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The cytokinin response factors modulate root and shoot growth and promote leaf senescence in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.950180707openalex-snapshot
Cytokinins in plant senescence: From spray and pray to clone and play
inferredcites →https://doi.org/10.1007/978-1-60761-765-5_12openalex-snapshot
Analysis of Root Meristem Size Development
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Phytochrome-Specific Type 5 Phosphatase Controls Light Signal Flux by Enhancing Phytochrome Stability and Affinity for a Signal Transducer
inferredcites →https://doi.org/10.1016/j.cell.2014.08.009openalex-snapshot
Determination and Inference of Eukaryotic Transcription Factor Sequence Specificity
inferredcites →https://doi.org/10.1016/j.cub.2004.12.079openalex-snapshot
Requirement of Homeobox Gene STIMPY/WOX9 for Arabidopsis Meristem Growth and Maintenance
inferredcites →https://doi.org/10.1016/j.cub.2007.02.047openalex-snapshot
Cytokinins Determine Arabidopsis Root-Meristem Size by Controlling Cell Differentiation
inferredcites →https://doi.org/10.1016/j.molcel.2009.11.018openalex-snapshot
The Incoherent Feedforward Loop Can Provide Fold-Change Detection in Gene Regulation
inferredcites →https://doi.org/10.1016/j.pbi.2010.08.006openalex-snapshot
Cytokinin signaling and transcriptional networks
inferredcites →https://doi.org/10.1016/j.pbi.2014.05.015openalex-snapshot
Cytokinin and the cell cycle
inferredcites →https://doi.org/10.1016/j.ydbio.2007.07.019openalex-snapshot
Combinations of WOX activities regulate tissue proliferation during Arabidopsis embryonic development
inferredcites →https://doi.org/10.1016/s1360-1385(02)02251-3openalex-snapshot
GATEWAY™ vectors for Agrobacterium-mediated plant transformation
inferredcites →https://doi.org/10.1021/ja01588a032openalex-snapshot
Isolation, Structure and Synthesis of Kinetin, a Substance Promoting Cell Division 1,2
inferredcites →https://doi.org/10.1021/ja01610a105openalex-snapshot
KINETIN, A CELL DIVISION FACTOR FROM DEOXYRIBONUCLEIC ACID1
inferredcites →https://doi.org/10.1038/35059117openalex-snapshot
Identification of CRE1 as a cytokinin receptor from Arabidopsis
inferredcites →https://doi.org/10.1038/nbt1385openalex-snapshot
Direct multiplexed measurement of gene expression with color-coded probe pairs
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1038/nprot.2008.195openalex-snapshot
Universal protein-binding microarrays for the comprehensive characterization of the DNA-binding specificities of transcription factors
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0505150103openalex-snapshot
Cytokinin-mediated control of leaf longevity by AHK3 through phosphorylation of ARR2 in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0602038103openalex-snapshot
A subset of Arabidopsis AP2 transcription factors mediates cytokinin responses in concert with a two-component pathway
inferredcites →https://doi.org/10.1073/pnas.0900060106openalex-snapshot
Cytokinin regulates root meristem activity via modulation of the polar auxin transport
inferredcites →https://doi.org/10.1073/pnas.1316278111openalex-snapshot
DNA-binding specificities of plant transcription factors and their potential to define target genes
inferredcites →https://doi.org/10.1073/pnas.171304098openalex-snapshot
Regulation of plant growth by cytokinin
inferredcites →https://doi.org/10.1073/pnas.94.13.7076openalex-snapshot
The AP2 domain of APETALA2 defines a large new family of DNA binding proteins in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.95.8.4766openalex-snapshot
Recessive and dominant mutations in the ethylene biosynthetic gene ACS 5 of Arabidopsis confer cytokinin insensitivity and ethylene overproduction, respectively
inferredcites →https://doi.org/10.1074/jbc.273.41.26857openalex-snapshot
Unique Mode of GCC Box Recognition by the DNA-binding Domain of Ethylene-responsive Element-binding Factor (ERF Domain) in Plant
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/jxb/erq206openalex-snapshot
The RAV1 transcription factor positively regulates leaf senescence in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/err199openalex-snapshot
CRFs form protein–protein interactions with each other and with members of the cytokinin signalling pathway in Arabidopsis via the CRF domain
