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The plant cytoskeleton takes center stage in abiotic stress responses and resilience
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cm.970270304openalex-snapshot
Microtubule converging centers and reorganization of the interphase cytoskeleton and the mitotic spindle in higher plant Haemanthus
inferredcites →https://doi.org/10.1007/bf01280302openalex-snapshot
The cytoskeleton and spatial control of cytokinesis in the plant life cycle
inferredcites →https://doi.org/10.1007/bf03017132openalex-snapshot
Philosophical Transactions of the Royal Society of London (A)
inferredcites →https://doi.org/10.1007/s00299-011-1007-0openalex-snapshot
Induced ectopic expression of At-CBF1 in marker-free transgenic tomatoes confers enhanced chilling tolerance
inferredcites →https://doi.org/10.1007/s00299-012-1348-3openalex-snapshot
Arabidopsis SOS3 plays an important role in salt tolerance by mediating calcium-dependent microfilament reorganization
inferredcites →https://doi.org/10.1007/s00344-012-9314-4openalex-snapshot
Protein Kinase LTRPK1 Influences Cold Adaptation and Microtubule Stability in Rice
inferredcites →https://doi.org/10.1007/s00425-012-1735-6openalex-snapshot
CHUP1 mediates actin-based light-induced chloroplast avoidance movement in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1007/s00425-015-2394-1openalex-snapshot
Heat stress affects the cytoskeleton and the delivery of sucrose synthase in tobacco pollen tubes
inferredcites →https://doi.org/10.1007/s00709-006-0239-2openalex-snapshot
Cell-type-specific disruption and recovery of the cytoskeleton in Arabidopsis thaliana epidermal root cells upon heat shock stress
inferredcites →https://doi.org/10.1007/s00709-007-0255-xopenalex-snapshot
The plant cytoskeleton – new jobs for a versatile network
inferredcites →https://doi.org/10.1007/s00709-009-0078-zopenalex-snapshot
Effect of heat stress on actin cytoskeleton and endoplasmic reticulum of tobacco BY-2 cultured cells and its inhibition by Co2+
inferredcites →https://doi.org/10.1007/s10725-015-0143-xopenalex-snapshot
Exogenous hydrogen sulfide alleviates salt stress in wheat seedlings by decreasing Na+ content
inferredcites →https://doi.org/10.1007/s10725-017-0353-5openalex-snapshot
Regulation of stomatal movement by cortical microtubule organization in response to darkness and ABA signaling in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-011-9860-3openalex-snapshot
Phytochrome B control of total leaf area and stomatal density affects drought tolerance in rice
inferredcites →https://doi.org/10.1007/s11103-014-0226-5openalex-snapshot
The CCCH zinc finger protein gene AtZFP1 improves salt resistance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11515-010-0027-4openalex-snapshot
Proteomics characteristics of rice leaves in response to environmental factors
inferredcites →https://doi.org/10.1007/s11738-009-0371-7openalex-snapshot
NaCl increases the activity of the plasma membrane H+-ATPase in C3 halophyte Suaeda salsa callus
inferredcites →https://doi.org/10.1007/s11738-015-1820-0openalex-snapshot
Drought-induced changes in the actin cytoskeleton of barley (Hordeum vulgare L.) leaves
inferredcites →https://doi.org/10.1007/s11738-016-2061-6openalex-snapshot
Heat stress induces actin cytoskeletal reorganization and transcript profiles of vegetative profilins and actin depolymerizing factors (ADFs) 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.cell.2015.08.028openalex-snapshot
A Mechanism for Sustained Cellulose Synthesis during Salt Stress
inferredcites →https://doi.org/10.1016/j.cub.2010.11.059openalex-snapshot
THRUMIN1 Is a Light-Regulated Actin-Bundling Protein Involved in Chloroplast Motility
inferredcites →https://doi.org/10.1016/j.cub.2013.07.035openalex-snapshot
Myosin XI-i Links the Nuclear Membrane to the Cytoskeleton to Control Nuclear Movement and Shape in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2013.08.006openalex-snapshot
An Atypical Tubulin Kinase Mediates Stress-Induced Microtubule Depolymerization in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2021.03.092openalex-snapshot
Cytoskeletal regulation of primary plant cell wall assembly
inferredcites →https://doi.org/10.1016/j.envexpbot.2012.02.009openalex-snapshot
Ecological stress memory and cross stress tolerance in plants in the face of climate extremes
inferredcites →https://doi.org/10.1016/j.heliyon.2022.e09248openalex-snapshot
The function and biosynthesis of callose in high plants
inferredcites →https://doi.org/10.1016/j.jgg.2011.05.006openalex-snapshot
