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Two-Component Signaling Elements and Histidyl-Aspartyl Phosphorelays†
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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.20343openalex-snapshot
Signal transduction in bacterial chemotaxis
inferredcites →https://doi.org/10.1007/bf00043870openalex-snapshot
The phytochrome apoprotein family inArabidopsis is encoded by five genes: the sequences and expression ofPHYD andPHYE
inferredcites →https://doi.org/10.1007/s00438-003-0858-7openalex-snapshot
The putative sensor histidine kinase CKI1 is involved in female gametophyte development in Arabidopsis
inferredcites →https://doi.org/10.1007/s00438-006-0177-xopenalex-snapshot
Genome-wide expression profiling of ARABIDOPSIS RESPONSE REGULATOR 7(ARR7) overexpression in cytokinin response
inferredcites →https://doi.org/10.1007/s004380000400openalex-snapshot
The response regulator ARR2: a pollen-specific transcription factor involved in the expression of nuclear genes for components of mitochondrial Complex I in Arabidopsis
inferredcites →https://doi.org/10.1016/0092-8674(93)90267-topenalex-snapshot
Signal transduction schemes of bacteria
inferredcites →https://doi.org/10.1016/0092-8674(95)90405-0openalex-snapshot
Protein kinases and phosphatases: The Yin and Yang of protein phosphorylation and signaling
inferredcites →https://doi.org/10.1016/0968-0004(94)90135-xopenalex-snapshot
Histidine and aspartate phosphorylation: two-component systems and the limits of homology
inferredcites →https://doi.org/10.1016/j.cub.2004.12.067openalex-snapshot
Overlapping and Distinct Roles of PRR7 and PRR9 in the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1016/j.cub.2006.04.030openalex-snapshot
Cytokinins Regulate a Bidirectional Phosphorelay Network in Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2007.11.005openalex-snapshot
Cytokinin signaling: two-components and more
inferredcites →https://doi.org/10.1016/s0014-5793(00)01860-3openalex-snapshot
Possible His to Asp phosphorelay signaling in an Arabidopsis two‐component system
inferredcites →https://doi.org/10.1016/s0014-5793(98)00418-9openalex-snapshot
Stress‐responsive expression of genes for two‐component response regulator‐like proteins in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0014-5793(98)00611-5openalex-snapshot
Expression of Arabidopsis response regulator homologs is induced by cytokinins and nitrate
inferredcites →https://doi.org/10.1016/s0014-5793(98)01188-0openalex-snapshot
Characterization of genes for two‐component phosphorelay mediators with a single HPt domain in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0021-9258(19)74354-3openalex-snapshot
Primary structure of pyruvate dehydrogenase kinase establishes a new family of eukaryotic protein kinases.
inferredcites →https://doi.org/10.1016/s0065-2296(00)32023-7openalex-snapshot
Histidine kinases and the role of two-component systems in plants
inferredcites →https://doi.org/10.1016/s0092-8674(00)80158-0openalex-snapshot
Signal Transduction via the Multi-Step Phosphorelay: Not Necessarily a Road Less Traveled
inferredcites →https://doi.org/10.1016/s0968-0004(01)01968-5openalex-snapshot
The CHASE domain: a predicted ligand-binding module in plant cytokinin receptors and other eukaryotic and bacterial receptors
inferredcites →https://doi.org/10.1016/s0968-0004(96)10068-2openalex-snapshot
The protein kinases of budding yeast: six score and more
inferredcites →https://doi.org/10.1016/s1360-1385(99)01427-2openalex-snapshot
Ethylene perception and signaling: an evolutionary perspective
inferredcites →https://doi.org/10.1016/s1360-1385(99)01542-3openalex-snapshot
Two-component systems in plant signal transduction
inferredcites →https://doi.org/10.1016/s1369-5266(03)00087-6openalex-snapshot
Cytokinin signal perception and transduction
inferredcites →https://doi.org/10.1038/35059117openalex-snapshot
Identification of CRE1 as a cytokinin receptor from Arabidopsis
inferredcites →https://doi.org/10.1038/35096500openalex-snapshot
Two-component circuitry in Arabidopsis cytokinin signal transduction
inferredcites →https://doi.org/10.1038/nature04270openalex-snapshot
WUSCHEL controls meristem function by direct regulation of cytokinin-inducible response regulators
inferredcites →https://doi.org/10.1038/sj.emboj.7600337openalex-snapshot
The response regulator 2 mediates ethylene signalling and hormone signal integration in Arabidopsis
inferredcites →https://doi.org/10.1042/0264-6021:3490195openalex-snapshot
Pyruvate dehydrogenase kinase from Arabidopsis thaliana: a protein histidine kinase that phosphorylates serine residues
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00909.xopenalex-snapshot
Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators
inferredcites →https://doi.org/10.1073/pnas.0237085100openalex-snapshot
Canonical histidine kinase activity of the transmitter domain of the ETR1 ethylene receptor from Arabidopsis is not required for signal transmission
inferredcites →https://doi.org/10.1073/pnas.0402887101openalex-snapshot
In planta functions of the Arabidopsis cytokinin receptor family
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.0706547105openalex-snapshot
Functional analysis of AHK1/ATHK1 and cytokinin receptor histidine kinases in response to abscisic acid, drought, and salt stress in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.232580499openalex-snapshot
An Arabidopsis histidine kinase is essential for megagametogenesis
inferredcites →https://doi.org/10.1073/pnas.95.10.5812openalex-snapshot
ETR2 is an ETR1 -like gene involved in ethylene signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.95.13.7825openalex-snapshot
Histidine kinase activity of the ETR1 ethylene receptor from Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.95.23.13976openalex-snapshot
Eukaryotic phytochromes: Light-regulated serine/threonine protein kinases with histidine kinase ancestry
inferredcites →https://doi.org/10.1073/pnas.95.5.2691openalex-snapshot
Response regulators implicated in His-to-Asp phosphotransfer signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.96.24.13603openalex-snapshot
The protein kinases of Caenorhabditis elegans : A model for signal transduction in multicellular organisms
inferredcites →https://doi.org/10.1074/jbc.m403100200openalex-snapshot
Autophosphorylation Activity of the Arabidopsis Ethylene Receptor Multigene Family
inferredcites →https://doi.org/10.1083/jcb.200301099openalex-snapshot
Yeast osmosensor Sln1 and plant cytokinin receptor Cre1 respond to changes in turgor pressure
inferredcites →https://doi.org/10.1093/dnares/4.2.161openalex-snapshot
Compilation of All Genes Encoding Two-component Phosphotransfer Signal Transducers in the Genome of Escherichia coli
inferredcites →https://doi.org/10.1093/jxb/erl205openalex-snapshot
Spatial and temporal expression of the response regulators ARR22 and ARR24 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/erm087openalex-snapshot
Functional cross-talk between two-component and phytochrome B signal transduction in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/28.1.231openalex-snapshot
SMART: a web-based tool for the study of genetically mobile domains
inferredcites →https://doi.org/10.1093/nar/29.1.111openalex-snapshot
PlantsP: a functional genomics database for plant phosphorylation
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029329openalex-snapshot
Histidine-Containing Phosphotransfer (HPt) Signal Transducers Implicated in His-to-Asp Phosphorelay in Arabidopsis
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029600openalex-snapshot
Compilation and Characterization of Arabiopsis thaliana Response Regulators Implicated in His-Asp Phosphorelay Signal Transduction
inferredcites →https://doi.org/10.1093/pcp/41.6.791openalex-snapshot
Genes Encoding Pseudo-Response Regulators: Insight into His-to-Asp Phosphorelay and Circadian Rhythm in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcd043openalex-snapshot
Circadian Waves of Expression of the APRR1/TOC1 Family of Pseudo-Response Regulators in Arabidopsis thaliana : Insight into the Plant Circadian Clock
inferredcites →https://doi.org/10.1093/pcp/pce015openalex-snapshot
Novel Family of Sensor Histidine Kinase Genes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pce036openalex-snapshot
Light Response of the Circadian Waves of the APRR1/TOC1 Quintet: When Does the Quintet Start Singing Rhythmically in Arabidopsis?
