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Overexpression of β‐expansin gene GmEXPB2 improves phosphorus efficiency in soybean

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What this work says

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

inferredcites →https://doi.org/10.1007/bf00730660openalex-snapshot
Chromosome doubling of mature haploid Brussels sprout plants by colchicine treatment
inferredcites →https://doi.org/10.1007/s00122-004-1751-4openalex-snapshot
Phosphorus deficiency-induced root elongation and its QTL in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s00299-011-1005-2openalex-snapshot
Root-targeted biotechnology to mediate hormonal signalling and improve crop stress tolerance
inferredcites →https://doi.org/10.1007/s00425-005-0204-xopenalex-snapshot
Expression of a plant expansin is involved in the establishment of root knot nematode parasitism in tomato
inferredcites →https://doi.org/10.1007/s11434-008-0521-0openalex-snapshot
Isolation and application of effective nitrogen fixation rhizobial strains on low-phosphorus acid soils in South China
inferredcites →https://doi.org/10.1016/j.gloenvcha.2008.10.009openalex-snapshot
The story of phosphorus: Global food security and food for thought
inferredcites →https://doi.org/10.1016/j.plaphy.2005.01.021openalex-snapshot
Fast changes in expression of expansin gene and leaf extensibility in osmotically stressed maize plants
inferredcites →https://doi.org/10.1016/s0003-2670(00)88444-5openalex-snapshot
A modified single solution method for the determination of phosphate in natural waters
inferredcites →https://doi.org/10.1016/s0378-4290(00)00098-8openalex-snapshot
Does assimilate supply limit leaf expansion in wheat grown in the field under low phosphorus availability?
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/10.1023/a:1004310217694openalex-snapshot
Plant leaf area expansion and assimilate production in wheat (Triticum aestivum L.) growing under low phosphorus conditions
inferredcites →https://doi.org/10.1023/a:1010621417854openalex-snapshot
Differential expression of α- and β-expansin genes in the elongating leaf of Festuca pratensis
inferredcites →https://doi.org/10.1023/b:euph.0000030670.36730.a4openalex-snapshot
The association of culm anatomy with lodging susceptibility in modern spring wheat genotypes
inferredcites →https://doi.org/10.1038/35030000openalex-snapshot
Loosening of plant cell walls by expansins
inferredcites →https://doi.org/10.1038/74531openalex-snapshot
Enhanced phosphorus uptake in transgenic tobacco plants that overproduce citrate
inferredcites →https://doi.org/10.1038/nature10622openalex-snapshot
Intermediates in the transformation of phosphonates to phosphate by bacteria
inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00514.xopenalex-snapshot
Leaf expansion – an integrating plant behaviour
inferredcites →https://doi.org/10.1073/pnas.160276997openalex-snapshot
Altered expression of expansin modulates leaf growth and pedicel abscission in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.191380498openalex-snapshot
Local expression of expansin induces the entire process of leaf development and modifies leaf shape
inferredcites →https://doi.org/10.1073/pnas.94.11.5955openalex-snapshot
Expression of a divergent expansin gene is fruit-specific and ripening-regulated
inferredcites →https://doi.org/10.1093/aob/mcq029openalex-snapshot
Genetic improvement for phosphorus efficiency in soybean: a radical approach
inferredcites →https://doi.org/10.1093/jexbot/53.368.473openalex-snapshot
Leaf initiation and development in soybean under phosphorus stress
inferredcites →https://doi.org/10.1093/jxb/45.9.1245openalex-snapshot
Partitioning of shoot and root dry matter and carbohydrates in bean plants suffering from phosphorus, potassium and magnesium deficiency
inferredcites →https://doi.org/10.1093/jxb/eri189openalex-snapshot
Is root growth under phosphorus deficiency affected by source or sink limitations?
