On the public citation graph

Fine-tuning of ABA responses by the protein kinase WNK8

https://doi.org/10.1101/251975

0 signed · 81 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/bies.201100086openalex-snapshot

FRET microscopy in the living cell: Different approaches, strengths and weaknesses

inferredcites →https://doi.org/10.1007/978-1-62703-580-4_33openalex-snapshot

Protein Fragment Bimolecular Fluorescence Complementation Analyses for the In vivo Study of Protein-Protein Interactions and Cellular Protein Complex Localizations

inferredcites →https://doi.org/10.1007/s00709-013-0595-7openalex-snapshot

FRET-FLIM applications in plant systems

inferredcites →https://doi.org/10.1007/s11103-012-9973-3openalex-snapshot

Direct interactions of ABA-insensitive(ABI)-clade protein phosphatase(PP)2Cs with calcium-dependent protein kinases and ABA response element-binding bZIPs may contribute to turning off ABA response

inferredcites →https://doi.org/10.1016/j.cell.2014.01.013openalex-snapshot

Reciprocal Encoding of Signal Intensity and Duration in a Glucose-Sensing Circuit

inferredcites →https://doi.org/10.1016/j.devcel.2014.04.004openalex-snapshot

A Mesoscale Abscisic Acid Hormone Interactome Reveals a Dynamic Signaling Landscape in Arabidopsis

inferredcites →https://doi.org/10.1016/j.febslet.2006.01.018openalex-snapshot

A WNK kinase binds and phosphorylates V‐ATPase subunit C

inferredcites →https://doi.org/10.1016/j.molcel.2011.05.011openalex-snapshot

The Molecular Basis of ABA-Independent Inhibition of PP2Cs by a Subclass of PYL Proteins

inferredcites →https://doi.org/10.1016/j.molp.2015.10.003openalex-snapshot

A Direct Link between Abscisic Acid Sensing and the Chromatin-Remodeling ATPase BRAHMA via Core ABA Signaling Pathway Components

inferredcites →https://doi.org/10.1016/j.pbi.2016.06.010openalex-snapshot

Integration of calcium and ABA signaling

inferredcites →https://doi.org/10.1016/j.pbi.2016.12.004openalex-snapshot

Shaping plant development through the SnRK1–TOR metabolic regulators

inferredcites →https://doi.org/10.1016/j.plantsci.2012.01.013openalex-snapshot

Functional roles of the protein phosphatase 2C, AtAIP1, in abscisic acid signaling and sugar tolerance in Arabidopsis

inferredcites →https://doi.org/10.1016/j.plaphy.2014.01.022openalex-snapshot

AtWNK9 is regulated by ABA and dehydration and is involved in drought tolerance in Arabidopsis

inferredcites →https://doi.org/10.1016/j.str.2004.04.014openalex-snapshot

Crystal Structure of the Kinase Domain of WNK1, a Kinase that Causes a Hereditary Form of Hypertension

inferredcites →https://doi.org/10.1016/j.tibs.2010.09.006openalex-snapshot

Protein kinases: evolution of dynamic regulatory proteins

inferredcites →https://doi.org/10.1016/j.tplants.2004.03.007openalex-snapshot

Plant PP2C phosphatases: emerging functions in stress signaling

inferredcites →https://doi.org/10.1016/j.tplants.2010.04.006openalex-snapshot

ABA perception and signalling

inferredcites →https://doi.org/10.1016/j.tplants.2013.01.007openalex-snapshot

ABA transport and transporters

inferredcites →https://doi.org/10.1016/s0014-5793(97)01558-5openalex-snapshot

ABI2, a second protein phosphatase 2C involved in abscisic acid signal transduction in Arabidopsis

inferredcites →https://doi.org/10.1016/s1369-5266(01)00225-4openalex-snapshot

ABA and sugar interactions regulating development: cross-talk or voices in a crowd?

