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

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What this work says

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

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GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.

inferredcites →https://doi.org/10.1007/bf00016490openalex-snapshot

Current advances in abscisic acid action and signalling

inferredcites →https://doi.org/10.1007/bf00027165openalex-snapshot

The expression of a rab-related gene, rab18, is induced by abscisic acid during the cold acclimation process of Arabidopsis thaliana (L.) Heynh

inferredcites →https://doi.org/10.1007/bf00040716openalex-snapshot

Phytohormone-regulated ?-amylase gene expression in rice

inferredcites →https://doi.org/10.1007/bf00272861openalex-snapshot

The isolation of abscisic acid (ABA) deficient mutants by selection of induced revertants in non-germinating gibberellin sensitive lines of Arabidopsis thaliana (L.) heynh.

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Aspects of recent developments in mutational studies of plant signaling pathways

inferredcites →https://doi.org/10.1016/s0092-8674(00)81606-2openalex-snapshot

Identification and Disruption of a Plant Shaker-like Outward Channel Involved in K+ Release into the Xylem Sap

inferredcites →https://doi.org/10.1016/s0968-0004(00)89118-5openalex-snapshot

The G-box: a ubiquitous regulatory DNA element in plants bound by the GBF family of bZIP proteins

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Genetic interactions between ABA, ethylene and sugar signaling pathways

inferredcites →https://doi.org/10.1023/a:1006058700720openalex-snapshot

Regulation of abscisic acid-induced transcription

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Arabidopsis mutants with reduced response to NaCI and osmotic stress

inferredcites →https://doi.org/10.1038/35066500openalex-snapshot

Guard cell abscisic acid signalling and engineering drought hardiness in plants

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Isolation and characterization of abscisic acid‐deficient Arabidopsis mutants at two new loci

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00231.xopenalex-snapshot

ICK1, a cyclin‐dependent protein kinase inhibitor fromArabidopsis thalianainteracts with both Cdc2a and CycD3, and its expression is induced by abscisic acid

inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00822.xopenalex-snapshot

The Arabidopsis SUCROSE UNCOUPLED‐6 gene is identical to ABSCISIC ACID INSENSITIVE‐4: involvement of abscisic acid in sugar responses

inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00833.xopenalex-snapshot

The Arabidopsis sugar‐insensitive mutants sis4 and sis5 are defective in abscisic acid synthesis and response

inferredcites →https://doi.org/10.1073/pnas.081594298openalex-snapshot

A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis

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/10.1073/pnas.85.19.7089openalex-snapshot

An evolutionarily conserved protein binding sequence upstream of a plant light-regulated gene.

inferredcites →https://doi.org/10.1073/pnas.89.9.3736openalex-snapshot

Functional expression of a probable Arabidopsis thaliana potassium channel in Saccharomyces cerevisiae.

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/jbc.m007303200openalex-snapshot

Guard Cell Inward K+ Channel Activity inArabidopsis Involves Expression of the Twin Channel Subunits KAT1 and KAT2

inferredcites →https://doi.org/10.1093/genetics/154.1.421openalex-snapshot

Genetic Analysis of Salt-Tolerant Mutants in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/jxb/46.1.143openalex-snapshot

Circumnutation and gravitropism cause root waving inArabidopsis thaliana

inferredcites →https://doi.org/10.1093/pcp/41.5.541openalex-snapshot

A Null Mutation in a bZIP Factor Confers ABA-Insensitivity in Arabidopsis thaliana

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

Plant bZIP proteins gather at ACGT elements

inferredcites →https://doi.org/10.1098/rstb.1998.0299openalex-snapshot

Signalling of abscisic acid to regulate plant growth

inferredcites →https://doi.org/10.1104/pp.104.2.761openalex-snapshot

Drought Rhizogenesis in Arabidopsis thaliana (Differential Responses of Hormonal Mutants)

inferredcites →https://doi.org/10.1104/pp.105.2.761openalex-snapshot

Characterization and Expression of Photosystem II Genes (psbE, psbF, and psbL) from the Facultative Crassulacean Acid Metabolism Plant Mesembryanthemum crystallinum

inferredcites →https://doi.org/10.1104/pp.111.2.363openalex-snapshot

The Interaction of Light and Abscisic Acid in the Regulation of Plant Gene Expression

inferredcites →https://doi.org/10.1104/pp.111.2.381openalex-snapshot

Abscisic Acid Induces the Alcohol Dehydrogenase Gene in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.115.2.327openalex-snapshot

