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GmPTF1 modifies root architecture responses to phosphate starvation primarily through regulating GmEXPB2 expression in soybean
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Comparison of yeast cell protein solubilization procedures for two-dimensional electrophoresis
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GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
inferredcites →https://doi.org/10.1002/pmic.201200263openalex-snapshot
Proteomics dissection of plant responses to mineral nutrient deficiency
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Applied Biochemistry and Biotechnology
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Plant Reporter Genes: The Gus Gene Fusion System
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Interdependence and nodule specificity of cis-acting regulatory elements in the soybean leghemoglobin lbc 3 and N23 gene promoters
inferredcites →https://doi.org/10.1007/bf01973757openalex-snapshot
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inferredcites →https://doi.org/10.1007/bf03184131openalex-snapshot
Characterization of root architecture in an applied core collection for phosphorus efficiency of soybean germplasm
inferredcites →https://doi.org/10.1007/pl00006494openalex-snapshot
Positional Dependence, Cliques, and Predictive Motifs in the bHLH Protein Domain
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GCTTCA as a novel motif for regulating mesocarp-specific expression of the oil palm (Elaeis guineensis Jacq.) stearoyl-ACP desaturase gene
inferredcites →https://doi.org/10.1007/s00425-002-0921-3openalex-snapshot
Molecular mechanisms of phosphate transport in plants
inferredcites →https://doi.org/10.1007/s00425-011-1368-1openalex-snapshot
Overexpression of transcription factor ZmPTF1 improves low phosphate tolerance of maize by regulating carbon metabolism and root growth
inferredcites →https://doi.org/10.1007/s00425-019-03227-xopenalex-snapshot
Functional characterization of a strong promoter of the early light-inducible protein gene from tomato
inferredcites →https://doi.org/10.1007/s00438-010-0511-1openalex-snapshot
Stable internal reference genes for normalization of real-time RT-PCR in tobacco (Nicotiana tabacum) during development and abiotic stress
inferredcites →https://doi.org/10.1007/s11103-005-0954-7openalex-snapshot
Identification of cis-elements for ethylene and circadian regulation of the Solanum melongena gene encoding cysteine proteinase
inferredcites →https://doi.org/10.1007/s12010-017-2420-9openalex-snapshot
Promoter Trapping and Deletion Analysis Show Arabidopsis thaliana APETALA2 Gene Promoter Is Bidirectional and Functions as a Pollen- and Ovule-Specific Promoter in the Reverse Orientation
inferredcites →https://doi.org/10.1016/b978-0-408-10649-8.50021-6openalex-snapshot
NUTRIENT INTERCEPTION AND TRANSPORT BY ROOT SYSTEMS
inferredcites →https://doi.org/10.1016/j.biotechadv.2009.02.006openalex-snapshot
Molecular mechanisms in response to phosphate starvation in rice
inferredcites →https://doi.org/10.1016/j.copbio.2012.03.002openalex-snapshot
Bioengineering and management for efficient phosphorus utilization in crops and pastures
inferredcites →https://doi.org/10.1016/j.molp.2015.12.012openalex-snapshot
Complex Regulation of Plant Phosphate Transporters and the Gap between Molecular Mechanisms and Practical Application: What Is Missing?
