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Shaping the root system architecture in plants for adaptation to drought stress
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781119525417.ch14openalex-snapshot
Simulating the Diversity and Plasticity of Root Systems Using 3D Models of the Root System Architecture
inferredcites →https://doi.org/10.1007/13562.0974-1275openalex-snapshot
Journal of Plant Biochemistry and Biotechnology
inferredcites →https://doi.org/10.1007/978-3-030-40277-8_2openalex-snapshot
Plant Responses and Tolerance to Combined Salt and Drought Stress
inferredcites →https://doi.org/10.1007/978-94-017-2923-9_5openalex-snapshot
Searching for quantitative trait loci controlling root traits in maize: a critical appraisal
inferredcites →https://doi.org/10.1007/978-981-15-0690-1_2openalex-snapshot
Promising Transcription Factors for Salt and Drought Tolerance in Plants
inferredcites →https://doi.org/10.1007/s00122-006-0357-4openalex-snapshot
Assessing the importance of genotype × environment interaction for root traits in rice using a mapping population II: conventional QTL analysis
inferredcites →https://doi.org/10.1007/s00122-010-1500-9openalex-snapshot
Identification of QTL for increased fibrous roots in soybean
inferredcites →https://doi.org/10.1007/s00122-011-1690-9openalex-snapshot
QTL for nodal root angle in sorghum (Sorghum bicolor L. Moench) co-locate with QTL for traits associated with drought adaptation
inferredcites →https://doi.org/10.1007/s00122-012-1963-yopenalex-snapshot
QTLs associated with root traits increase yield in upland rice when transferred through marker-assisted selection
inferredcites →https://doi.org/10.1007/s00122-013-2074-0openalex-snapshot
QTL for root angle and number in a population developed from bread wheats (Triticum aestivum) with contrasting adaptation to water-limited environments
inferredcites →https://doi.org/10.1007/s00122-016-2823-yopenalex-snapshot
Genome-wide association mapping and agronomic impact of cowpea root architecture
inferredcites →https://doi.org/10.1007/s00299-007-0441-5openalex-snapshot
Proteomic analysis of reactive oxygen species (ROS)-related proteins in rice roots
inferredcites →https://doi.org/10.1007/s00299-014-1573-zopenalex-snapshot
Balanced activity of microRNA166/165 and its target transcripts from the class III homeodomain-leucine zipper family regulates root growth in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00299-018-2364-8openalex-snapshot
An apple transcription factor, MdDREB76, confers salt and drought tolerance in transgenic tobacco by activating the expression of stress-responsive genes
inferredcites →https://doi.org/10.1007/s00299-021-02724-2openalex-snapshot
Phytohormone signalling and cross-talk to alleviate aluminium toxicity in plants
inferredcites →https://doi.org/10.1007/s00344-018-9788-9openalex-snapshot
Genome-Wide Identification and Expression Profiling of Ascorbate Peroxidase (APX) and Glutathione Peroxidase (GPX) Genes Under Drought Stress in Sorghum (Sorghum bicolor L.)
inferredcites →https://doi.org/10.1007/s00425-009-0994-3openalex-snapshot
Genome-wide survey of rice microRNAs and microRNA–target pairs in the root of a novel auxin-resistant mutant
inferredcites →https://doi.org/10.1007/s00425-017-2704-xopenalex-snapshot
ABP9, a maize bZIP transcription factor, enhances tolerance to salt and drought in transgenic cotton
inferredcites →https://doi.org/10.1007/s00425-019-03199-yopenalex-snapshot
Genome-wide survey and expression analyses of the GRAS gene family in Brassica napus reveals their roles in root development and stress response
inferredcites →https://doi.org/10.1007/s00438-014-0932-3openalex-snapshot
Genotyping-by-sequencing based intra-specific genetic map refines a ‘‘QTL-hotspot” region for drought tolerance in chickpea
inferredcites →https://doi.org/10.1007/s00709-010-0169-xopenalex-snapshot
Antioxidant response of wheat roots to drought acclimation
inferredcites →https://doi.org/10.1007/s10265-019-01100-2openalex-snapshot
A gene regulatory network for root hair development
inferredcites →https://doi.org/10.1007/s10681-012-0690-4openalex-snapshot
Mapping QTLs for seedling root traits in a doubled haploid wheat population under different water regimes
inferredcites →https://doi.org/10.1007/s10681-015-1574-1openalex-snapshot
Root traits contributing to drought tolerance of synthetic hexaploid wheat in a greenhouse study
inferredcites →https://doi.org/10.1007/s10681-018-2117-3openalex-snapshot
Identification of drought responsive QTLs during vegetative growth stage of rice using a saturated GBS-based SNP linkage map
inferredcites →https://doi.org/10.1007/s10725-011-9636-4openalex-snapshot
Sunflower root growth regulation: the role of jasmonic acid and its relation with auxins
inferredcites →https://doi.org/10.1007/s11032-009-9330-7openalex-snapshot
Identification of quantitative trait loci for specific mechanisms of resistance to Orobanche crenata Forsk. in pea (Pisum sativum L.)