Gene Expression and Signal Transduction in Water-Stress Response

inferredcites →https://doi.org/10.1104/pp.124.3.941openalex-snapshot

Genetic Analysis of Plant Salt Tolerance Using Arabidopsis

inferredcites →https://doi.org/10.1104/pp.96.1.291openalex-snapshot

Abscisic Acid Control of rbcS and cab Transcription in Tomato Leaves

inferredcites →https://doi.org/10.1105/tpc.10.6.1043openalex-snapshot

The Arabidopsis Abscisic Acid Response Locus ABI4 Encodes an APETALA2 Domain Protein

inferredcites →https://doi.org/10.1105/tpc.11.10.1897openalex-snapshot

ABI1 Protein Phosphatase 2C Is a Negative Regulator of Abscisic Acid Signaling

inferredcites →https://doi.org/10.1105/tpc.12.4.599openalex-snapshot

The Arabidopsis Abscisic Acid Response Gene ABI5 Encodes a Basic Leucine Zipper Transcription Factor

inferredcites →https://doi.org/10.1105/tpc.12.7.1103openalex-snapshot

Interactions between Abscisic Acid and Ethylene Signaling Cascades

inferredcites →https://doi.org/10.1105/tpc.12.7.1117openalex-snapshot

Regulation of Abscisic Acid Signaling by the Ethylene Response Pathway in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.4.10.1251openalex-snapshot

Isolation of the Arabidopsis ABI3 Gene by Positional Cloning

inferredcites →https://doi.org/10.1105/tpc.6.2.251openalex-snapshot

A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress.

inferredcites →https://doi.org/10.1105/tpc.9.1.5openalex-snapshot

Hexokinase as a Sugar Sensor in Higher Plants

inferredcites →https://doi.org/10.1105/tpc.9.5.759openalex-snapshot

The Arabidopsis ABSCISIC ACID-INSENSITIVE2 (ABI2) and ABI1 genes encode homologous protein phosphatases 2C involved in abscisic acid signal transduction.

inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot

A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

inferredcites →https://doi.org/10.1111/j.1399-3054.1984.tb06343.xopenalex-snapshot

The isolation and characterization of abscisic acid‐insensitive mutants of Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1399-3054.1995.tb05114.xopenalex-snapshot

Arabidopsis mutants with reduced response to NaCl and osmotic stress

inferredcites →https://doi.org/10.1126/science.250.4978.274openalex-snapshot

Reversible Root Tip Rotation in Arabidopsis Seedlings Induced by Obstacle-Touching Stimulus

inferredcites →https://doi.org/10.1126/science.282.5387.287openalex-snapshot

Role of Farnesyltransferase in ABA Regulation of Guard Cell Anion Channels and Plant Water Loss

inferredcites →https://doi.org/10.1126/science.3289117openalex-snapshot

The Leucine Zipper: A Hypothetical Structure Common to a New Class of DNA Binding Proteins

inferredcites →https://doi.org/10.1126/science.7910981openalex-snapshot

Arabidopsis ABA Response Gene ABI1 : Features of a Calcium-Modulated Protein Phosphatase

inferredcites →https://doi.org/10.1126/science.8197457openalex-snapshot

A Protein Phosphatase 2C Involved in ABA Signal Transduction in Arabidopsis thaliana

inferredcites →https://doi.org/10.1128/mcb.8.5.1985openalex-snapshot

Transcriptional regulation of the Arabidopsis thaliana chalcone synthase gene.

inferredcites →https://doi.org/10.1128/mcb.8.5.1985-1992.1988openalex-snapshot

Transcriptional Regulation of the Arabidopsis thaliana Chalcone Synthase Gene

inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.377openalex-snapshot

THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS

inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.199openalex-snapshot

ABSCISIC ACID SIGNAL TRANSDUCTION

inferredcites →https://doi.org/10.1146/annurev.pp.39.060188.002255openalex-snapshot

Metabolism And Physiology Of Abscisic Acid

inferredcites →https://doi.org/10.1385/0-89603-391-0:259openalex-snapshot

In Planta AgrobacteriumMediated Transformation of Adult Arabidopsis thaliana Plants by Vacuum Infiltration