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/pcg014openalex-snapshot
In Vivo and In Vitro Characterization of the ARR11 Response Regulator Implicated in the His-to-Asp Phosphorelay Signal Transduction in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcg108openalex-snapshot
The Type-A Response Regulator, ARR15, Acts as a Negative Regulator in the Cytokinin-Mediated Signal Transduction in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcg154openalex-snapshot
Comparative Studies on the Type-B Response Regulators Revealing their Distinctive Properties in the His-to-Asp Phosphorelay Signal Transduction of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pch128openalex-snapshot
Arabidopsis Response Regulator, ARR22, Ectopic Expression of Which Results in Phenotypes Similar to the wol Cytokinin-Receptor Mutant
inferredcites →https://doi.org/10.1093/pcp/pci033openalex-snapshot
Combinatorial Microarray Analysis Revealing Arabidopsis Genes Implicated in Cytokinin Responses through the His→Asp Phosphorelay Circuitry
inferredcites →https://doi.org/10.1093/pcp/pci061openalex-snapshot
The Arabidopsis Pseudo-response Regulators, PRR5 and PRR7, Coordinately Play Essential Roles for Circadian Clock Function
inferredcites →https://doi.org/10.1093/pcp/pci086openalex-snapshot
PSEUDO-RESPONSE REGULATORS, PRR9, PRR7 and PRR5, Together Play Essential Roles Close to the Circadian Clock of Arabidopsis thaliana
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/pcl063openalex-snapshot
ARR1 Directly Activates Cytokinin Response Genes that Encode Proteins with Diverse Regulatory Functions
inferredcites →https://doi.org/10.1093/pcp/pcl065openalex-snapshot
AHK5 Histidine Kinase Regulates Root Elongation Through an ETR1-Dependent Abscisic Acid and Ethylene Signaling Pathway in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcm122openalex-snapshot
Rhythmic and Light-Inducible Appearance of Clock-Associated Pseudo-Response Regulator Protein PRR9 Through Programmed Degradation in the Dark in 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/pcm178openalex-snapshot
Insight into Missing Genetic Links Between Two Evening-Expressed Pseudo-Response Regulator Genes TOC1 and PRR5 in the Circadian Clock-Controlled Circuitry in Arabidopsis thaliana
inferredcites →https://doi.org/10.1101/gad.189200openalex-snapshot
A novel two-component hybrid molecule regulates vascular morphogenesis of the Arabidopsis root
inferredcites →https://doi.org/10.1101/gad.3.11.1745openalex-snapshot
Novel phytochrome sequences in Arabidopsis thaliana: structure, evolution, and differential expression of a plant regulatory photoreceptor family.
inferredcites →https://doi.org/10.1104/pp.010773openalex-snapshot
Cytokinins. New Insights into a Classic Phytohormone
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.104.047126openalex-snapshot
Requirement of the Histidine Kinase Domain for Signal Transduction by the Ethylene Receptor ETR1
inferredcites →https://doi.org/10.1104/pp.104.050369openalex-snapshot
Arabidopsis Seedling Growth Response and Recovery to Ethylene. A Kinetic Analysis
inferredcites →https://doi.org/10.1104/pp.106.093666openalex-snapshot
Nomenclature for Two-Component Signaling Elements of Rice
inferredcites →https://doi.org/10.1104/pp.123.4.1449openalex-snapshot
Ethylene Perception by the ERS1 Protein 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.002733openalex-snapshot
Molecular Structure of the GARP Family of Plant Myb-Related DNA Binding Motifs of the Arabidopsis Response Regulators
inferredcites →https://doi.org/10.1105/tpc.015065openalex-snapshot
Arabidopsis PSEUDO-RESPONSE REGULATOR7 Is a Signaling Intermediate in Phytochrome-Regulated Seedling Deetiolation and Phasing of the Circadian Clock
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.021477openalex-snapshot
Histidine Kinase Homologs That Act as Cytokinin Receptors Possess Overlapping Functions in the Regulation of Shoot and Root Growth in Arabidopsis
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.10.8.1321openalex-snapshot
EIN4 and ERS2 Are Members of the Putative Ethylene Receptor Gene Family in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.029504openalex-snapshot
PSEUDO-RESPONSE REGULATOR 7 and 9 Are Partially Redundant Genes Essential for the Temperature Responsiveness of the Arabidopsis Circadian Clock
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.105.037994openalex-snapshot
Arabidopsis Response Regulators ARR3 and ARR4 Play Cytokinin-Independent Roles in the Control of Circadian Period
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.107.052662openalex-snapshot
Cytokinin Regulates Type-A Arabidopsis Response Regulator Activity and Protein Stability via Two-Component Phosphorelay
inferredcites →https://doi.org/10.1105/tpc.107.053033openalex-snapshot
Targeted Degradation of PSEUDO-RESPONSE REGULATOR5 by an SCF ZTL Complex Regulates Clock Function and Photomorphogenesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.107.054775openalex-snapshot
PRR3 Is a Vascular Regulator of TOC1 Stability in theArabidopsisCircadian Clock
inferredcites →https://doi.org/10.1105/tpc.11.9.1743openalex-snapshot
A Transmembrane Hybrid-Type Histidine Kinase in Arabidopsis Functions as an Osmosensor
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03258.xopenalex-snapshot
PRR7 protein levels are regulated by light and the circadian clock in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1438-8677.1999.tb00775.xopenalex-snapshot
Differential Expression and Nuclear Localization of Response Regulator‐Like Proteins from Arabidopsis thaliana1
inferredcites →https://doi.org/10.1111/j.1742-4658.2006.05467.xopenalex-snapshot
Analysis of protein interactions within the cytokinin‐signaling pathway of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1061320openalex-snapshot
Reciprocal Regulation Between TOC1 and LHY / CCA1 Within the Arabidopsis Circadian Clock
inferredcites →https://doi.org/10.1126/science.1065022openalex-snapshot
Interaction of the Response Regulator ARR4 with Phytochrome B in Modulating Red Light Signaling
inferredcites →https://doi.org/10.1126/science.1065201openalex-snapshot
