On the public citation graph
Phosphorylation‐dependent control of an RNA granule‐localized protein that fine‐tunes defence gene expression at a post‐transcriptional level
0 signed · 109 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known work and none has been retracted — and get a dated CiteStamped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/10.1007/978-1-4939-3591-8_12openalex-snapshot
Genome-Wide Profiling of RNA–Protein Interactions Using CLIP-Seq
inferredcites →https://doi.org/10.1016/j.ab.2012.05.015openalex-snapshot
A mutagenesis-based screen to rapidly identify phosphorylation sites in mitogen-activated protein kinase substrates
inferredcites →https://doi.org/10.1016/j.bbagrm.2013.02.003openalex-snapshot
Tristetraprolin (TTP): Interactions with mRNA and proteins, and current thoughts on mechanisms of action
inferredcites →https://doi.org/10.1016/j.cell.2006.03.037openalex-snapshot
Perception of the Bacterial PAMP EF-Tu by the Receptor EFR Restricts Agrobacterium-Mediated Transformation
inferredcites →https://doi.org/10.1016/j.molcel.2007.02.011openalex-snapshot
P Bodies and the Control of mRNA Translation and Degradation
inferredcites →https://doi.org/10.1016/j.molp.2014.12.022openalex-snapshot
Signaling Mechanisms in Pattern-Triggered Immunity (PTI)
inferredcites →https://doi.org/10.1016/j.pbi.2011.05.001openalex-snapshot
Endogenous peptide elicitors in higher plants
inferredcites →https://doi.org/10.1016/j.plantsci.2016.06.014openalex-snapshot
Arginine-rich motif-tandem CCCH zinc finger proteins in plant stress responses and post-transcriptional regulation of gene expression
inferredcites →https://doi.org/10.1016/j.tplants.2014.09.006openalex-snapshot
Modes of MAPK substrate recognition and control
inferredcites →https://doi.org/10.1038/emboj.2012.56openalex-snapshot
Dehydration stress activates Arabidopsis MPK6 to signal DCP1 phosphorylation
inferredcites →https://doi.org/10.1038/nature22371openalex-snapshot
Global translational reprogramming is a fundamental layer of immune regulation in plants
inferredcites →https://doi.org/10.1038/nmeth.3901openalex-snapshot
The Perseus computational platform for comprehensive analysis of (prote)omics data
inferredcites →https://doi.org/10.1038/nrm2694openalex-snapshot
RNA granules: post-transcriptional and epigenetic modulators of gene expression
inferredcites →https://doi.org/10.1042/bj20080625openalex-snapshot
Arabidopsis MAPKs: a complex signalling network involved in multiple biological processes
inferredcites →https://doi.org/10.1073/pnas.0810206106openalex-snapshot
Flg22 regulates the release of an ethylene response factor substrate from MAP kinase 6 in Arabidopsis thaliana via ethylene signaling
inferredcites →https://doi.org/10.1073/pnas.0906131106openalex-snapshot
Profiling translatomes of discrete cell populations resolves altered cellular priorities during hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1314851111openalex-snapshot
Selective mRNA sequestration by OLIGOURIDYLATE-BINDING PROTEIN 1 contributes to translational control during hypoxia in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.275.11.7521openalex-snapshot
Microbial Elicitors Induce Activation and Dual Phosphorylation of the Arabidopsis thaliana MAPK 6
inferredcites →https://doi.org/10.1074/jbc.m310486200openalex-snapshot
MAPKAP Kinase 2 Phosphorylates Tristetraprolin on in Vivo Sites Including Ser178, a Site Required for 14-3-3 Binding
inferredcites →https://doi.org/10.1074/mcp.m500007-mcp200openalex-snapshot
High Throughput Identification of Potential Arabidopsis Mitogen-activated Protein Kinases Substrates
inferredcites →https://doi.org/10.1080/15476286.2015.1017242openalex-snapshot
Probing the closed-loop model of mRNA translation in living cells
inferredcites →https://doi.org/10.1083/jcb.200502088openalex-snapshot
Stress granules and processing bodies are dynamically linked sites of mRNP remodeling
inferredcites →https://doi.org/10.1093/jxb/erw042openalex-snapshot
NB-LRR signaling induces translational repression of viral transcripts and the formation of RNA processing bodies through mechanisms differing from those activated by UV stress and RNAi
inferredcites →https://doi.org/10.1093/nar/gks285openalex-snapshot
