression profiles of a phosphate transporter gene (GmosPT) from the endomycorrhizal fungus Glomus mosseae
inferredcites →https://doi.org/10.1007/s11103-008-9380-yopenalex-snapshot
Plant hormones and nutrient signaling
inferredcites →https://doi.org/10.1007/s11104-004-2005-6openalex-snapshot
Phosphate Acquisition
inferredcites →https://doi.org/10.1007/s11104-010-0319-0openalex-snapshot
Root colonization by Piriformospora indica enhances grain yield in barley under diverse nutrient regimes by accelerating plant development
inferredcites →https://doi.org/10.1016/0038-0717(95)00047-iopenalex-snapshot
Growth and extracellular phosphatase activity of arbuscular mycorrhizal hyphae as influenced by soil organic matter
inferredcites →https://doi.org/10.1016/0048-4059(78)90017-6openalex-snapshot
Enzymatic studies on the metabolism of vesicular-arbuscular mycorrhiza II. Soluble alkaline phosphatase specific to mycorrhizal infection in onion roots
inferredcites →https://doi.org/10.1016/0378-1119(94)00814-9openalex-snapshot
A phosphate-repressible, high-affinity phosphate permease is encoded by the pho-5+ gene of Neurospora crassa
inferredcites →https://doi.org/10.1016/0959-440x(91)90034-qopenalex-snapshot
Families and superfamilies of transport proteins common to prokaryotes and eukaryotes
inferredcites →https://doi.org/10.1016/b978-0-12-370526-6.x5001-6openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/b978-0-12-652840-4.x5000-1openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/j.jplph.2004.08.012openalex-snapshot
Expression of a receptor kinase in Arabidopsis roots is stimulated by the basidiomycete Piriformospora indica and the protein accumulates in Triton X-100 insoluble plasma membrane microdomains
inferredcites →https://doi.org/10.1016/j.pbi.2005.03.016openalex-snapshot
Physiology and metabolism
inferredcites →https://doi.org/10.1016/j.tplants.2004.12.003openalex-snapshot
Symbiotic phosphate transport in arbuscular mycorrhizas
inferredcites →https://doi.org/10.1016/s0021-9258(18)47267-5openalex-snapshot
The cellular receptor for gibbon ape leukemia virus is a novel high affinity sodium-dependent phosphate transporter.
inferredcites →https://doi.org/10.1016/s0065-2113(10)07001-xopenalex-snapshot
Rhizosphere Processes and Management for Improving Nutrient Use Efficiency and Crop Productivity
inferredcites →https://doi.org/10.1016/s0074-7696(08)60159-xopenalex-snapshot
Regulation of Phosphate Transport and Homeostasis in Plant Cells
inferredcites →https://doi.org/10.1016/s0169-5347(00)89157-0openalex-snapshot
Multi-functionality and biodiversity in arbuscular mycorrhizas
inferredcites →https://doi.org/10.1016/s0953-7562(09)80248-7openalex-snapshot
In planta histochemical staining of fungal alkaline phosphatase activity for analysis of efficient arbuscular mycorrhizal infections
inferredcites →https://doi.org/10.1016/s0953-7562(09)81041-1openalex-snapshot
Biodiversity in arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1016/s1369-5266(03)00035-9openalex-snapshot
The role of nutrient availability in regulating root architecture
inferredcites →https://doi.org/10.1017/cbo9780511525421openalex-snapshot
The Physiology of Fungal Nutrition
inferredcites →https://doi.org/10.1017/cbo9780511600395.003openalex-snapshot
Phosphate starvation inducible enzymes and proteins in higher plants
inferredcites →https://doi.org/10.1023/a:1004305106426openalex-snapshot
Understanding allocation to shoot and root growth will require molecular information about which compounds act as signals for the plant nutrient status, and how meristem activity and cellular growth are regulated: Opinion
inferredcites →https://doi.org/10.1023/a:1013351617532openalex-snapshot
Bioavailability of soil inorganic P in the rhizosphere as affected by root-induced chemical changes: a review
inferredcites →https://doi.org/10.1023/a:1022932414788openalex-snapshot
Beyond the rhizosphere: growth and function of arbuscular mycorrhizal external hyphae in sands of varying pore sizes
inferredcites →https://doi.org/10.1038/35054664openalex-snapshot
A fern that hyperaccumulates arsenic
inferredcites →https://doi.org/10.1038/35078151openalex-snapshot
A fern that hyperaccumulates arsenic
inferredcites →https://doi.org/10.1038/35106601openalex-snapshot
A phosphate transporter expressed in arbuscule-containing cells in potato
inferredcites →https://doi.org/10.1038/378626a0openalex-snapshot
A phosphate transporter from the mycorrhizal fungus Glomus versiforme
inferredcites →https://doi.org/10.1038/461716aopenalex-snapshot
Environment: The disappearing nutrient
inferredcites →https://doi.org/10.1038/nature12042openalex-snapshot
Crystal Structure of a Eukaryotic Phosphate Transporter
inferredcites →https://doi.org/10.1038/ncomms1046openalex-snapshot
Mechanisms underlying beneficial plant–fungus interactions in mycorrhizal symbiosis
inferredcites →https://doi.org/10.1038/nrmicro1987openalex-snapshot
Arbuscular mycorrhiza: the mother of plant root endosymbioses
inferredcites →https://doi.org/10.1042/bj20112086openalex-snapshot
Mutational analysis of putative phosphate- and proton-binding sites in the Saccharomyces cerevisiae Pho84 phosphate:H+ transceptor and its effect on signalling to the PKA and PHO pathways
inferredcites →https://doi.org/10.1046/j.1365-3040.2001.00695.xopenalex-snapshot
Regulation of root hair density by phosphorus availability in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00963.xopenalex-snapshot
The spatial expression patterns of a phosphate transporter (MtPT1) from Medicago truncatula indicate a role in phosphate transport at the root/soil interface
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00729.xopenalex-snapshot
Functioning of mycorrhizal associations along the mutualism–parasitism continuum*
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00536.xopenalex-snapshot
A Lycopersicon esculentum phosphate transporter (LePT1) involved in phosphorus uptake from a vesicular–arbuscular mycorrhizal fungus
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00695.xopenalex-snapshot
Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource
inferredcites →https://doi.org/10.1071/s96047openalex-snapshot
Soil phosphorus: its measurement, and its uptake by plants
inferredcites →https://doi.org/10.1073/pnas.0306074101openalex-snapshot
Evolutionary conservation of a phosphate transporter in the arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1073/pnas.0504423102openalex-snapshot
The endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield
inferredcites →https://doi.org/10.1073/pnas.0906546107openalex-snapshot
Transport and signaling through the phosphate-binding site of the yeast Pho84 phosphate transceptor
inferredcites →https://doi.org/10.1073/pnas.1301653110openalex-snapshot
Host-related metabolic cues affect colonization strategies of a root endophyte
inferredcites →https://doi.org/10.1073/pnas.92.9.3884openalex-snapshot
Repressible cation-phosphate symporters in Neurospora crassa.