ARR1, a Transcription Factor for Genes Immediately Responsive to Cytokinins
inferredcites →https://doi.org/10.1126/science.1082971openalex-snapshot
Enhanced Fitness Conferred by Naturally Occurring Variation in the Circadian Clock
inferredcites →https://doi.org/10.1126/science.1118875openalex-snapshot
Cytokinin Signaling and Its Inhibitor AHP6 Regulate Cell Fate During Vascular Development
inferredcites →https://doi.org/10.1126/science.270.5243.1809openalex-snapshot
Ethylene-Binding Sites Generated in Yeast Expressing the Arabidopsis ETR1 Gene
inferredcites →https://doi.org/10.1126/science.274.5289.982openalex-snapshot
CKI1, a Histidine Kinase Homolog Implicated in Cytokinin Signal Transduction
inferredcites →https://doi.org/10.1126/science.283.5404.996openalex-snapshot
A Copper Cofactor for the Ethylene Receptor ETR1 from Arabidopsis
inferredcites →https://doi.org/10.1126/science.289.5480.768openalex-snapshot
Cloning of the Arabidopsis Clock Gene TOC1 , an Autoregulatory Response Regulator Homolog
inferredcites →https://doi.org/10.1126/science.7569898openalex-snapshot
Ethylene Insensitivity Conferred by Arabidopsis ERS Gene
inferredcites →https://doi.org/10.1126/science.7855595openalex-snapshot
Circadian Clock Mutants in Arabidopsis Identified by Luciferase Imaging
inferredcites →https://doi.org/10.1126/science.8211181openalex-snapshot
Arabidopsis Ethylene-Response Gene ETR1 : Similarity of Product to Two-Component Regulators
inferredcites →https://doi.org/10.1128/9781555818319.ch3openalex-snapshot
Two-Component Signal Transduction Systems: Structure-Function Relationships and Mechanisms of Catalysis
inferredcites →https://doi.org/10.1128/mmbr.53.4.450-490.1989openalex-snapshot
Protein phosphorylation and regulation of adaptive responses in bacteria
inferredcites →https://doi.org/10.1146/annurev.arplant.54.031902.134802openalex-snapshot
Perception and Signal Transduction of Cytokinins
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144208openalex-snapshot
PHYTOCHROME STRUCTURE AND SIGNALING MECHANISMS
inferredcites →https://doi.org/10.1146/annurev.biochem.69.1.183openalex-snapshot
Two-Component Signal Transduction
inferredcites →https://doi.org/10.1186/1471-2148-7-62openalex-snapshot
Evolutionary proteomics identifies amino acids essential for ligand-binding of the cytokinin receptor CHASE domain
inferredcites →https://doi.org/10.1199/tab.0112openalex-snapshot
Two-Component Signaling Elements and Histidyl-Aspartyl Phosphorelays†
inferredcites →https://doi.org/10.1242/dev.125.3.485openalex-snapshot
The short-period mutant, toc1-1, alters circadian clock regulation of multiple outputs throughout development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/jcs.110.10.1141openalex-snapshot
Histidine kinases in signal transduction pathways of eukaryotes
inferredcites →https://doi.org/10.1271/bbb.64.2482openalex-snapshot
Elongation Factor 2 in the Liver and Skeletal Muscle of Mice is Decreased by Starvation
inferredcites →https://doi.org/10.1271/bbb.64.2486openalex-snapshot
Compilation and Characterization of Histidine-Containing Phosphotransmitters Implicated in His-to-Asp Phosphorelay in Plants: AHP Signal Transducers of Arabidopsis thaliana
inferredcites →https://doi.org/10.1271/bbb.65.2113openalex-snapshot
Cellular Localization of the Signaling Components of Arabidopsis His-to-Asp Phosphorelay
inferredcites →https://doi.org/10.1271/bbb.68.1966openalex-snapshot
Rapid Response ofArabidopsisT87 Cultured Cells to Cytokinin through His-to-Asp Phosphorelay Signal Transduction
inferredcites →https://doi.org/10.1271/bbb.68.462openalex-snapshot
Comparative Studies of the AHP Histidine-containing Phosphotransmitters Implicated in His-to-Asp Phosphorelay inArabidopsis thaliana
inferredcites →https://doi.org/10.1271/bbb.69.2263openalex-snapshot
Two-Component Phosphorelay Signal Transduction Systems in Plants: from Hormone Responses to Circadian Rhythms
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.01.007zenodo-depositor-declared
Antibodies against CKI1RD, a receiver domain of the sensor histidine kinase in Arabidopsis thaliana: From antigen preparation to in planta immunolocalization
inferred← citeshttps://doi.org/10.1002/9780470015902.a0025266openalex-snapshot
Two‐Component Signalling in Plants
inferred← citeshttps://doi.org/10.1002/9781118223086.ch5openalex-snapshot
Perception of Ethylene by Plants – Ethylene Receptors
inferred← citeshttps://doi.org/10.1002/9781118764374.ch2openalex-snapshot
Drought tolerance mechanisms and their molecular basis
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0477openalex-snapshot
Perception of Ethylene by Plants – Ethylene Receptors
inferred← citeshttps://doi.org/10.1002/9783527694570.ch4openalex-snapshot
Crosstalk between Salt, Drought, and Cold Stress in Plants: Toward Genetic Engineering for Stress Tolerance
inferred← citeshttps://doi.org/10.1002/pld3.58openalex-snapshot
A role for two‐component signaling elements in the Arabidopsis growth recovery response to ethylene
inferred← citeshttps://doi.org/10.1002/pld3.70091openalex-snapshot
Molecular Characterization of Cytokinin Response Regulator ARR21 in Arabidopsis Seed Development
inferred← citeshttps://doi.org/10.1002/smtd.201900452openalex-snapshot
Amplification and Adaptation in the Ethylene Signaling Pathway
inferred← citeshttps://doi.org/10.1002/tpg2.20542openalex-snapshot
CRISPR‐mediated mutation of cytokinin signaling genes ( SlHP2 and SlHP3 ) in tomato: Morphological, physiological, and molecular characterization
inferred← citeshttps://doi.org/10.1007/978-1-4020-2686-7_16openalex-snapshot
Cytokinin Signal Transduction
inferred← citeshttps://doi.org/10.1007/978-1-4614-8824-8_14openalex-snapshot
Transcription Factors in Abiotic Stress Responses: Their Potentials in Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-3-030-80674-3_2openalex-snapshot
Osmosensing and Signalling in Plants: Potential Role in Crop Improvement Under Climate Change
inferred← citeshttps://doi.org/10.1007/978-3-319-42183-4_1openalex-snapshot
Physiological, Metabolic, and Molecular Responses of Plants to Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-642-25829-9_1openalex-snapshot
