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

https://doi.org/10.1007/s00299-015-1907-5
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What this work says

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

inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/bf00029852openalex-snapshot
The 5?-region of Arabidopsis thaliana cor15a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression
inferredcites →https://doi.org/10.1007/s00425-009-0895-5openalex-snapshot
Tolerance to various environmental stresses conferred by the salt-responsive rice gene ONAC063 in transgenic Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-011-1403-2openalex-snapshot
Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress
inferredcites →https://doi.org/10.1007/s10142-003-0088-4openalex-snapshot
Gene expression profiling of plant responses to abiotic stress
inferredcites →https://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
inferredcites →https://doi.org/10.1007/s11103-006-9089-8openalex-snapshot
A novel drought-inducible gene, ATAF1, encodes a NAC family protein that negatively regulates the expression of stress-responsive genes in Arabidopsis
inferredcites →https://doi.org/10.1007/s12374-013-0457-zopenalex-snapshot
CarNAC2, a novel NAC transcription factor in chickpea (Cicer arietinum L.), is associated with drought-response and various developmental processes in transgenic arabidopsis
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.08.004openalex-snapshot
AP2/ERF family transcription factors in plant abiotic stress responses
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.10.005openalex-snapshot
NAC transcription factors in plant abiotic stress responses
inferredcites →https://doi.org/10.1016/j.bbamem.2010.05.015openalex-snapshot
Interaction of two intrinsically disordered plant stress proteins (COR15A and COR15B) with lipid membranes in the dry state
inferredcites →https://doi.org/10.1016/j.bbrc.2008.09.030openalex-snapshot
Comparative analysis of ESTs in response to drought stress in chickpea (C. arietinum L.)
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.pbi.2006.01.019openalex-snapshot
Understanding regulatory networks and engineering for enhanced drought tolerance in plants
inferredcites →https://doi.org/10.1016/j.pbi.2009.07.016openalex-snapshot
cis-Regulatory elements in plant cell signaling
inferredcites →https://doi.org/10.1016/j.plantsci.2005.05.035openalex-snapshot
DNA-binding specificity and molecular functions of NAC transcription factors
inferredcites →https://doi.org/10.1016/j.plaphy.2009.09.002openalex-snapshot
Characterization of a chickpea (Cicer arietinum L.) NAC family gene, CarNAC5, which is both developmentally- and stress-regulated
inferredcites →https://doi.org/10.1016/j.tplants.2004.12.012openalex-snapshot
Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters
inferredcites →https://doi.org/10.1016/j.tplants.2010.02.006openalex-snapshot
WRKY transcription factors
inferredcites →https://doi.org/10.1016/s0076-6879(07)28006-1openalex-snapshot
Plant Gene Networks in Osmotic Stress Response: From Genes to Regulatory Networks
inferredcites →https://doi.org/10.1016/s0097-8485(01)00099-7openalex-snapshot
Application of a time-delay neural network to promoter annotation in the Drosophila melanogaster genome
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/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/10.1017/s0007114512000797openalex-snapshot
Nutritional quality and health benefits of chickpea (Cicer arietinumL.): a review
inferredcites →https://doi.org/10.1023/a:1008620002136openalex-snapshot
Diversity for abiotic and biotic stress resistance in the wild annual Cicer species
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/nbt.2491openalex-snapshot
