On the public citation graph

Biosynthesis and Signal Transduction of ABA, JA, and BRs in Response to Drought Stress of Kentucky Bluegrass

0 signed · 219 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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/s00216-006-0780-zopenalex-snapshot
Development of a monoclonal antibody-based enzyme-linked immunosorbent assay for the analysis of glycyrrhizic acid
inferredcites →https://doi.org/10.1007/s00299-018-2302-9openalex-snapshot
Overexpression of VaWRKY14 increases drought tolerance in Arabidopsis by modulating the expression of stress-related genes
inferredcites →https://doi.org/10.1007/s00344-014-9434-0openalex-snapshot
Drought Stress and Trinexapac-ethyl Modify Phytohormone Content Within Kentucky Bluegrass Leaves
inferredcites →https://doi.org/10.1007/s00709-016-0960-4openalex-snapshot
The ethylene response factor OsERF109 negatively affects ethylene biosynthesis and drought tolerance in rice
inferredcites →https://doi.org/10.1007/s10142-013-0356-xopenalex-snapshot
Drought stress responses in crops
inferredcites →https://doi.org/10.1007/s10535-013-0374-5openalex-snapshot
Brassinosteroids and their role in response of plants to abiotic stresses
inferredcites →https://doi.org/10.1007/s11032-014-0114-3openalex-snapshot
Transcriptional regulation of ABA core signaling component genes in sorghum (Sorghum bicolor L. Moench)
inferredcites →https://doi.org/10.1007/s11103-016-0568-2openalex-snapshot
The protein phosphatase 2C clade A protein OsPP2C51 positively regulates seed germination by directly inactivating OsbZIP10
inferredcites →https://doi.org/10.1007/s11105-012-0456-0openalex-snapshot
Cloning of Six ERF Family Transcription Factor Genes from Peanut and Analysis of their Expression during Abiotic Stress
inferredcites →https://doi.org/10.1007/s11356-016-6957-xopenalex-snapshot
Silicate application increases the photosynthesis and its associated metabolic activities in Kentucky bluegrass under drought stress and post-drought recovery
inferredcites →https://doi.org/10.1007/s11738-009-0302-7openalex-snapshot
Effect of 28-homobrassinolide on the drought stress-induced changes in photosynthesis and antioxidant system of Brassica juncea L.
inferredcites →https://doi.org/10.1007/s11738-014-1599-4openalex-snapshot
Exogenous ABA induces drought tolerance in upland rice: the role of chloroplast and ABA biosynthesis-related gene expression on photosystem II during PEG stress
inferredcites →https://doi.org/10.1007/s11816-015-0366-3openalex-snapshot
The soluble ABA receptor PYL8 regulates drought resistance by controlling ABA signaling in Arabidopsis
inferredcites →https://doi.org/10.1007/s12064-012-0162-3openalex-snapshot
Measurement of mRNA abundance using RNA-seq data: RPKM measure is inconsistent among samples
inferredcites →https://doi.org/10.1016/j.bbrc.2008.07.128openalex-snapshot
Overexpression of Arabidopsis ZEP enhances tolerance to osmotic stress
inferredcites →https://doi.org/10.1016/j.bbrc.2012.08.118openalex-snapshot
A mutation in Arabidopsis BSK5 encoding a brassinosteroid-signaling kinase protein affects responses to salinity and abscisic acid
inferredcites →https://doi.org/10.1016/j.bbrc.2017.01.104openalex-snapshot
Arabidopsis MAPKKK18 positively regulates drought stress resistance via downstream MAPKK3
inferredcites →https://doi.org/10.1016/j.jprot.2011.05.015openalex-snapshot
A proteomics view on the role of drought-induced senescence and oxidative stress defense in enhanced stem reserves remobilization in wheat
inferredcites →https://doi.org/10.1016/j.pbi.2011.02.001openalex-snapshot
Hormone balance and abiotic stress tolerance in crop plants
inferredcites →https://doi.org/10.1016/j.plaphy.2012.09.009openalex-snapshot
Transcriptomic analysis of oxylipin biosynthesis genes and chemical profiling reveal an early induction of jasmonates in chickpea roots under drought stress
inferredcites →https://doi.org/10.1016/j.plaphy.2012.10.012openalex-snapshot
Alginate oligosaccharides enhanced Triticum aestivum L. tolerance to drought stress
inferredcites →https://doi.org/10.1016/j.plaphy.2012.10.017openalex-snapshot
Hydrogen sulfide interacting with abscisic acid in stomatal regulation responses to drought stress in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2015.04.013openalex-snapshot
Molecular characterization of BZR transcription factor family and abiotic stress induced expression profiling in Brassica rapa
