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The Acid Growth Theory of auxin-induced cell elongation is alive and well.

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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/bf00201499openalex-snapshot
The pH profile for acid-induced elongation of coleoptile and epicotyl sections is consistent with the acid-growth theory
inferredcites →https://doi.org/10.1007/bf00201500openalex-snapshot
The outer epidermis of Avena and maize coleoptiles is not a unique target for auxin in elongation growth
inferredcites →https://doi.org/10.1016/s0070-2153(08)60746-2openalex-snapshot
Chapter 6 Control of Plant Cell Enlargement By Hydrogen Ions
inferredcites →https://doi.org/10.1104/pp.46.2.250openalex-snapshot
Enhancement of Wall Loosening and Elongation by Acid Solutions
inferredcites →https://doi.org/10.1104/pp.67.1.146openalex-snapshot
Auxin-regulated Wall Loosening and Sustained Growth in Elongation
inferredcites →https://doi.org/10.1104/pp.68.2.415openalex-snapshot
A Model for Predicting Ionic Equilibrium Concentrations in Cell Walls
inferredcites →https://doi.org/10.1104/pp.90.1.202openalex-snapshot
pH-Dependence of Extension Growth in Avena Coleoptiles and Its Implications for the Mechanism of Auxin Action
inferredcites →https://doi.org/10.1104/pp.93.2.432openalex-snapshot
Auxin Enhancement of mRNAs in Epidermis and Internal Tissues of the Pea Stem and Its Significance for Control of Elongation
inferredcites →https://doi.org/10.1104/pp.97.1.449openalex-snapshot
The Epidermis of the Pea Epicotyl Is Not a Unique Target Tissue for Auxin-Induced Growth
inferredcites →https://doi.org/10.1126/science.212.4490.70openalex-snapshot
Geotropism in Corn Roots: Evidence for Its Mediation by Differential Acid Efflux

What points at this work

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

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Mechanistic Insights into Indole-3-Acetic Acid-Promoting Wheat Root Phenanthrene Uptake: Transcriptomic Evidence
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Identification of the Bpexp1 Gene and its Upstream Factor Bpmyb4 Participating in the Xylem Development of Betula Platyphylla
inferred← citeshttps://doi.org/10.1002/047126363x.agr027openalex-snapshot
Auxins (Indole Auxins)
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001688.pub2openalex-snapshot
Plant Cell Growth and Elongation
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The Biosynthesis and Function of Polysaccharide Components of the Plant Cell Wall
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Bio‐Tribology and Bio‐Lubrication of Plant Cell Walls
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Polar auxin transport is implicated in vessel differentiation and spatial patterning during secondary growth in Populus
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Plant cell enlargement and the action of expansins
inferred← citeshttps://doi.org/10.1002/biot.202200134openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/etc.2760openalex-snapshot
Modulation of exogenous selenium in cadmium-induced changes in antioxidative metabolism, cadmium uptake, and photosynthetic performance in the 2 tobacco genotypes differing in cadmium tolerance
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Interactions between Inorganic Nitrogen Nutrition and Root Development
inferred← citeshttps://doi.org/10.1002/jpln.200800349openalex-snapshot
Decline in leaf growth under salt stress is due to an inhibition of H+‐pumping activity and increase in apoplastic pH of maize leaves
inferred← citeshttps://doi.org/10.1002/jpln.201200414openalex-snapshot
Potassium and stress alleviation: Physiological functions and management of cotton
inferred← citeshttps://doi.org/10.1002/jpln.201500228openalex-snapshot
Phosphorus speciation and high‐affinity transporters are influenced by humic substances
inferred← citeshttps://doi.org/10.1002/jpln.201700532openalex-snapshot
Wheat nutrition and growth as affected by humic acid‐phosphate interaction
inferred← citeshttps://doi.org/10.1002/jsfa.2740680407openalex-snapshot
Anisotropic swelling of cell walls of sugar beet tissue: Influence of ion‐exchange and sucrose
inferred← citeshttps://doi.org/10.1002/pld3.332openalex-snapshot
Differential abundance proteins associated with rapid growth of etiolated coleoptiles in maize
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BOTANICAL BRIEFING: The Function and Metabolism of Ascorbic Acid in Plants
inferred← citeshttps://doi.org/10.1006/anbo.1998.0686openalex-snapshot
Auxin Stimulates Cl−Uptake by Oat Coleoptiles
inferred← citeshttps://doi.org/10.1006/anbo.1998.0814openalex-snapshot
Changes in Auxin Patterns in Developing Gynophores of the Peanut Plant (Arachis hypogaeaL.)
