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Acid growth effects in maize roots: Evidence for a link between auxin-economy and proton extrusion in the control of root growth
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-642-66589-9_11openalex-snapshot
Auxins and the Regulation of Root Growth
inferredcites →https://doi.org/10.1007/978-3-642-66589-9_22openalex-snapshot
Geotropic Response Mechanisms in Roots and Shoots
inferredcites →https://doi.org/10.1007/bf00380852openalex-snapshot
Endogenous and exogenous auxin in the control of root growth
inferredcites →https://doi.org/10.1007/bf00385279openalex-snapshot
Abscisic acid as a root growth inhibitor: Physiological analyses
inferredcites →https://doi.org/10.1007/bf00386312openalex-snapshot
The in-vitro acid-growth response: Relation to in-vivo growth responses and auxin action
inferredcites →https://doi.org/10.1007/bf00386886openalex-snapshot
Versuche und Hypothese zur Prim�rwirkung des Auxins beim Streckungswachstum
inferredcites →https://doi.org/10.1007/bf00387107openalex-snapshot
Localization and identification of auxin in roots of Zea mays
inferredcites →https://doi.org/10.1007/bf00387886openalex-snapshot
Auxin gradient along the root of the maize seedling
inferredcites →https://doi.org/10.1007/bf00390285openalex-snapshot
Auxin-induced hydrogen-ion secretion in Avena coleoptiles and its implications
inferredcites →https://doi.org/10.1007/bf00390322openalex-snapshot
Indoleacetic acid movement in the root cap
inferredcites →https://doi.org/10.1007/bf00390819openalex-snapshot
Rapid growth responses of corn root segments: Effect of pH on elongation
inferredcites →https://doi.org/10.1007/bf00396184openalex-snapshot
Auxin inhibition of acid-and fusicoccin-induced elongation in lentil roots
inferredcites →https://doi.org/10.1007/bf00398262openalex-snapshot
Rapid-growth responses of corn root segments: Effect of citrate-phosphate buffer on elongation
inferredcites →https://doi.org/10.1016/0048-4059(76)90027-8openalex-snapshot
The development and function of roots
inferredcites →https://doi.org/10.1016/0304-4211(73)90042-4openalex-snapshot
Correlation between cell enlargement in pea internode segments and decrease in the pH of the medium of incubation
inferredcites →https://doi.org/10.1016/0304-4211(75)90055-3openalex-snapshot
Action of fusicoccin and abscisic acid on root growth
inferredcites →https://doi.org/10.1016/0304-4211(75)90105-4openalex-snapshot
Stimulation of H+ efflux and cation uptake by fusicoccin in barley roots
inferredcites →https://doi.org/10.1016/0304-4211(76)90075-4openalex-snapshot
Fusicoccin and auxin effects on root growth
inferredcites →https://doi.org/10.1016/0304-4211(76)90173-5openalex-snapshot
Fusicoccin-induced, K+-stimulated proton secretion and acid-induced growth of apical root segments
inferredcites →https://doi.org/10.1016/b978-0-08-025898-0.50009-xopenalex-snapshot
A CRITICAL ASSESSMENT OF THE CHOLODNY-WENT THEORY OF SHOOT GEOTROPISM
inferredcites →https://doi.org/10.1016/s0031-9422(00)91302-5openalex-snapshot
Indol-3yl-acetic acid in roots of Zea mays
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/10.1038/newbio244285a0openalex-snapshot
Effect of pH and Surface Charge on Cell Uptake of Auxin
inferredcites →https://doi.org/10.1073/pnas.67.4.1814openalex-snapshot
An In Vitro System That Simulates Plant Cell Extension Growth
inferredcites →https://doi.org/10.1093/jxb/29.5.1051openalex-snapshot
The Regulation of Root Growth in Cress Seedlings by Light and Gravity
inferredcites →https://doi.org/10.1104/pp.58.2.210openalex-snapshot
Kinetics of Hormone-induced H+ Excretion
inferredcites →https://doi.org/10.1104/pp.66.3.433openalex-snapshot
Evidence that Auxin-induced Growth of Soybean Hypocotyls Involves Proton Excretion
inferredcites →https://doi.org/10.1104/pp.67.5.1047openalex-snapshot
Some Aspects of the Control of Root Growth and Georeaction: The Involvement of Indoleacetic Acid and Abscisic Acid
inferredcites →https://doi.org/10.1111/j.1399-3054.1950.tb07508.xopenalex-snapshot
Studies on Growth and Metabolism of Roots. IV. Positive and Negative Auxin Effects on Cell Elongation
inferredcites →https://doi.org/10.1111/j.1399-3054.1964.tb09024.xopenalex-snapshot
The Role of Endogenous Auxin in the Elongation of Avena Leaf Sections
inferredcites →https://doi.org/10.1111/j.1399-3054.1975.tb03171.xopenalex-snapshot
Evidence for Three Different Systems of Movement of Indoleacetic Acid in Intact Roots of Phaseolus coccineus
inferredcites →https://doi.org/10.1111/j.1399-3054.1978.tb08611.xopenalex-snapshot
