On the public citation graph

Environmental stress and flowering time

0 signed · 174 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/s00122-005-0099-8openalex-snapshot

QTLs for drought escape and tolerance identified in a set of random introgression lines of rice

inferredcites →https://doi.org/10.1007/s00299-005-0061-xopenalex-snapshot

Involvement of GIGANTEA gene in the regulation of the cold stress response in Arabidopsis

inferredcites →https://doi.org/10.1016/0092-8674(95)90288-0openalex-snapshot

The CONSTANS gene of arabidopsis promotes flowering and encodes a protein showing similarities to zinc finger transcription factors

inferredcites →https://doi.org/10.1016/j.cub.2007.05.008openalex-snapshot

FT Protein Acts as a Long-Range Signal in Arabidopsis

inferredcites →https://doi.org/10.1016/j.cub.2007.05.009openalex-snapshot

Export of FT Protein from Phloem Companion Cells Is Sufficient for Floral Induction in Arabidopsis

inferredcites →https://doi.org/10.1016/j.cub.2011.03.038openalex-snapshot

FT, A Mobile Developmental Signal in Plants

inferredcites →https://doi.org/10.1016/j.fcr.2005.08.017openalex-snapshot

Improvement of rice drought tolerance through backcross breeding: Evaluation of donors and selection in drought nurseries

inferredcites →https://doi.org/10.1016/j.pbi.2009.09.007openalex-snapshot

Arabidopsis circadian clock and photoperiodism: time to think about location

inferredcites →https://doi.org/10.1016/j.pbi.2011.04.006openalex-snapshot

Drought, metabolites, and Arabidopsis natural variation: a promising combination for understanding adaptation to water-limited environments

inferredcites →https://doi.org/10.1016/j.scienta.2008.12.008openalex-snapshot

Water deficits promote flowering in Rhododendron via regulation of pre and post initiation development

inferredcites →https://doi.org/10.1016/s1016-8478(23)13012-3openalex-snapshot

Acceleration of Flowering by Overexpression of MFT (MOTHER OF FT AND TFL1)

inferredcites →https://doi.org/10.1038/35074138openalex-snapshot

CONSTANS mediates between the circadian clock and the control of flowering in Arabidopsis

inferredcites →https://doi.org/10.1038/nature01549openalex-snapshot

Adaptation of photoperiodic control pathways produces short-day flowering in rice

inferredcites →https://doi.org/10.1038/nature10928openalex-snapshot

Transcription factor PIF4 controls the thermosensory activation of flowering

inferredcites →https://doi.org/10.1038/ncomms2357openalex-snapshot

Release of SOS2 kinase from sequestration with GIGANTEA determines salt tolerance in Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00168.xopenalex-snapshot

Oxidative stress tolerance and longevity in Arabidopsis: the late‐flowering mutant gigantea is tolerant to paraquat

inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00663.xopenalex-snapshot

Interactions of the developmental regulator ABI3 with proteins identified from developing Arabidopsis seeds

inferredcites →https://doi.org/10.1073/pnas.0601620103openalex-snapshot

The tomato FT ortholog triggers systemic signals that regulate growth and flowering and substitute for diverse environmental stimuli

inferredcites →https://doi.org/10.1073/pnas.0608379104openalex-snapshot

Rapid evolution of flowering time by an annual plant in response to a climate fluctuation

inferredcites →https://doi.org/10.1073/pnas.1106771108openalex-snapshot

GIGANTEA directly activates Flowering Locus T in Arabidopsis thaliana

inferredcites →https://doi.org/10.1073/pnas.1118876109openalex-snapshot

FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.1308974110openalex-snapshot