Draft genome sequence of chickpea (Cicer arietinum) provides a resource for trait improvement
inferredcites →https://doi.org/10.1038/nbt766openalex-snapshot
Overexpression of a plasma membrane Na+/H+ antiporter gene improves salt tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1042/bj20091234openalex-snapshot
The Arabidopsis thaliana NAC transcription factor family: structure–function relationships and determinants of ANAC019 stress signalling
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00746.xopenalex-snapshot
Abscisic acid regulation of gene expression during water‐deficit stress in the era of the Arabidopsis genome
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.2003.01708.xopenalex-snapshot
Interaction between two cis ‐acting elements, ABRE and DRE, in ABA‐dependent expression of Arabidopsis rd29A gene in response to dehydration and high‐salinity stresses
inferredcites →https://doi.org/10.1074/jbc.m705217200openalex-snapshot
Identification of a Calmodulin-binding NAC Protein as a Transcriptional Repressor in Arabidopsis
inferredcites →https://doi.org/10.1093/dnares/10.6.239openalex-snapshot
Comprehensive Analysis of NAC Family Genes in Oryza sativa and Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/err462openalex-snapshot
TaNAC2, a NAC-type wheat transcription factor conferring enhanced multiple abiotic stress tolerances in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erv386openalex-snapshot
A stress-responsive NAC transcription factor SNAC3 confers heat and drought tolerance through modulation of reactive oxygen species in rice
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/nar/27.1.297openalex-snapshot
Plant cis-acting regulatory DNA elements (PLACE) database: 1999
inferredcites →https://doi.org/10.1093/pcp/pch037openalex-snapshot
A Combination of the Arabidopsis DREB1A Gene and Stress-Inducible rd29A Promoter Improved Drought- and Low-Temperature Stress Tolerance in Tobacco by Gene Transfer
inferredcites →https://doi.org/10.1093/pcp/pcp082openalex-snapshot
Physiological and Molecular Approaches to Improve Drought Resistance in Soybean
inferredcites →https://doi.org/10.1104/pp.009993openalex-snapshot
ACTCAT, a Novel cis-Acting Element for Proline- and Hypoosmolarity-Responsive Expression of theProDHGene Encoding Proline Dehydrogenase in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.041442openalex-snapshot
Pathogen- and NaCl-Induced Expression of the SCaM-4 Promoter Is Mediated in Part by a GT-1 Box That Interacts with a GT-1-Like Transcription Factor
inferredcites →https://doi.org/10.1104/pp.106.094292openalex-snapshot
Modulation of Ethylene Responses Affects Plant Salt-Stress Responses
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/10.1105/tpc.010362openalex-snapshot
Arabidopsis Basic Leucine Zipper Proteins That Mediate Stress-Responsive Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.10.8.1391openalex-snapshot
Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.104.022699openalex-snapshot
Isolation and Functional Analysis of Arabidopsis Stress-Inducible NAC Transcription Factors That Bind to a Drought-Responsivecis-Element in theearly responsive to dehydration stress 1Promoter[W]
inferredcites →https://doi.org/10.1105/tpc.105.035881openalex-snapshot
Functional Analysis of anArabidopsisTranscription Factor, DREB2A, Involved in Drought-Responsive Gene Expression
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.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.1365-313x.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.2011.04687.xopenalex-snapshot
Soybean NAC transcription factors promote abiotic stress tolerance and lateral root formation in transgenic plants
inferredcites →https://doi.org/10.1111/tpj.12173openalex-snapshot
A draft genome sequence of the pulse crop chickpea ( C icer arietinum L.)
