On the public citation graph
Integrated regulation of periclinal cell division by transcriptional module of BZR1‐SHR in Arabidopsis roots
0 signed · 112 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s003440010039openalex-snapshot
Gibberellin Metabolism and Its Regulation
inferredcites →https://doi.org/10.1016/j.cell.2008.02.001openalex-snapshot
Plant Stem Cell Niches: Standing the Test of Time
inferredcites →https://doi.org/10.1016/j.cell.2010.10.020openalex-snapshot
Transcriptional Regulation of ROS Controls Transition from Proliferation to Differentiation in the Root
inferredcites →https://doi.org/10.1016/j.cell.2016.01.044openalex-snapshot
Information Integration and Communication in Plant Growth Regulation
inferredcites →https://doi.org/10.1016/j.cub.2015.02.046openalex-snapshot
Spatiotemporal Brassinosteroid Signaling and Antagonism with Auxin Pattern Stem Cell Dynamics in Arabidopsis Roots
inferredcites →https://doi.org/10.1016/j.cub.2020.10.038openalex-snapshot
A PHABULOSA-Controlled Genetic Pathway Regulates Ground Tissue Patterning in the Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.devcel.2010.10.010openalex-snapshot
Integration of Brassinosteroid Signal Transduction with the Transcription Network for Plant Growth Regulation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.devcel.2014.05.020openalex-snapshot
Regulation of Plant Stem Cell Quiescence by a Brassinosteroid Signaling Module
inferredcites →https://doi.org/10.1016/j.molp.2016.02.009openalex-snapshot
Interplay between ABA and GA Modulates the Timing of Asymmetric Cell Divisions in the Arabidopsis Root Ground Tissue
inferredcites →https://doi.org/10.1016/j.molp.2019.06.006openalex-snapshot
BZR1 Family Transcription Factors Function Redundantly and Indispensably in BR Signaling but Exhibit BRI1-Independent Function in Regulating Anther Development in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2011.10.006openalex-snapshot
Growth and development of the root apical meristem
inferredcites →https://doi.org/10.1016/j.ydbio.2012.02.007openalex-snapshot
Surfing along the root ground tissue gene network
inferredcites →https://doi.org/10.1016/s0092-8674(00)80115-4openalex-snapshot
The SCARECROW Gene Regulates an Asymmetric Cell Division That Is Essential for Generating the Radial Organization of the Arabidopsis Root
inferredcites →https://doi.org/10.1016/s0092-8674(00)80357-8openalex-snapshot
A Putative Leucine-Rich Repeat Receptor Kinase Involved in Brassinosteroid Signal Transduction
inferredcites →https://doi.org/10.1016/s0092-8674(00)80865-xopenalex-snapshot
The SHORT-ROOT Gene Controls Radial Patterning of the Arabidopsis Root through Radial Signaling
inferredcites →https://doi.org/10.1038/35095061openalex-snapshot
Intercellular movement of the putative transcription factor SHR in root patterning
inferredcites →https://doi.org/10.1038/378062a0openalex-snapshot
Cell fate in the Arabidopsis root meristem determined by directional signalling
inferredcites →https://doi.org/10.1038/cr.2008.36openalex-snapshot
Is kinase activity essential for biological functions of BRI1?