inferredcites →https://doi.org/10.1016/j.plantsci.2008.06.007openalex-snapshot
Identification of temporally and spatially phosphate-starvation responsive genes in Glycine max
inferredcites →https://doi.org/10.1016/j.plantsci.2015.06.020openalex-snapshot
miRNA778 and SUVH6 are involved in phosphate homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2018.04.006openalex-snapshot
Adaptation to Phosphate Scarcity: Tips from Arabidopsis Roots
inferredcites →https://doi.org/10.1016/s0167-4781(02)00507-9openalex-snapshot
AhSL28, a senescence- and phosphate starvation-induced S-like RNase gene in Antirrhinum
inferredcites →https://doi.org/10.1016/s1360-1385(02)02241-0openalex-snapshot
Cluster roots – an underground adaptation for survival in extreme environments
inferredcites →https://doi.org/10.1016/s1360-1385(99)01418-1openalex-snapshot
Regulatory mechanism of plant gene transcription by GT-elements and GT-factors
inferredcites →https://doi.org/10.1023/a:1004824019289openalex-snapshot
Low-P tolerance by maize (Zea mays L.) genotypes: Significance of root growth, and organic acids and acid phosphatase root exudation
inferredcites →https://doi.org/10.1038/nprot.2007.141openalex-snapshot
Agrobacterium rhizogenes-mediated transformation of soybean to study root biology
inferredcites →https://doi.org/10.1042/bj20070102openalex-snapshot
BHLH32 modulates several biochemical and morphological processes that respond to Pi starvation in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01624.xopenalex-snapshot
Two different novel cis ‐acting elements of erd1 , a clpA homologous Arabidopsis gene function in induction by dehydration stress and dark‐induced senescence
inferredcites →https://doi.org/10.1073/pnas.1118876109openalex-snapshot
FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.2010241118openalex-snapshot
A critical role of the soybean evening complex in the control of photoperiod sensitivity and adaptation
inferredcites →https://doi.org/10.1093/aob/mcr246openalex-snapshot
Identification of soybean purple acid phosphatase genes and their expression responses to phosphorus availability and symbiosis
inferredcites →https://doi.org/10.1093/jxb/erh009openalex-snapshot
The transcriptional control of plant responses to phosphate limitation
inferredcites →https://doi.org/10.1093/jxb/ern130openalex-snapshot
Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
inferredcites →https://doi.org/10.1093/jxb/err446openalex-snapshot
Functional analysis of the Arabidopsis PLDZ2 promoter reveals an evolutionarily conserved low-Pi-responsive transcriptional enhancer element
inferredcites →https://doi.org/10.1093/jxb/erx292openalex-snapshot
GmPHR25, a GmPHR member up-regulated by phosphate starvation, controls phosphate homeostasis in soybean
inferredcites →https://doi.org/10.1093/jxb/erz307openalex-snapshot
The bHLH family member ZmPTF1 regulates drought tolerance in maize by promoting root development and abscisic acid synthesis
inferredcites →https://doi.org/10.1093/molbev/msg140openalex-snapshot
The Evolution of Transcriptional Regulation in Eukaryotes
inferredcites →https://doi.org/10.1093/mp/ssp120openalex-snapshot
Regulation of Phosphate Starvation Responses in Plants: Signaling Players and Cross-Talks
inferredcites →https://doi.org/10.1093/nar/27.1.297openalex-snapshot
Plant cis-acting regulatory DNA elements (PLACE) database: 1999
inferredcites →https://doi.org/10.1093/pcp/pcy051openalex-snapshot
Phosphite-Mediated Suppression of Anthocyanin Accumulation Regulated by Mitochondrial ATP Synthesis and Sugars in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.204401openalex-snapshot
A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae
inferredcites →https://doi.org/10.1104/pp.103.035998openalex-snapshot
A Novel Endo-β-Mannanase Gene in Tomato LeMAN5 Is Associated with Anther and Pollen Development
inferredcites →https://doi.org/10.1104/pp.105.063115openalex-snapshot
OsPTF1, a Novel Transcription Factor Involved in Tolerance to Phosphate Starvation in Rice
inferredcites →https://doi.org/10.1104/pp.106.079707openalex-snapshot
PHO2, MicroRNA399, and PHR1 Define a Phosphate-Signaling Pathway in Plants
inferredcites →https://doi.org/10.1104/pp.106.080580openalex-snapshot
Genome-Wide Analysis of Basic/Helix-Loop-Helix Transcription Factor Family in Rice and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot
WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.101691openalex-snapshot