inferredcites →https://doi.org/10.1007/s11032-011-9655-xopenalex-snapshot
QTL mapping and epistasis analysis of brace root traits in maize
inferredcites →https://doi.org/10.1007/s11032-014-0063-xopenalex-snapshot
Mapping quantitative trait loci associated with root penetration ability of wheat in contrasting environments
inferredcites →https://doi.org/10.1007/s11032-014-0122-3openalex-snapshot
Detection and validation of novel QTL for shoot and root traits in barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1007/s11033-009-9885-8openalex-snapshot
Overexpression of PgDREB2A transcription factor enhances abiotic stress tolerance and activates downstream stress-responsive genes
inferredcites →https://doi.org/10.1007/s11103-011-9793-xopenalex-snapshot
MicroRNAs as regulators of root development and architecture
inferredcites →https://doi.org/10.1007/s11103-011-9796-7openalex-snapshot
A dual role for MYB60 in stomatal regulation and root growth of Arabidopsis thaliana under drought stress
inferredcites →https://doi.org/10.1007/s11103-015-0301-6openalex-snapshot
Expression of SOD and APX genes positively regulates secondary cell wall biosynthesis and promotes plant growth and yield in Arabidopsis under salt stress
inferredcites →https://doi.org/10.1007/s11104-008-9843-6openalex-snapshot
Rooting depth and water use efficiency of tropical maize inbred lines, differing in drought tolerance
inferredcites →https://doi.org/10.1007/s11104-011-0735-9openalex-snapshot
A consensus map of QTLs controlling the root length of maize
inferredcites →https://doi.org/10.1007/s11104-011-1075-5openalex-snapshot
Novel QTLs for growth angle of seminal roots in wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1007/s11104-016-3092-xopenalex-snapshot
Modelling the interactions between root system architecture, root functions and reactive transport processes in soil
inferredcites →https://doi.org/10.1007/s11356-018-3364-5openalex-snapshot
Phytohormones enhanced drought tolerance in plants: a coping strategy
inferredcites →https://doi.org/10.1007/s11738-019-2939-1openalex-snapshot
Metabolomics reveals the drought-tolerance mechanism in wild soybean (Glycine soja)
inferredcites →https://doi.org/10.1007/s11816-014-0335-2openalex-snapshot
Overexpression of the rice basic leucine zipper transcription factor OsbZIP12 confers drought tolerance to rice and makes seedlings hypersensitive to ABA
inferredcites →https://doi.org/10.1007/s12033-014-9754-0openalex-snapshot
Overexpression of Horsegram (Macrotyloma uniflorum Lam.Verdc.) NAC Transcriptional Factor (MuNAC4) in Groundnut Confers Enhanced Drought Tolerance
inferredcites →https://doi.org/10.1007/s12284-009-9028-9openalex-snapshot
Rice Root Genetic Architecture: Meta-analysis from a Drought QTL Database
inferredcites →https://doi.org/10.1007/s12374-014-0349-xopenalex-snapshot
OsCML4 improves drought tolerance through scavenging of reactive oxygen species in rice
inferredcites →https://doi.org/10.1007/s13205-014-0257-2openalex-snapshot
Genome-wide transcriptomic comparison of cotton (Gossypium herbaceum) leaf and root under drought stress
inferredcites →https://doi.org/10.1007/s13562-020-00626-0openalex-snapshot
Role of abiotic stress responsive miRNAs in Arabidopsis root development
inferredcites →https://doi.org/10.1016/j.bbrc.2008.12.163openalex-snapshot
Overexpression of a NAC transcription factor enhances rice drought and salt tolerance
inferredcites →https://doi.org/10.1016/j.cell.2004.09.018openalex-snapshot
The PLETHORA Genes Mediate Patterning of the Arabidopsis Root Stem Cell Niche
inferredcites →https://doi.org/10.1016/j.cell.2009.06.031openalex-snapshot
The Sequential Action of miR156 and miR172 Regulates Developmental Timing in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2010.10.020openalex-snapshot
Transcriptional Regulation of ROS Controls Transition from Proliferation to Differentiation in the Root
inferredcites →https://doi.org/10.1016/j.cj.2019.08.006openalex-snapshot
OsABA8ox2, an ABA catabolic gene, suppresses root elongation of rice seedlings and contributes to drought response
inferredcites →https://doi.org/10.1016/j.fcr.2012.08.004openalex-snapshot
Genotype×environment interactions for root depth of wheat
inferredcites →https://doi.org/10.1016/j.gep.2016.01.001openalex-snapshot
MicroRNA expression profiles in response to drought stress in Sorghum bicolor
inferredcites →https://doi.org/10.1016/j.molp.2017.11.002openalex-snapshot
Crosstalk Complexities between Auxin, Cytokinin, and Ethylene in Arabidopsis Root Development: From Experiments to Systems Modeling, and Back Again
inferredcites →https://doi.org/10.1016/j.molp.2019.04.004openalex-snapshot
A Single-Cell RNA Sequencing Profiles the Developmental Landscape of Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.molp.2020.12.014openalex-snapshot
Transcriptional landscape of rice roots at the single-cell resolution
inferredcites →https://doi.org/10.1016/j.nbt.2015.12.005openalex-snapshot
Transgenic barley overexpressing a cytokinin dehydrogenase gene shows greater tolerance to drought stress
inferredcites →https://doi.org/10.1016/j.pbi.2015.10.012openalex-snapshot
Control of root growth and development by reactive oxygen species
inferredcites →https://doi.org/10.1016/j.plaphy.2014.06.008openalex-snapshot
Modulation of auxin content in Arabidopsis confers improved drought stress resistance
inferredcites →https://doi.org/10.1016/j.plaphy.2020.03.005openalex-snapshot
Revealing the complexity of protein abundance in chickpea root under drought-stress using a comparative proteomics approach
inferredcites →https://doi.org/10.1016/j.redox.2016.11.006openalex-snapshot
Reactive oxygen species signaling and stomatal movement: Current updates and future perspectives
inferredcites →https://doi.org/10.1016/j.scitotenv.2018.10.434openalex-snapshot
Crop yield sensitivity of global major agricultural countries to droughts and the projected changes in the future
inferredcites →https://doi.org/10.1016/j.tplants.2006.07.003openalex-snapshot
A novel role for abscisic acid emerges from underground
inferredcites →https://doi.org/10.1016/j.tplants.2007.08.012openalex-snapshot
Root system architecture: opportunities and constraints for genetic improvement of crops
inferredcites →https://doi.org/10.1016/j.tplants.2010.04.006openalex-snapshot
ABA perception and signalling
inferredcites →https://doi.org/10.1016/j.tplants.2015.06.008openalex-snapshot
Tuning plant signaling and growth to survive salt
inferredcites →https://doi.org/10.1016/j.ydbio.2006.12.037openalex-snapshot
Abscisic acid rescues the root meristem defects of the Medicago truncatula latd mutant
inferredcites →https://doi.org/10.1016/s0065-2296(07)46002-5openalex-snapshot
How the Environment Regulates Root Architecture in Dicots
inferredcites →https://doi.org/10.1016/s0092-8674(00)80865-xopenalex-snapshot
The SHORT-ROOT Gene Controls Radial Patterning of the Arabidopsis Root through Radial Signaling
inferredcites →https://doi.org/10.1016/s1360-1385(97)82562-9openalex-snapshot
Plant responses to water deficit
inferredcites →https://doi.org/10.1021/pr2008779openalex-snapshot