inferredcites →https://doi.org/10.1126/science.1166386openalex-snapshot
Trifurcate Feed-Forward Regulation of Age-Dependent Cell Death Involving miR164 in Arabidopsis
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.571openalex-snapshot
PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.463openalex-snapshot
P LANT C ELLULAR AND M OLECULAR R ESPONSES TO H IGH S ALINITY
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/10.1371/journal.pone.0114107openalex-snapshot
Genome-Wide Identification and Expression Analysis of the CaNAC Family Members in Chickpea during Development, Dehydration and ABA Treatments
inferredcites →https://doi.org/10.3389/fmicb.2013.00248openalex-snapshot
Roles of NAC transcription factors in the regulation of biotic and abiotic stress responses in plants

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.4135723openalex-extracted
Exploring Drought-Responsive Crucial Genes in Sorghum
inferred← citeshttps://doi.org/10.1002/9781394209965.ch5openalex-snapshot
Basic Bioinformatics for Identification and Analysis of Candidate Genes in Plants Toward Crop Improvement
inferred← citeshttps://doi.org/10.1002/agj2.20715openalex-snapshot
Comparative transcriptome analysis of Rosa chinensis ‘Old Blush’ provides insights into the crucial factors and signaling pathways in salt stress response
inferred← citeshttps://doi.org/10.1002/bies.201800018openalex-snapshot
May the Fittest Protein Evolve: Favoring the Plant‐Specific Origin and Expansion of NAC Transcription Factors
inferred← citeshttps://doi.org/10.1007/978-3-030-40277-8_14openalex-snapshot
NAC Transcription Factors in Drought and Salinity Tolerance
inferred← citeshttps://doi.org/10.1007/978-3-031-12990-2_9openalex-snapshot
The Role of Transcription Factors in Response to Biotic Stresses in Maize
inferred← citeshttps://doi.org/10.1007/978-981-15-6345-4_3openalex-snapshot
Arabidopsis thaliana: Model Plant for the Study of Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1007/s00299-016-1996-9openalex-snapshot
Identification and characterization of a novel NAC-like gene in chrysanthemum (Dendranthema lavandulifolium)
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/s00299-019-02461-7openalex-snapshot
Overexpression of CrCOMT from Carex rigescens increases salt stress and modulates melatonin synthesis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-025-03524-8openalex-snapshot
PgF3H gene enhances drought tolerance in transgenic Arabidopsis by regulating flavonoid biosynthesis and stress response
inferred← citeshttps://doi.org/10.1007/s00344-019-10056-5openalex-snapshot
Differential Gene Expression Pattern of Drought Responsive Transcription Factors in Chickpea: An Expressional Analysis
inferred← citeshttps://doi.org/10.1007/s00344-021-10463-7openalex-snapshot
The Role of PpNAC187 in Pear Drought and Salt Stress
inferred← citeshttps://doi.org/10.1007/s00344-022-10639-9openalex-snapshot
Enhancement of Drought Tolerance in Transgenic Arabidopsis thaliana Plants Overexpressing Chickpea Ca14-3-3 Gene
inferred← citeshttps://doi.org/10.1007/s00344-026-12140-zopenalex-snapshot
AlNAC2 Transcription Factor from a Halophyte Aeluropus lagopoides Confers Salinity and Drought Tolerance via Ion and ROS Homeostasis
inferred← citeshttps://doi.org/10.1007/s00425-016-2609-0openalex-snapshot
Arabidopsis AtNAP functions as a negative regulator via repression of AREB1 in salt stress response
inferred← citeshttps://doi.org/10.1007/s00425-020-03366-6openalex-snapshot
Engineering salinity tolerance in plants: progress and prospects
inferred← citeshttps://doi.org/10.1007/s10265-021-01270-yopenalex-snapshot
The biotechnological importance of the plant-specific NAC transcription factor family in crop improvement
inferred← citeshttps://doi.org/10.1007/s10535-017-0761-4openalex-snapshot
Osmotic stress affects growth, content of chlorophyll, abscisic acid, Na+, and K+, and expression of novel NAC genes in contrasting rice cultivars
