On the public citation graph
Root‐specific NF‐Y family transcription factor, PdNF‐YB21 , positively regulates root growth and drought resistance by abscisic acid‐mediated indoylacetic acid transport in Populu s
0 signed · 311 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1006/anbo.2001.1469openalex-snapshot
Effects of Flooding and Drought on the Anatomy of Paspalum dilatatum
inferredcites →https://doi.org/10.1007/978-1-4614-8591-9_10openalex-snapshot
Lignins and Abiotic Stress: An Overview
inferredcites →https://doi.org/10.1007/bf03195675openalex-snapshot
Differential expression of candidate genes for lignin biosynthesis under drought stress in maize leaves
inferredcites →https://doi.org/10.1007/s00425-008-0773-6openalex-snapshot
The Nuclear Factor Y subunits NF-YB2 and NF-YB3 play additive roles in the promotion of flowering by inductive long-day photoperiods in Arabidopsis
inferredcites →https://doi.org/10.1007/s11103-011-9790-0openalex-snapshot
Genome-wide comparison of two poplar genotypes with different growth rates
inferredcites →https://doi.org/10.1007/s11103-017-0661-1openalex-snapshot
Overexpression of the transcription factor NF-YC9 confers abscisic acid hypersensitivity in Arabidopsis
inferredcites →https://doi.org/10.1007/s11104-008-9843-6openalex-snapshot
Rooting depth and water use efficiency of tropical maize inbred lines, differing in drought tolerance
inferredcites →https://doi.org/10.1007/s11240-016-1088-0openalex-snapshot
Wheat nuclear factor Y (NF-Y) B subfamily gene TaNF-YB3;l confers critical drought tolerance through modulation of the ABA-associated signaling pathway
inferredcites →https://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot
Abiotic Stress Signaling and Responses in Plants
inferredcites →https://doi.org/10.1016/j.cell.2017.11.045openalex-snapshot
SnapShot: Abscisic Acid Signaling
inferredcites →https://doi.org/10.1016/j.devcel.2004.06.017openalex-snapshot
The Transcription Factor FUSCA3 Controls Developmental Timing in Arabidopsis through the Hormones Gibberellin and Abscisic Acid
inferredcites →https://doi.org/10.1016/j.envexpbot.2016.05.008openalex-snapshot
Effects of limited water availability on xylem transport in liana Humulus lupulus L
inferredcites →https://doi.org/10.1016/j.ijbiomac.2017.03.146openalex-snapshot
Structural variations of lignin macromolecule from different growth years of Triploid of Populus tomentosa Carr.
inferredcites →https://doi.org/10.1016/j.pbi.2008.06.015openalex-snapshot
Functional symmetry of the B3 network controlling seed development
inferredcites →https://doi.org/10.1016/j.pbi.2014.07.009openalex-snapshot
ABA-dependent and ABA-independent signaling in response to osmotic stress in plants
inferredcites →https://doi.org/10.1016/j.pbi.2018.05.015openalex-snapshot
NUCLEAR FACTOR-Y: still complex after all these years?
inferredcites →https://doi.org/10.1016/j.plaphy.2011.01.013openalex-snapshot
Over-expression of HAP3b enhances primary root elongation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2014.06.008openalex-snapshot
Modulation of auxin content in Arabidopsis confers improved drought stress resistance
inferredcites →https://doi.org/10.1016/j.soilbio.2005.06.027openalex-snapshot
Partitioning root and microbial contributions to soil respiration in Leymus chinensis populations
inferredcites →https://doi.org/10.1016/j.tplants.2013.08.009openalex-snapshot
Localised ABA signalling mediates root growth plasticity
inferredcites →https://doi.org/10.1016/j.tplants.2019.05.009openalex-snapshot
Advances in Imaging Plant Cell Walls
inferredcites →https://doi.org/10.1016/s0378-1119(99)00368-6openalex-snapshot
The molecular biology of the CCAAT-binding factor NF-Y
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1038/nprot.2009.1openalex-snapshot
Measurement of auxin transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nprot.2010.37openalex-snapshot
Quantitative analysis of major plant hormones in crude plant extracts by high-performance liquid chromatography–mass spectrometry
inferredcites →https://doi.org/10.1038/nprot.2014.147openalex-snapshot
A simple improved-throughput xylem protoplast system for studying wood formation
inferredcites →https://doi.org/10.1038/s41467-018-06430-8openalex-snapshot
Natural variation at XND1 impacts root hydraulics and trade-off for stress responses in Arabidopsis
inferredcites →https://doi.org/10.1038/s41477-018-0190-1openalex-snapshot
Rapid and reversible root growth inhibition by TIR1 auxin signalling
inferredcites →https://doi.org/10.1038/s41477-019-0361-8openalex-snapshot
Tuning water-use efficiency and drought tolerance in wheat using abscisic acid receptors
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00798.xopenalex-snapshot
Interaction with ethylene: changing views on the role of abscisic acid in root and shoot growth responses to water stress
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01096.xopenalex-snapshot
Regulation of drought tolerance by gene manipulation of 9‐ cis ‐epoxycarotenoid dioxygenase, a key enzyme in abscisic acid biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01708.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/10.1071/fp06055openalex-snapshot
The role of root architectural traits in adaptation of wheat to water-limited environments
inferredcites →https://doi.org/10.1073/pnas.0707193104openalex-snapshot
Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water-limited acres
inferredcites →https://doi.org/10.1073/pnas.1811491115openalex-snapshot
Arabidopsis thaliana NGATHA1 transcription factor induces ABA biosynthesis by activating NCED3 gene during dehydration stress
inferredcites →https://doi.org/10.1074/jbc.m209635200openalex-snapshot
The NF-YB/NF-YC Structure Gives Insight into DNA Binding and Transcription Regulation by CCAAT Factor NF-Y
inferredcites →https://doi.org/10.1078/0176-1617-00245openalex-snapshot
Cell wall peroxidase against ferulic acid, lignin, and NaCl-reduced root growth of rice seedlings
inferredcites →https://doi.org/10.1093/forestry/cpr012openalex-snapshot
Genome-wide responses to drought in forest trees