The alkaline tolerance in Arabidopsis requires stabilizing microfilament partially through inactivation of PKS5 kinase
inferredcites →https://doi.org/10.1016/j.jplph.2019.153015openalex-snapshot
Expression of protein synthesis elongation factors in winter wheat and oat in response to heat stress
inferredcites →https://doi.org/10.1016/j.pbi.2004.09.005openalex-snapshot
Plant organelle positioning
inferredcites →https://doi.org/10.1016/j.pbi.2004.09.017openalex-snapshot
MAPs in plant cells: delineating microtubule growth dynamics and organization
inferredcites →https://doi.org/10.1016/j.pbi.2008.02.005openalex-snapshot
Translational research impacting on crop productivity in drought-prone environments
inferredcites →https://doi.org/10.1016/j.pbi.2019.08.002openalex-snapshot
Understanding the functions and mechanisms of plant cytoskeleton in response to environmental signals
inferredcites →https://doi.org/10.1016/j.plantsci.2015.08.024openalex-snapshot
Drought stress delays endosperm development and misregulates genes associated with cytoskeleton organization and grain quality proteins in developing wheat seeds
inferredcites →https://doi.org/10.1016/j.plantsci.2016.02.017openalex-snapshot
OsBBX14 delays heading date by repressing florigen gene expression under long and short-day conditions in rice
inferredcites →https://doi.org/10.1016/j.plantsci.2017.09.004openalex-snapshot
MAP65-1 is required for the depolymerization and reorganization of cortical microtubules in the response to salt stress in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plantsci.2020.110589openalex-snapshot
Review: Microtubules monitor calcium and reactive oxygen species signatures in signal transduction
inferredcites →https://doi.org/10.1016/j.plantsci.2020.110629openalex-snapshot
GhVLN4 is involved in multiple stress responses and required for resistance to Verticillium wilt
inferredcites →https://doi.org/10.1016/j.plantsci.2022.111261openalex-snapshot
Binding of 14-3-3κ to ADF4 is involved in the regulation of hypocotyl growth and response to osmotic stress in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plipres.2016.01.002openalex-snapshot
Plant phospholipases D and C and their diverse functions in stress responses
inferredcites →https://doi.org/10.1016/j.sajb.2011.09.006openalex-snapshot
Overexpression of Suaeda salsa stroma ascorbate peroxidase in Arabidopsis chloroplasts enhances salt tolerance of plants
inferredcites →https://doi.org/10.1016/s0014-5793(98)01718-9openalex-snapshot
Gibberellic acid stabilises microtubules in maize suspension cells to cold and stimulates acetylation of α‐tubulin 1
inferredcites →https://doi.org/10.1016/s1097-2765(00)00139-8openalex-snapshot
Direct Binding of the Na–H Exchanger NHE1 to ERM Proteins Regulates the Cortical Cytoskeleton and Cell Shape Independently of H+ Translocation
inferredcites →https://doi.org/10.1016/s1369-5266(03)00085-2openalex-snapshot
Regulation of ion homeostasis under salt stress
inferredcites →https://doi.org/10.1023/a:1024674011448openalex-snapshot
Effects of Abscisic Acid, Low Temperature, and Plant Age on Cytoskeleton and Phosphorylated Proteins
inferredcites →https://doi.org/10.1038/35079128openalex-snapshot
MOR1 is essential for organizing cortical microtubules in plants
inferredcites →https://doi.org/10.1038/nsmb979openalex-snapshot
Translation elongation factor 1A is essential for regulation of the actin cytoskeleton and cell morphology
inferredcites →https://doi.org/10.1038/s41467-019-08780-3openalex-snapshot
The companion of cellulose synthase 1 confers salt tolerance through a Tau-like mechanism in plants
inferredcites →https://doi.org/10.1038/s41467-021-22455-yopenalex-snapshot
The E3 ligase MREL57 modulates microtubule stability and stomatal closure in response to ABA
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00845.xopenalex-snapshot
Early steps in cold sensing by plant cells: the role of actin cytoskeleton and membrane fluidity
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01052.xopenalex-snapshot
Cold‐activation of Brassica napus BN115 promoter is mediated by structural changes in membranes and cytoskeleton, and requires Ca2+ influx
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01142.xopenalex-snapshot
Reduced expression of α‐tubulin genes in Arabidopsis thaliana specifically affects root growth and morphology, root hair development and root gravitropism
inferredcites →https://doi.org/10.1071/pp9950875openalex-snapshot
Breeding for Salinity Resistance in Crop Plants: Where Next?
