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

https://doi.org/10.1007/s00299-016-2036-5
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Phylogenetic Analysis of Plant Basic Helix-Loop-Helix Proteins
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Plant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network
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CarNAC4, a NAC-type chickpea transcription factor conferring enhanced drought and salt stress tolerances in Arabidopsis
inferredcites →https://doi.org/10.1007/s00299-016-1935-9openalex-snapshot
Ectopic expression of phloem motor protein pea forisome PsSEO-F1 enhances salinity stress tolerance in tobacco
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/s00299-016-1954-6openalex-snapshot
Identification of the ASR gene family from Brachypodium distachyon and functional characterization of BdASR1 in response to drought stress
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Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance
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Function of wheat phosphate transporter gene TaPHT2;1 in Pi translocation and plant growth regulation under replete and limited Pi supply conditions
inferredcites →https://doi.org/10.1007/s11105-012-0548-xopenalex-snapshot
Overexpression of TaSRK2C1, a Wheat SNF1-Related Protein Kinase 2 Gene, Increases Tolerance to Dehydration, Salt, and Low Temperature in Transgenic Tobacco
inferredcites →https://doi.org/10.1016/j.cub.2012.11.022openalex-snapshot
The Stomatal Response to Reduced Relative Humidity Requires Guard Cell-Autonomous ABA Synthesis
inferredcites →https://doi.org/10.1016/j.envexpbot.2005.12.006openalex-snapshot
Roles of glycine betaine and proline in improving plant abiotic stress resistance
inferredcites →https://doi.org/10.1016/j.gene.2006.10.009openalex-snapshot
Deciphering the regulatory mechanisms of abiotic stress tolerance in plants by genomic approaches
inferredcites →https://doi.org/10.1016/j.gene.2008.10.016openalex-snapshot
Identification of ICE2, a gene involved in cold acclimation which determines freezing tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.plantsci.2003.10.024openalex-snapshot
Potential biochemical indicators of salinity tolerance in plants
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Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants
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PIF3, a Phytochrome-Interacting Factor Necessary for Normal Photoinduced Signal Transduction, Is a Novel Basic Helix-Loop-Helix Protein
inferredcites →https://doi.org/10.1016/s0958-1669(03)00030-2openalex-snapshot
Molecular responses to drought, salinity and frost: common and different paths for plant protection
inferredcites →https://doi.org/10.1016/s1360-1385(01)01983-5openalex-snapshot
Targeting detoxification pathways: an efficient approach to obtain plants with multiple stress tolerance?
inferredcites →https://doi.org/10.1016/s1369-5266(00)00067-4openalex-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(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)00289-3openalex-snapshot
Transcription factors in plant defense and stress responses
inferredcites →https://doi.org/10.1016/s1369-5266(03)00092-xopenalex-snapshot
Regulatory network of gene expression in the drought and cold stress responses
inferredcites →https://doi.org/10.1016/s1671-2927(12)60780-9openalex-snapshot
Molecular Characterization and Expression Analysis of TaZFP15, a C2H2-Type Zinc Finger Transcription Factor Gene in Wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1120204.xopenalex-snapshot
Role of the Arabidopsis CBF transcriptional activators in cold acclimation
inferredcites →https://doi.org/10.1038/7036openalex-snapshot
Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor
inferredcites →https://doi.org/10.1038/cr.2008.26openalex-snapshot
FIT interacts with AtbHLH38 and AtbHLH39 in regulating iron uptake gene expression for iron homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1038/nature08591openalex-snapshot
The abscisic acid receptor PYR1 in complex with abscisic acid
inferredcites →https://doi.org/10.1042/bj20091221openalex-snapshot
Threonine at position 306 of the KAT1 potassium channel is essential for channel activity and is a target site for ABA-activated SnRK2/OST1/SnRK2.6 protein kinase
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00754.xopenalex-snapshot
Osmolyte accumulation: can it really help increase crop yield under drought conditions?
