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Transport of exogenous auxin in two-branched dwarf pea seedlings (Pisum sativum L.)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1960.tb10618.xopenalex-snapshot
AUXIN RELATIONSHIPS IN THE ALASKA PEA (PISUM SATIVUM)
inferredcites →https://doi.org/10.1002/j.1537-2197.1967.tb06901.xopenalex-snapshot
THE ROLE OF AUXINS AND CYTOKININS IN THE RELEASE OF BUDS FROM DOMINANCE
inferredcites →https://doi.org/10.1007/bf00384778openalex-snapshot
The specificity of auxin transport in intact pea seedlings (Pisum sativum L.)
inferredcites →https://doi.org/10.1007/bf00384840openalex-snapshot
Auxin transport in intact pea seedlings (Pisum sativum L.): The inhibition of transport by 2,3,5-triiodobenzoic acid
inferredcites →https://doi.org/10.1007/bf00384993openalex-snapshot
Auxin-directed transport of radiophosphorus in stems
inferredcites →https://doi.org/10.1007/bf00385161openalex-snapshot
The role of roots, cytokinins and apical dominance in the control of lateral shoot form in Solanum andigena
inferredcites →https://doi.org/10.1007/bf00386984openalex-snapshot
The transport and metabolism of 14C-labelled indoleacetic acid in intact pea seedlings
inferredcites →https://doi.org/10.1007/bf00387722openalex-snapshot
Pathways of auxin transport in the intact pea seedling (Pisum sativum L.)
inferredcites →https://doi.org/10.1007/bf00390855openalex-snapshot
The rapid non-polar transport of auxin in the phloem of intact Coleus plants
inferredcites →https://doi.org/10.1007/bf00406647openalex-snapshot
Translokation radioaktiv markierter Indolyl-3-essigs�ure in Siebr�hren von Vicia faba
inferredcites →https://doi.org/10.1007/bf00429042openalex-snapshot
Transport, distribution et m�tabolisme de l'auxine dans la racine de Vicia faba L. apr�s application de[14C]AIA ou de [3H]AIA sur le bourgeon
inferredcites →https://doi.org/10.1007/bf01682534openalex-snapshot
Developmental changes in the secondary xylem ofAcer rubrum induced by various auxins and 2,3,5-tri-iodobenzoic acid
inferredcites →https://doi.org/10.1007/bf01682535openalex-snapshot
Developmental changes in the secondary xylem ofAcer rubrum induced by gibberellic acid, various auxins and 2,3,5-tri-iodobenzoic acid
inferredcites →https://doi.org/10.1016/b978-1-4832-2931-7.50023-9openalex-snapshot
The Role of Endogenous Hormones in Cambial Activity and Xylem Differentiation
inferredcites →https://doi.org/10.1016/b978-1-4832-2931-7.50024-0openalex-snapshot
Some Indirect Effects of Environment on Wood Formation
inferredcites →https://doi.org/10.1016/s0031-9422(00)85334-0openalex-snapshot
Physiology of Plant Growth and Development
inferredcites →https://doi.org/10.1038/1811744a0openalex-snapshot
Interaction between Indole-acetic Acid and Gibberellic Acid in Cambial Activity
inferredcites →https://doi.org/10.1038/201939a0openalex-snapshot
Release of Lateral Buds from Apical Dominance
inferredcites →https://doi.org/10.1093/jxb/23.2.346openalex-snapshot
Kinetin Transport to Axillary Buds of Dwarf Pea (Pisum sativumL.)