inferredcites →https://doi.org/10.1073/pnas.1007092107openalex-snapshot
Identification of a cellulose synthase-associated protein required for cellulose biosynthesis
inferredcites →https://doi.org/10.1073/pnas.1007836107openalex-snapshot
Two interacting coiled-coil proteins, WEB1 and PMI2, maintain the chloroplast photorelocation movement velocity in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.122224699openalex-snapshot
Regulation of SOS1, a plasma membrane Na + /H + exchanger in Arabidopsis thaliana , by SOS2 and SOS3
inferredcites →https://doi.org/10.1073/pnas.1317902111openalex-snapshot
Actin-dependent plastid movement is required for motive force generation in directional nuclear movement in plants
inferredcites →https://doi.org/10.1073/pnas.132092099openalex-snapshot
Reconstitution in yeast of the Arabidopsis SOS signaling pathway for Na + homeostasis
inferredcites →https://doi.org/10.1073/pnas.1510140112openalex-snapshot
At14a-Like1 participates in membrane-associated mechanisms promoting growth during drought in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1708087114openalex-snapshot
COP1 mediates dark-specific degradation of microtubule-associated protein WDL3 in regulating Arabidopsis hypocotyl elongation
inferredcites →https://doi.org/10.1073/pnas.94.9.4469openalex-snapshot
A 60-kDa plant microtubule-associated protein promotes the growth and stabilization of neurotubules in vitro
inferredcites →https://doi.org/10.1073/pnas.96.26.14931openalex-snapshot
The 65-kDa carrot microtubule-associated protein forms regularly arranged filamentous cross-bridges between microtubules
inferredcites →https://doi.org/10.1074/jbc.m008521200openalex-snapshot
Actin Directly Interacts with Phospholipase D, Inhibiting Its Activity
inferredcites →https://doi.org/10.1074/jbc.m111.275974openalex-snapshot
The Structure of Sucrose Synthase-1 from Arabidopsis thaliana and Its Functional Implications
inferredcites →https://doi.org/10.1080/14620316.2006.11512071openalex-snapshot
The effect of high temperatures on the expression and activity of sucrose-cleaving enzymes during tomato (Lycopersicon esculentum) anther development
inferredcites →https://doi.org/10.1091/mbc.e04-06-0459openalex-snapshot
Phospholipase D Is Involved in Myogenic Differentiation through Remodeling of Actin Cytoskeleton
inferredcites →https://doi.org/10.1093/emboj/21.6.1280openalex-snapshot
The cell morphogenesis gene ANGUSTIFOLIA encodes a CtBP/BARS‐like protein and is involved in the control of the microtubule cytoskeleton
inferredcites →https://doi.org/10.1093/jxb/eraa359openalex-snapshot
Involvement of Arabidopsis phospholipase D δ in regulation of ROS-mediated microtubule organization and stomatal movement upon heat shock
inferredcites →https://doi.org/10.1093/jxb/erh276openalex-snapshot
Root growth maintenance during water deficits: physiology to functional genomics
inferredcites →https://doi.org/10.1093/jxb/erm107openalex-snapshot
Microtubule dynamics in relation to osmotic stress-induced ABA accumulation in Zea mays roots
inferredcites →https://doi.org/10.1093/jxb/erv536openalex-snapshot
Gas exchange and leaf anatomy of a C3–CAM hybrid,Yucca gloriosa(Asparagaceae)
inferredcites →https://doi.org/10.1093/jxb/ery385openalex-snapshot
Arabidopsis ADF5 promotes stomatal closure by regulating actin cytoskeleton remodeling in response to ABA and drought stress
inferredcites →https://doi.org/10.1093/mp/ssp016openalex-snapshot
Prefoldins 3 and 5 Play an Essential Role in Arabidopsis Tolerance to Salt Stress
inferredcites →https://doi.org/10.1093/mp/sst062openalex-snapshot
A Bi-Functional Xyloglucan Galactosyltransferase Is an Indispensable Salt Stress Tolerance Determinant in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pce135openalex-snapshot
Cold Acclimation Can Induce Microtubular Cold Stability in a Manner Distinct from Abscisic Acid
inferredcites →https://doi.org/10.1093/pcp/pcf114openalex-snapshot
Hyperosmotic Stress Induces Formation of Tubulin Macrotubules in Root-Tip Cells of Triticum turgidum: Their Probable Involvement in Protoplast Volume Control
inferredcites →https://doi.org/10.1093/pcp/pcg097openalex-snapshot
Is Microtubule Disassembly a Trigger for Cold Acclimation?