inferredcites →https://doi.org/10.1016/j.plaphy.2017.08.025openalex-snapshot
Cloning and expression profiling of the PacSnRK2 and PacPP2C gene families during fruit development, ABA treatment, and dehydration stress in sweet cherry
inferredcites →https://doi.org/10.1016/j.scienta.2008.10.014openalex-snapshot
Reactive oxygen species, antioxidant enzyme activities and gene expression patterns in leaves and roots of Kentucky bluegrass in response to drought stress and recovery
inferredcites →https://doi.org/10.1016/j.scienta.2010.06.014openalex-snapshot
Effect of brassinosteroids on drought resistance and abscisic acid concentration in tomato under water stress
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/nature06006openalex-snapshot
The JAZ family of repressors is the missing link in jasmonate signalling
inferredcites →https://doi.org/10.1038/nature06543openalex-snapshot
Dual control of nuclear EIN3 by bifurcate MAPK cascades in C2H4 signalling
inferredcites →https://doi.org/10.1038/nmeth.4197openalex-snapshot
Salmon provides fast and bias-aware quantification of transcript expression
inferredcites →https://doi.org/10.1038/nprot.2013.084openalex-snapshot
De novo transcript sequence reconstruction from RNA-Seq: reference generation and analysis with Trinity
inferredcites →https://doi.org/10.1038/s41467-017-01239-3openalex-snapshot
Combining chemical and genetic approaches to increase drought resistance in plants
inferredcites →https://doi.org/10.1038/s41598-017-13464-3openalex-snapshot
Insights into grapevine defense response against drought as revealed by biochemical, physiological and RNA-Seq analysis
inferredcites →https://doi.org/10.1038/s41598-018-27274-8openalex-snapshot
NtLTP4, a lipid transfer protein that enhances salt and drought stresses tolerance in Nicotiana tabacum
inferredcites →https://doi.org/10.1038/srep28298openalex-snapshot
Overexpression of the brassinosteroid biosynthetic gene DWF4 in Brassica napus simultaneously increases seed yield and stress tolerance
inferredcites →https://doi.org/10.1071/bt16014openalex-snapshot
Changes in endogenous hormones and seed-coat phenolics during seed storage of two Suaeda salsa populations
inferredcites →https://doi.org/10.1071/fp11244openalex-snapshot
Water use, water use efficiency and drought resistance among warm-season turfgrasses in shallow soil profiles
inferredcites →https://doi.org/10.1073/pnas.0900349106openalex-snapshot
The primary signaling outputs of brassinosteroids are regulated by abscisic acid signaling
inferredcites →https://doi.org/10.1080/17429145.2012.752042openalex-snapshot
Physiological and comparative proteomic analyses of Thai jasmine rice and two check cultivars in response to drought stress
inferredcites →https://doi.org/10.1093/aobpla/plv023openalex-snapshot
Physiological, anatomical and transcriptional alterations in a rice mutant leading to enhanced water stress tolerance
inferredcites →https://doi.org/10.1093/jxb/erq331openalex-snapshot
The sucrose non-fermenting-1-related (SnRK) family of protein kinases: potential for manipulation to improve stress tolerance and increase yield
inferredcites →https://doi.org/10.1093/jxb/err252openalex-snapshot
Transcriptional regulation of SlPYL, SlPP2C, and SlSnRK2 gene families encoding ABA signal core components during tomato fruit development and drought stress
inferredcites →https://doi.org/10.1093/jxb/ers086openalex-snapshot
Cotton GhMKK5 affects disease resistance, induces HR-like cell death, and reduces the tolerance to salt and drought stress in transgenic Nicotiana benthamiana
inferredcites →https://doi.org/10.1093/jxb/ert185openalex-snapshot
Arabidopsis HEAT SHOCK TRANSCRIPTION FACTORA1b overexpression enhances water productivity, resistance to drought, and infection
inferredcites →https://doi.org/10.1093/nar/gkh063openalex-snapshot
The KEGG resource for deciphering the genome
inferredcites →https://doi.org/10.1093/nar/gkn176openalex-snapshot
High-throughput functional annotation and data mining with the Blast2GO suite
inferredcites →https://doi.org/10.1093/nar/gkv007openalex-snapshot
limma powers differential expression analyses for RNA-sequencing and microarray studies
inferredcites →https://doi.org/10.1093/pcp/pcf188openalex-snapshot
ABA-Activated SnRK2 Protein Kinase is Required for Dehydration Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1101/gr.103846.109openalex-snapshot
Optimization of de novo transcriptome assembly from next-generation sequencing data