inferred← citeshttps://doi.org/10.1007/1-4020-3589-6_9openalex-snapshot
Effects of Soil pH and Aluminum on Plant Respiration
inferred← citeshttps://doi.org/10.1007/3-540-27998-9_11openalex-snapshot
New insight into auxin perception, signal transduction and transport
inferred← citeshttps://doi.org/10.1007/7089_2006_070openalex-snapshot
Cellulose and Cell Elongation
inferred← citeshttps://doi.org/10.1007/7089_2006_071openalex-snapshot
Hemicelluloses and Cell Expansion
inferred← citeshttps://doi.org/10.1007/7089_2006_075openalex-snapshot
Redox and Wall-Restructuring
inferred← citeshttps://doi.org/10.1007/7089_2006_076openalex-snapshot
Mechanics of the Expanding Cell Wall
inferred← citeshttps://doi.org/10.1007/7089_2006_078openalex-snapshot
The Control of Cell Size and Rate of Elongation in the Arabidopsis Root
inferred← citeshttps://doi.org/10.1007/978-1-0716-1816-5_5openalex-snapshot
Postembryonic Organogenesis in Plants: Experimental Induction of New Shoot and Root Organs
inferred← citeshttps://doi.org/10.1007/978-1-0716-3511-7_7openalex-snapshot
Assaying the Effect of Peptide Treatment on H+-Pumping Activity in Plasma Membranes from Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.1007/978-1-4020-2686-7_10openalex-snapshot
Auxin and Cell Elongation
inferred← citeshttps://doi.org/10.1007/978-1-4020-2686-7_13openalex-snapshot
Expansins as Agents in Hormone Action
inferred← citeshttps://doi.org/10.1007/978-1-4020-5005-3_5openalex-snapshot
Plant Growth Regulators I: Introduction; Auxins, their Analogues and Inhibitors
inferred← citeshttps://doi.org/10.1007/978-1-4020-5725-0_3openalex-snapshot
How Well Understood Are the Processes that Create Dendroclimatic Records? A Mechanistic Model of the Climatic Control on Conifer Tree-Ring Growth Dynamics
inferred← citeshttps://doi.org/10.1007/978-1-4419-0987-9_14openalex-snapshot
The Cytoskeleton and Root Growth Behavior
inferred← citeshttps://doi.org/10.1007/978-1-4614-6108-1_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-33528-1_2openalex-snapshot
Insights into the Cell Wall and Cytoskeletal Regulation by Mechanical Forces in Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-41283-8_10openalex-snapshot
Mechanisms of Sugar Beet Response to Biotic and Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-3-030-71262-4_11openalex-snapshot
Zinc
inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_3openalex-snapshot
Seed Germination: Explicit Crosstalk Between Hormones and ROS
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_9openalex-snapshot
Membrane Delivery to the Vacuole and the Multifunctional Roles of Vacuoles
inferred← citeshttps://doi.org/10.1007/978-3-319-06710-0_15openalex-snapshot
Abiotic Stress Tolerance in Plants: Exploring the Role of Nitric Oxide and Humic Substances
inferred← citeshttps://doi.org/10.1007/978-3-319-19968-9_13openalex-snapshot
Aluminum-Induced Inhibition of Root Growth: Roles of Cell Wall Assembly, Structure, and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-56645-0_9openalex-snapshot
Molecular Mechanisms Regulating Root Hair Tip Growth: A Comparison with Pollen Tubes
inferred← citeshttps://doi.org/10.1007/978-3-319-79099-2_14openalex-snapshot
Cell Wall Expansion as Viewed by the Creep Method
inferred← citeshttps://doi.org/10.1007/978-3-540-37843-3_10openalex-snapshot
Electrogenic Pumps
inferred← citeshttps://doi.org/10.1007/978-3-540-78826-3_12openalex-snapshot
Ion Dynamics During the Polarized Growth of Arbuscular Mycorrhizal Fungi: From Presymbiosis to Symbiosis
inferred← citeshttps://doi.org/10.1007/978-3-540-89228-1_12openalex-snapshot
Signaling in Phototropism