Signal Transduction of Phytohormones Under Abiotic Stresses
inferred← citeshttps://doi.org/10.1007/978-981-13-8922-1_10openalex-snapshot
The Two-Component System: Transducing Environmental and Hormonal Signals
inferred← citeshttps://doi.org/10.1007/s00122-019-03331-2openalex-snapshot
Drought and heat stress-related proteins: an update about their functional relevance in imparting stress tolerance in agricultural crops
inferred← citeshttps://doi.org/10.1007/s00294-024-01302-9openalex-snapshot
Adaptative responses of Neurospora crassa by histidine kinases upon the attack of the arthropod Sinella curviseta
inferred← citeshttps://doi.org/10.1007/s00299-013-1424-3openalex-snapshot
Expression, purification, and characterization of cytokinin signaling intermediates: Arabidopsis histidine phosphotransfer protein 1 (AHP1) and AHP2
inferred← citeshttps://doi.org/10.1007/s00299-021-02677-6openalex-snapshot
Ectopic expression of GmHP08 enhances resistance of transgenic Arabidopsis toward drought stress
inferred← citeshttps://doi.org/10.1007/s00299-021-02727-zopenalex-snapshot
Two-component signaling system in plants: interaction network and specificity in response to stress and hormones
inferred← citeshttps://doi.org/10.1007/s00344-007-9000-0openalex-snapshot
Ethylene Receptors: Ethylene Perception and Signal Transduction
inferred← citeshttps://doi.org/10.1007/s00344-025-11696-6openalex-snapshot
Genome-Wide Identification and Expression Analysis of the Response Regulator (RR) Gene Family in Sacha Inchi
inferred← citeshttps://doi.org/10.1007/s00709-016-0944-4openalex-snapshot
Arabidopsis response regulator 22 inhibits cytokinin-regulated gene transcription in vivo
inferred← citeshttps://doi.org/10.1007/s10142-007-0063-6openalex-snapshot
Differential gene expression of rice two-component signaling elements during reproductive development and regulation by abiotic stress
inferred← citeshttps://doi.org/10.1007/s10142-014-0398-8openalex-snapshot
A multi-step phosphorelay two-component system impacts on tolerance against dehydration stress in common wheat
inferred← citeshttps://doi.org/10.1007/s10265-003-0094-6openalex-snapshot
Cytokinin signal transduction in plant cells
inferred← citeshttps://doi.org/10.1007/s11105-014-0825-yopenalex-snapshot
Differential Expression of Two-Component System–Related Drought-Responsive Genes in Two Contrasting Drought-Tolerant Soybean Cultivars DT51 and MTD720 Under Well-Watered and Drought Conditions
inferred← citeshttps://doi.org/10.1007/s11240-020-01779-5openalex-snapshot
Transcriptome profiling reveals cytokinin promoted callus regeneration in Brassica juncea
inferred← citeshttps://doi.org/10.1007/s11738-016-2213-8openalex-snapshot
Identification and expression analysis of cytokinin response regulators in Fragaria vesca
inferred← citeshttps://doi.org/10.1007/s11738-020-03085-1openalex-snapshot
Assessment of changes in the content of sulforaphane and expression levels of CYP79F1 and myrosinase genes and proteomic profile of Lepidium draba plant under water-deficit stress induced by polyethylene glycol
inferred← citeshttps://doi.org/10.1007/s12155-020-10092-0openalex-snapshot
Gene Expression and Physiological Differences in Neo-Octoploid Switchgrass Subjected to Drought Stress
inferred← citeshttps://doi.org/10.1007/s12298-023-01406-5openalex-snapshot
Characterization of Two-Component System gene (TCS) in melatonin-treated common bean under salt and drought stress
inferred← citeshttps://doi.org/10.1007/s13258-021-01039-6openalex-snapshot
Genome-wide identification of the ARRs gene family in tobacco (Nicotiana tabacum)
inferred← citeshttps://doi.org/10.1016/b978-0-12-822849-4.00002-4openalex-snapshot
Role of phytohormones as master regulators during the abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00017-8openalex-snapshot
Membrane-bound and endoplasmic reticulum-mediated cytokinin signaling: An update on abiotic stress responses
inferred← citeshttps://doi.org/10.1016/b978-1-891127-79-3.50002-0openalex-snapshot
Barley Grain: Development and Structure
inferred← citeshttps://doi.org/10.1016/j.bbagen.2024.130749openalex-snapshot
Shaping resilience: The critical role of plant response regulators in salinity stress
inferred← citeshttps://doi.org/10.1016/j.cub.2011.02.045openalex-snapshot
Two-Component Systems and Their Co-Option for Eukaryotic Signal Transduction
inferred← citeshttps://doi.org/10.1016/j.gene.2017.12.053openalex-snapshot
Transcriptomic analysis of topping-induced axillary shoot outgrowth in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.150026openalex-snapshot
Genome-wide analysis of the type-B ARRs gene family reveals key regulators of abiotic stress tolerance and hormone signaling in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116336openalex-snapshot
Genome-wide identification and analysis of the molecular evolution and expression of type-A response regulator genes in Populus deltoids
inferred← citeshttps://doi.org/10.1016/j.jarmap.2022.100441openalex-snapshot
Regulation of essential oil in aromatic plants under changing environment
inferred← citeshttps://doi.org/10.1016/j.jplph.2012.07.014openalex-snapshot
Characterization of a type-A response regulator differentially expressed during adventitious caulogenesis in Pinus pinaster
inferred← citeshttps://doi.org/10.1016/j.mod.2014.11.001openalex-snapshot
Understanding the shoot apical meristem regulation: A study of the phytohormones, auxin and cytokinin, in rice
inferred← citeshttps://doi.org/10.1016/j.parint.2017.03.003openalex-snapshot
Plant hormone cytokinins control cell cycle progression and plastid replication in apicomplexan parasites
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.05.006openalex-snapshot
Cytokinin and CLE signaling are highly intertwined developmental regulators across tissues and species
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110197openalex-snapshot
Specific TCP transcription factors interact with and stabilize PRR2 within different nuclear sub-domains
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112202openalex-snapshot
