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Ethylene Receptors Signal via a Noncanonical Pathway to Regulate Abscisic Acid Responses

https://doi.org/10.1104/pp.17.01321

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Molecular cloning, genomic organization, expression and evolution of 12S seed storage protein genes of Arabidopsis thaliana

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Effects of heavy metals on seed germination and early seedling growth of Arabidopsis thaliana

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Genetic analysis of involvement of ETR1 in plant response to salt and osmotic stress

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The Arabidopsis AtDi19 Gene Family Encodes a Novel Type of Cys2/His2 Zinc-finger Protein Implicated in ABA-independent Dehydration, High-salinity Stress and Light Signaling Pathways

inferredcites →https://doi.org/10.1007/s11103-006-9103-1openalex-snapshot

Different phosphorylation mechanisms are involved in the activation of sucrose non-fermenting 1 related protein kinases 2 by osmotic stresses and abscisic acid

inferredcites →https://doi.org/10.1007/s11103-007-9182-7openalex-snapshot

Arabidopsis EIN2 modulates stress response through abscisic acid response pathway

inferredcites →https://doi.org/10.1007/s11103-014-0251-4openalex-snapshot

Arabidopsis drought-induced protein Di19-3 participates in plant response to drought and high salinity stresses

inferredcites →https://doi.org/10.1007/s11240-011-0089-2openalex-snapshot

Expression of seed storage product genes (CRA1 and OLEO4) in embryogenic cultures of somatic tissues of Arabidopsis

inferredcites →https://doi.org/10.1007/s11738-012-0989-8openalex-snapshot

Ethylene antagonizes the inhibition of germination in Arabidopsis induced by salinity by modulating the concentration of hydrogen peroxide

inferredcites →https://doi.org/10.1007/s12038-010-0050-2openalex-snapshot

Interactions between ethylene, abscisic acid and cytokinin during germination and seedling establishment in Arabidopsis

inferredcites →https://doi.org/10.1016/0092-8674(93)90119-bopenalex-snapshot

CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases

inferredcites →https://doi.org/10.1016/j.cellsig.2009.01.033openalex-snapshot

Hedgehog signalling: Emerging evidence for non-canonical pathways

inferredcites →https://doi.org/10.1016/j.febslet.2012.11.030openalex-snapshot

Reducing jasmonic acid levels causes ein2 mutants to become ethylene responsive

inferredcites →https://doi.org/10.1016/j.tplants.2012.02.001openalex-snapshot

Auxin and ethylene: collaborators or competitors?

inferredcites →https://doi.org/10.1016/j.ygeno.2012.06.004openalex-snapshot

Expression profiling of ABA pathway transcripts indicates crosstalk between abiotic and biotic stress responses in Arabidopsis

inferredcites →https://doi.org/10.1016/s0014-5793(04)00238-8openalex-snapshot

Effect of salt and osmotic stress upon expression of the ethylene receptor ETR1 in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/s0092-8674(00)80300-1openalex-snapshot

Activation of the Ethylene Gas Response Pathway in Arabidopsis by the Nuclear Protein ETHYLENE-INSENSITIVE3 and Related Proteins

inferredcites →https://doi.org/10.1016/s0092-8674(00)81425-7openalex-snapshot

Ethylene Responses Are Negatively Regulated by a Receptor Gene Family in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/s0092-8674(03)00969-3openalex-snapshot

Plant Responses to Ethylene Gas Are Mediated by SCFEBF1/EBF2-Dependent Proteolysis of EIN3 Transcription Factor

inferredcites →https://doi.org/10.1016/s0960-9822(00)00657-6openalex-snapshot

Subcellular localization determines the availability of non-targeted proteins to plasmodesmatal transport

inferredcites →https://doi.org/10.1038/36285openalex-snapshot

Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

inferredcites →https://doi.org/10.1038/cr.2012.145openalex-snapshot

Activation of ethylene signaling is mediated by nuclear translocation of the cleaved EIN2 carboxyl terminus

inferredcites →https://doi.org/10.1038/emboj.2011.68openalex-snapshot

Central functions of bicarbonate in S‐type anion channel activation and OST1 protein kinase in CO2 signal transduction in guard cell