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A novel cold‐inducible zinc finger protein from soybean, SCOF‐1, enhances cold tolerance in transgenic plants
inferredcites →https://doi.org/10.1073/pnas.0401572101openalex-snapshot
Overexpression of a zinc-finger protein gene from rice confers tolerance to cold, dehydration, and salt stress in transgenic tobacco
inferredcites →https://doi.org/10.1073/pnas.0407107101openalex-snapshot
The phytochrome-interacting transcription factor, PIF3, acts early, selectively, and positively in light-induced chloroplast development
inferredcites →https://doi.org/10.1073/pnas.0907095106openalex-snapshot
Type 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0912021106openalex-snapshot
Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair
inferredcites →https://doi.org/10.1073/pnas.0912030107openalex-snapshot
Guard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca 2+ affinities
inferredcites →https://doi.org/10.1073/pnas.1018367108openalex-snapshot
Arabidopsis decuple mutant reveals the importance of SnRK2 kinases in osmotic stress responses in vivo
inferredcites →https://doi.org/10.1073/pnas.1118876109openalex-snapshot
FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS 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/10.1074/jbc.275.3.1723openalex-snapshot
ABFs, a Family of ABA-responsive Element Binding Factors
inferredcites →https://doi.org/10.1078/0176-1617-01065openalex-snapshot
Exogenous silicon (Si) increases antioxidant enzyme activity and reduces lipid peroxidation in roots of salt-stressed barley (Hordeum vulgareL.)
inferredcites →https://doi.org/10.1093/emboj/21.10.2441openalex-snapshot
PIF4, a phytochrome‐interacting bHLH factor, functions as a negative regulator of phytochrome B signaling in Arabidopsis
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/err210openalex-snapshot
Role of DREBs in regulation of abiotic stress responses in plants
inferredcites →https://doi.org/10.1093/jxb/err216openalex-snapshot
A bHLH transcription factor, DvIVS, is involved in regulation of anthocyanin synthesis in dahlia (Dahlia variabilis)
inferredcites →https://doi.org/10.1093/molbev/msp288openalex-snapshot
Origin and Diversification of Basic-Helix-Loop-Helix Proteins in Plants
inferredcites →https://doi.org/10.1093/pcp/pcr106openalex-snapshot
Achievements and Challenges in Understanding Plant Abiotic Stress Responses and Tolerance
inferredcites →https://doi.org/10.1101/gad.1077503openalex-snapshot
ICE1: a regulator of cold-induced transcriptome and freezing tolerance in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.14.4.391openalex-snapshot
Loss of PTEN facilitates HIF-1-mediated gene expression
inferredcites →https://doi.org/10.1101/gad.828000openalex-snapshot
Functional selectivity of recombinant mammalian SWI/SNF subunits
inferredcites →https://doi.org/10.1104/pp.006478openalex-snapshot
Transcription Factor CBF4 Is a Regulator of Drought Adaptation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.011021openalex-snapshot
Common Components, Networks, and Pathways of Cross-Tolerance to Stress. The Central Role of “Redox” and Abscisic Acid-Mediated Controls
inferredcites →https://doi.org/10.1104/pp.102.011007openalex-snapshot
Osmotic Stress Tolerance of Transgenic Tobacco Expressing a Gene Encoding a Membrane-Located Receptor-Like Protein from Tobacco Plants
inferredcites →https://doi.org/10.1104/pp.106.080580openalex-snapshot
Genome-Wide Analysis of Basic/Helix-Loop-Helix Transcription Factor Family in Rice and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.129791openalex-snapshot
Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses
inferredcites →https://doi.org/10.1104/pp.109.143867openalex-snapshot
Conservation of Lotus and Arabidopsis Basic Helix-Loop-Helix Proteins Reveals New Players in Root Hair Development
inferredcites →https://doi.org/10.1104/pp.111.190983openalex-snapshot
Co-Overexpression FIT with AtbHLH38 or AtbHLH39 in Arabidopsis-Enhanced Cadmium Tolerance via Increased Cadmium Sequestration in Roots and Improved Iron Homeostasis of Shoots
inferredcites →https://doi.org/10.1104/pp.112.210740openalex-snapshot
A Basic Helix-Loop-Helix Transcription Factor, PtrbHLH, of Poncirus trifoliata Confers Cold Tolerance and Modulates Peroxidase-Mediated Scavenging of Hydrogen Peroxide
inferredcites →https://doi.org/10.1104/pp.127.1.315openalex-snapshot
Hormonal Changes in the Grains of Rice Subjected to Water Stress during Grain Filling
inferredcites →https://doi.org/10.1105/tpc.006130openalex-snapshot
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling
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.013839openalex-snapshot
The Arabidopsis Basic/Helix-Loop-Helix Transcription Factor Family[W]
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Interaction between the bHLH Transcription Factor FIT and ETHYLENE INSENSITIVE3/ETHYLENE INSENSITIVE3-LIKE1 Reveals Molecular Linkage between the Regulation of Iron Acquisition and Ethylene Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.12.10.1863openalex-snapshot
The TT8 Gene Encodes a Basic Helix-Loop-Helix Domain Protein Required for Expression of DFR and BAN Genes in Arabidopsis Siliques
inferredcites →https://doi.org/10.1105/tpc.13.5.1035openalex-snapshot
Overexpression of the Tobacco Tsi1 Gene Encoding an EREBP/AP2–Type Transcription Factor Enhances Resistance against Pathogen Attack and Osmotic Stress in Tobacco
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.