A rapid method for assessing the RNA-binding potential of a protein
inferredcites →https://doi.org/10.1093/nar/gkv007openalex-snapshot
limma powers differential expression analyses for RNA-sequencing and microarray studies
inferredcites →https://doi.org/10.1093/pcp/pct175openalex-snapshot
The Arabidopsis Tandem Zinc Finger 9 Protein Binds RNA and Mediates Pathogen-Associated Molecular Pattern-Triggered Immune Responses
inferredcites →https://doi.org/10.1093/pcp/pcu074openalex-snapshot
Tandem CCCH Zinc Finger Proteins in Plant Growth, Development and Stress Response
inferredcites →https://doi.org/10.1094/mpmi-11-11-0281openalex-snapshot
Activation of the Arabidopsis thaliana Mitogen-Activated Protein Kinase MPK11 by the Flagellin-Derived Elicitor Peptide, flg22
inferredcites →https://doi.org/10.1094/mpmi-11-15-0246-ropenalex-snapshot
Arabidopsis TAF15b Localizes to RNA Processing Bodies and Contributes to snc1 -Mediated Autoimmunity
inferredcites →https://doi.org/10.1104/pp.109.145656openalex-snapshot
The Arabidopsis Tandem Zinc Finger Protein AtTZF1 Traffics between the Nucleus and Cytoplasmic Foci and Binds Both DNA and RNA
inferredcites →https://doi.org/10.1104/pp.17.01468openalex-snapshot
Polysomes, Stress Granules, and Processing Bodies: A Dynamic Triumvirate Controlling Cytoplasmic mRNA Fate and Function
inferredcites →https://doi.org/10.1105/tpc.104.026609openalex-snapshot
Phosphorylation of 1-Aminocyclopropane-1-Carboxylic Acid Synthase by MPK6, a Stress-Responsive Mitogen-Activated Protein Kinase, Induces Ethylene Biosynthesis in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.106.047605openalex-snapshot
Arabidopsis DCP2, DCP1, and VARICOSE Form a Decapping Complex Required for Postembryonic Development
inferredcites →https://doi.org/10.1105/tpc.112.109074openalex-snapshot
Phosphorylation of an ERF Transcription Factor by Arabidopsis MPK3/MPK6 Regulates Plant Defense Gene Induction and Fungal Resistance
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02617.xopenalex-snapshot
Gateway‐compatible vectors for plant functional genomics and proteomics
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03623.xopenalex-snapshot
Plant stress granules and mRNA processing bodies are distinct from heat stress granules
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02838.xopenalex-snapshot
GhZFP1, a novel CCCH‐type zinc finger protein from cotton, enhances salt stress tolerance and fungal disease resistance in transgenic tobacco by interacting with GZIRD21A and GZIPR5
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/nph.12817openalex-snapshot
The A rabidopsis thaliana mitogen‐activated protein kinases MPK 3 and MPK 6 target a subclass of ‘ VQ ‐motif’‐containing proteins to regulate immune responses
inferredcites →https://doi.org/10.1126/science.1162263openalex-snapshot
Arabidopsis Stomatal Initiation Is Controlled by MAPK-Mediated Regulation of the bHLH SPEECHLESS
inferredcites →https://doi.org/10.1128/mcb.00717-10openalex-snapshot
Phosphorylation of Tristetraprolin by MK2 Impairs AU-Rich Element mRNA Decay by Preventing Deadenylase Recruitment
inferredcites →https://doi.org/10.1128/mcb.26.6.2399-2407.2006openalex-snapshot
Mitogen-Activated Protein Kinase-Activated Protein Kinase 2 Regulates Tumor Necrosis Factor mRNA Stability and Translation Mainly by Altering Tristetraprolin Expression, Stability, and Binding to Adenine/Uridine-Rich Element
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112252openalex-snapshot
Mitogen-Activated Protein Kinase Signaling in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105346openalex-snapshot
A Renaissance of Elicitors: Perception of Microbe-Associated Molecular Patterns and Danger Signals by Pattern-Recognition Receptors
inferredcites →https://doi.org/10.1186/1471-2229-10-97openalex-snapshot
Regulation of Arabidopsis defense responses against Spodoptera littoralisby CPK-mediated calcium signaling
inferredcites →https://doi.org/10.1186/1746-4811-2-16openalex-snapshot
An improved method for preparing Agrobacterium cells that simplifies the Arabidopsis transformation protocol
inferredcites →https://doi.org/10.1186/s13059-017-1261-8openalex-snapshot