Quantitative phosphoproteomics identifies SnRK2 protein kinase substrates and reveals the effectors of abscisic acid action

inferredcites →https://doi.org/10.1073/pnas.170283997openalex-snapshot

GIGANTEA is a nuclear protein involved in phytochrome signaling in Arabidopsis

inferredcites →https://doi.org/10.1074/jbc.m112.394338openalex-snapshot

The E3 Ubiquitin Ligase HOS1 Regulates Arabidopsis Flowering by Mediating CONSTANS Degradation Under Cold Stress

inferredcites →https://doi.org/10.1093/aob/mcr160openalex-snapshot

Tests for the joint evolution of mating system and drought escape in Mimulus

inferredcites →https://doi.org/10.1093/emboj/18.17.4679openalex-snapshot

GIGANTEA: a circadian clock‐controlled gene that regulates photoperiodic flowering in Arabidopsis and encodes a protein with several possible membrane‐spanning domains

inferredcites →https://doi.org/10.1093/jxb/erl164openalex-snapshot

Gene networks involved in drought stress response and tolerance

inferredcites →https://doi.org/10.1093/jxb/err236openalex-snapshot

EDL3 is an F-box protein involved in the regulation of abscisic acid signalling in Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/mp/sst114openalex-snapshot

The Arabidopsis Floral Repressor BFT Delays Flowering by Competing with FT for FD Binding under High Salinity

inferredcites →https://doi.org/10.1093/pcp/pci151openalex-snapshot

TWIN SISTER OF FT (TSF) Acts as a Floral Pathway Integrator Redundantly with FT

inferredcites →https://doi.org/10.1093/pcp/pcn154openalex-snapshot

Long-Distance, Graft-Transmissible Action of Arabidopsis FLOWERING LOCUS T Protein to Promote Flowering

inferredcites →https://doi.org/10.1101/gad.1318705openalex-snapshot

The AIP2 E3 ligase acts as a novel negative regulator of ABA signaling by promoting ABI3 degradation

inferredcites →https://doi.org/10.1104/pp.103.022475openalex-snapshot

Viviparous1 Alters Global Gene Expression Patterns through Regulation of Abscisic Acid Signaling

inferredcites →https://doi.org/10.1104/pp.104.052811openalex-snapshot

Integration of Flowering Signals in Winter-Annual Arabidopsis

inferredcites →https://doi.org/10.1104/pp.105.067173openalex-snapshot

Independent Roles for EARLY FLOWERING 3 and ZEITLUPE in the Control of Circadian Timing, Hypocotyl Length, and Flowering Time

inferredcites →https://doi.org/10.1104/pp.111.187237openalex-snapshot

Phototropins But Not Cryptochromes Mediate the Blue Light-Specific Promotion of Stomatal Conductance, While Both Enhance Photosynthesis and Transpiration under Full Sunlight

inferredcites →https://doi.org/10.1104/pp.113.217729openalex-snapshot

GIGANTEA Enables Drought Escape Response via Abscisic Acid-Dependent Activation of the Florigens and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1

inferredcites →https://doi.org/10.1104/pp.113.217984openalex-snapshot

TWIN SISTER OF FT , GIGANTEA , and CONSTANS Have a Positive But Indirect Effect on Blue Light-Induced Stomatal Opening in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.105.033464openalex-snapshot

Distinct Roles of GIGANTEA in Promoting Flowering and Regulating Circadian Rhythms in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.107.054528openalex-snapshot

The GIGANTEA -Regulated MicroRNA172 Mediates Photoperiodic Flowering Independent of CONSTANS in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.108.063883openalex-snapshot

Crosstalk between Cold Response and Flowering in Arabidopsis Is Mediated through the Flowering-Time Gene SOC1 and Its Upstream Negative Regulator FLC

inferredcites →https://doi.org/10.1105/tpc.109.073072openalex-snapshot

MOTHER OF FT AND TFL1 Regulates Seed Germination through a Negative Feedback Loop Modulating ABA Signaling in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.110.081885openalex-snapshot

The Arabidopsis E3 Ubiquitin Ligase HOS1 Negatively Regulates CONSTANS Abundance in the Photoperiodic Control of Flowering

inferredcites →https://doi.org/10.1105/tpc.113.109355openalex-snapshot

Interlocking Feedback Loops Govern the Dynamic Behavior of the Floral Transition inArabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.115428openalex-snapshot

Flower Development under Drought Stress: Morphological and Transcriptomic Analyses Reveal Acute Responses and Long-Term Acclimation in Arabidopsis

inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01883.xopenalex-snapshot

THE ADAPTIVE SIGNIFICANCE OF DROUGHT ESCAPE IN AVENA BARBATA, AN ANNUAL GRASS

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03986.xopenalex-snapshot

Genetic and spatial interactions between FT , TSF and SVP during the early stages of floral induction in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04482.xopenalex-snapshot

