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Stress-related biomolecular condensates in plants

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What this work says

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

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Interactions with Aromatic Rings in Chemical and Biological Recognition
inferredcites →https://doi.org/10.1002/bies.201600042openalex-snapshot
Are aberrant phase transitions a driver of cellular aging?
inferredcites →https://doi.org/10.1002/jmr.1061openalex-snapshot
SVM based prediction of RNA‐binding proteins using binding residues and evolutionary information
inferredcites →https://doi.org/10.1007/164_2015_40openalex-snapshot
Discovery and Roles of 2′,3′-cAMP in Biological Systems
inferredcites →https://doi.org/10.1007/s40610-017-0053-yopenalex-snapshot
Assembly of Dynamic P450-Mediated Metabolons—Order Versus Chaos
inferredcites →https://doi.org/10.1016/j.bbadis.2016.12.022openalex-snapshot
Cytoplasmic stress granules: Dynamic modulators of cell signaling and disease
inferredcites →https://doi.org/10.1016/j.bbamem.2009.12.023openalex-snapshot
Vesicles with charged domains
inferredcites →https://doi.org/10.1016/j.cell.2012.04.016openalex-snapshot
Cell-free Formation of RNA Granules: Bound RNAs Identify Features and Components of Cellular Assemblies
inferredcites →https://doi.org/10.1016/j.cell.2013.05.039openalex-snapshot
The Hallmarks of Aging
inferredcites →https://doi.org/10.1016/j.cell.2015.07.047openalex-snapshot
A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation
inferredcites →https://doi.org/10.1016/j.cell.2015.12.038openalex-snapshot
ATPase-Modulated Stress Granules Contain a Diverse Proteome and Substructure
inferredcites →https://doi.org/10.1016/j.cell.2017.08.008openalex-snapshot
The Eukaryotic CO2-Concentrating Organelle Is Liquid-like and Exhibits Dynamic Reorganization
inferredcites →https://doi.org/10.1016/j.cell.2017.12.032openalex-snapshot
Context-Dependent and Disease-Specific Diversity in Protein Interactions within Stress Granules
inferredcites →https://doi.org/10.1016/j.cell.2018.06.006openalex-snapshot
A Molecular Grammar Governing the Driving Forces for Phase Separation of Prion-like RNA Binding Proteins
inferredcites →https://doi.org/10.1016/j.cell.2019.12.031openalex-snapshot
Modulation of RNA Condensation by the DEAD-Box Protein eIF4A
inferredcites →https://doi.org/10.1016/j.cell.2020.03.046openalex-snapshot
G3BP1 Is a Tunable Switch that Triggers Phase Separation to Assemble Stress Granules
inferredcites →https://doi.org/10.1016/j.cell.2020.03.050openalex-snapshot
Competing Protein-RNA Interaction Networks Control Multiphase Intracellular Organization
inferredcites →https://doi.org/10.1016/j.cell.2020.04.009openalex-snapshot
Condensation of Ded1p Promotes a Translational Switch from Housekeeping to Stress Protein Production
inferredcites →https://doi.org/10.1016/j.cell.2020.07.016openalex-snapshot
Formation of NPR1 Condensates Promotes Cell Survival during the Plant Immune Response
inferredcites →https://doi.org/10.1016/j.cell.2020.11.010openalex-snapshot
Single-Molecule Imaging Reveals Translation of mRNAs Localized to Stress Granules
inferredcites →https://doi.org/10.1016/j.cell.2021.06.009openalex-snapshot
A prion-like protein regulator of seed germination undergoes hydration-dependent phase separation
inferredcites →https://doi.org/10.1016/j.cell.2022.04.032openalex-snapshot
TIR domains of plant immune receptors are 2′,3′-cAMP/cGMP synthetases mediating cell death
inferredcites →https://doi.org/10.1016/j.celrep.2017.06.082openalex-snapshot
Glycolytic Enzymes Coalesce in G Bodies under Hypoxic Stress
inferredcites →https://doi.org/10.1016/j.cels.2018.05.002openalex-snapshot
Protein Phase Separation Provides Long-Term Memory of Transient Spatial Stimuli
inferredcites →https://doi.org/10.1016/j.cub.2019.12.020openalex-snapshot
UBAP2L Forms Distinct Cores that Act in Nucleating Stress Granules Upstream of G3BP1