inferredcites →https://doi.org/10.1093/pcp/pcj090openalex-snapshot
Salt Stress Affects Cortical Microtubule Organization and Helical Growth in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcl036openalex-snapshot
Disruption of Actin Filaments by Latrunculin B Affects Cell Wall Construction in Picea meyeri Pollen Tube by Disturbing Vesicle Trafficking
inferredcites →https://doi.org/10.1093/pcp/pcm095openalex-snapshot
Blue Light-Dependent Nuclear Positioning in Arabidopsis thaliana Leaf Cells
inferredcites →https://doi.org/10.1093/pcp/pcm123openalex-snapshot
Salt Tolerance Requires Cortical Microtubule Reorganization in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pct065openalex-snapshot
α-Tubulin is Rapidly Phosphorylated in Response to Hyperosmotic Stress in Rice and Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcy050openalex-snapshot
Cellulose Synthase Mutants Distinctively Affect Cell Growth and Cell Wall Integrity for Plant Biomass Production in Arabidopsis
inferredcites →https://doi.org/10.1093/plphys/kiaa083openalex-snapshot
HSP70-3 Interacts with Phospholipase Dδ and Participates in Heat Stress Defense
inferredcites →https://doi.org/10.1104/pp.102.010421openalex-snapshot
Na+/H+ Exchange Activity in the Plasma Membrane of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.031591openalex-snapshot
Reorganization and in Vivo Dynamics of Microtubules during Arabidopsis Root Hair Development
inferredcites →https://doi.org/10.1104/pp.104.051623openalex-snapshot
In Vivo Dynamics and Differential Microtubule-Binding Activities of MAP65 Proteins
inferredcites →https://doi.org/10.1104/pp.104.052159openalex-snapshot
The Cytoskeleton as a Regulator and Target of Biotic Interactions in Plants
inferredcites →https://doi.org/10.1104/pp.104.900130openalex-snapshot
The Cytoskeleton Becomes Multidisciplinary
inferredcites →https://doi.org/10.1104/pp.104.900133openalex-snapshot
New Views on the Plant Cytoskeleton
inferredcites →https://doi.org/10.1104/pp.105.061887openalex-snapshot
A Plant-Specific Protein Essential for Blue-Light-Induced Chloroplast Movements
inferredcites →https://doi.org/10.1104/pp.105.067371openalex-snapshot
An Auxilin-Like J-Domain Protein, JAC1, Regulates Phototropin-Mediated Chloroplast Movement in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.080333openalex-snapshot
Plastid Movement Impaired 2, a New Gene Involved in Normal Blue-Light-Induced Chloroplast Movements in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.130450openalex-snapshot
Microtubule-Associated Protein AtMPB2C Plays a Role in Organization of Cortical Microtubules, Stomata Patterning, and Tobamovirus Infectivity
inferredcites →https://doi.org/10.1104/pp.109.149526openalex-snapshot
Actin Reorganization Underlies Phototropin-Dependent Positioning of Nuclei in Arabidopsis Leaf Cells
inferredcites →https://doi.org/10.1104/pp.110.171371openalex-snapshot
Distribution of Callose Synthase, Cellulose Synthase, and Sucrose Synthase in Tobacco Pollen Tube Is Controlled in Dissimilar Ways by Actin Filaments and Microtubules
inferredcites →https://doi.org/10.1104/pp.113.217547openalex-snapshot
Abscisic Acid- and Stress-Induced Highly Proline-Rich Glycoproteins Regulate Root Growth in Rice
inferredcites →https://doi.org/10.1104/pp.125.1.360openalex-snapshot
Regulation of a Wheat Actin-Depolymerizing Factor during Cold Acclimation
inferredcites →https://doi.org/10.1104/pp.15.00214openalex-snapshot
PLASTID MOVEMENT IMPAIRED1 and PLASTID MOVEMENT IMPAIRED1-RELATED1 Mediate Photorelocation Movements of Both Chloroplasts and Nuclei
inferredcites →https://doi.org/10.1104/pp.17.01124openalex-snapshot
Ethylene Signaling Modulates Cortical Microtubule Reassembly in Response to Salt Stress
inferredcites →https://doi.org/10.1104/pp.18.00557openalex-snapshot
Actin Reorganization Triggers Rapid Cell Elongation in Roots
inferredcites →https://doi.org/10.1104/pp.18.01150openalex-snapshot
ANGUSTIFOLIA Regulates Actin Filament Alignment for Nuclear Positioning in Leaves