inferredcites →https://doi.org/10.1038/nature01984openalex-snapshot

Differential regulation of EIN3 stability by glucose and ethylene signalling in plants

inferredcites →https://doi.org/10.1038/nature08583openalex-snapshot

Structural basis of abscisic acid signalling

inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot

In vitro reconstitution of an abscisic acid signalling pathway

inferredcites →https://doi.org/10.1038/nature08613openalex-snapshot

A gate–latch–lock mechanism for hormone signalling by abscisic acid receptors

inferredcites →https://doi.org/10.1039/c1mb05159hopenalex-snapshot

Proteomic responses in Arabidopsis thaliana seedlings treated with ethylene

inferredcites →https://doi.org/10.1042/bj20091102openalex-snapshot

EIN2, the central regulator of ethylene signalling, is localized at the ER membrane where it interacts with the ethylene receptor ETR1

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00965.xopenalex-snapshot

The ABI1 and ABI2 protein phosphatases 2C act in a negative feedback regulatory loop of the abscisic acid signalling pathway

inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01966.xopenalex-snapshot

Gain‐of‐function and loss‐of‐function phenotypes of the protein phosphatase 2C HAB1 reveal its role as a negative regulator of abscisic acid signalling

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.0401698101openalex-snapshot

Arabidopsis EIN3-binding F-box 1 and 2 form ubiquitin-protein ligases that repress ethylene action and promote growth by directing EIN3 degradation

inferredcites →https://doi.org/10.1073/pnas.0402112101openalex-snapshot

Phospholipase Dα1-derived phosphatidic acid interacts with ABI1 phosphatase 2C and regulates abscisic acid signaling

inferredcites →https://doi.org/10.1073/pnas.0602239103openalex-snapshot

REVERSION-TO-ETHYLENE SENSITIVITY1 , a conserved gene that regulates ethylene receptor function in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.0811088106openalex-snapshot

Sumoylation of ABI5 by the Arabidopsis SUMO E3 ligase SIZ1 negatively regulates abscisic acid signaling

inferredcites →https://doi.org/10.1073/pnas.0903144106openalex-snapshot

Arabidopsis mutant deficient in 3 abscisic acid-activated protein kinases reveals critical roles in growth, reproduction, and stress

inferredcites →https://doi.org/10.1073/pnas.0907095106openalex-snapshot

Type 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.0912021106openalex-snapshot

Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair

inferredcites →https://doi.org/10.1073/pnas.1018367108openalex-snapshot

Arabidopsis decuple mutant reveals the importance of SnRK2 kinases in osmotic stress responses in vivo

inferredcites →https://doi.org/10.1073/pnas.1116590109openalex-snapshot

Reconstitution of abscisic acid activation of SLAC1 anion channel by CPK6 and OST1 kinases and branched ABI1 PP2C phosphatase action

inferredcites →https://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

inferredcites →https://doi.org/10.1073/pnas.1511701112openalex-snapshot

Noncanonical role of transferrin receptor 1 is essential for intestinal homeostasis

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.95.9.5401openalex-snapshot

Association of the Arabidopsis CTR1 Raf-like kinase with the ETR1 and ERS ethylene receptors

inferredcites →https://doi.org/10.1074/jbc.270.21.12526openalex-snapshot

The Ethylene Response Mediator ETR1 from Arabidopsis Forms a Disulfide-linked Dimer

inferredcites →https://doi.org/10.1074/jbc.m110.146605openalex-snapshot

Molecular Association of the Arabidopsis ETR1 Ethylene Receptor and a Regulator of Ethylene Signaling, RTE1

inferredcites →https://doi.org/10.1074/jbc.m112.383034openalex-snapshot

Ethylene Receptor 1 (ETR1) Is Sufficient and Has the Predominant Role in Mediating Inhibition of Ethylene Responses by Silver in Arabidopsis thaliana

inferredcites →https://doi.org/10.1074/jbc.m201286200openalex-snapshot

Localization of the Ethylene Receptor ETR1 to the Endoplasmic Reticulum of Arabidopsis