Amino acid permease OsAAP12 negatively regulates rice tillers and grain yield by transporting specific amino acids to affect nitrogen and cytokinin pathways
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.03.017openalex-snapshot
Genome-wide characterization of two-component system (TCS) genes in melon (Cucumis melo L.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.01.047openalex-snapshot
OsRR6, a type-A response regulator in rice, mediates cytokinin, light and stress responses when over-expressed in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pmpp.2013.12.002openalex-snapshot
Disruption of a phytochrome-like histidine kinase gene by homologous recombination leads to a significant reduction in vegetative growth, sclerotia production, and the pathogenicity of Botrytis cinerea
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112228openalex-snapshot
Ectopic expression of the apple cytokinin response regulator MdRR9 gene in tomatoes promotes shoot branching
inferred← citeshttps://doi.org/10.1016/j.tplants.2007.11.005openalex-snapshot
Cytokinin signaling: two-components and more
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.12.005openalex-snapshot
Cytokinins: metabolism and function in plant adaptation to environmental stresses
inferred← citeshttps://doi.org/10.1016/j.ygeno.2007.02.001openalex-snapshot
The two-component signal system in rice (Oryza sativa L.): A genome-wide study of cytokinin signal perception and transduction
inferred← citeshttps://doi.org/10.1016/j.ygeno.2019.08.006openalex-snapshot
Genome-wide identification and expression analysis of two component system genes in Cicer arietinum
inferred← citeshttps://doi.org/10.1016/s2095-3119(17)61720-9openalex-snapshot
Identification of salinity-related genes in ENO2 mutant (eno2) of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/nbt.3044openalex-snapshot
A load driver device for engineering modularity in biological networks
inferred← citeshttps://doi.org/10.1038/s41467-018-03921-6openalex-snapshot
A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development
inferred← citeshttps://doi.org/10.1038/s41598-017-07535-8openalex-snapshot
PRR2, a pseudo-response regulator, promotes salicylic acid and camalexin accumulation during plant immunity
inferred← citeshttps://doi.org/10.1038/s41598-017-08076-wopenalex-snapshot
Mapping the ‘Two-component system’ network in rice
inferred← citeshttps://doi.org/10.1038/s41598-020-80223-2openalex-snapshot
Characterization of CHARK, an unusual cytokinin receptor of rice
inferred← citeshttps://doi.org/10.1038/s42003-024-07091-8openalex-snapshot
Expression and functional divergence of a type-A response regulator paralog pair formed by dispersed duplication during Populus deltoides evolution
inferred← citeshttps://doi.org/10.1039/9781788012836-00253openalex-snapshot
Plant Ethylene Sensing and Signalling
inferred← citeshttps://doi.org/10.1071/cp21766openalex-snapshot
Genome-wide mining of B-type cytokinin response regulators in wheat reveals the involvement of
inferred← citeshttps://doi.org/10.1071/fp21153openalex-snapshot
Post-translational regulation of the membrane transporters contributing to salt tolerance in plants
inferred← citeshttps://doi.org/10.1071/fp24055openalex-snapshot
Computational analysis and expression profiling of two-component system (TCS) gene family members in mango (Mangifera indica) indicated their roles in stress response
inferred← citeshttps://doi.org/10.1073/pnas.1214848109openalex-snapshot
CTR1 phosphorylates the central regulator EIN2 to control ethylene hormone signaling from the ER membrane to the nucleus in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.1320660111openalex-snapshot
Intake and transformation to a glycoside of ( Z )-3-hexenol from infested neighbors reveals a mode of plant odor reception and defense
inferred← citeshttps://doi.org/10.1080/15592324.2018.1469360openalex-snapshot
Arabidopsis CKI1 mediated two-component signaling in the specification of female gametophyte
inferred← citeshttps://doi.org/10.1093/aobpla/plt010openalex-snapshot
Mechanisms of signal transduction by ethylene: overlapping and non-overlapping signalling roles in a receptor family
inferred← citeshttps://doi.org/10.1093/aobpla/plx067openalex-snapshot
Drought effects on the tissue- and cell-specific cytokinin activity in poplar
inferred← citeshttps://doi.org/10.1093/dnares/dsq021openalex-snapshot
Genome-Wide Analysis of Two-Component Systems and Prediction of Stress-Responsive Two-Component System Members in Soybean
inferred← citeshttps://doi.org/10.1093/dnares/dsq032openalex-snapshot
Genome-Wide Expression Profiling of Soybean Two-Component System Genes in Soybean Root and Shoot Tissues under Dehydration Stress
inferred← citeshttps://doi.org/10.1093/dnares/dsu004openalex-snapshot
Genome-Wide Identification, Phylogeny, Duplication, and Expression Analyses of Two-Component System Genes in Chinese Cabbage (Brassica rapa ssp. pekinensis)
inferred← citeshttps://doi.org/10.1093/gbe/evy213openalex-snapshot
Diversity and Evolution of Sensor Histidine Kinases in Eukaryotes
inferred← citeshttps://doi.org/10.1093/jxb/erad159openalex-snapshot
Cytokinin-inducible response regulator SlRR6 controls plant height through gibberellin and auxin pathways in tomato
inferred← citeshttps://doi.org/10.1093/jxb/erae335openalex-snapshot
Primary multistep phosphorelay activation comprises both cytokinin and abiotic stress responses: insights from comparative analysis of Brassica type-A response regulators
inferred← citeshttps://doi.org/10.1093/jxb/erag214openalex-snapshot
Beyond a plant hormone: ethylene receptors and signaling in microbes
inferred← citeshttps://doi.org/10.1093/jxb/erp204openalex-snapshot
Recent advances in ethylene research
inferred← citeshttps://doi.org/10.1093/jxb/ers354openalex-snapshot
Sensing the environment: key roles of membrane-localized kinases in plant perception and response to abiotic stress
inferred← citeshttps://doi.org/10.1093/jxb/erv172openalex-snapshot
Interactions between cytokinin signalling and abiotic stress responses
inferred← citeshttps://doi.org/10.1093/jxb/erv261openalex-snapshot
Illuminating light, cytokinin, and ethylene signalling crosstalk in plant development: Fig. 1.