inferredcites →https://doi.org/10.1104/pp.18.01314openalex-snapshot
Low Water Potential and At14a-Like1 (AFL1) Effects on Endocytosis and Actin Filament Organization
inferredcites →https://doi.org/10.1104/pp.19.01372openalex-snapshot
An Intrinsically Disordered Protein Interacts with the Cytoskeleton for Adaptive Root Growth under Stress
inferredcites →https://doi.org/10.1104/pp.20.00480openalex-snapshot
GLABRA2 Regulates Actin Bundling Protein VILLIN1 in Root Hair Growth in Response to Osmotic Stress
inferredcites →https://doi.org/10.1105/tpc.005892openalex-snapshot
Positioning of Nuclei in Arabidopsis Root Hairs
inferredcites →https://doi.org/10.1105/tpc.009837openalex-snapshot
The MUR3 Gene of Arabidopsis Encodes a Xyloglucan Galactosyltransferase That Is Evolutionarily Related to Animal Exostosins
inferredcites →https://doi.org/10.1105/tpc.010051openalex-snapshot
ADF Proteins Are Involved in the Control of Flowering and Regulate F-Actin Organization, Cell Expansion, and Organ Growth in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.017830openalex-snapshot
SPIRAL1Encodes a Plant-Specific Microtubule-Localized Protein Required for Directional Control of Rapidly Expanding Arabidopsis Cells[W]
inferredcites →https://doi.org/10.1105/tpc.104.023937openalex-snapshot
The Arabidopsis Microtubule-Associated Protein AtMAP65-1: Molecular Analysis of Its Microtubule Bundling Activity
inferredcites →https://doi.org/10.1105/tpc.104.161030openalex-snapshot
The Cortical Microtubule Array: From Dynamics to Organization
inferredcites →https://doi.org/10.1105/tpc.105.031930openalex-snapshot
KATAMARI1/MURUS3 Is a Novel Golgi Membrane Protein That Is Required for Endomembrane Organization in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.089920openalex-snapshot
Salt Stress–Induced Disassembly of Arabidopsis Cortical Microtubule Arrays Involves 26S Proteasome–Dependent Degradation of SPIRAL1
inferredcites →https://doi.org/10.1105/tpc.111.092684openalex-snapshot
MDP25, A Novel Calcium Regulatory Protein, Mediates Hypocotyl Cell Elongation by Destabilizing Cortical Microtubules inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.104182openalex-snapshot
Phosphatidic Acid Regulates Microtubule Organization by Interacting with MAP65-1 in Response to Salt Stress in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.112789openalex-snapshot
Light-Regulated Hypocotyl Elongation Involves Proteasome-Dependent Degradation of the Microtubule Regulatory Protein WDL3 in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.117887openalex-snapshot
The Actin-Related Protein2/3 Complex Regulates Mitochondrial-Associated Calcium Signaling during Salt Stress inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.4.807openalex-snapshot
A Katanin-like Protein Regulates Normal Cell Wall gBiosynthesis and Cell Elongation
inferredcites →https://doi.org/10.1105/tpc.16.00078openalex-snapshot
CASEIN KINASE1-LIKE PROTEIN2 Regulates Actin Filament Stability and Stomatal Closure via Phosphorylation of Actin Depolymerizing Factor
inferredcites →https://doi.org/10.1105/tpc.16.00847openalex-snapshot
Protein Phosphatase 2Cs and Microtubule-Associated Stress Protein 1 Control Microtubule Stability, Plant Growth, and Drought Response
inferredcites →https://doi.org/10.1111/j.0030-1299.2004.13255.xopenalex-snapshot
Impacts of multiple stressors on biodiversity and ecosystem functioning: the role of species co‐tolerance
inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02225.xopenalex-snapshot
OsRAN2, essential for mitosis, enhances cold tolerance in rice by promoting export of intranuclear tubulin and maintaining cell division under cold stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02115.xopenalex-snapshot
Interactions of tobacco microtubule‐associated protein MAP65‐1b with microtubules
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03153.xopenalex-snapshot
SB401, a pollen‐specific protein from Solanum berthaultii, binds to and bundles microtubules and F‐actin
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03444.xopenalex-snapshot
