On the public citation graph
Phosphoproteomics of Arabidopsis Highly ABA-Induced1 identifies AT-Hook Like10 phosphorylation required for stress growth regulation
0 signed · 60 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/pmic.201400072openalex-snapshot
Proteomic and phosphoproteomic analyses of chromatin‐associated proteins from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00425-010-1265-zopenalex-snapshot
Salicylate-mediated suppression of jasmonate-responsive gene expression in Arabidopsis is targeted downstream of the jasmonate biosynthesis pathway
inferredcites →https://doi.org/10.1007/s11103-004-3249-5openalex-snapshot
Identification of a novel plant MAR DNA binding protein localized on chromosomal surfaces
inferredcites →https://doi.org/10.1007/s11103-009-9507-9openalex-snapshot
Over-expression of an AT-hook gene, AHL22, delays flowering and inhibits the elongation of the hypocotyl in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11103-016-0458-7openalex-snapshot
ABA and cytokinins: challenge and opportunity for plant stress research
inferredcites →https://doi.org/10.1016/j.devcel.2011.09.009openalex-snapshot
Cell Identity Regulators Link Development and Stress Responses in the Arabidopsis Root
inferredcites →https://doi.org/10.1016/j.jprot.2012.10.018openalex-snapshot
A large-scale protein phosphorylation analysis reveals novel phosphorylation motifs and phosphoregulatory networks in Arabidopsis
inferredcites →https://doi.org/10.1016/j.tplants.2010.04.006openalex-snapshot
ABA perception and signalling
inferredcites →https://doi.org/10.1016/j.tplants.2016.04.004openalex-snapshot
The Role of MAPK Modules and ABA during Abiotic Stress Signaling
inferredcites →https://doi.org/10.1021/pr8000173openalex-snapshot
Site-Specific Phosphorylation Profiling of Arabidopsis Proteins by Mass Spectrometry and Peptide Chip Analysis
inferredcites →https://doi.org/10.1038/nbt.1800openalex-snapshot
Survival and growth of Arabidopsis plants given limited water are not equal
inferredcites →https://doi.org/10.1038/nbt0307-285openalex-snapshot
A curated compendium of phosphorylation motifs
inferredcites →https://doi.org/10.1038/srep30264openalex-snapshot
A novel gene OsAHL1 improves both drought avoidance and drought tolerance in rice
inferredcites →https://doi.org/10.1042/bj20111809openalex-snapshot
Determination of primary sequence specificity of Arabidopsis MAPKs MPK3 and MPK6 leads to identification of new substrates
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00245.xopenalex-snapshot
Allene oxide synthase: a major control point in Arabidopsis thaliana octadecanoid signalling
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00957.xopenalex-snapshot
DFL1, an auxin-responsive GH3 gene homologue, negatively regulates shoot cell elongation and lateral root formation, and positively regulates the light response of hypocotyl length
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.1219277110openalex-snapshot
Arabidopsis thaliana AHL family modulates hypocotyl growth redundantly by interacting with each other via the PPC/DUF296 domain
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.1702613114openalex-snapshot
Pathogen exploitation of an abscisic acid- and jasmonate-inducible MAPK phosphatase and its interception by Arabidopsis immunity
inferredcites →https://doi.org/10.1074/jbc.m610524200openalex-snapshot
GH3-mediated Auxin Homeostasis Links Growth Regulation with Stress Adaptation Response in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m800735200openalex-snapshot
An Arabidopsis Protein Phosphorylated in Response to Microbial Elicitation, AtPHOS32, Is a Substrate of MAP Kinases 3 and 6
inferredcites →https://doi.org/10.1074/mcp.m112.020560openalex-snapshot
Identification of Novel in vivo MAP Kinase Substrates in Arabidopsis thaliana Through Use of Tandem Metal Oxide Affinity Chromatography
inferredcites →https://doi.org/10.1074/mcp.m112.021220openalex-snapshot
Quantitative Phosphoproteomics after Auxin-stimulated Lateral Root Induction Identifies an SNX1 Protein Phosphorylation Site Required for Growth
inferredcites →https://doi.org/10.1074/mcp.m114.040352openalex-snapshot
Quantitative Phosphoproteomics of the Ataxia Telangiectasia-Mutated (ATM) and Ataxia Telangiectasia-Mutated and Rad3-related (ATR) Dependent DNA Damage Response in Arabidopsis thaliana*
inferredcites →https://doi.org/10.1074/mcp.m114.043307openalex-snapshot
Rapid Phosphoproteomic Effects of Abscisic Acid (ABA) on Wild-Type and ABA Receptor-Deficient A. thaliana Mutants*
inferredcites →https://doi.org/10.1074/mcp.m114.047183openalex-snapshot
Quantitative Circadian Phosphoproteomic Analysis of Arabidopsis Reveals Extensive Clock Control of Key Components in Physiological, Metabolic, and Signaling Pathways
inferredcites →https://doi.org/10.1074/mcp.m800466-mcp200openalex-snapshot