inferredcites →https://doi.org/10.1074/jbc.m305548200openalex-snapshot

Localization of the Raf-like Kinase CTR1 to the Endoplasmic Reticulum of Arabidopsis through Participation in Ethylene Receptor Signaling Complexes

inferredcites →https://doi.org/10.1074/jbc.m403100200openalex-snapshot

Autophosphorylation Activity of the Arabidopsis Ethylene Receptor Multigene Family

inferredcites →https://doi.org/10.1074/jbc.m509820200openalex-snapshot

The Regulatory Domain of SRK2E/OST1/SnRK2.6 Interacts with ABI1 and Integrates Abscisic Acid (ABA) and Osmotic Stress Signals Controlling Stomatal Closure in Arabidopsis

inferredcites →https://doi.org/10.1093/aobpla/plt010openalex-snapshot

Mechanisms of signal transduction by ethylene: overlapping and non-overlapping signalling roles in a receptor family

inferredcites →https://doi.org/10.1093/mp/ssm015openalex-snapshot

Subcellular Localization and In Vivo Interactions of the Arabidopsis thaliana Ethylene Receptor Family Members

inferredcites →https://doi.org/10.1093/mp/ssq036openalex-snapshot

New Insight in Ethylene Signaling: Autokinase Activity of ETR1 Modulates the Interaction of Receptors and EIN2

inferredcites →https://doi.org/10.1093/mp/sst031openalex-snapshot

Arabidopsis Di19 Functions as a Transcription Factor and Modulates PR1, PR2, and PR5 Expression in Response to Drought Stress

inferredcites →https://doi.org/10.1093/nar/gkq1019openalex-snapshot

The Sequence Read Archive

inferredcites →https://doi.org/10.1093/pcp/pce144openalex-snapshot

A Proteinase-Storing Body that Prepares for Cell Death or Stresses in the Epidermal Cells of Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pch078openalex-snapshot

A Novel Ethanol-Hypersensitive Mutant of Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcn075openalex-snapshot

Antagonistic Jacalin-Related Lectins Regulate the Size of ER Body-Type β-Glucosidase Complexes in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/pcp/pcp083openalex-snapshot

Three Arabidopsis SnRK2 Protein Kinases, SRK2D/SnRK2.2, SRK2E/SnRK2.6/OST1 and SRK2I/SnRK2.3, Involved in ABA Signaling are Essential for the Control of Seed Development and Dormancy

inferredcites →https://doi.org/10.1093/pcp/pcp107openalex-snapshot

Effects of Tobacco Ethylene Receptor Mutations on Receptor Kinase Activity, Plant Growth and Stress Responses

inferredcites →https://doi.org/10.1093/pcp/pcp147openalex-snapshot

Three SnRK2 Protein Kinases are the Main Positive Regulators of Abscisic Acid Signaling in Response to Water Stress in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcp157openalex-snapshot

Quantitative Analysis of ER Body Morphology in an Arabidopsis Mutant

inferredcites →https://doi.org/10.1093/pcp/pcq156openalex-snapshot

Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport

inferredcites →https://doi.org/10.1093/pcp/pcr113openalex-snapshot

Identification of Reference Genes for RT–qPCR Expression Analysis in Arabidopsis and Tomato Seeds

inferredcites →https://doi.org/10.1093/pcp/pct178openalex-snapshot

ATTED-II in 2014: Evaluation of Gene Coexpression in Agriculturally Important Plants

inferredcites →https://doi.org/10.1101/gad.12.23.3703openalex-snapshot

Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1

inferredcites →https://doi.org/10.1101/gad.1765709openalex-snapshot

Interplay between ethylene, ETP1/ETP2 F-box proteins, and degradation of EIN2 triggers ethylene responses in Arabidopsis

inferredcites →https://doi.org/10.1101/gr.1239303openalex-snapshot

Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks

inferredcites →https://doi.org/10.1104/pp.003780openalex-snapshot

Loss-of-Function Mutations in the Ethylene ReceptorETR1 Cause Enhanced Sensitivity and Exaggerated Response to Ethylene in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.010777openalex-snapshot