inferredcites →https://doi.org/10.1016/j.devcel.2020.09.010openalex-snapshot
Emerging Roles for Phase Separation in Plants
inferredcites →https://doi.org/10.1016/j.devcel.2020.09.023openalex-snapshot
Phase Separation—A Physical Mechanism for Organizing Information and Biochemical Reactions
inferredcites →https://doi.org/10.1016/j.devcel.2022.02.005openalex-snapshot
Liquid-liquid phase separation of RBGD2/4 is required for heat stress resistance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.febslet.2011.05.066openalex-snapshot
Förster resonance energy transfer demonstrates a flavonoid metabolon in living plant cells that displays competitive interactions between enzymes
inferredcites →https://doi.org/10.1016/j.jbc.2022.101845openalex-snapshot
Purine biosynthetic enzymes assemble into liquid-like condensates dependent on the activity of chaperone protein HSP90
inferredcites →https://doi.org/10.1016/j.jmb.2018.06.023openalex-snapshot
Mechanics, Structure and Function of Biopolymer Condensates
inferredcites →https://doi.org/10.1016/j.jmb.2018.08.003openalex-snapshot
Who's In and Who's Out—Compositional Control of Biomolecular Condensates
inferredcites →https://doi.org/10.1016/j.jmb.2018.08.005openalex-snapshot
Multiple Modes of Protein–Protein Interactions Promote RNP Granule Assembly
inferredcites →https://doi.org/10.1016/j.molcel.2015.01.013openalex-snapshot
Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles
inferredcites →https://doi.org/10.1016/j.molcel.2017.09.003openalex-snapshot
P-Body Purification Reveals the Condensation of Repressed mRNA Regulons
inferredcites →https://doi.org/10.1016/j.molcel.2019.06.044openalex-snapshot
Nucleo-cytoplasmic Partitioning of ARF Proteins Controls Auxin Responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.molcel.2019.09.014openalex-snapshot
Properties of Stress Granule and P-Body Proteomes
inferredcites →https://doi.org/10.1016/j.molcel.2019.12.026openalex-snapshot
Liquidity Is a Critical Determinant for Selective Autophagy of Protein Condensates
inferredcites →https://doi.org/10.1016/j.molcel.2020.10.032openalex-snapshot
Spatiotemporal Proteomic Analysis of Stress Granule Disassembly Using APEX Reveals Regulation by SUMOylation and Links to ALS Pathogenesis
inferredcites →https://doi.org/10.1016/j.molcel.2022.02.035openalex-snapshot
Lipid-mediated phase separation of AGO proteins on the ER controls nascent-peptide ubiquitination
inferredcites →https://doi.org/10.1016/j.molcel.2022.05.014openalex-snapshot
Stressful steps: Progress and challenges in understanding stress-induced mRNA condensation and accumulation in stress granules
inferredcites →https://doi.org/10.1016/j.neuron.2015.10.030openalex-snapshot
ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function
inferredcites →https://doi.org/10.1016/j.neuron.2019.05.048openalex-snapshot
Small-Molecule Modulation of TDP-43 Recruitment to Stress Granules Prevents Persistent TDP-43 Accumulation in ALS/FTD
inferredcites →https://doi.org/10.1016/j.pbi.2020.08.006openalex-snapshot
Biomolecular condensates in photosynthesis and metabolism
inferredcites →https://doi.org/10.1016/j.semcdb.2022.11.008openalex-snapshot
Composition and function of stress granules and P-bodies in plants
inferredcites →https://doi.org/10.1016/j.stem.2019.08.018openalex-snapshot
The RNA Helicase DDX6 Controls Cellular Plasticity by Modulating P-Body Homeostasis
inferredcites →https://doi.org/10.1016/j.tcb.2016.05.004openalex-snapshot
Principles and Properties of Stress Granules
inferredcites →https://doi.org/10.1016/j.tibs.2020.04.011openalex-snapshot
Making the Case for Disordered Proteins and Biomolecular Condensates in Bacteria
inferredcites →https://doi.org/10.1016/j.tips.2022.07.001openalex-snapshot
Biomolecular condensates: new opportunities for drug discovery and RNA therapeutics
inferredcites →https://doi.org/10.1016/s0021-9258(19)75707-xopenalex-snapshot
Further characterization of the Krebs tricarboxylic acid cycle metabolon.