inferred← citeshttps://doi.org/10.1093/mp/sss126openalex-snapshot
Structure–Function Analysis of Arabidopsis thaliana Histidine Kinase AHK5 Bound to Its Cognate Phosphotransfer Protein AHP1
inferred← citeshttps://doi.org/10.1093/mp/ssu074openalex-snapshot
The Interaction of the Arabidopsis Response Regulator ARR18 with bZIP63 Mediates the Regulation of PROLINE DEHYDROGENASE Expression
inferred← citeshttps://doi.org/10.1093/pcp/pci033openalex-snapshot
Combinatorial Microarray Analysis Revealing Arabidopsis Genes Implicated in Cytokinin Responses through the His→Asp Phosphorelay Circuitry
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1101/2023.11.14.567013openalex-snapshot
Primary multistep phosphorelay activation comprises both cytokinin and abiotic stress responses in Brassicaceae
inferred← citeshttps://doi.org/10.1104/pp.103.038109openalex-snapshot
Type-B Response Regulators Display Overlapping Expression Patterns in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.104.047126openalex-snapshot
Requirement of the Histidine Kinase Domain for Signal Transduction by the Ethylene Receptor ETR1
inferred← citeshttps://doi.org/10.1104/pp.110.161596openalex-snapshot
The Perception of Cytokinin: A Story 50 Years in the Making
inferred← citeshttps://doi.org/10.1104/pp.110.170621openalex-snapshot
Ethylene Receptor ETHYLENE RECEPTOR1 Domain Requirements for Ethylene Responses in Arabidopsis Seedlings
inferred← citeshttps://doi.org/10.1104/pp.111.192765openalex-snapshot
Characterization of Genes Involved in Cytokinin Signaling and Metabolism from Rice
inferred← citeshttps://doi.org/10.1104/pp.112.196790openalex-snapshot
Histidine Kinase Activity of the Ethylene Receptor ETR1 Facilitates the Ethylene Response in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.112.209791openalex-snapshot
Role of the Putative Osmosensor Arabidopsis Histidine Kinase1 in Dehydration Avoidance and Low-Water-Potential Response
inferred← citeshttps://doi.org/10.1104/pp.112.213207openalex-snapshot
Nomenclature for Members of the Two-Component Signaling Pathway of Plants
inferred← citeshttps://doi.org/10.1104/pp.113.228080openalex-snapshot
A Subfamily of Putative Cytokinin Receptors Is Revealed by an Analysis of the Evolution of the Two-Component Signaling System of Plants
inferred← citeshttps://doi.org/10.1104/pp.15.00415openalex-snapshot
Ethylene Inhibits Cell Proliferation of the Arabidopsis Root Meristem
inferred← citeshttps://doi.org/10.1104/pp.20.00609openalex-snapshot
Mutagenomics: A Rapid, High-Throughput Method to Identify Causative Mutations from a Genetic Screen
inferred← citeshttps://doi.org/10.1105/tpc.010444openalex-snapshot
Cytokinin Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.105.035451openalex-snapshot
Multiple Type-B Response Regulators Mediate Cytokinin Signal Transduction in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.105.037994openalex-snapshot
Arabidopsis Response Regulators ARR3 and ARR4 Play Cytokinin-Independent Roles in the Control of Circadian Period
inferred← citeshttps://doi.org/10.1105/tpc.107.055871openalex-snapshot
Analysis of theArabidopsisHistidine Kinase ATHK1 Reveals a Connection between Vegetative Osmotic Stress Sensing and Seed Maturation
inferred← citeshttps://doi.org/10.1105/tpc.111.087395openalex-snapshot
Analysis of Cytokinin Mutants and Regulation of Cytokinin Metabolic Genes Reveals Important Regulatory Roles of Cytokinins in Drought, Salt and Abscisic Acid Responses, and Abscisic Acid Biosynthesis
inferred← citeshttps://doi.org/10.1107/s174430911205186xopenalex-snapshot
Cloning, expression, purification, crystallization and preliminary X-ray diffraction analysis of AHP2, a signal transmitter protein fromArabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/febs.12363openalex-snapshot
M edicago truncatula histidine‐containing phosphotransfer protein
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2012.05101.xopenalex-snapshot
The Arabidopsis B‐type response regulator 18 homomerizes and positively regulates cytokinin responses
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.04033.xopenalex-snapshot
Arabidopsis histidine kinase 5 regulates salt sensitivity and resistance against bacterial and fungal infection
inferred← citeshttps://doi.org/10.1111/nph.19916openalex-snapshot
Marchantia polymorpha GOLDEN2 ‐ LIKE transcriptional factor; a central regulator of chloroplast and plant vegetative development
inferred← citeshttps://doi.org/10.1111/pbi.70322openalex-snapshot
Poplar Sex‐Determining Gene Directly Affects Tree Growth Through Regulating Cytokinin Signalling Pathway
inferred← citeshttps://doi.org/10.1111/pce.14586openalex-snapshot
Genetic regulation of nitrogen use efficiency in Gossypium spp
inferred← citeshttps://doi.org/10.1111/plb.13494openalex-snapshot
Genome‐wide identification and expression analysis of SlRR genes in response to abiotic stress in tomato
inferred← citeshttps://doi.org/10.1111/ppl.13696openalex-snapshot
Role of the type‐B authentic response regulator gene family in fragrant rice under alkaline salt stress
inferred← citeshttps://doi.org/10.1111/tpj.13097openalex-snapshot
The cytokinin response factors modulate root and shoot growth and promote leaf senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.14875openalex-snapshot
Barley HISTIDINE KINASE 1 (HvHK1) coordinates transfer cell specification in the young endosperm
inferred← citeshttps://doi.org/10.1128/ec.2.6.1151-1161.2003openalex-snapshot
Whole-Genome Analysis of Two-Component Signal Transduction Genes in Fungal Pathogens
inferred← citeshttps://doi.org/10.1128/msystems.00981-20openalex-snapshot
Pangenome Analytics Reveal Two-Component Systems as Conserved Targets in ESKAPEE Pathogens
inferred← citeshttps://doi.org/10.1134/s0026893324020067openalex-snapshot
The Molecular and Genetic Mechanisms of Sex Determination in Poplar
inferred← citeshttps://doi.org/10.1146/annurev-arplant-060625-095356openalex-snapshot
Structural Insights into Plant Hormone-Sensing Mechanisms
inferred← citeshttps://doi.org/10.1146/annurev-arplant-080720-093057openalex-snapshot
Histidine Kinases: Diverse Functions in Plant Development and Responses to Environmental Conditions
inferred← citeshttps://doi.org/10.1159/000458170openalex-snapshot
Genome-Wide Identification and Analysis of the Type-B Authentic Response Regulator Gene Family in Peach (Prunus persica)
inferred← citeshttps://doi.org/10.1186/s12864-019-6050-1openalex-snapshot
Genome-wide identification and interactome analysis of members of two-component system in Banana
inferred← citeshttps://doi.org/10.1186/s12864-025-11810-8openalex-snapshot
Genome-wide identification and analysis of SmRR gene family in eggplant (Solanum melongena L.) and their response to abiotic stress and auxin
inferred← citeshttps://doi.org/10.1186/s12870-022-03947-5openalex-snapshot
Systematic analysis of Histidine photosphoto transfer gene family in cotton and functional characterization in response to salt and around tolerance
inferred← citeshttps://doi.org/10.1186/s12870-025-06161-1openalex-snapshot
Genome-wide characterization of two-component system elements in barley enables the identification of grain-specific phosphorelay genes
inferred← citeshttps://doi.org/10.1186/s40659-022-00394-2openalex-snapshot
Structure and character analysis of cotton response regulator genes family reveals that GhRR7 responses to draught stress
inferred← citeshttps://doi.org/10.1199/tab.0106openalex-snapshot
The Protein Phosphatases and Protein Kinases of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1242/dev.149344openalex-snapshot
Cytokinin signaling in plant development
inferred← citeshttps://doi.org/10.1266/ggs.24-00068openalex-snapshot
Identification of abiotic stress-responsive genes: a genome-wide analysis of the cytokinin response regulator gene family in rice
inferred← citeshttps://doi.org/10.12677/ojns.2020.83014openalex-snapshot
Research Progress in Signal Transduction Mechanism of Cytokinin
inferred← citeshttps://doi.org/10.12703/p7-39openalex-snapshot
Ethylene receptors in plants - why so much complexity?
