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Hydrotropism in the primary roots of maize
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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/bf00202664openalex-snapshot
Hydrotropism in roots: sensing of a gradient in water potential by the root cap
inferredcites →https://doi.org/10.1007/pl00013906openalex-snapshot
A Spaceflight Experiment for the Study of Gravimorphogenesis and Hydrotropism in Cucumber Seedlings
inferredcites →https://doi.org/10.1007/s12374-009-9083-1openalex-snapshot
Accumulation of High Levels of ABA Regulates the Pleiotropic Response of the nhr1 Arabidopsis Mutant
inferredcites →https://doi.org/10.1016/j.cub.2017.07.015openalex-snapshot
Molecular Mechanisms of Root Gravitropism
inferredcites →https://doi.org/10.1016/j.envexpbot.2010.03.013openalex-snapshot
Transcriptome analysis of gene expression during the hydrotropic response in Arabidopsis seedlings
inferredcites →https://doi.org/10.1016/j.febslet.2012.01.008openalex-snapshot
MIZ1, an essential protein for root hydrotropism, is associated with the cytoplasmic face of the endoplasmic reticulum membrane in Arabidopsis root cells
inferredcites →https://doi.org/10.1016/j.molp.2016.02.001openalex-snapshot
Hydrotropism: Root Bending Does Not Require Auxin Redistribution
inferredcites →https://doi.org/10.1016/s0092-8674(00)80682-0openalex-snapshot
Regulation of Auxin Response by the Protein Kinase PINOID
inferredcites →https://doi.org/10.1038/nature22971openalex-snapshot
Improved maize reference genome with single-molecule technologies
inferredcites →https://doi.org/10.1038/nplants.2017.57openalex-snapshot
Root hydrotropism is controlled via a cortex-specific growth mechanism
inferredcites →https://doi.org/10.1038/nprot.2009.97openalex-snapshot
Mapping identifiers for the integration of genomic datasets with the R/Bioconductor package biomaRt
inferredcites →https://doi.org/10.1046/j.1365-3040.1997.d01-70.xopenalex-snapshot
Water potential, turgor and cell wall properties in elongating tissues of the hydrotropically bending roots of pea (Pisum sativum L.)
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.08010037.xopenalex-snapshot
An Arabidopsis thaliana root‐specific kinase homolog is induced by dehydration, ABA, and NaCl
inferredcites →https://doi.org/10.1071/fp06209openalex-snapshot
Ethylene modulates genetic, positional, and nutritional regulation of root plagiogravitropism
inferredcites →https://doi.org/10.1073/pnas.0609929104openalex-snapshot
A gene essential for hydrotropism in roots
inferredcites →https://doi.org/10.1073/pnas.1512748112openalex-snapshot
Activation of Big Grain1 significantly improves grain size by regulating auxin transport in rice
inferredcites →https://doi.org/10.1073/pnas.1804130115openalex-snapshot
MIZ1 regulates ECA1 to generate a slow, long-distance phloem-transmitted Ca 2+ signal essential for root water tracking in Arabidopsis
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/database/bar030openalex-snapshot
Ensembl BioMarts: a hub for data retrieval across taxonomic space
inferredcites →https://doi.org/10.1093/jxb/erg060openalex-snapshot
Electrophysiological responses of maize roots to low water potentials: relationship to growth and ABA accumulation
inferredcites →https://doi.org/10.1093/jxb/erl274openalex-snapshot
Auxin response, but not its polar transport, plays a role in hydrotropism of Arabidopsis roots
inferredcites →https://doi.org/10.1093/jxb/err031openalex-snapshot
Salicylic acid beyond defence: its role in plant growth and development
inferredcites →https://doi.org/10.1093/jxb/ers025openalex-snapshot
An altered hydrotropic response (ahr1) mutant of Arabidopsis recovers root hydrotropism with cytokinin
inferredcites →https://doi.org/10.1093/jxb/erx193openalex-snapshot
Auxin transport and response requirements for root hydrotropism differ between plant species
inferredcites →https://doi.org/10.1093/jxb/ery034openalex-snapshot
Hydrotropism: how roots search for water
inferredcites →https://doi.org/10.1093/nar/gkt214openalex-snapshot
The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029180openalex-snapshot
Calcium Requirement for the Induction of Hydrotropism and Enhancement of Calcium-Induced Curvature by Water Stress in Primary Roots of Pea, Pisum sativum L.