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a084088openalex-snapshot
Senescence of Inhibited Shoots of Peas and Apical Dominance
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a084089openalex-snapshot
Apical Dominance in Vicia faba
inferredcites →https://doi.org/10.1098/rspb.1931.0033openalex-snapshot
Experiments on growth and inhibition. I.—The increase of inhibition with distance
inferredcites →https://doi.org/10.1098/rspb.1934.0010openalex-snapshot
On the inhibition of bud development and other functions of growth substance in vicia faba
inferredcites →https://doi.org/10.1104/pp.48.2.146openalex-snapshot
Auxin Transport within Intact Dormant and Active White Ash Shoots
inferredcites →https://doi.org/10.1111/j.1469-8137.1937.tb06917.xopenalex-snapshot
ON THE NATURE OF CORRELATIVE INHIBITION
inferredcites →https://doi.org/10.1111/j.1469-8137.1972.tb01957.xopenalex-snapshot
THE INTERACTION BETWEEN GROWTH PROMOTERS IN APICAL DOMINANCE
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112365zenodo-depositor-declared
In silico characterization of the impact of mutation (LEU112PRO) on the structure and function of carotenoid cleavage dioxygenase 8 in Oryza sativa
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020122.pub2openalex-snapshot
Shoot Branching and Plant Architecture
inferred← citeshttps://doi.org/10.1002/9781118060766.ch7openalex-snapshot
Stock and Scion Growth Relationships and the Dwarfing Mechanism in Apple
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0640openalex-snapshot
Forbidden Fruit: Dominance Relationships and the Control of Shoot Architecture
inferred← citeshttps://doi.org/10.1006/anbo.1993.1028openalex-snapshot
Does Auxin Play a Role in the Release of Apical Dominance by Shoot Inversion in Ipomoea nil?
inferred← citeshttps://doi.org/10.1007/978-1-4757-9607-0_12openalex-snapshot
Axillary Bud Development in Pea: Apical Dominance, Growth Cycles, Hormonal Regulation and Plant Architecture
inferred← citeshttps://doi.org/10.1007/978-3-642-67731-1_4openalex-snapshot
Transport and Other Modes of Movement of Hormones (Mainly Auxins)
inferred← citeshttps://doi.org/10.1007/978-3-642-67734-2_2openalex-snapshot
Relation of Hormones to Nutrient Mobilization and the Internal Environment of the Plant: The Supply of Mineral Nutrients and Photosynthate
inferred← citeshttps://doi.org/10.1007/978-3-642-67734-2_7openalex-snapshot
Position as a Factor in Growth and Development Effects
inferred← citeshttps://doi.org/10.1007/978-3-642-71018-6_44openalex-snapshot
Apical Dominance and Correlations by Hormones
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_15openalex-snapshot
Computational Models of Auxin-Driven Development
inferred← citeshttps://doi.org/10.1007/bf00024103openalex-snapshot
The biosynthesis and translocation of 14C-IAA in Ricinus communis
inferred← citeshttps://doi.org/10.1007/bf00024773openalex-snapshot
The transport of radiolabeled indoleacetic acid and its conjugates in nodal stem segments of Phaseolus vulgaris L.
inferred← citeshttps://doi.org/10.1007/bf00024774openalex-snapshot
Effect of plant growth substances on the growth of axillary buds in cultured stem segments of Phaseolus vulgaris L.
inferred← citeshttps://doi.org/10.1007/bf00195190openalex-snapshot
Transfer of exogenous auxin from the phloem to the polar auxin transport pathway in pea (Pisum sativum L.)
inferred← citeshttps://doi.org/10.1007/bf00202333openalex-snapshot
The role of auxin efflux carriers in the reversible loss of polar auxin transport in the pea (Pisum sativum L.) stem
inferred← citeshttps://doi.org/10.1007/bf00380123openalex-snapshot
Accumulation of 14C from exogenous labelled auxin in lateral root primordia of intact pea seedlings (Pisum sativum L.)
inferred← citeshttps://doi.org/10.1007/bf00385444openalex-snapshot
Free tryptophan and indole-3-acetic acid levels in the leaves and vascular pathways of Ricinus communis L.
inferred← citeshttps://doi.org/10.1007/bf00388215openalex-snapshot
Components of auxin transport in stem segments of Pisum sativum L.
inferred← citeshttps://doi.org/10.1007/bf00388741openalex-snapshot
Effects of temperature and sink activity on the transport of 14C-labelled indol-3yl-acetic acid in the intact pea plant (Pisum sativum L.)
inferred← citeshttps://doi.org/10.1007/bf00388839openalex-snapshot
The effect of temperature on the velocity of exogenous auxin transport in intact chilling-sensitive and chilling-resistant plants
inferred← citeshttps://doi.org/10.1007/bf00402937openalex-snapshot
Non-uniform distribution and seasonal variation of endogenous indol-3yl-acetic acid in the cambial region of Pinus contorta Dougl.