Phosphate Homeostasis and Root Development in Arabidopsis Are Synchronized by the Zinc Finger Transcription Factor ZAT6
inferredcites →https://doi.org/10.1104/pp.109.138891openalex-snapshot
Overexpressing AtPAP15 Enhances Phosphorus Efficiency in Soybean
inferredcites →https://doi.org/10.1104/pp.112.199786openalex-snapshot
The High-Affinity Phosphate Transporter GmPT5 Regulates Phosphate Transport to Nodules and Nodulation in Soybean
inferredcites →https://doi.org/10.1104/pp.126.2.875openalex-snapshot
Phosphate Availability Regulates Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.01029openalex-snapshot
GmEXPB2, a Cell Wall β-Expansin Gene, Affects Soybean Nodulation through Modifying Root Architecture and Promoting Nodule Formation and Development
inferredcites →https://doi.org/10.1104/pp.15.01336openalex-snapshot
Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.17.01525openalex-snapshot
The Deubiquitinase OTU5 Regulates Root Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.17.01713openalex-snapshot
The ARF7 and ARF19 Transcription Factors Positively Regulate PHOSPHATE STARVATION RESPONSE1 in Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.18.01018openalex-snapshot
INCREASING NODULE SIZE1 Expression Is Required for Normal Rhizobial Symbiosis and Nodule Development
inferredcites →https://doi.org/10.1105/tpc.013839openalex-snapshot
The Arabidopsis Basic/Helix-Loop-Helix Transcription Factor Family[W]
inferredcites →https://doi.org/10.1105/tpc.106.045229openalex-snapshot
Functional Conservation of a Root Hair Cell-Specific cis -Element in Angiosperms with Different Root Hair Distribution Patterns
inferredcites →https://doi.org/10.1105/tpc.5.11.1529openalex-snapshot
An Arabidopsis myb homolog is induced by dehydration stress and its gene product binds to the conserved MYB recognition sequence.
inferredcites →https://doi.org/10.1111/j.1365-3040.1996.tb00386.xopenalex-snapshot
Stimulation of root hair elongation in Arabidopsis thaliana by low phosphorus availability
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02777.xopenalex-snapshot
Ternary complex formation between HvMYBS3 and other factors involved in transcriptional control in barley seeds
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04511.xopenalex-snapshot
A soybean β‐expansin geneGmEXPB2intrinsically involved in root system architecture responses to abiotic stresses
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01207.xopenalex-snapshot
Promoter deletion analysis elucidates the role of cis elements and 5'UTR intron in spatiotemporal regulation of AtPht1;4 expression in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1744-7909.2012.01143.xopenalex-snapshot
Overexpression of OsPAP10a, A Root‐Associated Acid Phosphatase, Increased Extracellular Organic Phosphorus Utilization in Rice
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1111/jipb.12434openalex-snapshot
Improving crop nutrient efficiency through root architecture modifications
inferredcites →https://doi.org/10.1111/jipb.12604openalex-snapshot
Characterization of the soybean GmALMT family genes and the function of GmALMT5 in response to phosphate starvation
inferredcites →https://doi.org/10.1111/ppl.12077openalex-snapshot
Overexpression of β‐expansin gene GmEXPB2 improves phosphorus efficiency in soybean
inferredcites →https://doi.org/10.1111/ppl.12467openalex-snapshot
TaZAT8, a C2H2‐ZFP type transcription factor gene in wheat, plays critical roles in mediating tolerance to Pi deprivation through regulating P acquisition, ROS homeostasis and root system establishment
inferredcites →https://doi.org/10.1128/mcb.20.2.429-440.2000openalex-snapshot
Helix-Loop-Helix Proteins: Regulators of Transcription in Eucaryotic Organisms
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103849openalex-snapshot
Signaling Network in Sensing Phosphate Availability in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141655openalex-snapshot
HOW DO CROP PLANTS TOLERATE ACID SOILS? MECHANISMS OF ALUMINUM TOLERANCE AND PHOSPHOROUS EFFICIENCY
inferredcites →https://doi.org/10.1186/s12870-019-1959-8openalex-snapshot
The PHOSPHATE1 genes participate in salt and Pi signaling pathways and play adaptive roles during soybean evolution
inferredcites →https://doi.org/10.1371/journal.pone.0134103openalex-snapshot
Proteomic Analysis Provides New Insights in Phosphorus Homeostasis Subjected to Pi (Inorganic Phosphate) Starvation in Tomato Plants (Solanum lycopersicum L.)