inferredcites →https://doi.org/10.1016/s1534-5807(01)00077-6openalex-snapshot
Auxin Signaling
inferredcites →https://doi.org/10.1021/acs.biochem.7b01162openalex-snapshot
P-Bodies: Composition, Properties, and Functions
inferredcites →https://doi.org/10.1021/acs.chemrev.1c00774openalex-snapshot
Conformational Dynamics of Intrinsically Disordered Proteins Regulate Biomolecular Condensate Chemistry
inferredcites →https://doi.org/10.1021/acs.chemrev.2c00608openalex-snapshot
A New Phase of Networking: The Molecular Composition and Regulatory Dynamics of Mammalian Stress Granules
inferredcites →https://doi.org/10.1021/cb500798yopenalex-snapshot
Classification of Chemical Chaperones Based on Their Effect on Protein Folding Landscapes
inferredcites →https://doi.org/10.1038/emboj.2012.20openalex-snapshot
Cytoplasmic Arabidopsis AGO7 accumulates in membrane‐associated siRNA bodies and is required for ta‐siRNA biogenesis
inferredcites →https://doi.org/10.1038/nature10879openalex-snapshot
Phase transitions in the assembly of multivalent signalling proteins
inferredcites →https://doi.org/10.1038/ncomms12399openalex-snapshot
Characterization of a recently evolved flavonol-phenylacyltransferase gene provides signatures of natural light selection in Brassicaceae
inferredcites →https://doi.org/10.1038/nrm.2017.7openalex-snapshot
Biomolecular condensates: organizers of cellular biochemistry
inferredcites →https://doi.org/10.1038/nrmicro.2018.10openalex-snapshot
Bacterial microcompartments
inferredcites →https://doi.org/10.1038/s41467-018-04543-8openalex-snapshot
The role of dynamic enzyme assemblies and substrate channelling in metabolic regulation
inferredcites →https://doi.org/10.1038/s41467-020-18234-wopenalex-snapshot
A moonlighting role for enzymes of glycolysis in the co-localization of mitochondria and chloroplasts
inferredcites →https://doi.org/10.1038/s41467-021-21181-9openalex-snapshot
Reentrant liquid condensate phase of proteins is stabilized by hydrophobic and non-ionic interactions
inferredcites →https://doi.org/10.1038/s41477-020-0681-8openalex-snapshot
DHH1/DDX6-like RNA helicases maintain ephemeral half-lives of stress-response mRNAs
inferredcites →https://doi.org/10.1038/s41477-021-00867-4openalex-snapshot
Ribosome stalling and SGS3 phase separation prime the epigenetic silencing of transposons
inferredcites →https://doi.org/10.1038/s41477-022-01175-1openalex-snapshot
ALBA proteins confer thermotolerance through stabilizing HSF messenger RNAs in cytoplasmic granules
inferredcites →https://doi.org/10.1038/s41556-021-00760-4openalex-snapshot
Reversible amyloids of pyruvate kinase couple cell metabolism and stress granule disassembly
inferredcites →https://doi.org/10.1038/s41556-022-00892-1openalex-snapshot
Membranes regulate biomolecular condensates
inferredcites →https://doi.org/10.1038/s41565-020-0731-4openalex-snapshot
Biomolecular condensates undergo a generic shear-mediated liquid-to-solid transition
inferredcites →https://doi.org/10.1038/s41573-022-00505-4openalex-snapshot
Modulating biomolecular condensates: a novel approach to drug discovery
inferredcites →https://doi.org/10.1038/s41580-020-00326-6openalex-snapshot
Biomolecular condensates at the nexus of cellular stress, protein aggregation disease and ageing
inferredcites →https://doi.org/10.1038/s41586-019-1165-8openalex-snapshot
Arabidopsis FLL2 promotes liquid–liquid phase separation of polyadenylation complexes
inferredcites →https://doi.org/10.1038/s41586-020-2256-2openalex-snapshot
Composition-dependent thermodynamics of intracellular phase separation
inferredcites →https://doi.org/10.1038/s41586-021-03572-6openalex-snapshot
A phase-separated nuclear GBPL circuit controls immunity in plants
inferredcites →https://doi.org/10.1038/s41586-022-04902-yopenalex-snapshot
Increasing the resilience of plant immunity to a warming climate
inferredcites →https://doi.org/10.1038/s41589-021-00801-xopenalex-snapshot
Mechanistic dissection of increased enzymatic rate in a phase-separated compartment
inferredcites →https://doi.org/10.1038/s41594-019-0250-xopenalex-snapshot
Molecular interactions underlying liquid−liquid phase separation of the FUS low-complexity domain
inferredcites →https://doi.org/10.1038/s41598-022-08130-2openalex-snapshot
Kinetic interplay between droplet maturation and coalescence modulates shape of aged protein condensates
inferredcites →https://doi.org/10.1073/pnas.1703139114openalex-snapshot
Arabidopsis m 6 A demethylase activity modulates viral infection of a plant virus and the m 6 A abundance in its genomic RNAs
inferredcites →https://doi.org/10.1073/pnas.1922284117openalex-snapshot