Cytokinin promotes flowering of Arabidopsis via transcriptional activation of the FT paralogue TSF

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04815.xopenalex-snapshot

PFT1, the MED25 subunit of the plant Mediator complex, promotes flowering through CONSTANS dependent and independent mechanisms in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03251.xopenalex-snapshot

The flowering time regulator CONSTANS is recruited to the FLOWERING LOCUS T promoter via a unique cis ‐element

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03603.xopenalex-snapshot

Plasticity and evolution in drought avoidance and escape in the annual plant Brassica rapa

inferredcites →https://doi.org/10.1111/mec.12344openalex-snapshot

Mass flowering of the tropical tree S horea beccariana was preceded by expression changes in flowering and drought‐responsive genes

inferredcites →https://doi.org/10.1126/science.1091761openalex-snapshot

Photoreceptor Regulation of CONSTANS Protein in Photoperiodic Flowering

inferredcites →https://doi.org/10.1126/science.1110586openalex-snapshot

FKF1 F-Box Protein Mediates Cyclic Degradation of a Repressor of CONSTANS in Arabidopsis

inferredcites →https://doi.org/10.1126/science.1114358openalex-snapshot

Integration of Spatial and Temporal Information During Floral Induction in Arabidopsis

inferredcites →https://doi.org/10.1126/science.1115983openalex-snapshot

FD, a bZIP Protein Mediating Signals from the Floral Pathway Integrator FT at the Shoot Apex

inferredcites →https://doi.org/10.1126/science.1118642openalex-snapshot

Integration of Plant Responses to Environmentally Activated Phytohormonal Signals

inferredcites →https://doi.org/10.1126/science.1141752openalex-snapshot

FT Protein Movement Contributes to Long-Distance Signaling in Floral Induction of Arabidopsis

inferredcites →https://doi.org/10.1126/science.1146994openalex-snapshot

FKF1 and GIGANTEA Complex Formation Is Required for Day-Length Measurement in Arabidopsis

inferredcites →https://doi.org/10.1126/science.286.5446.1960openalex-snapshot

A Pair of Related Genes with Antagonistic Roles in Mediating Flowering Signals

inferredcites →https://doi.org/10.1126/science.286.5446.1962openalex-snapshot

Activation Tagging of the Floral Inducer FT

inferredcites →https://doi.org/10.1242/dev.01231openalex-snapshot

CONSTANS acts in the phloem to regulate a systemic signal that induces photoperiodic flowering of Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pgen.0020106openalex-snapshot

Potent Induction of Arabidopsis thaliana Flowering by Elevated Growth Temperature

inferredcites →https://doi.org/10.4161/psb.5.9.12415openalex-snapshot

BROTHER OF FT AND TFL1(BFT), a member of theFT/TFL1family, shows distinct pattern of expression during the vegetative growth of Arabidopsis

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.4814706openalex-extracted

Analysis of the Function of the Anoectochilus Roxburghii Hd-Zip19 in Flower Development and Drought Responses

inferred← citeshttps://doi.org/10.2139/ssrn.4822669openalex-extracted

Analysis of the Function of the Anoectochilus Roxburghii Hd-Zip19 in Flower Development and Drought Responses

inferred← citeshttps://doi.org/10.1002/9781118951446.ch5openalex-snapshot

Structure and development of orchid mycorrhizas

inferred← citeshttps://doi.org/10.1002/cssc.201702007openalex-snapshot

Deep Eutectic Solvent Aqueous Solutions as Efficient Media for the Solubilization of Hardwood Xylans

inferred← citeshttps://doi.org/10.1002/pld3.70099openalex-snapshot

Parasitic‐Plant Parasite Rewires Flowering Pathways to Induce Stem‐Derived Galls

inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_6openalex-snapshot

Hormones in Photoperiodic Flower Induction

inferred← citeshttps://doi.org/10.1007/978-3-319-20517-5_8openalex-snapshot

Photoperiodism: The Calendar of Plants

inferred← citeshttps://doi.org/10.1007/978-981-10-7479-0_4openalex-snapshot

Reactive Oxygen Species (ROS): A Way to Stress Survival in Plants

inferred← citeshttps://doi.org/10.1007/978-981-19-5434-4_4openalex-snapshot

Inbred Line Development and Hybrid Breeding

inferred← citeshttps://doi.org/10.1007/s00344-025-11820-6openalex-snapshot

Nitric Oxide and Cyanide Enhance Flowering in Lemna gibba Through a Stress-Mediated Pathway Under Inductive Conditions