inferred← citeshttps://doi.org/10.1007/978-3-642-02550-1openalex-snapshot
Desert Plants : Biology and Biotechnology
inferred← citeshttps://doi.org/10.1007/978-3-642-02550-1_11openalex-snapshot
Parthenocarpy and Seed Production in Burseraceae
inferred← citeshttps://doi.org/10.1007/978-3-642-13431-9_3openalex-snapshot
The Plasma Membrane and the Cell Wall
inferred← citeshttps://doi.org/10.1007/978-3-642-20966-6_6openalex-snapshot
Signalling in Ectomycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.1007/978-3-642-29119-7_12openalex-snapshot
Membrane Excitation and Cytoplasmic Streaming as Modulators of Photosynthesis and Proton Flows in Characean Cells
inferred← citeshttps://doi.org/10.1007/978-3-642-40096-4_5openalex-snapshot
Types of Mycorrhizal Association
inferred← citeshttps://doi.org/10.1007/978-90-481-3195-2_32openalex-snapshot
Biochemistry of the Fiber
inferred← citeshttps://doi.org/10.1007/978-94-011-0239-1_15openalex-snapshot
Molecular genetics of auxin and cytokinin
inferred← citeshttps://doi.org/10.1007/978-94-011-0307-7_61openalex-snapshot
Oligosaccharides from Xyloglucan Affect the Development of Rubus Fruticosus Cell Suspension Culture
inferred← citeshttps://doi.org/10.1007/978-94-011-0473-9_10openalex-snapshot
Auxin and Cell Elongation
inferred← citeshttps://doi.org/10.1007/978-94-017-2664-1_16openalex-snapshot
Cell Wall Extensibility Changes by Hormonal and Non-Hormonal Factors
inferred← citeshttps://doi.org/10.1007/978-94-017-2687-0_6openalex-snapshot
Phytotoxins and Plant Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-94-017-2858-4_13openalex-snapshot
Nitrate uptake by bean (Phaseolus vulgaris L.) roots under phosphate deficiency
inferred← citeshttps://doi.org/10.1007/978-94-017-2858-4_3openalex-snapshot
Measurement of viscoelastic properties of root cell walls affected by low pH in lateral roots of Pisum sativum L.
inferred← citeshttps://doi.org/10.1007/978-94-017-3101-0_39openalex-snapshot
Inhibition of root growth by salinity stress: Toxicity or an adaptive biophysical response?
inferred← citeshttps://doi.org/10.1007/978-94-017-8783-3_2openalex-snapshot
Developmental Anatomy of Galls in the Neotropics: Arthropods Stimuli Versus Host Plant Constraints
inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_13openalex-snapshot
Cereals and Phytohormones Under Drought Stress
inferred← citeshttps://doi.org/10.1007/978-981-95-7033-1_3openalex-snapshot
Leaf Development
inferred← citeshttps://doi.org/10.1007/bf00016487openalex-snapshot
Molecular genetics of auxin and cytokinin
inferred← citeshttps://doi.org/10.1007/bf00019014openalex-snapshot
Hormonal regulation of S-adenosylmethionine synthase transcripts in pea ovaries
inferred← citeshttps://doi.org/10.1007/bf00024404openalex-snapshot
Developmental and genotypic differences in the response of pea stem segments to auxin
inferred← citeshttps://doi.org/10.1007/bf00192534openalex-snapshot
Uptake and decarboxylation of indole-3-acetic acid during auxin-induced growth in lupin hypocotyl segments
inferred← citeshttps://doi.org/10.1007/bf00195692openalex-snapshot
An oat coleoptile wall protein that induces wall extension in vitro and that is antigenically related to a similar protein from cucumber hypocotyls
inferred← citeshttps://doi.org/10.1007/bf00198577openalex-snapshot
Inhibition of Golgi-apparatus function by brefeldin A in maize coleoptiles and its consequences on auxin-mediated growth, cell-wall extensibility and secretion of cell-wall proteins
inferred← citeshttps://doi.org/10.1007/bf00198927openalex-snapshot
Effects of fusicoccin on intact cotton plants (Gossypium hirsutum L.)