inferredcites →https://doi.org/10.1073/pnas.93.19.10519openalex-snapshot
Phosphate transporters from the higher plant Arabidopsis thaliana.
inferredcites →https://doi.org/10.1073/pnas.94.13.7098openalex-snapshot
Overexpression of an Arabidopsis thaliana high-affinity phosphate transporter gene in tobacco cultured cells enhances cell growth under phosphate-limited conditions
inferredcites →https://doi.org/10.1074/jbc.m110.111021openalex-snapshot
A Phosphate Transporter from the Root Endophytic Fungus Piriformospora indica Plays a Role in Phosphate Transport to the Host Plant
inferredcites →https://doi.org/10.1093/genetics/160.2.463openalex-snapshot
RNA Interference in the Pathogenic Fungus Cryptococcus neoformans
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078367openalex-snapshot
Kinetic Characterization of Two Phosphate Uptake Systems with Different Affinities in Suspension-Cultured Catharanthus roseus Protoplasts
inferredcites →https://doi.org/10.1094/mpmi-20-9-1055openalex-snapshot
Laser Microdissection Reveals That Transcripts for Five Plant and One Fungal Phosphate Transporter Genes Are Contemporaneously Present in Arbusculated Cells
inferredcites →https://doi.org/10.1094/mpmi.1998.11.1.14openalex-snapshot
Cloning and Characterization of Two Phosphate Transporters from Medicago truncatula Roots: Regulation in Response to Phosphate and to Colonization by Arbuscular Mycorrhizal (AM) Fungi
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/10.1097/00010694-197007000-00015openalex-snapshot
The Nature and Properties of Soils
inferredcites →https://doi.org/10.1099/mic.0.019869-0openalex-snapshot
Antioxidant enzyme activities in maize plants colonized with Piriformospora indica
inferredcites →https://doi.org/10.1104/pp.105.060061openalex-snapshot
A Role for Auxin Redistribution in the Responses of the Root System Architecture to Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.1.7openalex-snapshot
Root Architecture and Plant Productivity
inferredcites →https://doi.org/10.1104/pp.110.161067openalex-snapshot
Quantitative Trait Loci, Epigenetics, Sugars, and MicroRNAs: Quaternaries in Phosphate Acquisition and Use
inferredcites →https://doi.org/10.1104/pp.111.174581openalex-snapshot
Roles of Arbuscular Mycorrhizas in Plant Phosphorus Nutrition: Interactions between Pathways of Phosphorus Uptake in Arbuscular Mycorrhizal Roots Have Important Implications for Understanding and Manipulating Plant Phosphorus Acquisition
inferredcites →https://doi.org/10.1104/pp.116.1.91openalex-snapshot
Tomato Phosphate Transporter Genes Are Differentially Regulated in Plant Tissues by Phosphorus1
inferredcites →https://doi.org/10.1104/pp.116.2.447openalex-snapshot
Phosphorus Uptake by Plants: From Soil to Cell
inferredcites →https://doi.org/10.1104/pp.67.4.797openalex-snapshot
Relationship between Energy-dependent Phosphate Uptake and the Electrical Membrane Potential in Lemna gibba G1
inferredcites →https://doi.org/10.1104/pp.89.4.1331openalex-snapshot
31P-Nuclear Magnetic Resonance Determination of Phosphate Compartmentation in Leaves of Reproductive Soybeans (Glycine max L.) as Affected by Phosphate Nutrition
inferredcites →https://doi.org/10.1104/pp.93.2.778openalex-snapshot
Phosphate Uptake by Excised Maize Root Tips Studied by in Vivo31P Nuclear Magnetic Resonance Spectroscopy
inferredcites →https://doi.org/10.1104/pp.99.2.672openalex-snapshot
Cytoplasmic Acidification Induced by Inorganic Phosphate Uptake in Suspension Cultured Catharanthus roseus Cells
inferredcites →https://doi.org/10.1105/tpc.004861openalex-snapshot
A Phosphate Transporter from Medicago truncatula Involved in the Acquisition of Phosphate Released by Arbuscular Mycorrhizal Fungi
inferredcites →https://doi.org/10.1105/tpc.11.4.677openalex-snapshot
Energization of Plant Cell Membranes by H + -Pumping ATPases: Regulation and Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.9.3.381openalex-snapshot
Two cDNAs from potato are able to complement a phosphate uptake-deficient yeast mutant: identification of phosphate transporters from higher plants.
