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Actin Reorganization Triggers Rapid Cell Elongation in Roots
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4939-1902-4_8openalex-snapshot
Vacuolar Staining Methods in Plant Cells
inferredcites →https://doi.org/10.1007/s00344-005-0044-8openalex-snapshot
Cell Elongation and Microtubule Behavior in the Arabidopsis Hypocotyl: Responses to Ethylene and Auxin
inferredcites →https://doi.org/10.1007/s00425-004-1381-8openalex-snapshot
Role of cytokinin in the regulation of root gravitropism
inferredcites →https://doi.org/10.1007/s11103-008-9398-1openalex-snapshot
ACTIN DEPOLYMERIZING FACTOR9 controls development and gene expression in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2004.12.026openalex-snapshot
Arabidopsis Interdigitating Cell Growth Requires Two Antagonistic Pathways with Opposing Action on Cell Morphogenesis
inferredcites →https://doi.org/10.1016/j.cub.2007.02.047openalex-snapshot
Cytokinins Determine Arabidopsis Root-Meristem Size by Controlling Cell Differentiation
inferredcites →https://doi.org/10.1016/j.cub.2013.07.051openalex-snapshot
Cytokinins Control Endocycle Onset by Promoting the Expression of an APC/C Activator in Arabidopsis Roots
inferredcites →https://doi.org/10.1016/j.devcel.2012.02.015openalex-snapshot
Genetic Framework of Cyclin-Dependent Kinase Function in Arabidopsis
inferredcites →https://doi.org/10.1016/j.devcel.2012.04.008openalex-snapshot
Role of Actin Cytoskeleton in Brassinosteroid Signaling and in Its Integration with the Auxin Response in Plants
inferredcites →https://doi.org/10.1016/j.pbi.2015.10.004openalex-snapshot
The cytoskeleton in the pollen tube
inferredcites →https://doi.org/10.1016/j.plantsci.2012.01.008openalex-snapshot
Control of the actin cytoskeleton in root hair development
inferredcites →https://doi.org/10.1016/j.tplants.2007.11.005openalex-snapshot
Cytokinin signaling: two-components and more
inferredcites →https://doi.org/10.1016/j.tplants.2010.04.007openalex-snapshot
Root apex transition zone: a signalling–response nexus in the root
inferredcites →https://doi.org/10.1016/s0960-9822(03)00493-7openalex-snapshot
Requirements for Arabidopsis ATARP2 and ATARP3 during Epidermal Development
inferredcites →https://doi.org/10.1016/s0960-9822(03)00533-5openalex-snapshot
Root-Specific CLE19 Overexpression and the sol1/2 Suppressors Implicate a CLV-like Pathway in the Control of Arabidopsis Root Meristem Maintenance
inferredcites →https://doi.org/10.1016/s1534-5807(01)00024-7openalex-snapshot
VACUOLELESS1 Is an Essential Gene Required for Vacuole Formation and Morphogenesis in Arabidopsis
inferredcites →https://doi.org/10.1021/bi00118a015openalex-snapshot
Mechanism of inhibition of microtubule polymerization by colchicine: inhibitory potencies of unliganded colchicine and tubulin-colchicine complexes
inferredcites →https://doi.org/10.1038/35059117openalex-snapshot
Identification of CRE1 as a cytokinin receptor from Arabidopsis
inferredcites →https://doi.org/10.1038/35096500openalex-snapshot
Two-component circuitry in Arabidopsis cytokinin signal transduction
inferredcites →https://doi.org/10.1038/380520a0openalex-snapshot
Control of root growth and development by cyclin expression
inferredcites →https://doi.org/10.1038/cr.2012.146openalex-snapshot
Cytokinin signaling regulates pavement cell morphogenesis in Arabidopsis
inferredcites →https://doi.org/10.1038/nature03184openalex-snapshot
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
inferredcites →https://doi.org/10.1038/s41598-018-22707-wopenalex-snapshot
Arabidopsis vegetative actin isoforms, AtACT2 and AtACT7, generate distinct filament arrays in living plant cells
inferredcites →https://doi.org/10.1038/srep02723openalex-snapshot
The boundary of the meristematic and elongation zones in roots: endoreduplication precedes rapid cell expansion
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10010107.xopenalex-snapshot
