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A Member of the 14-3-3 Gene Family in Brachypodium distachyon, BdGF14d, Confers Salt Tolerance in Transgenic Tobacco Plants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00299-016-1950-xopenalex-snapshot
Regulation of plant reactive oxygen species (ROS) in stress responses: learning from AtRBOHD
inferredcites →https://doi.org/10.1007/s00425-005-1564-yopenalex-snapshot
Expressing TERF1 in tobacco enhances drought tolerance and abscisic acid sensitivity during seedling development
inferredcites →https://doi.org/10.1007/s00425-011-1387-yopenalex-snapshot
Characterization of abiotic stress-responsive Arabidopsis thaliana RD29A and RD29B genes and evaluation of transgenes
inferredcites →https://doi.org/10.1007/s00709-012-0437-zopenalex-snapshot
Plant 14-3-3 proteins as spiders in a web of phosphorylation
inferredcites →https://doi.org/10.1007/s10265-011-0412-3openalex-snapshot
ABA-mediated transcriptional regulation in response to osmotic stress in plants
inferredcites →https://doi.org/10.1007/s10535-016-0584-8openalex-snapshot
Photosynthesis and antioxidative defense mechanisms in deciphering drought stress tolerance of crop plants
inferredcites →https://doi.org/10.1007/s11120-013-9813-6openalex-snapshot
Physiological and molecular mechanisms of plant salt tolerance
inferredcites →https://doi.org/10.1016/j.bbrc.2009.03.091openalex-snapshot
Knock-out of Arabidopsis AtNHX4 gene enhances tolerance to salt stress
inferredcites →https://doi.org/10.1016/j.copbio.2013.12.004openalex-snapshot
Salt resistant crop plants
inferredcites →https://doi.org/10.1016/j.devcel.2011.08.018openalex-snapshot
Dual Role of BKI1 and 14-3-3 s in Brassinosteroid Signaling to Link Receptor with Transcription Factors
inferredcites →https://doi.org/10.1016/j.febslet.2009.06.011openalex-snapshot
Interaction specificity of Arabidopsis 14‐3‐3 proteins with phototropin receptor kinases
inferredcites →https://doi.org/10.1016/j.jplph.2016.10.013openalex-snapshot
Overexpression of tomato SlGGP-LIKE gene improves tobacco tolerance to methyl viologen-mediated oxidative stress
inferredcites →https://doi.org/10.1016/j.pbi.2010.06.001openalex-snapshot
Plant phosphopeptide-binding proteins as signaling mediators
inferredcites →https://doi.org/10.1016/j.scienta.2013.12.034openalex-snapshot
Molecular cloning of a 14-3-3 protein gene from Lilium regale Wilson and overexpression of this gene in tobacco increased resistance to pathogenic fungi
inferredcites →https://doi.org/10.1016/j.semcdb.2011.08.006openalex-snapshot
14-3-3 proteins in plant physiology
inferredcites →https://doi.org/10.1016/j.semcdb.2011.09.001openalex-snapshot
Structural basis of 14-3-3 protein functions
inferredcites →https://doi.org/10.1016/j.tplants.2014.02.001openalex-snapshot
Plant salt-tolerance mechanisms
inferredcites →https://doi.org/10.1016/s0168-9452(02)00081-xopenalex-snapshot
14-3-3 Protein regulation of the antioxidant capacity of transgenic potato tubers
inferredcites →https://doi.org/10.1016/s1369-5266(03)00085-2openalex-snapshot
Regulation of ion homeostasis under salt stress
inferredcites →https://doi.org/10.1023/a:1021231805697openalex-snapshot
14-3-3 protein regulation of proton pumps and ion channels
inferredcites →https://doi.org/10.1034/j.1399-3054.2002.1160105.xopenalex-snapshot
Enhanced H+/ATP coupling ratio of H+‐ATPase and increased 14‐3‐3 protein content in plasma membrane of tomato cells upon osmotic shock
inferredcites →https://doi.org/10.1038/nature10272openalex-snapshot
14-3-3 proteins act as intracellular receptors for rice Hd3a florigen
inferredcites →https://doi.org/10.1038/sj.onc.1204777openalex-snapshot
14-3-3 proteins; bringing new definitions to scaffolding
inferredcites →https://doi.org/10.1074/jbc.275.3.1723openalex-snapshot
ABFs, a Family of ABA-responsive Element Binding Factors
inferredcites →https://doi.org/10.1074/mcp.m113.030171openalex-snapshot
