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Cadmium stress suppresses lateral root formation by interfering with the root clock
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4939-7747-5_13openalex-snapshot
Long-Term In Vivo Imaging of Luciferase-Based Reporter Gene Expression in Arabidopsis Roots
inferredcites →https://doi.org/10.1007/s00299-010-0902-0openalex-snapshot
Arabidopsis root growth dependence on glutathione is linked to auxin transport
inferredcites →https://doi.org/10.1016/j.cub.2010.09.007openalex-snapshot
A Novel Aux/IAA28 Signaling Cascade Activates GATA23-Dependent Specification of Lateral Root Founder Cell Identity
inferredcites →https://doi.org/10.1016/j.cub.2013.08.042openalex-snapshot
Halotropism Is a Response of Plant Roots to Avoid a Saline Environment
inferredcites →https://doi.org/10.1016/j.cub.2014.03.025openalex-snapshot
Programmed Cell Death Controlled by ANAC033/SOMBRERO Determines Root Cap Organ Size in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2015.03.046openalex-snapshot
Root Cap-Derived Auxin Pre-patterns the Longitudinal Axis of the Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.cub.2018.05.090openalex-snapshot
A Local Auxin Gradient Regulates Root Cap Self-Renewal and Size Homeostasis
inferredcites →https://doi.org/10.1016/j.cub.2018.07.074openalex-snapshot
The Xerobranching Response Represses Lateral Root Formation When Roots Are Not in Contact With Water
inferredcites →https://doi.org/10.1016/j.envexpbot.2013.10.001openalex-snapshot
Effects of iron deficiency on subcellular distribution and chemical forms of cadmium in peanut roots in relation to its translocation
inferredcites →https://doi.org/10.1016/j.jplph.2013.02.008openalex-snapshot
Cadmium interferes with maintenance of auxin homeostasis in Arabidopsis seedlings
inferredcites →https://doi.org/10.1016/j.pbi.2016.09.001openalex-snapshot
Dynamic control of lateral root positioning
inferredcites →https://doi.org/10.1016/j.plantsci.2018.05.018openalex-snapshot
A comparison of lateral root patterning among dicot and monocot plants
inferredcites →https://doi.org/10.1016/j.tplants.2013.04.006openalex-snapshot
Lateral root development in Arabidopsis: fifty shades of auxin
inferredcites →https://doi.org/10.1016/j.tplants.2018.05.011openalex-snapshot
Out of Shape During Stress: A Key Role for Auxin
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1038/ncb1316openalex-snapshot
Root gravitropism requires lateral root cap and epidermal cells for transport and response to a mobile auxin signal
inferredcites →https://doi.org/10.1038/ncomms7043openalex-snapshot
A fluorescent hormone biosensor reveals the dynamics of jasmonate signalling in plants
inferredcites →https://doi.org/10.1038/ncomms9821openalex-snapshot
A coherent transcriptional feed-forward motif model for mediating auxin-sensitive PIN3 expression during lateral root development
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00262.xopenalex-snapshot
The glutathione‐deficient, cadmium‐sensitive mutant,cad2–1, ofArabidopsis thalianais deficient in γ‐glutamylcysteine synthetase
inferredcites →https://doi.org/10.1073/pnas.0712307105openalex-snapshot
Auxin acts as a local morphogenetic trigger to specify lateral root founder cells
inferredcites →https://doi.org/10.1073/pnas.0906354106openalex-snapshot
The D-type cyclin CYCD4;1 modulates lateral root density in Arabidopsis by affecting the basal meristem region
inferredcites →https://doi.org/10.1073/pnas.1400966111openalex-snapshot
Plant roots use a patterning mechanism to position lateral root branches toward available water
inferredcites →https://doi.org/10.1073/pnas.1403016111openalex-snapshot
Periodic root branching in Arabidopsis requires synthesis of an uncharacterized carotenoid derivative
inferredcites →https://doi.org/10.1093/jxb/44.2.437openalex-snapshot
Aluminium Toxicity in Roots: An Investigation of Spatial Sensitivity and the Role of the Root Cap
inferredcites →https://doi.org/10.1093/jxb/erv295openalex-snapshot
The root cap: a short story of life and death
inferredcites →https://doi.org/10.1093/jxb/erv541openalex-snapshot
Priming and positioning of lateral roots in Arabidopsis. An approach for an integrating concept
inferredcites →https://doi.org/10.1098/rstb.2011.0239openalex-snapshot
Phloem-associated auxin response maxima determine radial positioning of lateral roots in maize
inferredcites →https://doi.org/10.1101/361709openalex-snapshot
Lateral Root Priming Synergystically Arises from Root Growth and Auxin Transport Dynamics
inferredcites →https://doi.org/10.1104/pp.011841openalex-snapshot
Ano hydrotropic responseRoot Mutant that Responds Positively to Gravitropism in Arabidopsis1,
inferredcites →https://doi.org/10.1104/pp.100.1.100openalex-snapshot
Cadmium-Sensitive Mutants of Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.107.2.315openalex-snapshot
Aluminum Toxicity and Tolerance in Plants
inferredcites →https://doi.org/10.1104/pp.107.4.1067openalex-snapshot