Shotgun Proteomic Analysis of Long-distance Drought Signaling in Rice Roots
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/ncomms6302openalex-snapshot
Coordinated regulation of photosynthesis in rice increases yield and tolerance to environmental stress
inferredcites →https://doi.org/10.1038/ncomms6833openalex-snapshot
Arabidopsis ERF109 mediates cross-talk between jasmonic acid and auxin biosynthesis during lateral root formation
inferredcites →https://doi.org/10.1038/ng.2725openalex-snapshot
Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions
inferredcites →https://doi.org/10.1038/s41598-018-37035-2openalex-snapshot
The cotton WRKY transcription factor (GhWRKY33) reduces transgenic Arabidopsis resistance to drought stress
inferredcites →https://doi.org/10.1038/s41598-020-68735-3openalex-snapshot
Comparative physiological and root proteome analyses of two sorghum varieties responding to water limitation
inferredcites →https://doi.org/10.1038/srep06829openalex-snapshot
Opposite metabolic responses of shoots and roots to drought
inferredcites →https://doi.org/10.1038/srep27177openalex-snapshot
The ABA receptor PYL9 together with PYL8 plays an important role in regulating lateral root growth
inferredcites →https://doi.org/10.1071/fp03255openalex-snapshot
Genetic mapping of basal root gravitropism and phosphorus acquisition efficiency in common bean
inferredcites →https://doi.org/10.1071/fp09150openalex-snapshot
Root phenomics of crops: opportunities and challenges
inferredcites →https://doi.org/10.1073/pnas.0604882103openalex-snapshot
Overexpressing a NAM, ATAF, and CUC (NAC) transcription factor enhances drought resistance and salt tolerance in rice
inferredcites →https://doi.org/10.1073/pnas.0707294104openalex-snapshot
Improvement of water use efficiency in rice by expression of HARDY , an Arabidopsis drought and salt tolerance gene
inferredcites →https://doi.org/10.1073/pnas.1711723115openalex-snapshot
Ethylene promotes root hair growth through coordinated EIN3/EIL1 and RHD6/RSL1 activity in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.171304098openalex-snapshot
Regulation of plant growth by cytokinin
inferredcites →https://doi.org/10.1073/pnas.2005911117openalex-snapshot
Root angle modifications by the DRO1 homolog improve rice yields in saline paddy fields
inferredcites →https://doi.org/10.1080/15592324.2018.1500069openalex-snapshot
Mechanisms for Abscisic Acid Inhibition of Primary Root Growth
inferredcites →https://doi.org/10.1086/297393openalex-snapshot
Jasmonic Acid: Effects on Growth and Development of Isolated Tomato Roots Cultured In vitro
inferredcites →https://doi.org/10.1093/dnares/dst019openalex-snapshot
Genome-Wide Organization and Expression Profiling of the NAC Transcription Factor Family in Potato (Solanum tuberosum L.)
inferredcites →https://doi.org/10.1093/jexbot/53.366.33openalex-snapshot
ABA, ethylene and the control of shoot and root growth under water stress
inferredcites →https://doi.org/10.1093/jxb/45.special_issue.1743openalex-snapshot
Confirmation that abscisic acid accumulation is required for maize primary root elongation at low water potentials
inferredcites →https://doi.org/10.1093/jxb/erp214openalex-snapshot
Overexpression of the soybean GmERF3 gene, an AP2/ERF type transcription factor for increased tolerances to salt, drought, and diseases in transgenic tobacco
inferredcites →https://doi.org/10.1093/jxb/err139openalex-snapshot
A conservative pattern of water use, rather than deep or profuse rooting, is critical for the terminal drought tolerance of chickpea
inferredcites →https://doi.org/10.1093/jxb/ers091openalex-snapshot
The pathway of auxin biosynthesis in plants
inferredcites →https://doi.org/10.1093/jxb/ert486openalex-snapshot
The effects of redox controls mediated by glutathione peroxidases on root architecture in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/eru232openalex-snapshot
Drought adaptation of stay-green sorghum is associated with canopy development, leaf anatomy, root growth, and water uptake
inferredcites →https://doi.org/10.1093/jxb/eru534openalex-snapshot
Plant hormone cross-talk: the pivot of root growth
inferredcites →https://doi.org/10.1093/jxb/erv512openalex-snapshot
Gene expression regulation in roots under drought
inferredcites →https://doi.org/10.1093/jxb/ery082openalex-snapshot
Genetic diversity of root system architecture in response to drought stress in grain legumes
inferredcites →https://doi.org/10.1093/jxb/erz263openalex-snapshot
The quest for osmosensors in plants
inferredcites →https://doi.org/10.1093/jxb/erz307openalex-snapshot
The bHLH family member ZmPTF1 regulates drought tolerance in maize by promoting root development and abscisic acid synthesis
inferredcites →https://doi.org/10.1093/jxb/erz490openalex-snapshot
WUSCHEL-related homeobox gene PagWOX11/12a responds to drought stress by enhancing root elongation and biomass growth in poplar
inferredcites →https://doi.org/10.1093/mp/ssr013openalex-snapshot
Overexpression of TaNAC69 Leads to Enhanced Transcript Levels of Stress Up-Regulated Genes and Dehydration Tolerance in Bread Wheat
inferredcites →https://doi.org/10.1093/pcp/pcu133openalex-snapshot
The Cotton WRKY Transcription Factor GhWRKY17 Functions in Drought and Salt Stress in Transgenic Nicotiana benthamiana Through ABA Signaling and the Modulation of Reactive Oxygen Species Production
inferredcites →https://doi.org/10.1098/rstb.1998.0295openalex-snapshot
The ethylene–receptor family from Arabidopsis : structure and function
inferredcites →https://doi.org/10.1098/rstb.2011.0234openalex-snapshot
Root system architecture: insights from Arabidopsis and cereal crops
inferredcites →https://doi.org/10.1104/pp.105.068254openalex-snapshot
The Zinc-Finger Protein Zat12 Plays a Central Role in Reactive Oxygen and Abiotic Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.091561openalex-snapshot
Auxin Biosynthesis by the YUCCA Genes in Rice
inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot
WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.144220openalex-snapshot
The MYB96 Transcription Factor Mediates Abscisic Acid Signaling during Drought Stress Response in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.154773openalex-snapshot
Root-Specific Expression of OsNAC10 Improves Drought Tolerance and Grain Yield in Rice under Field Drought Conditions
inferredcites →https://doi.org/10.1104/pp.111.177022openalex-snapshot
AtMYB2Regulates Whole Plant Senescence by Inhibiting Cytokinin-Mediated Branching at Late Stages of Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.187088openalex-snapshot
The Regulatory Activities of Plant MicroRNAs: A More Dynamic Perspective
inferredcites →https://doi.org/10.1104/pp.111.190389openalex-snapshot
Constitutive Activation of Transcription Factor OsbZIP46 Improves Drought Tolerance in Rice
inferredcites →https://doi.org/10.1104/pp.114.238873openalex-snapshot
The Emerging Role of Reactive Oxygen Species Signaling during Lateral Root Development
inferredcites →https://doi.org/10.1104/pp.126.2.759openalex-snapshot