inferred← citeshttps://doi.org/10.1007/bf00198931openalex-snapshot
Effect of brassinosteroids on growth and proton extrusion in the alga Chlorella vulgaris Beijerinck (Chlorophyceae)
inferred← citeshttps://doi.org/10.1007/bf00224794openalex-snapshot
Changing proton concentrations at the surfaces of gravistimulated Phleum roots
inferred← citeshttps://doi.org/10.1007/bf00620057openalex-snapshot
The electrical response ofAvena coleoptile cortex to auxins
inferred← citeshttps://doi.org/10.1007/bf00714467openalex-snapshot
Gibberellic acid induces cytoplasmic acidification in maize coleoptiles
inferred← citeshttps://doi.org/10.1007/bf01106764openalex-snapshot
An auxin-resistant mutant ofNicotiana plumbaginifolia Viv. is impaired in 1-naphthaleneacetic acid-induced hyperpolarization of hypocotyl cell membranes in intact seedlings
inferred← citeshttps://doi.org/10.1007/bf01280310openalex-snapshot
Cell biology and genetics of root hair formation inArabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/bf01281193openalex-snapshot
Localized membrane-wall adhesions inPelvetia zygotes
inferred← citeshttps://doi.org/10.1007/bf01288027openalex-snapshot
Protein synthesis and Golgi-mediated vesicle traffic is not required to maintain a polarised membrane voltage in the presence of auxin
inferred← citeshttps://doi.org/10.1007/bf02507161openalex-snapshot
Expansins.
inferred← citeshttps://doi.org/10.1007/bf02913986openalex-snapshot
The effects of electric field on the growth of intact seedlings and coleoptile segments ofZea mays L.
inferred← citeshttps://doi.org/10.1007/pl00000782openalex-snapshot
Life behind cell walls: paradigm lost, paradigm regained
inferred← citeshttps://doi.org/10.1007/pl00006980openalex-snapshot
The pro Gene Causes an Enhanced Cell Expansion Response to Fusicoccin in Tomato
inferred← citeshttps://doi.org/10.1007/pl00006983openalex-snapshot
Polyamine Sparing May Be Involved in the Prolongation of Cell Division Due to Inhibition of Phenylpropanoid Synthesis in Cytokinin-Starved Soybean Cells
inferred← citeshttps://doi.org/10.1007/pl00008101openalex-snapshot
Cellular mechanisms underlying growth asymmetry during stem gravitropism
inferred← citeshttps://doi.org/10.1007/s00122-010-1321-xopenalex-snapshot
Identification of differentially expressed genes at two key endosperm development stages using two maize inbreds with large and small grain and integration with detected QTL for grain weight
inferred← citeshttps://doi.org/10.1007/s00253-015-6534-0openalex-snapshot
Bacterial expansins and related proteins from the world of microbes
inferred← citeshttps://doi.org/10.1007/s00299-013-1426-1openalex-snapshot
Usual and unusual development of the dicot leaf: involvement of transcription factors and hormones
inferred← citeshttps://doi.org/10.1007/s00299-014-1728-yopenalex-snapshot
GA3 enhances root responsiveness to exogenous IAA by modulating auxin transport and signalling in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-015-1762-4openalex-snapshot
Plasma membrane H+-ATPase is involved in methyl jasmonate-induced root hair formation in lettuce (Lactuca sativa L.) seedlings
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/s00299-021-02803-4openalex-snapshot
The role of 14-3-3 proteins in plant growth and response to abiotic stress
inferred← citeshttps://doi.org/10.1007/s00299-026-03744-6openalex-snapshot
Dual impact of ambient pH on the virulence of Phytophthora nicotianae and resistance in tobacco
inferred← citeshttps://doi.org/10.1007/s00344-003-0009-8openalex-snapshot
Root Development and Absorption of Ammonium and Nitrate from the Rhizosphere
inferred← citeshttps://doi.org/10.1007/s00344-010-9180-xopenalex-snapshot
The Hormonal Regulation of Flower Development
inferred← citeshttps://doi.org/10.1007/s00344-012-9280-xopenalex-snapshot
Special Solutions to the Ortega Equation
inferred← citeshttps://doi.org/10.1007/s00344-012-9282-8openalex-snapshot
Apoplast Acidification in Growing Barley (Hordeum vulgare L.) Leaves
inferred← citeshttps://doi.org/10.1007/s00344-017-9714-6openalex-snapshot
Proteomic Analysis Demonstrates that Elongation of Below-Ear Internodes in Maize is Related to Three Different Hormones
inferred← citeshttps://doi.org/10.1007/s00344-019-10026-xopenalex-snapshot
Chemical Potential-Induced Wall State Transitions in Plant Cell Growth
inferred← citeshttps://doi.org/10.1007/s00344-020-10112-5openalex-snapshot