inferredcites →https://doi.org/10.1104/pp.008680openalex-snapshot
Transcriptional and Posttranscriptional Regulation of ArabidopsisTCH4 Expression by Diverse Stimuli. Roles of cis Regions and Brassinosteroids
inferredcites →https://doi.org/10.1104/pp.109.149856openalex-snapshot
A Raf-Like MAPKKK Gene DSM1 Mediates Drought Resistance through Reactive Oxygen Species Scavenging in Rice
inferredcites →https://doi.org/10.1104/pp.127.1.315openalex-snapshot
Hormonal Changes in the Grains of Rice Subjected to Water Stress during Grain Filling
inferredcites →https://doi.org/10.1105/tpc.104.027359openalex-snapshot
The Inheritance of Apomixis inPoa pratensisConfirms a Five Locus Model with Differences in Gene Expressivity and Penetrance
inferredcites →https://doi.org/10.1105/tpc.106.045443openalex-snapshot
C-23 Hydroxylation by Arabidopsis CYP90C1 and CYP90D1 Reveals a Novel Shortcut in Brassinosteroid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.106.046581openalex-snapshot
The Mitogen-Activated Protein Kinase Cascade MKK3–MPK6 Is an Important Part of the Jasmonate Signal Transduction Pathway in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.16.00171openalex-snapshot
MODD Mediates Deactivation and Degradation of OsbZIP46 to Negatively Regulate ABA Signaling and Drought Resistance in Rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03034.xopenalex-snapshot
Regulation and functional analysis of ZmDREB2A in response to drought and heat stresses in Zea mays L
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03052.xopenalex-snapshot
The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV‐B light, drought and cold stress responses
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04054.xopenalex-snapshot
PYR/PYL/RCAR family members are major in‐vivo ABI1 protein phosphatase 2C‐interacting proteins in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01635.xopenalex-snapshot
Pivotal role of the AREB/ABF‐SnRK2 pathway in ABRE‐mediated transcription in response to osmotic stress in plants
inferredcites →https://doi.org/10.1111/j.1467-7652.2010.00560.xopenalex-snapshot
Comparative analysis of drought‐responsive transcriptome inIndicarice genotypes with contrasting drought tolerance
inferredcites →https://doi.org/10.1111/pbi.12601openalex-snapshot
Os ASR 5 enhances drought tolerance through a stomatal closure pathway associated with ABA and H2O2 signalling in rice
inferredcites →https://doi.org/10.1111/pce.12351openalex-snapshot
Four A rabidopsis AREB / ABF transcription factors function predominantly in gene expression downstream of SnRK2 kinases in abscisic acid signalling in response to osmotic stress
inferredcites →https://doi.org/10.1111/pce.12806openalex-snapshot
Memory responses of jasmonic acid‐associated Arabidopsis genes to a repeated dehydration stress
inferredcites →https://doi.org/10.1111/pce.13031openalex-snapshot
CATALASE2 functions for seedling postgerminative growth by scavenging H 2 O 2 and stimulating ACX2/3 activity in Arabidopsis
inferredcites →https://doi.org/10.1111/ppl.12588openalex-snapshot
Transcriptional regulation of hormone‐synthesis and signaling pathways by overexpressing cytokinin‐synthesis contributes to improved drought tolerance in creeping bentgrass
inferredcites →https://doi.org/10.1186/1471-2164-9-432openalex-snapshot
Heat stress-responsive transcriptome analysis in heat susceptible and tolerant wheat (Triticum aestivum L.) by using Wheat Genome Array
inferredcites →https://doi.org/10.1186/1471-2229-10-192openalex-snapshot
Conservation between higher plants and the moss Physcomitrella patensin response to the phytohormone abscisic acid: a proteomics analysis
inferredcites →https://doi.org/10.1186/s12864-015-1799-3openalex-snapshot
RNA-seq for gene identification and transcript profiling in relation to root growth of bermudagrass (Cynodon dactylon) under salinity stress
inferredcites →https://doi.org/10.1186/s12864-016-2379-xopenalex-snapshot
Transcriptome profiling of Kentucky bluegrass (Poa pratensis L.) accessions in response to salt stress
inferredcites →https://doi.org/10.1186/s12864-018-4437-zopenalex-snapshot
Transcriptomic analysis reveals unique molecular factors for lipid hydrolysis, secondary cell-walls and oxidative protection associated with thermotolerance in perennial grass
inferredcites →https://doi.org/10.1186/s12870-015-0597-zopenalex-snapshot