inferredcites →https://doi.org/10.1093/pcp/pcf093openalex-snapshot
Hydrotropic Response and Expression Pattern of Auxin-Inducible Gene, CS-IAA1, in the Primary Roots of Clinorotated Cucumber Seedlings
inferredcites →https://doi.org/10.1093/pcp/pcp171openalex-snapshot
SIZ1 Controls Cell Growth and Plant Development in Arabidopsis Through Salicylic Acid
inferredcites →https://doi.org/10.1104/pp.106.2.607openalex-snapshot
Root Growth Maintenance at Low Water Potentials (Increased Activity of Xyloglucan Endotransglycosylase and Its Possible Regulation by Abscisic Acid)
inferredcites →https://doi.org/10.1104/pp.108.131003openalex-snapshot
GNOM-Mediated Vesicular Trafficking Plays an Essential Role in Hydrotropism of Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.111.179895openalex-snapshot
A Novel Image-Analysis Toolbox Enabling Quantitative Analysis of Root System Architecture
inferredcites →https://doi.org/10.1104/pp.111.3.765openalex-snapshot
Growth Maintenance of the Maize Primary Root at Low Water Potentials Involves Increases in Cell-Wall Extension Properties, Expansin Activity, and Wall Susceptibility to Expansins
inferredcites →https://doi.org/10.1104/pp.126.4.1471openalex-snapshot
Modification of Expansin Transcript Levels in the Maize Primary Root at Low Water Potentials
inferredcites →https://doi.org/10.1104/pp.17.01563openalex-snapshot
Comparative Analysis of Arabidopsis Ecotypes Reveals a Role for Brassinosteroids in Root Hydrotropism
inferredcites →https://doi.org/10.1105/tpc.105.037523openalex-snapshot
Physical and Functional Interactions between Pathogen-Induced Arabidopsis WRKY18, WRKY40, and WRKY60 Transcription Factors
inferredcites →https://doi.org/10.1111/j.1365-3040.1993.tb00850.xopenalex-snapshot
Intensity of hydrostimulation for the induction of root hydrotropism and its sensing by the root cap
inferredcites →https://doi.org/10.1111/nph.14689openalex-snapshot
Gravitropism interferes with hydrotropism via counteracting auxin dynamics in cucumber roots: clinorotation and spaceflight experiments
inferredcites →https://doi.org/10.1111/nph.15172openalex-snapshot
Back to basics: what is the function of an Aux/ IAA in auxin response?
inferredcites →https://doi.org/10.1111/nph.16487openalex-snapshot
A cell surface arabinogalactan‐peptide influences root hair cell fate
inferredcites →https://doi.org/10.1111/tpj.12479openalex-snapshot
Evolution and diversity of the 2–oxoglutarate‐dependent dioxygenase superfamily in plants
inferredcites →https://doi.org/10.1111/tpj.13296openalex-snapshot
Jasmonate‐mediated stomatal closure under elevated CO 2 revealed by time‐resolved metabolomics
inferredcites →https://doi.org/10.1126/science.230.4724.445openalex-snapshot
A Pea Mutant for the Study of Hydrotropism in Roots
inferredcites →https://doi.org/10.1134/s0006297912120024openalex-snapshot
Cytokinin oxidase is key enzyme of cytokinin degradation
inferredcites →https://doi.org/10.1134/s1021443715060084openalex-snapshot
Role of green light in physiological activity of plants
inferredcites →https://doi.org/10.1186/1471-2229-10-281openalex-snapshot
Roles of arabidopsis WRKY18, WRKY40 and WRKY60 transcription factors in plant responses to abscisic acid and abiotic stress
inferredcites →https://doi.org/10.1186/gb-2010-11-2-r14openalex-snapshot
Gene ontology analysis for RNA-seq: accounting for selection bias
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1269/jrr.07131openalex-snapshot
Effects of Locally Targeted Heavy-ion and Laser Microbeam on Root Hydrotropism in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0189827openalex-snapshot
Root-tip-mediated inhibition of hydrotropism is accompanied with the suppression of asymmetric expression of auxin-inducible genes in response to moisture gradients in cucumber roots
inferredcites →https://doi.org/10.3159/torrey-d-11-00040.1openalex-snapshot
Green light affects blue-light-based phototropism in hypocotyls of Arabidopsis thaliana1
inferredcites →https://doi.org/10.3389/fmolb.2017.00051openalex-snapshot
Metabolomics and Proteomics of Brassica napus Guard Cells in Response to Low CO2
inferredcites →https://doi.org/10.3389/fpls.2014.00563openalex-snapshot
Light and gravity signals synergize in modulating plant development
inferredcites →https://doi.org/10.3732/ajb.1200419openalex-snapshot
Molecular mechanisms of hydrotropism in seedling roots of Arabidopsis thaliana (Brassicaceae)
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.4621628openalex-extracted
Miz1 Modulates Root Hydrotropism by Involving Amyloplast Response
inferred← citeshttps://doi.org/10.1002/csc2.70084openalex-snapshot