Proteome and Phosphoproteome Characterization Reveals New Response and Defense Mechanisms of Brachypodium distachyon Leaves under Salt Stress
inferredcites →https://doi.org/10.1093/dnares/dsl001openalex-snapshot
The Rice 14-3-3 Gene Family and its Involvement in Responses to Biotic and Abiotic Stress
inferredcites →https://doi.org/10.1093/emboj/cdg104openalex-snapshot
Structural view of a fungal toxin acting on a 14‐3‐3 regulatory complex
inferredcites →https://doi.org/10.1093/jxb/erg057openalex-snapshot
Function and specificity of 14-3-3 proteins in the regulation of carbohydrate and nitrogen metabolism
inferredcites →https://doi.org/10.1093/jxb/erm370openalex-snapshot
Hydrogen peroxide generated by copper amine oxidase is involved in abscisic acid-induced stomatal closure in Vicia faba
inferredcites →https://doi.org/10.1093/jxb/erv149openalex-snapshot
Involvement of 14-3-3 protein GRF9 in root growth and response under polyethylene glycol-induced water stress
inferredcites →https://doi.org/10.1093/pcp/pch115openalex-snapshot
Overexpression of the Arabidopsis 14-3-3 Protein GF14λ in Cotton Leads to a “Stay-Green” Phenotype and Improves Stress Tolerance under Moderate Drought Conditions
inferredcites →https://doi.org/10.1093/pcp/pci179openalex-snapshot
The 14-3-3 Gene Expression Specificity in Response to Stress is Promoter-Dependent
inferredcites →https://doi.org/10.1093/pcp/pcs154openalex-snapshot
Overexpression of a Wheat Aquaporin Gene, TaAQP8, Enhances Salt Stress Tolerance in Transgenic Tobacco
inferredcites →https://doi.org/10.1093/pcp/pct161openalex-snapshot
A Glycine Soja 14-3-3 Protein GsGF14o Participates in Stomatal and Root Hair Development and Drought Tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.126.1.35openalex-snapshot
The Arabidopsis 14-3-3 Family of Signaling Regulators
inferredcites →https://doi.org/10.1104/pp.127.4.1539openalex-snapshot
Brachypodium distachyon. A New Model System for Functional Genomics in Grasses
inferredcites →https://doi.org/10.1105/tpc.104.024604openalex-snapshot
Involvement of 14-3-3 Signaling Protein Binding in the Functional Regulation of the Transcriptional Activator REPRESSION OF SHOOT GROWTH by Gibberellins
inferredcites →https://doi.org/10.1105/tpc.105.035626openalex-snapshot
Arabidopsis Protein Kinase PKS5 Inhibits the Plasma Membrane H + -ATPase by Preventing Interaction with 14-3-3 Protein
inferredcites →https://doi.org/10.1105/tpc.111.095273openalex-snapshot
Ion Exchangers NHX1 and NHX2 Mediate Active Potassium Uptake into Vacuoles to Regulate Cell Turgor and Stomatal Function in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.117069openalex-snapshot
Inhibition of the Arabidopsis Salt Overly Sensitive Pathway by 14-3-3 Proteins
inferredcites →https://doi.org/10.1105/tpc.15.00421openalex-snapshot
Aquaporins Contribute to ABA-Triggered Stomatal Closure through OST1-Mediated Phosphorylation
inferredcites →https://doi.org/10.1111/j.0031-9317.2004.0239.xopenalex-snapshot
14‐3‐3 proteins: regulation of signal‐induced events
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02955.xopenalex-snapshot
14‐3‐3 adaptor proteins are intermediates in ABA signal transduction during barley seed germination
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00534.xopenalex-snapshot
Antioxidant defense in the leaves of C3 and C4 plants under salinity stress
inferredcites →https://doi.org/10.1111/nph.13507openalex-snapshot
Chloride‐inducible transient apoplastic alkalinizations induce stomata closure by controlling abscisic acid distribution between leaf apoplast and guard cells in salt‐stressed Vicia faba
inferredcites →https://doi.org/10.1111/pbi.12498openalex-snapshot
The tomato mutant ars1 (altered response to salt stress 1) identifies an R1‐type MYB transcription factor involved in stomatal closure under salt acclimation