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002448openalex-snapshot
Two-Component Elements Mediate Interactions between Cytokinin and Salicylic Acid in Plant Immunity
inferred← citeshttps://doi.org/10.1371/journal.pone.0032124openalex-snapshot
Transcriptome Analyses of a Salt-Tolerant Cytokinin-Deficient Mutant Reveal Differential Regulation of Salt Stress Response by Cytokinin Deficiency
inferred← citeshttps://doi.org/10.1371/journal.pone.0041867openalex-snapshot
454 Transcriptome Sequencing Suggests a Role for Two-Component Signalling in Cellularization and Differentiation of Barley Endosperm Transfer Cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0047182openalex-snapshot
Induction of Glycerol Synthesis and Release in Cultured Symbiodinium
inferred← citeshttps://doi.org/10.1371/journal.pone.0212056openalex-snapshot
ARR22 overexpression can suppress plant Two-Component Regulatory Systems
inferred← citeshttps://doi.org/10.1614/ws-d-12-00175.1openalex-snapshot
BAC Library Development and Clone Characterization for Dormancy-Responsive DREB4A, DAM, and FT from Leafy Spurge (Euphorbia esula) Identifies Differential Splicing and Conserved Promoter Motifs
inferred← citeshttps://doi.org/10.16420/j.issn.0513-353x.2019-0761openalex-snapshot
Genome-wide Identification and Expression Analysis of miR396 Family During Adventitious Root Development in Apple
inferred← citeshttps://doi.org/10.17660/actahortic.2019.1256.17openalex-snapshot
Identification and quantification of the ethylene signalling components in tomato through targeted proteomics
inferred← citeshttps://doi.org/10.20935/acadmolbiogen8175openalex-snapshot
Liquid–liquid phase separation as a driver of abiogenesis and evolution
inferred← citeshttps://doi.org/10.2174/1389202918666170227150057openalex-snapshot
Transcription Factors and Their Roles in Signal Transduction in Plants under Abiotic Stresses
inferred← citeshttps://doi.org/10.2174/1389202921666210105154808openalex-snapshot
The Journey from Two-Step to Multi-Step Phosphorelay Signaling Systems
inferred← citeshttps://doi.org/10.29252/jcb.11.30.133openalex-snapshot
Transcription Factors Evaluation in a Transcriptome Analysis on Chickpea (Cicer arietinum L.) Under Drought Stress
inferred← citeshttps://doi.org/10.3109/07388551.2011.643463openalex-snapshot
Potentials toward genetic engineering of drought-tolerant soybean
inferred← citeshttps://doi.org/10.31857/s0026898424020021openalex-snapshot
Molecular and genetic mechanisms of sex determination in poplar
inferred← citeshttps://doi.org/10.32604/biocell.2022.018762openalex-snapshot
The molecular characteristics of soybean ARR-B transcription factors
inferred← citeshttps://doi.org/10.32607/20758251-2012-4-3-31-45openalex-snapshot
Receptor Properties and Features of Cytokinin Signaling
inferred← citeshttps://doi.org/10.3389/fgene.2023.1142544openalex-snapshot
Genome-wide identification and expression profiling of two-component system (TCS) genes in Brassica oleracea in response to shade stress
inferred← citeshttps://doi.org/10.3389/fpls.2014.00107openalex-snapshot
Transcriptomic signatures of transfer cells in early developing nematode feeding cells of Arabidopsis focused on auxin and ethylene signaling
inferred← citeshttps://doi.org/10.3389/fpls.2014.00108openalex-snapshot
Development of endosperm transfer cells in barley
inferred← citeshttps://doi.org/10.3389/fpls.2015.00711openalex-snapshot
Tissue specific and abiotic stress regulated transcription of histidine kinases in plants is also influenced by diurnal rhythm
inferred← citeshttps://doi.org/10.3389/fpls.2016.00067openalex-snapshot
Recent Advances in Utilizing Transcription Factors to Improve Plant Abiotic Stress Tolerance by Transgenic Technology
inferred← citeshttps://doi.org/10.3389/fpls.2016.00652openalex-snapshot
Tissue- and Cell-Specific Cytokinin Activity in Populus × canescens Monitored by ARR5::GUS Reporter Lines in Summer and Winter
inferred← citeshttps://doi.org/10.3389/fpls.2016.00899openalex-snapshot
Genome-Wide Identification of Two-Component System Genes in Cucurbitaceae Crops and Expression Profiling Analyses in Cucumber
inferred← citeshttps://doi.org/10.3389/fpls.2017.02212openalex-snapshot
No Time to Waste: Transcriptome Study Reveals that Drought Tolerance in Barley May Be Attributed to Stressed-Like Expression Patterns that Exist before the Occurrence of Stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.1006409openalex-snapshot
Genome-wide identification and expression analysis of the TaRRA gene family in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.3389/fpls.2022.1068961openalex-snapshot
Mining key genes related to root morphogenesis through genome-wide identification and expression analysis of RR gene family in citrus
inferred← citeshttps://doi.org/10.3389/fpls.2022.1091620openalex-snapshot
Genome-wide identification and expression analysis of two-component system genes in sweet potato (Ipomoea batatas L.)
