On the public citation graph
Pleiotropy in developmental regulation by flowering‐pathway genes: is it an evolutionary constraint?
0 signed · 294 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/jez.21008openalex-snapshot
Pleiotropic effects on mandibular morphology II: Differential epistasis and genetic variation in morphological integration
inferredcites →https://doi.org/10.1002/jez.b.21008openalex-snapshot
Pleiotropic effects on mandibular morphology II: Differential epistasis and genetic variation in morphological integration
inferredcites →https://doi.org/10.1006/anbo.1993.1029openalex-snapshot
The Impact of Atmospheric CO2 and Temperature Changes on Stomatal Density: Observation from Quercus robur Lammas Leaves
inferredcites →https://doi.org/10.1007/978-3-642-55974-7openalex-snapshot
Survival Strategies of Annual Desert Plants
inferredcites →https://doi.org/10.1007/s00425-005-0057-3openalex-snapshot
Loss of function of four DELLA genes leads to light- and gibberellin-independent seed germination in Arabidopsis
inferredcites →https://doi.org/10.1007/s10265-014-0639-xopenalex-snapshot
A promoter analysis of MOTHER OF FT AND TFL1 1 (JcMFT1), a seed-preferential gene from the biofuel plant Jatropha curcas
inferredcites →https://doi.org/10.1007/s11103-012-9991-1openalex-snapshot
Arabidopsis suppressor mutant of abh1 shows a new face of the already known players: ABH1 (CBP80) and ABI4—in response to ABA and abiotic stresses during seed germination
inferredcites →https://doi.org/10.1007/s12298-017-0458-3openalex-snapshot
Research progress on the autonomous flowering time pathway in Arabidopsis
inferredcites →https://doi.org/10.1016/j.bbrc.2017.11.149openalex-snapshot
Functional FRIGIDA allele enhances drought tolerance by regulating the P5CS1 pathway in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cub.2008.07.075openalex-snapshot
The Balance between CONSTANS and TEMPRANILLO Activities Determines FT Expression to Trigger Flowering
inferredcites →https://doi.org/10.1016/j.cub.2011.06.025openalex-snapshot
FLOWERING LOCUS T Regulates Stomatal Opening
inferredcites →https://doi.org/10.1016/j.cub.2012.03.044openalex-snapshot
High temperature exposure increases plant cooling capacity
inferredcites →https://doi.org/10.1016/j.cub.2018.11.006openalex-snapshot
A Tree Ortholog of SHORT VEGETATIVE PHASE Floral Repressor Mediates Photoperiodic Control of Bud Dormancy
inferredcites →https://doi.org/10.1016/j.pbi.2004.07.002openalex-snapshot
The autonomous pathway: epigenetic and post-transcriptional gene regulation in the control of Arabidopsis flowering time
inferredcites →https://doi.org/10.1016/j.pbi.2005.07.011openalex-snapshot
Ambient temperature perception in plants
inferredcites →https://doi.org/10.1016/j.tig.2010.09.001openalex-snapshot
Gene networks controlling the initiation of flower development
inferredcites →https://doi.org/10.1016/j.tig.2012.10.010openalex-snapshot
The many faces of pleiotropy
inferredcites →https://doi.org/10.1016/j.tplants.2017.08.008openalex-snapshot
Divergence in How Genetic Pathways Respond to Environments
inferredcites →https://doi.org/10.1016/j.tree.2006.05.001openalex-snapshot
Evo-devo and constraints on selection
inferredcites →https://doi.org/10.1016/j.tree.2012.01.016openalex-snapshot
A model of developmental evolution: selection, pleiotropy and compensation
inferredcites →https://doi.org/10.1016/j.ydbio.2017.03.024openalex-snapshot
Hormonal control of the floral transition: Can one catch them all?