inferred← citeshttps://doi.org/10.1007/s00709-018-1237-xopenalex-snapshot

Comparative analysis of transcriptome in two wheat genotypes with contrasting levels of drought tolerance

inferred← citeshttps://doi.org/10.1007/s00726-017-2501-7openalex-snapshot

Long photoperiod affects the maize transition from vegetative to reproductive stages: a proteomic comparison between photoperiod-sensitive inbred line and its recurrent parent

inferred← citeshttps://doi.org/10.1007/s10722-020-01000-8openalex-snapshot

Comparative in silico analysis of Eragrostis tef (Zucc.) Trotter with other species for elucidating presence of growth regulating factors (GRFs)

inferred← citeshttps://doi.org/10.1007/s11103-017-0624-6openalex-snapshot

The function of OsbHLH068 is partially redundant with its homolog, AtbHLH112, in the regulation of the salt stress response but has opposite functions to control flowering in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11103-018-0801-2openalex-snapshot

Transcription profiles reveal the regulatory mechanisms of spur bud changes and flower induction in response to shoot bending in apple (Malus domestica Borkh.)

inferred← citeshttps://doi.org/10.1007/s11103-020-01051-6openalex-snapshot

RdDM pathway components differentially modulate Tobamovirus symptom development

inferred← citeshttps://doi.org/10.1007/s11258-018-0796-4openalex-snapshot

Pitcher plant facilitates prey capture in a sympatric congener

inferred← citeshttps://doi.org/10.1007/s13562-021-00709-6openalex-snapshot

Identification, phylogeny and transcript profiling of ERF family genes during temperature stress treatment in Pea (Pisum sativum L.)

inferred← citeshttps://doi.org/10.1016/b978-0-12-821450-3.00004-4openalex-snapshot

Moth bean

inferred← citeshttps://doi.org/10.1016/bs.abr.2018.10.002openalex-snapshot

The Control of Bud Break and Flowering Time in Plants

inferred← citeshttps://doi.org/10.1016/j.apsoil.2017.09.001openalex-snapshot

Focus on mycorrhizal symbioses

inferred← citeshttps://doi.org/10.1016/j.chmed.2022.08.008openalex-snapshot

Transcriptome analysis of Saposhnikovia divaricata and mining of bolting and flowering genes

inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105541openalex-snapshot

Transcriptome uncovers BnaFBH3-mediated regulatory networks associated with tolerant to abiotic stress in Brassica napus

inferred← citeshttps://doi.org/10.1016/j.envexpbot.2026.106416openalex-snapshot

Premature tapetum degradation of Cakile maritima under drought and low or moderate salinity does not reduce its reproductive fitness

inferred← citeshttps://doi.org/10.1016/j.jare.2023.06.012openalex-snapshot

Exogenous abscisic acid represses rice flowering via SAPK8-ABF1-Ehd1/Ehd2 pathway

inferred← citeshttps://doi.org/10.1016/j.marpolbul.2017.10.037openalex-snapshot

Experimental evidence of warming-induced flowering in the Mediterranean seagrass Posidonia oceanica

inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112369openalex-snapshot

ArHDZ19 contributes to drought tolerance by advancing flowering time in Anoectochilus roxburghii

inferred← citeshttps://doi.org/10.1016/j.sciaf.2020.e00405openalex-snapshot

Clarity on frequently asked questions about drought measurements in plant physiology

inferred← citeshttps://doi.org/10.1016/j.stress.2025.100747openalex-snapshot

Genetic regulatory pathways of plant flowering time affected by abiotic stress

inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.013openalex-snapshot

Abscisic acid and its role in the modulation of plant growth, development, and yield stability

inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.03.024openalex-snapshot

Hormonal control of the floral transition: Can one catch them all?