What points at this work

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

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Tacdpk1-5a, a Calcium-Dependent Protein Kinase Gene in T. Aestivum, Positively Regulate Drought Response Through Modulating Distinct Osmotic Stress Responsive-Associated Processes

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Other Tropisms and their Relationship to Gravitropism

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Ethylene and Senescence Processes

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Transcription Factors and Hormone‐Mediated Mechanisms Regulate Stomata Development and Responses Under Abiotic Stresses: An Overview

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Phytohormones and Drought Stress: Plant Responses to Transcriptional Regulation

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CDK Inhibitors

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The Molecular Networks of Abiotic Stress Signaling

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Ethylene and Senescence Processes

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Abscisic Acid Regulates Fleshy Fruit Ripening and Stress Resistance

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The Molecular Networks of Abiotic Stress Signaling

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Emerging Trends in Functional Genomics for Stress Tolerance in Crop Plants

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Transcription Factors: Improving Abiotic Stress Tolerance in Plants

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Transcription Factors: Improving Abiotic Stress Tolerance in Plants

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Vegetable Crops (Chili Pepper and Onion): Approaches to Improve Crop Productivity and Abiotic Stress Tolerance

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Translational Biology Approaches to Improve Abiotic Stress Tolerance in Crops

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Developing Robust Crop Plants for Sustaining Growth and Yield Under Adverse Climatic Changes

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Role of Abscisic Acid Signaling in Drought Tolerance and Preharvest Sprouting Under Climate Change

inferred← citeshttps://doi.org/10.1002/9783527675265.ch22openalex-snapshot

Transcription Factors: Modulating Plant Adaption in the Scenario of Changing Climate

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Role of Transcription Factors in Abiotic Stress Tolerance in Crop Plants

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A Conserved DT2‐bZIP66‐NF‐YC4 Regulatory Module Confers Drought Tolerance in Rice and Arabidopsis

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Expression patterns of the ZmASR family during simulated drought stress in maize

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Transcription factors as tools to engineer enhanced drought stress tolerance in plants

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Factors that affect protein abundance of a positive regulator of abscisic acid signalling, the basic leucine zipper transcription factor ABRE‐binding factor 2 (ABF2)

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Transcriptomic analysis of sweet potato under dehydration stress identifies candidate genes for drought tolerance

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High‐throughput quantitative assessment of ABA‐responsive elements at single‐nucleotide resolution

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Mechanisms Underlying Plant Tolerance to Abiotic Stresses

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Salt Stress Signaling and Mechanisms of Plant Salt Tolerance

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Functional Genomics for Tolerance to Abiotic Stress in Cereals

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Transgenic Crops for Abiotic Stress Tolerance

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New insights into abiotic stress signalling in plants

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The Role of Hormones during Seed Development and Germination

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Biotechnology Approaches To Engineering Drought Tolerant Crop

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Plant Acclimation to Environmental Stress

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Role of DREB-Like Proteins in Improving Stress Tolerance of Transgenic Crops

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Crop Improvement Through Plant Tissue Culture

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Major Phytohormones Under Abiotic Stress

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Abiotic Stress in Crops: Candidate Genes, Osmolytes, Polyamines, and Biotechnological Intervention

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Drought Stress Responses and Signal Transduction in Plants

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Overview of Signal Transduction in Plants Under Salt and Drought Stresses

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Genomic Improvement of Rice for Drought, Aluminum, and Iron Toxicity Stress Tolerance

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Drought and Salt Stress in Cereals

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Nitric Oxide in Drought Stress Signalling and Tolerance in Plants

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Transgenic Approaches for Abiotic Stress Tolerance in Crop Plants

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Understanding How Plants Respond to Drought Stress at the Molecular and Whole Plant Levels

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Transcription Factors Involved in Plant Drought Tolerance Regulation

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Present Status and Future Prospects of Transgenic Approaches for Drought Tolerance

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Plant Molecular Adaptations and Strategies Under Drought Stress

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MicroRNAs: A Potential Resource and Tool in Enhancing Plant Tolerance to Drought

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Adaptation Strategies and Defence Mechanisms of Plants During Environmental Stress

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Transgenic Plants for Improved Salinity and Drought Tolerance

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Molecular responses of higher plants to dehydration

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Adaptation to a Changing Environment: The Regulatory Role of Small RNAs

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Identification of Traits, Genes, and Crops of the Future

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ABA Regulation of Plant Responses to Drought and Salt Stresses

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ABA Regulation of the Cold Stress Response in Plants

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ABA and the Floral Transition

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Drought-inducible—but ABA-independent—thaumatin-like protein from carrot (Daucus carota L.)