InsP 7 is a small-molecule regulator of NUDT3-mediated mRNA decapping and processing-body dynamics
inferredcites →https://doi.org/10.1073/pnas.2000223117openalex-snapshot
Identifying sequence perturbations to an intrinsically disordered protein that determine its phase-separation behavior
inferredcites →https://doi.org/10.1073/pnas.2017435118openalex-snapshot
Membrane bending by protein phase separation
inferredcites →https://doi.org/10.1073/pnas.96.22.12929openalex-snapshot
Interactions among enzymes of the Arabidopsis flavonoid biosynthetic pathway
inferredcites →https://doi.org/10.1074/jbc.ac117.001037openalex-snapshot
TAR DNA-binding protein 43 (TDP-43) liquid–liquid phase separation is mediated by just a few aromatic residues
inferredcites →https://doi.org/10.1074/jbc.m117.783050openalex-snapshot
Identification of a multienzyme complex for glucose metabolism in living cells
inferredcites →https://doi.org/10.1074/jbc.tm118.001192openalex-snapshot
The molecular language of membraneless organelles
inferredcites →https://doi.org/10.1083/jcb.201411047openalex-snapshot
YB-1 regulates stress granule formation and tumor progression by translationally activating G3BP1
inferredcites →https://doi.org/10.1083/jcb.201904141openalex-snapshot
Conserved metabolite regulation of stress granule assembly via AdoMet
inferredcites →https://doi.org/10.1083/jcb.202103175openalex-snapshot
Intracellular wetting mediates contacts between liquid compartments and membrane-bound organelles
inferredcites →https://doi.org/10.1083/jcb.202211015openalex-snapshot
Liquid–liquid phase separation drives herpesvirus assembly in the cytoplasm
inferredcites →https://doi.org/10.1091/mbc.e15-03-0136openalex-snapshot
P-body assembly requires DDX6 repression complexes rather than decay or Ataxin2/2L complexes
inferredcites →https://doi.org/10.1093/jmcb/mjaa075openalex-snapshot
Observation of an α-synuclein liquid droplet state and its maturation into Lewy body-like assemblies
inferredcites →https://doi.org/10.1093/jxb/erac497openalex-snapshot
Concentrating and sequestering biomolecules in condensates: impact on plant biology
inferredcites →https://doi.org/10.1093/nar/gku1003openalex-snapshot
STRING v10: protein–protein interaction networks, integrated over the tree of life
inferredcites →https://doi.org/10.1093/nar/gkv119openalex-snapshot
In plants, decapping prevents RDR6-dependent production of small interfering RNAs from endogenous mRNAs
inferredcites →https://doi.org/10.1093/nar/gkx353openalex-snapshot
A synergistic network of interactions promotes the formation of in vitro processing bodies and protects mRNA against decapping
inferredcites →https://doi.org/10.1093/nar/gky1085openalex-snapshot
eggNOG 5.0: a hierarchical, functionally and phylogenetically annotated orthology resource based on 5090 organisms and 2502 viruses
inferredcites →https://doi.org/10.1093/plcell/koac132openalex-snapshot
Arabidopsis RNA processing body components LSM1 and DCP5 aid in the evasion of translational repression during Cauliflower mosaic virus infection
inferredcites →https://doi.org/10.1093/plphys/kiab529openalex-snapshot
A NYN domain protein directly interacts with DECAPPING1 and is required for phyllotactic pattern
inferredcites →https://doi.org/10.1093/plphys/kiac013openalex-snapshot
2',3'-cAMP treatment mimics the stress molecular response in Arabidopsis thaliana.
inferredcites →https://doi.org/10.1098/rsob.210137openalex-snapshot
Higher-order organization of biomolecular condensates
inferredcites →https://doi.org/10.1104/pp.15.01407openalex-snapshot
Arabidopsis CML38, a Calcium Sensor That Localizes to Ribonucleoprotein Complexes under Hypoxia Stress
inferredcites →https://doi.org/10.1104/pp.18.00285openalex-snapshot
Interaction of 2',3'-cAMP with Rbp47b plays a role in stress granule formation
inferredcites →https://doi.org/10.1105/tpc.11.8.1537openalex-snapshot
Transgene-Mediated and Elicitor-Induced Perturbation of Metabolic Channeling at the Entry Point into the Phenylpropanoid Pathway
inferredcites →https://doi.org/10.1105/tpc.112.106989openalex-snapshot
Metabolic Fluxes in an Illuminated Arabidopsis Rosette
inferredcites →https://doi.org/10.1105/tpc.114.134494openalex-snapshot
Tudor Staphylococcal Nuclease Links Formation of Stress Granules and Processing Bodies with mRNA Catabolism in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.15.00867openalex-snapshot
The LSM1-7 Complex Differentially Regulates Arabidopsis Tolerance to Abiotic Stress Conditions by Promoting Selective mRNA Decapping
inferredcites →https://doi.org/10.1111/bph.14790openalex-snapshot
Stress granule: A promising target for cancer treatment
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02344.xopenalex-snapshot