inferredcites →https://doi.org/10.1111/j.1365-3040.1996.tb00253.xopenalex-snapshot
Studies on the distribution, re‐translocation and homeostasis of inorganic phosphate in barley leaves
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01617.xopenalex-snapshot
Phosphate in the arbuscular mycorrhizal symbiosis: transport properties and regulatory roles
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03749.xopenalex-snapshot
Two differentially regulated phosphate transporters from the symbiotic fungus Hebeloma cylindrosporum and phosphorus acquisition by ectomycorrhizal Pinus pinaster
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04170.xopenalex-snapshot
OsSPX1 suppresses the function of OsPHR2 in the regulation of expression of OsPT2 and phosphate homeostasis in shoots of rice
inferredcites →https://doi.org/10.1111/j.1399-3054.2004.00424.xopenalex-snapshot
Association of Piriformospora indica with Arabidopsis thaliana roots represents a novel system to study beneficial plant–microbe interactions and involves early plant protein modifications in the endoplasmic reticulum and at the plasma membrane
inferredcites →https://doi.org/10.1111/j.1469-8137.1978.tb01602.xopenalex-snapshot
TRANSLOCATION AND TRANSFER OF NUTRIENTS IN VESICULAR‐ARBUSCULAR MYCORRHIZAS
inferredcites →https://doi.org/10.1111/j.1469-8137.1979.tb07566.xopenalex-snapshot
ENZYMATIC STUDIES ON THE METABOLISM OF VESICULAR‐ARBUSCULAR MYCORRHIZA. III. ULTRASTRUCTURAL LOCALIZATION OF ACID AND ALKALINE PHOSPHATASE IN ONION ROOTS INFECTED BY GLOMUS MOSSEAE (NICOL. & GERD.)
inferredcites →https://doi.org/10.1111/j.1469-8137.1981.tb01728.xopenalex-snapshot
TRANSLOCATION AND TRANSFER OF NUTRIENTS IN VESICULAR‐ARBUSCULAR MYCORRHIZAS
inferredcites →https://doi.org/10.1111/j.1469-8137.1982.tb03238.xopenalex-snapshot
ENZYMATIC STUDIES ON THE METABOLISM OF VESICULAR–ARBUSCULAR MYCORRHIZAS
inferredcites →https://doi.org/10.1111/j.1469-8137.1990.tb00550.xopenalex-snapshot
Kinetics of phosphorus uptake by the germ‐tubes of the vesicular–arbuscular mycorrhizal fungus, Gigaspora margarita
inferredcites →https://doi.org/10.1111/j.1469-8137.1993.tb03839.xopenalex-snapshot
Symbiotic exchange of carbon and phosphorus between cucumber and three arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb02969.xopenalex-snapshot
The responses of plants to non‐uniform supplies of nutrients
inferredcites →https://doi.org/10.1111/j.1469-8137.1995.tb05726.xopenalex-snapshot
Root hair length determines beneficial effect of a Glomus species on shoot growth of some pasture species
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01512.xopenalex-snapshot
Rhizosphere geometry and heterogeneity arising from root‐mediated physical and chemical processes
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01558.xopenalex-snapshot
Nutrient availability and management in the rhizosphere: exploiting genotypic differences
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02326.xopenalex-snapshot
Conflict, cheats and the persistence of symbioses
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02753.xopenalex-snapshot
More than a carbon economy: nutrient trade and ecological sustainability in facultative arbuscular mycorrhizal symbioses
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03323.xopenalex-snapshot
Nitric oxide is involved in phosphorus deficiency‐induced cluster‐root development and citrate exudation in white lupin
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/10.1126/science.1208473openalex-snapshot
Reciprocal Rewards Stabilize Cooperation in the Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1128/jb.132.2.511-519.1977openalex-snapshot
Kinetic characterization of the two phosphate uptake systems in the fungus Neurospora crassa
inferredcites →https://doi.org/10.1128/mcb.11.6.3229openalex-snapshot
The PHO84 gene of Saccharomyces cerevisiae encodes an inorganic phosphate transporter.
inferredcites →https://doi.org/10.1128/mcb.11.6.3229-3238.1991openalex-snapshot
The PH084 Gene of Saccharomyces cerevisiae Encodes an Inorganic Phosphate Transporter
inferredcites →https://doi.org/10.1128/mmbr.54.3.266-292.1990openalex-snapshot
The fungal vacuole: composition, function, and biogenesis
inferredcites →https://doi.org/10.1128/mmbr.62.1.1-34.1998openalex-snapshot
Major Facilitator Superfamily
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.361openalex-snapshot
MOLECULAR AND CELLULAR ASPECTS OF THE ARBUSCULAR MYCORRHIZAL SYMBIOSIS
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1146/annurev.pp.24.060173.001301openalex-snapshot
Phosphate Pools, Phosphate Transport, and Phosphate Availability
inferredcites →https://doi.org/10.1152/ajpcell.1989.256.2.c322openalex-snapshot
Adaptation to Pi deprivation of cell Na-dependent Pi uptake: a widespread process
inferredcites →https://doi.org/10.1152/ajpregu.2001.280.2.r301openalex-snapshot
Evolution of the Na-Picotransport systems
inferredcites →https://doi.org/10.1186/s12870-014-0268-5openalex-snapshot
The beneficial fungus Piriformospora indica protects Arabidopsis from Verticillium dahliaeinfection by downregulation plant defense responses
inferredcites →https://doi.org/10.1201/9781420017113.ch7openalex-snapshot
The Rhizosphere
inferredcites →https://doi.org/10.1371/journal.ppat.1002290openalex-snapshot
Endophytic Life Strategies Decoded by Genome and Transcriptome Analyses of the Mutualistic Root Symbiont Piriformospora indica
inferredcites →https://doi.org/10.1890/0012-9658(2006)87[1627:msitam]2.0.co;2openalex-snapshot
MUTUALISTIC STABILITY IN THE ARBUSCULAR MYCORRHIZAL SYMBIOSIS: EXPLORING HYPOTHESES OF EVOLUTIONARY COOPERATION
inferredcites →https://doi.org/10.2134/1980.roleofphosphorus.c14openalex-snapshot
Evaluation and Utilization of Residual Phosphorus in Soils
inferredcites →https://doi.org/10.2134/agronj14.0122openalex-snapshot
Soil Application of Boron and Zinc Influence Fruit Yield and Quality of Satsuma Mandarin in Acidic Soils
inferredcites →https://doi.org/10.2136/sssaj1942.036159950006000c0029xopenalex-snapshot
The Mineralization of the Organic Phosphorus of Various Compounds in Soil
inferredcites →https://doi.org/10.2307/2960617openalex-snapshot
Mycorrhizal Symbiosis, 2nd edn.