Strong, constitutive expression of the Arabidopsis ACT2/ACT8 actin subclass in vegetative tissues
inferredcites →https://doi.org/10.1073/pnas.0402887101openalex-snapshot
In planta functions of the Arabidopsis cytokinin receptor family
inferredcites →https://doi.org/10.1073/pnas.1103584108openalex-snapshot
Programmed induction of endoreduplication by DNA double-strand breaks in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1401680111openalex-snapshot
Rice actin-binding protein RMD is a key link in the auxin–actin regulatory loop that controls cell growth
inferredcites →https://doi.org/10.1073/pnas.1517445113openalex-snapshot
Actin-dependent vacuolar occupancy of the cell determines auxin-induced growth repression
inferredcites →https://doi.org/10.1073/pnas.1600399113openalex-snapshot
Arabidopsis type B cytokinin response regulators ARR1, ARR10, and ARR12 negatively regulate plant responses to drought
inferredcites →https://doi.org/10.1073/pnas.1613979113openalex-snapshot
Cytoskeleton dynamics control the first asymmetric cell division in Arabidopsis zygote
inferredcites →https://doi.org/10.1073/pnas.1620749114openalex-snapshot
Cytokinin induces genome-wide binding of the type-B response regulator ARR10 to regulate growth and development in Arabidopsis
inferredcites →https://doi.org/10.1093/bioinformatics/btt276openalex-snapshot
TANGO: a generic tool for high-throughput 3D image analysis for studying nuclear organization
inferredcites →https://doi.org/10.1093/bioinformatics/btw413openalex-snapshot
MorphoLibJ: integrated library and plugins for mathematical morphology with ImageJ
inferredcites →https://doi.org/10.1093/emboj/18.16.4476openalex-snapshot
The mitotic inhibitor ccs52 is required for endoreduplication and ploidy‐dependent cell enlargement in plants
inferredcites →https://doi.org/10.1093/jxb/ert485openalex-snapshot
Hormonal control of cell division and elongation along differentiation trajectories in roots
inferredcites →https://doi.org/10.1093/jxb/erv308openalex-snapshot
Keeping it all together: auxin–actin crosstalk in plant development
inferredcites →https://doi.org/10.1093/pcp/pcl063openalex-snapshot
ARR1 Directly Activates Cytokinin Response Genes that Encode Proteins with Diverse Regulatory Functions
inferredcites →https://doi.org/10.1093/pcp/pcv176openalex-snapshot
Distinct Biochemical Properties ofArabidopsis thalianaActin Isoforms
inferredcites →https://doi.org/10.1101/gad.1829209openalex-snapshot
Endoreplication: polyploidy with purpose
inferredcites →https://doi.org/10.1104/pp.014068openalex-snapshot
Both Vegetative and Reproductive Actin Isovariants Complement the Stunted Root Hair Phenotype of the Arabidopsisact2-1 Mutation
inferredcites →https://doi.org/10.1104/pp.103.028563openalex-snapshot
The Putative Arabidopsis Arp2/3 Complex Controls Leaf Cell Morphogenesis
inferredcites →https://doi.org/10.1104/pp.104.040493openalex-snapshot
Disorganization of Cortical Microtubules Stimulates Tangential Expansion and Reduces the Uniformity of Cellulose Microfibril Alignment among Cells in the Root of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.055665openalex-snapshot
Cloning and Functional Characterization of a Formin-Like Protein (AtFH8) from Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.132449openalex-snapshot
FZR2/CCS52A1Expression Is a Determinant of Endoreduplication and Cell Expansion in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.175794openalex-snapshot
Cytokinin Interplay with Ethylene, Auxin, and Glucose Signaling Controls Arabidopsis Seedling Root Directional Growth
inferredcites →https://doi.org/10.1104/pp.124.4.1706openalex-snapshot
Characterization of the Response of the Arabidopsis Response Regulator Gene Family to Cytokinin
inferredcites →https://doi.org/10.1105/tpc.001537openalex-snapshot
The ROP2 GTPase Controls the Formation of Cortical Fine F-Actin and the Early Phase of Directional Cell Expansion during Arabidopsis Organogenesis