inferred← citeshttps://doi.org/10.1007/bf00571165openalex-snapshot
Cell length, light and14C-labelled indol-3yl-acetic acid transport inPisum satisum L. andPhaseolus vulgaris L
inferred← citeshttps://doi.org/10.1007/bf03030715openalex-snapshot
The serine proteinase inhibitor OsSerpin is a potent tillering regulator in rice
inferred← citeshttps://doi.org/10.1007/s00299-022-02956-wopenalex-snapshot
Auxin and CmAP1 regulate the reproductive development of axillary buds in Chinese chestnut (Castanea mollissima)
inferred← citeshttps://doi.org/10.1007/s00344-016-9638-6openalex-snapshot
The Roles of Auxin in Regulating “Shoot Branching” of Cremastra appendiculata
inferred← citeshttps://doi.org/10.1007/s00425-012-1697-8openalex-snapshot
AtGSNOR1 function is required for multiple developmental programs in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s004250050354openalex-snapshot
Dormancy-associated gene expression in pea axillary buds.
inferred← citeshttps://doi.org/10.1007/s10725-020-00581-9openalex-snapshot
Regulation by sugar and hormone signaling of the growth of Brassica napus L. axillary buds at the transcriptome level
inferred← citeshttps://doi.org/10.1007/s11103-004-4038-xopenalex-snapshot
The Plant Architecture of Rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1007/s11103-010-9599-2openalex-snapshot
Axillary bud outgrowth in herbaceous shoots: how do strigolactones fit into the picture?
inferred← citeshttps://doi.org/10.1007/s11103-010-9645-0openalex-snapshot
Over-expression of the IGI1 leading to altered shoot-branching development related to MAX pathway in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11105-009-0130-3openalex-snapshot
The Lateral Suppressor-Like Gene, DgLsL, Alternated the Axillary Branching in Transgenic Chrysanthemum (Chrysanthemum × morifolium) by Modulating IAA and GA Content
inferred← citeshttps://doi.org/10.1007/s44473-025-00035-yopenalex-snapshot
Unraveling the molecular mechanisms of phytohormonal regulation in safflower axillary bud outgrowth: insights from transcriptomics
inferred← citeshttps://doi.org/10.1016/b978-0-12-520920-5.50018-3openalex-snapshot
Whole Plant Senescence
inferred← citeshttps://doi.org/10.1016/b978-0-408-10767-9.50010-0openalex-snapshot
HORMONAL CONTROL OF PHOTOSYNTHESIS AND ASSIMILATE DISTRIBUTION
inferred← citeshttps://doi.org/10.1016/b978-0-443-13521-7.00006-3openalex-snapshot
Cross-talk of strigolactones with auxin and cytokinin
inferred← citeshttps://doi.org/10.1016/b978-012520915-1/50018-7openalex-snapshot
Whole Plant Senescence
inferred← citeshttps://doi.org/10.1016/j.cub.2004.10.017openalex-snapshot
Plant Signaling: Notes from the Underground
inferred← citeshttps://doi.org/10.1016/j.cub.2006.01.058openalex-snapshot
The Arabidopsis MAX Pathway Controls Shoot Branching by Regulating Auxin Transport
inferred← citeshttps://doi.org/10.1016/j.cub.2011.02.031openalex-snapshot
Auxin, Self-Organisation, and the Colonial Nature of Plants
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.01.009openalex-snapshot
MAX1 Encodes a Cytochrome P450 Family Member that Acts Downstream of MAX3/4 to Produce a Carotenoid-Derived Branch-Inhibiting Hormone
inferred← citeshttps://doi.org/10.1016/j.gde.2005.06.010openalex-snapshot
The fall and rise of apical dominance
inferred← citeshttps://doi.org/10.1016/j.gene.2018.01.101openalex-snapshot
Identification and expression analysis of the IPT and CKX gene families during axillary bud outgrowth in apple ( Malus domestica Borkh.)
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.03.002openalex-snapshot
Cloning and expression analysis of LoCCD8 during IAA-induced bulbils outgrowth in lily (Oriental Hybrid ‘Sorbonne’)
inferred← citeshttps://doi.org/10.1016/j.pbi.2005.07.010openalex-snapshot
Shoot and inflorescence branching
inferred← citeshttps://doi.org/10.1016/j.pbi.2007.08.005openalex-snapshot
Novel phytohormones involved in long-range signaling
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110880openalex-snapshot
Signaling network regulating plant branching: Recent advances and new challenges
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113717openalex-snapshot
Identification of an IAA conjugate resistant gene BraA07g034950.3C regulating primary rosette branching in flowering Chinese cabbage
inferred← citeshttps://doi.org/10.1016/j.tplants.2003.09.008openalex-snapshot
Regulation of shoot branching by auxin
inferred← citeshttps://doi.org/10.1016/s0044-328x(81)80032-3openalex-snapshot
Effets de l'acide indolyl-acétique exogène et son transport dans le gamétophyte d’une Fougére
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60469-xopenalex-snapshot
5 Reevaluating Concepts of Apical Dominance and the Control of Axillary Bud Outgrowth
inferred← citeshttps://doi.org/10.1016/s0168-9452(03)00008-6openalex-snapshot
Is auxin a diffusible signal mediating abscission of recessive sinks?