inferredcites →https://doi.org/10.2307/3761249openalex-snapshot
Specific Inhibitor and Substrate Specificity of Alkaline Phosphatase Expressed in the Symbiotic Phase of the Arbuscular Mycorrhizal Fungus, Glomus etunicatum
inferredcites →https://doi.org/10.2307/3761331openalex-snapshot
Piriformospora indica, gen. et sp. nov., a New Root-Colonizing Fungus
inferredcites →https://doi.org/10.2307/3870892openalex-snapshot
Energization of Plant Cell Membranes by H + -Pumping ATPases: Regulation and Biosynthesis
inferredcites →https://doi.org/10.4161/psb.6.5.15106openalex-snapshot
Piriformospora indica enhances plant growth by transferring phosphate

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4639606openalex-extracted
Changes in the P Pools of an Oxisol Over an Eight-Year Stand Rotation Under Eucalyptus Fertilized with Phosphate Sources of Different Solubility
inferred← citeshttps://doi.org/10.1002/9781119463665.ch14openalex-snapshot
The Root Endomutualist Piriformospora indica : A Promising Bio‐tool for Improving Crops under Salinity Stress
inferred← citeshttps://doi.org/10.1002/9781119463665.ch15openalex-snapshot
Root Endosymbiont‐mediated Priming of Host Plants for Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-030-19831-2_4openalex-snapshot
AM Fungi and Trichoderma Interaction for Biological Control of Soilborne Plant Pathogen Fusarium oxysporum
inferred← citeshttps://doi.org/10.1007/978-3-030-45971-0_9openalex-snapshot
Fungal Biofertilizers for Sustainable Agricultural Productivity
inferred← citeshttps://doi.org/10.1007/978-3-030-48474-3_1openalex-snapshot
Agriculturally Important Fungi for Crop Protection
inferred← citeshttps://doi.org/10.1007/978-3-030-76863-8_21openalex-snapshot
Impact of Climate Change on Functional AM Fungi in Rhizosphere
inferred← citeshttps://doi.org/10.1007/978-3-030-90649-8_14openalex-snapshot
Fungal Biofertilizer: An Alternative for Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-3-319-57849-1_13openalex-snapshot
Stimulated Growth of Lycopersicum esculentum CLA 1131 in Presence of Piriformospora indica and Vermicompost
inferred← citeshttps://doi.org/10.1007/978-3-319-57849-1_14openalex-snapshot
Promotion and Value Addition to Some Important Medicinal Plants Under Saline Condition by Intervention of a Novel Mycorrhizal Formulation
inferred← citeshttps://doi.org/10.1007/978-3-319-65897-1_3openalex-snapshot
Endophyte-Promoted Nutrient Acquisition: Phosphorus and Iron
inferred← citeshttps://doi.org/10.1007/978-3-319-68867-1_6openalex-snapshot
Arbuscular Mycorrhizal Symbiosis and Nutrient Resource Limitation: Predicting the Linkages and Effectiveness of Partnership
inferred← citeshttps://doi.org/10.1007/978-981-13-2772-8_3openalex-snapshot
Phosphorus Management in Agroecosytems and Role and Relevance of Microbes in Environmental Sustainability
inferred← citeshttps://doi.org/10.1007/978-981-15-8636-1_9openalex-snapshot
Biological Interventions Towards Management of Essential Elements in Crop Plants
inferred← citeshttps://doi.org/10.1007/978-981-95-1778-7_13openalex-snapshot
Economic Analysis of Mycorrhizal Applications and Their Potential for Enhancing Farm Profitability and Livelihoods
inferred← citeshttps://doi.org/10.1007/978-981-96-3534-4_11openalex-snapshot
Metabolomics: Towards Understanding of Plant-Microbe Interaction for Improved Productivity
inferred← citeshttps://doi.org/10.1007/978-981-96-4004-1_12openalex-snapshot
Plant Endophytic Fungi: Communication Mechanism to Deal with Biotic Stress
inferred← citeshttps://doi.org/10.1007/s00344-025-11953-8openalex-snapshot
Serendipita Indica Inoculation of Wheat (Triticum aestivum) Significantly Enhances Plant Growth and Salt Tolerance, Which is Coupled with a Concomitant Change in the Soil Rhizosphere Microbial Community
inferred← citeshttps://doi.org/10.1007/s00572-020-01006-1openalex-snapshot
Sorgoleone concentration influences mycorrhizal colonization in sorghum
inferred← citeshttps://doi.org/10.1007/s10265-024-01546-zopenalex-snapshot
Modulation of plant immunity and biotic interactions under phosphate deficiency
inferred← citeshttps://doi.org/10.1007/s11104-018-3624-7openalex-snapshot
The root endophytes Trametes versicolor and Piriformospora indica increase grain yield and P content in wheat
inferred← citeshttps://doi.org/10.1007/s11104-020-04618-wopenalex-snapshot
Alleviation of salinity stress in plants by endophytic plant-fungal symbiosis: Current knowledge, perspectives and future directions
inferred← citeshttps://doi.org/10.1007/s11104-023-06466-wopenalex-snapshot
Differential phosphorus acquisition strategies of nine cover crop species grown in a calcareous and a decalcified chernozem
inferred← citeshttps://doi.org/10.1007/s11274-024-04086-9openalex-snapshot
Prospects of phosphate solubilizing microorganisms in sustainable agriculture
inferred← citeshttps://doi.org/10.1007/s11274-025-04513-5openalex-snapshot
PiPho85, a cyclin-dependent kinase of Piriformospora indica rescue colonized maize plants grown under salt stress
inferred← citeshttps://doi.org/10.1007/s11356-023-28197-2openalex-snapshot
Plant invasion shifts soil microbiome and physico-chemical attributes along an elevational gradient in Kashmir Himalaya
inferred← citeshttps://doi.org/10.1007/s12649-025-03160-zopenalex-snapshot