inferredcites →https://doi.org/10.1105/tpc.010026openalex-snapshot
One Plant Actin Isovariant, ACT7, Is Induced by Auxin and Required for Normal Callus Formation
inferredcites →https://doi.org/10.1105/tpc.011676openalex-snapshot
Mutations in Actin-Related Proteins 2 and 3 Affect Cell Shape Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.018978openalex-snapshot
Type-A Arabidopsis Response Regulators Are Partially Redundant Negative Regulators of Cytokinin Signaling[W]
inferredcites →https://doi.org/10.1105/tpc.105.035451openalex-snapshot
Multiple Type-B Response Regulators Mediate Cytokinin Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.061960openalex-snapshot
A Single Vegetative Actin Isovariant Overexpressed under the Control of Multiple Regulatory Sequences Is Sufficient for NormalArabidopsisDevelopment
inferredcites →https://doi.org/10.1105/tpc.11.12.2331openalex-snapshot
Organized F-Actin Is Essential for Normal Trichome Morphogenesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.110.074856openalex-snapshot
Cytokinin Regulation of Auxin Synthesis in Arabidopsis Involves a Homeostatic Feedback Loop Regulated via Auxin and Cytokinin Signal Transduction
inferredcites →https://doi.org/10.1105/tpc.111.086546openalex-snapshot
The Plant-Specific Actin Binding Protein SCAB1 Stabilizes Actin Filaments and Regulates Stomatal Movement inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.087395openalex-snapshot
Analysis of Cytokinin Mutants and Regulation of Cytokinin Metabolic Genes Reveals Important Regulatory Roles of Cytokinins in Drought, Salt and Abscisic Acid Responses, and Abscisic Acid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.15.01003openalex-snapshot
Histone H3 Dynamics Reveal Domains with Distinct Proliferation Potential in the Arabidopsis Root
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02442.xopenalex-snapshot
Altered microtubule dynamics by expression of modified α ‐tubulin protein causes right‐handed helical growth in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02842.xopenalex-snapshot
Ethylene‐induced stomatal closure in Arabidopsis occurs via AtrbohF‐mediated hydrogen peroxide synthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03884.xopenalex-snapshot
The Arabidopsis cyclin‐dependent kinase‐activating kinase CDKF;1 is a major regulator of cell proliferation and cell expansion but is dispensable for CDKA activation
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04032.xopenalex-snapshot
Quantification and cluster analysis of actin cytoskeletal structures in plant cells: role of actin bundling in stomatal movement during diurnal cycles in Arabidopsis guard cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04367.xopenalex-snapshot
ABA promotes quiescence of the quiescent centre and suppresses stem cell differentiation in the Arabidopsis primary root meristem
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04372.xopenalex-snapshot
Vacuolar/pre-vacuolar compartment Qa-SNAREs VAM3/SYP22 and PEP12/SYP21 have interchangeable functions in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04843.xopenalex-snapshot
Cytokinin‐facilitated proteolysis of ARABIDOPSIS RESPONSE REGULATOR 2 attenuates signaling output in two‐component circuitry
inferredcites →https://doi.org/10.1111/nph.12473openalex-snapshot
My body is a cage: mechanisms and modulation of plant cell growth
inferredcites →https://doi.org/10.1111/tpj.13720openalex-snapshot
3D analysis of mitosis distribution highlights the longitudinal zonation and diarch symmetry in proliferation activity of the Arabidopsis thaliana root meristem
inferredcites →https://doi.org/10.1126/science.1065201openalex-snapshot
ARR1, a Transcription Factor for Genes Immediately Responsive to Cytokinins
inferredcites →https://doi.org/10.1126/science.1164147openalex-snapshot
A Genetic Framework for the Control of Cell Division and Differentiation in the Root Meristem