inferred← citeshttps://doi.org/10.1016/s0176-1617(99)80246-6openalex-snapshot
Auxin and Cytokinins in the Control of Apical Dominance in Pea — A Differential Response Due to Bud Position
inferred← citeshttps://doi.org/10.1016/s0254-6299(16)31085-7openalex-snapshot
The response of lateral buds of Pisum sativum to decapitation and selective bud excision
inferred← citeshttps://doi.org/10.1016/s1534-5807(02)00299-xopenalex-snapshot
Plant Development Makes Strides in Vermont
inferred← citeshttps://doi.org/10.1023/a:1010742721004openalex-snapshot
Mutual interaction of auxin and cytokinins in regulating correlative dominance
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1994.900133.xopenalex-snapshot
The role of hormones in apical dominance. New approaches to an old problem in plant development
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1999.106409.xopenalex-snapshot
Autoinhibition of indoleacetic acid transport in the shoots of two‐branched pea (Pisum sativum) plants and its relationship to correlative dominance
inferred← citeshttps://doi.org/10.1038/cr.2010.51openalex-snapshot
The BUD2 mutation affects plant architecture through altering cytokinin and auxin responses in Arabidopsis
inferred← citeshttps://doi.org/10.1038/srep41319openalex-snapshot
ERAMOSA controls lateral branching in snapdragon
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2000.00862.xopenalex-snapshot
The hormonal regulation of axillary bud growth in Arabidopsis
inferred← citeshttps://doi.org/10.1071/pp9820005openalex-snapshot
The Transport Behaviour of the Synthetic Auxin 2,4-Dichlorophenoxyacetic Acid in Decapitated Seedlings of Sunflower ( Helianthus annuus L.)
inferred← citeshttps://doi.org/10.1073/pnas.0509463102openalex-snapshot
MAX1 , a regulator of the flavonoid pathway, controls vegetative axillary bud outgrowth in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.0906696106openalex-snapshot
Control of bud activation by an auxin transport switch
inferred← citeshttps://doi.org/10.1073/pnas.2308587120openalex-snapshot
Tree architecture: A strigolactone-deficient mutant reveals a connection between branching order and auxin gradient along the tree stem
inferred← citeshttps://doi.org/10.1093/aob/mcr069openalex-snapshot
Auxin, cytokinin and the control of shoot branching
inferred← citeshttps://doi.org/10.1093/aob/mcs212openalex-snapshot
Defence on demand: mechanisms behind optimal defence patterns
inferred← citeshttps://doi.org/10.1093/aob/mcx113openalex-snapshot
Evolution and ecology of plant architecture: integrating insights from the fossil record, extant morphology, developmental genetics and phylogenies
inferred← citeshttps://doi.org/10.1093/hr/uhac224openalex-snapshot
PpTCP18 is upregulated by lncRNA5 and controls branch number in peach (Prunus persica) through positive feedback regulation of strigolactone biosynthesis
inferred← citeshttps://doi.org/10.1093/jhered/esl069openalex-snapshot
Genetic Interaction between 2 Tillering Genes, Reduced Culm Number 1 (rcn1) and Tillering Dwarf Gene d3, in Rice
inferred← citeshttps://doi.org/10.1093/jxb/erad048openalex-snapshot
Just enough fruit: understanding feedback mechanisms during sexual reproductive development
inferred← citeshttps://doi.org/10.1093/jxb/erad137openalex-snapshot
Lessons from a century of apical dominance research
inferred← citeshttps://doi.org/10.1093/jxb/erm134openalex-snapshot
Hormonal control of shoot branching
inferred← citeshttps://doi.org/10.1093/jxb/erq133openalex-snapshot
Strigolactone regulation of shoot branching in chrysanthemum (Dendranthema grandiflorum)
inferred← citeshttps://doi.org/10.1093/jxb/erq330openalex-snapshot
Existing branches correlatively inhibit further branching in Trifolium repens: possible mechanisms