inferredcites →https://doi.org/10.1371/journal.pone.0194628openalex-snapshot
Rice OsMYB5P improves plant phosphate acquisition by regulation of phosphate transporter
inferredcites →https://doi.org/10.2307/3869736openalex-snapshot
An Arabidopsis myb Homolog Is Induced by Dehydration Stress and Its Gene Product Binds to the Conserved MYB Recognition Sequence
inferredcites →https://doi.org/10.3389/fpls.2017.00817openalex-snapshot
Roles, Regulation, and Agricultural Application of Plant Phosphate Transporters
inferredcites →https://doi.org/10.3389/fpls.2017.01198openalex-snapshot
Functional Characterization of TaSnRK2.8 Promoter in Response to Abiotic Stresses by Deletion Analysis in Transgenic Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2018.01186openalex-snapshot
Overexpression of a Phosphate Starvation Response AP2/ERF Gene From Physic Nut in Arabidopsis Alters Root Morphological Traits and Phosphate Starvation-Induced Anthocyanin Accumulation
inferredcites →https://doi.org/10.3389/fpls.2019.00808openalex-snapshot
GmEXLB1, a Soybean Expansin-Like B Gene, Alters Root Architecture to Improve Phosphorus Acquisition in Arabidopsis
inferredcites →https://doi.org/10.4161/psb.3.9.5781openalex-snapshot
Role of OsPHR2 on phosphorus homoestasis and root hairs development in rice (Oryza sativaL.)
inferredcites →https://doi.org/10.4238/2014.february.19.3openalex-snapshot
GmPTF1, a novel transcription factor gene, is involved in conferring soybean tolerance to phosphate starvation
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.4854565openalex-extracted
Tabahd35-1b Positively Regulates Phosphate Starvation Response in Wheat
inferred← citeshttps://doi.org/10.1007/978-3-031-32967-8_13openalex-snapshot
Genetic Engineering Aiming to Improve the Use of Phosphorus in Agriculture
inferred← citeshttps://doi.org/10.1007/s00122-024-04667-0openalex-snapshot
Exploring the phosphorus–starch content balance mechanisms in maize grains using GWAS population and transcriptome data
inferred← citeshttps://doi.org/10.1007/s00122-026-05233-6openalex-snapshot
Identification of nodule number-related loci and the candidate gene GmbHLH135 in soybean under low phosphorus stress
inferred← citeshttps://doi.org/10.1007/s00299-023-02978-yopenalex-snapshot
Development of transgenic composite Stylosanthes plants to study root growth regulated by a β-expansin gene, SgEXPB1, under phosphorus deficiency
inferred← citeshttps://doi.org/10.1007/s00344-025-11791-8openalex-snapshot
Unfolding of Minerals Acquisition in Plants: The Role of Secondary Messengers, Phytohormones and Epigenetics Under Dehydration Stress
inferred← citeshttps://doi.org/10.1007/s00438-022-01895-1openalex-snapshot
Genome-wide association analysis discovered new loci and candidate genes associated with low-phosphorus tolerance based on shoot mineral elements concentrations in soybean
inferred← citeshttps://doi.org/10.1007/s11032-022-01301-zopenalex-snapshot
Functional study and elite haplotype identification of soybean phosphate starvation response transcription factors GmPHR14 and GmPHR32
inferred← citeshttps://doi.org/10.1007/s11104-022-05564-5openalex-snapshot
The promotion of legume nodulation in plant-soil-microbe systems under phosphorus-limited conditions
inferred← citeshttps://doi.org/10.1007/s11104-024-06990-3openalex-snapshot
Rhizosphere microbial carbon utilization stimulates soil phosphorus fraction transformation in response to maize (Zea mays L.) and soybean (Glycine max.) interspecific interactions