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Calcium-Activated K+ Channels and Calcium-Induced Calcium Release by Slow Vacuolar Ion Channels in Guard Cell Vacuoles Implicated in the Control of Stomatal Closure.
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Differential abscisic acid regulation of guard cell slow anion channels in Arabidopsis wild-type and abi1 and abi2 mutants.
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Reactive oxygen species homeostasis and signalling during drought and salinity stresses
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Drought, ozone, ABA and ethylene: new insights from cell to plant to community
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ABA signal transduction at the crossroad of biotic and abiotic stress responses
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The bHLH transcription factor MdbHLH3 promotes anthocyanin accumulation and fruit colouration in response to low temperature in apples
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Disruption of AtMRP4, a guard cell plasma membrane ABCC‐type ABC transporter, leads to deregulation of stomatal opening and increased drought susceptibility
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04477.xopenalex-snapshot
OsbHLH148, a basic helix‐loop‐helix protein, interacts with OsJAZ proteins in a jasmonate signaling pathway leading to drought tolerance in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04887.xopenalex-snapshot
Epoxycarotenoid cleavage by NCED5 fine‐tunes ABA accumulation and affects seed dormancy and drought tolerance with other NCED family members
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The role of abscisic acid and auxin in the response of poplar to abiotic stress
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03718.xopenalex-snapshot
MtbHLH1, a bHLH transcription factor involved in Medicago truncatula nodule vascular patterning and nodule to plant metabolic exchanges
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/10.1126/science.290.5499.2105openalex-snapshot
Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112122openalex-snapshot
Abscisic Acid: Emergence of a Core Signaling Network
inferredcites →https://doi.org/10.1146/annurev.arplant.44.1.357openalex-snapshot
Quaternary Ammonium and Tertiary Sulfonium Compounds in Higher Plants
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S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.56.032604.144046openalex-snapshot
ABSCISIC ACID BIOSYNTHESIS AND CATABOLISM
inferredcites →https://doi.org/10.1186/1471-2229-12-22openalex-snapshot
The cold-induced basic helix-loop-helix transcription factor gene MdCIbHLH1encodes an ICE-like protein in apple
inferredcites →https://doi.org/10.1201/9780367812140openalex-snapshot
Cellular and Molecular Physiology of Cell Volume Regulation
inferredcites →https://doi.org/10.1242/dev.00880openalex-snapshot
The bHLH genes GLABRA3 (GL3) and ENHANCER OF GLABRA3(EGL3) specify epidermal cell fate in the Arabidopsis root
inferredcites →https://doi.org/10.1371/journal.pone.0044843openalex-snapshot
Arabidopsis bHLH100 and bHLH101 Control Iron Homeostasis via a FIT-Independent Pathway
inferredcites →https://doi.org/10.1371/journal.pone.0078997openalex-snapshot
Evolution of the bHLH Genes Involved in Stomatal Development: Implications for the Expansion of Developmental Complexity of Stomata in Land Plants
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Calcium-Activated K + Channels and Calcium-Induced Calcium Release by Slow Vacuolar Ion Channels in Guard Cell Vacuoles Implicated in the Control of Stomatal Closure
inferredcites →https://doi.org/10.3390/ijms160715251openalex-snapshot
Function of ABA in Stomatal Defense against Biotic and Drought Stresses

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4681119openalex-extracted
Cloning and Expression Analysis of the Transcription Factor Tabhlh35
inferred← citeshttps://doi.org/10.2139/ssrn.4765684openalex-extracted
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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Molecular Breeding and Omics Approaches for Food Quality and Functional Food
inferred← citeshttps://doi.org/10.1007/978-3-032-24001-9_8openalex-snapshot
Effectiveness of Foliar Spray of Stress-Mitigating Chemicals in Salinity Stress Management
inferred← citeshttps://doi.org/10.1007/978-981-19-5121-3_12openalex-snapshot
Cereals and Phytohormones Under Salt Stress
inferred← citeshttps://doi.org/10.1007/s00122-025-05019-2openalex-snapshot
ZmWAK3-mediated cell wall remodeling and stomatal dynamics modulate drought tolerance in maize seedlings