inferred← citeshttps://doi.org/10.1093/jxb/err094openalex-snapshot
YUCCA6 over-expression demonstrates auxin function in delaying leaf senescence in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erv047openalex-snapshot
Sucrose is an early modulator of the key hormonal mechanisms controlling bud outgrowth in Rosa hybrida
inferred← citeshttps://doi.org/10.1093/jxb/ery117openalex-snapshot
Auxin–cytokinin interactions in the regulation of correlative inhibition in two-branched pea seedlings
inferred← citeshttps://doi.org/10.1093/mp/ssn007openalex-snapshot
Interactions between Axillary Branches of Arabidopsis
inferred← citeshttps://doi.org/10.1093/mp/ssu058openalex-snapshot
CONSTANS-LIKE 7 (COL7) Is Involved in Phytochrome B (phyB)-Mediated Light-Quality Regulation of Auxin Homeostasis
inferred← citeshttps://doi.org/10.1093/oxfordjournals.aob.a087684openalex-snapshot
The Role of Basipetal Auxin Transport in the Positional Control of Abscission Sites Induced in Impatiens sultani Stem Explants
inferred← citeshttps://doi.org/10.1093/pcp/pci183openalex-snapshot
A PIN1 Family Gene, OsPIN1, involved in Auxin-dependent Adventitious Root Emergence and Tillering in Rice
inferred← citeshttps://doi.org/10.1093/pcp/pcv089openalex-snapshot
Gibberellin Promotes Shoot Branching in the Perennial Woody PlantJatropha curcas
inferred← citeshttps://doi.org/10.1093/plphys/kiae088openalex-snapshot
Far-red light-enhanced apical dominance stimulates flower and fruit abortion in sweet pepper
inferred← citeshttps://doi.org/10.1098/rspb.1978.0098openalex-snapshot
The position of regenerating cambia: auxin/sucrose ratio and the gradient induction hypothesis
inferred← citeshttps://doi.org/10.1101/2025.05.26.656108openalex-snapshot
A BRC1-modulated switch in auxin transport accounts for the competition between Arabidopsis axillary buds
inferred← citeshttps://doi.org/10.1101/gad.256603openalex-snapshot
MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea
inferred← citeshttps://doi.org/10.1104/pp.104.058743openalex-snapshot
Auxin Dynamics after Decapitation Are Not Correlated with the Initial Growth of Axillary Buds
inferred← citeshttps://doi.org/10.1104/pp.106.086868openalex-snapshot
Apical Dominance and Shoot Branching. Divergent Opinions or Divergent Mechanisms?
inferred← citeshttps://doi.org/10.1104/pp.108.134783openalex-snapshot
Strigolactone Acts Downstream of Auxin to Regulate Bud Outgrowth in Pea and Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.109.135475openalex-snapshot
Roles for Auxin, Cytokinin, and Strigolactone in Regulating Shoot Branching
inferred← citeshttps://doi.org/10.1104/pp.111.177022openalex-snapshot
AtMYB2Regulates Whole Plant Senescence by Inhibiting Cytokinin-Mediated Branching at Late Stages of Development in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.113.218461openalex-snapshot
Using Arabidopsis to Study Shoot Branching in Biomass Willow
inferred← citeshttps://doi.org/10.1104/pp.115.3.1251openalex-snapshot
The rms1 Mutant of Pea Has Elevated Indole-3-Acetic Acid Levels and Reduced Root-Sap Zeatin Riboside Content but Increased Branching Controlled by Graft-Transmissible Signal(s)
inferred← citeshttps://doi.org/10.1104/pp.121.3.839openalex-snapshot
AXR1 Acts after Lateral Bud Formation to Inhibit Lateral Bud Growth in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.123.2.689openalex-snapshot
Auxin Inhibition of Decapitation-Induced Branching Is Dependent on Graft-Transmissible Signals Regulated by GenesRms1andRms2
inferred← citeshttps://doi.org/10.1104/pp.126.1.203openalex-snapshot
Long-Distance Signaling and the Control of Branching in therms1 Mutant of Pea
inferred← citeshttps://doi.org/10.1104/pp.15.00014openalex-snapshot
Strigolactone Inhibition of Branching Independent of Polar Auxin Transport
