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Genome wide identification of NAC transcription factors and their role in abiotic stress tolerance in Chenopodium quinoa
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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/jmbi.2000.4315openalex-snapshot
Predicting transmembrane protein topology with a hidden markov model: application to complete genomes11Edited by F. Cohen
inferredcites →https://doi.org/10.1007/s00299-011-1068-0openalex-snapshot
Plant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network
inferredcites →https://doi.org/10.1007/s00425-007-0498-yopenalex-snapshot
Two NAC domain transcription factors, SND1 and NST1, function redundantly in regulation of secondary wall synthesis in fibers of Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-016-2609-0openalex-snapshot
Arabidopsis AtNAP functions as a negative regulator via repression of AREB1 in salt stress response
inferredcites →https://doi.org/10.1007/s12155-009-9047-9openalex-snapshot
A Bioinformatic Analysis of NAC Genes for Plant Cell Wall Development in Relation to Lignocellulosic Bioenergy Production
inferredcites →https://doi.org/10.1016/j.devcel.2008.09.019openalex-snapshot
The NAC Domain Transcription Factors FEZ and SOMBRERO Control the Orientation of Cell Division Plane in Arabidopsis Root Stem Cells
inferredcites →https://doi.org/10.1016/j.envexpbot.2012.07.004openalex-snapshot
Salt tolerance mechanisms in quinoa (Chenopodium quinoa Willd.)
inferredcites →https://doi.org/10.1016/j.gene.2010.06.008openalex-snapshot
Genome-wide analysis of NAC transcription factor family in rice
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.plantsci.2014.07.003openalex-snapshot
The Arabidopsis NAC transcription factor NTL4 participates in a positive feedback loop that induces programmed cell death under heat stress conditions
inferredcites →https://doi.org/10.1016/j.tplants.2004.12.010openalex-snapshot
NAC transcription factors: structurally distinct, functionally diverse
inferredcites →https://doi.org/10.1016/j.ympev.2016.04.009openalex-snapshot
Molecular and cytogenetic evidence for an allotetraploid origin of Chenopodium quinoa and C. berlandieri (Amaranthaceae)
inferredcites →https://doi.org/10.1016/s0092-8674(00)80902-2openalex-snapshot
A Homolog of NO APICAL MERISTEM Is an Immediate Target of the Floral Homeotic Genes APETALA3/PISTILLATA
inferredcites →https://doi.org/10.1016/s0092-8674(00)81093-4openalex-snapshot
The No Apical Meristem Gene of Petunia Is Required for Pattern Formation in Embryos and Flowers and Is Expressed at Meristem and Primordia Boundaries
inferredcites →https://doi.org/10.1038/cr.2009.108openalex-snapshot
Dual function of Arabidopsis ATAF1 in abiotic and biotic stress responses
inferredcites →https://doi.org/10.1038/nplants.2016.13openalex-snapshot
Arabidopsis NAC transcription factor JUB1 regulates GA/BR metabolism and signalling
inferredcites →https://doi.org/10.1038/nrg928openalex-snapshot
Splitting pairs: the diverging fates of duplicated genes
inferredcites →https://doi.org/10.1038/s41598-017-03435-zopenalex-snapshot
Genome-wide survey of switchgrass NACs family provides new insights into motif and structure arrangements and reveals stress-related and tissue-specific NACs
inferredcites →https://doi.org/10.1038/sj.embor.7400093openalex-snapshot
Structure of the conserved domain of ANAC, a member of the NAC family of transcription factors
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.1365-313x.2002.01359.xopenalex-snapshot
Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high‐salinity stresses using a full‐length cDNA microarray
inferredcites →https://doi.org/10.1073/pnas.0505266102openalex-snapshot
A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation
inferredcites →https://doi.org/10.1073/pnas.0810304106openalex-snapshot
Suppressor of gamma response 1 ( SOG1 ) encodes a putative transcription factor governing multiple responses to DNA damage
inferredcites →https://doi.org/10.1081/fri-120018872openalex-snapshot
The Resistance of Quinoa ( Chenopodium quinoa Willd.) to Adverse Abiotic Factors
inferredcites →https://doi.org/10.1081/fri-120018884openalex-snapshot
Nutritional Value and Use of the Andean Crops Quinoa (Chenopodium quinoa) and Kañiwa (Chenopodium pallidicaule)