inferred← citeshttps://doi.org/10.1016/s1875-5364(18)30078-5openalex-snapshot

Transcriptomic analysis identifies differentially expressed genes (DEGs) associated with bolting and flowering in Saposhnikovia divaricata

inferred← citeshttps://doi.org/10.1038/s41438-021-00652-6openalex-snapshot

AaWRKY17, a positive regulator of artemisinin biosynthesis, is involved in resistance to Pseudomonas syringae in Artemisia annua

inferred← citeshttps://doi.org/10.1038/s41598-020-78417-9openalex-snapshot

The vascular targeted citrus FLOWERING LOCUS T3 gene promotes non-inductive early flowering in transgenic Carrizo rootstocks and grafted juvenile scions

inferred← citeshttps://doi.org/10.1038/srep37309openalex-snapshot

Novel Genomic and Evolutionary Insight of WRKY Transcription Factors in Plant Lineage

inferred← citeshttps://doi.org/10.1071/cp18117openalex-snapshot

Modelled impacts of extreme heat and drought on maize yield in South Africa

inferred← citeshttps://doi.org/10.1080/11263504.2025.2527242openalex-snapshot

Photoperiodic regulation of rice leaf proteome reveals a splicing boost under short days

inferred← citeshttps://doi.org/10.1080/15592324.2021.1877005openalex-snapshot

Plant drought tolerance provided through genome editing of the trehalase gene

inferred← citeshttps://doi.org/10.1093/botlinnean/boad007openalex-snapshot

Architectural traits underlie growth form diversity and polycarpic versus monocarpic life histories inCerberiopsis(Apocynaceae)

inferred← citeshttps://doi.org/10.1093/jxb/eraa089openalex-snapshot

Molecular genetic analyses of abiotic stress responses during plant reproductive development

inferred← citeshttps://doi.org/10.1093/jxb/erad228openalex-snapshot

Reduction in PLANT DEFENSIN 1 expression in Arabidopsis thaliana results in increased resistance to pathogens and zinc toxicity

inferred← citeshttps://doi.org/10.1093/jxb/eraf090openalex-snapshot

New insights into nutrient- and drought-responsive flowering

inferred← citeshttps://doi.org/10.1093/jxb/erv441openalex-snapshot

The link between flowering time and stress tolerance

inferred← citeshttps://doi.org/10.1093/jxb/erv450openalex-snapshot

Overexpression of soybean miR172c confers tolerance to water deficit and salt stress, but increases ABA sensitivity in transgenic Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/jxb/erw272openalex-snapshot

Stress-induced flowering: the third category of flowering response

inferred← citeshttps://doi.org/10.1093/jxb/erw384openalex-snapshot

ABA-dependent control of GIGANTEA signalling enables drought escape via up-regulation of FLOWERING LOCUS T in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/jxb/erx055openalex-snapshot

Floral transitions in wheat and barley: interactions between photoperiod, abiotic stresses, and nutrient status

inferred← citeshttps://doi.org/10.1093/pcp/pcaa121openalex-snapshot

Analysis of the Function of the Alfalfa Mslea-D34 Gene in Abiotic Stress Responses and Flowering Time

inferred← citeshttps://doi.org/10.1093/pcp/pcy007openalex-snapshot

Toward a Molecular Understanding of Abscisic Acid Actions in Floral Transition

inferred← citeshttps://doi.org/10.1093/plcell/koae090openalex-snapshot

CONSTANS, a HUB for all seasons: How photoperiod pervades plant physiology regulatory circuits

inferred← citeshttps://doi.org/10.1093/plphys/kiab231openalex-snapshot

LATERAL ORGAN BOUNDARIES DOMAIN 25 functions as a key regulator of haustorium development in dodders

inferred← citeshttps://doi.org/10.1098/rstb.2020.0384openalex-snapshot

Natural disturbances and masting: from mechanisms to fitness consequences

inferred← citeshttps://doi.org/10.1101/2021.01.04.425251openalex-snapshot

CcLBD25 functions as a key regulator of haustorium development in Cuscuta campestris

inferred← citeshttps://doi.org/10.1101/2024.10.17.618901openalex-snapshot

Parasitic-plant parasite utilizes flowering pathways at unconventional stages to form stem-derived galls

inferred← citeshttps://doi.org/10.1101/443424openalex-snapshot

Non-functional and weak alleles of FRIGIDA and FLOWERING LOCUS C reduce lifetime water-use independent of leaf-level water-use-efficiency traits in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1105/tpc.15.00619openalex-snapshot