Effects of pH on Georeaction and Elongation of Maize Root Segments
inferredcites →https://doi.org/10.1111/j.1438-8677.1935.tb01879.xopenalex-snapshot
8. A. Th. Czaja: Wurzelwachstum, Wuchsstoff und die Theorie der Wuchsstoffwirkung
inferredcites →https://doi.org/10.1139/b67-080openalex-snapshot
UPTAKE AND METABOLISM OF INDOLEACETIC ACID, NAPHTHALENEACETIC ACID, AND 2,4-DICHLOROPHENOXYACETIC ACID BY PEA ROOT SEGMENTS IN RELATION TO GROWTH INHIBITION DURING AND AFTER AUXIN APPLICATION
inferredcites →https://doi.org/10.1146/annurev.pp.22.060171.001213openalex-snapshot
Cell Wall Extension
inferredcites →https://doi.org/10.1146/annurev.pp.25.060174.001211openalex-snapshot
Rapid Responses to Plant Hormones
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.4664810openalex-extracted
Mechanistic Insights into Indole-3-Acetic Acid-Promoting Wheat Root Phenanthrene Uptake: Transcriptomic Evidence
inferred← citeshttps://doi.org/10.1007/bf00197737openalex-snapshot
Computer-based video digitizer analysis of surface extension in maize roots
inferred← citeshttps://doi.org/10.1007/bf00391031openalex-snapshot
Gradients in maize roots: local elongation and pH
inferred← citeshttps://doi.org/10.1007/bf00393311openalex-snapshot
Transmembrane electrical potentials in growing maize roots
inferred← citeshttps://doi.org/10.1007/bf00394984openalex-snapshot
Auxin binding in roots: A comparison between maize roots and coleoptiles
inferred← citeshttps://doi.org/10.1007/bf00397731openalex-snapshot
Growth distribution and surface pH patterns along maize roots
inferred← citeshttps://doi.org/10.1007/bf00446364openalex-snapshot
Distribution of growth and proton efflux in gravireactive roots of maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1007/bf00744985openalex-snapshot
The proton pumps of the plasmalemma and the tonoplast of higher plants
inferred← citeshttps://doi.org/10.1007/bf02878158openalex-snapshot
Purification and immunohistochemical localization of the auxin binding site i protein from maize coleoptiles
inferred← citeshttps://doi.org/10.1007/s00299-015-1870-1openalex-snapshot
Growth regulating properties of isoprene and isoprenoid-based essential oils
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/s00425-010-1106-0openalex-snapshot
Nitric oxide mediates humic acids-induced root development and plasma membrane H+-ATPase activation
inferred← citeshttps://doi.org/10.1007/s10725-015-0091-5openalex-snapshot
Morphological and physiological effects of trans-cinnamic acid and its hydroxylated derivatives on maize root types
inferred← citeshttps://doi.org/10.1007/s11103-017-0623-7openalex-snapshot
A novel AP2/ERF family transcription factor from Glycine soja, GsERF71, is a DNA binding protein that positively regulates alkaline stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/0167-4889(83)90129-5openalex-snapshot
31P-NMR study of turnip seed germination and sprout growth inhibition by peroxydisulfate ion
inferred← citeshttps://doi.org/10.1016/0168-9452(88)90053-2openalex-snapshot
Kinetics of proton secretion and growth in maize roots: action of various plant growth effectors
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.06.142openalex-snapshot
Narrow leaf 1 (NAL1) regulates leaf shape by affecting cell expansion in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.124522openalex-snapshot
Indole-3-acetic acid enhances the co-transport of proton and phenanthrene mediated by TaSAUR80-5A in wheat roots
inferred← citeshttps://doi.org/10.1016/j.jgg.2022.05.007openalex-snapshot
The molecular mechanism of plasma membrane H+-ATPases in plant responses to abiotic stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2006.11.008openalex-snapshot
Cell division versus cell elongation: The control of radicle elongation during thermoinhibition of Tagetes minuta achenes
inferred← citeshttps://doi.org/10.1016/j.plantsci.2005.01.021openalex-snapshot
The plasma membrane H+-ATPase of maize embryos localizes in regions that are critical during the onset of germination
inferred← citeshttps://doi.org/10.1038/s41586-021-03976-4openalex-snapshot
TMK-based cell-surface auxin signalling activates cell-wall acidification
inferred← citeshttps://doi.org/10.1038/srep04556openalex-snapshot
Suppression of Elongation and Growth of Tomato Seedlings by Auxin Biosynthesis Inhibitors and Modeling of the Growth and Environmental Response
inferred← citeshttps://doi.org/10.1073/pnas.1613499114openalex-snapshot