inferred← citeshttps://doi.org/10.1007/s00299-020-02590-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-023-03115-5openalex-snapshot
Functional analysis of sweet cherry PavbHLH106 in the regulation of cold stress
inferred← citeshttps://doi.org/10.1007/s00299-024-03344-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-025-03428-7openalex-snapshot
A bHLH transcription factor RrUNE12 regulates salt tolerance and promotes ascorbate synthesis
inferred← citeshttps://doi.org/10.1007/s00299-025-03506-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10142-026-02032-6openalex-snapshot
Heterologous expression of DobHLH25 from Dendrobium officinale enhances drought tolerance in Arabidopsis
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Identification of QTLs related to cadmium tolerance from wild rice (Oryza nivara) using a high-density genetic map for a set of introgression lines
inferred← citeshttps://doi.org/10.1007/s11033-026-11613-4openalex-snapshot
Genetic architecture and breeding strategies for enhancing wheat (Triticum aestivum L.) tolerance to combined heat, drought, and salinity stresses
inferred← citeshttps://doi.org/10.1007/s11103-018-0761-6openalex-snapshot
Transcriptional regulation of osmotic stress tolerance in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1007/s11105-025-01627-wopenalex-snapshot
Dissecting Root-Specific Drought Responses in Contrasting Wheat Genotypes Through RNA-Seq and qRT-PCR Validation
inferred← citeshttps://doi.org/10.1007/s12298-024-01433-wopenalex-snapshot
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Heterologous expression of the maize transcription factor ZmbHLH36 enhances abiotic stress tolerance in Arabidopsis
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Integrative multi-omics approaches for crop abiotic stress tolerance
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Signaling Molecules in Ecophysiological Response Mechanisms of Salt-Stressed Plants
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Plant transcription factors and osmotic stress
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Wheat kinase TaSnRK2.4 forms a functional module with phosphatase TaPP2C01 and transcription factor TaABF2 to regulate drought response
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104523openalex-snapshot
MdCIB1, an apple bHLH transcription factor, plays a positive regulator in response to drought stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105291openalex-snapshot
Surviving the enemies: Regulatory mechanisms of stomatal function in response to drought and salt stress
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ZFP37, C3H, NAC94, and bHLH148 transcription factors regulate cultivar-specific drought response by modulating r40C1 gene expression in rice
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Basic Helix-Loop-Helix (bHLH) transcription factor family in Yellow horn (Xanthoceras sorbifolia Bunge): Genome-wide characterization, chromosome location, phylogeny, structures and expression patterns
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144093openalex-snapshot
Functional analysis of AobHLH88 involved in anthocyanin synthesis using multi-omics data in Asparagus officinalis
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154449openalex-snapshot
Isolation of OSCAs in wheat and over-expression of TaOSCA14D increased salt stress tolerance
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112495openalex-snapshot
Transcriptome sequence reveal the roles of MaGME777 and MabHLH770 in drought tolerance in Musa acuminata
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113338openalex-snapshot
ZnO nanoparticles alleviate salinity stress through transcriptional and antioxidant regulation in chickpea
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.07.036openalex-snapshot
TaNF-YA7-5B, a gene encoding nuclear factor Y (NF–Y) subunit A in Triticum aestivum, confers plant tolerance to PEG-inducing dehydration simulating drought through modulating osmotic stress-associated physiological processes
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Exogenous strigolactones alleviate drought stress in wheat (Triticum aestivum L.) by promoting cell wall biogenesis to optimize root architecture
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Active oxygen generation induced by the glucose sensor TaHXK7-1A decreased the drought resistance of transgenic Arabidopsis and wheat (Triticum aestivum L.)
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Transcription factor gene TaWRKY76 confers plants improved drought and salt tolerance through modulating stress defensive-associated processes in Triticum aestivum L.
