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VlbZIP30 of grapevine functions in drought tolerance via the abscisic acid core signaling pathway

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

inferredcites →https://doi.org/10.1007/bf00039429openalex-snapshot

Analysis of an ABA-responsive rice gene promoter in transgenic tobacco

inferredcites →https://doi.org/10.1007/s00299-015-1910-xopenalex-snapshot

Overexpression of VaPAT1, a GRAS transcription factor from Vitis amurensis, confers abiotic stress tolerance in Arabidopsis

inferredcites →https://doi.org/10.1007/s00299-016-2040-9openalex-snapshot

Drastic anthocyanin increase in response to PAP1 overexpression in fls1 knockout mutant confers enhanced osmotic stress tolerance in Arabidopsis thaliana

inferredcites →https://doi.org/10.1007/s00425-008-0731-3openalex-snapshot

Soybean GmbZIP44, GmbZIP62 and GmbZIP78 genes function as negative regulator of ABA signaling and confer salt and freezing tolerance in transgenic Arabidopsis

inferredcites →https://doi.org/10.1007/s00425-010-1147-4openalex-snapshot

A tomato bZIP transcription factor, SlAREB, is involved in water deficit and salt stress response

inferredcites →https://doi.org/10.1007/s00425-011-1540-7openalex-snapshot

Characterization of StABF1, a stress-responsive bZIP transcription factor from Solanum tuberosum L. that is phosphorylated by StCDPK2 in vitro

inferredcites →https://doi.org/10.1007/s00425-015-2285-5openalex-snapshot

A fungal transcription factor gene is expressed in plants from its own promoter and improves drought tolerance

inferredcites →https://doi.org/10.1007/s10265-011-0437-7openalex-snapshot

Opening a new era of ABA research

inferredcites →https://doi.org/10.1007/s11033-010-0124-0openalex-snapshot

Ectopic expression of a grapevine transcription factor VvWRKY11 contributes to osmotic stress tolerance in Arabidopsis

inferredcites →https://doi.org/10.1007/s11103-006-9079-xopenalex-snapshot

A rice dehydration-inducible SNF1-related protein kinase 2 phosphorylates an abscisic acid responsive element-binding factor and associates with ABA signaling

inferredcites →https://doi.org/10.1007/s11103-008-9298-4openalex-snapshot

A bZIP transcription factor, OsABI5, is involved in rice fertility and stress tolerance

inferredcites →https://doi.org/10.1007/s11103-008-9344-2openalex-snapshot

A small plant-specific protein family of ABI five binding proteins (AFPs) regulates stress response in germinating Arabidopsis seeds and seedlings

inferredcites →https://doi.org/10.1007/s11103-011-9732-xopenalex-snapshot

Maize ABP9 enhances tolerance to multiple stresses in transgenic Arabidopsis by modulating ABA signaling and cellular levels of reactive oxygen species

inferredcites →https://doi.org/10.1007/s11103-011-9738-4openalex-snapshot

The soybean GmbZIP1 transcription factor enhances multiple abiotic stress tolerances in transgenic plants

inferredcites →https://doi.org/10.1007/s11103-012-9956-4openalex-snapshot

The homeodomain-leucine zipper (HD-Zip) class I transcription factors ATHB7 and ATHB12 modulate abscisic acid signalling by regulating protein phosphatase 2C and abscisic acid receptor gene activities

inferredcites →https://doi.org/10.1007/s11103-013-0054-zopenalex-snapshot

Functional characterization of an abiotic stress-inducible transcription factor AtERF53 in Arabidopsis thaliana

inferredcites →https://doi.org/10.1007/s11103-013-0115-3openalex-snapshot

OsbZIP71, a bZIP transcription factor, confers salinity and drought tolerance in rice

inferredcites →https://doi.org/10.1007/s11103-015-0378-yopenalex-snapshot

Ectopic expression of a hot pepper bZIP-like transcription factor in potato enhances drought tolerance without decreasing tuber yield

inferredcites →https://doi.org/10.1007/s11105-013-0627-7openalex-snapshot

Overexpression of VaCBF4, a Transcription Factor from Vitis amurensis, Improves Cold Tolerance Accompanying Increased Resistance to Drought and Salinity in Arabidopsis

inferredcites →https://doi.org/10.1007/s11105-014-0723-3openalex-snapshot

Evolutionary and Expression Analyses of Basic Zipper Transcription Factors in the Highly Homozygous Model Grape PN40024 (Vitis vinifera L.)