inferredcites →https://doi.org/10.1093/jxb/43.12.1583openalex-snapshot
Maize Root Plasma Membranes Isolated by Aqueous Polymer Two-phase Partitioning: Assessment of Residual Tonoplast ATPase and Pyrophosphatase Activities
inferredcites →https://doi.org/10.1093/jxb/45.special_issue.1743openalex-snapshot
Confirmation that abscisic acid accumulation is required for maize primary root elongation at low water potentials
inferredcites →https://doi.org/10.1093/jxb/erh276openalex-snapshot
Root growth maintenance during water deficits: physiology to functional genomics
inferredcites →https://doi.org/10.1093/jxb/erq463openalex-snapshot
An arginine decarboxylase gene PtADC from Poncirus trifoliata confers abiotic stress tolerance and promotes primary root growth in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/ers400openalex-snapshot
Manipulation of arginase expression modulates abiotic stress tolerance in Arabidopsis: effect on arginine metabolism and ROS accumulation
inferredcites →https://doi.org/10.1093/jxb/ert262openalex-snapshot
Overexpression of the poplar NF-YB7 transcription factor confers drought tolerance and improves water-use efficiency in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erw472openalex-snapshot
Root xylem plasticity to improve water use and yield in water-stressed soybean
inferredcites →https://doi.org/10.1093/jxb/erx233openalex-snapshot
SnRK1 phosphorylation of FUSCA3 positively regulates embryogenesis, seed yield, and plant growth at high temperature in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erx488openalex-snapshot
A leu-rich repeat receptor-like protein kinase, FaRIPK1, interacts with the ABA receptor, FaABAR, to regulate fruit ripening in strawberry
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/pcp/pcm180openalex-snapshot
Programmed Proteome Response for Drought Avoidance/Tolerance in the Root of a C3 Xerophyte (Wild Watermelon) Under Water Deficits
inferredcites →https://doi.org/10.1093/treephys/27.7.985openalex-snapshot
Seasonal change in the drought response of wood cell development in poplar
inferredcites →https://doi.org/10.1093/treephys/tpw048openalex-snapshot
Responses of hydraulics at the whole-plant level to simulated nitrogen deposition of different levels inFraxinus mandshurica
inferredcites →https://doi.org/10.1093/treephys/tpx054openalex-snapshot
Genes and gene clusters related to genotype and drought-induced variation in saccharification potential, lignin content and wood anatomical traits in Populus nigra†
inferredcites →https://doi.org/10.1093/treephys/tpx093openalex-snapshot
PtoMYB170 positively regulates lignin deposition during wood formation in poplar and confers drought tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.028357openalex-snapshot
Xylem Wall Collapse in Water-Stressed Pine Needles
inferredcites →https://doi.org/10.1104/pp.104.047266openalex-snapshot
AtGA3ox2, a Key Gene Responsible for Bioactive Gibberellin Biosynthesis, Is Regulated during Embryogenesis by LEAFY COTYLEDON2 and FUSCA3 in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.073130openalex-snapshot
Progressive Inhibition by Water Deficit of Cell Wall Extensibility and Growth along the Elongation Zone of Maize Roots Is Related to Increased Lignin Metabolism and Progressive Stelar Accumulation of Wall Phenolics
inferredcites →https://doi.org/10.1104/pp.106.080895openalex-snapshot
The turnip Mutant of Arabidopsis Reveals That LEAFY COTYLEDON1 Expression Mediates the Effects of Auxin and Sugars to Promote Embryonic Cell Identity
inferredcites →https://doi.org/10.1104/pp.108.129494openalex-snapshot
NaCl-Induced Alternations of Cellular and Tissue Ion Fluxes in Roots of Salt-Resistant and Salt-Sensitive Poplar Species
inferredcites →https://doi.org/10.1104/pp.114.253328openalex-snapshot
Does Morphological and Anatomical Plasticity during the Vegetative Stage Make Wheat More Tolerant of Water Deficit Stress Than Rice?
inferredcites →https://doi.org/10.1104/pp.122.3.967openalex-snapshot
Abscisic Acid Accumulation Maintains Maize Primary Root Elongation at Low Water Potentials by Restricting Ethylene Production
inferredcites →https://doi.org/10.1104/pp.15.01011openalex-snapshot
MicroRNA857 Is Involved in the Regulation of Secondary Growth of Vascular Tissues in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.16.00379openalex-snapshot
Overexpression of the OsERF71 Transcription Factor Alters Rice Root Structure and Drought Resistance
inferredcites →https://doi.org/10.1104/pp.19.00391openalex-snapshot
NF-YB2 and NF-YB3 Have Functionally Diverged and Differentially Induce Drought and Heat Stress-Specific Genes
inferredcites →https://doi.org/10.1104/pp.93.4.1329openalex-snapshot
Increased Endogenous Abscisic Acid Maintains Primary Root Growth and Inhibits Shoot Growth of Maize Seedlings at Low Water Potentials
inferredcites →https://doi.org/10.1105/tpc.007542openalex-snapshot
Auxin Acts in Xylem-Associated or Medullary Cells to Mediate Apical Dominance
inferredcites →https://doi.org/10.1105/tpc.108.059444openalex-snapshot
The Arabidopsis NFYA5 Transcription Factor Is Regulated Transcriptionally and Posttranscriptionally to Promote Drought Resistance
inferredcites →https://doi.org/10.1105/tpc.112.096289openalex-snapshot
CellSeT: Novel Software to Extract and Analyze Structured Networks of Plant Cells from Confocal Images
inferredcites →https://doi.org/10.1105/tpc.15.00531openalex-snapshot
Transcriptional and Hormonal Regulation of Gravitropism of Woody Stems inPopulus
inferredcites →https://doi.org/10.1105/tpc.16.00864openalex-snapshot
CONSTANS Imparts DNA Sequence Specificity to the Histone Fold NF-YB/NF-YC Dimer
inferredcites →https://doi.org/10.1105/tpc.18.00018openalex-snapshot
Integrated Regulation of Apical Hook Development by Transcriptional Coupling of EIN3/EIL1 and PIFs in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02009.xopenalex-snapshot
Adaptation of plasma membrane H + ‐ATPase of rice roots to low pH as related to ammonium nutrition
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02099.xopenalex-snapshot
Root cortical aerenchyma improves the drought tolerance of maize ( Zea mays L.)