inferred← citeshttps://doi.org/10.1007/s10725-017-0295-yopenalex-snapshot
Genome-wide identification, classification and expression analysis of NAC family of genes in sorghum [Sorghum bicolor (L.) Moench]
inferred← citeshttps://doi.org/10.1007/s11032-023-01433-wopenalex-snapshot
OsNAC74 affects grain protein content and various biological traits by regulating OsAAP6 expression in rice
inferred← citeshttps://doi.org/10.1007/s11103-017-0643-3openalex-snapshot
The Glycine soja NAC transcription factor GsNAC019 mediates the regulation of plant alkaline tolerance and ABA sensitivity
inferred← citeshttps://doi.org/10.1007/s11103-018-0792-zopenalex-snapshot
Picea wilsonii transcription factor NAC2 enhanced plant tolerance to abiotic stress and participated in RFCP1-regulated flowering time
inferred← citeshttps://doi.org/10.1007/s11103-020-01091-yopenalex-snapshot
GmNAC06, a NAC domain transcription factor enhances salt stress tolerance in soybean
inferred← citeshttps://doi.org/10.1007/s11105-016-1004-0openalex-snapshot
A chickpea NAC-type transcription factor, CarNAC6, confers enhanced dehydration tolerance in Arabidopsis
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/s11240-018-1486-6openalex-snapshot
Overexpression of two cold-responsive ATAF-like NAC transcription factors from fine-stem stylo (Stylosanthes guianensis var. intermedia) enhances cold tolerance in tobacco plants
inferred← citeshttps://doi.org/10.1007/s11627-020-10105-9openalex-snapshot
An NAC transcription factor gene from Malus baccata, MbNAC29, increases cold and high salinity tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11676-017-0399-2openalex-snapshot
A novel cold-inducible promoter, PThCAP from Tamarix hispida, confers cold tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11738-019-2929-3openalex-snapshot
Altered physiological responses of LlaNAC gene of Lepidium latifolium over-expressing tobacco plants
inferred← citeshttps://doi.org/10.1007/s12042-024-09354-4openalex-snapshot
Transcriptional Regulation of Biotic and Abiotic Stress Responses: Challenges and Potential Mechanism for Stress Tolerance and Chickpea Improvement
inferred← citeshttps://doi.org/10.1007/s12298-021-00996-2openalex-snapshot
The SlNAC2 transcription factor from tomato confers tolerance to drought stress in transgenic tobacco plants
inferred← citeshttps://doi.org/10.1007/s13205-023-03643-7openalex-snapshot
Salt stress responses and alleviation strategies in legumes: a review of the current knowledge
inferred← citeshttps://doi.org/10.1007/s13562-021-00749-yopenalex-snapshot
Balancing yield trade-off in legumes during multiple stress tolerance via strategic crosstalk by native NAC transcription factors
inferred← citeshttps://doi.org/10.1007/s13580-022-00443-5openalex-snapshot
Genome-wide identification and expression analysis of the SlNAC gene family in tomato based on a high-quality genome
inferred← citeshttps://doi.org/10.1016/b978-0-12-812689-9.00016-9openalex-snapshot
Dynamic Proline Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-813066-7.00014-0openalex-snapshot
Single-Versus Multigene Transfer Approaches for Crop Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-323-98332-7.00013-5openalex-snapshot
Role of abscisic acid in regulating plant's physiological and molecular aspects under abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-443-13236-0.00010-5openalex-snapshot
Defensins in plants: Diversity and role in plant defense
inferred← citeshttps://doi.org/10.1016/b978-0-444-63661-4.00005-0openalex-snapshot
Drought-Tolerant Plants
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.06.026openalex-snapshot
Phosphorylation of ZmNAC84 at Ser-113 enhances the drought tolerance by directly modulating ZmSOD2 expression in maize
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2019.107186openalex-snapshot
Genome-wide analysis of NAC transcription factors and their response to abiotic stress in celery (Apium graveolens L.)