inferredcites →https://doi.org/10.1007/s11240-016-0969-6openalex-snapshot

Expression of a grape bZIP transcription factor, VqbZIP39, in transgenic Arabidopsis thaliana confers tolerance of multiple abiotic stresses

inferredcites →https://doi.org/10.1007/s11248-012-9645-8openalex-snapshot

Co-expression of AtbHLH17 and AtWRKY28 confers resistance to abiotic stress in Arabidopsis

inferredcites →https://doi.org/10.1016/j.biotechadv.2013.09.006openalex-snapshot

The role of ABA and MAPK signaling pathways in plant abiotic stress responses

inferredcites →https://doi.org/10.1016/j.febslet.2006.04.062openalex-snapshot

Constitutive expression of abiotic stress‐inducible hot pepper CaXTH3 , which encodes a xyloglucan endotransglucosylase/hydrolase homolog, improves drought and salt tolerance in transgenic Arabidopsis plants

inferredcites →https://doi.org/10.1016/j.jplph.2010.03.001openalex-snapshot

Photosynthesis and photoprotection in coffee leaves is affected by nitrogen and light availabilities in winter conditions

inferredcites →https://doi.org/10.1016/j.jplph.2013.01.017openalex-snapshot

Three ERF transcription factors from Chinese wild grapevine Vitis pseudoreticulata participate in different biotic and abiotic stress-responsive pathways

inferredcites →https://doi.org/10.1016/j.jplph.2013.03.008openalex-snapshot

AtFtsH heterocomplex-mediated degradation of apoproteins of the major light harvesting complex of photosystem II (LHCII) in response to stresses

inferredcites →https://doi.org/10.1016/j.molp.2016.04.001openalex-snapshot

Dissecting Abscisic Acid Signaling Pathways Involved in Cuticle Formation

inferredcites →https://doi.org/10.1016/j.plantsci.2016.08.011openalex-snapshot

Expression of a grape (Vitis vinifera) bZIP transcription factor, VlbZIP36, in Arabidopsis thaliana confers tolerance of drought stress during seed germination and seedling establishment

inferredcites →https://doi.org/10.1016/j.tibtech.2004.02.001openalex-snapshot

Engineering grapevine for increased resistance to fungal pathogens without compromising wine stability

inferredcites →https://doi.org/10.1016/j.tplants.2004.03.007openalex-snapshot

Plant PP2C phosphatases: emerging functions in stress signaling

inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot

MYB transcription factors in Arabidopsis

inferredcites →https://doi.org/10.1016/s1360-1385(01)02223-3openalex-snapshot

bZIP transcription factors in Arabidopsis

inferredcites →https://doi.org/10.1016/s1369-5266(00)80068-0openalex-snapshot

Molecular responses to dehydration and low temperature: differences and cross-talk between two stress signaling pathways

inferredcites →https://doi.org/10.1016/s1369-5266(02)00282-0openalex-snapshot

Hydrogen peroxide signalling

inferredcites →https://doi.org/10.1016/s1534-5807(01)00087-9openalex-snapshot

Modulation of Abscisic Acid Signal Transduction and Biosynthesis by an Sm-like Protein in Arabidopsis

inferredcites →https://doi.org/10.1038/srep17587openalex-snapshot

An ABA down-regulated bHLH transcription repressor gene, bHLH129 regulates root elongation and ABA response when overexpressed in Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot

Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00965.xopenalex-snapshot

The ABI1 and ABI2 protein phosphatases 2C act in a negative feedback regulatory loop of the abscisic acid signalling pathway

inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01096.xopenalex-snapshot

Regulation of drought tolerance by gene manipulation of 9‐ cis ‐epoxycarotenoid dioxygenase, a key enzyme in abscisic acid biosynthesis in Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01874.xopenalex-snapshot

AtAGP30, an arabinogalactan‐protein in the cell walls of the primary root, plays a role in root regeneration and seed germination

inferredcites →https://doi.org/10.1073/pnas.0505667103openalex-snapshot

Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1

inferredcites →https://doi.org/10.1073/pnas.0707193104openalex-snapshot

Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water-limited acres

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.190309197openalex-snapshot

Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity conditions

inferredcites →https://doi.org/10.1074/jbc.m109.051938openalex-snapshot

Overproduction of the Membrane-bound Receptor-like Protein Kinase 1, RPK1, Enhances Abiotic Stress Tolerance in Arabidopsis

inferredcites →https://doi.org/10.1080/15592324.2016.1139277openalex-snapshot

Regulation of Arabidopsis MAPKKK18 by ABI1 and SnRK2, components of the ABA signaling pathway

inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot

edgeR : a Bioconductor package for differential expression analysis of digital gene expression data

inferredcites →https://doi.org/10.1093/dnares/dsw061openalex-snapshot

Genome-wide analysis of cis-regulatory element structure and discovery of motif-driven gene co-expression networks in grapevine

inferredcites →https://doi.org/10.1093/jxb/erm364openalex-snapshot

Water deficits and heat shock effects on photosynthesis of a transgenic Arabidopsis thaliana constitutively expressing ABP9, a bZIP transcription factor

inferredcites →https://doi.org/10.1093/jxb/ern014openalex-snapshot

Development of abiotic stress tolerance via bZIP-type transcription factor LIP19 in common wheat

inferredcites →https://doi.org/10.1093/jxb/err210openalex-snapshot

Role of DREBs in regulation of abiotic stress responses in plants

inferredcites →https://doi.org/10.1093/jxb/err236openalex-snapshot

EDL3 is an F-box protein involved in the regulation of abscisic acid signalling in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/jxb/eru270openalex-snapshot

MSRB7 reverses oxidation of GSTF2/3 to confer tolerance of Arabidopsis thaliana to oxidative stress

inferredcites →https://doi.org/10.1093/jxb/erv301openalex-snapshot

PtrABF ofPoncirus trifoliatafunctions in dehydration tolerance by reducing stomatal density and maintaining reactive oxygen species homeostasis

inferredcites →https://doi.org/10.1093/jxb/erv312openalex-snapshot

Salt-induced transcription factor MYB74 is regulated by the RNA-directed DNA methylation pathway in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/erw122openalex-snapshot

Expression ofVitis amurensis NAC26in Arabidopsis enhances drought tolerance by modulating jasmonic acid synthesis

inferredcites →https://doi.org/10.1093/jxb/erw347openalex-snapshot

Functional characterization of the Arabidopsis transcription factor bZIP29 reveals its role in leaf and root development

inferredcites →https://doi.org/10.1093/mp/ssr030openalex-snapshot

AtPUB19, a U-Box E3 Ubiquitin Ligase, Negatively Regulates Abscisic Acid and Drought Responses in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/mp/sst031openalex-snapshot

Arabidopsis Di19 Functions as a Transcription Factor and Modulates PR1, PR2, and PR5 Expression in Response to Drought Stress

inferredcites →https://doi.org/10.1093/nar/25.17.3389openalex-snapshot

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

inferredcites →https://doi.org/10.1093/pcp/pcf188openalex-snapshot

ABA-Activated SnRK2 Protein Kinase is Required for Dehydration Stress Signaling in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcp075openalex-snapshot

Functional Analysis of Transcription Factors in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcp083openalex-snapshot