inferredcites →https://doi.org/10.1016/s0092-8674(01)00460-3openalex-snapshot
An mRNA Cap Binding Protein, ABH1, Modulates Early Abscisic Acid Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1016/s0140-1963(18)31739-7openalex-snapshot
Seed coat permeability as a function of photoperiodical treatments of the mother plants during seed maturation in the desert annual plant: Trigonella arabica, del
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/10.1016/s1369-5266(99)00041-2openalex-snapshot
Response of plant development to environment: control of flowering by daylength and temperature
inferredcites →https://doi.org/10.1017/s0960258500000696openalex-snapshot
The effects of the parent environment on seed germinability
inferredcites →https://doi.org/10.1017/s0960258500004256openalex-snapshot
Phytochromes and seed germination
inferredcites →https://doi.org/10.1038/360273a0openalex-snapshot
Molecular characterization of the Arabidopsis floral homeotic gene APETALA1
inferredcites →https://doi.org/10.1038/nature02195openalex-snapshot
Vernalization in Arabidopsis thaliana is mediated by the PHD finger protein VIN3
inferredcites →https://doi.org/10.1038/nature02269openalex-snapshot
Vernalization requires epigenetic silencing of FLC by histone methylation
inferredcites →https://doi.org/10.1038/nature06756openalex-snapshot
Pleiotropic scaling of gene effects and the ‘cost of complexity’
inferredcites →https://doi.org/10.1038/nature08800openalex-snapshot
Genome-wide association study of 107 phenotypes in Arabidopsis thaliana inbred lines
inferredcites →https://doi.org/10.1038/ncomms3186openalex-snapshot
Two FLX family members are non-redundantly required to establish the vernalization requirement in Arabidopsis
inferredcites →https://doi.org/10.1038/ng1085openalex-snapshot
A thermosensory pathway controlling flowering time in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/ng1298openalex-snapshot
A genetic link between cold responses and flowering time through FVE in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nrg2949openalex-snapshot
The pleiotropic structure of the genotype–phenotype map: the evolvability of complex organisms
inferredcites →https://doi.org/10.1038/nrg3291openalex-snapshot
The genetic basis of flowering responses to seasonal cues
inferredcites →https://doi.org/10.1038/s41477-018-0253-3openalex-snapshot
Molecular basis of flowering under natural long-day conditions in Arabidopsis
inferredcites →https://doi.org/10.1046/j.0960-7412.2001.01210.xopenalex-snapshot
FLC, a repressor of flowering, is regulated by genes in different inductive pathways
inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00746.xopenalex-snapshot
The evolution of maladaptation
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.7040543.xopenalex-snapshot
Arabidopsis late‐flowering fve mutants are affected in both vegetative and reproductive development
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00980.xopenalex-snapshot
Gibberellin response mutants identified by luciferase imaging
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01380.xopenalex-snapshot
The VERNALIZATION INDEPENDENCE 4 gene encodes a novel regulator of FLOWERING LOCUS C
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01430.xopenalex-snapshot
ABI5 acts downstream of ABI3 to execute an ABA‐dependent growth arrest during germination
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01674.xopenalex-snapshot
Phytochrome control of flowering is temperature sensitive and correlates with expression of the floral integrator FT
inferredcites →https://doi.org/10.1046/j.1420-9101.1988.1010045.xopenalex-snapshot
The influence of variation and of developmental constraints on the rate of multivariate phenotypic evolution
inferredcites →https://doi.org/10.1071/fp16368openalex-snapshot
Effect of FLOWERING LOCUS C on seed germination depends on dormancy
inferredcites →https://doi.org/10.1073/pnas.0402377101openalex-snapshot
Floral homeotic genes are targets of gibberellin signaling in flower development
inferredcites →https://doi.org/10.1073/pnas.0437826100openalex-snapshot