inferred← citeshttps://doi.org/10.1104/pp.17.01691openalex-snapshot
Cytokinin Targets Auxin Transport to Promote Shoot Branching
inferred← citeshttps://doi.org/10.1104/pp.18.00519openalex-snapshot
Initial Bud Outgrowth Occurs Independent of Auxin Flow from Out of Buds
inferred← citeshttps://doi.org/10.1105/tpc.007542openalex-snapshot
Auxin Acts in Xylem-Associated or Medullary Cells to Mediate Apical Dominance
inferred← citeshttps://doi.org/10.1105/tpc.104.026716openalex-snapshot
The Branching Gene RAMOSUS1 Mediates Interactions among Two Novel Signals and Auxin in Pea
inferred← citeshttps://doi.org/10.1105/tpc.106.048934openalex-snapshot
Arabidopsis BRANCHED1 Acts as an Integrator of Branching Signals within Axillary Buds
inferred← citeshttps://doi.org/10.1105/tpc.109.065987openalex-snapshot
DWARF27, an Iron-Containing Protein Required for the Biosynthesis of Strigolactones, Regulates Rice Tiller Bud Outgrowth
inferred← citeshttps://doi.org/10.1105/tpc.109.069013openalex-snapshot
Computational Modeling and Molecular Physiology Experiments Reveal New Insights into Shoot Branching in Pea
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2009.01930.xopenalex-snapshot
The control of shoot branching: an example of plant information processing
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2006.02722.xopenalex-snapshot
Transitions in the functioning of the shoot apical meristem in birch ( Betula pendula ) involve ethylene
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2007.03032.xopenalex-snapshot
MAX2 participates in an SCF complex which acts locally at the node to suppress shoot branching
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2010.04443.xopenalex-snapshot
Competitive canalization of PIN‐dependent auxin flow from axillary buds controls pea bud outgrowth
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1982.tb04542.xopenalex-snapshot
The apical control of lateral bud development in excised shoot tips of Cuscuta reflexa cultured in vitro
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1989.tb05487.xopenalex-snapshot
Dominance among fruits/sinks and the search for a correlative signal
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2009.00267.xopenalex-snapshot
The polycotyledon (pct1-2) mutant of tomato shows enhanced accumulation of PIN1 auxin transport facilitator protein
inferred← citeshttps://doi.org/10.1111/j.1439-037x.1987.tb01155.xopenalex-snapshot
Wirkstoffeffekte auf das Speichersystem Weizenähre in Abhängigkeit von den Bedingungen zwischen Anthese und Reife
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02724.xopenalex-snapshot
Rice shoot branching requires an ATP‐binding cassette subfamily G protein
inferred← citeshttps://doi.org/10.1111/jipb.12665openalex-snapshot
Non‐dormant Axillary Bud 1 regulates axillary bud outgrowth in sorghum
inferred← citeshttps://doi.org/10.1111/nph.12217openalex-snapshot
The role of the potato ( S olanum tuberosum ) CCD8 gene in stolon and tuber development
inferred← citeshttps://doi.org/10.1111/nph.17398openalex-snapshot
Callose accumulation in specific phloem cell types reduces axillary bud growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.19664openalex-snapshot
The activation of Arabidopsis axillary buds involves a switch from slow to rapid committed outgrowth regulated by auxin and strigolactone
inferred← citeshttps://doi.org/10.1111/nph.70480openalex-snapshot
Basal axillary buds in pea are hydraulically connected to the stem but are protected during drought by osmotic adjustment
inferred← citeshttps://doi.org/10.1111/pbi.13228openalex-snapshot
Knockout of two Bna MAX 1 homologs by CRISPR /Cas9‐targeted mutagenesis improves plant architecture and increases yield in rapeseed ( Brassica napus L.)