inferredcites →https://doi.org/10.1093/jxb/err238openalex-snapshot
Evidence for the localization of the Arabidopsis cytokinin receptors AHK3 and AHK4 in the endoplasmic reticulum
inferredcites →https://doi.org/10.1093/pcp/pce037openalex-snapshot
The Arabidopsis Sensor His-kinase, AHK4, Can Respond to Cytokinins
inferredcites →https://doi.org/10.1093/pcp/pce094openalex-snapshot
The AHK4 Gene Involved in the Cytokinin-Signaling Pathway as a Direct Receptor Molecule in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pce127openalex-snapshot
The Arabidopsis AHK4 Histidine Kinase is a Cytokinin-Binding Receptor that Transduces Cytokinin Signals Across the Membrane
inferredcites →https://doi.org/10.1093/pcp/pcl040openalex-snapshot
Type-B ARR Transcription Factors, ARR10 and ARR12, are Implicated in Cytokinin-Mediated Regulation of Protoxylem Differentiation in Roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcm165openalex-snapshot
Three Type-B Response Regulators, ARR1, ARR10 and ARR12, Play Essential but Redundant Roles in Cytokinin Signal Transduction Throughout the Life Cycle of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pct049openalex-snapshot
Cytokinin Response Factor 6 Negatively Regulates Leaf Senescence and is Induced in Response to Cytokinin and Numerous Abiotic Stresses
inferredcites →https://doi.org/10.1104/pp.103.021436openalex-snapshot
Expression Profiling of Cytokinin Action in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.038109openalex-snapshot
Type-B Response Regulators Display Overlapping Expression Patterns in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.046367openalex-snapshot
GENEVESTIGATOR. Arabidopsis Microarray Database and Analysis Toolbox
inferredcites →https://doi.org/10.1104/pp.107.4.1075openalex-snapshot
Cytokinin Action Is Coupled to Ethylene in Its Effects on the Inhibition of Root and Hypocotyl Elongation in Arabidopsis thaliana Seedlings
inferredcites →https://doi.org/10.1104/pp.111.180539openalex-snapshot
The Cytokinin Receptors of Arabidopsis Are Located Mainly to the Endoplasmic Reticulum
inferredcites →https://doi.org/10.1104/pp.113.217026openalex-snapshot
Identification of Cytokinin-Responsive Genes Using Microarray Meta-Analysis and RNA-Seq in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.124.4.1706openalex-snapshot
Characterization of the Response of the Arabidopsis Response Regulator Gene Family to Cytokinin
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.018978openalex-snapshot
Type-A Arabidopsis Response Regulators Are Partially Redundant Negative Regulators of Cytokinin Signaling[W]
inferredcites →https://doi.org/10.1105/tpc.10.6.1009openalex-snapshot
Two Genes with Similarity to Bacterial Response Regulators Are Rapidly and Specifically Induced by Cytokinin in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.035451openalex-snapshot
Multiple Type-B Response Regulators Mediate Cytokinin Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.037796openalex-snapshot
ArabidopsisCytokinin Receptor Mutants Reveal Functions in Shoot Growth, Leaf Senescence, Seed Size, Germination, Root Development, and Cytokinin Metabolism
inferredcites →https://doi.org/10.1105/tpc.106.045674openalex-snapshot
The Arabidopsis Histidine Phosphotransfer Proteins Are Redundant Positive Regulators of Cytokinin Signaling
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.108.059584openalex-snapshot
Type B Response Regulators of Arabidopsis Play Key Roles in Cytokinin Signaling and Plant Development
inferredcites →https://doi.org/10.1105/tpc.109.072678openalex-snapshot
Phosphorylation of Conserved PIN Motifs Directs Arabidopsis PIN1 Polarity and Auxin Transport
inferredcites →https://doi.org/10.1105/tpc.113.110106openalex-snapshot
14-3-3 Regulates 1-Aminocyclopropane-1-Carboxylate Synthase Protein Turnover in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.133595openalex-snapshot
The Yin-Yang of Hormones: Cytokinin and Auxin Interactions in Plant Development
inferredcites →https://doi.org/10.1105/tpc.12.3.393openalex-snapshot
Arabidopsis Ethylene-Responsive Element Binding Factors Act as Transcriptional Activators or Repressors of GCC Box–Mediated Gene Expression
inferredcites →https://doi.org/10.1105/tpc.3.7.647openalex-snapshot
Delayed Leaf Senescence in Tobacco Plants Transformed with tmr, a Gene for Cytokinin Production in Agrobacterium.