inferredcites →https://doi.org/10.1126/science.1244454openalex-snapshot
A Peptide Hormone and Its Receptor Protein Kinase Regulate Plant Cell Expansion
inferredcites →https://doi.org/10.1146/annurev.cellbio.21.122303.114901openalex-snapshot
SPATIAL CONTROL OF CELL EXPANSION BY THE PLANT CYTOSKELETON
inferredcites →https://doi.org/10.1242/dev.00549openalex-snapshot
Arabidopsis CROOKEDencodes for the smallest subunit of the ARP2/3 complex and controls cell shape by region specific fine F-actin formation
inferredcites →https://doi.org/10.1242/dev.126.24.5559openalex-snapshot
The actin cytoskeleton is required to elaborate and maintain spatial patterning during trichome cell morphogenesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1263/jbb.104.34openalex-snapshot
Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation
inferredcites →https://doi.org/10.1371/journal.pone.0000718openalex-snapshot
An “Electronic Fluorescent Pictograph” Browser for Exploring and Analyzing Large-Scale Biological Data Sets
inferredcites →https://doi.org/10.1371/journal.pone.0065867openalex-snapshot
Comparative Proteomic Analysis of Embryos between a Maize Hybrid and Its Parental Lines during Early Stages of Seed Germination
inferredcites →https://doi.org/10.2307/3870959openalex-snapshot
Organized F-Actin Is Essential for Normal Trichome Morphogenesis in Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2015.01178openalex-snapshot
Epigenetic Control of Cell Division and Cell Differentiation in the Root Apex
inferredcites →https://doi.org/10.4161/psb.1.6.3511openalex-snapshot
The Root Apex ofArabidopsis thalianaConsists of Four Distinct Zones of Growth Activities
inferredcites →https://doi.org/10.5685/plmorphol.29.15openalex-snapshot
Quantitative evaluation of cytoskeletal organizations by microscopic image analysis
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.4837604openalex-extracted
Dynamic Changes and Transcriptome Analyses Reveal the Microfilament Skeleton Response to Water Stress in Thalli of Neopyropia Yezoensis Inhabiting the Intertidal Zone
inferred← citeshttps://doi.org/10.1007/978-3-030-33528-1_5openalex-snapshot
Actin Cytoskeleton and Action Potentials: Forgotten Connections
inferred← citeshttps://doi.org/10.1007/s00122-024-04601-4openalex-snapshot
A large presence/absence variation in the promotor of the ClLOG gene determines trichome elongation in watermelon
inferred← citeshttps://doi.org/10.1007/s00344-023-11046-4openalex-snapshot
Endogenous Serotonin Accumulation Coincides with Reorganization of Auxin Efflux Protein (PIN1) and Actin (ACT8) Accompanying Primary Root Growth Inhibition in NaCl-Stress-Induced Etiolated Sunflower (Helianthus annuus; cv. KBSH 44) Seedlings
inferred← citeshttps://doi.org/10.1007/s00425-022-03914-2openalex-snapshot
Exogenous 6-benzylaminopurine inhibits tip growth and cytokinesis via regulating actin dynamics in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.1007/s10265-021-01333-0openalex-snapshot
Arabidopsis thaliana subclass I ACTIN DEPOLYMERIZING FACTORs and vegetative ACTIN2/8 are novel regulators of endoreplication
inferred← citeshttps://doi.org/10.1007/s10265-023-01438-8openalex-snapshot
Novel whole-mount FISH analysis for intact root of Arabidopsis thaliana with spatial reference to 3D visualization
inferred← citeshttps://doi.org/10.1007/s11427-024-3067-yopenalex-snapshot
Cytoskeletal control of development and environmental adaptation in plants
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114844openalex-snapshot
Actin-mediated avoidance of tricellular junction influences global topology at the Arabidopsis shoot apical meristem
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.04.004openalex-snapshot
A Self-Organized PLT/Auxin/ARR-B Network Controls the Dynamics of Root Zonation Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.113085openalex-snapshot