Implications of ethylene biosynthesis and signaling in soybean drought stress tolerance
inferredcites →https://doi.org/10.1186/s12870-016-0764-xopenalex-snapshot
Contrasting transcriptional responses of PYR1/PYL/RCAR ABA receptors to ABA or dehydration stress between maize seedling leaves and roots
inferredcites →https://doi.org/10.1186/s12870-017-1078-3openalex-snapshot
GaMYB85, an R2R3 MYB gene, in transgenic Arabidopsis plays an important role in drought tolerance
inferredcites →https://doi.org/10.1371/journal.pone.0124382openalex-snapshot
Transcriptomic Analysis of Drought Stress Responses in Ammopiptanthus mongolicus Leaves Using the RNA-Seq Technique
inferredcites →https://doi.org/10.1371/journal.pone.0197870openalex-snapshot
Drought-tolerant and drought-sensitive genotypes of maize (Zea mays L.) differ in contents of endogenous brassinosteroids and their drought-induced changes
inferredcites →https://doi.org/10.21273/hortsci.44.2.459openalex-snapshot
Correlations of Leaf Relative Water Content, Canopy Temperature, and Spectral Reflectance in Perennial Ryegrass Under Water Deficit Conditions
inferredcites →https://doi.org/10.21273/hortsci.46.7.1027openalex-snapshot
Drought Tolerance Associated with Proline and Hormone Metabolism in Two Tall Fescue Cultivars
inferredcites →https://doi.org/10.21273/jashs.136.4.247openalex-snapshot
Antioxidant Enzyme Activities and Gene Expression Patterns in Leaves of Kentucky Bluegrass in Response to Drought and Post-drought Recovery
inferredcites →https://doi.org/10.2135/cropsci2012.05.0284openalex-snapshot
Effects of Cytokinin and Potassium on Stomatal and Photosynthetic Recovery of Kentucky Bluegrass from Drought Stress
inferredcites →https://doi.org/10.3389/fpls.2016.01080openalex-snapshot
Identification of Drought Tolerant Mechanisms in Maize Seedlings Based on Transcriptome Analysis of Recombination Inbred Lines
inferredcites →https://doi.org/10.3389/fpls.2017.00625openalex-snapshot
Overexpression of a Tartary Buckwheat Gene, FtbHLH3, Enhances Drought/Oxidative Stress Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2017.00983openalex-snapshot
Effects of Nitrogen Supply on Water Stress and Recovery Mechanisms in Kentucky Bluegrass Plants
inferredcites →https://doi.org/10.3390/ijms160715811openalex-snapshot
Plant MYB Transcription Factors: Their Role in Drought Response Mechanisms
inferredcites →https://doi.org/10.3390/ijms18091834openalex-snapshot
Genome-Wide Identification and Characterization of the GmSnRK2 Family in Soybean

What points at this work

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

inferred← citeshttps://doi.org/10.1002/ece3.8281zenodo-depositor-declared
Comparing whole‐genome shotgun sequencing and DNA metabarcoding approaches for species identification and quantification of pollen species mixtures
inferred← citeshttps://doi.org/10.1002/csc2.21412openalex-snapshot
Transcriptomic and metabolomic analysis reveal differentially expressed genes and metabolic pathways in bermudagrass under drought stress
inferred← citeshttps://doi.org/10.1002/its2.25openalex-snapshot
Gene expression differences for drought stress response in three cool‐season turfgrasses
inferred← citeshttps://doi.org/10.1002/jsfa.11597openalex-snapshot
Role of abscisic acid in modulating drought acclimation, agronomic characteristics and β‐N‐oxalyl‐L‐α , β‐ diaminopropionic acid ( β‐ODAP ) accumulation in grass pea (Lathyrus sativus L. )
inferred← citeshttps://doi.org/10.1007/s00299-026-03725-9openalex-snapshot
PpCML14 from Kentucky bluegrass confers drought and salinity tolerance in transgenic rice
inferred← citeshttps://doi.org/10.1007/s00344-021-10533-wopenalex-snapshot
High Concentration of CO2 Improve the Pb Resistance of Oryza sativa L. Seedlings by Enhancing Photosynthesis and Regulating Plant Endogenous Hormones
inferred← citeshttps://doi.org/10.1007/s00709-025-02112-7openalex-snapshot
A validation study by integrated analysis of physiological, biochemical, and meta-gene expression responses to drought stress in sorghum (Sorghum bicolor L.)
inferred← citeshttps://doi.org/10.1007/s10725-024-01189-zopenalex-snapshot
Metabolomics and related genes analysis revealed the distinct mechanism of drought resistance in novel buckwheat and cultivated species
inferred← citeshttps://doi.org/10.1007/s11240-023-02508-4openalex-snapshot
Cloning, characterization and expression analysis of a brassinosteroids biosynthetic gene VvDET2 in Cabernet Sauvignon (Vitis vinifera L.)