Transcriptional Mechanism of Jasmonate Receptor COI1-Mediated Delay of Flowering Time in Arabidopsis

inferred← citeshttps://doi.org/10.1111/jipb.13956openalex-snapshot

GIGANTEA‐LATE ELONGATED HYPOCOTYL complex regulates citrus drought tolerance and drought induced flowering

inferred← citeshttps://doi.org/10.1111/mec.15089openalex-snapshot

Heat‐stress induced flowering can be a potential adaptive response to ocean warming for the iconic seagrass Posidonia oceanica

inferred← citeshttps://doi.org/10.1111/nph.16839openalex-snapshot

Beyond flowering time: diverse roles of an APETALA2‐like transcription factor in shoot architecture and perennial traits

inferred← citeshttps://doi.org/10.1111/nph.18711openalex-snapshot

Changes in phenology can alter patterns of natural selection: the joint evolution of germination time and postgermination traits

inferred← citeshttps://doi.org/10.1111/pbi.12212openalex-snapshot

Validation of A integumenta as a gene to modify floral size in ornamental plants

inferred← citeshttps://doi.org/10.1111/pce.12775openalex-snapshot

How specialized volatiles respond to chronic and short‐term physiological and shock heat stress in Brassica nigra

inferred← citeshttps://doi.org/10.1111/pce.13527openalex-snapshot

Accelerated flowering time reduces lifetime water use without penalizing reproductive performance in Arabidopsis

inferred← citeshttps://doi.org/10.1111/pce.13546openalex-snapshot

Complex interactions between day length and diurnal patterns of gene expression drive photoperiodic responses in a perennial C4 grass

inferred← citeshttps://doi.org/10.1111/ppl.70731openalex-snapshot

Methodologies and Considerations in Evaluating Heat Stress Response and Thermotolerance of Pollen Grains

inferred← citeshttps://doi.org/10.1111/tpj.15783openalex-snapshot

BrABF3 promotes flowering through the direct activation of CONSTANS transcription in pak choi

inferred← citeshttps://doi.org/10.1177/0748730416679307openalex-snapshot

Geographic Variation of Plant Circadian Clock Function in Natural and Agricultural Settings

inferred← citeshttps://doi.org/10.1186/s12864-017-4324-zopenalex-snapshot

Transcriptomics analysis of the flowering regulatory genes involved in the herbicide resistance of Asia minor bluegrass (Polypogon fugax)

inferred← citeshttps://doi.org/10.1186/s12870-018-1555-3openalex-snapshot

Comparative RNA-sequencing-based transcriptome profiling of buds from profusely flowering ‘Qinguan’ and weakly flowering ‘Nagafu no. 2’ apple varieties reveals novel insights into the regulatory mechanisms underlying floral induction

inferred← citeshttps://doi.org/10.1186/s12870-019-1967-8openalex-snapshot

Understanding the molecular mechanisms underlying graft success in grapevine

inferred← citeshttps://doi.org/10.1186/s12870-022-03873-6openalex-snapshot

Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.1371/journal.pone.0127699openalex-snapshot

Investigating the Association between Flowering Time and Defense in the Arabidopsis thaliana-Fusarium oxysporum Interaction

inferred← citeshttps://doi.org/10.15252/embr.201744862openalex-snapshot

Antisense transcription represses Arabidopsis seed dormancy QTL DOG1 to regulate drought tolerance

inferred← citeshttps://doi.org/10.3389/fpls.2016.00682openalex-snapshot

Transcriptomic Analysis Identifies Differentially Expressed Genes (DEGs) Associated with Bolting and Flowering in Radish (Raphanus sativus L.)