Three Arabidopsis SnRK2 Protein Kinases, SRK2D/SnRK2.2, SRK2E/SnRK2.6/OST1 and SRK2I/SnRK2.3, Involved in ABA Signaling are Essential for the Control of Seed Development and Dormancy

inferredcites →https://doi.org/10.1093/pcp/pcp147openalex-snapshot

Three SnRK2 Protein Kinases are the Main Positive Regulators of Abscisic Acid Signaling in Response to Water Stress in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcq155openalex-snapshot

RD20, a Stress-Inducible Caleosin, Participates in Stomatal Control, Transpiration and Drought Tolerance in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/pcp/pcw084openalex-snapshot

Ectopic Expression of DREB Transcription Factor, AtDREB1A, Confers Tolerance to Drought in TransgenicSalvia miltiorrhiza

inferredcites →https://doi.org/10.1093/pcp/pcw147openalex-snapshot

MYB94 and MYB96 Additively Activate Cuticular Wax Biosynthesis in Arabidopsis

inferredcites →https://doi.org/10.1096/fasebj.8.2.8119490openalex-snapshot

Plant bZIP proteins gather at ACGT elements

inferredcites →https://doi.org/10.1104/pp.003566openalex-snapshot

Arabidopsis ABI5 Subfamily Members Have Distinct DNA-Binding and Transcriptional Activities

inferredcites →https://doi.org/10.1104/pp.102.019273openalex-snapshot

Integration of Wounding and Osmotic Stress Signals Determines the Expression of the AtMYB102 Transcription Factor Gene

inferredcites →https://doi.org/10.1104/pp.104.052084openalex-snapshot

The Arabidopsis Trehalose-6-P SynthaseAtTPS1Gene Is a Regulator of Glucose, Abscisic Acid, and Stress Signaling

inferredcites →https://doi.org/10.1104/pp.105.070128openalex-snapshot

ABA-Hypersensitive Germination3Encodes a Protein Phosphatase 2C (AtPP2CA) That Strongly Regulates Abscisic Acid Signaling during Germination among Arabidopsis Protein Phosphatase 2Cs

inferredcites →https://doi.org/10.1104/pp.106.081018openalex-snapshot

Enhancement of Abscisic Acid Sensitivity and Reduction of Water Consumption in Arabidopsis by Combined Inactivation of the Protein Phosphatases Type 2C ABI1 and HAB1

inferredcites →https://doi.org/10.1104/pp.106.094532openalex-snapshot

Overexpression of an R1R2R3 MYB Gene, OsMYB3R - 2 , Increases Tolerance to Freezing, Drought, and Salt Stress in Transgenic Arabidopsis

inferredcites →https://doi.org/10.1104/pp.108.118208openalex-snapshot

Chaperone Activity of ERD10 and ERD14, Two Disordered Stress-Related Plant Proteins

inferredcites →https://doi.org/10.1104/pp.110.161182openalex-snapshot

TaCHP: A Wheat Zinc Finger Protein Gene Down-Regulated by Abscisic Acid and Salinity Stress Plays a Positive Role in Stress Tolerance

inferredcites →https://doi.org/10.1104/pp.110.164152openalex-snapshot

Linking the Salt Transcriptome with Physiological Responses of a Salt-Resistant Populus Species as a Strategy to Identify Genes Important for Stress Acclimation

inferredcites →https://doi.org/10.1104/pp.111.190389openalex-snapshot

Constitutive Activation of Transcription Factor OsbZIP46 Improves Drought Tolerance in Rice

inferredcites →https://doi.org/10.1104/pp.112.196725openalex-snapshot

Systematic Identification of Functional Plant Modules through the Integration of Complementary Data Sources

inferredcites →https://doi.org/10.1104/pp.112.202408openalex-snapshot

Unique Drought Resistance Functions of theHighly ABA-InducedClade A Protein Phosphatase 2Cs