inferred← citeshttps://doi.org/10.1007/s11240-026-03420-3openalex-snapshot
Functional analysis of PpOSK4 in Kentucky bluegrass: molecular basis for inhibiting Arabidopsis growth and enhancing drought resistance in Kentucky bluegrass
inferred← citeshttps://doi.org/10.1007/s11738-021-03202-8openalex-snapshot
Exogenous application of acetic acid improves the survival rate of cotton by increasing abscisic acid and jasmonic acid contents under drought stress
inferred← citeshttps://doi.org/10.1007/s13258-023-01460-zopenalex-snapshot
Comparative transcriptome analysis of two contrasting genotypes provides new insights into the drought response mechanism in pigeon pea (Cajanus cajan L. Millsp.)
inferred← citeshttps://doi.org/10.1007/s13562-023-00865-xopenalex-snapshot
Biochemical, physiological and molecular responses of rice to terminal drought stress: transcriptome profiling of leaf and root reveals the key stress-responsive genes
inferred← citeshttps://doi.org/10.1007/s13580-024-00640-4openalex-snapshot
Enhancing blueberry drought resilience: ABA and MeJA hormonal formulations unveil water-saving strategies
inferred← citeshttps://doi.org/10.1016/b978-0-443-18927-2.00009-1openalex-snapshot
Plant growth coordination during stress conditions: Role of phytohormones
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119100openalex-snapshot
Transcriptomic evidence of Dicranopteris pedata’s specialized defense systems against REEs stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104571openalex-snapshot
Transcript responses to drought in Kentucky bluegrass (Poa pratensis L.) germplasm varying in their tolerance to drought stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105184openalex-snapshot
Physiological and transcriptomic analyses of the effects of coronatine on drought tolerance in Carex leucochlora
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.06.006openalex-snapshot
The role of PYL genes as core components of abscisic acid signaling in plant abiotic stress response
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115858openalex-snapshot
Physiological and transcriptomic analyses of roots from Panax ginseng C. A. Meyer under drought stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154634openalex-snapshot
PpbZIP23 from a native Kentucky bluegrass (Poa pratensis L.) regulates osmotic stress tolerance in transgenic rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154708openalex-snapshot
A calmodulin-like protein from Kentucky bluegrass PpCML29 confers drought tolerance through activating antioxidant defense to maintain ROS homeostasis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113006openalex-snapshot
Potato transcription factor StMYB19 enhances drought tolerance by regulating ROS homeostasis and JA signalling pathway
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.01.034openalex-snapshot
Physiological, biochemical and gene-expressional responses to water deficit in apple subjected to partial root-zone drying (PRD)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.09.044openalex-snapshot
Physiological and transcriptomic analyses of the effects of exogenous melatonin on drought tolerance in maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.06.011openalex-snapshot
ZmBSK1 positively regulates BR-induced H2O2 production via NADPH oxidase and functions in oxidative stress tolerance in maize
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108679openalex-snapshot
Integrated anatomical structure, physiological, and transcriptomic analyses to identify differential cold tolerance responses of Ziziphus jujuba mill. ‘Yueguang’ and its autotetraploid ‘Hongguang’
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108814openalex-snapshot
Adaptive strategies to drought stress in grasses of the poaceae family under climate change: Physiological, genetic and molecular perspectives: A review
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.112832openalex-snapshot
Brassinosteroids alleviate postharvest water deficit stress in cut Dendrobium 'Khao Sanan' orchid through modulation of protective mechanisms, osmotic regulation, and endogenous hormonal levels
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.113430openalex-snapshot
Effects of preharvest alginate oligosaccharides treatment on water stress-induced cracking of sweet cherry fruit
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110315openalex-snapshot
Nitrogen assimilation and gene regulation of two Kentucky bluegrass cultivars differing in response to nitrate supply
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100516openalex-snapshot
Understanding abiotic stress tolerance mechanisms in non-food grass species through omics approaches
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100979openalex-snapshot
Transcriptomic and physiological analyses revealed the effects of exogenous MeJA on the antioxidant system and hormone signaling network in apple roots (Malus baccata L.) in response to suboptimal low root-zone temperature stress
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c09429openalex-snapshot
Synthesis, Plant Growth Regulatory Activity, and Transcriptome Analysis of Novel Opabactin Analogs
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c09519openalex-snapshot