inferred← citeshttps://doi.org/10.1111/pce.14758openalex-snapshot
Far‐red light inhibits lateral bud growth mainly through enhancing apical dominance independently of strigolactone synthesis in tomato
inferred← citeshttps://doi.org/10.1111/ppl.70509openalex-snapshot
Transcriptome Analysis Reveals the Mechanism of Early Branching of Balsa ( Ochroma lagopus Swartz)
inferred← citeshttps://doi.org/10.1111/tpj.12488openalex-snapshot
Strigolactones and the control of plant development: lessons from shoot branching
inferred← citeshttps://doi.org/10.1111/tpj.12862openalex-snapshot
Cytokinin is required for escape but not release from auxin mediated apical dominance
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-101011-155741openalex-snapshot
Hormonal Interactions in the Regulation of Plant Development
inferred← citeshttps://doi.org/10.1146/annurev.arplant.56.032604.144122openalex-snapshot
SHOOT BRANCHING
inferred← citeshttps://doi.org/10.1146/annurev.arplant.59.032607.092902openalex-snapshot
Molecular Basis of Plant Architecture
inferred← citeshttps://doi.org/10.1186/s12870-021-03217-wopenalex-snapshot
Down-expression of TaPIN1s Increases the Tiller Number and Grain Yield in Wheat
inferred← citeshttps://doi.org/10.1186/s13104-015-0989-zopenalex-snapshot
Using 2-deoxy-2-[18F]fluoro-D-glucose ([18F]FDG) to study carbon allocation in plants after herbivore attack
inferred← citeshttps://doi.org/10.1242/dev.051987openalex-snapshot
Strigolactones enhance competition between shoot branches by dampening auxin transport
inferred← citeshttps://doi.org/10.1242/dev.145649openalex-snapshot
BRC1expression regulates bud activation potential, but is not necessary or sufficient for bud growth inhibition in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pbio.1002446openalex-snapshot
Connective Auxin Transport in the Shoot Facilitates Communication between Shoot Apices
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003395openalex-snapshot
A BRC1-modulated switch in auxin efflux accounts for the competition between Arabidopsis axillary buds
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008023openalex-snapshot
Connective auxin transport contributes to strigolactone-mediated shoot branching control independent of the transcription factor BRC1
inferred← citeshttps://doi.org/10.14264/uql.2020.1007openalex-snapshot
A synthetic biology toolbox for examining and engineering strigolactone biosynthesis
inferred← citeshttps://doi.org/10.1614/ws-05-066r1.1openalex-snapshot
Transcriptome analysis of paradormancy release in root buds of leafy spurge (Euphorbia esula)
inferred← citeshttps://doi.org/10.3389/fpls.2014.00741openalex-snapshot
Multiple pathways regulate shoot branching
inferred← citeshttps://doi.org/10.3389/fpls.2017.01874openalex-snapshot
A Growing Stem Inhibits Bud Outgrowth – The Overlooked Theory of Apical Dominance
inferred← citeshttps://doi.org/10.3389/fpls.2019.00076openalex-snapshot
BRANCHED1: A Key Hub of Shoot Branching
inferred← citeshttps://doi.org/10.3389/fpls.2019.01296openalex-snapshot
Light Regulation of Axillary Bud Outgrowth Along Plant Axes: An Overview of the Roles of Sugars and Hormones
inferred← citeshttps://doi.org/10.3389/fpls.2020.572193openalex-snapshot
Functional Analysis of the teosinte branched 1 Gene in the Tetraploid Switchgrass (Panicum virgatum L.) by CRISPR/Cas9-Directed Mutagenesis
inferred← citeshttps://doi.org/10.3390/plants12203628openalex-snapshot
Unlocking the Multifaceted Mechanisms of Bud Outgrowth: Advances in Understanding Shoot Branching
inferred← citeshttps://doi.org/10.3390/plants15142197openalex-snapshot
Phytohormones and Shoot Branching: A Mini-Review of Molecular Regulatory Networks and Mechanisms
inferred← citeshttps://doi.org/10.3732/ajb.89.11.1764openalex-snapshot
Is auxin the repressor signal of branch growth in apical control?
inferred← citeshttps://doi.org/10.4236/ojf.2015.57056openalex-snapshot
Stimulation of Multiple Leader Formation in Some Genotypes of Acacia mangium and Acacia auriculiformis with 6-Benzylaminopurine (BAP)
inferred← citeshttps://doi.org/10.4238/gmr15049320openalex-snapshot
NtBRC1 suppresses axillary branching in tobacco after decapitation
inferred← citeshttps://doi.org/10.70675/3a64f17eze0d5z4c45zabc2z96a2e3eec1a6openalex-snapshot
Study of the role of sugars, in interaction with hormones, in light intensity modulation of bud outgrowth
inferred← citeshttps://doi.org/10.7554/elife.06808openalex-snapshot
Three ancient hormonal cues co-ordinate shoot branching in a moss
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