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02480.xopenalex-snapshot
EgMYB2, a new transcriptional activator from Eucalyptus xylem, regulates secondary cell wall formation and lignin biosynthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02520.xopenalex-snapshot
Virus‐induced gene silencing is an effective tool for assaying gene function in the basal eudicot species Papaver somniferum (opium poppy)
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04367.xopenalex-snapshot
ABA promotes quiescence of the quiescent centre and suppresses stem cell differentiation in the Arabidopsis primary root meristem
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01351.xopenalex-snapshot
Relationships between xylem anatomy, root hydraulic conductivity, leaf/root ratio and transpiration in citrus trees on different rootstocks
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03304.xopenalex-snapshot
The challenge of tree height in Eucalyptus regnans: when xylem tapering overcomes hydraulic resistance
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00892.xopenalex-snapshot
Abiotic and Biotic Stresses and Changes in the Lignin Content and Composition in Plants
inferredcites →https://doi.org/10.1111/nph.12004openalex-snapshot
Abscisic acid accumulation modulates auxin transport in the root tip to enhance proton secretion for maintaining root growth under moderate water stress
inferredcites →https://doi.org/10.1111/nph.12735openalex-snapshot
A mi R 169 isoform regulates specific NF ‐ YA targets and root architecture in A rabidopsis
inferredcites →https://doi.org/10.1111/nph.13034openalex-snapshot
Root structural and functional dynamics in terrestrial biosphere models – evaluation and recommendations
inferredcites →https://doi.org/10.1111/nph.13882openalex-snapshot
Abscisic acid regulates root growth under osmotic stress conditions via an interacting hormonal network with cytokinin, ethylene and auxin
inferredcites →https://doi.org/10.1111/pbi.12011openalex-snapshot
OsNAC5 overexpression enlarges root diameter in rice plants leading to enhanced drought tolerance and increased grain yield in the field
inferredcites →https://doi.org/10.1111/pbi.12270openalex-snapshot
Overexpression of a NF ‐ YC transcription factor from bermudagrass confers tolerance to drought and salinity in transgenic rice
inferredcites →https://doi.org/10.1111/pbi.12358openalex-snapshot
Arabidopsis EDT 1 / HDG 11 improves drought and salt tolerance in cotton and poplar and increases cotton yield in the field
inferredcites →https://doi.org/10.1111/pbi.12951openalex-snapshot
Overexpression of OsTF1L, a rice HD‐Zip transcription factor, promotes lignin biosynthesis and stomatal closure that improves drought tolerance
inferredcites →https://doi.org/10.1111/pce.12410openalex-snapshot
Role of aquaporins in determining transpiration and photosynthesis in water‐stressed plants: crop water‐use efficiency, growth and yield
inferredcites →https://doi.org/10.1111/pce.12777openalex-snapshot
An ecophysiological and developmental perspective on variation in vessel diameter
inferredcites →https://doi.org/10.1111/tpj.12554openalex-snapshot
Both CRISPR / C as‐based nucleases and nickases can be used efficiently for genome engineering in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13413openalex-snapshot
Poplar Ptab ZIP 1‐like enhances lateral root formation and biomass growth under drought stress
inferredcites →https://doi.org/10.1126/science.1128691openalex-snapshot
The Genome of Black Cottonwood, Populus trichocarpa (Torr. & Gray)
inferredcites →https://doi.org/10.1126/science.1227491openalex-snapshot
How Does Plant Cell Wall Nanoscale Architecture Correlate with Enzymatic Digestibility?
inferredcites →https://doi.org/10.1126/science.aag1550openalex-snapshot
A transcription factor hierarchy defines an environmental stress response network
inferredcites →https://doi.org/10.1186/1753-6561-5-s1-o8openalex-snapshot
Chikungunya, a new threat propagated by the cosmopolite Aedes albopictus
inferredcites →https://doi.org/10.1186/1753-6561-5-s7-p103openalex-snapshot
Drought stress and changes in the lignin content and composition in Eucalyptus
inferredcites →https://doi.org/10.1242/dev.159202openalex-snapshot
Continuous root xylem formation and vascular acclimation to water deficit involves endodermal ABA signalling via miR165
inferredcites →https://doi.org/10.2307/2413665openalex-snapshot
MEGA: Molecular Evolutionary Genetics Analysis, Version 1.02.
inferredcites →https://doi.org/10.3389/fpls.2015.00547openalex-snapshot
How tree roots respond to drought
inferredcites →https://doi.org/10.3389/fpls.2017.01493openalex-snapshot
The Biphasic Root Growth Response to Abscisic Acid in Arabidopsis Involves Interaction with Ethylene and Auxin Signalling Pathways
inferredcites →https://doi.org/10.3389/fpls.2018.01875openalex-snapshot
Engineering Drought Resistance in Forest Trees
inferredcites →https://doi.org/10.3389/fpls.2018.01979openalex-snapshot
GmWRKY16 Enhances Drought and Salt Tolerance Through an ABA-Mediated Pathway in Arabidopsis thaliana
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.4876979openalex-extracted
Systematic Identification and Characterization of the Apple Nf-Y Genes Reveal Mdnf-Yb14 Confers Drought Tolerance in Transformed Arabidopsis Thaliana
inferred← citeshttps://doi.org/10.1002/bies.70023openalex-snapshot
NF‐Y Transcription Factors: Key Players in Biotic and Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/978-1-0716-4358-7_19openalex-snapshot
CRISPR-Cas in Woody Perennial Plants: Methods, Efficiency, Applications, and Challenges to Creating Commercial Varieties with High Ecological and Economic Value
inferred← citeshttps://doi.org/10.1007/978-3-031-26669-0_18openalex-snapshot
Tweaking CRISPR/Cas for Developing Salt and Drought Tolerant Crop Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-46150-7_20openalex-snapshot
Genome Editing in Forest Trees
inferred← citeshttps://doi.org/10.1007/978-3-031-50787-8_11openalex-snapshot
Applied Genomics in Poplar: Genome Editing and Modifications
inferred← citeshttps://doi.org/10.1007/978-981-97-4363-6_13openalex-snapshot
Understanding Host Plant Resistance to Insect Pests and Strategies to Incorporate It in Forest Trees
inferred← citeshttps://doi.org/10.1007/978-981-99-9338-3_12openalex-snapshot
The Use of Gene Editing Technology to Introduce Targeted Modifications in Woody Plants