Mechanisms Underlying Allelopathic Disturbance of Herbicide Imazethapyr on Wheat and Its Neighboring Ryegrass ( Lolium perenne )
inferred← citeshttps://doi.org/10.1071/cp21610openalex-snapshot
Transcriptome analysis of maize pollen grains under drought stress during flowering
inferred← citeshttps://doi.org/10.1089/dna.2021.0337openalex-snapshot
Transcriptional Regulation of Different Rhizome Parts Reveal the Candidate Genes That Regulate Rhizome Development in Poa pratensis
inferred← citeshttps://doi.org/10.1093/hr/uhac040openalex-snapshot
Hierarchical transcription factor and regulatory network for drought response in Betula platyphylla
inferred← citeshttps://doi.org/10.1093/treephys/tpac034openalex-snapshot
Exogenous application of acetic acid enhances drought tolerance by influencing the MAPK signaling pathway induced by ABA and JA in apple plants
inferred← citeshttps://doi.org/10.1186/s12864-022-08684-5openalex-snapshot
Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.1186/s12870-020-02785-7openalex-snapshot
Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.1186/s12870-021-03334-6openalex-snapshot
Integrated transcriptome and small RNA sequencing analyses reveal a drought stress response network in Sophora tonkinensis
inferred← citeshttps://doi.org/10.1186/s12870-022-04019-4openalex-snapshot
Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.1186/s12870-023-04206-xopenalex-snapshot
Transcriptome and metabolome analysis reveals key genes and secondary metabolites of Casuarina equisetifolia ssp. incana in response to drought stress
inferred← citeshttps://doi.org/10.1186/s12870-025-06554-2openalex-snapshot
Identification of key genes and signaling pathways in coconut (Cocos nucifera L.) under drought stress via comparative transcriptome analysis
inferred← citeshttps://doi.org/10.1186/s12870-025-07995-5openalex-snapshot
Candidate genes and molecular mechanisms regulating tiller development in wild Kentucky bluegrass
inferred← citeshttps://doi.org/10.1186/s12870-025-08090-5openalex-snapshot
PpZAT12 from a native Kentucky bluegrass (Poa pratensis L.) confers drought tolerance through regulating antioxidant defense system and multiple metabolic pathways
inferred← citeshttps://doi.org/10.1186/s12870-026-08154-0openalex-snapshot
Physiological and transcriptomic cooperative regulatory mechanisms of Cotinus Coggygria in response to drought and rewatering processes
inferred← citeshttps://doi.org/10.1186/s12870-026-09056-xopenalex-snapshot
Functional characterization of PpGS2 promoter in response to hormonal and environmental signals in Kentucky bluegrass
inferred← citeshttps://doi.org/10.1186/s13717-024-00496-7openalex-snapshot
Transcriptomic responses to drought stress in the Patagonian southern beech Nothofagus alpina
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1507914/v1openalex-snapshot
Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.21203/rs.3.rs-41819/v1openalex-snapshot
Comparative Study on Nitrogen Assimilation and Gene Regulation of different Kentucky bluegrass Cultivars in response to Nitrate supply
inferred← citeshttps://doi.org/10.3389/fgene.2024.1474259openalex-snapshot
Integrated PacBio SMRT and Illumina sequencing uncovers transcriptional and physiological responses to drought stress in whole-plant Nitraria tangutorum
inferred← citeshttps://doi.org/10.3389/fmicb.2020.556118openalex-snapshot
Beneficial Effects of Mixing Kentucky Bluegrass With Red Fescue via Plant-Soil Interactions in Black Soil of Northeast China
inferred← citeshttps://doi.org/10.3389/fpls.2021.717563openalex-snapshot
Comparative Transcriptome Analysis Revealed Candidate Genes Potentially Related to Desiccation Sensitivity of Recalcitrant Quercus variabilis Seeds
inferred← citeshttps://doi.org/10.3389/fpls.2021.720452openalex-snapshot
Secondary Metabolism and Hormone Response Reveal the Molecular Mechanism of Triploid Mulberry (Morus Alba L.) Trees Against Drought
inferred← citeshttps://doi.org/10.3389/fpls.2021.808772openalex-snapshot
Differential Metabolomic Responses of Kentucky Bluegrass Cultivars to Low Nitrogen Stress
inferred← citeshttps://doi.org/10.3389/fpls.2022.894710openalex-snapshot
Overexpression of a Zea mays Brassinosteroid-Signaling Kinase Gene ZmBSK1 Confers Salt Stress Tolerance in Maize
inferred← citeshttps://doi.org/10.3389/fpls.2022.961680openalex-snapshot
Brassinosteroids induced drought resistance of contrasting drought-responsive genotypes of maize at physiological and transcriptomic levels
inferred← citeshttps://doi.org/10.3389/fpls.2023.1139162openalex-snapshot
Contents of endogenous brassinosteroids and the response to drought and/or exogenously applied 24-epibrassinolide in two different maize leaves
inferred← citeshttps://doi.org/10.3389/fpls.2023.1158035openalex-snapshot
Mining of long non-coding RNAs with target genes in response to rust based on full-length transcriptome in Kentucky bluegrass
inferred← citeshttps://doi.org/10.3389/fpls.2025.1629615openalex-snapshot
Association mapping and candidate gene identification for drought tolerance in sorghum
inferred← citeshttps://doi.org/10.3390/agriculture13101860openalex-snapshot
Advances in Crop Genetic Improvement to Overcome Drought Stress: Bibliometric and Meta-Analysis
inferred← citeshttps://doi.org/10.3390/agronomy14112543openalex-snapshot
Transcriptomic Analysis Reveals the Molecular Defense Mechanisms of Poa pratensis Against Powdery Mildew Fungus Blumeria graminis f. sp. Poae