inferredcites →https://doi.org/10.1038/nature09143openalex-snapshot
Spatiotemporal regulation of cell-cycle genes by SHORTROOT links patterning and growth
inferredcites →https://doi.org/10.1038/ncb2546openalex-snapshot
Brassinosteroid, gibberellin and phytochrome impinge on a common transcription module in Arabidopsis
inferredcites →https://doi.org/10.1038/nrm2164openalex-snapshot
Stem-cell niches: nursery rhymes across kingdoms
inferredcites →https://doi.org/10.1038/s41467-018-03463-xopenalex-snapshot
Hydrogen peroxide positively regulates brassinosteroid signaling through oxidation of the BRASSINAZOLE-RESISTANT1 transcription factor
inferredcites →https://doi.org/10.1038/s41586-019-1819-6openalex-snapshot
RGF1 controls root meristem size through ROS signalling
inferredcites →https://doi.org/10.1038/s41586-020-3016-zopenalex-snapshot
An SHR–SCR module specifies legume cortical cell fate to enable nodulation
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00137.xopenalex-snapshot
Genetic evidence that the endodermis is essential for shoot gravitropism in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00915.xopenalex-snapshot
Promotive effect of brassinosteroids on cell division involves a distinct CycD3‐induction pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0811633106openalex-snapshot
Steroids are required for epidermal cell fate establishment in Arabidopsis roots
inferredcites →https://doi.org/10.1073/pnas.1012215108openalex-snapshot
Funneling of gibberellin signaling by the GRAS transcription regulator SCARECROW-LIKE 3 in the Arabidopsis root
inferredcites →https://doi.org/10.1073/pnas.1012232108openalex-snapshot
SCARECROW-LIKE 3 promotes gibberellin signaling by antagonizing master growth repressor DELLA in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1119992109openalex-snapshot
Molecular mechanism for the interaction between gibberellin and brassinosteroid signaling pathways in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1205579109openalex-snapshot
The SHORT-ROOT protein acts as a mobile, dose-dependent signal in patterning the ground tissue
inferredcites →https://doi.org/10.1073/pnas.2018565117openalex-snapshot
BAM1/2 receptor kinase signaling drives CLE peptide-mediated formative cell divisions in Arabidopsis roots
inferredcites →https://doi.org/10.1093/jxb/eru099openalex-snapshot
Arabidopsis thaliana RALF1 opposes brassinosteroid effects on root cell elongation and lateral root formation
inferredcites →https://doi.org/10.1093/jxb/erv316openalex-snapshot
Brassinazole resistant 1 (BZR1)-dependent brassinosteroid signalling pathway leads to ectopic activation of quiescent cell division and suppresses columella stem cell differentiation
inferredcites →https://doi.org/10.1093/mp/ssu106openalex-snapshot
SPINDLY, ERECTA, and Its Ligand STOMAGEN Have a Role in Redox-Mediated Cortex Proliferation in the Arabidopsis Root
inferredcites →https://doi.org/10.1101/gad.239335.114openalex-snapshot
Root growth is modulated by differential hormonal sensitivity in neighboring cells
inferredcites →https://doi.org/10.1101/gad.440307openalex-snapshot
Arabidopsis JACKDAW and MAGPIE zinc finger proteins delimit asymmetric cell division and stabilize tissue boundaries by restricting SHORT-ROOT action
inferredcites →https://doi.org/10.1104/pp.103.036897openalex-snapshot
Brassinosteroids Interact with Auxin to Promote Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.058362openalex-snapshot
Maturation of the Ground Tissue of the Root Is Regulated by Gibberellin and SCARECROW and Requires SHORT-ROOT
inferredcites →https://doi.org/10.1104/pp.105.062414openalex-snapshot
Nodulation Phenotypes of Gibberellin and Brassinosteroid Mutants of Pea
inferredcites →https://doi.org/10.1104/pp.111.183178openalex-snapshot
Genome-Wide Direct Target Analysis Reveals a Role for SHORT-ROOT in Root Vascular Patterning through Cytokinin Homeostasis
inferredcites →https://doi.org/10.1104/pp.114.256313openalex-snapshot
Interaction between Glucose and Brassinosteroid during the Regulation of Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.00533openalex-snapshot
Binary 2in1 Vectors Improve in Planta (Co)localization and Dynamic Protein Interaction Studies
inferredcites →https://doi.org/10.1104/pp.15.01501openalex-snapshot
SEUSS Integrates Gibberellin Signaling with Transcriptional Inputs from the SHR-SCR-SCL3 Module to Regulate Middle Cortex Formation in the Arabidopsis Root
inferredcites →https://doi.org/10.1104/pp.17.00814openalex-snapshot