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.03.017openalex-snapshot
The soybean transcription factor GmNAC085 enhances drought tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104824openalex-snapshot
Latest biotechnology tools and targets for improving abiotic stress tolerance in protein legumes
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105289openalex-snapshot
Triacylglycerol Lipase A10 (Sltgla10) Gene Negatively Regulates Cold Tolerance, Vegetative and Reproductive Growth in Tomato
inferred← citeshttps://doi.org/10.1016/j.gene.2016.04.028openalex-snapshot
The Miscanthus NAC transcription factor MlNAC9 enhances abiotic stress tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.gene.2017.11.021openalex-snapshot
Transcriptome – Scale characterization of salt responsive bean TCP transcription factors
inferred← citeshttps://doi.org/10.1016/j.gene.2018.04.012openalex-snapshot
The SlNAC8 gene of the halophyte Suaeda liaotungensis enhances drought and salt stress tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.gene.2018.06.075openalex-snapshot
The chrysanthemum leaf and root transcript profiling in response to salinity stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2017.04.007openalex-snapshot
Overexpression of a tartary buckwheat R2R3-MYB transcription factor gene, FtMYB9, enhances tolerance to drought and salt stresses in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2017.05.002openalex-snapshot
The Reaumuria trigyna transcription factor RtWRKY1 confers tolerance to salt stress in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111282openalex-snapshot
Interaction between MdWRKY55 and MdNAC17-L enhances salt tolerance in apple by activating MdNHX1 expression
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111425openalex-snapshot
Inducible expression of truncated NAC62 provides tolerance against Alternaria brassicicola and imparts developmental changes in Indian mustard
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.10.022openalex-snapshot
Tartary buckwheat FtMYB10 encodes an R2R3-MYB transcription factor that acts as a novel negative regulator of salt and drought response in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.06.020openalex-snapshot
Effects, tolerance mechanisms and management of salt stress in grain legumes
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.09.012openalex-snapshot
A R2R3-MYB transcription factor gene, FtMYB13, from Tartary buckwheat improves salt/drought tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.03.028openalex-snapshot
Overexpression of grapevine VvNAC08 enhances drought tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.04.008openalex-snapshot
Ectopic expression of HaNAC1, an ATAF transcription factor from Haloxylon ammodendron, improves growth and drought tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.01.004openalex-snapshot
Overexpression of the wheat NAC transcription factor TaSNAC4-3A gene confers drought tolerance in transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110075openalex-snapshot
PbARP1 enhances salt tolerance of ‘Duli’ pear (Pyrus betulifolia Bunge) through abscisic acid signalling pathway
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110449openalex-snapshot
CaNAC67, a stress-responsive NAC transcription factor-encoding gene from chickpea (Cicer arietinum), improves drought tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111449openalex-snapshot
Sunflower NAC84 confers plant salt and drought tolerance and yield-increasing potential
inferred← citeshttps://doi.org/10.1016/j.plgene.2017.06.003openalex-snapshot
Plant NAC transcription factors responsive to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101406openalex-snapshot
Advances, challenges, and opportunities to improve drought tolerance in chickpea
inferred← citeshttps://doi.org/10.1093/aob/mcaf037openalex-snapshot
Evolution of drought resistance strategies following the introduction of white clover ( Trifolium repens L.)
inferred← citeshttps://doi.org/10.1093/database/baw099openalex-snapshot
SorghumFDB: sorghum functional genomics database with multidimensional network analysis
inferred← citeshttps://doi.org/10.1093/hr/uhae061openalex-snapshot
Phosphorylation of birch BpNAC90 improves the activation of gene expression to confer drought tolerance
inferred← citeshttps://doi.org/10.1093/plphys/kiac508openalex-snapshot
The unique sweet potato NAC transcription factor IbNAC3 modulates combined salt and drought stresses
inferred← citeshttps://doi.org/10.1093/plphys/kiac600openalex-snapshot
Growth-regulating factor 15-mediated gene regulatory network enhances salt tolerance in poplar
inferred← citeshttps://doi.org/10.1111/jpi.12850openalex-snapshot
Genetic and evolutionary dissection of melatonin response signaling facilitates the regulation of plant growth and stress responses
inferred← citeshttps://doi.org/10.1111/nph.17761openalex-snapshot
ZmMPK5 phosphorylates ZmNAC49 to enhance oxidative stress tolerance in maize
inferred← citeshttps://doi.org/10.1111/pbi.14112openalex-snapshot
MdNAC104 positively regulates apple cold tolerance via CBF‐dependent and CBF‐independent pathways
inferred← citeshttps://doi.org/10.1111/plb.13486openalex-snapshot
Genome‐wide identification and expression analysis of NAC family genes in Ginkgo biloba L.
inferred← citeshttps://doi.org/10.1111/ppl.12613openalex-snapshot
Three stress‐responsive NAC transcription factors from Populus euphratica differentially regulate salt and drought tolerance in transgenic plants
inferred← citeshttps://doi.org/10.1186/s12864-020-06913-3openalex-snapshot
Integrated small RNA and Degradome sequencing provide insights into salt tolerance in sesame (Sesamum indicum L.)