inferred← citeshttps://doi.org/10.1007/s00299-026-03745-5openalex-snapshot
MdNF-YB14, an apple NF-Y transcription factor, acts as a positive regulator of drought tolerance
inferred← citeshttps://doi.org/10.1007/s00344-020-10287-xopenalex-snapshot
Transcriptomic Profiling Revealed Genes Involved in Response to Drought Stress in Alfalfa
inferred← citeshttps://doi.org/10.1007/s00344-022-10807-xopenalex-snapshot
Role of Root Hydraulics in Plant Drought Tolerance
inferred← citeshttps://doi.org/10.1007/s00344-024-11395-8openalex-snapshot
Gene Editing: Paving the Way for Enhancing Plant Tolerance to Abiotic Stresses-Mechanisms, Breakthroughs, and Future Prospects
inferred← citeshttps://doi.org/10.1007/s00344-026-12055-9openalex-snapshot
Study on the Response and Adaptation Mechanism of Phlomoides rotata to Drought Stress
inferred← citeshttps://doi.org/10.1007/s00425-022-04030-xopenalex-snapshot
Five NUCLEAR FACTOR-Y subunit B genes in rapeseed (Brassica napus) promote flowering and root elongation in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00425-025-04887-8openalex-snapshot
Overexpression of CsNF-YA5 enhances drought tolerance in citrus rootstocks and grafted plants: a biotechnological strategy for crop resilience
inferred← citeshttps://doi.org/10.1007/s10142-025-01607-zopenalex-snapshot
Durum wheat nuclear factor Y (NF-Y) a subfamily: structure, phylogeny, and expression analysis in response to hormones and abiotic stresses
inferred← citeshttps://doi.org/10.1007/s10725-021-00704-wopenalex-snapshot
CRISPR technology for abiotic stress resistant crop breeding
inferred← citeshttps://doi.org/10.1007/s10725-021-00711-xopenalex-snapshot
Roles of cytokinins in root growth and abiotic stress response of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10725-023-01096-9openalex-snapshot
Ascorbate oxidation stimulates rice root growth via effects on auxin and abscisic acid levels
inferred← citeshttps://doi.org/10.1007/s11103-025-01674-7openalex-snapshot
MsCCoAOMTh3 confers drought tolerance by mediating lignin content and ROS scavenging
inferred← citeshttps://doi.org/10.1007/s11240-021-02014-5openalex-snapshot
Tuning drought resistance by using a root-specific expression transcription factor PdNF-YB21 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11240-021-02178-0openalex-snapshot
Increased abscisic acid sensitivity and drought tolerance of Arabidopsis by overexpression of poplar abscisic acid receptors
inferred← citeshttps://doi.org/10.1007/s11240-025-03003-8openalex-snapshot
Review of biotechnological advances in mahogany (Swietenia macrophylla King): in vitro culture and genetic transformation
inferred← citeshttps://doi.org/10.1007/s11295-025-01698-6openalex-snapshot
Trends in tree improvement methods: from classical breeding to genomic technologies
inferred← citeshttps://doi.org/10.1007/s11676-026-02117-9openalex-snapshot
Genetic and genomic improvement of Quercus alba productivity and resilience: a synthesis of breeding systems in white oaks (Quercus sect. Quercus)
inferred← citeshttps://doi.org/10.1007/s11816-022-00764-yopenalex-snapshot
Heterologous expression of ZmNF-YA12 confers tolerance to drought and salt stress in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s13580-021-00418-yopenalex-snapshot
Identification of hub salt-responsive genes in Cucumis sativus using a long non-coding RNA and mRNA interaction network
inferred← citeshttps://doi.org/10.1007/s13580-024-00643-1openalex-snapshot
Nuclear factor NF-YA4a regulates salt stress tolerance and juvenile-adult phase transition in Pyrus
inferred← citeshttps://doi.org/10.1007/s44154-022-00048-zopenalex-snapshot
Regulatory network established by transcription factors transmits drought stress signals in plant
inferred← citeshttps://doi.org/10.1007/s44154-024-00199-1openalex-snapshot
CsLAC4, regulated by CsmiR397a, confers drought tolerance to the tea plant by enhancing lignin biosynthesis
inferred← citeshttps://doi.org/10.1007/s44372-026-00494-3openalex-snapshot
Beneficial networking between AMF and plants leads to improved stress tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00015-xopenalex-snapshot
Signaling crosstalk between cytokinins and abscisic acid in plant defense, growth, and development
inferred← citeshttps://doi.org/10.1016/b978-0-443-13229-2.00001-6openalex-snapshot
CRISPR genome editing of woody trees: Current status and future prospects
inferred← citeshttps://doi.org/10.1016/b978-0-443-18444-4.00001-6openalex-snapshot
CRISPR/Cas genome editing and applications in forest tree breeding
inferred← citeshttps://doi.org/10.1016/b978-0-443-24135-2.00013-xopenalex-snapshot
CRISPR plants against oxidative stress: Methods and applications
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115770openalex-snapshot
HIPP26L-NF-YC9-SRMT module regulates drought response in poplar
inferred← citeshttps://doi.org/10.1016/j.cj.2023.03.005openalex-snapshot
Genome-wide analysis of nuclear factor Y genes and functional investigation of watermelon ClNF-YB9 during seed development
inferred← citeshttps://doi.org/10.1016/j.cj.2023.10.011openalex-snapshot
The BEL1-like transcription factor GhBLH5-A05 participates in cotton response to drought stress
inferred← citeshttps://doi.org/10.1016/j.cj.2023.12.001openalex-snapshot
The ABA synthesis enzyme allele OsNCED2 promotes dryland adaptation in upland rice
inferred← citeshttps://doi.org/10.1016/j.cj.2024.04.008openalex-snapshot
Overexpression of the peroxidase gene ZmPRX1 increases maize seedling drought tolerance by promoting root development and lignification
inferred← citeshttps://doi.org/10.1016/j.cub.2024.12.003openalex-snapshot
ABA-auxin cascade regulates crop root angle in response to drought
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115608openalex-snapshot
Transcriptomic analysis revealing the molecular response to arsenic stress in desert Eremostachys moluccelloides Bunge
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105515openalex-snapshot
Transcriptome profiles reveal NF-YC1-regulated pathways in adaption to salt stress in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105686openalex-snapshot
A novel Populus euphratica DUB gene, PeMINDY3, enhances drought and salt tolerance by promoting ROS scavenging
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.106015openalex-snapshot
A putative NF-Y complex interacting with ERD15 may positively regulate the expression of a peroxidase gene in response to stress in rapeseed (Brassica napus L.)