Cell-Fate Specification in Arabidopsis Roots Requires Coordinative Action of Lineage Instruction and Positional Reprogramming
inferredcites →https://doi.org/10.1105/tpc.10.2.231openalex-snapshot
The DWF4 Gene of Arabidopsis Encodes a Cytochrome P450 That Mediates Multiple 22α-Hydroxylation Steps in Brassinosteroid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.107.056069openalex-snapshot
High-Resolution Whole-Mount Imaging of Three-Dimensional Tissue Organization and Gene Expression Enables the Study of Phloem Development and Structure in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.132092openalex-snapshot
Brassinosteroid Regulates Cell Elongation by Modulating Gibberellin Metabolism in Rice
inferredcites →https://doi.org/10.1105/tpc.114.132407openalex-snapshot
Arabidopsis BIRD Zinc Finger Proteins Jointly Stabilize Tissue Boundaries by Confining the Cell Fate Regulator SHORT-ROOT and Contributing to Fate Specification
inferredcites →https://doi.org/10.1105/tpc.15.00433openalex-snapshot
Brassinosteroids Are Master Regulators of Gibberellin Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.19.00587openalex-snapshot
Brassinosteroid and Hydrogen Peroxide Interdependently Induce Stomatal Opening by Promoting Guard Cell Starch Degradation
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb17159.xopenalex-snapshot
Diphenylene iodonium as an inhibitor of the NADPH oxidase complex of bovine neutrophils
inferredcites →https://doi.org/10.1111/j.1747-0765.2005.tb00044.xopenalex-snapshot
Systemic Effect of a Brassinosteroid on Root Nodule Formation in Soybean as Revealed by the Application of Brassinolide and Brassinazole
inferredcites →https://doi.org/10.1111/nph.12036openalex-snapshot
Brassinosteroid production and signaling differentially control cell division and expansion in the leaf
inferredcites →https://doi.org/10.1111/nph.16824openalex-snapshot
Hydrogen peroxide homeostasis provides beneficial micro‐environment for SHR‐mediated periclinal division in Arabidopsis root
inferredcites →https://doi.org/10.1111/tpj.14672openalex-snapshot
Brassinosteroid‐mediated reactive oxygen species are essential for tapetum degradation and pollen fertility in tomato
inferredcites →https://doi.org/10.1126/science.1065769openalex-snapshot
Regulation of Brassinosteroid Signaling by a GSK3/SHAGGY-Like Kinase
inferredcites →https://doi.org/10.1126/science.1139531openalex-snapshot
An Evolutionarily Conserved Mechanism Delimiting SHR Movement Defines a Single Layer of Endodermis in Plants
inferredcites →https://doi.org/10.1126/science.1240667openalex-snapshot
ERF115 Controls Root Quiescent Center Cell Division and Stem Cell Replenishment
inferredcites →https://doi.org/10.1126/science.272.5260.398openalex-snapshot
A Role for Brassinosteroids in Light-Dependent Development of Arabidopsis
inferredcites →https://doi.org/10.1126/science.aad1171openalex-snapshot
Transcriptional control of tissue formation throughout root development
inferredcites →https://doi.org/10.1126/scisignal.2002908openalex-snapshot
An Interaction Between BZR1 and DELLAs Mediates Direct Signaling Crosstalk Between Brassinosteroids and Gibberellins in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev-genet-102209-163450openalex-snapshot
Brassinosteroid Signaling Network and Regulation of Photomorphogenesis
inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.427openalex-snapshot
BRASSINOSTEROIDS: Essential Regulators of Plant Growth and Development
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103830openalex-snapshot
Gibberellin Receptor and Its Role in Gibberellin Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092804openalex-snapshot
Gibberellin Metabolism and its Regulation
inferredcites →https://doi.org/10.1242/dev.057331openalex-snapshot
Brassinosteroids control meristem size by promoting cell cycle progression in Arabidopsis roots
inferredcites →https://doi.org/10.1242/dev.061804openalex-snapshot
Brassinosteroid perception in the epidermis controls root meristem size
inferredcites →https://doi.org/10.1242/dev.119.1.71openalex-snapshot
Cellular organisation of the Arabidopsis thaliana root
inferredcites →https://doi.org/10.1242/dev.120.9.2475openalex-snapshot
Embryonic origin of the Arabidopsis primary root and root meristem initials
inferredcites →https://doi.org/10.1242/dev.122.5.1589openalex-snapshot
Two independent and polarized processes of cell elongation regulate leaf blade expansion in Arabidopsis thaliana (L.) Heynh.