Rapid Accumulation of Phosphatidylinositol 4,5-Bisphosphate and Inositol 1,4,5-Trisphosphate Correlates with Calcium Mobilization in Salt-Stressed Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.00415openalex-snapshot
Ethylene Inhibits Cell Proliferation of the Arabidopsis Root Meristem
inferredcites →https://doi.org/10.1104/pp.16.00191openalex-snapshot
ROS Regulation of Polar Growth in Plant Cells
inferredcites →https://doi.org/10.1104/pp.16.00379openalex-snapshot
Overexpression of the OsERF71 Transcription Factor Alters Rice Root Structure and Drought Resistance
inferredcites →https://doi.org/10.1104/pp.18.00199openalex-snapshot
Root Engineering in Barley: Increasing Cytokinin Degradation Produces a Larger Root System, Mineral Enrichment in the Shoot and Improved Drought Tolerance
inferredcites →https://doi.org/10.1104/pp.18.00436openalex-snapshot
ZmbZIP4 Contributes to Stress Resistance in Maize by Regulating ABA Synthesis and Root Development
inferredcites →https://doi.org/10.1105/tpc.003285openalex-snapshot
Spatiotemporal Patterning of Reactive Oxygen Production and Ca2+ Wave Propagation in Fucus Rhizoid Cells
inferredcites →https://doi.org/10.1105/tpc.012393openalex-snapshot
CBL1, a Calcium Sensor That Differentially Regulates Salt, Drought, and Cold Responses in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.014928openalex-snapshot
Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity
inferredcites →https://doi.org/10.1105/tpc.105.030841openalex-snapshot
MicroRNA Directs mRNA Cleavage of the Transcription Factor NAC1 to Downregulate Auxin Signals for Arabidopsis Lateral Root Development
inferredcites →https://doi.org/10.1105/tpc.105.033076openalex-snapshot
Control of Root Cap Formation by MicroRNA-Targeted Auxin Response Factors in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.055863openalex-snapshot
Cytokinins Act Directly on Lateral Root Founder Cells to Inhibit Root Initiation
inferredcites →https://doi.org/10.1105/tpc.108.058263openalex-snapshot
Activated Expression of an Arabidopsis HD-START Protein Confers Drought Tolerance with Improved Root System and Reduced Stomatal Density
inferredcites →https://doi.org/10.1105/tpc.109.071316openalex-snapshot
Perturbation of Indole-3-Butyric Acid Homeostasis by the UDP-GlucosyltransferaseUGT74E2ModulatesArabidopsisArchitecture and Water Stress Tolerance
inferredcites →https://doi.org/10.1105/tpc.109.072694openalex-snapshot
Root-Specific Reduction of Cytokinin Causes Enhanced Root Growth, Drought Tolerance, and Leaf Mineral Enrichment inArabidopsisand Tobacco
inferredcites →https://doi.org/10.1105/tpc.111.089870openalex-snapshot
The Basic Helix-Loop-Helix Transcription Factor MYC2 Directly Represses PLETHORA Expression during Jasmonate-Mediated Modulation of the Root Stem Cell Niche in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.097006openalex-snapshot
IAA-Ala Resistant3 , an Evolutionarily Conserved Target of miR167, Mediates Arabidopsis Root Architecture Changes during High Osmotic Stress
inferredcites →https://doi.org/10.1105/tpc.112.103044openalex-snapshot
Spatiotemporal Regulation of Lateral Root Organogenesis in Arabidopsis by Cytokinin
inferredcites →https://doi.org/10.1105/tpc.12.7.1103openalex-snapshot
Interactions between Abscisic Acid and Ethylene Signaling Cascades
inferredcites →https://doi.org/10.1105/tpc.15.00080openalex-snapshot
Ethylene Responses in Rice Roots and Coleoptiles Are Differentially Regulated by a Carotenoid Isomerase-Mediated Abscisic Acid Pathway
inferredcites →https://doi.org/10.1105/tpc.15.00227openalex-snapshot
The Interaction between Rice ERF3 and WOX11 Promotes Crown Root Development by Regulating Gene Expression Involved in Cytokinin Signaling
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02331.xopenalex-snapshot
Ethylene‐binding activity, gene expression levels, and receptor system output for ethylene receptor family members from Arabidopsis and tomato†
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04129.xopenalex-snapshot
Getting to the root of plant biology: impact of the Arabidopsis genome sequence on root research
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.2011.04610.xopenalex-snapshot
The auxin responsive AP2/ERF transcription factor CROWN ROOTLESS5 is involved in crown root initiation in rice through the induction of OsRR1, a type‐A response regulator of cytokinin signaling
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04698.xopenalex-snapshot
OsIAA23‐mediated auxin signaling defines postembryonic maintenance of QC in rice
inferredcites →https://doi.org/10.1111/j.1432-1033.2004.04334.xopenalex-snapshot
Cytokinin oxidase/dehydrogenase genes in barley and wheat
inferredcites →https://doi.org/10.1111/j.1439-0523.2010.01801.xopenalex-snapshot
Drought tolerance of barley varieties in relation to their root system size
inferredcites →https://doi.org/10.1111/j.1467-7652.2012.00697.xopenalex-snapshot
The overexpression ofOsNAC9alters the root architecture of rice plants enhancing drought resistance and grain yield under field conditions
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.01995.xopenalex-snapshot
Distribution of superoxide and hydrogen peroxide in Arabidopsis root and their influence on root development: possible interaction with peroxidases
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02472.xopenalex-snapshot
Branching out in new directions: the control of root architecture by lateral root formation
inferredcites →https://doi.org/10.1111/jipb.12109openalex-snapshot
Quantifying relationships between rooting traits and water uptake under drought in Mediterranean barley and durum wheat
inferredcites →https://doi.org/10.1111/nph.12735openalex-snapshot
A mi R 169 isoform regulates specific NF ‐ YA targets and root architecture in A rabidopsis
inferredcites →https://doi.org/10.1111/nph.13882openalex-snapshot
Abscisic acid regulates root growth under osmotic stress conditions via an interacting hormonal network with cytokinin, ethylene and auxin
inferredcites →https://doi.org/10.1111/nph.16524openalex-snapshot
Root‐specific NF‐Y family transcription factor, PdNF‐YB21 , positively regulates root growth and drought resistance by abscisic acid‐mediated indoylacetic acid transport in Populu s
inferredcites →https://doi.org/10.1111/pbi.12011openalex-snapshot
OsNAC5 overexpression enlarges root diameter in rice plants leading to enhanced drought tolerance and increased grain yield in the field
inferredcites →https://doi.org/10.1111/pbi.12673openalex-snapshot
The rice Os NAC 6 transcription factor orchestrates multiple molecular mechanisms involving root structural adaptions and nicotianamine biosynthesis for drought tolerance
inferredcites →https://doi.org/10.1111/pbi.12688openalex-snapshot
Drought coping strategies in cotton: increased crop per drop
inferredcites →https://doi.org/10.1111/pbi.12716openalex-snapshot
Overexpression of Os ERF 48 causes regulation of Os CML 16 , a calmodulin‐like protein gene that enhances root growth and drought tolerance
inferredcites →https://doi.org/10.1111/pce.12467openalex-snapshot
OsAUX 1 controls lateral root initiation in rice ( O ryza sativa L .)