Low-Nitrogen Stress Stimulates Lateral Root Initiation and Nitrogen Assimilation in Wheat: Roles of Phytohormone Signaling
inferred← citeshttps://doi.org/10.1007/s00344-021-10459-3openalex-snapshot
Expansive Growth vs. pH Reflects a Poisson Point Process of Binding/Unbinding Events in Plant Cell Walls
inferred← citeshttps://doi.org/10.1007/s003440000042openalex-snapshot
Halogenated Auxins Affect Microtubules and Root Elongation in Lactuca sativa
inferred← citeshttps://doi.org/10.1007/s00424-008-0457-xopenalex-snapshot
The plant plasma membrane proton pump ATPase: a highly regulated P-type ATPase with multiple physiological roles
inferred← citeshttps://doi.org/10.1007/s00425-001-0690-4openalex-snapshot
Photosynthetic control of the plasma membrane H + -ATPase in Vallisneria leaves. II. Presence of putative isogenes and a protein equipped with a C-terminal autoinhibitory domain
inferred← citeshttps://doi.org/10.1007/s00425-003-0993-8openalex-snapshot
Extensibility of isolated cell walls in the giant tip-growing cells of the xanthophycean alga Vaucheria terrestris
inferred← citeshttps://doi.org/10.1007/s00425-004-1274-xopenalex-snapshot
Mannan transglycosylase: a novel enzyme activity in cell walls of higher plants
inferred← citeshttps://doi.org/10.1007/s00425-004-1456-6openalex-snapshot
Relationship between expression of the PM H+-ATPase, growth and ion partitioning in the leaves of salt-treated Medicago species
inferred← citeshttps://doi.org/10.1007/s00425-005-0152-5openalex-snapshot
Loss of stability, pH, and the anisotropic extensibility of Chara cell walls
inferred← citeshttps://doi.org/10.1007/s00425-006-0372-3openalex-snapshot
The cyclic nucleotide-gated calmodulin-binding channel AtCNGC10 localizes to the plasma membrane and influences numerous growth responses and starch accumulation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-006-0454-2openalex-snapshot
Indolacetic and humic acids induce lateral root development through a concerted plasmalemma and tonoplast H+ pumps activation
inferred← citeshttps://doi.org/10.1007/s00425-008-0876-0openalex-snapshot
An anionic class III peroxidase from zucchini may regulate hypocotyl elongation through its auxin oxidase activity
inferred← citeshttps://doi.org/10.1007/s00425-013-1941-xopenalex-snapshot
Rapid auxin-induced root growth inhibition requires the TIR and AFB auxin receptors
inferred← citeshttps://doi.org/10.1007/s00425-016-2571-xopenalex-snapshot
Expression of a constitutively activated plasma membrane H+-ATPase in Nicotiana tabacum BY-2 cells results in cell expansion
inferred← citeshttps://doi.org/10.1007/s00425-020-03376-4openalex-snapshot
The physiological mechanism underlying root elongation in response to nitrogen deficiency in crop plants
inferred← citeshttps://doi.org/10.1007/s00425-022-03826-1openalex-snapshot
Interaction between fructan metabolism and plant growth regulators
inferred← citeshttps://doi.org/10.1007/s00425-024-04463-6openalex-snapshot
Ectopic expression of OsWOX9A alters leaf anatomy and plant architecture in rice
inferred← citeshttps://doi.org/10.1007/s004250050672openalex-snapshot
Identification and expression of three new Nicotiana plumbaginifolia genes which encode isoforms of a plasma-membrane H + -ATPase, and one of which is induced by mechanical stress
inferred← citeshttps://doi.org/10.1007/s004250050703openalex-snapshot
Submergence induces expansin gene expression in flooding-tolerant Rumex palustris and not in flooding-intolerant R. acetosa
inferred← citeshttps://doi.org/10.1007/s004250050747openalex-snapshot
Effects of NH 4 + , NO 3 − and HCO 3 − on apoplast pH in the outer cortex of root zones of maize, as measured by the fluorescence ratio of fluorescein boronic acid
inferred← citeshttps://doi.org/10.1007/s00427-016-0572-1openalex-snapshot
The vascular plants: open system of growth
inferred← citeshttps://doi.org/10.1007/s00468-019-01940-4openalex-snapshot
The role of plant hormones in tree-ring formation
inferred← citeshttps://doi.org/10.1007/s00572-008-0204-3openalex-snapshot
Arbuscular mycorrhizal fungi induce differential activation of the plasma membrane and vacuolar H+ pumps in maize roots
inferred← citeshttps://doi.org/10.1007/s00709-010-0172-2openalex-snapshot
Expansin-regulated cell elongation is involved in the drought tolerance in wheat
inferred← citeshttps://doi.org/10.1007/s00709-021-01697-zopenalex-snapshot
Plant root development: is the classical theory for auxin-regulated root growth false?