MAPK-triggered chromatin reprogramming by histone deacetylase in plant innate immunity
inferredcites →https://doi.org/10.1371/journal.pgen.1002767openalex-snapshot
Dual-Level Regulation of ACC Synthase Activity by MPK3/MPK6 Cascade and Its Downstream WRKY Transcription Factor during Ethylene Induction in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0009588openalex-snapshot
Phosphorylation of Human Tristetraprolin in Response to Its Interaction with the Cbl Interacting Protein CIN85
inferredcites →https://doi.org/10.1371/journal.pone.0041313openalex-snapshot
Tristetraprolin Inhibits Poly(A)-Tail Synthesis in Nuclear mRNA that Contains AU-Rich Elements by Interacting with Poly(A)-Binding Protein Nuclear 1
inferredcites →https://doi.org/10.1371/journal.pone.0151574openalex-snapshot
Plant Tandem CCCH Zinc Finger Proteins Interact with ABA, Drought, and Stress Response Regulators in Processing-Bodies and Stress Granules
inferredcites →https://doi.org/10.15252/embj.201488645openalex-snapshot
The mRNA decay factor PAT1 functions in a pathway including MAP kinase 4 and immune receptor SUMM2
inferredcites →https://doi.org/10.3389/fpls.2014.00201openalex-snapshot
Composition and function of P bodies in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2014.00554openalex-snapshot
Sustained mitogen-activated protein kinase activation reprograms defense metabolism and phosphoprotein profile in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2015.00940openalex-snapshot
Cellular reprogramming through mitogen-activated protein kinases
inferredcites →https://doi.org/10.3389/fpls.2016.00061openalex-snapshot
Regulation of WRKY46 Transcription Factor Function by Mitogen-Activated Protein Kinases in Arabidopsis thaliana
inferredcites →https://doi.org/10.4161/15592324.2014.976155openalex-snapshot
Identification of additional MAP kinases activated upon PAMP treatment
inferredcites →https://doi.org/10.4161/psb.5.2.10988openalex-snapshot
AtTZF gene family localizes to cytoplasmic foci
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4771969openalex-extracted
Modulation of Stress Granule Dynamics by Phosphorylation and Ubiquitination in Plants
inferred← citeshttps://doi.org/10.2139/ssrn.4871974openalex-extracted
Modulation of Stress Granule Dynamics by Phosphorylation and Ubiquitination in Plants
inferred← citeshttps://doi.org/10.1002/tpg2.20510openalex-snapshot
Genome‐wide association study uncovers pea candidate genes and metabolic pathways involved in rust resistance
inferred← citeshttps://doi.org/10.1002/wrna.1597openalex-snapshot
Translational gene regulation in plants: A green new deal
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111162openalex-snapshot
Modulation of stress granule dynamics by phosphorylation and ubiquitination in plants
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.105018openalex-snapshot
Arabidopsis translation initiation factor binding protein CBE1 negatively regulates accumulation of the NADPH oxidase respiratory burst oxidase homolog D
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.09.006openalex-snapshot
Noncanonical mono(ADP-ribosyl)ation of zinc finger SZF proteins counteracts ubiquitination for protein homeostasis in plant immunity
inferred← citeshttps://doi.org/10.1016/j.molp.2020.09.024openalex-snapshot
Reshaping of the Arabidopsis thaliana Proteome Landscape and Co-regulation of Proteins in Development and Immunity
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102374openalex-snapshot
Biomolecular condensates tunes immune signaling at the Host–Pathogen interface
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.006openalex-snapshot
Hydrogen peroxide is involved in strigolactone induced low temperature stress tolerance in rape seedlings (Brassica rapa L.)
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101633openalex-snapshot
Liquid–liquid phase separation at the frontline of plant–pathogen battles
inferred← citeshttps://doi.org/10.1038/s41477-025-02154-yopenalex-snapshot
Pathogen-induced condensation of the guard cell RNA-binding protein SAIR1 fine-tunes translation for immunity
inferred← citeshttps://doi.org/10.1042/ebc20210088openalex-snapshot
What’s new in protein kinase/phosphatase signalling in the control of plant immunity?