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An abiotic stress-responsive bZIP transcription factor from wild and cultivated tomatoes regulates stress-related genes

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Salt tolerance in soybean WF-7 is partially regulated by ABA and ROS signaling and involves withholding toxic Cl− ions from aerial tissues

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Cross-talk between abscisic acid-dependent and abscisic acid-independent pathways during abiotic stress

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ABA signaling in stress-response and seed development

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Expression patterns of WRKY genes in di-haploid Populus simonii × P. nigra in response to salinity stress revealed by quantitative real-time PCR and RNA sequencing

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AtERF15 is a positive regulator of ABA response

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CarNAC4, a NAC-type chickpea transcription factor conferring enhanced drought and salt stress tolerances in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s00299-016-2036-5openalex-snapshot

Wheat bHLH-type transcription factor gene TabHLH1 is crucial in mediating osmotic stresses tolerance through modulating largely the ABA-associated pathway

inferred← citeshttps://doi.org/10.1007/s00299-020-02512-4openalex-snapshot

ABA-dependent bZIP transcription factor, CsbZIP18, from Camellia sinensis negatively regulates freezing tolerance in Arabidopsis

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Phytohormone signaling and crosstalk in regulating drought stress response in plants

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TaCDPK1-5A positively regulates drought response through modulating osmotic stress responsive-associated processes in wheat (Triticum aestivum)

inferred← citeshttps://doi.org/10.1007/s00344-018-9817-8openalex-snapshot

Identification of Wheat d-Cysteine Desulfhydrase (TaD-CDes) Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Stomatal Closure in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s00344-023-11175-wopenalex-snapshot

Ectopic Expression of the Potato StD26 Encoding a Ribosomal Protein S27 Enhances Salt Tolerance in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1007/s00425-003-1105-5openalex-snapshot

Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance

inferred← citeshttps://doi.org/10.1007/s00425-004-1444-xopenalex-snapshot

The ABI2-dependent abscisic acid signalling controls HrpN-induced drought tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s00425-006-0302-4openalex-snapshot

Functional roles of the pepper pathogen-induced bZIP transcription factor, CAbZIP1, in enhanced resistance to pathogen infection and environmental stresses

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1007/s00425-008-0837-7openalex-snapshot

Functional roles of the pepper antimicrobial protein gene, CaAMP1, in abscisic acid signaling, and salt and drought tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s00425-008-0857-3openalex-snapshot

Identification of OsbZIP72 as a positive regulator of ABA response and drought tolerance in rice

inferred← citeshttps://doi.org/10.1007/s00425-010-1271-1openalex-snapshot

A tomato glutaredoxin gene SlGRX1 regulates plant responses to oxidative, drought and salt stresses

inferred← citeshttps://doi.org/10.1007/s00425-011-1403-2openalex-snapshot

Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress

inferred← citeshttps://doi.org/10.1007/s00425-011-1496-7openalex-snapshot

Cloning and characterization of a maize bZIP transcription factor, ZmbZIP72, confers drought and salt tolerance in transgenic Arabidopsis

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1007/s00425-011-1580-zopenalex-snapshot

The pepper extracellular peroxidase CaPO2 is required for salt, drought and oxidative stress tolerance as well as resistance to fungal pathogens

inferred← citeshttps://doi.org/10.1007/s00425-012-1820-xopenalex-snapshot

Isolation of an abscisic acid senescence and ripening inducible gene from litchi and functional characterization under water stress

inferred← citeshttps://doi.org/10.1007/s00425-013-1979-9openalex-snapshot

Genomic surveys and expression analysis of bZIP gene family in castor bean (Ricinus communis L.)

