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Local Positive Feedback Regulation Determines Cell Shape in Root Hair Cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0006-291x(89)92189-xopenalex-snapshot
Calyculin A and okadaic acid: Inhibitors of protein phosphatase activity
inferredcites →https://doi.org/10.1016/j.biochi.2007.01.012openalex-snapshot
NOX family NADPH oxidases: Not just in mammals
inferredcites →https://doi.org/10.1016/j.jmb.2006.03.066openalex-snapshot
Structural Basis for Diversity of the EF-hand Calcium-binding Proteins
inferredcites →https://doi.org/10.1016/j.tplants.2006.10.002openalex-snapshot
Vesicular trafficking, cytoskeleton and signalling in root hairs and pollen tubes
inferredcites →https://doi.org/10.1016/s0021-9258(17)34550-7openalex-snapshot
Characterization of ionomycin as a calcium ionophore.
inferredcites →https://doi.org/10.1038/nature01485openalex-snapshot
Reactive oxygen species produced by NADPH oxidase regulate plant cell growth
inferredcites →https://doi.org/10.1038/nature04198openalex-snapshot
A RhoGDP dissociation inhibitor spatially regulates growth in root hair cells
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.12020427.xopenalex-snapshot
Cytoplasmic free calcium distributions during the development of root hairs of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00136.xopenalex-snapshot
Six Arabidopsis thaliana homologues of the human respiratory burst oxidase (gp91phox)
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00415.xopenalex-snapshot
Microtubules regulate tip growth and orientation in root hairs of Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m103034200openalex-snapshot
A Ca2+-activated NADPH Oxidase in Testis, Spleen, and Lymph Nodes
inferredcites →https://doi.org/10.1074/jbc.m708106200openalex-snapshot
Synergistic Activation of the Arabidopsis NADPH Oxidase AtrbohD by Ca2+ and Phosphorylation
inferredcites →https://doi.org/10.1093/emboj/20.11.2779openalex-snapshot
Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control polar growth
inferredcites →https://doi.org/10.1104/pp.005777openalex-snapshot
ACTIN2 Is Essential for Bulge Site Selection and Tip Growth during Root Hair Development of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.011569openalex-snapshot
Brefeldin A: Deciphering an Enigmatic Inhibitor of Secretion
inferredcites →https://doi.org/10.1105/tpc.010359openalex-snapshot
The Arabidopsis Rop2 GTPase Is a Positive Regulator of Both Root Hair Initiation and Tip Growth
inferredcites →https://doi.org/10.1105/tpc.10.2.255openalex-snapshot
A Plant Homolog of the Neutrophil NADPH Oxidase gp91phox Subunit Gene Encodes a Plasma Membrane Protein with Ca2+ Binding Motifs
inferredcites →https://doi.org/10.1105/tpc.104.028449openalex-snapshot
Dissection of Arabidopsis ADP-RIBOSYLATION FACTOR 1 Function in Epidermal Cell Polarity
inferredcites →https://doi.org/10.1105/tpc.105.035972openalex-snapshot
PINOID Positively Regulates Auxin Efflux inArabidopsisRoot Hair Cells and Tobacco Cells
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03192.xopenalex-snapshot
Quantitative phosphoproteomic analysis of plasma membrane proteins reveals regulatory mechanisms of plant innate immune responses
inferredcites →https://doi.org/10.1146/annurev.cellbio.17.1.159openalex-snapshot
Polarized Cell Growth in Higher Plants
inferredcites →https://doi.org/10.1242/dev.129.1.123openalex-snapshot
Cell specification in theArabidopsisroot epidermis requires the activity ofECTOPIC ROOT HAIR 3– a katanin-p60 protein
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/978-1-4614-7881-2_19-1openalex-snapshot
ROP GTPases and Cell Shape
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Humic Substances and Plant Defense Metabolism
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Regulation in Biological Systems
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Programmed Cell Death in Plant Immunity: Cellular Reorganization, Signaling, and Cell Cycle Dependence in Cultured Cells as a Model System
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The Function of Cellular Redox Homeostasis and Reactive Oxygen Species (ROS) in Plants Tolerance to Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-3-319-56645-0_9openalex-snapshot
Molecular Mechanisms Regulating Root Hair Tip Growth: A Comparison with Pollen Tubes
inferred← citeshttps://doi.org/10.1007/978-3-319-75910-4_3openalex-snapshot
Root Hair Growth and Development in Response to Nutrients and Phytohormones
inferred← citeshttps://doi.org/10.1007/978-3-540-79405-9_15openalex-snapshot