inferredcites →https://doi.org/10.1016/s1534-5807(02)00229-0openalex-snapshot

A Calcium Sensor and Its Interacting Protein Kinase Are Global Regulators of Abscisic Acid Signaling in Arabidopsis

inferredcites →https://doi.org/10.1021/pr101065jopenalex-snapshot

Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment

inferredcites →https://doi.org/10.1038/msb.2011.66openalex-snapshot

Arabidopsis G‐protein interactome reveals connections to cell wall carbohydrates and morphogenesis

inferredcites →https://doi.org/10.1038/nature08591openalex-snapshot

The abscisic acid receptor PYR1 in complex with abscisic acid

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

In vitro reconstitution of an abscisic acid signalling pathway

inferredcites →https://doi.org/10.1038/nbt.1511openalex-snapshot

MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification

inferredcites →https://doi.org/10.1038/nbt1037openalex-snapshot

Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein

inferredcites →https://doi.org/10.1038/ncb2568openalex-snapshot

Endocytosis of the seven-transmembrane RGS1 protein activates G-protein-coupled signalling in Arabidopsis

inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot

Fiji: an open-source platform for biological-image analysis

inferredcites →https://doi.org/10.1038/nprot.2006.468openalex-snapshot

In-gel digestion for mass spectrometric characterization of proteins and proteomes

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.0910601106openalex-snapshot

A protein kinase-phosphatase pair interacts with an ion channel to regulate ABA signaling in plant guard cells

inferredcites →https://doi.org/10.1073/pnas.1308974110openalex-snapshot

Quantitative phosphoproteomics identifies SnRK2 protein kinase substrates and reveals the effectors of abscisic acid action

inferredcites →https://doi.org/10.1073/pnas.1322085111openalex-snapshot

Abscisic acid sensor RCAR7/PYL13, specific regulator of protein phosphatase coreceptors

inferredcites →https://doi.org/10.1073/pnas.1608449113openalex-snapshot

FERONIA interacts with ABI2-type phosphatases to facilitate signaling cross-talk between abscisic acid and RALF peptide in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.2034853100openalex-snapshot

A novel domain in the protein kinase SOS2 mediates interaction with the protein phosphatase 2C ABI2

inferredcites →https://doi.org/10.1074/jbc.275.22.16795openalex-snapshot

WNK1, a Novel Mammalian Serine/Threonine Protein Kinase Lacking the Catalytic Lysine in Subdomain II

inferredcites →https://doi.org/10.1074/jbc.m111.279331openalex-snapshot

Phosphorylation of Calcineurin B-like (CBL) Calcium Sensor Proteins by Their CBL-interacting Protein Kinases (CIPKs) Is Required for Full Activity of CBL-CIPK Complexes toward Their Target Proteins

inferredcites →https://doi.org/10.1074/jbc.m115.711309openalex-snapshot

The Arabidopsis AtPP2CA Protein Phosphatase Inhibits the GORK K+ Efflux Channel and Exerts a Dominant Suppressive Effect on Phosphomimetic-activating Mutations

inferredcites →https://doi.org/10.1093/jxb/erl035openalex-snapshot

RACK1 mediates multiple hormone responsiveness and developmental processes in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/erp221openalex-snapshot

RACK1 is a negative regulator of ABA responses in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/erx263openalex-snapshot

T-DNA alleles of the receptor kinase THESEUS1 with opposing effects on cell wall integrity signaling

inferredcites →https://doi.org/10.1093/mp/ssr031openalex-snapshot

Mechanistic Analysis of AKT1 Regulation by the CBL–CIPK–PP2CA Interactions

inferredcites →https://doi.org/10.1093/mp/sst065openalex-snapshot

A New β-Estradiol-Inducible Vector Set that Facilitates Easy Construction and Efficient Expression of Transgenes Reveals CBL3-Dependent Cytoplasm to Tonoplast Translocation of CIPK5

inferredcites →https://doi.org/10.1093/pcp/pch171openalex-snapshot

Isolation and Characterization of Novel Mutants Affecting the Abscisic Acid Sensitivity of Arabidopsis Germination and Seedling Growth

inferredcites →https://doi.org/10.1101/gad.1953910openalex-snapshot

Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions

inferredcites →https://doi.org/10.1101/pdb.prot4995openalex-snapshot

In Planta Visualization of Protein Interactions Using Bimolecular Fluorescence Complementation (BiFC)

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.110.160663openalex-snapshot