Mutational Analysis of the Ethylene Receptor ETR1. Role of the Histidine Kinase Domain in Dominant Ethylene Insensitivity

inferredcites →https://doi.org/10.1104/pp.102.019182openalex-snapshot

Ethylene Modulates Root-Wave Responses in Arabidopsis

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.104.050393openalex-snapshot

Short-Term Growth Responses to Ethylene in Arabidopsis Seedlings Are EIN3/EIL1 Independent

inferredcites →https://doi.org/10.1104/pp.104.056994openalex-snapshot

A Role for ETR1 in Hydrogen Peroxide Signaling in Stomatal Guard Cells

inferredcites →https://doi.org/10.1104/pp.104.2.363openalex-snapshot

The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A

inferredcites →https://doi.org/10.1104/pp.105.070128openalex-snapshot

ABA-Hypersensitive Germination3Encodes a Protein Phosphatase 2C (AtPP2CA) That Strongly Regulates Abscisic Acid Signaling during Germination among Arabidopsis Protein Phosphatase 2Cs

inferredcites →https://doi.org/10.1104/pp.105.070318openalex-snapshot

The Protein Phosphatase AtPP2CA Negatively Regulates Abscisic Acid Signal Transduction in Arabidopsis, and Effects of abh1 on AtPP2CA mRNA

inferredcites →https://doi.org/10.1104/pp.106.080523openalex-snapshot

Subcellular Localization and Membrane Topology of the Melon Ethylene Receptor CmERS1

inferredcites →https://doi.org/10.1104/pp.106.087858openalex-snapshot

Ethylene Stimulates Nutations That Are Dependent on the ETR1 Receptor

inferredcites →https://doi.org/10.1104/pp.109.137174openalex-snapshot

Triple Loss of Function of Protein Phosphatases Type 2C Leads to Partial Constitutive Response to Endogenous Abscisic Acid

inferredcites →https://doi.org/10.1104/pp.110.170621openalex-snapshot

Ethylene Receptor ETHYLENE RECEPTOR1 Domain Requirements for Ethylene Responses in Arabidopsis Seedlings

inferredcites →https://doi.org/10.1104/pp.111.188623openalex-snapshot

Selective Inhibition of Clade A Phosphatases Type 2C by PYR/PYL/RCAR Abscisic Acid Receptors

inferredcites →https://doi.org/10.1104/pp.112.193979openalex-snapshot

Arabidopsis RTE1 Is Essential to Ethylene Receptor ETR1 Amino-Terminal Signaling Independent of CTR1

inferredcites →https://doi.org/10.1104/pp.112.196790openalex-snapshot

Histidine Kinase Activity of the Ethylene Receptor ETR1 Facilitates the Ethylene Response in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.112.202408openalex-snapshot

Unique Drought Resistance Functions of theHighly ABA-InducedClade A Protein Phosphatase 2Cs

inferredcites →https://doi.org/10.1104/pp.114.241695openalex-snapshot

The Ethylene Receptors ETHYLENE RESPONSE1 and ETHYLENE RESPONSE2 Have Contrasting Roles in Seed Germination of Arabidopsis during Salt Stress

inferredcites →https://doi.org/10.1104/pp.15.00233openalex-snapshot

An Ancestral Role for CONSTITUTIVE TRIPLE RESPONSE1 Proteins in Both Ethylene and Abscisic Acid Signaling

inferredcites →https://doi.org/10.1104/pp.15.00575openalex-snapshot

Identification of Open Stomata1-Interacting Proteins Reveals Interactions with Sucrose Non-fermenting1-Related Protein Kinases2 and with Type 2A Protein Phosphatases That Function in Abscisic Acid Responses

inferredcites →https://doi.org/10.1104/pp.15.00626openalex-snapshot

Identification of Regions in the Receiver Domain of the ETHYLENE RESPONSE1 Ethylene Receptor of Arabidopsis Important for Functional Divergence

inferredcites →https://doi.org/10.1104/pp.15.00724openalex-snapshot

Ethylene and Hormonal Cross Talk in Vegetative Growth and Development

inferredcites →https://doi.org/10.1104/pp.58.3.268openalex-snapshot

A Potent Inhibitor of Ethylene Action in Plants

inferredcites →https://doi.org/10.1105/tpc.007906openalex-snapshot

Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production

inferredcites →https://doi.org/10.1105/tpc.019000openalex-snapshot

Microarray Expression Analyses of Arabidopsis Guard Cells and Isolation of a Recessive Abscisic Acid Hypersensitive Protein Phosphatase 2C Mutant[W]