inferredcites →https://doi.org/10.1111/pce.14137openalex-snapshot
ABA regulation of root growth during soil drying and recovery can involve auxin response
inferredcites →https://doi.org/10.1111/ppl.13201openalex-snapshot
Root system architecture, physiological and transcriptional traits of soybean ( Glycine max L.) in response to water deficit: A review
inferredcites →https://doi.org/10.1111/ppl.13382openalex-snapshot
Alleviating aluminum toxicity in plants: Implications of reactive oxygen species signaling and crosstalk with other signaling pathways
inferredcites →https://doi.org/10.1111/tpj.12919openalex-snapshot
The role of miR156/ SPL s modules in Arabidopsis lateral root development
inferredcites →https://doi.org/10.1111/tpj.12958openalex-snapshot
Transcription factor WRKY 46 modulates the development of Arabidopsis lateral roots in osmotic/salt stress conditions via regulation of ABA signaling and auxin homeostasis
inferredcites →https://doi.org/10.1111/tpj.13413openalex-snapshot
Poplar Ptab ZIP 1‐like enhances lateral root formation and biomass growth under drought stress
inferredcites →https://doi.org/10.1126/science.1146265openalex-snapshot
A High-Resolution Root Spatiotemporal Map Reveals Dominant Expression Patterns
inferredcites →https://doi.org/10.1146/annurev-arplant-042817-040322openalex-snapshot
Reactive Oxygen Species in Plant Signaling
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141701openalex-snapshot
REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction
inferredcites →https://doi.org/10.1175/jamc-d-18-0174.1openalex-snapshot
Global Patterns of Crop Production Losses Associated with Droughts from 1983 to 2009
inferredcites →https://doi.org/10.1186/1471-2164-10-276openalex-snapshot
Improved resolution in the position of drought-related QTLs in a single mapping population of rice by meta-analysis
inferredcites →https://doi.org/10.1186/1471-2164-11-630openalex-snapshot
Comparative transcriptomics of drought responses in Populus: a meta-analysis of genome-wide expression profiling in mature leaves and root apices across two genotypes
inferredcites →https://doi.org/10.1186/1471-2164-13-680openalex-snapshot
Comparative transcriptomic analysis of roots of contrasting Gossypium herbaceum genotypes revealing adaptation to drought
inferredcites →https://doi.org/10.1186/1471-2164-14-216openalex-snapshot
CAMTA 1 regulates drought responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2164-14-647openalex-snapshot
Comprehensive transcriptomic study on horse gram (Macrotyloma uniflorum): De novo assembly, functional characterization and comparative analysis in relation to drought stress
inferredcites →https://doi.org/10.1186/1471-2229-8-32openalex-snapshot
Spatial distribution of transcript changes in the maize primary root elongation zone at low water potential
inferredcites →https://doi.org/10.1186/gb-2012-13-6-r47openalex-snapshot
Apple miRNAs and tasiRNAs with novel regulatory networks
inferredcites →https://doi.org/10.1186/s12864-015-1334-6openalex-snapshot
Genetic variants in root architecture-related genes in a Glycine soja accession, a potential resource to improve cultivated soybean
inferredcites →https://doi.org/10.1186/s12870-016-0771-yopenalex-snapshot
Plant hormone-mediated regulation of stress responses
inferredcites →https://doi.org/10.1186/s12870-018-1488-xopenalex-snapshot
MiR393 and miR390 synergistically regulate lateral root growth in rice under different conditions
inferredcites →https://doi.org/10.1186/s12870-019-2159-2openalex-snapshot
A MYB-related transcription factor from sheepgrass, LcMYB2, promotes seed germination and root growth under drought stress
inferredcites →https://doi.org/10.12688/f1000research.7678.1openalex-snapshot
Plant adaptation to drought stress
inferredcites →https://doi.org/10.1270/jsbbs.18068openalex-snapshot
Identification and mapping of QTLs associated with drought tolerance traits in rice by a cross between Super Basmati and IR55419-04
inferredcites →https://doi.org/10.1270/jsbbs.64.193openalex-snapshot
Molecular mapping of the brace root traits in sorghum (Sorghum bicolor L. Moench)
inferredcites →https://doi.org/10.1371/journal.pgen.1004701openalex-snapshot
Ethylene-Induced Inhibition of Root Growth Requires Abscisic Acid Function in Rice (Oryza sativa L.) Seedlings
inferredcites →https://doi.org/10.1371/journal.pgen.1005300openalex-snapshot
Multilayered Organization of Jasmonate Signalling in the Regulation of Root Growth
inferredcites →https://doi.org/10.1371/journal.pgen.1006889openalex-snapshot
Genetic control of the root system in rice under normal and drought stress conditions by genome-wide association study
inferredcites →https://doi.org/10.1371/journal.pone.0030039openalex-snapshot
OsTIR1 and OsAFB2 Downregulation via OsmiR393 Overexpression Leads to More Tillers, Early Flowering and Less Tolerance to Salt and Drought in Rice
inferredcites →https://doi.org/10.1371/journal.pone.0078037openalex-snapshot
Genome-Wide Association Mapping of Root Traits in a Japonica Rice Panel
inferredcites →https://doi.org/10.1371/journal.pone.0084886openalex-snapshot
Functional Analysis of Water Stress-Responsive Soybean GmNAC003 and GmNAC004 Transcription Factors in Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0137098openalex-snapshot
Overexpression of EcbHLH57 Transcription Factor from Eleusine coracana L. in Tobacco Confers Tolerance to Salt, Oxidative and Drought Stress
inferredcites →https://doi.org/10.1371/journal.pone.0156814openalex-snapshot
MicroRNA Signatures of Drought Signaling in Rice Root
inferredcites →https://doi.org/10.1371/journal.pone.0213502openalex-snapshot
Comparative metabolomic profiling in the roots and leaves in contrasting genotypes reveals complex mechanisms involved in post-anthesis drought tolerance in wheat
inferredcites →https://doi.org/10.1534/g3.114.011080openalex-snapshot
Abscisic Acid Regulates Root Elongation Through the Activities of Auxin and Ethylene inArabidopsis thaliana
inferredcites →https://doi.org/10.2135/cropsci2016.02.0116openalex-snapshot
BRACE: A Method for High Throughput Maize Phenotyping of Root Traits for Short‐Season Drought Tolerance
inferredcites →https://doi.org/10.2135/cropsci2018.01.0076openalex-snapshot
Root System Architecture and Its Association with Yield under Different Water Regimes in Durum Wheat
inferredcites →https://doi.org/10.21608/jpp.2010.86384openalex-snapshot
THE ROLE OF ROOT SYSTEM TRAITS IN THE DROUGHT TOLERANCE OF RICE ( Oryza sativa L.)