Involvement of Arabidopsis RACK1 in Protein Translation and Its Regulation by Abscisic Acid

inferredcites →https://doi.org/10.1104/pp.114.247460openalex-snapshot

Arabidopsis Receptor of Activated C Kinase1 Phosphorylation by WITH NO LYSINE8 KINASE

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/10.1105/tpc.000943openalex-snapshot

Physical and Functional Interaction of the Arabidopsis K+ Channel AKT2 and Phosphatase AtPP2CA

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.113.114066openalex-snapshot

ABI1 and PP2CA Phosphatases Are Negative Regulators of Snf1-Related Protein Kinase1 Signaling in Arabidopsis

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.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.2008.03454.xopenalex-snapshot

Nuclear localization of the mutant protein phosphatase abi1 is required for insensitivity towards ABA responses in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03981.xopenalex-snapshot

EXPRESSION OF CONCERN: Modulation of drought resistance by the abscisic acid receptor PYL5 through inhibition of clade A PP2Cs

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04169.xopenalex-snapshot

The Arabidopsis defense component EDM2 affects the floral transition in an FLC-dependent manner

inferredcites →https://doi.org/10.1111/j.1399-3054.1984.tb06343.xopenalex-snapshot

The isolation and characterization of abscisic acid‐insensitive mutants of Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00072.xopenalex-snapshot

The plant WNK gene family and regulation of flowering time in Arabidopsis

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.1181829openalex-snapshot

Structural Mechanism of Abscisic Acid Binding and Signaling by Dimeric PYR1

inferredcites →https://doi.org/10.1126/science.1251358openalex-snapshot

Border Control—A Membrane-Linked Interactome of Arabidopsis

inferredcites →https://doi.org/10.1126/science.8197457openalex-snapshot

A Protein Phosphatase 2C Involved in ABA Signal Transduction in Arabidopsis thaliana

inferredcites →https://doi.org/10.1126/scisignal.2003509openalex-snapshot

Genetics and Phosphoproteomics Reveal a Protein Phosphorylation Network in the Abscisic Acid Signaling Pathway in Arabidopsis thaliana

inferredcites →https://doi.org/10.1126/scisignal.aaa4829openalex-snapshot

Nitrate sensing and uptake in Arabidopsis are enhanced by ABI2, a phosphatase inactivated by the stress hormone abscisic acid

inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112122openalex-snapshot

Abscisic Acid: Emergence of a Core Signaling Network

inferredcites →https://doi.org/10.1146/annurev.biophys.37.032807.125842openalex-snapshot

Bimolecular Fluorescence Complementation (BiFC) Analysis as a Probe of Protein Interactions in Living Cells

inferredcites →https://doi.org/10.1155/2008/420747openalex-snapshot

Genevestigator V3: A Reference Expression Database for the Meta‐Analysis of Transcriptomes

inferredcites →https://doi.org/10.1371/journal.pone.0000718openalex-snapshot

An “Electronic Fluorescent Pictograph” Browser for Exploring and Analyzing Large-Scale Biological Data Sets

inferredcites →https://doi.org/10.1371/journal.pone.0083043openalex-snapshot

GreenGate - A Novel, Versatile, and Efficient Cloning System for Plant Transgenesis

inferredcites →https://doi.org/10.1385/0-89603-254-x:9openalex-snapshot

Isolation of DNA from Plants

inferredcites →https://doi.org/10.3389/fpls.2015.01090openalex-snapshot

The Receptor for Activated C Kinase in Plant Signaling: Tale of a Promiscuous Little Molecule

inferredcites →https://doi.org/10.3390/ijms14047032openalex-snapshot

Disruption of AtWNK8 Enhances Tolerance of Arabidopsis to Salt and Osmotic Stresses via Modulating Proline Content and Activities of Catalase and Peroxidase

inferredcites →https://doi.org/10.7554/elife.01917openalex-snapshot

Fluorescent sensors for activity and regulation of the nitrate transceptor CHL1/NRT1.1 and oligopeptide transporters

inferredcites →https://doi.org/10.7554/elife.03599openalex-snapshot

Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells

inferredcites →https://doi.org/10.7554/elife.05828openalex-snapshot

SnRK1-triggered switch of bZIP63 dimerization mediates the low-energy response in plants

inferredcites →https://doi.org/10.7554/elife.10328openalex-snapshot

Correction: Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.