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Rice annexin OsANN4 interacting with OsCDPK24, reduces root aerenchyma formation by modulating H 2 O 2 under ABA treatment

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

inferredcites →https://doi.org/10.1007/bf00016490openalex-snapshot
Current advances in abscisic acid action and signalling
inferredcites →https://doi.org/10.1007/bf00397407openalex-snapshot
Electron microscopy of gas space (aerenchyma) formation in adventitious roots of Zea mays L. subjected to oxygen shortage
inferredcites →https://doi.org/10.1007/s00299-011-1201-0openalex-snapshot
Identification and characterization of annexin gene family in rice
inferredcites →https://doi.org/10.1007/s00709-016-0968-9openalex-snapshot
Cadmium-induced changes in antioxidative systems and differentiation in roots of contrasted Medicago truncatula lines
inferredcites →https://doi.org/10.1007/s12298-011-0093-3openalex-snapshot
Lysigenous aerenchyma formation involves non-apoptotic programmed cell death in rice (Oryza sativa L.) roots
inferredcites →https://doi.org/10.1016/j.ceca.2014.10.013openalex-snapshot
Increasing complexity and versatility: How the calcium signaling toolkit was shaped during plant land colonization
inferredcites →https://doi.org/10.1016/j.celrep.2016.11.015openalex-snapshot
L-Met Activates Arabidopsis GLR Ca2+ Channels Upstream of ROS Production and Regulates Stomatal Movement
inferredcites →https://doi.org/10.1016/j.molcel.2017.12.002openalex-snapshot
Reciprocal Regulation of the TOR Kinase and ABA Receptor Balances Plant Growth and Stress Response
inferredcites →https://doi.org/10.1016/j.pbi.2008.06.014openalex-snapshot
The ABA receptors – we report you decide
inferredcites →https://doi.org/10.1016/j.sbi.2010.09.007openalex-snapshot
Thirsty plants and beyond: structural mechanisms of abscisic acid perception and signaling
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot
ROS signaling: the new wave?
inferredcites →https://doi.org/10.1016/s0305-7364(05)80010-1openalex-snapshot
Characterization of maize lines differing in leaf abscisic acid content in the field. 1 abscisic acid physiology
inferredcites →https://doi.org/10.1016/s0981-9428(98)80010-7openalex-snapshot
Immunological and biochemical evidence for nuclear localization of annexin in peas
inferredcites →https://doi.org/10.1016/s1369-5266(03)00090-6openalex-snapshot
Relay and control of abscisic acid signaling
inferredcites →https://doi.org/10.1038/aps.2014.5openalex-snapshot
Abscisic acid perception and signaling: structural mechanisms and applications
inferredcites →https://doi.org/10.1038/cr.2013.149openalex-snapshot
The unique mode of action of a divergent member of the ABA-receptor protein family in ABA and stress signaling
inferredcites →https://doi.org/10.1038/nature08599openalex-snapshot
In vitro reconstitution of an abscisic acid signalling pathway
inferredcites →https://doi.org/10.1038/nature10536openalex-snapshot
Oxygen sensing in plants is mediated by an N-end rule pathway for protein destabilization
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00194.xopenalex-snapshot
Immunolocalization of a novel annexin‐like protein encoded by a stress and abscisic acid responsive gene in alfalfa
inferredcites →https://doi.org/10.1093/aob/mcf114openalex-snapshot
Aerenchyma and an Inducible Barrier to Radial Oxygen Loss Facilitate Root Aeration in Upland, Paddy and Deep-water Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1093/aob/mcq221openalex-snapshot
Contrasting dynamics of radial O2-loss barrier induction and aerenchyma formation in rice roots of two lengths
inferredcites →https://doi.org/10.1093/jxb/erf090openalex-snapshot
Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves
inferredcites →https://doi.org/10.1093/jxb/erm293openalex-snapshot
Nitric oxide, stomatal closure, and abiotic stress
inferredcites →https://doi.org/10.1093/jxb/erq151openalex-snapshot
ABA receptors: the START of a new paradigm in phytohormone signalling
inferredcites →https://doi.org/10.1093/jxb/ers366openalex-snapshot
ZmCPK11 is involved in abscisic acid-induced antioxidant defence and functions upstream of ZmMPK5 in abscisic acid signalling in maize
inferredcites →https://doi.org/10.1093/jxb/ert371openalex-snapshot
Ethylene and reactive oxygen species are involved in root aerenchyma formation and adaptation of wheat seedlings to oxygen-deficient conditions
inferredcites →https://doi.org/10.1093/jxb/erv099openalex-snapshot
ROS and RNS in plant physiology: an overview
inferredcites →https://doi.org/10.1093/jxb/erv294openalex-snapshot
A calcium-binding protein, rice annexin OsANN1, enhances heat stress tolerance by modulating the production of H2O2
inferredcites →https://doi.org/10.1093/jxb/erw297openalex-snapshot
Rice putative methyltransferase gene OsTSD2 is required for root development involving pectin modification
inferredcites →https://doi.org/10.1093/pcp/pcq156openalex-snapshot
Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport
inferredcites →https://doi.org/10.1104/pp.109.145458openalex-snapshot
Annexins: Components of the Calcium and Reactive Oxygen Signaling Network
inferredcites →https://doi.org/10.1104/pp.15.00879openalex-snapshot