inferredcites →https://doi.org/10.1111/ppl.12046openalex-snapshot
Ectopic expression of wheat TaCIPK14 , encoding a calcineurin B‐like protein‐interacting protein kinase, confers salinity and cold tolerance in tobacco
inferredcites →https://doi.org/10.1111/tpj.12391openalex-snapshot
Xanthomonas euvesicatoria type III effector X op Q interacts with tomato and pepper 14–3–3 isoforms to suppress effector‐triggered immunity
inferredcites →https://doi.org/10.1111/tpj.12677openalex-snapshot
Light modulated activity of root alkaline/neutral invertase involves the interaction with 14‐3‐3 proteins
inferredcites →https://doi.org/10.1126/science.285.5431.1256openalex-snapshot
Salt Tolerance Conferred by Overexpression of a Vacuolar Na + /H + Antiport in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112226openalex-snapshot
Guard Cell Signal Transduction Network: Advances in Understanding Abscisic Acid, CO2, and Ca2+Signaling
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092844openalex-snapshot
14-3-3 and FHA Domains Mediate Phosphoprotein Interactions
inferredcites →https://doi.org/10.1186/1471-2164-12-216openalex-snapshot
Common and unique elements of the ABA-regulated transcriptome of Arabidopsis guard cells
inferredcites →https://doi.org/10.1186/1752-0509-5-192openalex-snapshot
Determining novel functions of Arabidopsis14-3-3 proteins in central metabolic processes
inferredcites →https://doi.org/10.1186/s12870-015-0644-9openalex-snapshot
TaNAC29, a NAC transcription factor from wheat, enhances salt and drought tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1186/s12870-015-0657-4openalex-snapshot
Identification and comprehensive analyses of the CBL and CIPK gene families in wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1371/journal.pone.0013935openalex-snapshot
The Arabidopsis ABA-Activated Kinase OST1 Phosphorylates the bZIP Transcription Factor ABF3 and Creates a 14-3-3 Binding Site Involved in Its Turnover
inferredcites →https://doi.org/10.1371/journal.pone.0046744openalex-snapshot
Genome-Wide Identification and Analysis of MAPK and MAPKK Gene Families in Brachypodium distachyon
inferredcites →https://doi.org/10.1371/journal.pone.0069881openalex-snapshot
TaCIPK29, a CBL-Interacting Protein Kinase Gene from Wheat, Confers Salt Stress Tolerance in Transgenic Tobacco
inferredcites →https://doi.org/10.1371/journal.pone.0090764openalex-snapshot
Specificity of ε and Non-ε Isoforms of Arabidopsis 14-3-3 Proteins Towards the H+-ATPase and Other Targets
inferredcites →https://doi.org/10.1371/journal.pone.0129589openalex-snapshot
TaPP2C1, a Group F2 Protein Phosphatase 2C Gene, Confers Resistance to Salt Stress in Transgenic Tobacco
inferredcites →https://doi.org/10.3389/fpls.2015.00615openalex-snapshot
Expression of TaWRKY44, a wheat WRKY gene, in transgenic tobacco confers multiple abiotic stress tolerances
inferredcites →https://doi.org/10.3389/fpls.2015.01210openalex-snapshot
14-3-3 Proteins in Guard Cell Signaling
inferredcites →https://doi.org/10.3389/fpls.2016.00548openalex-snapshot
Tuning of Redox Regulatory Mechanisms, Reactive Oxygen Species and Redox Homeostasis under Salinity Stress
inferredcites →https://doi.org/10.3389/fpls.2016.01099openalex-snapshot
Molecular Characterization of the 14-3-3 Gene Family in Brachypodium distachyon L. Reveals High Evolutionary Conservation and Diverse Responses to Abiotic Stresses
inferredcites →https://doi.org/10.5483/bmbrep.2007.40.3.349openalex-snapshot
Molecular Analysis and Expression Patterns of the 14-3-3 Gene Family from Oryza Sativa
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s00299-021-02803-4openalex-snapshot
The role of 14-3-3 proteins in plant growth and response to abiotic stress
inferred← citeshttps://doi.org/10.1007/s00299-023-03035-4openalex-snapshot
Evolution of the 14–3–3 gene family in monocotyledons and dicotyledons and validation of MdGRF13 function in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-025-03689-2openalex-snapshot