inferredcites →https://doi.org/10.1093/jxb/err399openalex-snapshot
How genetic modification of roots affects rhizosphere processes and plant performance
inferredcites →https://doi.org/10.1093/pcp/pcd029openalex-snapshot
Overexpression of Mitochondrial Citrate Synthase in Arabidopsis thaliana Improved Growth on a Phosphorus-Limited Soil
inferredcites →https://doi.org/10.1104/pp.009902openalex-snapshot
Expression of an Expansin Gene Is Correlated with Root Elongation in Soybean
inferredcites →https://doi.org/10.1104/pp.010934openalex-snapshot
Phosphate Availability Alters Architecture and Causes Changes in Hormone Sensitivity in the Arabidopsis Root System
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.105.076497openalex-snapshot
Phosphorus and Aluminum Interactions in Soybean in Relation to Aluminum Tolerance. Exudation of Specific Organic Acids from Different Regions of the Intact Root System
inferredcites →https://doi.org/10.1104/pp.106.078626openalex-snapshot
Molecular Cloning and Characterization of β-Expansin Gene Related to Root Hair Formation in Barley
inferredcites →https://doi.org/10.1104/pp.106.087494openalex-snapshot
Association of Specific Expansins with Growth in Maize Leaves Is Maintained under Environmental, Genetic, and Developmental Sources of Variation
inferredcites →https://doi.org/10.1104/pp.106.092130openalex-snapshot
Differential Effects of Sucrose and Auxin on Localized Phosphate Deficiency-Induced Modulation of Different Traits of Root System Architecture in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.138891openalex-snapshot
Overexpressing AtPAP15 Enhances Phosphorus Efficiency in Soybean
inferredcites →https://doi.org/10.1104/pp.111.175281openalex-snapshot
Metabolic Adaptations of Phosphate-Starved Plants
inferredcites →https://doi.org/10.1104/pp.125.4.1901openalex-snapshot
Induction of a Major Leaf Acid Phosphatase Does Not Confer Adaptation to Low Phosphorus Availability in Common Bean
inferredcites →https://doi.org/10.1104/pp.89.1.225openalex-snapshot
Influence of Phosphorus Nutrition on Growth and Carbon Partitioning in Glycine max
inferredcites →https://doi.org/10.1105/tpc.006437openalex-snapshot
Regulation of Root Hair Initiation and Expansin Gene Expression in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.011965openalex-snapshot
Regulation of Expansin Gene Expression Affects Growth and Development in Transgenic Rice Plants
inferredcites →https://doi.org/10.1105/tpc.11.11.2203openalex-snapshot
Modification of Expansin Protein Abundance in Tomato Fruit Alters Softening and Cell Wall Polymer Metabolism during Ripening
inferredcites →https://doi.org/10.1105/tpc.4.11.1425openalex-snapshot
Two Endogenous Proteins That Induce Cell Wall Extension in Plants
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.1365-3040.2004.01194.xopenalex-snapshot
The decrease in growth of phosphorus‐deficient maize leaves is related to a lower cell production
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.1365-313x.2011.04533.xopenalex-snapshot
Root hair‐specific expansins modulate root hair elongation in rice
inferredcites →https://doi.org/10.1111/j.1467-7652.2009.00403.xopenalex-snapshot
Transgenic barley (Hordeum vulgare L.) expressing the wheat aluminium resistance gene (TaALMT1) shows enhanced phosphorus nutrition and grain production when grown on an acid soil
inferredcites →https://doi.org/10.1111/j.1747-0765.2008.00329.xopenalex-snapshot
Overexpression of theLASAP2gene for secretory acid phosphatase in white lupin improves the phosphorus uptake and growth of tobacco 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/10.1525/bio.2011.61.2.1openalex-snapshot
Peak Phosphorus
inferredcites →https://doi.org/10.2134/agronj1998.00021962009000020008xopenalex-snapshot
Phosphorus Nutrition Affects Wheat Response to Water Deficit
inferredcites →https://doi.org/10.2135/cropsci1991.0011183x003100020031xopenalex-snapshot
Vegetative Growth of the Common Bean in Response to Phosphorus Nutrition
inferredcites →https://doi.org/10.2135/cropsci1996.0011183x003600040020xopenalex-snapshot
Utilization of Phosphorus Substrates by Contrasting Common Bean Genotypes

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/10.1002/9781118958841.ch2openalex-snapshot