Genomics‐based selection and functional characterization of triterpene glycosyltransferases from the model legume Medicago truncatula
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04655.xopenalex-snapshot
CBP60g and SARD1 play partially redundant critical roles in salicylic acid signaling
inferredcites →https://doi.org/10.1111/nph.15690openalex-snapshot
Protein and metabolite composition of Arabidopsis stress granules
inferredcites →https://doi.org/10.1111/nph.17865openalex-snapshot
Stress granule‐associated TaMBF1c confers thermotolerance through regulating specific mRNA translation in wheat ( Triticum aestivum )
inferredcites →https://doi.org/10.1111/pce.12666openalex-snapshot
Lipid signalling in plant responses to abiotic stress
inferredcites →https://doi.org/10.1111/tpj.12388openalex-snapshot
Enhancement of oxidative and drought tolerance in Arabidopsis by overaccumulation of antioxidant flavonoids
inferredcites →https://doi.org/10.1111/tpj.14022openalex-snapshot
The UPF1 interactome reveals interaction networks between RNA degradation and translation repression factors in Arabidopsis
inferredcites →https://doi.org/10.1111/tra.12704openalex-snapshot
Biomolecular condensates in neurodegeneration and cancer
inferredcites →https://doi.org/10.1126/science.1172046openalex-snapshot
Germline P Granules Are Liquid Droplets That Localize by Controlled Dissolution/Condensation
inferredcites →https://doi.org/10.1126/science.aad9964openalex-snapshot
Phase separation of signaling molecules promotes T cell receptor signal transduction
inferredcites →https://doi.org/10.1126/science.aaf6846openalex-snapshot
ATP as a biological hydrotrope
inferredcites →https://doi.org/10.1126/science.aaz4427openalex-snapshot
Partitioning of cancer therapeutics in nuclear condensates
inferredcites →https://doi.org/10.1140/epje/s10189-021-00118-6openalex-snapshot
Non-equilibrium phase separation in mixtures of catalytically active particles: size dispersity and screening effects
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120129openalex-snapshot
The Structure of Photosystem II and the Mechanism of Water Oxidation in Photosynthesis
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120233openalex-snapshot
The Spatial Organization of Metabolism Within the Plant Cell
inferredcites →https://doi.org/10.1242/jcs.054437openalex-snapshot
Unravelling the ultrastructure of stress granules and associated P-bodies in human cells
inferredcites →https://doi.org/10.1371/journal.pbio.3002305openalex-snapshot
SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.ppat.1006213openalex-snapshot
A calmodulin-like protein suppresses RNA silencing and promotes geminivirus infection by degrading SGS3 via the autophagy pathway in Nicotiana benthamiana
inferredcites →https://doi.org/10.15252/embj.2020105043openalex-snapshot
Tudor staphylococcal nuclease is a docking platform for stress granule components and is essential for SnRK1 activation in Arabidopsis
inferredcites →https://doi.org/10.15252/embj.2021109952openalex-snapshot
On the role of phase separation in the biogenesis of membraneless compartments
inferredcites →https://doi.org/10.15252/embj.2022111885openalex-snapshot
An actin remodeling role for Arabidopsis processing bodies revealed by their proximity interactome
inferredcites →https://doi.org/10.3389/fpls.2017.02093openalex-snapshot
Plant RNA Regulatory Network and RNA Granules in Virus Infection
inferredcites →https://doi.org/10.3389/fpls.2020.595792openalex-snapshot
Identification and Characterization of the Heat-Induced Plastidial Stress Granules Reveal New Insight Into Arabidopsis Stress Response
inferredcites →https://doi.org/10.3389/fpls.2021.722643openalex-snapshot
Plant Stress Granules: Trends and Beyond
inferredcites →https://doi.org/10.3389/fpls.2021.722940openalex-snapshot
Arabidopsis CALMODULIN-LIKE 38 Regulates Hypoxia-Induced Autophagy of SUPPRESSOR OF GENE SILENCING 3 Bodies
inferredcites →https://doi.org/10.3389/fpls.2022.1032045openalex-snapshot
Landscape of biomolecular condensates in heat stress responses
inferredcites →https://doi.org/10.3390/ijms22126287openalex-snapshot
Arabidopsis thaliana G3BP Ortholog Rescues Mammalian Stress Granule Phenotype across Kingdoms
inferredcites →https://doi.org/10.3390/plants9091122openalex-snapshot
Dynamics and Functions of Stress Granules and Processing Bodies in Plants
inferredcites →https://doi.org/10.4161/rna.26851openalex-snapshot
Screening of small molecules affecting mammalian P-body assembly uncovers links with diverse intracellular processes and organelle physiology
inferredcites →https://doi.org/10.7554/elife.18413openalex-snapshot