Genetics of Root Hair Formation
inferred← citeshttps://doi.org/10.1007/978-3-540-89228-1_10openalex-snapshot
Ionic Loops and Rebounds: Oxygen-Deprivation Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-3-540-89228-1_7openalex-snapshot
Signaling to the Actin Cytoskeleton During Cell Morphogenesis and Patterning
inferred← citeshttps://doi.org/10.1007/978-3-642-00390-5_10openalex-snapshot
The ROS Signaling Network of Cells
inferred← citeshttps://doi.org/10.1007/978-3-642-00390-5_13openalex-snapshot
ROS and Plant Membrane Rafts
inferred← citeshttps://doi.org/10.1007/978-3-642-00390-5_3openalex-snapshot
Reactive Oxygen Species in Growth and Development
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3-Phosphoinositide-Dependent Protein Kinase is a Switchboard from Signaling Lipids to Protein Phosphorylation Cascades
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Reactive Oxygen Species and Cognate Redox Signaling System in Plant Innate Immunity
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Reactive Oxygen Species: Role in Senescence and Signal Transduction
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Disrupted actin dynamics trigger an increment in the reactive oxygen species levels in the Arabidopsis root under salt stress
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inferred← citeshttps://doi.org/10.1016/b978-0-323-90943-3.00014-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2011.03.015openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2019.04.059openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2019.09.021openalex-snapshot
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Saline and osmotic stress differentially affects apoplastic and intracellular reactive oxygen species production, curling and death of root hair during Glycine max L.–Bradyrhizobium japonicum interaction
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2012.05.003openalex-snapshot
Interactions between hormone and redox signalling pathways in the control of growth and cross tolerance to stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.05.016openalex-snapshot
Down-regulation of a Phaseolus vulgaris annexin impairs rhizobial infection and nodulation
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.07.015openalex-snapshot
Genome-wide analysis and expression profiling of respiratory burst oxidase homologue gene family in Glycine max
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.11.020openalex-snapshot
The loss of RBOHD function modulates root adaptive responses to combined hypoxia and salinity stress in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104279openalex-snapshot
Respiratory burst oxidases and apoplastic peroxidases facilitate ammonium syndrome development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104813openalex-snapshot
Cadmium enhances root hair elongation through reactive oxygen species in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105514openalex-snapshot
The mechanism of Ca2+ signal transduction in plants responding to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.febslet.2013.12.011openalex-snapshot
Rotenone induces neurotoxicity through Rac1‐dependent activation of NADPH oxidase in SHSY‐5Y cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.07.027openalex-snapshot
Nox enzymes from fungus to fly to fish and what they tell us about Nox function in mammals
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.09.027openalex-snapshot
Urothelial cells produce hydrogen peroxide through the activation of Duox1
inferred← citeshttps://doi.org/10.1016/j.gde.2008.05.001openalex-snapshot
Root layers: complex regulation of developmental patterning
inferred← citeshttps://doi.org/10.1016/j.gene.2018.03.099openalex-snapshot
De novo transcriptomic analysis to identify differentially expressed genes during the process of aerenchyma formation in Typha angustifolia leaves
inferred← citeshttps://doi.org/10.1016/j.hal.2020.101938openalex-snapshot
Nutrient deficiency stimulates the production of superoxide in the noxious red-tide-forming raphidophyte Chattonella antiqua
inferred← citeshttps://doi.org/10.1016/j.hal.2024.102712openalex-snapshot
Production of extracellular superoxide contributes to photosynthesis via elimination of reducing power and regeneration of NADP+ in the red-tide-forming raphidophyte Chattonella marina complex
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.125900openalex-snapshot
Selenium nanoparticles ameliorate Brassica napus L. cadmium toxicity by inhibiting the respiratory burst and scavenging reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.128217openalex-snapshot