inferred← citeshttps://doi.org/10.1080/07388551.2024.2344584openalex-snapshot
A close-up of regulatory networks and signaling pathways of MKK5 in biotic and abiotic stresses
inferred← citeshttps://doi.org/10.1080/15592324.2020.1862564openalex-snapshot
High temperature-mediated disturbance of carbohydrate metabolism and gene expressional regulation in rice: a review
inferred← citeshttps://doi.org/10.1093/hr/uhac177openalex-snapshot
StMPK7 phosphorylates and stabilizes a potato RNA-binding protein StUBA2a/b to enhance plant defence responses
inferred← citeshttps://doi.org/10.1093/jxb/erad050openalex-snapshot
Arabidopsis translation factor eEF1Bγ impacts plant development and is associated with heat-induced cytoplasmic foci
inferred← citeshttps://doi.org/10.1093/plcell/koab240openalex-snapshot
The emerging role of biomolecular condensates in plant immunity
inferred← citeshttps://doi.org/10.1093/plphys/kiac387openalex-snapshot
The trans-Golgi-localized protein BICAT3 regulates manganese allocation and matrix polysaccharide biosynthesis
inferred← citeshttps://doi.org/10.1093/plphys/kiag134openalex-snapshot
DDX6-like RNA helicases compromise salt-stress tolerance by facilitating mRNA decapping activity in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2022.01.27.478037openalex-snapshot
Arabidopsis CONSERVED BINDING OF EIF4E1 negatively regulates the NADPH oxidase RESPIRATORY BURST OXIDASE HOMOLOG D
inferred← citeshttps://doi.org/10.1101/2023.03.31.535076openalex-snapshot
Changes in Protein Turn-over rates Regulate Tryptophan and Glucosinolate Biosynthesis, IAA Transport and Photosynthesis in Arabidopsis Growth and Defense Transitions
inferred← citeshttps://doi.org/10.1111/nph.70593openalex-snapshot
The role of post‐translational modifications in the dynamics of cytoplasmic biomolecular condensates in plants
inferred← citeshttps://doi.org/10.1111/pce.14374openalex-snapshot
Comparative analysis of wild‐type accessions reveals novel determinants of Arabidopsis seed longevity
inferred← citeshttps://doi.org/10.1111/tpj.14738openalex-snapshot
Believe your GFP: cytoplasmic RNA granules play a role in plant defence
inferred← citeshttps://doi.org/10.1186/s12915-023-01739-3openalex-snapshot
Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.15252/embr.202051656openalex-snapshot
Get closer and make hotspots: liquid–liquid phase separation in plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.802337openalex-snapshot
RNA Binding Protein OsTZF7 Traffics Between the Nucleus and Processing Bodies/Stress Granules and Positively Regulates Drought Stress in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2022.932793openalex-snapshot
Highly Overexpressed AtC3H18 Impairs Microgametogenesis via Promoting the Continuous Assembly of mRNP Granules
inferred← citeshttps://doi.org/10.3390/genes11111287openalex-snapshot
Overexpression of Two CCCH-type Zinc-Finger Protein Genes Leads to Pollen Abortion in Brassica campestris ssp. chinensis
inferred← citeshttps://doi.org/10.3390/ijms21176428openalex-snapshot
BcMF30a and BcMF30c, Two Novel Non-Tandem CCCH Zinc-Finger Proteins, Function in Pollen Development and Pollen Germination in Brassica campestris ssp. chinensis
inferred← citeshttps://doi.org/10.3390/ijms242316862openalex-snapshot
Heterologous Expression of Two Brassica campestris CCCH Zinc-Finger Proteins in Arabidopsis Induces Cytoplasmic Foci and Causes Pollen Abortion
inferred← citeshttps://doi.org/10.3390/plants9091122openalex-snapshot
Dynamics and Functions of Stress Granules and Processing Bodies in Plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.24531942openalex-snapshot
Additional file 1 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.24532326openalex-snapshot
Additional file 2 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637633openalex-snapshot
Additional file 3 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637636openalex-snapshot
Additional file 4 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637639openalex-snapshot
Additional file 5 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637642openalex-snapshot
Additional file 6 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637645openalex-snapshot
Additional file 7 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637648openalex-snapshot
Additional file 8 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637651openalex-snapshot
Additional file 9 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637654openalex-snapshot
Additional file 10 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637657openalex-snapshot
Additional file 11 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637660openalex-snapshot
Additional file 12 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637663openalex-snapshot
Additional file 13 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26637666openalex-snapshot
Additional file 14 of Changing turn-over rates regulate abundance of tryptophan, GS biosynthesis, IAA transport and photosynthesis proteins in Arabidopsis growth defense transitions
inferred← citeshttps://doi.org/10.64898/2026.08.19.745790openalex-snapshot
MO25 binds CBL-interacting protein kinases associated with ribonucleoprotein condensates and regulates meiotic exit
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.