inferred← citeshttps://doi.org/10.3389/fpls.2017.01786openalex-snapshot

Accelerated Generation of Selfed Pure Line Plants for Gene Identification and Crop Breeding

inferred← citeshttps://doi.org/10.3389/fpls.2017.02212openalex-snapshot

No Time to Waste: Transcriptome Study Reveals that Drought Tolerance in Barley May Be Attributed to Stressed-Like Expression Patterns that Exist before the Occurrence of Stress

inferred← citeshttps://doi.org/10.3389/fpls.2020.00708openalex-snapshot

Modeling of Root Nitrate Responses Suggests Preferential Foraging Arises From the Integration of Demand, Supply and Local Presence Signals

inferred← citeshttps://doi.org/10.3389/fpls.2022.877908openalex-snapshot

Identification of Flowering Regulatory Networks and Hub Genes Expressed in the Leaves of Elymus sibiricus L. Using Comparative Transcriptome Analysis

inferred← citeshttps://doi.org/10.3389/fpls.2025.1751953openalex-snapshot

From natural induction to artificial regulation: a review on the mechanisms and techniques of flowering in pineapple

inferred← citeshttps://doi.org/10.3390/agronomy13123034openalex-snapshot

The Role of Drought and Temperature Stress in the Regulation of Flowering Time in Annuals and Perennials

inferred← citeshttps://doi.org/10.3390/genes11101142openalex-snapshot

Gigantea: Uncovering New Functions in Flower Development

inferred← citeshttps://doi.org/10.3390/horticulturae7070171openalex-snapshot

Comparative Transcriptomic Analysis of Differentially Expressed Transcripts Associated with Flowering Time of Loquat (Eriobotya japonica Lindl.)

inferred← citeshttps://doi.org/10.3390/horticulturae7120579openalex-snapshot

The Responses of Physiological Characteristics and Flowering Related Gene to the Different Water Stress Levels of Red-Flesh Pummelo Cultivars (Citrus grandis (L.) Osbeck) Own-Rooted by Air Layering Propagation under Two Growing Conditions

inferred← citeshttps://doi.org/10.3390/ijms22041723openalex-snapshot

Genomic Architecture of Phenotypic Plasticity in Response to Water Stress in Tetraploid Wheat

inferred← citeshttps://doi.org/10.3390/ijms262211120openalex-snapshot

Response of Plants to Touch Stress at Morphological, Physiological and Molecular Levels

inferred← citeshttps://doi.org/10.3390/life12081271openalex-snapshot

Circadian Rhythm Regulates Reactive Oxygen Species Production and Inhibits Al-Induced Programmed Cell Death in Peanut

inferred← citeshttps://doi.org/10.3390/plants12020264openalex-snapshot

PEBP Signaling Network in Tubers and Tuberous Root Crops

inferred← citeshttps://doi.org/10.3390/plants13162190openalex-snapshot

CIRCADIAN CLOCK-ASSOCIATED1 Delays Flowering by Directly Inhibiting the Transcription of BcSOC1 in Pak-choi

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397956openalex-snapshot

Additional file 10 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397959openalex-snapshot

Additional file 11 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397962openalex-snapshot

Additional file 12 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397965openalex-snapshot

Additional file 13 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397968openalex-snapshot

Additional file 14 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397971openalex-snapshot

Additional file 15 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397974openalex-snapshot

Additional file 16 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397977openalex-snapshot

Additional file 17 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397980openalex-snapshot

Additional file 18 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397983openalex-snapshot

Additional file 19 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397989openalex-snapshot

Additional file 1 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397992openalex-snapshot

Additional file 2 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397995openalex-snapshot

Additional file 3 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21397998openalex-snapshot

Additional file 4 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21398001openalex-snapshot

Additional file 5 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21398004openalex-snapshot

Additional file 6 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21398007openalex-snapshot

Additional file 7 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21398010openalex-snapshot

Additional file 8 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.6084/m9.figshare.21398013openalex-snapshot

Additional file 9 of Comparison of anther transcriptomes in response to cold stress at the reproductive stage between susceptible and resistant Japonica rice varieties

inferred← citeshttps://doi.org/10.64898/2026.08.05.743098openalex-snapshot

Warming and precipitation change alter flowering phenology and coflowering networks in California serpentine grasslands

inferred← citeshttps://doi.org/10.7554/elife.06100openalex-snapshot

Planting molecular functions in an ecological context with Arabidopsis thaliana

inferred← citeshttps://doi.org/10.7717/peerj.1339openalex-snapshot

Variation in the flowering time orthologs BrFLC and BrSOC1 in a natural population of Brassica rapa

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.