Plasticity of maize (Zea mays L.) roots in water‐deficient and nitrogen‐limited soil
inferred← citeshttps://doi.org/10.1007/s00425-023-04262-5openalex-snapshot
Zoom-in to molecular mechanisms underlying root growth and function under heterogeneous soil environment and abiotic stresses
inferred← citeshttps://doi.org/10.1007/s11103-025-01646-xopenalex-snapshot
Unearthing the hidden organ: vital role of the root in drought tolerance of plants
inferred← citeshttps://doi.org/10.1007/s11356-022-20719-8openalex-snapshot
Effect of formulation on the indoxacarb and lufenuron dissipation in maize and risk assessment
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108198openalex-snapshot
Light-Dark Modulates Root Hydrotropism Associated with Gravitropism by Involving Amyloplast Response in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104732openalex-snapshot
An integrated analysis of transcriptome and metabolome provides insights into the responses of maize (Zea mays L.) roots to different straw and fertilizer conditions
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154224openalex-snapshot
Amyloplast is involved in the MIZ1-modulated root hydrotropism
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108386openalex-snapshot
Unlocking dynamic root phenotypes for simultaneous enhancement of water and phosphorus uptake
inferred← citeshttps://doi.org/10.1021/jasms.5c00293openalex-snapshot
Improving Metabolite Annotations in On-Tissue Chemical Derivatization Mass Spectrometry Imaging by Functional Group Filtering and Hydrogen–Deuterium Exchange
inferred← citeshttps://doi.org/10.1093/jxb/eraf063openalex-snapshot
Roles of hormones in regulating root growth–water interactions
inferred← citeshttps://doi.org/10.1093/plcell/koae055openalex-snapshot
Not so hidden anymore: Advances and challenges in understanding root growth under water deficits
inferred← citeshttps://doi.org/10.1093/plcell/koae279openalex-snapshot
Arabidopsis calcium-dependent protein kinases 4/5/6/11 negatively regulate hydrotropism via phosphorylation of MIZU-KUSSEI1
inferred← citeshttps://doi.org/10.1101/2022.03.11.483958openalex-snapshot
The asymmetric ABA response on both sides of root tip is important for tomato root hydrotropism by mediating proton efflux and cell elongation
inferred← citeshttps://doi.org/10.1111/pce.14720openalex-snapshot
ABA is required for differential cell wall acidification associated with root hydrotropic bending in tomato
inferred← citeshttps://doi.org/10.1111/ppl.70505openalex-snapshot
Water as a Compass: Hydrostimulation‐Triggered Aerial Root Growth in Phalaenopsis aphrodite
inferred← citeshttps://doi.org/10.1146/annurev-arplant-102820-114551openalex-snapshot
H + -ATPases in Plant Growth and Stress Responses
inferred← citeshttps://doi.org/10.1186/s12864-024-10219-zopenalex-snapshot
Integrated meta-analysis and transcriptomics pinpoint genomic loci and novel candidate genes associated with submergence tolerance in rice
inferred← citeshttps://doi.org/10.1186/s12915-026-02503-zopenalex-snapshot
Shaping with water: linking moisture perception to development in plant roots
inferred← citeshttps://doi.org/10.1186/s13007-024-01178-3openalex-snapshot
A system for the study of roots 3D kinematics in hydroponic culture: a study on the oscillatory features of root tip
inferred← citeshttps://doi.org/10.3389/fpls.2022.939544openalex-snapshot
Genome-wide association, RNA-seq and iTRAQ analyses identify candidate genes controlling radicle length of wheat
inferred← citeshttps://doi.org/10.3390/plants15101571openalex-snapshot
Genotypic Variation in Maize Root Hydrotropism and Its Association with Shoot Growth and Water Use Efficiency Under Partial Root–Zone Drying
inferred← citeshttps://doi.org/10.48130/frures-0025-0019openalex-snapshot
Physiological and transcriptome analysis of Roucongbing disease in Chinese bayberry (Morella rubra Sieb. et Zucc)
inferred← citeshttps://doi.org/10.6084/m9.figshare.26702005openalex-snapshot
Additional file 1 of Integrated meta-analysis and transcriptomics pinpoint genomic loci and novel candidate genes associated with submergence tolerance in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.26702008openalex-snapshot
Additional file 2 of Integrated meta-analysis and transcriptomics pinpoint genomic loci and novel candidate genes associated with submergence tolerance in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.26702011openalex-snapshot
Additional file 3 of Integrated meta-analysis and transcriptomics pinpoint genomic loci and novel candidate genes associated with submergence tolerance in rice
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