inferredcites →https://doi.org/10.1242/dev.145623openalex-snapshot
Brassinosteroid signaling directs formative cell divisions and protophloem differentiation in Arabidopsis root meristems
inferredcites →https://doi.org/10.1242/dev.151894openalex-snapshot
Brassinosteroid signaling in plant development and adaptation to stress
inferredcites →https://doi.org/10.3390/ijms20122941openalex-snapshot
MtBZR1 Plays an Important Role in Nodule Development in Medicago truncatula
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.4822288openalex-extracted
Real-Time Live Imaging of Cytosolic Reactive Oxygen Species and Ca2+ of Marchantia Polymorpha Gemmalings Reveal Immediate Initial Responses of Plant Cells Triggered by Nonthermal Plasma Irradiation
inferred← citeshttps://doi.org/10.1007/s11104-024-07150-3openalex-snapshot
Arbuscular mycorrhizal fungi affect root morphology locally but not systemically through altering nutrient- and phytohormone-related gene expressions at low soil P level
inferred← citeshttps://doi.org/10.1007/s11240-025-03278-xopenalex-snapshot
Effects of brassinolide and chitosan on the growth and medicinal value of Astragalus membranaceus callus
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115751openalex-snapshot
Hormonal regulation of primary root development
inferred← citeshttps://doi.org/10.1016/j.cub.2024.09.074openalex-snapshot
Three RLKs integrate SHR-SCR and gibberellins to regulate root ground tissue patterning in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.11.019openalex-snapshot
Plant thiol peroxidases as redox sensors and signal transducers in abiotic stress acclimation
inferred← citeshttps://doi.org/10.1016/j.jia.2025.12.073openalex-snapshot
Brassinosteroid signaling drives floral transition defects in Camellia sinensis ‘Ziyang 1’ via CsBZR2-mediated suppression of CsFLC
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154833openalex-snapshot
Genetic and environmental factors in determining rice panicle morphogenesis
inferred← citeshttps://doi.org/10.1016/j.molp.2026.07.009openalex-snapshot
A CLV3–WUS positive feedback loop in individual cells enhances shoot stem cell thermotolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102879openalex-snapshot
Natura non facit saltus: Conserved and rewired molecular pathways underpinning root ground tissue evolution in vascular plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109172openalex-snapshot
Real-time live imaging of cytosolic hydrogen peroxide and Ca2+ of Marchantia polymorpha gemmalings reveal immediate initial responses of plant cells triggered by nonthermal plasma irradiation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110825openalex-snapshot
Genome-wide identification and expression analysis of BES1/BZR1 gene family in melon (Cucumis melo L.) and functional characteristics of CmBES1-3
inferred← citeshttps://doi.org/10.1016/j.tplants.2024.10.015openalex-snapshot
The whole and its parts: cell-specific functions of brassinosteroids
inferred← citeshttps://doi.org/10.1038/s41598-024-53104-1openalex-snapshot
Growth control of Marchantia polymorpha gemmae using nonthermal plasma irradiation
inferred← citeshttps://doi.org/10.1038/s44319-025-00433-5openalex-snapshot
BZR1 promotes pluripotency acquisition and callus development through direct regulation of ARF7 and ARF19
inferred← citeshttps://doi.org/10.1080/15592324.2025.2577402openalex-snapshot
ROS-mediated interplay between brassinosteroids and gibberellic acids antagonistically modulates asymmetric periclinal cell division leading to middle cortex formation in Arabidopsis roots