inferred← citeshttps://doi.org/10.1016/j.gene.2021.146089openalex-snapshot
Genome-wide screening and identification of nuclear Factor-Y family genes and exploration their function on regulating abiotic and biotic stress in potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.01.012openalex-snapshot
The glutamate receptor gene GLR3.3: A bridge of calcium-mediated root development in poplar
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.10.240openalex-snapshot
Genome-wide analysis of autophagy-related gene family and PagATG18a enhances salt tolerance by regulating ROS homeostasis in poplar
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.139361openalex-snapshot
Genome-wide identification of the papaya-like cysteine protease family in poplar and determination of the functional role of PeRD19A in conferring salt tolerance
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.142321openalex-snapshot
Lignin synthesis plays an essential role in the adaptation of Haloxylon ammodendron to adverse environments
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.113609openalex-snapshot
PdNF-YB21 positively regulated root lignin structure in poplar
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116441openalex-snapshot
Male and female poplars exhibited sex-specific differences in metabolic and transcriptional responses to two levels of water deficit
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117945openalex-snapshot
Genome-wide identification of poplar GSTU gene family and its PtrGSTU23 and PtrGSTU40 to improve salt tolerance in poplar
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.118476openalex-snapshot
Integrated transcriptomic and metabolomic analyses reveals the molecular bases of alfalfa regrowth processes of new shoots after cutting under different water and nitrogen availability
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120664openalex-snapshot
Increased genome editing efficiency in poplar by optimizing sgRNA length and copy number
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121350openalex-snapshot
Revolutionizing poplar biotechnology: Genetic transformation and CRISPR/Cas strategies
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.122735openalex-snapshot
Genome-wide identification of MADS-box gene family members in poplar and functional characterization of PagMADS23a in the regulation of stomatal density
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123329openalex-snapshot
Identification of salinity-tolerance in Satureja khuzistanica populations through growth, physiological and essential oil responses
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123558openalex-snapshot
Genome-wide analysis of plasma membrane H+ -ATPases in Populus tomentosa reveals the roles of PtoPHA14D in regulating adventitious root development
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110603openalex-snapshot
Programmed cell death (PCD) control in plants: New insights from the Arabidopsis thaliana deathosome
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111209openalex-snapshot
Exogenous sucrose influences KEA1 and KEA2 to regulate abscisic acid-mediated primary root growth in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112502openalex-snapshot
Overexpression of maize transcription factor ZmNF-YC14 positively regulates drought and salt stress responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.03.057openalex-snapshot
Analysis of Populus glycosyl hydrolase family I members and their potential role in the ABA treatment and drought stress response
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.09.004openalex-snapshot
PtoMPO1, a negative mediator, functions in poplar drought tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108129openalex-snapshot
Roles of abscisic acid and auxin in plants during drought: A molecular point of view
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110517openalex-snapshot
Identification of a nuclear transcription factor-Y (NF-Y) gene family in pepper and analysis of a CaNF-YC1-CaTIFY7-CaCBF1a/b transcription factor module under cold stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110762openalex-snapshot
Genome-wide identification of NF-Y genes in kiwifruit genome and the role of AcNF-YC22 in response to heat stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110951openalex-snapshot
The BpNF-YC9-BpbHLH80 module: A key regulator of salt stress in birch revealed via hierarchical gene regulatory networks
inferred← citeshttps://doi.org/10.1016/j.rhisph.2024.100922openalex-snapshot
Physiological, hormonal and molecular dynamics of root system architectural response to drought stress signaling in crops
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.06.004openalex-snapshot
OsNF-YA8 promotes starch accumulation and influences seed traits by positively regulating starch biosynthesis in rice
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100658openalex-snapshot
Comparative analysis of the NF-Y transcription factor family identifies VaNF-YA6 as a positive regulator of salt and drought tolerance in grapevine
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100698openalex-snapshot
WITHDRAWN: Selected cell wall remodeling mechanisms orchestrating plant drought tolerance
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100417openalex-snapshot
Engineering drought and salinity tolerance traits in crops through CRISPR-mediated genome editing: Targets, tools, challenges, and perspectives
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101425openalex-snapshot
Sophisticated crosstalk of tryptophan-derived metabolites in plant stress responses
inferred← citeshttps://doi.org/10.1073/pnas.2010911118openalex-snapshot
Abscisic acid regulates secondary cell-wall formation and lignin deposition in Arabidopsis thaliana through phosphorylation of NST1
inferred← citeshttps://doi.org/10.1080/15592324.2025.2451700openalex-snapshot
Genome-wide identification and analysis of the NF-Y transcription factor family reveal its potential roles in tobacco ( Nicotiana tabacum L.)
inferred← citeshttps://doi.org/10.1080/15592324.2025.2608488openalex-snapshot
TdNF-YA2A-1 transcription factor confers salt and osmotic stress tolerance in tobacco through regulation of the antioxidant defense system
inferred← citeshttps://doi.org/10.1093/hr/uhae347openalex-snapshot
The AREB transcription factor SaAREB6 promotes drought stress-induced santalol biosynthesis in sandalwood
inferred← citeshttps://doi.org/10.1093/hr/uhaf304openalex-snapshot
Large-scale comparative analysis of the nuclear factor-Y transcription factors across 320 horticultural and other plants
inferred← citeshttps://doi.org/10.1093/insilicoplants/diae007openalex-snapshot
A multi-tissue genome-scale model of Populus trichocarpa elucidates overexpression targets for improving drought tolerance
inferred← citeshttps://doi.org/10.1093/jpe/rtaf172openalex-snapshot