The role of NADPH oxidases in regulating leaf gas exchange and ion homeostasis in Arabidopsis plants under cadmium stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2010.09.004openalex-snapshot
Phosphatidic acid production in chitosan-elicited tomato cells, via both phospholipase D and phospholipase C/diacylglycerol kinase, requires nitric oxide
inferred← citeshttps://doi.org/10.1016/j.jplph.2012.05.014openalex-snapshot
NADPH oxidase activity in pollen tubes is affected by calcium ions, signaling phospholipids and Rac/Rop GTPases
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153887openalex-snapshot
Multicopper oxidases GbAO and GbSKS are involved in the Verticillium dahliae resistance in Gossypium barbadense
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154082openalex-snapshot
ROS: Important factor in plant stem cell fate regulation
inferred← citeshttps://doi.org/10.1016/j.molp.2015.01.023openalex-snapshot
Calcium Signaling during Reproduction and Biotrophic Fungal Interactions in Plants
inferred← citeshttps://doi.org/10.1016/j.molp.2019.12.014openalex-snapshot
The RALF1–FERONIA Complex Phosphorylates eIF4E1 to Promote Protein Synthesis and Polar Root Hair Growth
inferred← citeshttps://doi.org/10.1016/j.molp.2020.11.017openalex-snapshot
A positive feedback circuit for ROP-mediated polar growth
inferred← citeshttps://doi.org/10.1016/j.molp.2024.04.002openalex-snapshot
FERONIA-mediated TIR1/AFB2 oxidation stimulates auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.niox.2010.12.008openalex-snapshot
Regulatory mechanisms of nitric oxide and reactive oxygen species generation and their role in plant immunity
inferred← citeshttps://doi.org/10.1016/j.pbi.2008.10.002openalex-snapshot
Tip growth: signaling in the apical dome
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.08.002openalex-snapshot
The exploring root—root growth responses to local environmental conditions
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.10.005openalex-snapshot
Plant cells taking shape: new insights into cytoplasmic control
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.07.014openalex-snapshot
Respiratory burst oxidases: the engines of ROS signaling
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.09.005openalex-snapshot
Calcium regulation of tip growth: new genes for old mechanisms
inferred← citeshttps://doi.org/10.1016/j.peptides.2021.170599openalex-snapshot
CASPARIAN STRIP INTEGRITY FACTOR (CIF) family peptides - regulator of plant extracellular barriers
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.08.016openalex-snapshot
Pectins, ROS homeostasis and UV-B responses in plant roots
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.09.016openalex-snapshot
Reactive oxygen species in cell wall metabolism and development in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.01.014openalex-snapshot
Arabidopsis NADPH oxidases, AtrbohD and AtrbohF, are essential for jasmonic acid-induced expression of genes regulated by MYC2 transcription factor
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.08.012openalex-snapshot
The control of root growth by reactive oxygen species in Salix nigra Marsh. seedlings
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.11.006openalex-snapshot
Reverse function of ROS-induced CBL10 during salt and drought stress responses
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.03.004openalex-snapshot
Mutual interplay of Ca2+ and ROS signaling in plant immune response
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.110824openalex-snapshot
The apple MdPTI1L kinase is phosphorylated by MdOXI1 during S-RNase-induced reactive oxygen species signaling in pollen tubes
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111071openalex-snapshot
MxRop1-MxrbohD1 interaction mediates ROS signaling in response to iron deficiency in the woody plant Malus xiaojinensis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111500openalex-snapshot
Molecular hydrogen positively influences lateral root formation by regulating hydrogen peroxide signaling
inferred← citeshttps://doi.org/10.1016/j.plaphy.2012.02.016openalex-snapshot
ROS signaling as common element in low oxygen and heat stresses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.08.017openalex-snapshot
Spectral phasor analysis reveals altered membrane order and function of root hair cells in Arabidopsis dry2/sqe1-5 drought hypersensitive mutant
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.05.020openalex-snapshot