inferred← citeshttps://doi.org/10.1186/s12864-020-6479-2openalex-snapshot
Genome-wide analysis of the NAC transcription factor family in broomcorn millet (Panicum miliaceum L.) and expression analysis under drought stress
inferred← citeshttps://doi.org/10.1186/s12870-016-0882-5openalex-snapshot
Comprehensive analysis and discovery of drought-related NAC transcription factors in common bean
inferred← citeshttps://doi.org/10.1186/s12870-020-02396-2openalex-snapshot
Cloning and molecular characterization of Triticum aestivum ornithine amino transferase (TaOAT) encoding genes
inferred← citeshttps://doi.org/10.1371/journal.pone.0162556openalex-snapshot
The Salinity Responsive Mechanism of a Hydroxyproline-Tolerant Mutant of Peanut Based on Digital Gene Expression Profiling Analysis
inferred← citeshttps://doi.org/10.1371/journal.pone.0199262openalex-snapshot
Genome-wide identification and comprehensive analysis of the NAC transcription factor family in Sesamum indicum
inferred← citeshttps://doi.org/10.1371/journal.pone.0199774openalex-snapshot
RNA-Seq analysis revealed genes associated with drought stress response in kabuli chickpea (Cicer arietinum L.)
inferred← citeshttps://doi.org/10.2174/1874070701812010204openalex-snapshot
Heterologous Expression of Transcription Factor AtWRKY57 Alleviates Salt Stress-Induced Oxidative Damage
inferred← citeshttps://doi.org/10.29252/jcb.11.30.133openalex-snapshot
Transcription Factors Evaluation in a Transcriptome Analysis on Chickpea (Cicer arietinum L.) Under Drought Stress
inferred← citeshttps://doi.org/10.29252/jcb.9.24.1openalex-snapshot
Transcriptome Analysis of Iranian Local Chickpea in Response to Drought Stress
inferred← citeshttps://doi.org/10.32604/phyton.2022.023738openalex-snapshot
Chickpea C2H2-Type Zinc Finger Protein ZF2 is a Positive Regulator in Drought Response in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2017.00635openalex-snapshot
ThNAC13, a NAC Transcription Factor from Tamarix hispida, Confers Salt and Osmotic Stress Tolerance to Transgenic Tamarix and Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2019.00290openalex-snapshot
Overexpression of Chickpea Defensin Gene Confers Tolerance to Water-Deficit Stress in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2019.00890openalex-snapshot
OoNAC72, a NAC-Type Oxytropis ochrocephala Transcription Factor, Conferring Enhanced Drought and Salt Stress Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2022.833326openalex-snapshot
GmWRKY21, a Soybean WRKY Transcription Factor Gene, Enhances the Tolerance to Aluminum Stress in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2022.868142openalex-snapshot
De novo Transcriptome Analysis of Drought-Adapted Cluster Bean (Cultivar RGC-1025) Reveals the Wax Regulatory Genes Involved in Drought Resistance
inferred← citeshttps://doi.org/10.3389/fpls.2024.1353365openalex-snapshot
GhBRX.1, GhBRX.2, and GhBRX4.3 improve resistance to salt and cold stress in upland cotton
inferred← citeshttps://doi.org/10.3390/antiox11020395openalex-snapshot
Dynamic Responses of Antioxidant and Glyoxalase Systems to Seed Aging Based on Full-Length Transcriptome in Oat (Avena sativa L.)