The roles of the cytoskeleton during cellulose deposition at the secondary cell wall
inferredcites →https://doi.org/10.1111/j.1438-8677.2009.00201.xopenalex-snapshot
The microfilament cytoskeleton plays a vital role in salt and osmotic stress tolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00922.xopenalex-snapshot
The Actin Cytoskeleton and Signaling Network during Pollen Tube Tip Growth
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00981.xopenalex-snapshot
Microfilament Dynamics is Required for Root Growth under Alkaline Stress in Arabidopsis
inferredcites →https://doi.org/10.1111/jipb.12445openalex-snapshot
From filaments to function: The role of the plant actin cytoskeleton in pathogen perception, signaling and immunity
inferredcites →https://doi.org/10.1111/jipb.13046openalex-snapshot
Regulation of cytoskeleton‐associated protein activities: Linking cellular signals to plant cytoskeletal function
inferredcites →https://doi.org/10.1111/jipb.13264openalex-snapshot
MDP25 mediates the fine‐tuning of microtubule organization in response to salt stress
inferredcites →https://doi.org/10.1111/nph.14920openalex-snapshot
Elucidating the molecular mechanisms mediating plant salt‐stress responses
inferredcites →https://doi.org/10.1111/pce.12905openalex-snapshot
A ROP2‐RIC1 pathway fine‐tunes microtubule reorganization for salt tolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.13023openalex-snapshot
Phospholipase Dδ negatively regulates plant thermotolerance by destabilizing cortical microtubules in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.13066openalex-snapshot
Cold sensing in grapevine—Which signals are upstream of the microtubular “thermometer”
inferredcites →https://doi.org/10.1111/pce.13326openalex-snapshot
HOP family plays a major role in long‐term acquired thermotolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.12102openalex-snapshot
Microtubules, signalling and abiotic stress
inferredcites →https://doi.org/10.1111/tpj.14775openalex-snapshot
Arabidopsis RING E3 ubiquitin ligase JUL1 participates in ABA‐mediated microtubule depolymerization, stomatal closure, and tolerance response to drought stress
inferredcites →https://doi.org/10.1126/science.1126551openalex-snapshot
Visualization of Cellulose Synthase Demonstrates Functional Association with Microtubules
inferredcites →https://doi.org/10.1126/science.1245533openalex-snapshot
A Mechanism for Reorientation of Cortical Microtubule Arrays Driven by Microtubule Severing
inferredcites →https://doi.org/10.1126/science.42.1074.161openalex-snapshot
The Proceedings of the National Academy of Sciences
inferredcites →https://doi.org/10.1134/s1990519x17040083openalex-snapshot
Reorganization of interphase microtubules in root cells of Medicago sativa L. during acclimation to osmotic and salt stress
inferredcites →https://doi.org/10.1146/annurev-phyto-080516-035632openalex-snapshot
Understanding Cytoskeletal Dynamics During the Plant Immune Response
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.463openalex-snapshot
P LANT C ELLULAR AND M OLECULAR R ESPONSES TO H IGH S ALINITY
inferredcites →https://doi.org/10.1155/2012/835836openalex-snapshot
Roles of Protein Synthesis Elongation Factor EF-Tu in Heat Tolerance in Plants
inferredcites →https://doi.org/10.1155/2018/8517018openalex-snapshot
Roles of C-Repeat Binding Factors-Dependent Signaling Pathway in Jasmonates-Mediated Improvement of Chilling Tolerance of Postharvest Horticultural Commodities
inferredcites →https://doi.org/10.1186/1471-2229-13-79openalex-snapshot
The cell morphogenesis ANGUSTIFOLIA (AN) gene, a plant homolog of CtBP/BARS, is involved in abiotic and biotic stress response in higher plants
inferredcites →https://doi.org/10.1186/1939-8433-5-33openalex-snapshot
Comprehensive analysis of differentially expressed rice actin depolymerizing factor gene family and heterologous overexpression of OsADF3 confers Arabidopsis Thaliana drought tolerance
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