inferredcites →https://doi.org/10.1104/pp.113.231977openalex-snapshot

The Basic Leucine Zipper Transcription Factor ABSCISIC ACID RESPONSE ELEMENT-BINDING FACTOR2 Is an Important Transcriptional Regulator of Abscisic Acid-Dependent Grape Berry Ripening Processes

inferredcites →https://doi.org/10.1104/pp.114.251116openalex-snapshot

A STRESS-RESPONSIVE NAC1-Regulated Protein Phosphatase Gene Rice Protein Phosphatase18 Modulates Drought and Oxidative Stress Tolerance through Abscisic Acid-Independent Reactive Oxygen Species Scavenging in Rice

inferredcites →https://doi.org/10.1104/pp.16.00035openalex-snapshot

The Raf-like kinase ILK1 and the high affinity K+ transporter HAK5 are required for Innate Immunity and Abiotic Stress Response

inferredcites →https://doi.org/10.1104/pp.16.00421openalex-snapshot

Coordinate Regulation of Metabolite Glycosylation and Stress Hormone Biosynthesis by TT8 in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.16.00860openalex-snapshot

The heat-stress factor HSFA6b connects ABA signaling and ABA-mediated heat responses

inferredcites →https://doi.org/10.1104/pp.17.00273openalex-snapshot

Cooperative Regulatory Functions of miR858 and MYB83 during Cyst Nematode Parasitism

inferredcites →https://doi.org/10.1104/pp.17.01086openalex-snapshot

The G-Box Transcriptional Regulatory Code in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.005272openalex-snapshot

Abscisic Acid–Induced Transcription Is Mediated by Phosphorylation of an Abscisic Acid Response Element Binding Factor, TRAB1

inferredcites →https://doi.org/10.1105/tpc.010362openalex-snapshot

Arabidopsis Basic Leucine Zipper Proteins That Mediate Stress-Responsive Abscisic Acid Signaling

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

Abscisic Acid Signaling in Seeds and Seedlings

inferredcites →https://doi.org/10.1105/tpc.105.035659openalex-snapshot

AREB1 Is a Transcription Activator of Novel ABRE-Dependent ABA Signaling That Enhances Drought Stress Tolerance in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.108.059444openalex-snapshot

The Arabidopsis NFYA5 Transcription Factor Is Regulated Transcriptionally and Posttranscriptionally to Promote Drought Resistance

inferredcites →https://doi.org/10.1105/tpc.111.083485openalex-snapshot

The MYB96 Transcription Factor Regulates Cuticular Wax Biosynthesis under Drought Conditions inArabidopsis

inferredcites →https://doi.org/10.1105/tpc.112.098574openalex-snapshot

Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid

inferredcites →https://doi.org/10.1105/tpc.15.00222openalex-snapshot

The Arabidopsis Transcription Factor NAC016 Promotes Drought Stress Responses by Repressing AREB1 Transcription through a Trifurcate Feed-Forward Regulatory Loop Involving NAP

inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01524.xopenalex-snapshot

Three grape CBF/DREB1 genes respond to low temperature, drought and abscisic acid

inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02220.xopenalex-snapshot

The transcription factor SlAREB1 confers drought, salt stress tolerance and regulates biotic and abiotic stress‐related genes in tomato

inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02334.xopenalex-snapshot

Vitis CBF1 and Vitis CBF4 differ in their effect on Arabidopsis abiotic stress tolerance, development and gene expression

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02171.xopenalex-snapshot

A dehydration‐induced NAC protein, RD26, is involved in a novel ABA‐dependent stress‐signaling pathway

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02192.xopenalex-snapshot

ABF2, an ABRE‐binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02583.xopenalex-snapshot

Abscisic acid‐activated SNRK2 protein kinases function in the gene‐regulation pathway of ABA signal transduction by phosphorylating ABA response element‐binding factors

inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02678.xopenalex-snapshot

Identification of AtHD2C as a novel regulator of abscisic acid responses in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04092.xopenalex-snapshot