inferredcites →https://doi.org/10.1105/tpc.8.2.137openalex-snapshot
The AINTEGUMENTA gene of Arabidopsis required for ovule and female gametophyte development is related to the floral homeotic gene APETALA2.
inferredcites →https://doi.org/10.1110/ps.051718605openalex-snapshot
Gateway vectors for the production of combinatorially‐tagged His6‐MBP fusion proteins in the cytoplasm and periplasm of Escherichia coli
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.01940.xopenalex-snapshot
Environmental perception avenues: the interaction of cytokinin and environmental response pathways
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02016.xopenalex-snapshot
mapman : a user‐driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02219.xopenalex-snapshot
Visualization of protein interactions in living plant cells using bimolecular fluorescence complementation
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02641.xopenalex-snapshot
The WAG1 and WAG2 protein kinases negatively regulate root waving in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04165.xopenalex-snapshot
The subcellular distribution of the Arabidopsis histidine phosphotransfer proteins is independent of cytokinin signaling
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04519.xopenalex-snapshot
Improved protein‐binding microarrays for the identification of DNA‐binding specificities of transcription factors
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04668.xopenalex-snapshot
Type‐A response regulators are required for proper root apical meristem function through post‐transcriptional regulation of PIN auxin efflux carriers
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/nph.12291openalex-snapshot
APETALA 2/Ethylene Responsive Factor ( AP 2/ ERF ) transcription factors: mediators of stress responses and developmental programs
inferredcites →https://doi.org/10.1111/tpj.12084openalex-snapshot
Cytokinin‐dependent specification of the functional megaspore in the Arabidopsis female gametophyte
inferredcites →https://doi.org/10.1126/science.1164147openalex-snapshot
A Genetic Framework for the Control of Cell Division and Differentiation in the Root Meristem
inferredcites →https://doi.org/10.1126/science.270.5244.1986openalex-snapshot
Inhibition of Leaf Senescence by Autoregulated Production of Cytokinin
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105503openalex-snapshot
Cytokinin Signaling Networks
inferredcites →https://doi.org/10.1186/1471-2229-10-74openalex-snapshot
The CRF domain defines Cytokinin Response Factor proteins in plants
inferredcites →https://doi.org/10.1186/1471-2229-12-112openalex-snapshot
Transcript profiling of cytokinin action in Arabidopsis roots and shoots discovers largely similar but also organ-specific responses
inferredcites →https://doi.org/10.1186/gb-2009-10-12-248openalex-snapshot
The WUS homeobox-containing (WOX) protein family
inferredcites →https://doi.org/10.1186/gb-2009-10-3-r25openalex-snapshot
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
inferredcites →https://doi.org/10.1199/tab.0112openalex-snapshot
Two-Component Signaling Elements and Histidyl-Aspartyl Phosphorelays†
inferredcites →https://doi.org/10.1242/dev.041426openalex-snapshot
STIMPY mediates cytokinin signaling during shoot meristem establishment in Arabidopsis seedlings
inferredcites →https://doi.org/10.1242/dev.052456openalex-snapshot
Plasma membrane-bound AGC3 kinases phosphorylate PIN auxin carriers at TPRXS(N/S) motifs to direct apical PIN recycling
inferredcites →https://doi.org/10.2307/3869246openalex-snapshot
Delayed Leaf Senescence in Tobacco Plants Transformed with tmr, a Gene for Cytokinin Production in Agrobacterium
inferredcites →https://doi.org/10.3389/fpls.2012.00008openalex-snapshot
Gene Regulation by Cytokinin in Arabidopsis
inferredcites →https://doi.org/10.4161/psb.24737openalex-snapshot
Cytokinin inhibition of leaf senescence
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Controlled Atmosphere Storage Induces Hypoxia Stress to Delay Postharvest Senescence in Cabbage
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Genome‐wide binding analysis of AtGNC and AtCGA1 demonstrates their cross‐regulation and common and specific functions
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Gene expression changes occurring at bolting time are associated with leaf senescence in Arabidopsis
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Exploring Plant Co-Expression and Gene-Gene Interactions with CORNET 3.0
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Effects of Aromatic Cytokinins on Senescence-Induced Alterations in Photosynthesis
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Exogenous kinetin mitigates arsenic-induced oxidative stress by regulating ROS homeostasis and antioxidant defense in Ocimum basilicum L.