inferred← citeshttps://doi.org/10.1007/s00425-013-1985-yopenalex-snapshot

A systems biology perspective on the role of WRKY transcription factors in drought responses in plants

inferred← citeshttps://doi.org/10.1007/s00425-013-2001-2openalex-snapshot

Heterologous expression of Arabidopsis ABF4 gene in potato enhances tuberization through ABA-GA crosstalk regulation

inferred← citeshttps://doi.org/10.1007/s00425-019-03104-7openalex-snapshot

OsbZIP42 is a positive regulator of ABA signaling and confers drought tolerance to rice

inferred← citeshttps://doi.org/10.1007/s00425-023-04232-xopenalex-snapshot

A pervasive phosphorylation cascade modulation of plant transcription factors in response to abiotic stress

inferred← citeshttps://doi.org/10.1007/s00438-007-0306-1openalex-snapshot

SAZ, a new SUPERMAN-like protein, negatively regulates a subset of ABA-responsive genes in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s00438-008-0385-7openalex-snapshot

Systematic analysis of NPK1-like genes in rice reveals a stress-inducible gene cluster co-localized with a quantitative trait locus of drought resistance

inferred← citeshttps://doi.org/10.1007/s00438-009-0432-zopenalex-snapshot

Identification and functional validation of a unique set of drought induced genes preferentially expressed in response to gradual water stress in peanut

inferred← citeshttps://doi.org/10.1007/s10059-009-0058-3openalex-snapshot

An ARIA-Interacting AP2 Domain Protein Is a Novel Component of ABA Signaling

inferred← citeshttps://doi.org/10.1007/s10059-010-0070-7openalex-snapshot

AtNEK6 interacts with ARIA and is involved in ABA response during seed germination

inferred← citeshttps://doi.org/10.1007/s10059-011-0300-7openalex-snapshot

Overexpression of AtMYB52 Confers ABA Hypersensitivity and Drought Tolerance

inferred← citeshttps://doi.org/10.1007/s10059-012-0080-8openalex-snapshot

Overexpression of Arabidopsis Translationally Controlled Tumor Protein Gene AtTCTP Enhances Drought Tolerance with Rapid ABA-Induced Stomatal Closure

inferred← citeshttps://doi.org/10.1007/s10059-013-0036-7openalex-snapshot

Abiotic Stress Responsive Rice ASR1 and ASR3 Exhibit Different Tissue-Dependent Sugar and Hormone-Sensitivities

inferred← citeshttps://doi.org/10.1007/s10059-013-2245-5openalex-snapshot

ATHB17 Is a Positive Regulator of Abscisic Acid Response during Early Seedling Growth

inferred← citeshttps://doi.org/10.1007/s10142-004-0119-9openalex-snapshot

Effect of herbicidal application of 2,4-dichlorophenoxyacetic acid in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s10142-010-0187-yopenalex-snapshot

Modulation of transcription factor and metabolic pathway genes in response to water-deficit stress in rice

inferred← citeshttps://doi.org/10.1007/s10142-014-0394-zopenalex-snapshot

ABI-like transcription factor gene TaABL1 from wheat improves multiple abiotic stress tolerances in transgenic plants

inferred← citeshttps://doi.org/10.1007/s10265-011-0412-3openalex-snapshot

ABA-mediated transcriptional regulation in response to osmotic stress in plants

inferred← citeshttps://doi.org/10.1007/s10265-011-0448-4openalex-snapshot

The Arabidopsis AtbZIP1 transcription factor is a positive regulator of plant tolerance to salt, osmotic and drought stresses

inferred← citeshttps://doi.org/10.1007/s10265-021-01330-3openalex-snapshot

Plant adaptability in karst regions

inferred← citeshttps://doi.org/10.1007/s10528-012-9546-9openalex-snapshot

Sensitivity of Translation Initiation Factor eIF1 as a Molecular Target of Salt Toxicity to Sodic-Alkaline Stress in the Halophytic Grass Leymus chinensis

inferred← citeshttps://doi.org/10.1007/s10535-006-0141-yopenalex-snapshot

Transgenic plants with improved dehydration-stress tolerance: Progress and future prospects

inferred← citeshttps://doi.org/10.1007/s10535-010-0038-7openalex-snapshot

Transcription factors in plants and ABA dependent and independent abiotic stress signalling

inferred← citeshttps://doi.org/10.1007/s10535-017-0734-7openalex-snapshot

Overexpression of ERF96, a small ethylene response factor gene, enhances salt tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s10709-013-9702-0openalex-snapshot