Distinct stages in stress granule assembly and disassembly
inferredcites →https://doi.org/10.7554/elife.31486openalex-snapshot
Pi-Pi contacts are an overlooked protein feature relevant to phase separation
inferredcites →https://doi.org/10.7554/elife.48480openalex-snapshot
RNA promotes phase separation of glycolysis enzymes into yeast G bodies in hypoxia

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/agt2.725openalex-snapshot
A Vanillin‐Derived Inhibitor of Aggregates via Targeting Intrinsically Disordered Regions of Phytoviral Nucleocapsid Protein
inferred← citeshttps://doi.org/10.1002/bies.202400043openalex-snapshot
Subcellular dynamics of ethylene signaling drive plant plasticity to growth and stress
inferred← citeshttps://doi.org/10.1007/978-1-0716-3973-3_4openalex-snapshot
Isolation and Visualization of Plant Stress Granule-Associated Components via On-Beads Digestion and Co-localization Analysis
inferred← citeshttps://doi.org/10.1007/s11084-026-09721-zopenalex-snapshot
MAPK signaling modulates the partition of DCP1 between processing bodies and stress granules in plant cells
inferred← citeshttps://doi.org/10.1007/s44154-023-00141-xopenalex-snapshot
Liquid-liquid phase separation as a major mechanism of plant abiotic stress sensing and responses
inferred← citeshttps://doi.org/10.1016/j.bbagen.2025.130787openalex-snapshot
Compartmentation of multiple metabolic enzymes and their preparation in vitro and in cellulo
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2026.109051openalex-snapshot
Environmental stress drives dynamic remodeling of the plant condensatome
inferred← citeshttps://doi.org/10.1016/j.bpj.2025.11.2681openalex-snapshot
Biomolecular condensates as cellular memory modules: Thermodynamic principles and plant stress adaptation
inferred← citeshttps://doi.org/10.1016/j.chom.2024.07.013openalex-snapshot
Alleviating protein-condensation-associated damage at the endoplasmic reticulum enhances plant disease tolerance
inferred← citeshttps://doi.org/10.1016/j.chom.2026.02.007openalex-snapshot
Immune activation reprograms growth mRNA stability to shape plant growth-defense trade-offs
inferred← citeshttps://doi.org/10.1016/j.cub.2023.09.037openalex-snapshot
Plant metabolism: A protein map of the photosynthetic organelle
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.12.009openalex-snapshot
FKF1 nuclear condensates control anti-florigen turnover and flowering onset in response to nitrogen availability in monocots
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.2026.111456openalex-snapshot
The Pof1 nicotinamide mononucleotide adenylyl transferase has a non-canonical role in NAD+ metabolism in the budding yeast Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.01.007openalex-snapshot
Transcriptional, epigenetic, and post-translational regulation of plant autophagy
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.137170openalex-snapshot
Nanoplastic-induced antibody liquid-liquid phase separation: Insights into potential immunotoxic implications
inferred← citeshttps://doi.org/10.1016/j.mib.2024.102467openalex-snapshot
Proteomic composition of eukaryotic and bacterial RNA decay condensates suggests convergent evolution
inferred← citeshttps://doi.org/10.1016/j.mocell.2024.100167openalex-snapshot
The disordered effector RipAO of Ralstonia solanacearum destabilizes microtubule networks in Nicotiana benthamiana cells
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.07.033openalex-snapshot
Proteasome resides in and dismantles plant heat stress granules constitutively
inferred← citeshttps://doi.org/10.1016/j.molp.2024.02.016openalex-snapshot
Plant RNA-binding proteins: Phase separation dynamics and functional mechanisms underlying plant development and stress responses
inferred← citeshttps://doi.org/10.1016/j.molp.2025.06.013openalex-snapshot
Targeted protein and protein-condensate degradation in plant science research and crop breeding
inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102697openalex-snapshot
Biomolecular condensates at the plasma membrane: Insights into plant cell signaling
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102881openalex-snapshot
Genetic and epigenetic mechanisms underlying male reproductive thermotolerance
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112200openalex-snapshot
Stress induced factor 2 is a dual regulator for defense and seed germination in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112413openalex-snapshot
Mechanistic insights into DXO1 and XRN3: regulatory roles of RNA stability, transcription, and liquid-liquid phase separation in Arabidopsis thaliana (L.) Heynh.