inferred← citeshttps://doi.org/10.1093/aob/mcad016openalex-snapshot
Uncovering genetic control of primary root length variation inBrassica napususing QTL-seq. A commentary on: ‘Rapid identification of a major locusqPRL-C06affecting primary root length inBrassica napusby QTL-seq’
inferred← citeshttps://doi.org/10.1093/hr/uhaf158openalex-snapshot
CrWRKY57 and CrABF3 cooperatively activate CrCYCD6;1 to modulate drought tolerance and root development
inferred← citeshttps://doi.org/10.1093/plcell/koae047openalex-snapshot
MAC3A and MAC3B mediate degradation of the transcription factor ERF13 and thus promote lateral root emergence
inferred← citeshttps://doi.org/10.1093/plcell/koae172openalex-snapshot
Transcription factors BZR1 and PAP1 cooperate to promote anthocyanin biosynthesis in Arabidopsis shoots
inferred← citeshttps://doi.org/10.1111/jipb.13817openalex-snapshot
Dual regulation of stomatal development by brassinosteroid in Arabidopsis hypocotyls
inferred← citeshttps://doi.org/10.1111/ppl.13684openalex-snapshot
Delving deeper into the link between sugar transport, sugar signaling, and vascular system development
inferred← citeshttps://doi.org/10.1111/tpj.16527openalex-snapshot
Comparative analysis of BZR1 / BES1 family transcription factors in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.70736openalex-snapshot
Abscisic acid promotes RBOH ‐dependent reactive oxygen species production and lignin biosynthesis in pears via the PuABI5 ‐ PuMYB169 module
inferred← citeshttps://doi.org/10.1126/sciadv.ade2493openalex-snapshot
Auxin promotes hypocotyl elongation by enhancing BZR1 nuclear accumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1126/science.adu9798openalex-snapshot
Unlocking the potential of brassinosteroids: A path to precision plant engineering
inferred← citeshttps://doi.org/10.2139/ssrn.5077806openalex-snapshot
Hydrogen Peroxide Modulates Auxin Transport and Root Apical Meristem Activity in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.1069996openalex-snapshot
(Don’t) Look Up!: Is short-root just a short‐root plant?
inferred← citeshttps://doi.org/10.3389/fpls.2025.1705659openalex-snapshot
Integrative regulation of middle cortex formation: from classic modules to emerging pathways
inferred← citeshttps://doi.org/10.3389/fpls.2026.1830107openalex-snapshot
Molecular mechanisms of root expansion in medicinal plants
inferred← citeshttps://doi.org/10.3390/agronomy14102287openalex-snapshot
Genome-Wide Identification and Expression Profiling of the BES1 Gene Family in Medicago sativa
inferred← citeshttps://doi.org/10.3390/antiox13050554openalex-snapshot
Hydrogen Peroxide Signaling in the Maintenance of Plant Root Apical Meristem Activity
inferred← citeshttps://doi.org/10.3390/f14122413openalex-snapshot
Effects of a New Plant Growth Regulator on Callus Induction from Immature Embryo Explants of Korean Pine (Pinus koraiensis)
inferred← citeshttps://doi.org/10.3390/ijms23116025openalex-snapshot
Maize ZmBES1/BZR1-3 and -9 Transcription Factors Negatively Regulate Drought Tolerance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms231710149openalex-snapshot
BES1/BZR1 Family Transcription Factors Regulate Plant Development via Brassinosteroid-Dependent and Independent Pathways
inferred← citeshttps://doi.org/10.3390/ijms25136836openalex-snapshot
Interaction of the Transcription Factors BES1/BZR1 in Plant Growth and Stress Response
inferred← citeshttps://doi.org/10.3390/plants11233278openalex-snapshot
Convergence between Development and Stress: Ectopic Xylem Formation in Arabidopsis Hypocotyl in Response to 24-Epibrassinolide and Cadmium
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.