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.105.035659openalex-snapshot

AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.106.048538openalex-snapshot

Identification of Two Protein Kinases Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Gene Expression in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.107.050153openalex-snapshot

PIL5, a Phytochrome-Interacting bHLH Protein, Regulates Gibberellin Responsiveness by Binding Directly to theGAIandRGAPromoters inArabidopsisSeeds

inferredcites →https://doi.org/10.1105/tpc.108.063065openalex-snapshot

Cellulose Binding Protein from the Parasitic Nematode Heterodera schachtii Interacts with Arabidopsis Pectin Methylesterase: Cooperative Cell Wall Modification during Parasitism

inferredcites →https://doi.org/10.1105/tpc.109.069179openalex-snapshot

Protein Phosphatases 2C Regulate the Activation of the Snf1-Related Kinase OST1 by Abscisic Acid in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.11.10.1897openalex-snapshot

ABI1 Protein Phosphatase 2C Is a Negative Regulator of Abscisic Acid Signaling

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.12.7.1117openalex-snapshot

Regulation of Abscisic Acid Signaling by the Ethylene Response Pathway in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.16.01050openalex-snapshot

S-type Anion Channels SLAC1 and SLAH3 Function as Essential Negative Regulators of Inward K+ Channels and Stomatal Opening in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.2.6.513openalex-snapshot

Exploiting the Triple Response of Arabidopsis to Identify Ethylene-Related Mutants

inferredcites →https://doi.org/10.1105/tpc.5.5.553openalex-snapshot

Developmental and age-related processes that influence the longevity and senescence of photosynthetic tissues in arabidopsis.

inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02243.xopenalex-snapshot

Separating parental environment from seed size effects on next generation growth and development in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03107.xopenalex-snapshot

ABA‐Hypersensitive Germination1 encodes a protein phosphatase 2C, an essential component of abscisic acid signaling in Arabidopsis seed

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03339.xopenalex-snapshot

Subcellular co‐localization of Arabidopsis RTE1 and ETR1 supports a regulatory role for RTE1 in ETR1 ethylene signaling

inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03424.xopenalex-snapshot

PYK10, a β‐glucosidase located in the endoplasmatic reticulum, is crucial for the beneficial interaction between Arabidopsis thaliana and the endophytic fungus Piriformospora indica

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04092.xopenalex-snapshot

AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation

inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot

A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03610.xopenalex-snapshot

Ethylene‐dependent/ethylene‐independent ABA regulation of tomato plants colonized by arbuscular mycorrhiza fungi

inferredcites →https://doi.org/10.1111/nph.13436openalex-snapshot

Membrane‐associated transcription factor peptidase, site‐2 protease, antagonizes ABA signaling in Arabidopsis

inferredcites →https://doi.org/10.1111/nph.13466openalex-snapshot

Dominant gain‐of‐function mutations in transmembrane domain III of ERS 1 and ETR 1 suggest a novel role for this domain in regulating the magnitude of ethylene response in Arabidopsis

inferredcites →https://doi.org/10.1111/pbi.12652openalex-snapshot

Post‐translational control of ABA signalling: the roles of protein phosphorylation and ubiquitination

inferredcites →https://doi.org/10.1111/pce.12351openalex-snapshot

Four A rabidopsis AREB / ABF transcription factors function predominantly in gene expression downstream of SnRK2 kinases in abscisic acid signalling in response to osmotic stress

