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A theoretical study on the cross-talk of stress regulatory pathways in root cells

https://doi.org/10.1016/j.bpc.2018.06.004

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What this work says

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

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Systems Biology in Practice

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The dynamics of cell cycle regulation

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Stochastic ecological kinetics of regime shifts in a time‐delayed lake eutrophication ecosystem

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Crosstalk between ABA and auxin signaling pathways in roots of Arabidopsis thaliana (L.) Heynh.

inferredcites →https://doi.org/10.1007/s11103-008-9308-6openalex-snapshot

Interaction between sugar and abscisic acid signalling during early seedling development in Arabidopsis

inferredcites →https://doi.org/10.1007/s11103-008-9389-2openalex-snapshot

Cross-regulatory mechanisms in hormone signaling

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Hormone interactions during lateral root formation

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Plant hormones in interactions with the environment

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Identification of the Molecular Mechanisms for Cell-Fate Selection in Budding Yeast through Mathematical Modeling

inferredcites →https://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot

Abiotic Stress Signaling and Responses in Plants

inferredcites →https://doi.org/10.1016/j.cub.2007.05.018openalex-snapshot

A Receptor-like Kinase Mediates the Response of Arabidopsis Cells to the Inhibition of Cellulose Synthesis

inferredcites →https://doi.org/10.1016/j.ecocom.2015.02.005openalex-snapshot

Noises-induced regime shifts and -enhanced stability under a model of lake approaching eutrophication

inferredcites →https://doi.org/10.1016/j.ecolmodel.2012.03.025openalex-snapshot

Noise and large time delay: Accelerated catastrophic regime shifts in ecosystems

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

ABA perception and signalling

inferredcites →https://doi.org/10.1016/s0092-8674(00)00112-4openalex-snapshot

Signaling Networks

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Sniffers, buzzers, toggles and blinkers: dynamics of regulatory and signaling pathways in the cell

inferredcites →https://doi.org/10.1016/s1360-1385(03)00051-7openalex-snapshot

Dissecting Arabidopsis lateral root development

inferredcites →https://doi.org/10.1038/nature08102openalex-snapshot

Unlimited multistability in multisite phosphorylation systems

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

In vitro reconstitution of an abscisic acid signalling pathway

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.2641043.xopenalex-snapshot

Impaired sucrose‐induction mutants reveal the modulation of sugar‐induced starch biosynthetic gene expression by abscisic acid signalling

inferredcites →https://doi.org/10.1049/iet-syb.2014.0061openalex-snapshot

Crosstalk between pathways enhances the controllability of signalling networks

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.1212547109openalex-snapshot

FERONIA receptor kinase pathway suppresses abscisic acid signaling in Arabidopsis by activating ABI2 phosphatase

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.1609626113openalex-snapshot

Receptor kinase complex transmits RALF peptide signal to inhibit root growth in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.181141598openalex-snapshot

Receptor-like kinases from Arabidopsis form a monophyletic gene family related to animal receptor kinases

inferredcites →https://doi.org/10.1073/pnas.96.14.7821openalex-snapshot

Kinase interaction domain of kinase-associated protein phosphatase, a phosphoprotein-binding domain

inferredcites →https://doi.org/10.1088/1742-5468/2014/12/p12015openalex-snapshot

Delay and noise induced regime shift and enhanced stability in gene expression dynamics

inferredcites →https://doi.org/10.1093/jxb/eru442openalex-snapshot

A mechanism of growth inhibition by abscisic acid in germinating seeds of Arabidopsis thaliana based on inhibition of plasma membrane H+-ATPase and decreased cytosolic pH, K+, and anions

inferredcites →https://doi.org/10.1093/mp/ssu010openalex-snapshot

FERONIA Receptor Kinase Controls Seed Size in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/pcp/pcx048openalex-snapshot

FERONIA Receptor Kinase at the Crossroads of Hormone Signaling and Stress Responses

inferredcites →https://doi.org/10.1101/gad.1945410openalex-snapshot

Classic and contemporary approaches to modeling biochemical reactions

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/gad.220402openalex-snapshot

The Arabidopsis kinase-associated protein phosphatase controls internalization of the somatic embryogenesis receptor kinase 1

inferredcites →https://doi.org/10.1104/pp.105.063503openalex-snapshot

Ethylene Inhibits Abscisic Acid-Induced Stomatal Closure in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.17.01206openalex-snapshot

The sHSP22 Heat Shock Protein Requires the ABI1 Protein Phosphatase to Modulate Polar Auxin Transport and Downstream Responses

inferredcites →https://doi.org/10.1104/pp.90.2.463openalex-snapshot

In Vivo Inhibition of Seed Development and Reserve Protein Accumulation in Recombinants of Abscisic Acid Biosynthesis and Responsiveness Mutants in Arabidopsis thaliana

inferredcites →https://doi.org/10.1105/tpc.010441openalex-snapshot

Abscisic Acid Signaling in Seeds and Seedlings

inferredcites →https://doi.org/10.1105/tpc.112.098707openalex-snapshot

DEXH Box RNA Helicase–Mediated Mitochondrial Reactive Oxygen Species Production in Arabidopsis Mediates Crosstalk between Abscisic Acid and Auxin Signaling

inferredcites →https://doi.org/10.1105/tpc.112.100107openalex-snapshot

A Plasma Membrane Receptor Kinase, GHR1, Mediates Abscisic Acid- and Hydrogen Peroxide-Regulated Stomatal Movement 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.1244454openalex-snapshot

A Peptide Hormone and Its Receptor Protein Kinase Regulate Plant Cell Expansion

inferredcites →https://doi.org/10.1142/s0217979214502233openalex-snapshot

Noises-induced toggle switch and stability in a gene regulation network

inferredcites →https://doi.org/10.1142/s0218339007002295openalex-snapshot

GENERIC ENZYMATIC RATE EQUATION UNDER LIVING CONDITIONS

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-arplant-042811-105449openalex-snapshot

Growth Control and Cell Wall Signaling in Plants

inferredcites →https://doi.org/10.1186/1471-2202-7-s1-s10openalex-snapshot

Mathematical modeling of intracellular signaling pathways

inferredcites →https://doi.org/10.1186/1752-0509-6-146openalex-snapshot

Compound stress response in stomatal closure: a mathematical model of ABA and ethylene interaction in guard cells

inferredcites →https://doi.org/10.1242/dev.02027openalex-snapshot

Functional redundancy of PIN proteins is accompanied by auxin-dependent cross-regulation of PIN expression

inferredcites →https://doi.org/10.1371/journal.pgen.1006947openalex-snapshot

SCFAtPP2-B11 modulates ABA signaling by facilitating SnRK2.3 degradation in Arabidopsis thaliana

inferredcites →https://doi.org/10.1371/journal.pone.0171065openalex-snapshot

A mathematical model of the interaction of abscisic acid, ethylene and methyl jasmonate on stomatal closure in plants

inferredcites →https://doi.org/10.1529/biophysj.106.090084openalex-snapshot

Mathematical Models of Specificity in Cell Signaling

inferredcites →https://doi.org/10.3389/fpls.2014.00113openalex-snapshot

Sugar sensing and signaling in plants

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.4693224openalex-extracted

1+1<2: Evidence from Combined Stress of Sesuvium Portulacastrum L

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109404openalex-snapshot

1+1<2: Combined effect of low temperature stress and salt stress on Sesuvium portulacastrum L.

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