inferredcites →https://doi.org/10.3389/fchem.2017.00106openalex-snapshot
Drought Response in Wheat: Key Genes and Regulatory Mechanisms Controlling Root System Architecture and Transpiration Efficiency
inferredcites →https://doi.org/10.3389/fpls.2016.01108openalex-snapshot
Analysis of Drought-Induced Proteomic and Metabolomic Changes in Barley (Hordeum vulgare L.) Leaves and Roots Unravels Some Aspects of Biochemical Mechanisms Involved in Drought Tolerance
inferredcites →https://doi.org/10.3389/fpls.2016.01335openalex-snapshot
Roots Withstanding their Environment: Exploiting Root System Architecture Responses to Abiotic Stress to Improve Crop Tolerance
inferredcites →https://doi.org/10.3389/fpls.2017.01763openalex-snapshot
Genetic Loci Governing Grain Yield and Root Development under Variable Rice Cultivation Conditions
inferredcites →https://doi.org/10.3389/fpls.2018.00229openalex-snapshot
QTL-By-Environment Interaction in the Response of Maize Root and Shoot Traits to Different Water Regimes
inferredcites →https://doi.org/10.3389/fpls.2019.00436openalex-snapshot
A Major Root Architecture QTL Responding to Water Limitation in Durum Wheat
inferredcites →https://doi.org/10.3389/fpls.2019.01030openalex-snapshot
Shaping Ethylene Response: The Role of EIN3/EIL1 Transcription Factors
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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/10.1093/plphys/kiae605openalex-snapshot
Advancing our understanding of root development: Technologies and insights from diverse studies
inferred← citeshttps://doi.org/10.1093/plphys/kiaf432openalex-snapshot
Integrating 3D imaging, GWAS, and single-cell transcriptome approaches to elucidate root system architecture in Populus
inferred← citeshttps://doi.org/10.1093/treephys/tpac107openalex-snapshot
Basic helix-loop-helix transcription factor PxbHLH02 enhances drought tolerance in Populus (Populus simonii × P. nigra)
inferred← citeshttps://doi.org/10.1101/2022.07.15.500193openalex-snapshot
The role of GmXTH1 , a new xyloglucan endotransglycosylase/hydrolase from soybean, in regulating soybean root growth at seedling stage
inferred← citeshttps://doi.org/10.1111/aab.12835openalex-snapshot
Low water supply differentially affects the growth, yield and mineral profile of kabuli and desi chickpeas (Cicer arietinum)
inferred← citeshttps://doi.org/10.1111/jipb.13827openalex-snapshot
The interaction of nutrient uptake with biotic and abiotic stresses in plants
inferred← citeshttps://doi.org/10.1111/pbi.70432openalex-snapshot
RrMYB2 Regulates Drought Stress via RrJMJ12 ‐Dependent Epigenetic Modification in Rosa rugosa
inferred← citeshttps://doi.org/10.1111/pce.15163openalex-snapshot
PeFUS3 Drives Lateral Root Growth Via Auxin and ABA Signalling Under Drought Stress in Populus
inferred← citeshttps://doi.org/10.1111/plb.70141openalex-snapshot
Heterologous expression of α‐AtCAH1 improves resistance to drought stress and increases tuber yield in potato ( Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1111/ppl.13730openalex-snapshot
Raising crops for dry and saline lands: Challenges and the way forward
inferred← citeshttps://doi.org/10.1111/ppl.13787openalex-snapshot
Integrating advancements in root phenotyping and genome‐wide association studies to open the root genetics gateway
inferred← citeshttps://doi.org/10.1111/ppl.14151openalex-snapshot
Plant hormone ethylene: A leading edge in conferring drought stress tolerance
inferred← citeshttps://doi.org/10.1111/ppl.71023openalex-snapshot
Exogenous Pyrroloquinoline Quinone Application Enhances Low‐Phosphorus Adaptation in Rice by Modulating Redox Homeostasis Under Variable Light
inferred← citeshttps://doi.org/10.1134/s1021443724608395openalex-snapshot
Exogenous Spermidine Enhanced the Drought Tolerance in the Root of Hordeum jubatum by Modulating Root System Architecture and Anatomical Structure
inferred← citeshttps://doi.org/10.1139/cjfr-2023-0288openalex-snapshot
Effect of 3-year amendment measures on coastal saline–alkali soil conditions during the growing season
inferred← citeshttps://doi.org/10.1186/s12284-025-00800-9openalex-snapshot
WOX11-OsPRX130 module confers rice drought tolerance by maintaining ROS homeostasis in rice root
inferred← citeshttps://doi.org/10.1186/s12870-022-04006-9openalex-snapshot
Integrated transcriptome and methylome analyses reveal the molecular regulation of drought stress in wild strawberry (Fragaria nilgerrensis)
inferred← citeshttps://doi.org/10.1186/s12870-024-05699-wopenalex-snapshot
Effects of different karst fissures and rainfall distribution on the biomass, mineral nutrient elements, antioxidant substances, and photosynthesis of two coniferous seedlings
inferred← citeshttps://doi.org/10.1186/s12870-025-07346-4openalex-snapshot
Optimizing root spatial distribution during the flower-boll stage can reduce yield losses from square stage drought in cotton
inferred← citeshttps://doi.org/10.1186/s12870-026-08321-3openalex-snapshot
Physiological and metabolic responses of dill to nano-silica and nano-zinc under drought stress: implications for yield and essential oil quality
inferred← citeshttps://doi.org/10.1186/s12870-026-08478-xopenalex-snapshot