Sensing, signaLling, and CONTROL of phosphate starvation in plants: molecular players and applications
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0517openalex-snapshot
Sensing, Signalling, and Control of Phosphate Starvation in Plants: Molecular Players and Applications
inferred← citeshttps://doi.org/10.1002/9781119525417.ch2openalex-snapshot
Genetic and Molecular Regulation of Root Growth and Development
inferred← citeshttps://doi.org/10.1007/124_2016_11openalex-snapshot
Physiology and Spatio-temporal Relations of Nutrient Acquisition by Roots and Root Symbionts
inferred← citeshttps://doi.org/10.1007/978-3-030-84985-6_2openalex-snapshot
Root Architectural Plasticity in Changing Nutrient Availability
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/10.1007/978-3-031-75678-8_19openalex-snapshot
Genetic Engineering and Genome Editing for Enhancing Nutritional Quality of Legumes
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Root System Architecture and Phenotyping for Improved Resource Use Efficiency in Crops
inferred← citeshttps://doi.org/10.1007/s00284-020-02258-yopenalex-snapshot
Regulation of c-di-GMP in Biofilm Formation of Klebsiella pneumoniae in Response to Antibiotics and Probiotic Supernatant in a Chemostat System
inferred← citeshttps://doi.org/10.1007/s00299-014-1669-5openalex-snapshot
A comparison study of Agrobacterium-mediated transformation methods for root-specific promoter analysis in soybean
inferred← citeshttps://doi.org/10.1007/s00299-016-1948-4openalex-snapshot
Expansins: roles in plant growth and potential applications in crop improvement
inferred← citeshttps://doi.org/10.1007/s00299-021-02749-7openalex-snapshot
Genetic transformation of legumes: an update
inferred← citeshttps://doi.org/10.1007/s00425-024-04348-8openalex-snapshot
Identification of GmPT proteins and investigation of their expressions in response to abiotic stress in soybean
inferred← citeshttps://doi.org/10.1007/s00438-015-1133-4openalex-snapshot
Genome-wide identification and expression analysis of the expansin gene family in tomato
inferred← citeshttps://doi.org/10.1007/s00438-016-1226-8openalex-snapshot
Genome-wide identification of the expansin gene family in tobacco (Nicotiana tabacum)
inferred← citeshttps://doi.org/10.1007/s10529-020-02968-0openalex-snapshot
Overexpression of a Eutrema salsugineum phosphate transporter gene EsPHT1;4 enhances tolerance to low phosphorus stress in soybean
inferred← citeshttps://doi.org/10.1007/s10529-021-03079-0openalex-snapshot
Correction to: Overexpression of a Eutrema salsugineum phosphate transporter gene EsPHT1;4 enhances tolerance to low phosphorus stress in soybean
inferred← citeshttps://doi.org/10.1007/s10709-021-00136-4openalex-snapshot
Genome-wide identification of expansin gene family in barley and drought-related expansins identification based on RNA-seq
inferred← citeshttps://doi.org/10.1007/s10725-017-0313-0openalex-snapshot
Cloning and characterization of an expansin gene AbEXP from Achyranthes bidentata
inferred← citeshttps://doi.org/10.1007/s10725-020-00588-2openalex-snapshot
Blue and red light upregulate α-expansin 1 (EXPA1) in transgenic Brassica rapa and its overexpression promotes leaf and root growth in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s12033-017-0020-0openalex-snapshot
Extracellular Secretion of Phytase from Transgenic Wheat Roots Allows Utilization of Phytate for Enhanced Phosphorus Uptake
inferred← citeshttps://doi.org/10.1007/s13205-020-02293-3openalex-snapshot
Genome-wide identification, characterization, and expression analysis of the expansin gene family in watermelon (Citrullus lanatus)
inferred← citeshttps://doi.org/10.1007/s13205-021-03106-xopenalex-snapshot
Genome-wide identification, characterization of expansin gene family of banana and their expression pattern under various stresses
inferred← citeshttps://doi.org/10.1016/b978-0-12-811308-0.00018-1openalex-snapshot
Transgenic approaches for improving phosphorus use efficiency in plants
inferred← citeshttps://doi.org/10.1016/bs.agron.2024.08.002openalex-snapshot
Interaction of phosphorus supply and water deficits on the yield, protein and oil content, and nitrogen fixation of soybean (Glycine max (L.) Merr.)