The RING-H2 finger gene 1 (RHF1) encodes an E3 ubiquitin ligase and participates in drought stress response in Nicotiana tabacum

inferred← citeshttps://doi.org/10.1007/s10725-010-9475-8openalex-snapshot

Genomic analysis of allelopathic response to low nitrogen and barnyardgrass competition in rice (Oryza sativa L.)

inferred← citeshttps://doi.org/10.1007/s10725-012-9727-xopenalex-snapshot

Maize (Zea mays L.) homologue of ABA-insensitive (ABI) 5 gene plays a negative regulatory role in abiotic stresses response

inferred← citeshttps://doi.org/10.1007/s10725-015-0095-1openalex-snapshot

Expression patterns of WRKY genes in di-haploid Populus simonii × P. nigra in response to osmotic stress and ABA treatment

inferred← citeshttps://doi.org/10.1007/s10725-015-0124-0openalex-snapshot

A chickpea stress-responsive NAC transcription factor, CarNAC5, confers enhanced tolerance to drought stress in transgenic Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11032-009-9341-4openalex-snapshot

Constitutive expression of the barley HvWRKY38 transcription factor enhances drought tolerance in turf and forage grass (Paspalum notatum Flugge)

inferred← citeshttps://doi.org/10.1007/s11032-011-9576-8openalex-snapshot

Expression of the Arabidopsis AtMYB44 gene confers drought/salt-stress tolerance in transgenic soybean

inferred← citeshttps://doi.org/10.1007/s11032-012-9793-9openalex-snapshot

Down-regulation of OsPDCD5, a homolog of the mammalian PDCD5, increases rice tolerance to salt stress

inferred← citeshttps://doi.org/10.1007/s11032-015-0374-6openalex-snapshot

EcbZIP60, a basic leucine zipper transcription factor from Eleusine coracana L. improves abiotic stress tolerance in tobacco by activating unfolded protein response pathway

inferred← citeshttps://doi.org/10.1007/s11032-016-0470-2openalex-snapshot

A ramie (Boehmeria nivea) bZIP transcription factor BnbZIP3 positively regulates drought, salinity and heavy metal tolerance

inferred← citeshttps://doi.org/10.1007/s11032-017-0758-xopenalex-snapshot

Guard-cell-specific expression of Arabidopsis ABF4 improves drought tolerance of tomato and tobacco

inferred← citeshttps://doi.org/10.1007/s11033-010-0664-3openalex-snapshot

Abscisic acid response element binding factor 1 is required for establishment of Arabidopsis seedlings during winter

inferred← citeshttps://doi.org/10.1007/s11033-012-1550-yopenalex-snapshot

Over-expression of TaMYB33 encoding a novel wheat MYB transcription factor increases salt and drought tolerance in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11033-012-1758-xopenalex-snapshot

Isolation and characterization of two ABRE-binding proteins: EABF and EABF1 from the oil palm

inferred← citeshttps://doi.org/10.1007/s11033-012-2481-3openalex-snapshot

Isolation and functional characterization of a salt responsive transcriptional factor, LrbZIP from lotus root (Nelumbo nucifera Gaertn)

inferred← citeshttps://doi.org/10.1007/s11033-013-3001-9openalex-snapshot

Overexpression of the Malus hupehensis MhNPR1 gene increased tolerance to salt and osmotic stress in transgenic tobacco

inferred← citeshttps://doi.org/10.1007/s11033-020-05451-1openalex-snapshot

Phosphatase AtDBP1 negatively regulates drought and salt tolerance through altering leaf surface permeability in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11103-004-0417-6openalex-snapshot

The ethylene-responsive factor like protein 1 (CaERFLP1) of hot pepper (Capsicum annuum L.) interacts in vitro with both GCC and DRE/CRT sequences with different binding affinities: Possible biological roles of CaERFLP1 in response to pathogen infection and high salinity conditions in transgenic…

inferred← citeshttps://doi.org/10.1007/s11103-004-1581-4openalex-snapshot

The homeobox genes ATHB12 and ATHB7encode potential regulators of growth in response to water deficit in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11103-005-2418-5openalex-snapshot

Transcriptional Regulation of ABI3- and ABA-responsive Genes Including RD29B and RD29A in Seeds, Germinating Embryos, and Seedlings of Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11103-005-7294-5openalex-snapshot