A Cadmium-Sensitive, Glutathione-Deficient Mutant of Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.112.4.1471openalex-snapshot
Accumulation of Al in Root Mucilage of an Al-Resistant and an Al-Sensitive Cultivar of Wheat
inferredcites →https://doi.org/10.1104/pp.15.00415openalex-snapshot
Ethylene Inhibits Cell Proliferation of the Arabidopsis Root Meristem
inferredcites →https://doi.org/10.1105/tpc.004960openalex-snapshot
Auxin-Mediated Cell Cycle Activation during Early Lateral Root Initiation
inferredcites →https://doi.org/10.1105/tpc.107.052126openalex-snapshot
Ethylene Regulates Root Growth through Effects on Auxin Biosynthesis and Transport-Dependent Auxin Distribution
inferredcites →https://doi.org/10.1105/tpc.109.071225openalex-snapshot
Interplay between the NADP-Linked Thioredoxin and Glutathione Systems in Arabidopsis Auxin Signaling
inferredcites →https://doi.org/10.1105/tpc.109.072272openalex-snapshot
SOMBRERO, BEARSKIN1, and BEARSKIN2 Regulate Root Cap Maturation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.127993openalex-snapshot
TAA1-Regulated Local Auxin Biosynthesis in the Root-Apex Transition Zone Mediates the Aluminum-Induced Inhibition of Root Growth in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.134874openalex-snapshot
PIN-Dependent Auxin Transport: Action, Regulation, and Evolution
inferredcites →https://doi.org/10.1105/tpc.16.00182openalex-snapshot
Growing Out of Stress: The Role of Cell- and Organ-Scale Growth Control in Plant Water-Stress Responses
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01318.xopenalex-snapshot
Auxin and ethylene interactions control mitotic activity of the quiescent centre, root cap size, and pattern of cap cell differentiation in maize
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03495.xopenalex-snapshot
Ethylene regulates lateral root formation and auxin transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/pce.12172openalex-snapshot
A new role for glutathione in the regulation of root architecture linked to strigolactones
inferredcites →https://doi.org/10.1111/pce.12597openalex-snapshot
Inhibition of root meristem growth by cadmium involves nitric oxide‐mediated repression of auxin accumulation and signalling in Arabidopsis
inferredcites →https://doi.org/10.1111/pce.13361openalex-snapshot
Ethylene promotes cadmium‐induced root growth inhibition through EIN3 controlled XTH33 and LSU1 expression in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1160158openalex-snapshot
Receptor-Like Kinase ACR4 Restricts Formative Cell Divisions in the Arabidopsis Root
inferredcites →https://doi.org/10.1126/science.1191937openalex-snapshot
Oscillating Gene Expression Determines Competence for Periodic Arabidopsis Root Branching
inferredcites →https://doi.org/10.1126/science.1245871openalex-snapshot
A Spatial Accommodation by Neighboring Cells Is Required for Organ Initiation in Arabidopsis
inferredcites →https://doi.org/10.1126/science.aad2776openalex-snapshot
Cyclic programmed cell death stimulates hormone signaling and root development in Arabidopsis
inferredcites →https://doi.org/10.1186/s12870-014-0214-6openalex-snapshot
Cadmium-induced ethylene production and responses in Arabidopsis thaliana rely on ACS2 and ACS6 gene expression
inferredcites →https://doi.org/10.1242/dev.065102openalex-snapshot
Ethylene inhibits lateral root development, increases IAA transport and expression of PIN3 and PIN7 auxin efflux carriers
inferredcites →https://doi.org/10.1242/dev.090548openalex-snapshot
To branch or not to branch: the role of pre-patterning in lateral root formation
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.169839openalex-snapshot
The plant hormone auxin beats the time for oscillating light-regulated lateral root induction
inferredcites →https://doi.org/10.3389/fpls.2016.00081openalex-snapshot
Salt Stress Affects the Redox Status of Arabidopsis Root Meristems
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.4868367openalex-extracted
Elucidating the Interactive and Toxicological Effects of Maize Seedlings Under Combined Exposure of Cadmium and Cerium: Insights from Morphological, Physiological, and Molecular Docking Analyses
inferred← citeshttps://doi.org/10.1007/s42729-025-02787-0openalex-snapshot
Arbuscular Mycorrhizal Fungi (Glomus macrocarpum) and ZnO Nanoparticles Synergistically Improved the Growth of Wheat (Triticum aestivum L.) and Decreased Cadmium Uptake in Cd Contaminated Soil
inferred← citeshttps://doi.org/10.1016/b978-0-443-34104-5.00011-6openalex-snapshot
Toxicity and detoxification of cadmium in plants
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115414openalex-snapshot
A rhizobacterium-secreted protein induces lateral root development through the IAA34-PUCHI pathway
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.055openalex-snapshot
Periodic root branching is influenced by light through an HY1-HY5-auxin pathway
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.109744openalex-snapshot