Rooting for survival: ABA-mediated hormonal integration driving primary root elongation under drought stress
inferred← citeshttps://doi.org/10.1093/jxb/erac190openalex-snapshot
The transcription factor GNC optimizes nitrogen use efficiency and growth by up-regulating the expression of nitrate uptake and assimilation genes in poplar
inferred← citeshttps://doi.org/10.1093/plphys/kiad532openalex-snapshot
IbMYB73 targets abscisic acid-responsive IbGER5 to regulate root growth and stress tolerance in sweet potato
inferred← citeshttps://doi.org/10.1093/plphys/kiae381openalex-snapshot
Nuclear factors NF-YC3 and NF-YBs positively regulate arbuscular mycorrhizal symbiosis in tomato
inferred← citeshttps://doi.org/10.1093/plphys/kiaf584openalex-snapshot
The MhNF-YA3-like-MhMSI4-like module regulates apple drought tolerance by activating the expression of MhAAO3
inferred← citeshttps://doi.org/10.1093/plphys/kiag462openalex-snapshot
A CsNF-YB4-CsWAT1-CsARF9 regulatory cascade mediates auxin-dependent suppression of lignin biosynthesis and resistance to Colletotrichum camelliae in tea plants
inferred← citeshttps://doi.org/10.1093/plphys/kiag488openalex-snapshot
The NAC17–PUB30 module enhances drought stress tolerance by regulating adventitious root development in apple
inferred← citeshttps://doi.org/10.1093/plphys/kiag508openalex-snapshot
MhNF-YC6 and MhCOL4 synergistically promote abscisic acid biosynthesis to combat drought stress in apple
inferred← citeshttps://doi.org/10.1093/treephys/tpab140openalex-snapshot
The yellowhornAGLtranscription factor geneXsAGL22contributes to ABA biosynthesis and drought tolerance in poplar
inferred← citeshttps://doi.org/10.1093/treephys/tpac106openalex-snapshot
PePYL4 enhances drought tolerance by modulating water-use efficiency and ROS scavenging in Populus
inferred← citeshttps://doi.org/10.1093/treephys/tpaf147openalex-snapshot
SaRac1 , a small GTPase, plays an essential role in haustorium development in the root parasite sandalwood ( Santalum album )
inferred← citeshttps://doi.org/10.1101/2020.06.11.146092openalex-snapshot
An ABA Synthesis Enzyme Allele OsNCED2 Promotes the Aerobic Adaption in Upland Rice
inferred← citeshttps://doi.org/10.1111/jipb.13201openalex-snapshot
CmNF‐YB8 affects drought resistance in chrysanthemum by altering stomatal status and leaf cuticle thickness
inferred← citeshttps://doi.org/10.1111/jipb.13732openalex-snapshot
A pair of nuclear factor Y transcription factors act as positive regulators in jasmonate signaling and disease resistance in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.17301openalex-snapshot
PdGNC confers drought tolerance by mediating stomatal closure resulting from NO and H 2 O 2 production via the direct regulation of PdHXK1 expression in Populus
inferred← citeshttps://doi.org/10.1111/nph.17799openalex-snapshot
PuC3H35 confers drought tolerance by enhancing lignin and proanthocyanidin biosynthesis in the roots of Populus ussuriensis
inferred← citeshttps://doi.org/10.1111/nph.19251openalex-snapshot
The AP2 / ERF transcription factor PtoERF15 confers drought tolerance via JA ‐mediated signaling in Populus
inferred← citeshttps://doi.org/10.1111/nph.19533openalex-snapshot
The ABI4‐RGL2 module serves as a double agent to mediate the antagonistic crosstalk between ABA and GA signals
inferred← citeshttps://doi.org/10.1111/nph.71520openalex-snapshot
The PtoERF1 ‐ PtomiR393a ‐ PtoFBL4 module confers drought tolerance via ABA –auxin crosstalk in Populus
inferred← citeshttps://doi.org/10.1111/pbi.13752openalex-snapshot
Transcriptional activation of rice CINNAMOYL‐CoA REDUCTASE 10 by OsNAC5, contributes to drought tolerance by modulating lignin accumulation in roots
inferred← citeshttps://doi.org/10.1111/pbi.14349openalex-snapshot
Soybean steroids improve crop abiotic stress tolerance and increase yield
inferred← citeshttps://doi.org/10.1111/pbi.14355openalex-snapshot
NF‐YC15 transcription factor activates ethylene biosynthesis and improves cassava disease resistance
inferred← citeshttps://doi.org/10.1111/pce.15163openalex-snapshot
PeFUS3 Drives Lateral Root Growth Via Auxin and ABA Signalling Under Drought Stress in Populus
inferred← citeshttps://doi.org/10.1111/pce.15495openalex-snapshot
The PagAFP2a‐PagAREB1 Module Form a Negative Feedback Loop to Regulate Salt Tolerance in Populus
inferred← citeshttps://doi.org/10.1111/pce.70029openalex-snapshot
MhNF‐YA1‐Like‐MhDnaJC76‐MhAAO3 Transcriptional Cascade Enhances ABA Biosynthesis and Drought Tolerance in Apple
inferred← citeshttps://doi.org/10.1111/ppl.13651openalex-snapshot
Shaping the root system architecture in plants for adaptation to drought stress
inferred← citeshttps://doi.org/10.1111/ppl.13668openalex-snapshot
Genome‐wide characterization of nuclear factor Y transcription factors in Fagopyrum tataricum
inferred← citeshttps://doi.org/10.1111/ppl.13751openalex-snapshot
Overexpression of PeNAC122 gene promotes wood formation and tolerance to osmotic stress in poplars
inferred← citeshttps://doi.org/10.1111/ppl.70202openalex-snapshot
MhNF ‐ YA2 modulates drought tolerance by triggering MhHSP70 ‐3 expression in Malus hupehensis
inferred← citeshttps://doi.org/10.1111/ppl.70255openalex-snapshot
Future‐proofing ornamental plants: Cutting‐edge strategies for drought resistance and sustainability
inferred← citeshttps://doi.org/10.1111/ppl.70516openalex-snapshot
HvNF‐YB7 : A Key Regulator of the HvGSTF13.1 ‐Mediated Glutathione Antioxidant System in Drought‐Tolerant Barley
inferred← citeshttps://doi.org/10.1111/tpj.16588openalex-snapshot
The transcription factor PtoMYB142 enhances drought tolerance in Populus tomentosa by regulating gibberellin catabolism
inferred← citeshttps://doi.org/10.1111/tpj.70023openalex-snapshot
Cytokinin mediates age‐dependent drought response by regulating the removal reactive oxygen species in apple
inferred← citeshttps://doi.org/10.1111/tpj.70089openalex-snapshot
BpMAPK3‐mediated BpWRKY53 phosphorylation enhances Betula platyphylla drought stress tolerance by increasing flavonoid content
inferred← citeshttps://doi.org/10.1111/tpj.70893openalex-snapshot
Apple microRNA477b‐MsDELLA‐like‐MsNF‐YC9 module enhances osmotic stress tolerance by regulating abscisic acid biosynthesis
inferred← citeshttps://doi.org/10.1186/s12864-023-09556-2openalex-snapshot
Aspartyl tRNA-synthetase (AspRS) gene family enhances drought tolerance in poplar through BABA-PtrIBIs-PtrVOZ signaling module
inferred← citeshttps://doi.org/10.1186/s12864-024-10531-8openalex-snapshot
Genomic determinants, architecture, and constraints in drought-related traits in Corymbia calophylla
inferred← citeshttps://doi.org/10.1186/s12870-024-05932-6openalex-snapshot
Overexpression of an NF-YB gene family member, EaNF-YB2, enhances drought tolerance in sugarcane (Saccharum Spp. Hybrid)
inferred← citeshttps://doi.org/10.1186/s12870-026-08191-9openalex-snapshot
Study on the positive regulation of drought tolerance by PdMYB2R032 based on R2R3-MYB gene family analysis in Populus deltoides