In Silico Analysis of Phosphoproteome Data Suggests a Rich-get-richer Process of Phosphosite Accumulation over Evolution
inferredcites →https://doi.org/10.1080/17429145.2012.749433openalex-snapshot
Arabidopsis casein kinase 1-like 2 involved in abscisic acid signal transduction pathways
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/10.1101/gad.299347.117openalex-snapshot
Ectopic application of the repressive histone modification H3K9me2 establishes post-zygotic reproductive isolation in Arabidopsis thaliana
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.109.138677openalex-snapshot
Large-Scale Arabidopsis Phosphoproteome Profiling Reveals Novel Chloroplast Kinase Substrates and Phosphorylation Networks
inferredcites →https://doi.org/10.1104/pp.110.157347openalex-snapshot
Large-Scale Comparative Phosphoproteomics Identifies Conserved Phosphorylation Sites in Plants
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.112.202408openalex-snapshot
Unique Drought Resistance Functions of theHighly ABA-InducedClade A Protein Phosphatase 2Cs
inferredcites →https://doi.org/10.1104/pp.16.00405openalex-snapshot
SUPPRESSOR OF PHYTOCHROME B4-#3 Represses Genes Associated with Auxin Signaling to Modulate Hypocotyl Growth
inferredcites →https://doi.org/10.1104/pp.16.01825openalex-snapshot
Reconstitution of Abscisic Acid Signaling from the Receptor to DNA via bHLH Transcription Factors
inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot
Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid
inferredcites →https://doi.org/10.1105/tpc.16.00078openalex-snapshot
CASEIN KINASE1-LIKE PROTEIN2 Regulates Actin Filament Stability and Stomatal Closure via Phosphorylation of Actin Depolymerizing Factor
inferredcites →https://doi.org/10.1105/tpc.16.00847openalex-snapshot
Protein Phosphatase 2Cs and Microtubule-Associated Stress Protein 1 Control Microtubule Stability, Plant Growth, and Drought Response
inferredcites →https://doi.org/10.1105/tpc.17.00875openalex-snapshot
EAR1 Negatively Regulates ABA Signaling by Enhancing 2C Protein Phosphatase Activity
inferredcites →https://doi.org/10.1105/tpc.18.00250openalex-snapshot
Two Abscisic Acid-Responsive Plastid Lipase Genes Involved in Jasmonic Acid Biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02593.xopenalex-snapshot
Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03488.xopenalex-snapshot
A versatile strategy to define the phosphorylation preferences of plant protein kinases and screen for putative substrates
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04819.xopenalex-snapshot
An efficient Agrobacterium ‐mediated transient transformation of Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.13651openalex-snapshot
Identification and characterization of the phosphatidic acid‐binding A. thaliana phosphoprotein PLD rp1 that is regulated by PLD α1 in a stress‐dependent manner
inferredcites →https://doi.org/10.1126/science.1191132openalex-snapshot
Secreted Peptide Signals Required for Maintenance of Root Stem Cell Niche in Arabidopsis
inferredcites →https://doi.org/10.1126/science.7910981openalex-snapshot
Arabidopsis ABA Response Gene ABI1 : Features of a Calcium-Modulated Protein Phosphatase
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/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1186/s12864-015-1753-4openalex-snapshot
Integrating Phosphoproteomics and Bioinformatics to Study Brassinosteroid-Regulated Phosphorylation Dynamics in Arabidopsis
inferredcites →https://doi.org/10.1199/tab.0166openalex-snapshot
Abscisic Acid Synthesis and Response
inferredcites →https://doi.org/10.1242/dev.119.3.823openalex-snapshot
Formation of the shoot apical meristem in Arabidopsis thaliana: an analysis of development in the wild type and in the shoot meristemless mutant
inferredcites →https://doi.org/10.1371/journal.pone.0181804openalex-snapshot
Coordination of matrix attachment and ATP-dependent chromatin remodeling regulate auxin biosynthesis and Arabidopsis hypocotyl elongation
inferredcites →https://doi.org/10.2144/000113941openalex-snapshot
A 2in1 Cloning System Enables Ratiometric Bimolecular Fluorescence Complementation (rBiFC)
inferredcites →https://doi.org/10.3389/fpls.2015.00484openalex-snapshot
Dynamic proline metabolism: importance and regulation in water limited environments
inferredcites →https://doi.org/10.3389/fpls.2017.00523openalex-snapshot
Comparative Analysis of Phosphoproteome Remodeling After Short Term Water Stress and ABA Treatments versus Longer Term Water Stress Acclimation
inferredcites →https://doi.org/10.3389/fpls.2017.02050openalex-snapshot
Combined 15N-Labeling and TandemMOAC Quantifies Phosphorylation of MAP Kinase Substrates Downstream of MKK7 in Arabidopsis
inferredcites →https://doi.org/10.7554/elife.07811openalex-snapshot
Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems
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.