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2016.06.001openalex-snapshot
Genetic modification of plant cell walls to enhance biomass yield and biofuel production in bioenergy 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.envexpbot.2019.05.024openalex-snapshot
Transient silencing of an expansin HvEXPA1 inhibits root cell elongation and reduces Al accumulation in root cell wall of Tibetan wild barley
inferred← citeshttps://doi.org/10.1016/j.fcr.2016.06.023openalex-snapshot
Root plasticity for maintenance of productivity under abiotic stressed soil environments in rice: Progress and prospects
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.139313openalex-snapshot
Phosphorylation of cellulose synthases in plant responses to environmental changes
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.05.014openalex-snapshot
Plant expansins: diversity and interactions with plant cell walls
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.06.008openalex-snapshot
Food for thought: how nutrients regulate root system architecture
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.02.022openalex-snapshot
Wheat expansin gene TaEXPA2 is involved in conferring plant tolerance to Cd toxicity
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
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112779openalex-snapshot
Understanding the mechanistic insight and relevance of root hair-driven rhizobia for developing climate-smart crops
inferred← citeshttps://doi.org/10.1016/j.scienta.2014.07.037openalex-snapshot
Overexpression of the rice phosphate transporter gene OsPT6 enhances tolerance to low phosphorus stress in vegetable soybean
inferred← citeshttps://doi.org/10.1016/s2095-3119(17)61709-xopenalex-snapshot
Transgenic approaches for improving use efficiency of nitrogen, phosphorus and potassium in crops
inferred← citeshttps://doi.org/10.1080/00103624.2019.1654506openalex-snapshot
Contribution of Roots and Mycorrhizal Hyphae on Phosphorus Efficiency of Maize(Zea mays, L.) Genotypes Grown on Calcareous Soil—A Mechanistic Modeling Approach
inferred← citeshttps://doi.org/10.1080/00380768.2014.970116openalex-snapshot
Influence of transgenic ath-miR399d tomato lines on microbial community and diversity in rhizosphere soil
inferred← citeshttps://doi.org/10.1080/15226514.2023.2295354openalex-snapshot
Phytoremediation ability and selected genetic transcription in Hydrocotyle umbellata -under cadmium stress
inferred← citeshttps://doi.org/10.1101/830612openalex-snapshot
GmPTF1 Modifies Root Architecture Responses to Phosphate Starvation in Soybean
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/jipb.12243openalex-snapshot
Effects of transgenic soybean on growth and phosphorus acquisition in mixed culture system
inferred← citeshttps://doi.org/10.1111/jipb.13433openalex-snapshot
Understandings and future challenges in soybean functional genomics and molecular breeding
inferred← citeshttps://doi.org/10.1111/pce.70796openalex-snapshot
Expansins: Molecular Mediators of Cell Wall Extensibility in Plant Development and Stress Adaptation
inferred← citeshttps://doi.org/10.1111/ppl.12492openalex-snapshot
Ectopic expression of wheat expansin gene TaEXPA2 improved the salt tolerance of transgenic tobacco by regulating Na+/K+ and antioxidant competence
inferred← citeshttps://doi.org/10.1111/ppl.12524openalex-snapshot
The purple acid phosphatase GmPAP21 enhances internal phosphorus utilization and possibly plays a role in symbiosis with rhizobia in soybean
inferred← citeshttps://doi.org/10.1111/tpj.13237openalex-snapshot
An Al‐inducible expansin gene, Os EXPA 10 is involved in root cell elongation of rice
inferred← citeshttps://doi.org/10.1111/tpj.15307openalex-snapshot
GmPTF1 modifies root architecture responses to phosphate starvation primarily through regulating GmEXPB2 expression in soybean