TaGF14g, a wheat 14-3-3 protein, acts as a positive regulator of drought and salt tolerance
inferred← citeshttps://doi.org/10.1007/s00344-022-10639-9openalex-snapshot
Enhancement of Drought Tolerance in Transgenic Arabidopsis thaliana Plants Overexpressing Chickpea Ca14-3-3 Gene
inferred← citeshttps://doi.org/10.1007/s00425-017-2779-4openalex-snapshot
RETRACTED ARTICLE: Molecular characterization of the 14-3-3 gene family in rice and its expression studies under abiotic stress
inferred← citeshttps://doi.org/10.1007/s00425-018-2887-9openalex-snapshot
Expression of TaGF14b, a 14-3-3 adaptor protein gene from wheat, enhances drought and salt tolerance in transgenic tobacco
inferred← citeshttps://doi.org/10.1007/s11738-018-2787-4openalex-snapshot
Functional roles of two 14-3-3s in response to salt stress in common bean
inferred← citeshttps://doi.org/10.1007/s12374-021-09333-2openalex-snapshot
Overexpression of BdASR2 Plays a Positive Role in Response to Salt Tolerance in Brachypodium distachyon
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105665openalex-snapshot
Mt14-3-3, interacting with MtNAC2, is involved in floral transition and multiple abiotic stress pathways
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.122122openalex-snapshot
Transcriptome and proteome analyses reveal selenium mediated amelioration of arsenic toxicity in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154685openalex-snapshot
Overexpression of mango GF14I1 and GF14I2 promotes early flowering and enhances abiotic stress tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110215openalex-snapshot
Overexpression of 14-3-3 proteins enhances cold tolerance and increases levels of stress-responsive proteins of Arabidopsis plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110219openalex-snapshot
MdGRF11, an apple 14-3-3 protein, acts as a positive regulator of drought and salt tolerance
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110689openalex-snapshot
The BTB-TAZ protein MdBT2 negatively regulates the drought stress response by interacting with the transcription factor MdNAC143 in apple
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111782openalex-snapshot
MdGRF11-MdARF19-2 module acts as a positive regulator of drought resistance in apple rootstock
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112403openalex-snapshot
The 14–3–3 gene AaGRF1 positively regulates cold tolerance in kiwifruit
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108007openalex-snapshot
Drought priming modulates ABF, GRFs, related microRNAs and induce metabolic adjustment during heat stress in chickpea
inferred← citeshttps://doi.org/10.1071/fp21022openalex-snapshot
Comprehensive analysis of 14-3-3 family genes and their responses to cold and drought stress in cucumber
inferred← citeshttps://doi.org/10.1080/15592324.2024.2359257openalex-snapshot
The 14-3-3 protein nt GF14e interacts with CIPK2 and increases low potassium stress in tobacco
inferred← citeshttps://doi.org/10.1080/17429145.2022.2045370openalex-snapshot
Genome-wide analysis of the GRF gene family and their expression profiling in peach ( Prunus persica )
inferred← citeshttps://doi.org/10.1093/jxb/erab392openalex-snapshot
OsATL38 mediates mono-ubiquitination of the 14-3-3 protein OsGF14d and negatively regulates the cold stress response in rice
inferred← citeshttps://doi.org/10.1093/plphys/kiad621openalex-snapshot
The 14-3-3 protein GRF8 modulates salt stress tolerance in apple via the WRKY18- SOS pathway
inferred← citeshttps://doi.org/10.1111/pce.14520openalex-snapshot
A 14‐3‐3 protein positively regulates rice salt tolerance by stabilizing phospholipase C1
inferred← citeshttps://doi.org/10.1128/spectrum.02456-21openalex-snapshot
Arbuscular Mycorrhizal Fungi Enhanced Drought Resistance of Populus cathayana by Regulating the 14-3-3 Family Protein Genes