inferredcites →https://doi.org/10.1126/science.1172408openalex-snapshot

Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors

inferredcites →https://doi.org/10.1126/science.1173041openalex-snapshot

Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins

inferredcites →https://doi.org/10.1126/science.1181276openalex-snapshot

Becoming T. rex

inferredcites →https://doi.org/10.1126/science.1181829openalex-snapshot

Structural Mechanism of Abscisic Acid Binding and Signaling by Dimeric PYR1

inferredcites →https://doi.org/10.1126/science.1215106openalex-snapshot

Molecular Mimicry Regulates ABA Signaling by SnRK2 Kinases and PP2C Phosphatases

inferredcites →https://doi.org/10.1126/science.1225974openalex-snapshot

Processing and Subcellular Trafficking of ER-Tethered EIN2 Control Response to Ethylene Gas

inferredcites →https://doi.org/10.1126/science.241.4869.1086openalex-snapshot

Insensitivity to Ethylene Conferred by a Dominant Mutation in Arabidopsis thaliana

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.283.5404.996openalex-snapshot

A Copper Cofactor for the Ethylene Receptor ETR1 from Arabidopsis

inferredcites →https://doi.org/10.1126/science.284.5423.2148openalex-snapshot

EIN2, a Bifunctional Transducer of Ethylene and Stress Responses in Arabidopsis

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/10.1146/annurev-arplant-042809-112122openalex-snapshot

Abscisic Acid: Emergence of a Core Signaling Network

inferredcites →https://doi.org/10.1172/jci20195openalex-snapshot

Interspecies communication in bacteria

inferredcites →https://doi.org/10.1186/1471-2229-10-60openalex-snapshot

Genetic and transformation studies reveal negative regulation of ERS1 ethylene receptor signaling in Arabidopsis

inferredcites →https://doi.org/10.1186/1471-2229-7-3openalex-snapshot

A strong constitutive ethylene-response phenotype conferred on Arabidopsis plants containing null mutations in the ethylene receptors ETR1 and ERS1

inferredcites →https://doi.org/10.1186/gb-2007-8-4-r49openalex-snapshot

Integration of Arabidopsis thaliana stress-related transcript profiles, promoter structures, and cell-specific expression

inferredcites →https://doi.org/10.1201/9781351075763openalex-snapshot

The Plant Hormone Ethylene

inferredcites →https://doi.org/10.1371/journal.pgen.1006194openalex-snapshot

The Molecular Mechanism of Ethylene-Mediated Root Hair Development Induced by Phosphate Starvation

inferredcites →https://doi.org/10.1371/journal.pone.0125168openalex-snapshot

ABA Inducible Rice Protein Phosphatase 2C Confers ABA Insensitivity and Abiotic Stress Tolerance in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pone.0154072openalex-snapshot

Comprehensive Analysis of ABA Effects on Ethylene Biosynthesis and Signaling during Tomato Fruit Ripening

inferredcites →https://doi.org/10.1534/g3.114.011080openalex-snapshot

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inferredcites →https://doi.org/10.3389/fpls.2014.00433openalex-snapshot

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inferredcites →https://doi.org/10.3389/fpls.2014.00744openalex-snapshot

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inferredcites →https://doi.org/10.3389/fpls.2017.00161openalex-snapshot

Abscisic Acid Signaling and Abiotic Stress Tolerance in Plants: A Review on Current Knowledge and Future Prospects

What points at this work

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inferred← citeshttps://doi.org/10.7287/peerj.14282v0.1/reviews/1openalex-snapshot

Peer Review #1 of "SES1 is vital for seedling establishment and post-germination growth under high-potassium stress conditions in Arabidopsis thaliana (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.14282v0.1/reviews/2openalex-snapshot

Peer Review #2 of "SES1 is vital for seedling establishment and post-germination growth under high-potassium stress conditions in Arabidopsis thaliana (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.14282v0.1/reviews/3openalex-snapshot

Peer Review #3 of "SES1 is vital for seedling establishment and post-germination growth under high-potassium stress conditions in Arabidopsis thaliana (v0.1)"

inferred← citeshttps://doi.org/10.7717/peerj.14282openalex-snapshot

SES1 is vital for seedling establishment and post-germination growth under high-potassium stress conditions in Arabidopsis thaliana

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