inferred← citeshttps://doi.org/10.1186/s13059-022-02718-7openalex-snapshot
PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.1186/s13595-022-01143-xopenalex-snapshot
Closing the gap between phenotyping and genotyping: review of advanced, image-based phenotyping technologies in forestry
inferred← citeshttps://doi.org/10.1360/tb-2023-1125openalex-snapshot
Application of CRISPR/Cas genome editing in woody plant trait improvement
inferred← citeshttps://doi.org/10.21203/rs.3.rs-122486/v1openalex-snapshot
Transcriptome profiling provides new insights into florets number difference of inflorescence in L.angustifolia
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2344198/v1openalex-snapshot
Identification and phylogenetic analysis of R2R3-MYB subfamily in Brassica napus
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4649597/v1openalex-snapshot
Growth responses and accumulation of osmoprotectants under salinity and drought in woody plants: insights from Parkinsonia praecox (Ruiz & Pav.) Hawkins
inferred← citeshttps://doi.org/10.2139/ssrn.5383643openalex-snapshot
Study on the Positive Regulation of Drought Tolerance by Pdmyb2r032 in Populus Deltoides Based on R2r3-Myb Gene Family Analysis
inferred← citeshttps://doi.org/10.22207/jpam.19.1.02openalex-snapshot
Comparative Study of Trichoderma BHU-1 Mediated Drought Alleviation of Susceptible and Tolerant Rice Cultivars
inferred← citeshttps://doi.org/10.32615/bp.2022.032openalex-snapshot
Abscisic acid affects the floret numbers of inflorescence by regulating indole-3-acetic acid transport and accumulation in Lavandula angustifolia
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1067427openalex-snapshot
NF-YB family transcription factors in Arabidopsis: Structure, phylogeny, and expression analysis in biotic and abiotic stresses
inferred← citeshttps://doi.org/10.3389/fpls.2020.00672openalex-snapshot
Analysis of Dynamic Global Transcriptional Atlas Reveals Common Regulatory Networks of Hormones and Photosynthesis Across Nicotiana Varieties in Response to Long-Term Drought
inferred← citeshttps://doi.org/10.3389/fpls.2020.572137openalex-snapshot
Transcriptional Regulation of Drought Response in Arabidopsis and Woody Plants
inferred← citeshttps://doi.org/10.3389/fpls.2021.738301openalex-snapshot
Morpho-Anatomical Traits and Soluble Sugar Concentration Largely Explain the Responses of Three Deciduous Tree Species to Progressive Water Stress
inferred← citeshttps://doi.org/10.3389/fpls.2021.749688openalex-snapshot
Genome-Wide Analysis of NF-Y Genes in Potato and Functional Identification of StNF-YC9 in Drought Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2021.786328openalex-snapshot
Advances and Perspectives of Transgenic Technology and Biotechnological Application in Forest Trees
inferred← citeshttps://doi.org/10.3389/fpls.2021.788938openalex-snapshot
AnDHN, a Dehydrin Protein From Ammopiptanthus nanus, Mitigates the Negative Effects of Drought Stress in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.1085409openalex-snapshot
Responses of root system architecture to water stress at multiple levels: A meta-analysis of trials under controlled conditions
inferred← citeshttps://doi.org/10.3389/fpls.2022.809723openalex-snapshot
Physio-Morphological, Biochemical and Transcriptomic Analyses Provide Insights Into Drought Stress Responses in Mesona chinensis Benth
inferred← citeshttps://doi.org/10.3389/fpls.2022.884456openalex-snapshot
Overexpression of Pennisetum purpureum CCoAOMT Contributes to Lignin Deposition and Drought Tolerance by Promoting the Accumulation of Flavonoids in Transgenic Tobacco
inferred← citeshttps://doi.org/10.3389/fpls.2023.1163939openalex-snapshot
OsOLP1 contributes to drought tolerance in rice by regulating ABA biosynthesis and lignin accumulation
inferred← citeshttps://doi.org/10.3389/fpls.2023.1255436openalex-snapshot
Transcription factors NF-YB involved in embryogenesis and hormones responses in Dimocarpus Longan Lour
inferred← citeshttps://doi.org/10.3389/fpls.2025.1635078openalex-snapshot
Advanced imaging-enabled understanding of cell wall remodeling mechanisms mediating plant drought stress tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2025.1661547openalex-snapshot
Deep short-read sequences facilitated identification of seven putative drought tolerance genes in a genome-wide association study in soybean
inferred← citeshttps://doi.org/10.3389/fpls.2025.1708920openalex-snapshot
Reference based transcriptome assembly of Piper nigrum L. reveals novel genes and transcripts in drought tolerance
inferred← citeshttps://doi.org/10.3389/fsufs.2025.1670566openalex-snapshot
Engineering resilience in woody plants: multi-omics, genome editing, and microbiome strategies to boost abiotic stress tolerance
inferred← citeshttps://doi.org/10.3390/biology12071037openalex-snapshot
Recent Developments in CRISPR/Cas9 Genome-Editing Technology Related to Plant Disease Resistance and Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.3390/cimb48090946openalex-snapshot
Abscisic Acid-Mediated Drought Tolerance in Populus: Physiological, Molecular, and Biotechnological Perspectives
inferred← citeshttps://doi.org/10.3390/f13122116openalex-snapshot
The Development of Forest Genetic Breeding and the Application of Genome Selection and CRISPR/Cas9 in Forest Breeding
inferred← citeshttps://doi.org/10.3390/f14020191openalex-snapshot
Overexpression of the Poplar WRKY51 Transcription Factor Enhances Salt Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/f14091784openalex-snapshot
Responses of Physiological, Morphological and Anatomical Traits to Abiotic Stress in Woody Plants
inferred← citeshttps://doi.org/10.3390/f16020361openalex-snapshot
Genome-Wide Identification and Expression Profile Analysis of the NF-Y Transcription Factor Gene Family in Eucalyptus grandis
inferred← citeshttps://doi.org/10.3390/genes11080919openalex-snapshot
Brassinosteroid Priming Improves Peanut Drought Tolerance via Eliminating Inhibition on Genes in Photosynthesis and Hormone Signaling
inferred← citeshttps://doi.org/10.3390/genes16080855openalex-snapshot
Transcriptomic Identification of Key Genes Responding to High Heat Stress in Moso Bamboo (Phyllostachys edulis)
inferred← citeshttps://doi.org/10.3390/horticulturae10080798openalex-snapshot
Genome and Transcriptome Analysis of NF-Y Transcription Factors in Sweet Potato under Salt Stress
inferred← citeshttps://doi.org/10.3390/horticulturae9010070openalex-snapshot
Genome-Wide Identification and Analysis of NF-Y Gene Family Reveal Its Potential Roles in Stress-Resistance in Chrysanthemum
inferred← citeshttps://doi.org/10.3390/horticulturae9080901openalex-snapshot
Effects of Crystal Lime Sulfur Fumigation and Application of Root-Growth-Promoting Agents on the Control of Apple Replant Disease
inferred← citeshttps://doi.org/10.3390/ijms22189777openalex-snapshot