Fungal Cultivation in a Dairy Side Stream: Valorisation Potential of Whey into Added-Value Biomass and By-Products
inferred← citeshttps://doi.org/10.1007/s12892-021-00128-yopenalex-snapshot
Assessing NPK use efficiency of commercial inoculants in cassava (Manihot esculenta Cratz): an application of data envelopment analysis
inferred← citeshttps://doi.org/10.1007/s13199-025-01060-3openalex-snapshot
Endophytic fungi mediated alleviation of salinity stress in crop plants: an insight and future prospect
inferred← citeshttps://doi.org/10.1007/s42729-019-00060-9openalex-snapshot
P Pools in Barley Detritusphere Are Influenced by N and P Addition to the Soil
inferred← citeshttps://doi.org/10.1007/s42729-023-01526-7openalex-snapshot
Significance and Exploitation of Rhizosphere Chemical Signaling Metabolites for Enhancing Soil Nutrient Transformation
inferred← citeshttps://doi.org/10.1007/s42729-025-02412-0openalex-snapshot
Effects of Phosphate Solubility on Soil P Pools, Nutrition, and Growth of Eucalyptus Over an Eight-Year Rotation
inferred← citeshttps://doi.org/10.1007/s44378-026-00215-yopenalex-snapshot
Dynamics of potassium and phosphorus uptake in soybean cultivated on oxisol amended with biotite schist and potassium chloride
inferred← citeshttps://doi.org/10.1016/b978-0-12-804312-7.00007-3openalex-snapshot
Fungal and Plant Tools for the Uptake of Nutrients in Arbuscular Mycorrhizas
inferred← citeshttps://doi.org/10.1016/b978-0-323-85797-0.00011-2openalex-snapshot
Role of legumes in phytoremediation of heavy metals
inferred← citeshttps://doi.org/10.1016/b978-0-443-24863-4.00007-8openalex-snapshot
Significance of arbuscular mycorrhizal fungi in improving growth, chemical profile, and biological activities of medicinal and aromatic plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-34104-5.00007-4openalex-snapshot
Role of mycorrhiza in cadmium uptake and detoxification
inferred← citeshttps://doi.org/10.1016/b978-0-443-45130-0.00013-8openalex-snapshot
Enhancing metal tolerance in plants through arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/j.biteb.2024.101854openalex-snapshot
An investigation into the ability of three fungi and one yeast to grow and capture nutrients in cheese whey
inferred← citeshttps://doi.org/10.1016/j.crbiot.2023.100158openalex-snapshot
Exploring the potential: Can mycorrhizal fungi and hyphosphere silicate-solubilizing bacteria synergistically alleviate cadmium stress in plants?
inferred← citeshttps://doi.org/10.1016/j.crmicr.2022.100107openalex-snapshot
Aspects, problems and utilization of Arbuscular Mycorrhizal (AM) application as bio-fertilizer in sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.cub.2019.04.061openalex-snapshot
Mycorrhizal Fungi Respond to Resource Inequality by Moving Phosphorus from Rich to Poor Patches across Networks
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105633openalex-snapshot
Unveiling the complex molecular dynamics of arbuscular mycorrhizae: A comprehensive exploration and future perspectives in harnessing phosphate-solubilizing microorganisms for sustainable progress
inferred← citeshttps://doi.org/10.1016/j.foreco.2022.120340openalex-snapshot
Influence of stand age and site conditions on ectomycorrhizal fungal dynamics in Cistus ladanifer-dominated scrubland ecosystems
inferred← citeshttps://doi.org/10.1016/j.molp.2016.05.007openalex-snapshot
Arabidopsis Farms Colletotrichum tofieldiae for Phosphate Uptake
inferred← citeshttps://doi.org/10.1016/j.pep.2024.106559openalex-snapshot
Biochemical characterization of a high affinity phosphate transporter (PiPT) from root endophyte fungus Piriformospora indica
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.02.007openalex-snapshot
Metabolomic responses triggered by arbuscular mycorrhiza enhance tolerance to water stress in wheat cultivars
inferred← citeshttps://doi.org/10.1016/j.pmpp.2019.02.010openalex-snapshot
Piriformospora indica colonization reprograms plants to improved P-uptake, enhanced crop performance, and biotic/abiotic stress tolerance
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112081openalex-snapshot
Micropropagated walnut dependency on phosphate fertilization and arbuscular mycorrhiza for growth, nutrition and quality differ between rootstocks both after acclimatization and post-acclimatization
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.138366openalex-snapshot
The role of rice (Oryza sativa L.) in sequestering phosphorus compounds and trace elements: Speciation and dynamics
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.176034openalex-snapshot
Biochar and arbuscular mycorrhizal fungi promote rapid-cycling Brassica napus growth under cadmium stress
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.03.024openalex-snapshot
Effects of arbuscular mycorrhizal fungi and P-solubilizing Pseudomonas fluorescence (ATCC-17400) on morphological traits and mineral content of sesame
inferred← citeshttps://doi.org/10.1016/j.sjbs.2023.103911openalex-snapshot
Diversity, Distribution, and applications of arbuscular mycorrhizal fungi in the Arabian Peninsula
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.07.010openalex-snapshot
Take a Trip Through the Plant and Fungal Transportome of Mycorrhiza