inferred← citeshttps://doi.org/10.1186/s12864-022-09037-yopenalex-snapshot
Genome-wide identification and gene expression analysis of the 14–3-3 gene family in potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-32624/v1openalex-snapshot
Identification of peach growth regulating-factors and their expression under UVB
inferred← citeshttps://doi.org/10.3389/fmicb.2022.934964openalex-snapshot
Effect of arbuscular mycorrhizal fungi and phosphorus on drought-induced oxidative stress and 14-3-3 proteins gene expression of Populus cathayana
inferred← citeshttps://doi.org/10.3389/fpls.2018.00105openalex-snapshot
Overexpression of PvGF14c from Phyllostachys violascens Delays Flowering Time in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2018.02003openalex-snapshot
TaSnRK2.9, a Sucrose Non-fermenting 1-Related Protein Kinase Gene, Positively Regulates Plant Response to Drought and Salt Stress in Transgenic Tobacco
inferred← citeshttps://doi.org/10.3389/fpls.2020.568489openalex-snapshot
Overexpression of NtDOG1L-T Improves Heat Stress Tolerance by Modulation of Antioxidant Capability and Defense-, Heat-, and ABA-Related Gene Expression in Tobacco
inferred← citeshttps://doi.org/10.3389/fpls.2021.831883openalex-snapshot
PpNUDX8, a Peach NUDIX Hydrolase, Plays a Negative Regulator in Response to Drought Stress
inferred← citeshttps://doi.org/10.3390/genes9020110openalex-snapshot
Genome-Wide Analysis of the GRF Family Reveals Their Involvement in Abiotic Stress Response in Cassava
inferred← citeshttps://doi.org/10.3390/ijms18102040openalex-snapshot
Genome-Wide Analysis of CCA1-Like Proteins in Soybean and Functional Characterization of GmMYB138a
inferred← citeshttps://doi.org/10.3390/ijms20071758openalex-snapshot
Transcriptional and Metabolomic Analyses Indicate that Cell Wall Properties are Associated with Drought Tolerance in Brachypodium distachyon
inferred← citeshttps://doi.org/10.3390/ijms22041904openalex-snapshot
Genome-Wide Identification and Characterization of Wheat 14-3-3 Genes Unravels the Role of TaGRF6-A in Salt Stress Tolerance by Binding MYB Transcription Factor
inferred← citeshttps://doi.org/10.3390/ijms25063432openalex-snapshot
Genome-Wide Identification of the 14-3-3 Gene Family and Its Involvement in Salt Stress Response through Interaction with NsVP1 in Nitraria sibirica Pall
inferred← citeshttps://doi.org/10.3390/ijms252212304openalex-snapshot
Functional Characterization of the 14-3-3 Gene Family in Alfalfa and the Role of MsGRF2 in Drought Response Mechanisms
inferred← citeshttps://doi.org/10.3390/plants12152887openalex-snapshot
14-3-3 Proteins and the Plasma Membrane H+-ATPase Are Involved in Maize (Zea mays) Magnetic Induction
inferred← citeshttps://doi.org/10.3390/plants12233975openalex-snapshot
A 14-3-3 Protein-Encoding Gene, BdGF14g, Confers Better Drought Tolerance by Regulating ABA Biosynthesis and Signaling
inferred← citeshttps://doi.org/10.3390/plants13020245openalex-snapshot
The 14-3-3 Protein BdGF14a Increases the Transcriptional Regulation Activity of BdbZIP62 to Confer Drought and Salt Resistance in Tobacco
inferred← citeshttps://doi.org/10.3390/plants14233568openalex-snapshot
Functional 14-3-3 Proteins: Master Regulators in Plant Responses to Salt Stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.22612445openalex-snapshot
Additional file 1 of Genome-wide identification and gene expression analysis of the 14–3-3 gene family in potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22612448openalex-snapshot
Additional file 2 of Genome-wide identification and gene expression analysis of the 14–3-3 gene family in potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.22612451openalex-snapshot
Additional file 3 of Genome-wide identification and gene expression analysis of the 14–3-3 gene family in potato (Solanum tuberosum L.)
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