AREB1, AREB2, and ABF3 are master transcription factors that cooperatively regulate ABRE-dependent ABA signaling involved in drought stress tolerance and require ABA for full activation

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04248.xopenalex-snapshot

ABO3, a WRKY transcription factor, mediates plant responses to abscisic acid and drought tolerance in Arabidopsis

inferredcites →https://doi.org/10.1111/mpp.12290openalex-snapshot

LTP3 contributes to disease susceptibility in A rabidopsis by enhancing abscisic acid ( ABA ) biosynthesis

inferredcites →https://doi.org/10.1111/pbi.12731openalex-snapshot

Overexpression of an Arabidopsis thaliana galactinol synthase gene improves drought tolerance in transgenic rice and increased grain yield in the field

inferredcites →https://doi.org/10.1111/pce.12228openalex-snapshot

Functional characterization of A rabidopsis HsfA6a as a heat‐shock transcription factor under high salinity and dehydration conditions

inferredcites →https://doi.org/10.1111/pce.12351openalex-snapshot

Four A rabidopsis AREB / ABF transcription factors function predominantly in gene expression downstream of SnRK2 kinases in abscisic acid signalling in response to osmotic stress

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.53.091401.143329openalex-snapshot

S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS

inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105444openalex-snapshot

TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES

inferredcites →https://doi.org/10.1186/1471-2105-7-535openalex-snapshot

PageMan: An interactive ontology tool to generate, display, and annotate overview graphs for profiling experiments

inferredcites →https://doi.org/10.1186/1471-2229-13-151openalex-snapshot

The bZIP protein from Tamarix hispida, ThbZIP1, is ACGT elements binding factor that enhances abiotic stress signaling in transgenic Arabidopsis

inferredcites →https://doi.org/10.1186/gb-2013-14-4-r36openalex-snapshot

TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions

inferredcites →https://doi.org/10.1186/s12870-016-0911-4openalex-snapshot

Transcriptomic comparison between two Vitis vinifera L. varieties (Trincadeira and Touriga Nacional) in abiotic stress conditions

inferredcites →https://doi.org/10.1371/journal.pone.0059481openalex-snapshot

NUCLEAR FACTOR Y Transcription Factors Have Both Opposing and Additive Roles in ABA-Mediated Seed Germination

inferredcites →https://doi.org/10.1371/journal.pone.0059924openalex-snapshot

Ectopic Expression of Arabidopsis Glycosyltransferase UGT85A5 Enhances Salt Stress Tolerance in Tobacco

inferredcites →https://doi.org/10.1371/journal.pone.0070771openalex-snapshot

The Effects of Glucosinolates and Their Breakdown Products on Necrotrophic Fungi

inferredcites →https://doi.org/10.1371/journal.pone.0111988openalex-snapshot

HemI: A Toolkit for Illustrating Heatmaps

inferredcites →https://doi.org/10.3389/fpls.2015.00025openalex-snapshot

The regulatory network of ThbZIP1 in response to abscisic acid treatment

inferredcites →https://doi.org/10.3389/fpls.2017.01093openalex-snapshot

Abscisic Acid Is a Major Regulator of Grape Berry Ripening Onset: New Insights into ABA Signaling Network

inferredcites →https://doi.org/10.7150/ijbs.13538openalex-snapshot

Wheat Transcription Factor TaAREB3 Participates in Drought and Freezing Tolerances in Arabidopsis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/978-981-15-0690-1_2openalex-snapshot

Promising Transcription Factors for Salt and Drought Tolerance in Plants

inferred← citeshttps://doi.org/10.21203/rs.3.rs-289346/v1openalex-snapshot

Abscisic Acid Metabolism in Leaves and Roots of Four Vitis Species in Response to Water Deficit

inferred← citeshttps://doi.org/10.4236/oalib.1109969openalex-snapshot

Effect of Overexpression of SlbZIP39 on Plant Architecture and Fruit Size in Tomato (Solanum lycopersicum L.)

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