inferredcites →https://doi.org/10.1093/bioinformatics/btu817openalex-snapshot
GSDS 2.0: an upgraded gene feature visualization server
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/dnares/dsr015openalex-snapshot
Genome-Wide Survey and Expression Analysis of the Plant-Specific NAC Transcription Factor Family in Soybean During Development and Dehydration Stress
inferredcites →https://doi.org/10.1093/jxb/erq257openalex-snapshot
Ionic and osmotic relations in quinoa (Chenopodium quinoa Willd.) plants grown at various salinity levels
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/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkl1068openalex-snapshot
Exploring membrane-associated NAC transcription factors in Arabidopsis : implications for membrane biology in genome regulation
inferredcites →https://doi.org/10.1093/nar/gkw982openalex-snapshot
PlantTFDB 4.0: toward a central hub for transcription factors and regulatory interactions in plants
inferredcites →https://doi.org/10.1093/pcp/pch101openalex-snapshot
VOZ; Isolation and Characterization of Novel Vascular Plant Transcription Factors with a One-Zinc Finger from Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pct204openalex-snapshot
The NAC Family Transcription Factor OsNAP Confers Abiotic Stress Response Through the ABA Pathway
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.108.132795openalex-snapshot
Expansion and Diversification of thePopulusR2R3-MYB Family of Transcription Factors
inferredcites →https://doi.org/10.1105/tpc.012203openalex-snapshot
The CUP-SHAPED COTYLEDON3 Gene Is Required for Boundary and Shoot Meristem Formation 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.106.043018openalex-snapshot
A Membrane-Bound NAC Transcription Factor Regulates Cell Division inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.045716openalex-snapshot
Arabidopsis CUP-SHAPED COTYLEDON3 Regulates Postembryonic Shoot Meristem and Organ Boundary Formation
inferredcites →https://doi.org/10.1105/tpc.111.084913openalex-snapshot
The Arabidopsis NAC Transcription Factor VNI2 Integrates Abscisic Acid Signals into Leaf Senescence via the COR / RD Genes
inferredcites →https://doi.org/10.1105/tpc.113.118927openalex-snapshot
The Protein Phosphatase RCF2 and Its Interacting Partner NAC019 Are Critical for Heat Stress–Responsive Gene Regulation and Thermotolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.9.6.841openalex-snapshot
Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01608.xopenalex-snapshot
Genome‐wide reprogramming of metabolism and regulatory networks of Arabidopsis in response to phosphorus
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02488.xopenalex-snapshot
The transcription factor ATAF2 represses the expression of pathogenesis‐related genes in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02575.xopenalex-snapshot
AtNAC2, a transcription factor downstream of ethylene and auxin signaling pathways, is involved in salt stress response and lateral root development
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04859.xopenalex-snapshot
Dual involvement of a Medicago truncatula NAC transcription factor in root abiotic stress response and symbiotic nodule senescence
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01356.xopenalex-snapshot
Dissecting the plant transcriptome and the regulatory responses to phosphate deprivation
inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00088.xopenalex-snapshot
Transcription factors regulating leaf senescence in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/jipb.12085openalex-snapshot
Analyses of the NAC Transcription Factor Gene Family in Gossypium raimondii Ulbr.: Chromosomal Location, Structure, Phylogeny, and Expression Patterns
inferredcites →https://doi.org/10.1111/jipb.12379openalex-snapshot
ANAC005 is a membrane‐associated transcription factor and regulates vascular development inArabidopsis
inferredcites →https://doi.org/10.1111/nph.15127openalex-snapshot
Transcription factor RD 26 is a key regulator of metabolic reprogramming during dark‐induced senescence
inferredcites →https://doi.org/10.1111/pbi.12776openalex-snapshot
NAC transcription factor JUNGBRUNNEN 1 enhances drought tolerance in tomato