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108700openalex-snapshot
A synchronized symphony: Intersecting roles of ubiquitin proteasome system and autophagy in cellular degradation
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2026.114171openalex-snapshot
Comprehensive lipidomics analysis reveals the ceramides play an essential role in chilling injury of bell peppers
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100810openalex-snapshot
The role of membrane-biomolecular condensate interactions in stress
inferred← citeshttps://doi.org/10.1016/j.tibtech.2026.03.005openalex-snapshot
Utilizing biomolecular condensates as electrochemical reactors
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.12.010openalex-snapshot
Viral condensates orchestrate plant infection
inferred← citeshttps://doi.org/10.1016/j.tplants.2026.06.010openalex-snapshot
Emerging roles of biomolecular condensation in plant membrane biology
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100663openalex-snapshot
Liquid–liquid phase separation in plants: Advances and perspectives from model species to crops
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101180openalex-snapshot
Nucleo-cytoplasmic distribution of SAP18 reveals its dual function in splicing regulation and heat-stress response in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101229openalex-snapshot
RNA modifications in plant adaptation to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101879openalex-snapshot
The dehydrin protein COR15 enhances antiviral RNA silencing by preventing viral protein-mediated SGS3 degradation and promoting SGS3 condensate formation
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.102024openalex-snapshot
Cell wall dynamics and their regulation by biomolecular condensates in plants
inferred← citeshttps://doi.org/10.1038/s41418-025-01555-yopenalex-snapshot
The role of plant metacaspases in cell death and survival
inferred← citeshttps://doi.org/10.1038/s41422-025-01133-4openalex-snapshot
FUSTer than stress granules: a prion-like domain warns plants of heat
inferred← citeshttps://doi.org/10.1038/s41467-025-56570-xopenalex-snapshot
Genetically-encoded targeted protein degradation technology to remove endogenous condensation-prone proteins and improve crop performance
inferred← citeshttps://doi.org/10.1038/s41467-025-57306-7openalex-snapshot
The adaptor protein AP-3β disassembles heat-induced stress granules via 19S regulatory particle in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41467-025-60771-9openalex-snapshot
Chromatin heterogeneity modulates nuclear condensate dynamics and phase behavior
inferred← citeshttps://doi.org/10.1038/s41467-025-62395-5openalex-snapshot
Viral proteins suppress rice defenses by boosting OsTSN1 RNA decay via phase separation and multimerization
inferred← citeshttps://doi.org/10.1038/s41477-023-01497-8openalex-snapshot
Silencing translation with phenolic acids
inferred← citeshttps://doi.org/10.1038/s41580-026-00977-xopenalex-snapshot
Principles and mechanisms of plant acclimation to heat stress
inferred← citeshttps://doi.org/10.1038/s41586-025-09704-6openalex-snapshot
Florigen activation complex forms via multifaceted assembly in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s44323-025-00036-2openalex-snapshot
Regulatory links between the circadian clock and stress-induced biomolecular condensates
inferred← citeshttps://doi.org/10.1073/pnas.2425689122openalex-snapshot
Biomolecular condensation of ERC1 recruits ATG8 and NBR1 to drive autophagosome formation for plant heat tolerance
inferred← citeshttps://doi.org/10.1093/9780197846032.001.0001openalex-snapshot
Populations of Individuals
inferred← citeshttps://doi.org/10.1093/9780197846032.002.0004openalex-snapshot
Foreword
inferred← citeshttps://doi.org/10.1093/9780197846032.002.0005openalex-snapshot
Preface
inferred← citeshttps://doi.org/10.1093/9780197846032.002.0006openalex-snapshot
Epigraph
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0001openalex-snapshot
Populations of Individuals
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0002openalex-snapshot
Population-based Threshold Models
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0003openalex-snapshot
Origin and Integration of Biological Processes
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0004openalex-snapshot
Microorganisms
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0005openalex-snapshot
Plants
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0006openalex-snapshot
Animals
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0007openalex-snapshot
Developmental Plasticity, Ecology and Evolution
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0008openalex-snapshot
Implications and Anticipations
inferred← citeshttps://doi.org/10.1093/9780197846032.005.0001openalex-snapshot
Methods
inferred← citeshttps://doi.org/10.1093/jxb/erae171openalex-snapshot
Thermal adaptation in plants: understanding the dynamics of translation factors and condensates
inferred← citeshttps://doi.org/10.1093/jxb/eraf190openalex-snapshot
Interplay between membrane system and biomolecular condensates in plant
inferred← citeshttps://doi.org/10.1093/nar/gkaf1522openalex-snapshot
DNA binding and dimerization of the SOG1 NAC domain are functionally linked with its ability to undergo liquid–liquid phase separation
inferred← citeshttps://doi.org/10.1093/plcell/koad172openalex-snapshot