Integrative multi-trait phenotyping reveals coordinated root and antioxidant responses underlying drought tolerance in soybean
inferred← citeshttps://doi.org/10.1186/s13007-025-01479-1openalex-snapshot
Automatic root measurement: a lightweight method for measuring pea root length
inferred← citeshttps://doi.org/10.1371/journal.pone.0309353openalex-snapshot
Genome-wide identification and characterization of FORMIN gene family in potato (Solanum tuberosum L.) and their expression profiles in response to drought stress condition
inferred← citeshttps://doi.org/10.1371/journal.pone.0336637openalex-snapshot
Quantitative evaluation of soil anti-erodibility in the fluctuation zones of rooted soil in a large reservoir, southwest of China
inferred← citeshttps://doi.org/10.1590/1984-70332025v25n2a23openalex-snapshot
Which common bean root phenotyping method is best? This depends on the phenological growth stage
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3369465/v1openalex-snapshot
Phenotypic characterisation and comparative non-targeted GC-MS-based metabolomic profiling of two contrasting seedling fonio millet (Digitaria exilis) accessions: an insight to drought tolerance in small millets
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7702056/v1openalex-snapshot
AhDTF1, a novel R2R3-MYB transcription factor, involves in drought tolerance and seed color
inferred← citeshttps://doi.org/10.2139/ssrn.4974436openalex-snapshot
Xanthophyll Cycle and Photosynthetic Electron Transport Enhanced by Galactolipid Modification Alleviate Drought-Induced Leaf Senescence
inferred← citeshttps://doi.org/10.2139/ssrn.5180644openalex-snapshot
Ahdtf1, a Peanut R2r3-Myb Transcription Factor, Involves in Drought Tolerance and Seed Coat Color
inferred← citeshttps://doi.org/10.2139/ssrn.6067037openalex-snapshot
Root Morphological Plasticity and Carbon Trade-offs in Mesua ferrea Saplings Under Progressive Droughts in Northeast India, Indo-Burma Biodiversity Hotspots
inferred← citeshttps://doi.org/10.2139/ssrn.7075324openalex-snapshot
Regulatory insights and first report of fructan accumulation in early vegetative sunflower lines contrasting in osmotic adjustment under water deficit
inferred← citeshttps://doi.org/10.22541/essoar.167347082.25216669/v1openalex-snapshot
Prospects Of Developing Drought Resilience In Crop Plants Through Strategic Modifications In Root System Architecture
inferred← citeshttps://doi.org/10.2478/sg-2023-0017openalex-snapshot
Drought stress-induced Picea abies transcriptome changes in the context of functional interactions
inferred← citeshttps://doi.org/10.3389/fgene.2026.1822936openalex-snapshot
Enhancing cereal productivity via nitrogen use efficiency: from conventional breeding to modern genomics
inferred← citeshttps://doi.org/10.3389/fpls.2022.1085409openalex-snapshot
Responses of root system architecture to water stress at multiple levels: A meta-analysis of trials under controlled conditions
inferred← citeshttps://doi.org/10.3389/fpls.2022.836063openalex-snapshot
Expression of Potato StDRO1 in Arabidopsis Alters Root Architecture and Drought Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2024.1403922openalex-snapshot
Lentil adaptation to drought stress: response, tolerance, and breeding approaches
inferred← citeshttps://doi.org/10.3389/fpls.2025.1515819openalex-snapshot
Physiological and molecular responses of two contrasting drought resistance pistachio interspecific hybrid rootstocks
inferred← citeshttps://doi.org/10.3389/fpls.2025.1630935openalex-snapshot
Root plasticity and xylem modifications drive drought resilience in okra [Abelmoschus esculentus (L.) Moench] at the seedling stage
inferred← citeshttps://doi.org/10.3389/fpls.2025.1716676openalex-snapshot
A two-tier strategy for developing water deficit stress tolerant maize: hydroponics-based root phenotyping followed by rainfed field validation
inferred← citeshttps://doi.org/10.3389/fpls.2026.1738299openalex-snapshot
Epigenetic modifications in plant abiotic stress adaptation: towards climate-resilient and sustainable crop improvement
inferred← citeshttps://doi.org/10.3389/fpls.2026.1783318openalex-snapshot
Integrating multi-omics approaches to shape legume root system architecture under drought stress: a comprehensive review
inferred← citeshttps://doi.org/10.3389/fpls.2026.1796736openalex-snapshot
Assessing the effect of deficit irrigation and biochar application on soil water depletion, root distribution, and water productivity of cucumber in semi-arid West Texas
inferred← citeshttps://doi.org/10.3389/fpls.2026.1855949openalex-snapshot
Morphological, physiological, and root metabolomic responses of Hemerocallis minor Mill. to drought stress
inferred← citeshttps://doi.org/10.3390/agronomy13092241openalex-snapshot
Identification and Fine Mapping of Osdsm3, a Drought-Sensitive Gene in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.3390/agronomy13123069openalex-snapshot
Effect of Partial Root-Zone Irrigation on Plant Growth, Root Morphological Traits and Leaf Elemental Stoichiometry of Tomato under Elevated CO2
inferred← citeshttps://doi.org/10.3390/agronomy14040788openalex-snapshot
How Does Irrigation with Wastewater Affect the Physical Soil Properties and the Root Growth of Sugarcane under Subsurface Drip?