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111123openalex-snapshot
Distinct transcriptional programs control polyethylene glycol (PEG)-induced drought stress responses in oat (Avena sativa L.) shoot and roots
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Crop gene regulatory networks for precision breeding in saline environments
inferred← citeshttps://doi.org/10.1016/j.plgene.2017.07.003openalex-snapshot
Abscisic acid: A key regulator of abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.ygeno.2020.07.011openalex-snapshot
Identification and characterization of differentially expressed genes in the rice root following exogenous application of spermidine during salt stress
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c09665openalex-snapshot
Functions of Basic Helix–Loop–Helix (bHLH) Proteins in the Regulation of Plant Responses to Cold, Drought, Salt, and Iron Deficiency: A Comprehensive Review
inferred← citeshttps://doi.org/10.1080/17429145.2021.1925759openalex-snapshot
Insight into abscisic acid perception and signaling to increase plant tolerance to abiotic stress
inferred← citeshttps://doi.org/10.1093/jxb/erz307openalex-snapshot
The bHLH family member ZmPTF1 regulates drought tolerance in maize by promoting root development and abscisic acid synthesis
inferred← citeshttps://doi.org/10.1093/treephys/tpac087openalex-snapshot
Molecular plasticity to soil water deficit differs between sessile oak ( Quercus Petraea (Matt.) Liebl.) high- and low-water use efficiency genotypes
inferred← citeshttps://doi.org/10.1093/treephys/tpaf146openalex-snapshot
MhORG2, a novel negative modulator, regulates drought tolerance in apple by repressing the expression of MhAAO3 and antioxidant enzyme genes
inferred← citeshttps://doi.org/10.1111/nph.18549openalex-snapshot
TaERF87 and TaAKS1 synergistically regulate TaP5CS1 / TaP5CR1 ‐mediated proline biosynthesis to enhance drought tolerance in wheat
inferred← citeshttps://doi.org/10.1111/pce.70038openalex-snapshot
Wheat miRNA TaMIR5062‐5A Targets Calmodulin TaCML31 That Cooperates With MYB Member TaMYB77 to Modulate Drought and Salt Responses
inferred← citeshttps://doi.org/10.1111/tpj.16332openalex-snapshot
Multi‐omics atlas of combinatorial abiotic stress responses in wheat
inferred← citeshttps://doi.org/10.1111/tpj.16953openalex-snapshot
PbGBF3 enhances salt response in pear by upregulating PbAPL2 and PbSDH1 and reducing ABA‐mediated salt sensitivity
inferred← citeshttps://doi.org/10.1111/tpj.70589openalex-snapshot
The MAPK regulatory module TaMPKKK18 ‐ 3B / TaMPKK1 .2‐ 6B / TaMPK2 ‐ 1D / TaNAC2 ‐ 5B regulates low‐P stress response in Triticum aestivum
inferred← citeshttps://doi.org/10.1186/s12864-023-09911-3openalex-snapshot
Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.1186/s12864-025-11657-zopenalex-snapshot
Genome-wide analysis of the Tritipyrum bHLH gene family and the response of TtbHLH310 in salt-tolerance
inferred← citeshttps://doi.org/10.1186/s12870-018-1529-5openalex-snapshot
Comparative functional genomics analysis of bHLH gene family in rice, maize and wheat
inferred← citeshttps://doi.org/10.1186/s12870-020-02474-5openalex-snapshot
Transcription factor TabHLH49 positively regulates dehydrin WZY2 gene expression and enhances drought stress tolerance in wheat
inferred← citeshttps://doi.org/10.1186/s12870-020-02732-6openalex-snapshot
MfbHLH38, a Myrothamnus flabellifolia bHLH transcription factor, confers tolerance to drought and salinity stresses in Arabidopsis
inferred← citeshttps://doi.org/10.1186/s12870-021-02862-5openalex-snapshot
Genome-wide identification of PbrbHLH family genes, and expression analysis in response to drought and cold stresses in pear (Pyrus bretschneideri)
inferred← citeshttps://doi.org/10.1186/s12870-021-03318-6openalex-snapshot
The bHLH transcription factor AhbHLH112 improves the drought tolerance of peanut
inferred← citeshttps://doi.org/10.1186/s12870-022-03799-zopenalex-snapshot
TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.13005/bbra/3072openalex-snapshot
Potential of Molecular Plant Breeding for Sustaining the Global Food Security
inferred← citeshttps://doi.org/10.1515/biol-2018-0052openalex-snapshot
Overexpression of Zinc Finger Transcription Factor ZAT6 Enhances Salt Tolerance
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1741352/v1openalex-snapshot
TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2192486/v1openalex-snapshot
Construction of Cinnamomun bodinieri cDNA library and screening of upstream regulators of CbP5CS using yeast one hybrid