inferred← citeshttps://doi.org/10.1007/s007090200007openalex-snapshot
A role for actin-driven secretion in auxin-induced growth
inferred← citeshttps://doi.org/10.1007/s10265-003-0110-xopenalex-snapshot
Role of the plasma membrane H + -ATPase in auxin-induced elongation growth: historical and new aspects
inferred← citeshttps://doi.org/10.1007/s10265-008-0176-6openalex-snapshot
pH and expansin action on single suspension-cultured tomato (Lycopersicon esculentum) cells
inferred← citeshttps://doi.org/10.1007/s10535-007-0015-yopenalex-snapshot
Estimation of endogenous contents of phytohormones during internode development in Merremia emarginata
inferred← citeshttps://doi.org/10.1007/s10535-007-0147-0openalex-snapshot
Effect of cadmium on growth, proton extrusion and membrane potential in maize coleoptile segments
inferred← citeshttps://doi.org/10.1007/s10725-007-9184-0openalex-snapshot
Effect of temperature on growth, proton extrusion and membrane potential in maize (Zea mays L.) coleoptile segments
inferred← citeshttps://doi.org/10.1007/s10725-013-9855-yopenalex-snapshot
Cellular responses to naphthoquinones: juglone as a case study
inferred← citeshttps://doi.org/10.1007/s10725-017-0325-9openalex-snapshot
A comparison of the effects of 1,4-naphthoquinone and 2-hydroxy-1,4-naphthoquinone (lawsone) on indole-3-acetic acid (IAA)-induced growth of maize coleoptile cells
inferred← citeshttps://doi.org/10.1007/s10725-018-0453-xopenalex-snapshot
Emerging functions of chromatin modifications in auxin biosynthesis in response to environmental alterations
inferred← citeshttps://doi.org/10.1007/s10725-019-00522-1openalex-snapshot
Study of auxin regulation of pollen tube growth through calcium channels in Pyrus pyrifolia
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/s11033-021-06589-2openalex-snapshot
The Arabidopsis expansin gene (AtEXPA18) is capable to ameliorate drought stress tolerance in transgenic tobacco plants
inferred← citeshttps://doi.org/10.1007/s11103-004-3474-yopenalex-snapshot
Differential expression profiles of growth-related genes in the elongation zone of maize primary roots
inferred← citeshttps://doi.org/10.1007/s11103-016-0476-5openalex-snapshot
Auxin response under osmotic stress
inferred← citeshttps://doi.org/10.1007/s11104-020-04459-7openalex-snapshot
Magnesium alleviates aluminum toxicity by promoting polar auxin transport and distribution and root alkalization in the root apex in populus
inferred← citeshttps://doi.org/10.1007/s11104-022-05852-0openalex-snapshot
Water-dispersible carbon nanomaterials improve lettuce (Latuca sativa) growth and enhance soil biochemical quality at low to medium application rates
inferred← citeshttps://doi.org/10.1007/s11104-023-06297-9openalex-snapshot
Calcifuge and soil-indifferent Proteaceae from south-western Australia: novel strategies in a calcareous habitat
inferred← citeshttps://doi.org/10.1007/s11183-005-0073-yopenalex-snapshot
The Effects of H+-ATPase Activator and Inhibitors on Cell Growth in the Maize Root
inferred← citeshttps://doi.org/10.1007/s11183-005-0101-yopenalex-snapshot
Mechanisms Coordinating Wheat Seedling Growth Response as Affected by Shoot/Root Ratio
inferred← citeshttps://doi.org/10.1007/s11240-017-1235-2openalex-snapshot
Phototropic bending of intact and wounded potato shoots
inferred← citeshttps://doi.org/10.1007/s11356-017-0795-3openalex-snapshot
Recycling of wastes from fish beneficiation by composting: chemical characteristics of the compost and efficiency of their humic acids in stimulating the growth of lettuce
inferred← citeshttps://doi.org/10.1007/s11515-018-1518-yopenalex-snapshot
Phototropism in land plants: Molecules and mechanism from light perception to response
inferred← citeshttps://doi.org/10.1007/s11627-000-0053-zopenalex-snapshot
A novel cottong ovule culture: Induction, growth, and characterization of submerged cotton fibers (Gossypium hirsutum L.)