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Comprehensive Insights into Flavonoids: Biosynthesis, Stress Modulation, and Plant Growth Regulation
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OsMADS29, a Monocot-Specific Transcription Factor Modulates Cytokinin-Auxin Homeostasis Across the Land Plants
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Maleic hydrazide elicits global transcriptomic changes in chemically topped tobacco to influence shoot bud development
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Dissecting chickpea genomic loci associated with the root penetration responsive traits in compacted soil
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Cytokinin response factor 1 acts as a negative regulator of cytokinin-mediated developmental pathways in Arabidopsis
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Roles of potential plant hormones and transcription factors in controlling leaf senescence and drought tolerance
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Interactions between plant hormones and thiol-related heavy metal chelators
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Versatile effect of cytokinin on detached senescing leaves of Arabidopsis in the light
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Identification of a novel dwarfing gene, Rht_m097, on chromosome 4BS in common wheat
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Opposite roles of the Arabidopsis cytokinin receptors AHK2 and AHK3 in the expression of plastid genes and genes for the plastid transcriptional machinery during senescence
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Effect of Planting Patterns and Fertilization Optimization on Hormonal Profile, Leaf Senescence and Yield in Maize
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Metabolic Control of Gametophore Shoot Formation through Arginine in the Moss Physcomitrium patens
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Cytokinin functions as an asymmetric and anti-gravitropic signal in lateral roots
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Lineage specific conservation of cis-regulatory elements in Cytokinin Response Factors
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Molecular framework integrating nitrate sensing in root and auxin-guided shoot adaptive responses
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Deciphering the molecular mechanisms of leaf senescence: from nutrient remobilization to stress tolerance improvement
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Advances in AP2/ERF super-family transcription factors in plant
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Development of sugar beet leaves: contents of hormones, localization of abscisic acid, and the level of products of photosynthesis
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Crosstalk among plant hormone regulates the root development
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Weed-induced changes in the maize root transcriptome reveal transcription factors and physiological processes impacted early in crop–weed interactions
inferred← citeshttps://doi.org/10.1093/g3journal/jkae026openalex-snapshot
GWAS supported by computer vision identifies large numbers of candidate regulators of in planta regeneration in Populus trichocarpa
inferred← citeshttps://doi.org/10.1093/jxb/erac079openalex-snapshot
PUCHI represses early meristem formation in developing lateral roots of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erae005openalex-snapshot
TARGET OF MONOPTEROS: key transcription factors orchestrating plant development and environmental response
inferred← citeshttps://doi.org/10.1093/jxb/erx287openalex-snapshot
New insights into the regulation of leaf senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcz100openalex-snapshot
Cytokinin Signaling Is Essential for Organ Formation in Marchantia polymorpha
inferred← citeshttps://doi.org/10.1093/plcell/koad327openalex-snapshot