Calcium affects uranium responses in Arabidopsis thaliana: From distribution to toxicity
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108273openalex-snapshot
The hidden harmony: Exploring ROS-phytohormone nexus for shaping plant root architecture in response to environmental cues
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109137openalex-snapshot
Actin cytoskeleton and plasma membrane aquaporins are involved in different drought response of Arabidopsis rhd2 and der1 root hair mutants
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.plgene.2019.100173openalex-snapshot
Reactive oxygen species-mediated signaling during abiotic stress
inferred← citeshttps://doi.org/10.1016/j.pmpp.2016.03.004openalex-snapshot
Hierarchical regulation of NADPH oxidase by protein kinases in plant immunity
inferred← citeshttps://doi.org/10.1016/j.pmpp.2023.102000openalex-snapshot
Dynamics of plant immune MAPK activity and ROS signaling in response to invaders
inferred← citeshttps://doi.org/10.1016/j.redox.2017.05.008openalex-snapshot
Non-linear actions of physiological agents: Finite disarrangements elicit fitness benefits
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109577openalex-snapshot
Exogenous salicylic acid alleviates salt stress by improving leaf photosynthesis and root system architecture in cucumber seedlings
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.06.004openalex-snapshot
Rapid tip growth: Insights from pollen tubes
inferred← citeshttps://doi.org/10.1016/j.stress.2022.100108openalex-snapshot
Chilling-induced H2O2 signaling activates the antioxidant enzymes in alleviating the photooxidative damage caused by loss of function of 2-Cys peroxiredoxin in watermelon
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100164openalex-snapshot
Reactive oxygen species: Connecting eustress, hormesis, and allostasis in plants
inferred← citeshttps://doi.org/10.1016/j.tcb.2009.02.005openalex-snapshot
Feeling green: mechanosensing in plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2010.08.010openalex-snapshot
Root hair systems biology
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot
ROS signaling: the new wave?
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.10.001openalex-snapshot
A burst of plant NADPH oxidases
inferred← citeshttps://doi.org/10.1016/j.tplants.2012.12.002openalex-snapshot
Plant mechanosensing and Ca2+ transport
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.02.008openalex-snapshot
How Does pH Fit in with Oscillating Polar Growth?
inferred← citeshttps://doi.org/10.1016/j.xplc.2021.100246openalex-snapshot
The hidden half comes into the spotlight: Peeking inside the black box of root developmental phases
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100451openalex-snapshot
Signaling network controlling ROP-mediated tip growth in Arabidopsis and beyond
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101350openalex-snapshot
Enhanced auxin signaling promotes root-hair growth at moderately low temperature in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101483openalex-snapshot
A GhSnRK10–GhRopGEF5–GhROP10 signaling pathway regulates cotton fiber cell growth
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101972openalex-snapshot
Cytokinin-activated DIRIGENT13 promotes lignan synthesis to regulate root growth and abiotic stress tolerance by modulating ROS homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.ygeno.2011.12.008openalex-snapshot
Identification of differentially expressed genes in cucumber (Cucumis sativus L.) root under waterlogging stress by digital gene expression profile
inferred← citeshttps://doi.org/10.1016/j.ygeno.2019.08.010openalex-snapshot
Systematic study of the stress-responsive Rboh gene family in Nicotiana tabacum: Genome-wide identification, evolution and role in disease resistance
inferred← citeshttps://doi.org/10.1016/s0065-2296(10)52002-0openalex-snapshot
Chapter 2 Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.9b00028openalex-snapshot
RBOH-Dependent ROS Synthesis and ROS Scavenging by Plant Specialized Metabolites To Modulate Plant Development and Stress Responses
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c02146openalex-snapshot
Interaction between TaNOX7 and TaCDPK13 Contributes to Plant Fertility and Drought Tolerance by Regulating ROS Production
inferred← citeshttps://doi.org/10.1021/acs.jafc.8b02178openalex-snapshot
Melatonin: A Multifunctional Molecule That Triggers Defense Responses against High Light and Nitrogen Starvation Stress in Haematococcus pluvialis
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