inferred← citeshttps://doi.org/10.3390/agronomy14123006openalex-snapshot
Field Application of Mycorrhizal Inoculant Influences Growth, Nutrition, and Physiological Parameters of Corn Plants and Affects Soil Microbiological Attributes
inferred← citeshttps://doi.org/10.3390/agronomy16050575openalex-snapshot
Phenotypic and Physiological Characterization of Rice Recombinant Inbred Lines with Enhanced Drought Tolerance at Vegetative and Reproductive Stages
inferred← citeshttps://doi.org/10.3390/agronomy16111099openalex-snapshot
The Regulatory Effect of Integrated Agronomic Management on the Root and Shoot Growth Relationship of Shallow-Buried Drip Irrigation Maize in the West Liaohe Plain
inferred← citeshttps://doi.org/10.3390/agronomy16191977openalex-snapshot
Abiotic Factors as Functional Drivers of Plant Growth-Promoting Rhizobacteria: Interconnections in Agricultural Systems
inferred← citeshttps://doi.org/10.3390/biology13121033openalex-snapshot
ROS, an Important Plant Growth Regulator in Root Growth and Development: Functional Genes and Mechanism
inferred← citeshttps://doi.org/10.3390/f14040731openalex-snapshot
Organic Materials and AMF Addition Promote Growth of Taxodium ‘zhongshanshan’ by Improving Soil Structure
inferred← citeshttps://doi.org/10.3390/f15111895openalex-snapshot
Spatial Distribution of Fine Roots in Pinus tabuliformis and Populus tomentosa and Their Competition in Soils Response to Nutrient Availability and Proximity
inferred← citeshttps://doi.org/10.3390/f16121869openalex-snapshot
Evaluation of Soil Health of Panax notoginseng Forest Plantations Based on Minimum Data Set
inferred← citeshttps://doi.org/10.3390/horticulturae11091092openalex-snapshot
Comparative Analysis of Cabernet Sauvignon (Vitis vinifera L.) and Kober 5BB (V. berlandieri × V. riparia) Root Transcriptomes Reveals Multiple Processes Associated with Drought Tolerance in Grapevines
inferred← citeshttps://doi.org/10.3390/ijms24087406openalex-snapshot
Modifying the Expression of Cysteine Protease Gene PCP Affects Pollen Development, Germination and Plant Drought Tolerance in Maize
inferred← citeshttps://doi.org/10.3390/ijms252413733openalex-snapshot
Studies on the Physiological Response of Hemerocallis middendorffii to Two Types of Drought Stresses
inferred← citeshttps://doi.org/10.3390/ijms26115274openalex-snapshot
Resilience of Maize to Environmental Stress: Insights into Drought and Heat Tolerance
inferred← citeshttps://doi.org/10.3390/ijms27177616openalex-snapshot
Genome-Wide Analysis of Triticum aestivum Root Meristem Growth Factor (RGF) Gene Family Highlights TaRGF5 as a Putative Component of Root-Associated Signaling
inferred← citeshttps://doi.org/10.3390/ijms27177822openalex-snapshot
Functional Characterization of the Oat (Avena sativa L.) TCP Transcription Factor AsTCP38 Reveals Its Role in Low-Nitrogen Stress Tolerance
inferred← citeshttps://doi.org/10.3390/ijpb17080065openalex-snapshot
Development of Salt and Drought Tolerance Classification in the Kazakhstan Cotton Collection Using Optimal Phenotypic Traits
inferred← citeshttps://doi.org/10.3390/metabo16060401openalex-snapshot
Phytohormonal Regulation of Plant Responses to Major Abiotic Stresses: From Signaling Pathways to Hormonal Crosstalk
inferred← citeshttps://doi.org/10.3390/plants11172256openalex-snapshot
Roots’ Drought Adaptive Traits in Crop Improvement
inferred← citeshttps://doi.org/10.3390/plants12183329openalex-snapshot
Effects of Salt Tolerance Training on Multidimensional Root Distribution and Root-Shoot Characteristics of Summer Maize under Brackish Water Irrigation
inferred← citeshttps://doi.org/10.3390/plants12233948openalex-snapshot
Abiotic Stress in Rice: Visiting the Physiological Response and Its Tolerance Mechanisms
inferred← citeshttps://doi.org/10.3390/plants13060860openalex-snapshot
The Receptor Kinases DRUS1 and DRUS2 Behave Distinctly in Osmotic Stress Tolerance by Modulating the Root System Architecture via Auxin Signaling
inferred← citeshttps://doi.org/10.3390/plants13121620openalex-snapshot
Transcriptome Analysis of Early Lateral Root Formation in Tomato
inferred← citeshttps://doi.org/10.3390/plants14101461openalex-snapshot
Comparative Study on the Effects of Silicon Nanoparticles and Cellulose Nanocrystals on Drought Tolerance in Tall Fescue (Festuca arundinacea Schreb.)
inferred← citeshttps://doi.org/10.3390/plants14111726openalex-snapshot
Seed Nanopriming with ZnO and SiO2 Enhances Germination, Seedling Vigor, and Antioxidant Defense Under Drought Stress
inferred← citeshttps://doi.org/10.3390/plants14233587openalex-snapshot
2,4-Epibrassinolide Enhances Drought Tolerance in Prunella vulgaris by Improving Photosynthesis, Redox Homeostasis, and Secondary Metabolism
inferred← citeshttps://doi.org/10.3390/plants14243842openalex-snapshot
Competitive Interactions Among Populus euphratica Seedlings Intensify Under Drought and Salt Stresses
inferred← citeshttps://doi.org/10.3390/plants15010077openalex-snapshot
Citrus Genotype Modulates Rhizosphere Microbiome Structure and Function Under Drought Stress
inferred← citeshttps://doi.org/10.3390/plants15060935openalex-snapshot
Diversity of Root System Architecture in Mediterranean Maize Inbred Lines Provides New Breeding Opportunities to Improve Stress Resilience and Resource Efficiency
inferred← citeshttps://doi.org/10.3390/plants15162537openalex-snapshot
Photosynthetic Performance of Green Alder (Alnus alnobetula) in Experimental Drought
inferred← citeshttps://doi.org/10.3390/plants15172693openalex-snapshot
Endangered Salvia daiguii Has Evolved Drought Tolerance Through Photosynthetic, Antioxidant, and Respiratory Adaptations: Implications for Ex Situ Propagule Reintroduction
inferred← citeshttps://doi.org/10.34133/plantphenomics.0098openalex-snapshot
Phenotyping of Salvia miltiorrhiza Roots Reveals Associations between Root Traits and Bioactive Components
inferred← citeshttps://doi.org/10.4025/actasciagron.v48i1.74585openalex-snapshot
Ora-pro-nóbis (Pereskia aculeata Mill.) propagated by seeds and cuttings under water deficit and biological indicators of soil quality
inferred← citeshttps://doi.org/10.5772/intechopen.1011411openalex-snapshot
Perspective Chapter: Unlocking Root Architecture Plasticity – Enhancing Crop Productivity and Resilience to Abiotic Stresses
inferred← citeshttps://doi.org/10.5772/intechopen.1014325openalex-snapshot
Molecular and Physiological Responses of Plants to Salinity and Drought Stress: Implications for Crop Improvement and Climate Resilience
inferred← citeshttps://doi.org/10.5772/intechopen.113928openalex-snapshot
The Modification of Abscisic Acid and Cytokinin Signaling with Genome Editing to Increase Plant Drought Tolerance
inferred← citeshttps://doi.org/10.6084/m9.figshare.22610998openalex-snapshot
Additional file 1 of Integrated transcriptome and methylome analyses reveal the molecular regulation of drought stress in wild strawberry (Fragaria nilgerrensis)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22611001openalex-snapshot
Additional file 2 of Integrated transcriptome and methylome analyses reveal the molecular regulation of drought stress in wild strawberry (Fragaria nilgerrensis)
inferred← citeshttps://doi.org/10.7717/peerj.17684openalex-snapshot
Comprehensive identification and expression analysis of FAR1/FHY3 genes under drought stress in maize (Zea mays L.)
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