Cytokinin: From autoclaved DNA to two-component signaling
inferred← citeshttps://doi.org/10.1093/plcell/koae312openalex-snapshot
KNUCKLES regulates floral meristem termination by controlling auxin distribution and cytokinin activity
inferred← citeshttps://doi.org/10.1093/plphys/kiab180openalex-snapshot
CYTOKININ-RESPONSIVE GROWTH REGULATOR regulates cell expansion and cytokinin-mediated cell cycle progression
inferred← citeshttps://doi.org/10.1093/plphys/kiac445openalex-snapshot
Spatiotemporal dynamics of the tomato fruit transcriptome under prolonged water stress
inferred← citeshttps://doi.org/10.1093/treephys/tpad156openalex-snapshot
A cytokinin response factor PtCRF1 is involved in the regulation of wood formation in poplar
inferred← citeshttps://doi.org/10.1101/2020.02.06.937342openalex-snapshot
The Arabidopsis gene RGO mediates cytokinin responses and increases seed yield
inferred← citeshttps://doi.org/10.1101/2022.06.08.495082openalex-snapshot
GWAS identifies candidate regulators of in planta regeneration in Populus trichocarpa
inferred← citeshttps://doi.org/10.1101/2025.08.06.668818openalex-snapshot
An in planta single-cell screen to accelerate functional genetics
inferred← citeshttps://doi.org/10.1105/tpc.15.00909openalex-snapshot
CYTOKININ RESPONSE FACTOR2 (CRF2) and CRF3 Regulate Lateral Root Development in Response to Cold Stress in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.15291openalex-snapshot
ORESARA15, a PLATZ transcription factor, mediates leaf growth and senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.16071openalex-snapshot
Genome‐wide identification of EMBRYO ‐ DEFECTIVE ( EMB ) genes required for growth and development in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.17833openalex-snapshot
Isoprene enhances leaf cytokinin metabolism and induces early senescence
inferred← citeshttps://doi.org/10.1111/pbi.12958openalex-snapshot
The developmental dynamics of the Populus stem transcriptome
inferred← citeshttps://doi.org/10.1111/pce.13021openalex-snapshot
Redox regulation at the site of primary growth: auxin, cytokinin and ROS crosstalk
inferred← citeshttps://doi.org/10.1111/tpj.13816openalex-snapshot
WD 40‐ REPEAT 5a represses root meristem growth by suppressing auxin synthesis through changes of nitric oxide accumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.13962openalex-snapshot
Role of BASIC PENTACYSTEINE transcription factors in a subset of cytokinin signaling responses
inferred← citeshttps://doi.org/10.1111/tpj.13995openalex-snapshot
Premature leaf senescence 3, encoding a methyltransferase, is required for melatonin biosynthesis in rice
inferred← citeshttps://doi.org/10.1111/tpj.14537openalex-snapshot
A unique chromosome translocation disrupting ClWIP1 leads to gynoecy in watermelon
inferred← citeshttps://doi.org/10.1111/tpj.15386openalex-snapshot
Meta‐analysis of transcriptomic studies of cytokinin‐treated rice roots defines a core set of cytokinin response genes
inferred← citeshttps://doi.org/10.1111/tpj.15433openalex-snapshot
Arabidopsis WRKY71 regulates ethylene‐mediated leaf senescence by directly activating EIN2 , ORE1 and ACS2 genes
inferred← citeshttps://doi.org/10.1111/tpj.16039openalex-snapshot
RAV1 mediates cytokinin signaling for regulating primary root growth in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.17156openalex-snapshot
Laser dissection‐assisted phloem transcriptomics highlights the metabolic and physiological changes accompanying clubroot disease progression in oilseed rape
inferred← citeshttps://doi.org/10.1111/tpj.70130openalex-snapshot
A space for time. Exploring temporal regulation of plant development across spatial scales
inferred← citeshttps://doi.org/10.1134/s102144372106008xopenalex-snapshot
Inactivation of the Cytokinin Membrane Receptor AHK2 Gene Causes Differential Expression of Genes of Trans-Factors Involved in Regulation of Senescence in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1139/cjb-2018-0052openalex-snapshot
Transcriptome profiling of rice roots in early response to Bacillus subtilis (RR4) colonization