inferred← citeshttps://doi.org/10.1007/s11104-024-07125-4openalex-snapshot
Interactions between plant-soil feedbacks and climate control root symbioses
inferred← citeshttps://doi.org/10.1007/s11738-025-03783-8openalex-snapshot
Genome analysis, identification, and expression analysis of nitrogen and potassium responsive genes in cassava
inferred← citeshttps://doi.org/10.1007/s12298-024-01479-wopenalex-snapshot
Opportunity for genome engineering to enhance phosphate homeostasis in crops
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2025.108686openalex-snapshot
Understanding low-phosphate stress responses in plants: Opportunities for genome editing to improve phosphorous use efficiency (PUE)
inferred← citeshttps://doi.org/10.1016/j.cj.2022.12.003openalex-snapshot
Diverse functions of GmNLA1 members in controlling phosphorus homeostasis highlight coordinate response of soybean to nitrogen and phosphorus availability
inferred← citeshttps://doi.org/10.1016/j.cj.2023.04.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cj.2023.05.011openalex-snapshot
Maize–soybean relay cropping increases soybean yield synergistically by extending the post-anthesis leaf stay-green period and accelerating grain filling
inferred← citeshttps://doi.org/10.1016/j.cj.2026.06.017openalex-snapshot
Activation of GmGCS1 by GmPHR1 modulates root architecture and phosphorus acquisition in soybean
inferred← citeshttps://doi.org/10.1016/j.copbio.2024.103180openalex-snapshot
Bioengineering and management for efficient and sustainable utilization of phosphorus in crops
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104810openalex-snapshot
Carbon metabolic adjustment in soybean nodules in response to phosphate limitation: A metabolite perspective
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105120openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105646openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105762openalex-snapshot
The inhibition of N2 fixation by nitrogen is attenuated by the P supply, altering the plant metabolism
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Regulation of SmEXPA13 expression by SmMYB1R1-L enhances salt tolerance in Salix matsudana Koidz
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Molecular mechanisms underlying plant responses to low phosphate stress and potential applications in crop improvement
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111148openalex-snapshot
GmWRKY46, a WRKY transcription factor, negatively regulates phosphorus tolerance primarily through modifying root morphology in soybean
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112469openalex-snapshot
GmEXPA11 facilitates nodule enlargement and nitrogen fixation via interaction with GmNOD20 under regulation of GmPTF1 in soybean
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Characterization of SgALMT genes reveals the function of SgALMT2 in conferring aluminum tolerance in Stylosanthes guianensis through the mediation of malate exudation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110230openalex-snapshot
A novel glycerophosphodiester phosphodiesterase 13 is involved in the phosphate starvation-induced phospholipid degradation in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110386openalex-snapshot
Overexpression of MdTGA1 enhances the adaptability to nitrogen and phosphorus deficiency in apple (Malus domestica Borkh.)