inferred← citeshttps://doi.org/10.3390/biology13090673openalex-snapshot
Regulatory Dynamics of Plant Hormones and Transcription Factors under Salt Stress
inferred← citeshttps://doi.org/10.3390/f13081304openalex-snapshot
Picea wilsonii Transcription Factor PwNAC38 Promotes Drought and Salt Tolerance in Transgenic Arabidopsis and Apple Calli
inferred← citeshttps://doi.org/10.3390/genes15091176openalex-snapshot
RNA-Seq and WGCNA Analyses Reveal Key Regulatory Modules and Genes for Salt Tolerance in Cotton
inferred← citeshttps://doi.org/10.3390/ijms19061634openalex-snapshot
Revisiting the Role of Plant Transcription Factors in the Battle against Abiotic Stress
inferred← citeshttps://doi.org/10.3390/ijms20040799openalex-snapshot
Grain Legumes and Fear of Salt Stress: Focus on Mechanisms and Management Strategies
inferred← citeshttps://doi.org/10.3390/ijms21010286openalex-snapshot
The Soybean GmNAC019 Transcription Factor Mediates Drought Tolerance in Arabidopsis in an Abscisic Acid-Dependent Manner
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/ijms25042396openalex-snapshot
Expression Patterns and Molecular Mechanisms Regulating Drought Tolerance of Soybean [Glycine max (L.) Merr.] Conferred by Transcription Factor Gene GmNAC19
inferred← citeshttps://doi.org/10.3390/ijms25074088openalex-snapshot
Overexpression of a Fragaria vesca NAM, ATAF, and CUC (NAC) Transcription Factor Gene (FvNAC29) Increases Salt and Cold Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/life12111846openalex-snapshot
Molecular Breeding and Drought Tolerance in Chickpea
inferred← citeshttps://doi.org/10.3390/metabo11070457openalex-snapshot
Plant Responses to Abiotic Stresses and Rhizobacterial Biostimulants: Metabolomics and Epigenetics Perspectives
inferred← citeshttps://doi.org/10.3732/ajb.1600419openalex-snapshot
Autopolyploidization, geographic origin, and metabolome evolution in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12218921openalex-snapshot
Additional file 1 of Cloning and molecular characterization of Triticum aestivum ornithine amino transferase (TaOAT) encoding genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.12218927openalex-snapshot
Additional file 2 of Cloning and molecular characterization of Triticum aestivum ornithine amino transferase (TaOAT) encoding genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.12218933openalex-snapshot
Additional file 3 of Cloning and molecular characterization of Triticum aestivum ornithine amino transferase (TaOAT) encoding genes
inferred← citeshttps://doi.org/10.70675/bfef7490z999dz4b16z9f53ze499c532079dopenalex-snapshot
Analyse des facteurs de transcription de la famille NAC chez le blé tendre (Triticum aestivum L.) et leur implication dans la réponse à des stress abiotiques
inferred← citeshttps://doi.org/10.7287/peerj.12921v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Transcriptomics analysis of field-droughted pear (Pyrus spp.) reveals potential drought stress genes and metabolic pathways (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12921v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Transcriptomics analysis of field-droughted pear (Pyrus spp.) reveals potential drought stress genes and metabolic pathways (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12921v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Transcriptomics analysis of field-droughted pear (Pyrus spp.) reveals potential drought stress genes and metabolic pathways (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12921v0.3/reviews/2openalex-snapshot
Peer Review #2 of "Transcriptomics analysis of field-droughted pear (Pyrus spp.) reveals potential drought stress genes and metabolic pathways (v0.3)"
inferred← citeshttps://doi.org/10.7287/peerj.12921v0.4/reviews/3openalex-snapshot
Peer Review #3 of "Transcriptomics analysis of field-droughted pear (Pyrus spp.) reveals potential drought stress genes and metabolic pathways (v0.4)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7211v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Transcription factors involved in abiotic stress responses in Maize (Zea mays L.) and their roles in enhanced productivity in the post genomics era (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.12921openalex-snapshot
Transcriptomics analysis of field-droughted pear ( Pyrus spp. ) reveals potential drought stress genes and metabolic pathways
inferred← citeshttps://doi.org/10.7717/peerj.7211openalex-snapshot
Transcription factors involved in abiotic stress responses in Maize ( Zea mays L.) and their roles in enhanced productivity in the post genomics era
inferred← citeshttps://doi.org/10.7717/peerj.7319openalex-snapshot
Selection of reliable reference genes for quantitative RT-PCR in garlic under salt stress
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