inferred← citeshttps://doi.org/10.1139/gen-2021-0083openalex-snapshot
Molecular analysis of nematode-responsive defence genes CRF1, WRKY45, and PR7 in Solanum lycopersicum tissues during the infection of plant-parasitic nematode species of the genus Meloidogyne
inferred← citeshttps://doi.org/10.11623/frj.2024.32.3.06openalex-snapshot
Functional Analysis of Transcription Factor PhERF039 for Enhancing Water Stress Tolerance in Petunia × hybrida ‘Mitchell Diploid’
inferred← citeshttps://doi.org/10.1186/s12864-018-5114-yopenalex-snapshot
Comparative analysis of cytokinin response factors in Brassica diploids and amphidiploids and insights into the evolution of Brassica species
inferred← citeshttps://doi.org/10.1186/s12870-026-08588-6openalex-snapshot
Genome-wide identification of AP2/ERF transcription factors in Populus trichocarpa: structural analysis, expression patterns, and response to Melampsora larici-populina
inferred← citeshttps://doi.org/10.1242/dev.143545openalex-snapshot
Cytokinin response factors integrate auxin and cytokinin pathways for female reproductive organ development
inferred← citeshttps://doi.org/10.1242/dev.149344openalex-snapshot
Cytokinin signaling in plant development
inferred← citeshttps://doi.org/10.15252/embr.201948967openalex-snapshot
Transcription factor CDF4 promotes leaf senescence and floral organ abscission by regulating abscisic acid and reactive oxygen species pathways in Arabidopsis
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2017-0365openalex-snapshot
Overexpression of salt-induced protein (salT) delays leaf senescence in rice
inferred← citeshttps://doi.org/10.1590/3085-89092025444openalex-snapshot
Application of Indole-3-butyric acid in cacao scion: Effects on the grafting
inferred← citeshttps://doi.org/10.20868/upm.thesis.77361openalex-snapshot
Molecular and physiological analyses of DOF/TCP factors in Systemic Nitrogen Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.2139/ssrn.7238303openalex-snapshot
Histone Lysine Methyltransferase SDG26 Is Involved in Leaf-size Control through Regulation of Cytokinins Related Genes Expression in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.22302/iribb.jur.mp.v84i1.201openalex-snapshot
The Hevea brasiliensis AP2/ERF superfamily: from ethylene signalling to latex harvesting and physiological disease response
inferred← citeshttps://doi.org/10.22302/ppbbi.jur.mp.v84i1.201openalex-snapshot
The Hevea brasiliensis AP2/ERF superfamily: from ethylene signalling to latex harvesting and physiological disease response
inferred← citeshttps://doi.org/10.31163/2618-964x-2018-1-1-14-24openalex-snapshot
HORMONE CONTENT AND ABSCISIC ACID LOCALIZATION IN LEAVES OF DIFFERENT AGE OF SUGAR BEET
inferred← citeshttps://doi.org/10.3389/fgene.2024.1377204openalex-snapshot
CRF transcription factors in the trade-off between abiotic stress response and plant developmental processes
inferred← citeshttps://doi.org/10.3389/fpls.2017.01614openalex-snapshot
CHASE-Containing Histidine Kinase Receptors in Apple Tree: From a Common Receptor Structure to Divergent Cytokinin Binding Properties and Specific Functions
inferred← citeshttps://doi.org/10.3389/fpls.2017.01697openalex-snapshot
Dancing with Hormones: A Current Perspective of Nitrate Signaling and Regulation in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.788996openalex-snapshot
Multiple Layers of Regulation on Leaf Senescence: New Advances and Perspectives
inferred← citeshttps://doi.org/10.3389/fpls.2022.923136openalex-snapshot
New Advances in the Regulation of Leaf Senescence by Classical and Peptide Hormones
inferred← citeshttps://doi.org/10.3389/fpls.2022.983650openalex-snapshot
An APETALA2/ethylene responsive factor transcription factor GmCRF4a regulates plant height and auxin biosynthesis in soybean
inferred← citeshttps://doi.org/10.3390/agronomy8100234openalex-snapshot
Impact of Genetic Background on the Leaf-Protective Enzyme Activity and Hormone Levels of Maize
inferred← citeshttps://doi.org/10.3390/cells10081971openalex-snapshot