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Revealing the Mechanistic Basis of Regulation of Phosphorus Uptake in Soybean (Glycine max) Roots by Molybdenum: An Integrated Omics Approach
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Biomass formation and yield performance in diverse multicrops and their potential for biofuel use in short-growing boreal climate conditions
inferred← citeshttps://doi.org/10.1071/fp25045openalex-snapshot
The gibberellic acid responsive GmbHLHm1 transcription factor influences nodule development, nitrogen fixation activity and shoot nitrogen content in soybean (Glycine max)
inferred← citeshttps://doi.org/10.1080/01904167.2026.2657809openalex-snapshot
Root architectural and physiological traits drive adaptation to low phosphorus in Bambara groundnut
inferred← citeshttps://doi.org/10.1093/plphys/kiad170openalex-snapshot
Transcription factors GmERF1 and GmWRKY6 synergistically regulate low phosphorus tolerance in soybean
inferred← citeshttps://doi.org/10.1093/plphys/kiae478openalex-snapshot
The soybean NUCLEAR FACTOR-Y C4 and α-EXPANSIN 7 module influences phosphorus uptake by regulating root morphology
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Phenylalanine ammonia-lyase 2 regulates secondary metabolism and confers manganese tolerance in Stylosanthes guianensis
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Understandings and future challenges in soybean functional genomics and molecular breeding
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Decoding stress resilience in soybean: Regulatory networks and precision breeding under climate change
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Cooperative interactions between nitrogen fixation and phosphorus nutrition in legumes
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Molecular module GmPTF1a / b‐GmNPLa regulates rhizobia infection and nodule formation in soybean
inferred← citeshttps://doi.org/10.1111/pbi.14592openalex-snapshot
Natural variation in the GmVPE1 promoter contributes to phosphorus re‐translocation to seeds and improves soybean yield
inferred← citeshttps://doi.org/10.1111/pce.14497openalex-snapshot
GmEIL4 enhances soybean (Glycine max) phosphorus efficiency by improving root system development
inferred← citeshttps://doi.org/10.1111/pce.14715openalex-snapshot
Impaired glycosylation of GmPAP15a, a root‐associated purple acid phosphatase, inhibits extracellular phytate‐P utilization in soybean
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-111822-115334openalex-snapshot
Plant Cell Wall Loosening by Expansins
inferred← citeshttps://doi.org/10.1186/s12870-022-03556-2openalex-snapshot
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DoSPX1 and DoMYB37 regulate the expression of DoCSLA6 in Dendrobium officinale during phosphorus starvation
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GmAux/IAA16 exerts a positive regulatory role in enhancing low-phosphorus stress tolerance in plants
inferred← citeshttps://doi.org/10.1360/tb-2023-0376openalex-snapshot
Research progress on alleviating aluminum stress of soybean in acidic soil
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011135openalex-snapshot
ZmARF1 positively regulates low phosphorus stress tolerance via modulating lateral root development in maize
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7860168/v1openalex-snapshot
Genome-wide Identification of JAZ Family and Functional Analysis of GmJAZ6 in Response to Phosphorus Deficiency in Soybean
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ZmEXPB7, a β-expansin gene, contributes to drought tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1094157openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/agriculture16181947openalex-snapshot
The Aspartate Kinase GmAK1 Controls Low-Phosphate Tolerance and Seed Oil Content in Soybean
inferred← citeshttps://doi.org/10.3390/agronomy15010016openalex-snapshot
GsEXPA8 Enhances Soybean Tolerance of NaHCO3 Stress by Regulating Root Morphology
inferred← citeshttps://doi.org/10.3390/agronomy15040836openalex-snapshot
Responses of Nitrogen Metabolism Pathways to Low-Phosphorus Stress: Decrease in Nitrogen Accumulation and Alterations in Protein Metabolism in Soybeans
inferred← citeshttps://doi.org/10.3390/biom15010118openalex-snapshot
Role of Environmental Factors in Legume-Rhizobium Symbiosis: A Review
inferred← citeshttps://doi.org/10.3390/ijms23094592openalex-snapshot
Mechanisms Underlying Soybean Response to Phosphorus Deficiency through Integration of Omics Analysis
inferred← citeshttps://doi.org/10.3390/ijms23148026openalex-snapshot
Overexpression of AcEXPA23 Promotes Lateral Root Development in Kiwifruit
inferred← citeshttps://doi.org/10.3390/ijms25031802openalex-snapshot
Unregulated GmAGL82 due to Phosphorus Deficiency Positively Regulates Root Nodule Growth in Soybean
inferred← citeshttps://doi.org/10.3390/plants12152865openalex-snapshot
Subcellular Proteomics to Elucidate Soybean Response to Abiotic Stress
inferred← citeshttps://doi.org/10.3390/plants15081201openalex-snapshot
Breeding Climate-Resilient Soybeans for 2050 and Beyond: Leveraging Novel Technologies to Mitigate Yield Stagnation and Climate Change Impacts
inferred← citeshttps://doi.org/10.48130/forres-0024-0014openalex-snapshot
Phosphorus uptake, transport, and signaling in woody and model plants
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