Transcriptome profiling of Bupleurum chinense DC. root provides new insights into the continuous inflorescence removal induced improvements to root growth and saikosaponin biosynthesis
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110414openalex-snapshot
Pleiotropic regulatory locus 1 maintains actin cytoskeleton integrity and cellular homeostasis to enable Arabidopsis root growth
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.04.003openalex-snapshot
Endoreplication as a potential driver of cell wall modifications
inferred← citeshttps://doi.org/10.1016/j.pbi.2020.08.005openalex-snapshot
Arabidopsis primary root growth: let it grow, can't hold it back anymore!
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110233openalex-snapshot
Poplar PdRabG3f inhibits root elongation and increases salt tolerance by enhancing endogenous abscisic acid synthesis
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.108974openalex-snapshot
Herbicides act as restrictive factors in rice-watermelon rotation
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100762openalex-snapshot
Dynamic changes and transcriptome analyses reveal the microfilament skeleton response to water stress in thalli of Neopyropia yezoensis inhabiting the intertidal zone
inferred← citeshttps://doi.org/10.1080/15592324.2019.1578632openalex-snapshot
ABA inhibits root cell elongation through repressing the cytokinin signaling
inferred← citeshttps://doi.org/10.1080/15592324.2021.1876348openalex-snapshot
Latrunculin B facilitates gravitropic curvature of Arabidopsis root by inhibiting cell elongation, especially the cells in the lower flanks of the transition and elongation zones
inferred← citeshttps://doi.org/10.1080/15592324.2026.2726829openalex-snapshot
Root hair initiation-dependent and -independent nuclear movements during root hair development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1091/mbc.e24-06-0248openalex-snapshot
Morphometric analysis of actin networks
inferred← citeshttps://doi.org/10.1093/aob/mcaf087openalex-snapshot
Hormonal regulation of root growth under moderately elevated temperatures
inferred← citeshttps://doi.org/10.1093/hr/uhad125openalex-snapshot
GWAS identifies candidate genes controlling adventitious rooting in Populus trichocarpa
inferred← citeshttps://doi.org/10.1093/jxb/erab360openalex-snapshot
Hormonal orchestration of root apical meristem formation and maintenance in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erac280openalex-snapshot
Actin isovariant ACT7 controls root meristem development in Arabidopsis through modulating auxin and ethylene responses
inferred← citeshttps://doi.org/10.1093/jxb/erad091openalex-snapshot
Cytokinin signaling promotes root hair growth by directly regulating RSL4 expression
inferred← citeshttps://doi.org/10.1093/jxb/eraf346openalex-snapshot
Mutations adjacent to the nucleotide-binding cleft of Arabidopsis thaliana ACTIN7 confer resistance to the actin-disrupting compound latrunculin B
inferred← citeshttps://doi.org/10.1093/pcp/pcaf027openalex-snapshot
Arabidopsis thaliana ACTIN DEPOLYMERIZING FACTOR s play a role in leaf senescence regulation
inferred← citeshttps://doi.org/10.1093/pcp/pcz217openalex-snapshot
Nickel Toxicity Targets Cell Wall-Related Processes and PIN2-Mediated Auxin Transport to Inhibit Root Elongation and Gravitropic Responses in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiac590openalex-snapshot
A brassinosteroid transcriptional regulatory network participates in regulating fiber elongation in cotton
inferred← citeshttps://doi.org/10.1093/plphys/kiad228openalex-snapshot
Hormone-regulated expansins: Expression, localization, and cell wall biomechanics in Arabidopsis root growth
inferred← citeshttps://doi.org/10.1093/plphys/kiaf303openalex-snapshot
The transcriptional repressors IAA5 and IAA29 participate in DNA damage-induced stem cell death in Arabidopsis roots
inferred← citeshttps://doi.org/10.1093/plphys/kiaf495openalex-snapshot
Intracellular MIZU-KUSSEI1 movement and hydrotropism in Arabidopsis require F-actin organization