inferred← citeshttps://doi.org/10.3389/fpls.2023.1138048openalex-snapshot
Omics-assisted characterization of two-component system genes from Gossypium Raimondii in response to salinity and molecular interaction with abscisic acid
inferred← citeshttps://doi.org/10.3389/fpls.2023.1309802openalex-snapshot
Genome-wide identification and expression profiles analysis of the authentic response regulator gene family in licorice
inferred← citeshttps://doi.org/10.3389/fpls.2024.1511713openalex-snapshot
Identification of the AHP family reveals their critical response to cytokinin regulation during adventitious root formation in apple rootstock
inferred← citeshttps://doi.org/10.3389/fpls.2025.1537021openalex-snapshot
ARR1 and AHP interactions in the multi-step phosphorelay system
inferred← citeshttps://doi.org/10.3389/fpls.2025.1721349openalex-snapshot
Genome-wide identification and functional characterization of the two-component system gene family in petunia reveals roles in hormone signaling and stress response
inferred← citeshttps://doi.org/10.3390/agronomy13040989openalex-snapshot
Comparative Omics-Based Identification and Expression Analysis of a Two-Component System in Vigna radiata in Drought Stress
inferred← citeshttps://doi.org/10.3390/cimb45070332openalex-snapshot
Transcriptome Analysis of Embryogenic and Non-Embryogenic Callus of Picea Mongolica
inferred← citeshttps://doi.org/10.3390/genes14081638openalex-snapshot
Exploring the Binding Affinity of the ARR2 GARP DNA Binding Domain via Comparative Methods
inferred← citeshttps://doi.org/10.3390/genes16040409openalex-snapshot
Resequencing and Transcriptome Analyses Reveal Variations and Expression Patterns of the RR Gene Family in Cucumber
inferred← citeshttps://doi.org/10.3390/horticulturae10121294openalex-snapshot
Genome-Wide Identification and Expression Analysis of Pseudo-Response Regulators (PRRs) in the Tea Plant Camellia sinensis (L.) O. Kuntze
inferred← citeshttps://doi.org/10.3390/horticulturae9020191openalex-snapshot
Genome-Wide Analysis of the AP2/ERF Family in Oily Persimmon (Diospyros oleifera) and Their Preliminary Roles Exploration in Response to Polyamines for Adventitious Root Formation in Cultivated Persimmon (D. kaki)
inferred← citeshttps://doi.org/10.3390/ijms17081204openalex-snapshot
Genome-Wide Identification and Expression Analysis of Two-Component System Genes in Tomato
inferred← citeshttps://doi.org/10.3390/ijms17122061openalex-snapshot
Functional Divergence of Poplar Histidine-Aspartate Kinase HK1 Paralogs in Response to Osmotic Stress
inferred← citeshttps://doi.org/10.3390/ijms21113896openalex-snapshot
Expression and Role of Response Regulating, Biosynthetic and Degrading Genes for Cytokinin Signaling during Clubroot Disease Development
inferred← citeshttps://doi.org/10.3390/ijms21144898openalex-snapshot
The Interaction Network and Signaling Specificity of Two-Component System in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms21186574openalex-snapshot
Research Progress on the Roles of Cytokinin in Plant Response to Stress
inferred← citeshttps://doi.org/10.3390/ijms22073320openalex-snapshot
Cytokinin Type-B Response Regulators Promote Bulbil Initiation in Lilium lancifolium
inferred← citeshttps://doi.org/10.3390/ijms22073647openalex-snapshot
Reconstitution of Cytokinin Signaling in Rice Protoplasts
inferred← citeshttps://doi.org/10.3390/ijms242417308openalex-snapshot
Two-Component System Genes in Brassica napus: Identification, Analysis, and Expression Patterns in Response to Abiotic and Biotic Stresses
inferred← citeshttps://doi.org/10.3390/ijms26157161openalex-snapshot
Genomic Insights into ARR Genes: Key Role in Cotton Leaf Abscission Formation
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/plants14101485openalex-snapshot
Non-Canonical Inter-Protein Interactions of Key Proteins Belonging to Cytokinin Signaling Pathways
inferred← citeshttps://doi.org/10.3390/plants9020166openalex-snapshot
Role of the Cytokinin-Activated Type-B Response Regulators in Hormone Crosstalk
inferred← citeshttps://doi.org/10.3390/plants9040422openalex-snapshot
Role and Regulation of Cytokinins in Plant Response to Drought Stress
inferred← citeshttps://doi.org/10.3390/plants9111409openalex-snapshot
Genome-Wide Characterization and Expression of Two-Component System Genes in Cytokinin-Regulated Gall Formation in Zizania latifolia
inferred← citeshttps://doi.org/10.3929/ethz-a-006690303openalex-snapshot
The mevalonate pathway: a monitoring approach in plants by systems biology tools
inferred← citeshttps://doi.org/10.4137/bbi.s38425openalex-snapshot
Survey of Genes Involved in Biosynthesis, Transport, and Signaling of Phytohormones with Focus on Solanum lycopersicum
inferred← citeshttps://doi.org/10.4161/psb.21293openalex-snapshot
Overlapping and lineage-specific roles for the type-B response regulators of monocots and dicots
inferred← citeshttps://doi.org/10.4161/psb.5.2.10411openalex-snapshot
Role of cytokinin responsive two-component system in ABA and osmotic stress signalings
inferred← citeshttps://doi.org/10.4236/as.2018.94032openalex-snapshot
Genome-Wide Identification of Two-Component Signal Transduction System Genes in Melon (Cucumis melon L.)
inferred← citeshttps://doi.org/10.5451/unibas-003138022openalex-snapshot
Characterization of flagellin perception in "Arabidopsis thaliana"
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/d9985fa0z7eddz401dzbecfz50d805b64d14openalex-snapshot
Molecular mechanisms of plant-xenobiotic interactions : involvement of stress, development and hormone signaling regulations
inferred← citeshttps://doi.org/10.70675/e43c6957zaa89z424az8de7zd5a8db943afeopenalex-snapshot
Contribution et régulation de PRR2, un facteur de transcription spécifique aux plantes, dans l'immunité végétale
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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