Expression of the Malus sieversii NF-YB21 Encoded Gene Confers Tolerance to Osmotic Stresses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms221910354openalex-snapshot
Identification and Comprehensive Analysis of the Nuclear Factor-Y Family Genes Reveal Their Multiple Roles in Response to Nutrient Deficiencies in Brassica napus
inferred← citeshttps://doi.org/10.3390/ijms23126426openalex-snapshot
Genome-Wide Identification and Analysis of the NF-Y Transcription Factor Family Reveal Its Potential Roles in Salt Stress in Alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.3390/ijms23158159openalex-snapshot
The AP2/ERF GmERF113 Positively Regulates the Drought Response by Activating GmPR10-1 in Soybean
inferred← citeshttps://doi.org/10.3390/ijms231710175openalex-snapshot
CRISPR-Based Genome Editing and Its Applications in Woody Plants
inferred← citeshttps://doi.org/10.3390/ijms232415778openalex-snapshot
The NF-Y Transcription Factor Family in Watermelon: Re-Characterization, Assembly of ClNF-Y Complexes, Hormone- and Pathogen-Inducible Expression and Putative Functions in Disease Resistance
inferred← citeshttps://doi.org/10.3390/ijms24054426openalex-snapshot
Crucial Abiotic Stress Regulatory Network of NF-Y Transcription Factor in Plants
inferred← citeshttps://doi.org/10.3390/ijms24086934openalex-snapshot
Genome-Wide Identification and Chilling Stress Analysis of the NF-Y Gene Family in Melon
inferred← citeshttps://doi.org/10.3390/ijms24108910openalex-snapshot
Comprehensive Analysis of the NF-YB Gene Family and Expression under Abiotic Stress and Hormone Treatment in Larix kaempferi
inferred← citeshttps://doi.org/10.3390/ijms241511898openalex-snapshot
Genome-Wide Identification of the NF-Y Gene Family and Their Involvement in Bolting and Flowering in Flowering Chinese Cabbage
inferred← citeshttps://doi.org/10.3390/ijms241914655openalex-snapshot
The miRNA-mRNA Regulatory Modules of Pinus massoniana Lamb. in Response to Drought Stress
inferred← citeshttps://doi.org/10.3390/ijms25020836openalex-snapshot
Genome-Wide Analysis of Nuclear factor-YC Genes in the Tea Plant (Camellia sinensis) and Functional Identification of CsNF-YC6
inferred← citeshttps://doi.org/10.3390/ijms252312832openalex-snapshot
Genome-Wide Identification and Expression Profiles of Nuclear Factor Y A Transcription Factors in Blueberry Under Abiotic Stress
inferred← citeshttps://doi.org/10.3390/ijms26010038openalex-snapshot
Plant Nuclear Factor Y (NF-Y) Transcription Factors: Evolving Insights into Biological Functions and Gene Expansion
inferred← citeshttps://doi.org/10.3390/ijms26083884openalex-snapshot
The Role of Phytohormones in Mediating Drought Stress Responses in Populus Species
inferred← citeshttps://doi.org/10.3390/ijms27062540openalex-snapshot
Design and Testing of Root-Specific Synthetic Promoters by Machine Learning
inferred← citeshttps://doi.org/10.3390/ijms27198853openalex-snapshot
Physiological and Molecular Mechanisms of Tree Responses to Combined Drought and Low-Nitrogen Stress: A Review
inferred← citeshttps://doi.org/10.3390/life13010242openalex-snapshot
High Efficiency Regeneration System from Blueberry Leaves and Stems
inferred← citeshttps://doi.org/10.3390/life13020533openalex-snapshot
Responses to Drought Stress in Poplar: What Do We Know and What Can We Learn?
inferred← citeshttps://doi.org/10.3390/plants10010016openalex-snapshot
Genomic Organization, Phylogenetic Comparison, and Differential Expression of the Nuclear Factor-Y Gene Family in Apple (Malus Domestica)
inferred← citeshttps://doi.org/10.3390/plants10122769openalex-snapshot
Molecular and Physiological Perspectives of Abscisic Acid Mediated Drought Adjustment Strategies
inferred← citeshttps://doi.org/10.3390/plants12040886openalex-snapshot
Identification and Phylogenetic Analysis of the R2R3-MYB Subfamily in Brassica napus
inferred← citeshttps://doi.org/10.3390/plants12050978openalex-snapshot
Comparative Transcriptome Profiling Reveals Key MicroRNAs and Regulatory Mechanisms for Aluminum Tolerance in Olive
inferred← citeshttps://doi.org/10.3390/plants12091892openalex-snapshot
The Potential of CRISPR/Cas Technology to Enhance Crop Performance on Adverse Soil Conditions
inferred← citeshttps://doi.org/10.3390/plants13070953openalex-snapshot
Alfalfa Responses to Intensive Soil Compaction: Effects on Plant and Root Growth, Phytohormones and Internal Gene Expression
inferred← citeshttps://doi.org/10.3390/plants14030438openalex-snapshot
Genome-Wide Identification and Expression Pattern Analysis of Nuclear Factor Y B/C Genes in Pinus koraiensis, and Functional Identification of LEAFY COTYLEDON 1
inferred← citeshttps://doi.org/10.3390/plants15162466openalex-snapshot
Genome-Wide Characterization of Nuclear Factor Y (NF-Y) Transcription Factors in Allohexaploid Oat
inferred← citeshttps://doi.org/10.34133/2020/7914051openalex-snapshot
Plant Biosystems Design for a Carbon-Neutral Bioeconomy
inferred← citeshttps://doi.org/10.34133/2021/9798714openalex-snapshot
Biological Parts for Plant Biodesign to Enhance Land-Based Carbon Dioxide Removal
inferred← citeshttps://doi.org/10.48130/fr-2022-0006openalex-snapshot
Progress and challenges in applying CRISPR/Cas techniques to the genome editing of trees
inferred← citeshttps://doi.org/10.5958/0974-4479.2021.00016.2openalex-snapshot
Understanding Transcription Factors in Plant Response to Drought Stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267330openalex-snapshot
Additional file 10 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267333openalex-snapshot
Additional file 11 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267336openalex-snapshot
Additional file 12 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267339openalex-snapshot
Additional file 13 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267342openalex-snapshot
Additional file 14 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267345openalex-snapshot
Additional file 15 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267348openalex-snapshot
Additional file 1 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267351openalex-snapshot
Additional file 2 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267354openalex-snapshot
Additional file 3 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267357openalex-snapshot
Additional file 4 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267360openalex-snapshot
Additional file 5 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267363openalex-snapshot
Additional file 6 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267366openalex-snapshot
Additional file 7 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
inferred← citeshttps://doi.org/10.6084/m9.figshare.20267369openalex-snapshot
Additional file 8 of PtoNF-YC9-SRMT-PtoRD26 module regulates the high saline tolerance of a triploid poplar
showing the first 200 of 209 · page through all 209
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.