inferred← citeshttps://doi.org/10.3390/agronomy16030337openalex-snapshot
Physiological and Transcriptomic Responses of Asterothamnus centraliasiaticus Leaves to Drought Stress
inferred← citeshttps://doi.org/10.3390/biology11081192openalex-snapshot
Application of 2,4-Epibrassinolide Improves Drought Tolerance in Tobacco through Physiological and Biochemical Mechanisms
inferred← citeshttps://doi.org/10.3390/genes10121041openalex-snapshot
Transcriptome Profiling, Biochemical and Physiological Analyses Provide New Insights towards Drought Tolerance in Nicotiana tabacum L.
inferred← citeshttps://doi.org/10.3390/genes16070760openalex-snapshot
AdBSK1-Mediated Hormone Signaling Regulates Flowering Transition in Actinidia deliciosa ‘Guichang’
inferred← citeshttps://doi.org/10.3390/horticulturae10101029openalex-snapshot
Molecular and Physiological Responses of Toona ciliata to Simulated Drought Stress
inferred← citeshttps://doi.org/10.3390/ijms20092360openalex-snapshot
OsbZIP81, A Homologue of Arabidopsis VIP1, May Positively Regulate JA Levels by Directly Targetting the Genes in JA Signaling and Metabolism Pathway in Rice
inferred← citeshttps://doi.org/10.3390/ijms21010167openalex-snapshot
RNA-seq and ChIP-seq as Complementary Approaches for Comprehension of Plant Transcriptional Regulatory Mechanism
inferred← citeshttps://doi.org/10.3390/ijms23042374openalex-snapshot
Current Studies of the Effects of Drought Stress on Root Exudates and Rhizosphere Microbiomes of Crop Plant Species
inferred← citeshttps://doi.org/10.3390/ijms24054458openalex-snapshot
PtrVCS2 Regulates Drought Resistance by Changing Vessel Morphology and Stomatal Closure in Populus trichocarpa
inferred← citeshttps://doi.org/10.3390/ijms242216228openalex-snapshot
Drought Stress Alleviator Melatonin Reconfigures Water-Stressed Barley (Hordeum vulgare L.) Plants’ Photosynthetic Efficiency, Antioxidant Capacity, and Endogenous Phytohormone Profile
inferred← citeshttps://doi.org/10.3390/ijms25042250openalex-snapshot
Transcriptome Analysis Reveals the Mechanism by Which Exogenous Melatonin Treatment Delays Leaf Senescence of Postharvest Chinese Kale (Brassica oleracea var. alboglabra)
inferred← citeshttps://doi.org/10.3390/ijms25158499openalex-snapshot
Genome-Wide Identification of the Brassinosteroid Signal Kinase Gene Family and Its Profiling under Salinity Stress
inferred← citeshttps://doi.org/10.3390/ijms25179653openalex-snapshot
Transcriptome Regulation Mechanisms Difference between Female and Male Buchloe dactyloides in Response to Drought Stress and Rehydration
inferred← citeshttps://doi.org/10.3390/plants12233971openalex-snapshot
Transcriptome Analysis of Native Kentucky Bluegrass (Poa pratensis L.) in Response to Osmotic Stress
inferred← citeshttps://doi.org/10.3390/plants13020309openalex-snapshot
Transcriptome Analysis Reveals Key Genes Involved in the Response of Pyrus betuleafolia to Drought and High-Temperature Stress
inferred← citeshttps://doi.org/10.3390/plants14243758openalex-snapshot
Isolation of Endophytic Bacteria from Kentucky Bluegrass and the Biocontrol Effects of Neobacillus sp. 718 on Powdery Mildew
inferred← citeshttps://doi.org/10.3390/w17192849openalex-snapshot
Modeling the Ecological Preferences and Adaptive Capacities of Kentucky Bluegrass Based on Water Availability Using Various Machine Learning Algorithms
inferred← citeshttps://doi.org/10.48130/frures-2023-0019openalex-snapshot
Transcriptome analysis revealed MAPK and hormone pathway involving in exogenous melatonin-regulated salt tolerance in sour jujube
inferred← citeshttps://doi.org/10.48130/gr-2021-0011openalex-snapshot
Exploring the salt- and drought-tolerant genes of alfalfa through expression library screening strategy
inferred← citeshttps://doi.org/10.48130/grares-0026-0006openalex-snapshot
ABA and MAPK signaling-mediated transcriptional regulation of drought and salinity responses in grasses
inferred← citeshttps://doi.org/10.54393/fbt.v5i2.177openalex-snapshot
Potential of Plant Bioactive Compounds for the Treatment of Cancer
inferred← citeshttps://doi.org/10.5772/intechopen.93709openalex-snapshot
Plant Growth and Morphophysiological Modifications in Perennial Ryegrass under Environmental Stress
inferred← citeshttps://doi.org/10.5772/intechopen.93812openalex-snapshot
A Review on Kentucky Bluegrass Responses and Tolerance to Drought Stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515604openalex-snapshot
Additional file 1 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515607openalex-snapshot
Additional file 2 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515610openalex-snapshot
Additional file 3 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515613openalex-snapshot
Additional file 4 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515616openalex-snapshot
Additional file 5 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515619openalex-snapshot
Additional file 6 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.13515622openalex-snapshot
Additional file 7 of Transcriptome profiling reveals the effects of drought tolerance in Giant Juncao
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106585openalex-snapshot
Additional file 1 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106588openalex-snapshot