inferred← citeshttps://doi.org/10.21203/rs.3.rs-53464/v1openalex-snapshot
Genome-Wide Analysis of Basic Helix-Loop-Helix (bHLH) TFs in Sea Buckthorn (Hippophae rhamnoides)
inferred← citeshttps://doi.org/10.3389/fagro.2021.661932openalex-snapshot
Salinity Stress in Wheat (Triticum aestivum L.) in the Changing Climate: Adaptation and Management Strategies
inferred← citeshttps://doi.org/10.3389/fgene.2021.602528openalex-snapshot
Transcriptome and Comparative Chloroplast Genome Analysis of Vincetoxicum versicolor: Insights Into Molecular Evolution and Phylogenetic Implication
inferred← citeshttps://doi.org/10.3389/fpls.2018.00734openalex-snapshot
Abiotic Stress Signaling in Wheat – An Inclusive Overview of Hormonal Interactions During Abiotic Stress Responses in Wheat
inferred← citeshttps://doi.org/10.3389/fpls.2021.677611openalex-snapshot
Regulatory Mechanisms of bHLH Transcription Factors in Plant Adaptive Responses to Various Abiotic Stresses
inferred← citeshttps://doi.org/10.3389/fpls.2022.1067076openalex-snapshot
Transcriptomic and metabolic regulatory network characterization of drought responses in tobacco
inferred← citeshttps://doi.org/10.3389/fpls.2022.901128openalex-snapshot
Systematic Analysis of bHLH Transcription Factors in Cassava Uncovers Their Roles in Postharvest Physiological Deterioration and Cyanogenic Glycosides Biosynthesis
inferred← citeshttps://doi.org/10.3389/fpls.2023.1193284openalex-snapshot
Drought and recovery in barley: key gene networks and retrotransposon response
inferred← citeshttps://doi.org/10.3389/fpls.2024.1338169openalex-snapshot
Comparative transcriptome analysis reveals nicotine metabolism is a critical component for enhancing stress response intensity of innate immunity system in tobacco
inferred← citeshttps://doi.org/10.3389/fpls.2025.1653650openalex-snapshot
Whole-genome identification and functional analysis of grape bHLH transcription factors: new insights into the regulation of monoterpene biosynthesis
inferred← citeshttps://doi.org/10.3390/agronomy10060788openalex-snapshot
The Role of Stress-Responsive Transcription Factors in Modulating Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.3390/agronomy13122918openalex-snapshot
The Agropyron mongolicum bHLH Gene AmbHLH148 Positively Involved in Transgenic Nicotiana benthamiana Adaptive Response to Drought Stress
inferred← citeshttps://doi.org/10.3390/biology15060459openalex-snapshot
Deciphering the Temporal Transcriptional Dynamics and Key Regulatory Networks of Pyrus betulifolia in Response to PEG-Induced Osmotic Stress
inferred← citeshttps://doi.org/10.3390/biology8040080openalex-snapshot
Wheat Yellow Mosaic Virus NIb Interacting with Host Light Induced Protein (LIP) Facilitates Its Infection through Perturbing the Abscisic Acid Pathway in Wheat
inferred← citeshttps://doi.org/10.3390/biom11060788openalex-snapshot
Improving Performance of Salt-Grown Crops by Exogenous Application of Plant Growth Regulators
inferred← citeshttps://doi.org/10.3390/f15112051openalex-snapshot
The bHLH Transcription Factor PubHLH66 Improves Salt Tolerance in Daqing Poplar (Populus ussuriensis)
inferred← citeshttps://doi.org/10.3390/genes15050573openalex-snapshot
Insights into Salinity Tolerance in Wheat
inferred← citeshttps://doi.org/10.3390/ijms22094921openalex-snapshot
Current Understanding of bHLH Transcription Factors in Plant Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.3390/ijms23052537openalex-snapshot
CabHLH79 Acts Upstream of CaNAC035 to Regulate Cold Stress in Pepper
inferred← citeshttps://doi.org/10.3390/ijms23105546openalex-snapshot
Heterologous Expression of Dehydration-Inducible MfbHLH145 of Myrothamnus flabellifoli Enhanced Drought and Salt Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms232315053openalex-snapshot
A Novel bHLH Transcription Factor PtrbHLH66 from Trifoliate Orange Positively Regulates Plant Drought Tolerance by Mediating Root Growth and ROS Scavenging
inferred← citeshttps://doi.org/10.3390/ijms24097969openalex-snapshot
Wheat ABA Receptor TaPYL5 Constitutes a Signaling Module with Its Downstream Partners TaPP2C53/TaSnRK2.1/TaABI1 to Modulate Plant Drought Response
inferred← citeshttps://doi.org/10.3390/ijms26010331openalex-snapshot
Genetic Variation in Wheat Root Transcriptome Responses to Salinity: A Comparative Study of Tolerant and Sensitive Genotypes
inferred← citeshttps://doi.org/10.3390/ijms26115145openalex-snapshot
Molecular Mechanism of Exogenous GABA in Regulating Salt Tolerance in Tomato (Solanum lycopersicum L.)