inferredcites →https://doi.org/10.1126/science.1133649openalex-snapshot
A NAC Gene Regulating Senescence Improves Grain Protein, Zinc, and Iron Content in Wheat
inferredcites →https://doi.org/10.1186/1471-2148-3-17openalex-snapshot
Genome-wide comparative phylogenetic analysis of the rice and Arabidopsis Dof gene families
inferredcites →https://doi.org/10.1186/1471-2148-5-1openalex-snapshot
The WRKY transcription factor superfamily: its origin in eukaryotes and expansion in plants
inferredcites →https://doi.org/10.1186/1471-2164-9-44openalex-snapshot
Genome-wide analysis of CCCH zinc finger family in Arabidopsis and rice
inferredcites →https://doi.org/10.1186/1471-2229-10-145openalex-snapshot
Comprehensive Analysis of NAC Domain Transcription Factor Gene Family in Populus trichocarpa
inferredcites →https://doi.org/10.1186/1756-0500-4-302openalex-snapshot
Characterization of barley (Hordeum vulgare L.) NAC transcription factors suggests conserved functions compared to both monocots and dicots
inferredcites →https://doi.org/10.1186/s12864-019-5500-0openalex-snapshot
Genome-wide analysis of the NAC transcription factor family in Tartary buckwheat (Fagopyrum tataricum)
inferredcites →https://doi.org/10.1186/s12870-015-0644-9openalex-snapshot
TaNAC29, a NAC transcription factor from wheat, enhances salt and drought tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1186/s12870-018-1367-5openalex-snapshot
Comprehensive analysis of NAC transcription factors uncovers their roles during fiber development and stress response in cotton
inferredcites →https://doi.org/10.1186/s12896-016-0261-1openalex-snapshot
Over-expression of a NAC 67 transcription factor from finger millet (Eleusine coracana L.) confers tolerance against salinity and drought stress in rice
inferredcites →https://doi.org/10.1371/journal.pone.0105726openalex-snapshot
Arabidopsis NAC Domain Proteins, VND1 to VND5, Are Transcriptional Regulators of Secondary Wall Biosynthesis in Vessels
inferredcites →https://doi.org/10.1371/journal.pone.0135667openalex-snapshot
The Wheat NAC Transcription Factor TaNAC2L Is Regulated at the Transcriptional and Post-Translational Levels and Promotes Heat Stress Tolerance in Transgenic Arabidopsis
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
inferredcites →https://doi.org/10.3390/genes10020131openalex-snapshot
Evolution and Identification of the WRKY Gene Family in Quinoa (Chenopodium quinoa)
inferredcites →https://doi.org/10.3390/genes9020035openalex-snapshot
Genome-Wide Characterization of Heat-Shock Protein 70s from Chenopodium quinoa and Expression Analyses of Cqhsp70s in Response to Drought Stress
inferredcites →https://doi.org/10.4161/15592324.2014.989746openalex-snapshot
TheArabidopsisNAC transcription factor NST2 functions together with SND1 and NST1 to regulate secondary wall biosynthesis in fibers of inflorescence stems
inferredcites →https://doi.org/10.4161/psb.2.1.3606openalex-snapshot
Membrane Regulation of Cytokinin-Mediated Cell Division inArabidopsis
inferredcites →https://doi.org/10.4161/psb.22092openalex-snapshot
Arabidopsis NAC transcription factor JUNGBRUNNEN1 affects thermomemory-associated genes and enhances heat stress tolerance in primed and unprimed conditions
inferredcites →https://doi.org/10.4161/psb.6.8.15792openalex-snapshot
Auxin modulation of salt stress signaling in Arabidopsis seed germination
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-981-16-6361-1_5openalex-snapshot
Breeding Efforts for Crop Productivity in Abiotic Stress Environment
inferred← citeshttps://doi.org/10.1007/s11240-020-01830-5openalex-snapshot
Ectopic expression of AmNAC1 from Avicennia marina (Forsk.) Vierh. confers multiple abiotic stress tolerance in yeast and tobacco
inferred← citeshttps://doi.org/10.1016/b978-0-443-13490-6.00033-3openalex-snapshot
Thermo-primed cellular networks for plant stress management
inferred← citeshttps://doi.org/10.1038/s42003-023-05613-4openalex-snapshot
A chromosome-scale assembly of the quinoa genome provides insights into the structure and dynamics of its subgenomes
inferred← citeshttps://doi.org/10.3389/fpls.2022.866409openalex-snapshot
Thermo-Priming Mediated Cellular Networks for Abiotic Stress Management in Plants
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