inferred← citeshttps://doi.org/10.1007/s11738-002-0035-3openalex-snapshot
Influence of gibberellic acid on auxin biosynthesis and their effects on coleoptile elongation in garlic
inferred← citeshttps://doi.org/10.1007/s11738-010-0669-5openalex-snapshot
Level of ascorbic acid in transgenic rice for l-galactono-1,4-lactone dehydrogenase overexpressing or suppressed is associated with plant growth and seed set
inferred← citeshttps://doi.org/10.1007/s11738-011-0803-zopenalex-snapshot
Effect of thiosulphinates contained in garlic extract on growth, proton fluxes and membrane potential in maize (Zea mays L.) coleoptile segments
inferred← citeshttps://doi.org/10.1007/s11738-018-2674-zopenalex-snapshot
Effects of potassium deficiency on the enzymatic changes in developing cotton fibers
inferred← citeshttps://doi.org/10.1007/s11738-022-03413-7openalex-snapshot
Root system responses to phosphate nutrition involve plasma membrane H+-ATPases in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s12042-010-9048-zopenalex-snapshot
Papaya Fruit Softening: Role of Hydrolases
inferred← citeshttps://doi.org/10.1007/s12374-022-09363-4openalex-snapshot
The Comparison of Temporal Transcriptome Changes Between Morning-Opening and Afternoon-Opening Iris Flowers Reveals the Candidate Genes Regulating Flower Opening and Closing
inferred← citeshttps://doi.org/10.1007/s12892-026-00354-2openalex-snapshot
Optimisation of cotyledonary node-based tissue culture workflow for Agrobacterium-mediated transformation in soybean (Glycine max)
inferred← citeshttps://doi.org/10.1007/s40626-019-00145-xopenalex-snapshot
Plant electrome: the electrical dimension of plant life
inferred← citeshttps://doi.org/10.1007/s42729-023-01486-yopenalex-snapshot
Effects of Potassium and Nanocapsule of Potassium on Pepper Growth and Physiological Changes in High-Temperature Stress
inferred← citeshttps://doi.org/10.1016/0014-5793(93)81424-xopenalex-snapshot
Structure, function and regulation of plasma membrane H+‐ATPase
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00886-1openalex-snapshot
Proton pump activation and growth promotion by cinchomeronic acid in radish
inferred← citeshttps://doi.org/10.1016/0168-9452(93)90078-eopenalex-snapshot
o-Hydroxyphenylacetic acid-enhanced rice coleoptile elongation
inferred← citeshttps://doi.org/10.1016/0955-0674(94)90095-7openalex-snapshot
The plant extracellular matrix: in a new expansive mood
inferred← citeshttps://doi.org/10.1016/b978-0-08-057455-4.50082-7openalex-snapshot
Plant Cell Physiology
inferred← citeshttps://doi.org/10.1016/b978-0-12-387692-8.00002-3openalex-snapshot
Recent Advances in Understanding the Regulation of Whole-Plant Growth Inhibition by Salinity, Drought and Colloid Stress
inferred← citeshttps://doi.org/10.1016/b978-0-12-419987-3.00019-4openalex-snapshot
References
inferred← citeshttps://doi.org/10.1016/b978-0-12-656970-4.50056-7openalex-snapshot
Plant Cell Physiology
inferred← citeshttps://doi.org/10.1016/b978-0-12-656971-1.50056-8openalex-snapshot
Plant Cell Physiology
inferred← citeshttps://doi.org/10.1016/b978-0-12-800132-5.00003-1openalex-snapshot
The Physiology of Potassium in Crop Production
inferred← citeshttps://doi.org/10.1016/b978-0-12-816365-8.00003-8openalex-snapshot
Water relations and nutrient uptake
inferred← citeshttps://doi.org/10.1016/b978-0-12-816365-8.09993-0openalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1016/b978-0-323-91314-0.00016-8openalex-snapshot
Zinc and plant hormones: an updated review
inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00001-xopenalex-snapshot
Signaling crosstalk between auxins—abscisic acid in plant defense, growth, and development
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00015-4openalex-snapshot
Auxin receptors: Pivotal regulators of plant development