Arabidopsis ERF4 is a transcriptional repressor capable of modulating ethylene and abscisic acid responses

inferred← citeshttps://doi.org/10.1007/s11103-005-7306-5openalex-snapshot

Expression profiling reveals COI1 to be a key regulator of genes involved in wound- and methyl jasmonate-induced secondary metabolism, defence, and hormone interactions

inferred← citeshttps://doi.org/10.1007/s11103-005-8767-2openalex-snapshot

Redundant and Distinct Functions of the ABA Response Loci ABA-INSENSITIVE(ABI)5 and ABRE-BINDING FACTOR (ABF)3

inferred← citeshttps://doi.org/10.1007/s11103-006-0055-2openalex-snapshot

Differential gene expression of wheat progeny with contrasting levels of transpiration efficiency

inferred← citeshttps://doi.org/10.1007/s11103-006-9072-4openalex-snapshot

Transcriptional activator TSRF1 reversely regulates pathogen resistance and osmotic stress tolerance in tobacco

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1007/s11103-007-9182-7openalex-snapshot

Arabidopsis EIN2 modulates stress response through abscisic acid response pathway

inferred← citeshttps://doi.org/10.1007/s11103-008-9298-4openalex-snapshot

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

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1007/s11103-008-9451-0openalex-snapshot

Characterization of promoter elements required for expression and induction by sucrose of the Arabidopsis COX5b-1 nuclear gene, encoding the zinc-binding subunit of cytochrome c oxidase

inferred← citeshttps://doi.org/10.1007/s11103-009-9538-2openalex-snapshot

Ectopic over-expression of BhHsf1, a heat shock factor from the resurrection plant Boea hygrometrica, leads to increased thermotolerance and retarded growth in transgenic Arabidopsis and tobacco

inferred← citeshttps://doi.org/10.1007/s11103-009-9575-xopenalex-snapshot

Overexpression of soybean ubiquitin-conjugating enzyme gene GmUBC2 confers enhanced drought and salt tolerance through modulating abiotic stress-responsive gene expression in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11103-009-9592-9openalex-snapshot

The bZIP transcription factor OsABF1 is an ABA responsive element binding factor that enhances abiotic stress signaling in rice

inferred← citeshttps://doi.org/10.1007/s11103-010-9629-0openalex-snapshot

The pepper oxidoreductase CaOXR1 interacts with the transcription factor CaRAV1 and is required for salt and osmotic stress tolerance

inferred← citeshttps://doi.org/10.1007/s11103-010-9684-6openalex-snapshot

Two cotton Cys2/His2-type zinc-finger proteins, GhDi19-1 and GhDi19-2, are involved in plant response to salt/drought stress and abscisic acid signaling

inferred← citeshttps://doi.org/10.1007/s11103-010-9717-1openalex-snapshot

Functional characterisation of OsCPK21, a calcium-dependent protein kinase that confers salt tolerance in rice

inferred← citeshttps://doi.org/10.1007/s11103-011-9738-4openalex-snapshot

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

inferred← citeshttps://doi.org/10.1007/s11103-011-9854-1openalex-snapshot

A transcriptomic analysis reveals the nature of salinity tolerance of a wheat introgression line

inferred← citeshttps://doi.org/10.1007/s11103-013-0040-5openalex-snapshot

GmNFYA3, a target gene of miR169, is a positive regulator of plant tolerance to drought stress

inferred← citeshttps://doi.org/10.1007/s11103-013-0082-8openalex-snapshot

Cochaperonin CPN20 negatively regulates abscisic acid signaling in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11103-013-0115-3openalex-snapshot

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

inferred← citeshttps://doi.org/10.1007/s11103-014-0242-5openalex-snapshot

Identification and functional roles of CaDIN1 in abscisic acid signaling and drought sensitivity

inferred← citeshttps://doi.org/10.1007/s11103-014-0251-4openalex-snapshot

Arabidopsis drought-induced protein Di19-3 participates in plant response to drought and high salinity stresses

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1007/s11103-015-0411-1openalex-snapshot

Overexpression of the MYB37 transcription factor enhances abscisic acid sensitivity, and improves both drought tolerance and seed productivity in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1007/s11103-016-0514-3openalex-snapshot