inferred← citeshttps://doi.org/10.1101/2020.06.19.160838openalex-snapshot
DNA damage inhibits root growth by enhancing cytokinin biosynthesis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2020.06.25.170969openalex-snapshot
Expansin-controlled cell wall stiffness regulates root growth in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2021.09.16.460643openalex-snapshot
AHK5 mediates ETR1-initiated multistep phosphorelay in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.09.02.506394openalex-snapshot
Local induction of IAA5 and IAA29 promotes DNA damage-triggered stem cell death in Arabidopsis roots
inferred← citeshttps://doi.org/10.1101/2023.02.28.530538openalex-snapshot
Pleiotropic Regulatory Locus1 maintains actin microfilament integrity and concomitant cellular homeostasis facilitating root development in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.07.20.604417openalex-snapshot
A high-resolution model of gene expression during Gossypium hirsutum (cotton) fiber development
inferred← citeshttps://doi.org/10.1101/2025.08.18.670899openalex-snapshot
Actin Counters Geometry to Guide Plant Cell Division
inferred← citeshttps://doi.org/10.1104/pp.18.01314openalex-snapshot
Low Water Potential and At14a-Like1 (AFL1) Effects on Endocytosis and Actin Filament Organization
inferred← citeshttps://doi.org/10.1104/pp.19.00064openalex-snapshot
An Auxin Transport Inhibitor Targets Villin-Mediated Actin Dynamics to Regulate Polar Auxin Transport
inferred← citeshttps://doi.org/10.1105/tpc.18.00973openalex-snapshot
Cryo-EM Structure of Actin Filaments from Zea mays Pollen
inferred← citeshttps://doi.org/10.1111/nph.17936openalex-snapshot
May the dark be with roots: a perspective on how root illumination may bias in vitro research on plant–environment interactions
inferred← citeshttps://doi.org/10.1111/pbi.70311openalex-snapshot
Mapping the Phosphorylation Regulatory Network of Single‐Celled Fibre Elongation Mediated by GhBIN2 in Cotton
inferred← citeshttps://doi.org/10.1111/pce.14450openalex-snapshot
The plant cytoskeleton takes center stage in abiotic stress responses and resilience
inferred← citeshttps://doi.org/10.1111/tpj.14986openalex-snapshot
Dual‐color 3D‐dSTORM colocalization and quantification of ROXY1 and RNAPII variants throughout the transcription cycle in root meristem nuclei
inferred← citeshttps://doi.org/10.1126/sciadv.abg0993openalex-snapshot
Alterations in hormonal signals spatially coordinate distinct responses to DNA double-strand breaks inArabidopsisroots
inferred← citeshttps://doi.org/10.1126/sciadv.abn5057openalex-snapshot
Arabidopsis TIE1 and TIE2 transcriptional repressors dampen cytokinin response during root development
inferred← citeshttps://doi.org/10.1126/sciadv.aeb8498openalex-snapshot
The actin cytoskeleton is required to maintain plant cell division orientation against cellular geometry
inferred← citeshttps://doi.org/10.1186/s12864-025-11360-zopenalex-snapshot
A high-resolution model of gene expression during Gossypium hirsutum (cotton) fiber development
inferred← citeshttps://doi.org/10.1186/s40659-020-00321-3openalex-snapshot
Actin filaments mediated root growth inhibition by changing their distribution under UV-B and hydrogen peroxide exposure in Arabidopsis
inferred← citeshttps://doi.org/10.1242/dev.200899openalex-snapshot
A mutation in THREONINE SYNTHASE 1 uncouples proliferation and transition domains of the root apical meristem: experimental evidence and in silico proposed mechanism
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010338openalex-snapshot
Actin depolymerizing factor ADF7 inhibits actin bundling protein VILLIN1 to regulate root hair formation in response to osmotic stress in Arabidopsis
inferred← citeshttps://doi.org/10.2142/biophys.64.132openalex-snapshot
“Cell Wall” “Large Vacuole” & “Cytoplasmic Streaming”: How Do Cytoskeletons Build Plant Cells with Unique Physical Properties?