inferred← citeshttps://doi.org/10.1016/b978-0-443-33006-3.00007-3openalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1016/b978-0-444-89608-7.50017-4openalex-snapshot
Leaf cell expansion
inferred← citeshttps://doi.org/10.1016/b978-012378260-1/50006-3openalex-snapshot
Nitrogen as a Limiting Factor: Crop Acquisition of Ammonium and Nitrate
inferred← citeshttps://doi.org/10.1016/b978-012652840-4/50019-xopenalex-snapshot
References
inferred← citeshttps://doi.org/10.1016/b978-012656976-6/50155-4openalex-snapshot
Plant Cell Physiology
inferred← citeshttps://doi.org/10.1016/b978-012660570-9/50157-xopenalex-snapshot
Hormonal Regulation of Cell Division and Cell Growth
inferred← citeshttps://doi.org/10.1016/bs.abr.2026.07.012openalex-snapshot
Sugarcane management with biostimulants and plant growth regulators
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.10.003openalex-snapshot
Patterning at the shoot apical meristem and phyllotaxis
inferred← citeshttps://doi.org/10.1016/j.abb.2013.10.025openalex-snapshot
Phosphorylation-related modification at the dimer interface of 14-3-3ω dramatically alters monomer interaction dynamics
inferred← citeshttps://doi.org/10.1016/j.actaastro.2018.12.036openalex-snapshot
Plant cell development and aging may accelerate in microgravity
inferred← citeshttps://doi.org/10.1016/j.algal.2019.101547openalex-snapshot
Effects of an auxin-producing symbiotic bacterium on cell growth of the microalga Haematococcus pluvialis: Elevation of cell density and prolongation of exponential stage
inferred← citeshttps://doi.org/10.1016/j.bbagen.2015.03.007openalex-snapshot
The imbalance of redox homeostasis in arthropod-induced plant galls: Mechanisms of stress generation and dissipation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.149507openalex-snapshot
Arabidopsis plasma membrane H+-ATPase interacts with auxin to regulate Danger-Associated Peptide Pep1-induced root growth inhibition
inferred← citeshttps://doi.org/10.1016/j.biombioe.2026.109806openalex-snapshot
Sugarcane filter cake-derived humic acid modulates phosphorus acquisition and transporter response in tomato under low-phosphorus conditions
inferred← citeshttps://doi.org/10.1016/j.biortech.2017.03.149openalex-snapshot
Selective enrichment of Eicosapentaenoic acid (20:5n-3) in N. oceanica CASA CC201 by natural auxin supplementation
inferred← citeshttps://doi.org/10.1016/j.biortech.2021.125139openalex-snapshot
Enhanced enzymatic hydrolysis of cellulose by endoglucanase via expansin pretreatment and the addition of zinc ions
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2026.108930openalex-snapshot
Expansins and expansin-like proteins revisited: Untangling the ‘Gordian’ knots
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.11.014openalex-snapshot
A Statistical Model of Expansive Growth in Plant and Fungal Cells: The Case of Phycomyces
inferred← citeshttps://doi.org/10.1016/j.ceca.2016.06.006openalex-snapshot
The role of Ca2+ and Ca2+ channels in the gametophytic self-incompatibility of Pyrus pyrifolia
inferred← citeshttps://doi.org/10.1016/j.cell.2022.07.012openalex-snapshot
Extracellular pH sensing by plant cell-surface peptide-receptor complexes
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.143059openalex-snapshot
Valorization of sewage sludge incineration ash as a novel soilless growing medium for urban agriculture and greenery
inferred← citeshttps://doi.org/10.1016/j.cj.2017.08.007openalex-snapshot
Cell signaling mechanisms and metabolic regulation of germination and dormancy in barley seeds
inferred← citeshttps://doi.org/10.1016/j.cj.2020.03.006openalex-snapshot
Map-based cloning of a novel QTL qBN-1 influencing branch number in soybean [Glycine max (L.) Merr.]
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