inferred← citeshttps://doi.org/10.1021/acs.est.5c08760openalex-snapshot
Phytate-Mediated Arsenic Hyperaccumulation in Pteris vittata : Synthesis, Sequestration, and Exudation
inferred← citeshttps://doi.org/10.1021/acs.est.9b04819openalex-snapshot
Localized Intensification of Arsenic Release within the Emergent Rice Rhizosphere
inferred← citeshttps://doi.org/10.1021/acsearthspacechem.0c00302openalex-snapshot
Arsenic Accumulation in Hydroponically Grown Schizachyrium scoparium (Little Bluestem) Amended with Root-Colonizing Endophytes
inferred← citeshttps://doi.org/10.1038/s41598-025-02511-zopenalex-snapshot
Using zeolite, molasses, and PGP microorganisms to improve apatite solubility and increase phosphorus uptake by Sorghum bicolor L. (Speedfed cultivar)
inferred← citeshttps://doi.org/10.1038/srep36765openalex-snapshot
PiHOG1, a stress regulator MAP kinase from the root endophyte fungus Piriformospora indica, confers salinity stress tolerance in rice plants
inferred← citeshttps://doi.org/10.1073/pnas.1617799114openalex-snapshot
Phosphate is the third nutrient monitored by TOR in Candida albicans and provides a target for fungal-specific indirect TOR inhibition
inferred← citeshttps://doi.org/10.1080/00380768.2019.1704180openalex-snapshot
Combining the phosphate solubilizing microorganisms with biochar types in order to improve safflower yield and soil enzyme activity
inferred← citeshttps://doi.org/10.1080/00380768.2022.2164675openalex-snapshot
Responses of rubber tree seedlings ( Hevea brasiliensis ) to phosphorus deficient soils
inferred← citeshttps://doi.org/10.1080/01490451.2019.1616857openalex-snapshot
Understanding How Pochonia chlamydosporia Increases Phosphorus Availability
inferred← citeshttps://doi.org/10.1080/01490451.2021.1956648openalex-snapshot
Arsenic and Nickel Stress Response, Their Bioremediation Potential and Mechanism of Trichoderma lixii Isolated from Electroplating Wastewater
inferred← citeshttps://doi.org/10.1080/01904167.2023.2191638openalex-snapshot
Unraveling arbuscular mycorrhizal fungi interaction in rice for plant growth development and enhancing phosphorus use efficiency through recent development of regulatory genes
inferred← citeshttps://doi.org/10.1080/15592324.2019.1632688openalex-snapshot
Piriformospora indica-induced phytohormone changes and root colonization strategies are highly host-specific
inferred← citeshttps://doi.org/10.1080/15592324.2022.2030082openalex-snapshot
Sulfur nutrition and its role in plant growth and development
inferred← citeshttps://doi.org/10.1093/plcell/koab006openalex-snapshot
Sulfur transfer from the endophytic fungus Serendipita indica improves maize growth and requires the sulfate transporter SiSulT
inferred← citeshttps://doi.org/10.1093/treephys/tpaa100openalex-snapshot
Metabolome adjustments in ectomycorrhizal Populus × canescens associated with strong promotion of plant growth by Paxillus involutus despite a very low root colonization rate
inferred← citeshttps://doi.org/10.1101/2020.01.07.897710openalex-snapshot
Role of Sulphate Transporter (PiSulT) of Endophytic Fungus Serendipita indica in Plant Growth and Development
inferred← citeshttps://doi.org/10.1101/317933openalex-snapshot
Intersection of phosphate transport, oxidative stress and TOR signalling in Candida albicans virulence
inferred← citeshttps://doi.org/10.1104/pp.17.01423openalex-snapshot
A Poly(A) Ribonuclease Controls the Cellotriose-Based Interaction between Piriformospora indica and Its Host Arabidopsis
inferred← citeshttps://doi.org/10.1111/1365-2435.70022openalex-snapshot
Nutrient‐induced changes in root respiration in 10 woody plant species
inferred← citeshttps://doi.org/10.1111/1365-2745.70335openalex-snapshot
Realistic species loss has little effect on local resource depletion and competitive pressure in a temperate wet meadow
inferred← citeshttps://doi.org/10.1111/jipb.12559openalex-snapshot
Engineering crop nutrient efficiency for sustainable agriculture
inferred← citeshttps://doi.org/10.1111/nph.17058openalex-snapshot
Carbohydrate depletion in roots impedes phosphorus nutrition in young forest trees
inferred← citeshttps://doi.org/10.1111/pce.14421openalex-snapshot
The mycorrhizal symbiosis alters the plant defence strategy in a model legume plant
inferred← citeshttps://doi.org/10.1111/raq.12980openalex-snapshot
Implications of Microalgal–Bacterial Interactions in Modern Aquaculture Practices: A Review of the Current Knowledge
inferred← citeshttps://doi.org/10.1111/tpj.16184openalex-snapshot
Role of mycorrhizas and root exudates in plant uptake of soil nutrients (calcium, iron, magnesium, and potassium): has the puzzle been completely solved?
inferred← citeshttps://doi.org/10.11606/d.11.2022.tde-08062022-152300openalex-snapshot
Resposta do >i /i< à aplicação de fontes fosfatadas com diferentes solubilidades
inferred← citeshttps://doi.org/10.11648/j.abb.20241204.11openalex-snapshot
Associations of Arbuscular Mycorrhizal Fungi (AMF) for Enhancements in Soil Fertility and Promotion of Plant Growth: A Review
inferred← citeshttps://doi.org/10.1186/s12870-024-05405-wopenalex-snapshot
Characterization and stress-responsive regulation of CmPHT1 genes involved in phosphate uptake and transport in Melon (Cucumis melo L.)