PopulusPtERF85 Balances Xylem Cell Expansion and Secondary Cell Wall Formation in Hybrid Aspen
inferred← citeshttps://doi.org/10.3390/cells9122576openalex-snapshot
Interplay between Hormones and Several Abiotic Stress Conditions on Arabidopsis thaliana Primary Root Development
inferred← citeshttps://doi.org/10.3390/genes11060633openalex-snapshot
Nitrate Signaling, Functions, and Regulation of Root System Architecture: Insights from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/horticulturae9080850openalex-snapshot
Callus Induction and Adventitious Root Regeneration of Cotyledon Explants in Peach Trees
inferred← citeshttps://doi.org/10.3390/ijms20082043openalex-snapshot
AHK3-Mediated Cytokinin Signaling Is Required for the Delayed Leaf Senescence Induced by SSPP
inferred← citeshttps://doi.org/10.3390/ijms21103660openalex-snapshot
Genome-Wide Dissection of the CRF Gene Family in Brassica napus Indicates that BnaCRF8s Specifically Regulate Root Architecture and Phosphate Homeostasis against Phosphate Fluctuation in Plants
inferred← citeshttps://doi.org/10.3390/ijms22031226openalex-snapshot
Transcriptomics Reveals Fast Changes in Salicylate and Jasmonate Signaling Pathways in Shoots of Carbonate-Tolerant Arabidopsis thaliana under Bicarbonate Exposure
inferred← citeshttps://doi.org/10.3390/ijms22031282openalex-snapshot
Convergence and Divergence of Sugar and Cytokinin Signaling in Plant Development
inferred← citeshttps://doi.org/10.3390/ijms222111890openalex-snapshot
Early Sucrose Degradation and the Dominant Sucrose Cleavage Pattern Influence Lycoris sprengeri Bulblet Regeneration In Vitro
inferred← citeshttps://doi.org/10.3390/molecules26040782openalex-snapshot
Transcriptome Changes Reveal the Molecular Mechanisms of Humic Acid-Induced Salt Stress Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3390/plants14020208openalex-snapshot
Dressed Up to the Nines: The Interplay of Phytohormones Signaling and Redox Metabolism During Plant Response to Drought
inferred← citeshttps://doi.org/10.3390/plants14030418openalex-snapshot
Effects of Cytokinins on Morphogenesis, Total (Poly)Phenolic Content and Antioxidant Capacity of In Vitro-Cultured Hop Plantlets, cvs. Cascade and Columbus
inferred← citeshttps://doi.org/10.3390/plants14213288openalex-snapshot
Identification of Auxin, Cytokinin, Transcription Factors, and Other Zygotic Embryogenesis-Related Genes in Persea americana: A Transcriptomic-Based Study
inferred← citeshttps://doi.org/10.3390/plants14243858openalex-snapshot
Pangenome-Wide Identification, Evolutionary Analysis of Maize ZmPLD Gene Family, and Functional Validation of ZmPLD15 in Cold Stress Tolerance
inferred← citeshttps://doi.org/10.33915/etd.7390openalex-snapshot
Enhancing Water Stress Tolerance in Floriculture Crops
inferred← citeshttps://doi.org/10.5958/0975-928x.2019.00133.9openalex-snapshot
Radiation effect on germination and seedling traits in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.64898/2026.08.07.743468openalex-snapshot
DigiAra Computationally Designs Plant Mutants for Resistance to Microbial Infection in Arabidopsis
inferred← citeshttps://doi.org/10.70675/052c5654z7a9ez4582zb1ffz7c7130c67970openalex-snapshot
The role of auxin in cell differentiation in meristems
inferred← citeshttps://doi.org/10.70675/678142dcz99ecz4c75zb811zbab4d041a3a8openalex-snapshot
Caractérisation fonctionnelle de facteurs de transcription associés à la signalisation des cytokinines et impliqués dans la nodulation symbiotique chez Medicago truncatula
inferred← citeshttps://doi.org/10.70675/91c4211bze9a7z4f23z9812z2d7a91671584openalex-snapshot
Development of a novel experimental platform for the study of Cytokinin perception and signalling pathway
inferred← citeshttps://doi.org/10.70675/f85357e5z174ez49c5zb51ezcefbc580e017openalex-snapshot
"Coupable par association" : exploitation de ressources transcriptomiques pour la construction de réseaux de co-expression de gènes dédiés à l'élucidation de voies cellulaires
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