The RING Finger Ubiquitin E3 Ligase OsHTAS Enhances Heat Tolerance by Promoting H2O2-Induced Stomatal Closure in Rice
inferredcites →https://doi.org/10.1104/pp.16.01862openalex-snapshot
A Novel Chemical Inhibitor of ABA Signaling Targets All ABA Receptors
inferredcites →https://doi.org/10.1105/tpc.021683openalex-snapshot
Proteomic Identification of Annexins, Calcium-Dependent Membrane Binding Proteins That Mediate Osmotic Stress and Abscisic Acid Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.044230openalex-snapshot
An Arabidopsis Glutathione Peroxidase Functions as Both a Redox Transducer and a Scavenger in Abscisic Acid and Drought Stress Responses
inferredcites →https://doi.org/10.1105/tpc.106.048884openalex-snapshot
Calcium-Dependent Protein Kinases Regulate the Production of Reactive Oxygen Species by Potato NADPH Oxidase
inferredcites →https://doi.org/10.1105/tpc.107.050666openalex-snapshot
Two Calcium-Dependent Protein Kinases, CPK4 and CPK11, Regulate Abscisic Acid Signal Transduction inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.090480openalex-snapshot
Transcriptomic Analysis Reveals Calcium Regulation of Specific Promoter Motifs in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.16.00976openalex-snapshot
An NADPH Oxidase RBOH Functions in Rice Roots during Lysigenous Aerenchyma Formation under Oxygen-Deficient Conditions
inferredcites →https://doi.org/10.1105/tpc.18.00506openalex-snapshot
Abscisic Acid Inhibits Rice Protein Phosphatase PP45 via H 2 O 2 and Relieves Repression of the Ca 2+ /CaM-Dependent Protein Kinase DMI3
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02041.xopenalex-snapshot
Reactive oxygen species homeostasis and signalling during drought and salinity stresses
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02671.xopenalex-snapshot
Protein–protein interactions of tandem affinity purification‐tagged protein kinases in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03433.xopenalex-snapshot
AtMKK1 mediates ABA‐induced CAT1 expression and H2O2 production via AtMPK6‐coupled signaling 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.2009.04054.xopenalex-snapshot
PYR/PYL/RCAR family members are major in‐vivo ABI1 protein phosphatase 2C‐interacting proteins in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04766.xopenalex-snapshot
A rice calcium‐dependent protein kinase OsCPK12 oppositely modulates salt‐stress tolerance and blast disease resistance
inferredcites →https://doi.org/10.1111/j.1438-8677.2011.00496.xopenalex-snapshot
Abscisic acid‐regulated responses of aba2‐1 under osmotic stress: the abscisic acid‐inducible antioxidant defence system and reactive oxygen species production
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02364.xopenalex-snapshot
Oxygen dynamics in submerged rice (Oryza sativa)
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02431.xopenalex-snapshot
Guard‐cell signalling for hydrogen peroxide and abscisic acid
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03535.xopenalex-snapshot
Identification of genes expressed in maize root cortical cells during lysigenous aerenchyma formation using laser microdissection and microarray analyses
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04308.xopenalex-snapshot
Evolutionary adaptation of plant annexins has diversified their molecular structures, interactions and functional roles
inferredcites →https://doi.org/10.1111/j.1744-7909.2011.01034.xopenalex-snapshot
Characterization of a Novel Annexin Gene from Cotton (Gossypium hirsutum cv CRI 35) and Antioxidative Role of its Recombinant Protein
inferredcites →https://doi.org/10.1111/jipb.12614openalex-snapshot
The calcium‐dependent kinase OsCPK24 functions in cold stress responses in rice
inferredcites →https://doi.org/10.1111/nph.14966openalex-snapshot
Advances and current challenges in calcium signaling
inferredcites →https://doi.org/10.1111/pbi.12427openalex-snapshot
Zm ABA 2, an interacting protein of Zm MPK 5, is involved in abscisic acid biosynthesis and functions
inferredcites →https://doi.org/10.1111/pce.12829openalex-snapshot
OsDi19‐4 acts downstream of OsCDPK14 to positively regulate ABA response in rice
inferredcites →https://doi.org/10.1111/ppl.12011openalex-snapshot
Molecular elements of low‐oxygen signaling in plants
inferredcites →https://doi.org/10.1111/tpj.12372openalex-snapshot
Annexin 1 regulates the H 2 O 2‐induced calcium signature in A rabidopsis thaliana roots
inferredcites →https://doi.org/10.1111/tpj.12708openalex-snapshot
The single‐subunit RING ‐type E3 ubiquitin ligase RSL 1 targets PYL 4 and PYR 1 ABA receptors in plasma membrane to modulate abscisic acid signaling
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/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1152/physrev.00038.2011openalex-snapshot
Ion Channels in Plants
inferredcites →https://doi.org/10.1186/gb-2004-5-4-219openalex-snapshot
The annexins.
inferredcites →https://doi.org/10.1199/tab.0166openalex-snapshot
Abscisic Acid Synthesis and Response
inferredcites →https://doi.org/10.1371/journal.pone.0095246openalex-snapshot
Identification and Characterization of ABA Receptors in Oryza sativa
inferredcites →https://doi.org/10.4161/psb.19647openalex-snapshot
Insight into plant annexin function
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