inferred← citeshttps://doi.org/10.1186/s13007-022-00854-6openalex-snapshot
Determination of phosphorus compounds in plant tissues: from colourimetry to advanced instrumental analytical chemistry
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002726openalex-snapshot
Hyphae of the fungus Aspergillus nidulans demonstrate chemotropism to nutrients and pH
inferred← citeshttps://doi.org/10.1371/journal.pone.0210538openalex-snapshot
Nitrogen- and phosphorus-starved Triticum aestivum show distinct belowground microbiome profiles
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007076openalex-snapshot
Intersection of phosphate transport, oxidative stress and TOR signalling in Candida albicans virulence
inferred← citeshttps://doi.org/10.14393/ufu.te.2023.8044openalex-snapshot
Fertilizantes especiais na cultura do cafeeiro (Coffea arábica L.)
inferred← citeshttps://doi.org/10.1590/0034-737x202370040015openalex-snapshot
Nitrogen and phosphorus fertilization in upland rice in the municipality of Humaitá at Amazonas State
inferred← citeshttps://doi.org/10.18502/kls.v7i3.11105openalex-snapshot
Native Endomycorrhiza With Tolerance to Heavy Metal Contamination in Organic Culture Media
inferred← citeshttps://doi.org/10.20546/ijcrbp.2020.709.002openalex-snapshot
Effectiveness of organic culture media combination on propagation of Gigaspora sp. indigenous to Sorowako, Indonesia
inferred← citeshttps://doi.org/10.20956/ijas.v7i2.1918openalex-snapshot
Native Mycorrhizal Fungi in Land Contaminated Cr, Co and Cu
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8238189/v1openalex-snapshot
Genome sequence and annotation of Botrytis cinerea UCA992 strain
inferred← citeshttps://doi.org/10.2139/ssrn.4865443openalex-snapshot
Biochar/ Arbuscular Mycorrhizal Fungi Regulate the Physiology and Biochemistry of Rapid-Cycling Brassica Napus Under Cadmium Stress
inferred← citeshttps://doi.org/10.24966/amr-694x/vol6iss1openalex-snapshot
inferred← citeshttps://doi.org/10.28940/terra.v38i3.671openalex-snapshot
Efecto de ácidos húmicos, micorrizas y quitosano en indicadores del crecimiento de dos cultivares de tomate (Solanum lycopersicum L.)
inferred← citeshttps://doi.org/10.31692/a8tmrs67openalex-snapshot
VARIABILIDADE ESPACIAL DA COLONIZAÇÃO MICORRÍZICA EM RAÍZES DE PLANTAS COLETADAS EM SOLO SOB SISTEMA DE PLANTIO DIRETO NO CERRADO SUL-MATO-GROSS
inferred← citeshttps://doi.org/10.31849/jip.v20i2.10901openalex-snapshot
Combination of bio-organo-mineral fertilizers on optimizing the growth and production of tomatoes (Solanum lycopersicum L.) in dryland environment
inferred← citeshttps://doi.org/10.32604/phyton.2021.016174openalex-snapshot
Pathways of Phosphorus Absorption and Early Signaling between the Mycorrhizal Fungi and Plants
inferred← citeshttps://doi.org/10.3389/ffgc.2020.00054openalex-snapshot
Mycorrhizal Phosphorus Efficiencies and Microbial Competition Drive Root P Uptake
inferred← citeshttps://doi.org/10.3389/fmicb.2016.00332openalex-snapshot
Piriformospora indica: Potential and Significance in Plant Stress Tolerance
inferred← citeshttps://doi.org/10.3389/fmicb.2017.00754openalex-snapshot
Endophytic Fungi Piriformospora indica Mediated Protection of Host from Arsenic Toxicity
inferred← citeshttps://doi.org/10.3389/fmicb.2019.02076openalex-snapshot
The pH Signaling Transcription Factor PAC-3 Regulates Metabolic and Developmental Processes in Pathogenic Fungi
inferred← citeshttps://doi.org/10.3389/fmicb.2021.739844openalex-snapshot
Rhizosphere Microbial Communities Are Significantly Affected by Optimized Phosphorus Management in a Slope Farming System
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1558567openalex-snapshot
Effects and molecular mechanism of endophytic elicitors on the accumulation of secondary metabolites in medicinal plants
inferred← citeshttps://doi.org/10.3389/fphar.2018.00191openalex-snapshot
Multiple Transceptors for Macro- and Micro-Nutrients Control Diverse Cellular Properties Through the PKA Pathway in Yeast: A Paradigm for the Rapidly Expanding World of Eukaryotic Nutrient Transceptors Up to Those in Human Cells
inferred← citeshttps://doi.org/10.3389/fpls.2016.00912openalex-snapshot
Cooperation through Competition—Dynamics and Microeconomics of a Minimal Nutrient Trade System in Arbuscular Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.3389/fpls.2018.00463openalex-snapshot
Forest Soil Phosphorus Resources and Fertilization Affect Ectomycorrhizal Community Composition, Beech P Uptake Efficiency, and Photosynthesis
inferred← citeshttps://doi.org/10.3389/fpls.2019.01158openalex-snapshot
Structure–Function Analysis Reveals Amino Acid Residues of Arabidopsis Phosphate Transporter AtPHT1;1 Crucial for Its Activity
inferred← citeshttps://doi.org/10.3389/fpls.2021.699618openalex-snapshot
Contribution of Arbuscular Mycorrhizal Fungi, Phosphate–Solubilizing Bacteria, and Silicon to P Uptake by Plant
inferred← citeshttps://doi.org/10.3389/fpls.2023.1145830openalex-snapshot
Benefits of biological nitrification inhibition of Leymus chinensis under alkaline stress: the regulatory function of ammonium-N exceeds its nutritional function