Additional file 2 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106591openalex-snapshot
Additional file 3 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106594openalex-snapshot
Additional file 4 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106597openalex-snapshot
Additional file 5 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106600openalex-snapshot
Additional file 6 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.20106603openalex-snapshot
Additional file 7 of Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606279openalex-snapshot
Additional file 1 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606282openalex-snapshot
Additional file 2 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606285openalex-snapshot
Additional file 3 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606288openalex-snapshot
Additional file 4 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606291openalex-snapshot
Additional file 5 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606294openalex-snapshot
Additional file 6 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606297openalex-snapshot
Additional file 7 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606300openalex-snapshot
Additional file 8 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606303openalex-snapshot
Additional file 9 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606306openalex-snapshot
Additional file 10 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606309openalex-snapshot
Additional file 11 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606312openalex-snapshot
Additional file 12 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606315openalex-snapshot
Additional file 13 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606318openalex-snapshot
Additional file 14 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606321openalex-snapshot
Additional file 15 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606324openalex-snapshot
Additional file 16 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606327openalex-snapshot
Additional file 17 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22606330openalex-snapshot
Additional file 18 of Iris lactea var. chinensis plant drought tolerance depends on the response of proline metabolism, transcription factors, transporters and the ROS-scavenging system
inferred← citeshttps://doi.org/10.6084/m9.figshare.22649336openalex-snapshot
Additional file 1 of Transcriptome and metabolome analysis reveals key genes and secondary metabolites of Casuarina equisetifolia ssp. incana in response to drought stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26716450openalex-snapshot
Additional file 1 of Transcriptomic responses to drought stress in the Patagonian southern beech Nothofagus alpina
inferred← citeshttps://doi.org/10.6084/m9.figshare.26716453openalex-snapshot
Additional file 2 of Transcriptomic responses to drought stress in the Patagonian southern beech Nothofagus alpina
inferred← citeshttps://doi.org/10.7287/peerj.12252v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Turf performance and physiological responses of native Poa species to summer stress in Northeast China (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12252v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Turf performance and physiological responses of native Poa species to summer stress in Northeast China (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12252v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Turf performance and physiological responses of native Poa species to summer stress in Northeast China (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.12252v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Turf performance and physiological responses of native Poa species to summer stress in Northeast China (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13077v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Functional analysis of ARF1 from Cymbidium goeringii in IAA response during leaf development (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13077v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Functional analysis of ARF1 from Cymbidium goeringii in IAA response during leaf development (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13077v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Functional analysis of ARF1 from Cymbidium goeringii in IAA response during leaf development (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13077v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Functional analysis of ARF1 from Cymbidium goeringii in IAA response during leaf development (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13077v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Functional analysis of ARF1 from Cymbidium goeringii in IAA response during leaf development (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.13077v0.2/reviews/3openalex-snapshot
Peer Review #3 of "Functional analysis of ARF1 from Cymbidium goeringii in IAA response during leaf development (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.12252openalex-snapshot
Turf performance and physiological responses of native Poa species to summer stress in Northeast China
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.