Auxin steers root cell expansion via apoplastic pH regulation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1080/07352688509382200openalex-snapshot
The action of auxin on plant cell elongation
inferred← citeshttps://doi.org/10.1080/07352689509701924openalex-snapshot
Mineral Nitrogen in Plant Physiology and Plant Nutrition
inferred← citeshttps://doi.org/10.1093/jxb/err313openalex-snapshot
In Posidonia oceanica cadmium induces changes in DNA methylation and chromatin patterning
inferred← citeshttps://doi.org/10.1093/jxb/ers259openalex-snapshot
PIN2 is required for the adaptation of Arabidopsis roots to alkaline stress by modulating proton secretion
inferred← citeshttps://doi.org/10.1093/jxb/erx040openalex-snapshot
Arabidopsis plasma membrane H+-ATPase genes AHA2 and AHA7 have distinct and overlapping roles in the modulation of root tip H+ efflux in response to low-phosphorus stress
inferred← citeshttps://doi.org/10.1094/mpmi-07-16-0138-ropenalex-snapshot
Trichoderma asperellum Induces Maize Seedling Growth by Activating the Plasma Membrane H+-ATPase
inferred← citeshttps://doi.org/10.1098/rsbl.2021.0629openalex-snapshot
Aerial (+)-borneol modulates root morphology, auxin signalling and meristematic activity in Arabidopsis roots
inferred← citeshttps://doi.org/10.1101/2022.03.11.483958openalex-snapshot
The asymmetric ABA response on both sides of root tip is important for tomato root hydrotropism by mediating proton efflux and cell elongation
inferred← citeshttps://doi.org/10.1101/2023.08.22.554241openalex-snapshot
Jasmonates regulate auxin-mediated root growth inhibition in response to rhizospheric pH in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.100.2.614openalex-snapshot
Electric Current Precedes Emergence of a Lateral Root in Higher Plants
inferred← citeshttps://doi.org/10.1104/pp.112.196428openalex-snapshot
Auxin Activates the Plasma Membrane H+-ATPase by Phosphorylation during Hypocotyl Elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.113.224758openalex-snapshot
The Tomato 14-3-3 Protein TFT4 Modulates H+ Efflux, Basipetal Auxin Transport, and the PKS5-J3 Pathway in the Root Growth Response to Alkaline Stress
inferred← citeshttps://doi.org/10.1104/pp.121.3.905openalex-snapshot
The Correlation of Profiles of Surface pH and Elongation Growth in Maize Roots
inferred← citeshttps://doi.org/10.1104/pp.125.3.1419openalex-snapshot
Salinity-Induced Inhibition of Leaf Elongation in Maize Is Not Mediated by Changes in Cell Wall Acidification Capacity
inferred← citeshttps://doi.org/10.1104/pp.77.1.190openalex-snapshot
Inhibitory Effects of Water Deficit on Maize Leaf Elongation
inferred← citeshttps://doi.org/10.1104/pp.83.4.801openalex-snapshot
Auxin Effect on the Transmembrane Potential Difference of Wild-Type and Mutant Tobacco Protoplasts Exhibiting a Differential Sensitiity to Auxin
inferred← citeshttps://doi.org/10.1105/tpc.13.4.907openalex-snapshot
Changes in Root Cap pH Are Required for the Gravity Response of the Arabidopsis Root
inferred← citeshttps://doi.org/10.1105/tpc.15.01057openalex-snapshot
The Effects of High Steady State Auxin Levels on Root Cell Elongation in Brachypodium
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1983.tb06275.xopenalex-snapshot
Effects of a brassinosteroid on growth and electrogenic proton extrusion in maize root segments
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2006.00870.xopenalex-snapshot
Hormone growth responses of roots of shoot height mutants of pea
inferred← citeshttps://doi.org/10.1111/j.1469-8137.1994.tb04255.xopenalex-snapshot
The control of cell expansion in roots
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02656.xopenalex-snapshot
A pH signaling mechanism involved in the spatial distribution of calcium and anion fluxes in ectomycorrhizal roots
inferred← citeshttps://doi.org/10.1111/pbi.13435openalex-snapshot
HD‐ZIP IV gene Roc8 regulates the size of bulliform cells and lignin content in rice
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ABA is required for differential cell wall acidification associated with root hydrotropic bending in tomato
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Jasmonates Regulate Auxin‐Mediated Root Growth Inhibition in Response to Rhizospheric pH in Arabidopsis thaliana
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Studies on the control of cell-wall extension. Three year progress report, September 1, 1978-June 30, 1981
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Calcium: The Missing Link in Auxin Action
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