inferred← citeshttps://doi.org/10.3390/ijms26209915openalex-snapshot
bHLH Transcription Factors in Cereal Crops: Diverse Functions in Regulating Growth, Development and Stress Responses
inferred← citeshttps://doi.org/10.3390/plants13131835openalex-snapshot
PagbHLH35 Enhances Salt Tolerance through Improving ROS Scavenging in Transgenic Poplar
inferred← citeshttps://doi.org/10.3390/plants13162315openalex-snapshot
Functions and Regulatory Mechanisms of bHLH Transcription Factors during the Responses to Biotic and Abiotic Stresses in Woody Plants
inferred← citeshttps://doi.org/10.3390/plants14060882openalex-snapshot
Identification of the bHLH Transcription Factor Family in Orah Mandarin and the Response of CrbHLH46 to Low-Temperature Stress
inferred← citeshttps://doi.org/10.3390/stresses2040033openalex-snapshot
Involvement of Nitric Oxide in Methyl Jasmonate-Mediated Regulation of Water Metabolism in Wheat Plants under Drought Stress
inferred← citeshttps://doi.org/10.34016/pjbt.2023.20.02.817openalex-snapshot
GENETIC ANALYSIS IN VARIOUS GENOTYPES OF BREAD WHEAT UNDER NORMAL AND HEAT-STRESS ENVIRONMENTS
inferred← citeshttps://doi.org/10.6084/m9.figshare.13843558openalex-snapshot
Additional file 2 of Genome-wide identification of PbrbHLH family genes, and expression analysis in response to drought and cold stresses in pear (Pyrus bretschneideri)
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787032openalex-snapshot
Additional file 10 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787035openalex-snapshot
Additional file 11 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787038openalex-snapshot
Additional file 12 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787041openalex-snapshot
Additional file 13 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787044openalex-snapshot
Additional file 14 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787047openalex-snapshot
Additional file 15 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787050openalex-snapshot
Additional file 1 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787053openalex-snapshot
Additional file 2 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787056openalex-snapshot
Additional file 3 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787059openalex-snapshot
Additional file 4 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787062openalex-snapshot
Additional file 5 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787068openalex-snapshot
Additional file 6 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787071openalex-snapshot
Additional file 7 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787074openalex-snapshot
Additional file 8 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.20787077openalex-snapshot
Additional file 9 of TaPYL4, an ABA receptor gene of wheat, positively regulates plant drought adaptation through modulating the osmotic stress-associated processes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668623openalex-snapshot
Additional file 1 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668626openalex-snapshot
Additional file 2 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668629openalex-snapshot
Additional file 3 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668632openalex-snapshot
Additional file 4 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668635openalex-snapshot
Additional file 5 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668638openalex-snapshot
Additional file 6 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668641openalex-snapshot
Additional file 7 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668644openalex-snapshot
Additional file 8 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668647openalex-snapshot
Additional file 9 of Basic helix-loop-helix (bHLH) gene family in rye (Secale cereale L.): genome-wide identification, phylogeny, evolutionary expansion and expression analyses
inferred← citeshttps://doi.org/10.7717/peerj.6519openalex-snapshot
Transcriptome analysis of osmotic-responsive genes in ABA-dependent and -independent pathways in wheat (Triticum aestivum L.) roots
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