Arabidopsismetacaspase MC1 localizes in stress granules, clears protein aggregates, and delays senescence
inferred← citeshttps://doi.org/10.1093/plcell/koad182openalex-snapshot
Focus on biomolecular condensates
inferred← citeshttps://doi.org/10.1093/plcell/koad254openalex-snapshot
Biomolecular condensates in plant RNA silencing: insights into formation, function, and stress responses
inferred← citeshttps://doi.org/10.1093/plcell/koad288openalex-snapshot
A proxitome-RNA-capture approach reveals that processing bodies repress coregulated hub genes
inferred← citeshttps://doi.org/10.1093/plcell/koae129openalex-snapshot
Erasing marks: Functions of plant deubiquitylating enzymes in modulating the ubiquitin code
inferred← citeshttps://doi.org/10.1093/plcell/koae145openalex-snapshot
A prion-like domain is required for phase separation and chloroplast RNA processing during cold acclimation in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koag019openalex-snapshot
The terminal uridylyltransferase URT1 regulates the transcriptome and primary dormancy of seeds
inferred← citeshttps://doi.org/10.1093/plcell/koag028openalex-snapshot
Molecular determinants underlying NPH3 condensation and function in phototropism: an integrative approach
inferred← citeshttps://doi.org/10.1093/plcell/koag254openalex-snapshot
OsGRP3 deacetylation drives nuclear condensate assembly and transcriptional reprogramming under salt stress
inferred← citeshttps://doi.org/10.1098/rsos.250132openalex-snapshot
Translational reprogramming under heat stress: a plant’s perspective
inferred← citeshttps://doi.org/10.1101/2023.09.29.560215openalex-snapshot
The prion-like domain of the chloroplast RNA binding protein CP29A is required for cold-induced phase separation next to nucleoids and supports RNA splicing and translation during cold acclimation
inferred← citeshttps://doi.org/10.1101/2023.12.13.571504openalex-snapshot
Phosphorylation Promotes Liquid-Liquid Phase Separation of GRP8 and Its Assembly into Stress Granules Upon Salinity Stress in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.01.12.575397openalex-snapshot
Stress Granule Protein TZF1 Enhances Salt Stress Tolerance by Targeting ACA11 mRNA for Degradation in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.10.31.621288openalex-snapshot
MAPK Signaling Modulates the Partition of DCP1 Between P-Bodies and Stress Granules in Plant Cells
inferred← citeshttps://doi.org/10.1101/2024.12.19.629392openalex-snapshot
The TUTase URT1 regulates the transcriptome of seeds and their primary dormancy
inferred← citeshttps://doi.org/10.1111/jipb.13781openalex-snapshot
Reading m6A marks in mRNA: A potent mechanism of gene regulation in plants
inferred← citeshttps://doi.org/10.1111/nph.70524openalex-snapshot
Guanylate‐binding proteins: emerging critical functions in plant development, immunity and stress response
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/nph.71172openalex-snapshot
PWO proteins are associated with PRC2 since their emergence in vascular plants
inferred← citeshttps://doi.org/10.1111/pbi.70082openalex-snapshot
Localising enzymes to biomolecular condensates increases their accumulation and benefits engineered metabolic pathway performance in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1111/pce.70124openalex-snapshot
WRKY Transcription Factors in Rice: Key Regulators Orchestrating Development and Stress Resilience
inferred← citeshttps://doi.org/10.1111/pce.70750openalex-snapshot
Emerging Roles of Biomolecular Condensates and Phase Separation in Plant Stress Adaptation and Gene Regulation
inferred← citeshttps://doi.org/10.1111/tpj.70987openalex-snapshot
PERSPECTIVE : organelle positioning as a principle of metabolic regulation and stress tolerance
inferred← citeshttps://doi.org/10.1126/sciadv.ads3653openalex-snapshot
Phase separation of the poplar microtubule-associated protein PagPCaP1a aids microtubule depolymerization in response to high salt
inferred← citeshttps://doi.org/10.1142/s1793048024300019openalex-snapshot
Biophysical Mechanisms of Liquid–Liquid Phase Separation in Biological Systems
inferred← citeshttps://doi.org/10.1146/annurev-arplant-070725-083459openalex-snapshot
A Multidimensional View of Biomolecular Condensates in Plant Biology
inferred← citeshttps://doi.org/10.1186/s12870-024-05492-9openalex-snapshot
Spermidine augments salt stress resilience in rice roots potentially by enhancing OsbZIP73’s RNA binding capacity
inferred← citeshttps://doi.org/10.3389/fpls.2024.1375478openalex-snapshot
Overexpression of stress granule protein TZF1 enhances salt stress tolerance by targeting ACA11 mRNA for degradation in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2026.1880044openalex-snapshot
Post-transcriptional regulation of light-stress responses and predictive modeling in vegetable Solanaceae Crops
inferred← citeshttps://doi.org/10.3390/ijms27052497openalex-snapshot
From Shared Mechanisms to Precision Breeding: Engineering Cold and Drought Cross-Tolerance in Crops
inferred← citeshttps://doi.org/10.3390/plants15010052openalex-snapshot
Protein Post-Translational Modifications in Plant Abiotic Stress Responses
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
inferred← citeshttps://doi.org/10.70675/47d2b811z34e2z4f02z86f7z13a4b75b907fopenalex-snapshot
Analysis of the response of the nucleus of Arabidopsis thaliana to heat stress
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