inferred← citeshttps://doi.org/10.2142/biophysico.bppb-v22.0013openalex-snapshot
Cytoskeleton as a generator of characteristic physical properties of plant cells: ‘cell wall,’ ‘large vacuole,’ and ‘cytoplasmic streaming’
inferred← citeshttps://doi.org/10.31274/td-20240329-570openalex-snapshot
Parallelism and convergence during independent domestication of cotton species
inferred← citeshttps://doi.org/10.3389/fpls.2021.659155openalex-snapshot
Integrative Roles of Phytohormones on Cell Proliferation, Elongation and Differentiation in the Arabidopsis thaliana Primary Root
inferred← citeshttps://doi.org/10.3389/fpls.2021.777119openalex-snapshot
Bundling up the Role of the Actin Cytoskeleton in Primary Root Growth
inferred← citeshttps://doi.org/10.3389/fpls.2022.862171openalex-snapshot
The Root Hair Development of Pectin Polygalacturonase PGX2 Activation Tagging Line in Response to Phosphate Deficiency
inferred← citeshttps://doi.org/10.3389/fpls.2023.1146802openalex-snapshot
Cotton fiber as a model for understanding shifts in cell development under domestication
inferred← citeshttps://doi.org/10.3390/ijms22115739openalex-snapshot
Sound Waves Promote Arabidopsis thaliana Root Growth by Regulating Root Phytohormone Content
inferred← citeshttps://doi.org/10.3390/ijms24044143openalex-snapshot
At the Nexus between Cytoskeleton and Vacuole: How Plant Cytoskeletons Govern the Dynamics of Large Vacuoles
inferred← citeshttps://doi.org/10.3390/ijms242015480openalex-snapshot
Exploring the Role of the Plant Actin Cytoskeleton: From Signaling to Cellular Functions
inferred← citeshttps://doi.org/10.3390/plants12244076openalex-snapshot
Arabidopsis Root Development Regulation by the Endogenous Folate Precursor, Para-Aminobenzoic Acid, via Modulation of the Root Cell Cycle
inferred← citeshttps://doi.org/10.36987/jpbn.v10i1.5325openalex-snapshot
Effectiveness of Bottle Size Variation on the Growth of Dendrobium Striaenopsis Orchid Plantlets
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.24.1103aopenalex-snapshot
Whole-mount immunostaining that avoids cross-reaction between antibodies from different host species for simultaneous visualization of actin filaments and microtubules
inferred← citeshttps://doi.org/10.70675/7b853c4aze25az4f8bzb66fz32664a7f750dopenalex-snapshot
Le Root Extracellular Trap (RET), un réseau au coeur de la défense racinaire : caractérisation moléculaire et fonctionnelle chez deux légumineuses, Glycine max (Merr.) L. et Pisum sativum (L.)
inferred← citeshttps://doi.org/10.70675/984322fdz7e95z4225z80dbz154bfb36bed7openalex-snapshot
Cell fate and blade patterning during the early growth of Saccharina latissima sporophytes
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