inferred← citeshttps://doi.org/10.3389/fpls.2025.1526041openalex-snapshot
Recent advances in understanding the mechanisms of plant cadmium accumulation as affected by grafting in vegetable production
inferred← citeshttps://doi.org/10.3389/fsufs.2021.754853openalex-snapshot
Prospects for Abiotic Stress Tolerance in Crops Utilizing Phyto- and Bio-Stimulants
inferred← citeshttps://doi.org/10.3390/agriculture9030051openalex-snapshot
Inoculation with Mycorrhizal Fungi and Other Microbes to Improve the Morpho-Physiological and Floral Traits of Gazania rigens (L.) Gaertn
inferred← citeshttps://doi.org/10.3390/agronomy10060815openalex-snapshot
Arbuscular Mycorrhizal Fungi as Potential Agents in Ameliorating Heavy Metal Stress in Plants
inferred← citeshttps://doi.org/10.3390/agronomy11112267openalex-snapshot
Unravelling the Role of Rhizosphere Microbiome and Root Traits in Organic Phosphorus Mobilization for Sustainable Phosphorus Fertilization. A Review
inferred← citeshttps://doi.org/10.3390/agronomy14061109openalex-snapshot
Phosphorus Supply to Plants of Vaccinium L. Genus: Proven Patterns and Unexplored Issues
inferred← citeshttps://doi.org/10.3390/agronomy16161541openalex-snapshot
Application of Straw-Decomposing Microbial Inoculant JN01 Modifies Soil Microbial Communities, Enhances Nutrient Availability, and Improves Growth in a Pot-Based Early- and Late-Season Rice System with Straw Retention
inferred← citeshttps://doi.org/10.3390/biology8040093openalex-snapshot
Transcriptome Analysis of Wheat Roots Reveals a Differential Regulation of Stress Responses Related to Arbuscular Mycorrhizal Fungi and Soil Disturbance
inferred← citeshttps://doi.org/10.3390/f10020167openalex-snapshot
Soil Physicochemical Properties and the Rhizosphere Soil Fungal Community in a Mulberry (Morus alba L.)/Alfalfa (Medicago sativa L.) Intercropping System
inferred← citeshttps://doi.org/10.3390/ijms23169194openalex-snapshot
Is Endophytic Colonization of Host Plants a Method of Alleviating Drought Stress? Conceptualizing the Hidden World of Endophytes.
inferred← citeshttps://doi.org/10.3390/jof9010088openalex-snapshot
Variability in Nutrient Use by Orchid Mycorrhizal Fungi in Two Medium Types
inferred← citeshttps://doi.org/10.3390/life14010006openalex-snapshot
Advances in Identifying the Mechanisms by Which Microorganisms Improve Barley Salt Tolerance
inferred← citeshttps://doi.org/10.3390/microorganisms13020423openalex-snapshot
Enhancing Sorghum Growth: Influence of Arbuscular Mycorrhizal Fungi and Sorgoleone
inferred← citeshttps://doi.org/10.3390/plants14121878openalex-snapshot
The Growth-Promoting Effects of Piriformospora indica on Banana Under Different Concentrations of Phosphorus and Potassium Treatments
inferred← citeshttps://doi.org/10.3390/plants15172575openalex-snapshot
Functional Roles of Arbuscular Mycorrhizal Fungi and Plant Growth-Promoting Rhizobacteria in Pistachio: Implications for Stress Tolerance, Nutrient Acquisition and Disease Suppression
inferred← citeshttps://doi.org/10.3390/su16146001openalex-snapshot
Phosphorus Flow Analysis in Lithuania
inferred← citeshttps://doi.org/10.35537/10915/99599openalex-snapshot
Micorrizas arbusculares
inferred← citeshttps://doi.org/10.36560/15920221583openalex-snapshot
Morphophysiological aspects of bean plants cultivated with natural reactive phosphate and solubilizing and growth promoting microorganisms
inferred← citeshttps://doi.org/10.3732/ajb.1600142openalex-snapshot
Common mycelial networks impact competition in an invasive grass
inferred← citeshttps://doi.org/10.3856/vol52-issue3-fulltext-3127openalex-snapshot
Comparing lettuce and cucumber production using hydroponics and aquaponic (tilapia) systems
inferred← citeshttps://doi.org/10.4018/979-8-3693-8201-1.ch006openalex-snapshot
Enhancing Soil Fertility and Nutrient Cycling
inferred← citeshttps://doi.org/10.4238/gmr18469openalex-snapshot
Research Article Morphological, biochemical and molecular characterization of sorghum (Sorghum bicolor) genotypes contrasting for phosphate-use efficiency
inferred← citeshttps://doi.org/10.4314/gjass.v21i1.11openalex-snapshot
The effect of amf (glomus clarum) on tomato resistance to early leaf blight (alternaria solani) on tomato
inferred← citeshttps://doi.org/10.47328/ufvbbt.2022.587openalex-snapshot
Influência do cobre na anatomia foliar e no crescimento de Joannesia princeps Vell. (Euphorbiaceae) associado a um inóculo micorrízico
inferred← citeshttps://doi.org/10.53550/pr.2022.v41i01.046openalex-snapshot
ARSENIC CONTAMINATION: SOURCES, EXTENT AND IMPACT ON THE ENVIRONMENT
inferred← citeshttps://doi.org/10.6084/m9.figshare.26360960openalex-snapshot
Additional file 1 of Characterization and stress-responsive regulation of CmPHT1 genes involved in phosphate uptake and transport in Melon (Cucumis melo L.)
inferred← citeshttps://doi.org/10.70675/de48c447zb9f5z478dz9687zb191256d01ebopenalex-snapshot
Rôles du porte-greffe et du greffon dans la réponse à la disponibilité en phosphore chez la Vigne
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.