Repression of ARF10 by microRNA160 plays an important role in the mediation of leaf water loss

inferred← citeshttps://doi.org/10.1007/s11103-017-0693-6openalex-snapshot

Structural characterization of a novel full-length transcript promoter from Horseradish Latent Virus (HRLV) and its transcriptional regulation by multiple stress responsive transcription factors

inferred← citeshttps://doi.org/10.1007/s11103-018-0713-1openalex-snapshot

The wheat TabZIP2 transcription factor is activated by the nutrient starvation-responsive SnRK3/CIPK protein kinase

inferred← citeshttps://doi.org/10.1007/s11103-018-0729-6openalex-snapshot

Role of Arabidopsis ABF1/3/4 during det1 germination in salt and osmotic stress conditions

inferred← citeshttps://doi.org/10.1007/s11103-018-0769-yopenalex-snapshot

Expression of the Arabidopsis ABF4 gene in potato increases tuber yield, improves tuber quality and enhances salt and drought tolerance

inferred← citeshttps://doi.org/10.1007/s11103-019-00951-6openalex-snapshot

Maize NCP1 negatively regulates drought and ABA responses through interacting with and inhibiting the activity of transcription factor ABP9

inferred← citeshttps://doi.org/10.1007/s11105-014-0704-6openalex-snapshot

Gene Family Analysis of the Arabidopsis NF-YA Transcription Factors Reveals Opposing Abscisic Acid Responses During Seed Germination

inferred← citeshttps://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.)

inferred← citeshttps://doi.org/10.1007/s11105-023-01412-7openalex-snapshot

Accumulated Endogenous Abscisic Acid Contributes to the Cold Tolerance of Pre-planted Cultivated Tobacco

inferred← citeshttps://doi.org/10.1007/s11240-005-3800-3openalex-snapshot

Overexpression of Arabidopsis ABF3 gene enhances tolerance to droughtand cold in transgenic lettuce (Lactuca sativa)

inferred← citeshttps://doi.org/10.1007/s11240-006-9143-xopenalex-snapshot

Transgenic Agrostis mongolica Roshev. with enhanced tolerance to drought and heat stresses obtained from Agrobacterium-mediated transformation

inferred← citeshttps://doi.org/10.1007/s11240-012-0258-yopenalex-snapshot

Molecular characterization of a stress-response bZIP transcription factor in banana

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1007/s11240-017-1335-zopenalex-snapshot

Over-expression of a grape WRKY transcription factor gene, VlWRKY48, in Arabidopsis thaliana increases disease resistance and drought stress tolerance

inferred← citeshttps://doi.org/10.1007/s11240-017-1348-7openalex-snapshot

Overexpression of an alfalfa (Medicago sativa) gene, MsDUF, negatively impacted seed germination and response to osmotic stress in transgenic tobacco

inferred← citeshttps://doi.org/10.1007/s11240-018-01546-7openalex-snapshot

Arabidopsis zinc finger homeodomain protein ZHD5 promotes shoot regeneration and confers other cytokinin-related phenotypes when overexpressed

inferred← citeshttps://doi.org/10.1007/s11248-005-5076-0openalex-snapshot

Hahb-4, a sunflower homeobox-leucine zipper gene, is a developmental regulator and confers drought tolerance to Arabidopsis thaliana plants

inferred← citeshttps://doi.org/10.1007/s11295-017-1109-0openalex-snapshot

Enhanced vacuolar invertase activity and capability for carbohydrate import in GA-treated inflorescence correlate with increased fruit set in grapevine

inferred← citeshttps://doi.org/10.1007/s11356-021-12649-8openalex-snapshot

Nexus on climate change: agriculture and possible solution to cope future climate change stresses

inferred← citeshttps://doi.org/10.1007/s11427-012-4332-9openalex-snapshot

Arabidopsis F-box gene FOA1 involved in ABA signaling

inferred← citeshttps://doi.org/10.1007/s11434-013-5941-9openalex-snapshot

Functional analysis of the ABA-responsive protein family in ABA and stress signal transduction in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11738-012-0969-zopenalex-snapshot

Analysis and application of RD29 genes in abiotic stress response

inferred← citeshttps://doi.org/10.1007/s11738-015-1889-5openalex-snapshot

The soybean gene, GmMYBJ2, encodes a R2R3-type transcription factor involved in drought stress tolerance in Arabidopsis thaliana

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