inferred← citeshttps://doi.org/10.1128/spectrum.02456-21openalex-snapshot
Arbuscular Mycorrhizal Fungi Enhanced Drought Resistance of Populus cathayana by Regulating the 14-3-3 Family Protein Genes
inferred← citeshttps://doi.org/10.1134/s1022795420040109openalex-snapshot
Identification and Characterization of the Expansin Genes in Triticum urartu in Response to Various Phytohormones
inferred← citeshttps://doi.org/10.1186/s13020-023-00867-wopenalex-snapshot
Identification and expression analysis of expansin gene family in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1371/journal.pone.0153494openalex-snapshot
Overexpression of the Wheat Expansin Gene TaEXPA2 Improved Seed Production and Drought Tolerance in Transgenic Tobacco Plants
inferred← citeshttps://doi.org/10.1371/journal.pone.0195138openalex-snapshot
Genome-wide identification of wheat (Triticum aestivum) expansins and expansin expression analysis in cold-tolerant and cold-sensitive wheat cultivars
inferred← citeshttps://doi.org/10.1515/biolog-2016-0015openalex-snapshot
Characterization and expression analysis of the expansin gene NnEXPA1 in lotus Nelumbo nucifera
inferred← citeshttps://doi.org/10.22034/jpbb.2021.302209.1014openalex-snapshot
In Silico Evaluation of Expansin-Gene Function in Softening and Fruit Ripening
inferred← citeshttps://doi.org/10.3389/fpls.2017.01376openalex-snapshot
Nitrate Uptake Affects Cell Wall Synthesis and Modeling
inferred← citeshttps://doi.org/10.3389/fpls.2019.00808openalex-snapshot
GmEXLB1, a Soybean Expansin-Like B Gene, Alters Root Architecture to Improve Phosphorus Acquisition in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1094157openalex-snapshot
Improving phosphorus acquisition efficiency through modification of root growth responses to phosphate starvation in legumes
inferred← citeshttps://doi.org/10.3390/agronomy11112354openalex-snapshot
Regulation of Phosphorus Supply on Nodulation and Nitrogen Fixation in Soybean Plants with Dual-Root Systems
inferred← citeshttps://doi.org/10.3390/ijms20215259openalex-snapshot
Cell Wall Proteins Play Critical Roles in Plant Adaptation to Phosphorus Deficiency
inferred← citeshttps://doi.org/10.3390/ijms252111814openalex-snapshot
Origin, Evolution, and Diversification of the Expansin Family in Plants
inferred← citeshttps://doi.org/10.3390/plants13121656openalex-snapshot
Overexpression of Wild Soybean Expansin Gene GsEXLB14 Enhanced the Tolerance of Transgenic Soybean Hairy Roots to Salt and Drought Stresses
inferred← citeshttps://doi.org/10.3390/plants4020334openalex-snapshot
Root Traits and Phenotyping Strategies for Plant Improvement
inferred← citeshttps://doi.org/10.3390/su18073198openalex-snapshot
Novel Developments in Nano Fertilizer for Sustainable Crop Production to Promote Global Food Security
inferred← citeshttps://doi.org/10.3906/bot-1502-40openalex-snapshot
Overexpression of a soybean expansin gene, GmEXP1, improvesdrought tolerance in transgenic tobacco
inferred← citeshttps://doi.org/10.5772/intechopen.1002885openalex-snapshot
Breeding for Macronutrient Use Efficiency (NTUE) in Legumes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26676743openalex-snapshot
Additional file 1 of Identification and expression analysis of expansin gene family in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.6084/m9.figshare.26676746openalex-snapshot
Additional file 2 of Identification and expression analysis of expansin gene family in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.6084/m9.figshare.26676749openalex-snapshot
Additional file 3 of Identification and expression analysis of expansin gene family in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.7868/s0002188117070122openalex-snapshot
ИСПОЛЬЗОВАНИЕ ПРИЗНАКОВ КОРНЕВЫХ СИСТЕМ ПОЛЕВЫХ КУЛЬТУР В СЕЛЕКЦИИ НА УРОЖАЙНОСТЬ И УСТОЙЧИВОСТЬ К СТРЕССОРАМ
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