Transcriptome analysis reveals comprehensive responses to cadmium stress in maize inoculated with arbuscular mycorrhizal fungi
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.2025.106122openalex-snapshot
Dimethyl sulfoxide synergistically mitigates cadmium-induced oxidative damage in pak choi by activating antioxidant and autophagy mechanisms
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131933openalex-snapshot
Interactive effect of silicon and zinc on cadmium toxicity alleviation in wheat plants
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.166644openalex-snapshot
Auxin is involved in cadmium accumulation in rice through controlling nitric oxide production and the ability of cell walls to bind cadmium
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101301openalex-snapshot
Molecular mechanisms of cadmium uptake, translocation and detoxification in rice: Implications for breeding Cd-safe varieties
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c08812openalex-snapshot
Effect of Exogenous STTM397 and miRNA397 on Cadmium Uptake and Accumulation in Water Spinach ( Ipomoea aquatica )
inferred← citeshttps://doi.org/10.1038/s41477-023-01494-xopenalex-snapshot
Plastid-localized amino acid metabolism coordinates rice ammonium tolerance and nitrogen use efficiency
inferred← citeshttps://doi.org/10.1093/jxb/erab444openalex-snapshot
Potential use of arbuscular mycorrhizal fungi for simultaneous mitigation of arsenic and cadmium accumulation in rice
inferred← citeshttps://doi.org/10.1093/jxb/erad366openalex-snapshot
IAR4 mutation enhances cadmium toxicity by disturbing auxin homeostasis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/pcp/pcaa150openalex-snapshot
Cadmium Inhibits Lateral Root Emergence in Rice by Disrupting OsPIN-Mediated Auxin Distribution and the Protective Effect of OsHMA3
inferred← citeshttps://doi.org/10.1111/pce.14021openalex-snapshot
Volatile compounds from beneficial rhizobacteria Bacillus spp. promote periodic lateral root development in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14230openalex-snapshot
The volatile cedrene from Trichoderma guizhouense modulates Arabidopsis root development through auxin transport and signalling
inferred← citeshttps://doi.org/10.1111/plb.13348openalex-snapshot
Mechanism of cadmium tolerance in Salicornia europaea at optimum levels of NaCl
inferred← citeshttps://doi.org/10.1242/dev.181446openalex-snapshot
The dynamic nature and regulation of the root clock
inferred← citeshttps://doi.org/10.15666/aeer/1904_26492666openalex-snapshot
BIOCHEMICAL AND DNA DAMAGE RESPONSES OF HYDROPONICALLY GROWN ELANDS SOURFIG (CARPOBROTUS ACINACIFORMIS L.) LEAVES TO CADMIUM STRESS CONDITIONS
inferred← citeshttps://doi.org/10.20868/upm.thesis.72036openalex-snapshot
Identificación y perturbación de la señalización auxínica por el factor Aux/IAA POTENT en el Reloj de la Raíz y la formación de raíces laterales
inferred← citeshttps://doi.org/10.20868/upm.thesis.72239openalex-snapshot
Unraveling new mechanisms of postembryonic organ formation in Arabidopsis thaliana roots through computational and in vivo approaches
inferred← citeshttps://doi.org/10.2139/ssrn.5384937openalex-snapshot
Ntgcn2 Orchestrates Multilayer Cadmium Tolerance in Tobacco Via Coordinated Transcriptional Regulation of Growth, Antioxidant, and Detoxification Pathways
inferred← citeshttps://doi.org/10.33540/1293openalex-snapshot
Underground decision making; where to grow, when to branch
inferred← citeshttps://doi.org/10.3389/fpls.2022.886700openalex-snapshot
The Root Clock as a Signal Integrator System: Ensuring Balance for Survival
inferred← citeshttps://doi.org/10.3389/fpls.2026.1927917openalex-snapshot
Exogenous γ-aminobutyric acid mitigates physiological and transcriptomic responses of Prunus mongolica under combined alkali salt and cadmium stress
inferred← citeshttps://doi.org/10.3389/fsufs.2026.1925087openalex-snapshot
Dose-dependent exposure of magnesium oxide nanoparticles promoted yield of pea with improved storage stability and germination efficiency of harvested seeds
inferred← citeshttps://doi.org/10.3390/agriculture12050637openalex-snapshot
Developmental and Physiological Responses of Pisum sativum L. after Short- and Long-Time Cadmium Exposure
inferred← citeshttps://doi.org/10.3390/antiox10091494openalex-snapshot
Peroxisomal PEX7 Receptor Affects Cadmium-Induced ROS and Auxin Homeostasis in Arabidopsis Root System
inferred← citeshttps://doi.org/10.3390/ijms23020825openalex-snapshot
Brassinosteroids Mitigate Cadmium Effects in Arabidopsis Root System without Any Cooperation with Nitric Oxide
inferred← citeshttps://doi.org/10.36632/mejar/2023.12.2.19openalex-snapshot
Physiological Effects of Cadmium on Plants: A review
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.21.0130aopenalex-snapshot
A novel petal up-regulated PhXTH7 promoter analysis in Petunia hybrida by using bioluminescence reporter gene
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