Regulation of photoperiodic flowering by Arabidopsis photoreceptors
inferredcites →https://doi.org/10.1073/pnas.0607142103openalex-snapshot
The wheat and barley vernalization gene VRN3 is an orthologue of FT
inferredcites →https://doi.org/10.1073/pnas.0607877103openalex-snapshot
Cloning of DOG1 , a quantitative trait locus controlling seed dormancy in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0806446105openalex-snapshot
Phylogenetic patterns of species loss in Thoreau's woods are driven by climate change
inferredcites →https://doi.org/10.1073/pnas.081594298openalex-snapshot
A postgermination developmental arrest checkpoint is mediated by abscisic acid and requires the ABI5 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0901367106openalex-snapshot
Major flowering time gene, FLOWERING LOCUS C , regulates seed germination in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1116325108openalex-snapshot
Dormancy cycling in Arabidopsis seeds is controlled by seasonally distinct hormone-signaling pathways
inferredcites →https://doi.org/10.1073/pnas.1301647110openalex-snapshot
Differential control of seed primary dormancy in Arabidopsis ecotypes by the transcription factor SPATULA
inferredcites →https://doi.org/10.1073/pnas.1412274111openalex-snapshot
Maternal temperature history activates Flowering Locus T in fruits to control progeny dormancy according to time of year
inferredcites →https://doi.org/10.1073/pnas.1531467100openalex-snapshot
Attenuation of FLOWERING LOCUS C activity as a mechanism for the evolution of summer-annual flowering behavior in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1600558113openalex-snapshot
DELAY OF GERMINATION1 ( DOG1 ) regulates both seed dormancy and flowering time through microRNA pathways
inferredcites →https://doi.org/10.1073/pnas.1700536114openalex-snapshot
Establishment of a vernalization requirement in Brachypodium distachyon requires REPRESSOR OF VERNALIZATION1
inferredcites →https://doi.org/10.1073/pnas.97.7.3753openalex-snapshot
The molecular basis of vernalization: The central role of FLOWERING LOCUS C ( FLC )
inferredcites →https://doi.org/10.1086/282900openalex-snapshot
Dispersion and Population Interactions
inferredcites →https://doi.org/10.1086/284220openalex-snapshot
Ontogeny, Timing of Development, and Genetic Variance-Covariances Structure
inferredcites →https://doi.org/10.1086/513111openalex-snapshot
Fitness Effects Associated with the Major Flowering Time GeneFRIGIDAinArabidopsis thalianain the Field
inferredcites →https://doi.org/10.1086/679439openalex-snapshot
Modeling the Influence of Genetic and Environmental Variation on the Expression of Plant Life Cycles across Landscapes
inferredcites →https://doi.org/10.1093/aob/mcr301openalex-snapshot
Co-adaptation of seed dormancy and flowering time in the arable weed Capsella bursa-pastoris (shepherd's purse)
inferredcites →https://doi.org/10.1093/aob/mcu032openalex-snapshot
Molecular control of seasonal flowering in rice, arabidopsis and temperate cereals
inferredcites →https://doi.org/10.1093/aob/mcw166openalex-snapshot
Contrasting germination responses to vegetative canopies experienced in pre- vs. post-dispersal environments
inferredcites →https://doi.org/10.1093/aob/mcx132openalex-snapshot
The autonomous flowering-time pathway pleiotropically regulates seed germination in Arabidopsis thaliana
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/genetics/124.3.773openalex-snapshot
Pleiotropic models of quantitative variation.
inferredcites →https://doi.org/10.1093/genetics/148.2.885openalex-snapshot
Genetic Interactions Among Late-Flowering Mutants of Arabidopsis
inferredcites →https://doi.org/10.1093/genetics/154.4.1419openalex-snapshot
The Genetical Theory of Natural Selection
inferredcites →https://doi.org/10.1093/genetics/164.1.347openalex-snapshot
Genetic Analysis of Early Flowering Mutants in Arabidopsis Defines a Class of Pleiotropic Developmental Regulator Required for Expression of the Flowering-Time Switch Flowering Locus C
inferredcites →https://doi.org/10.1093/genetics/164.2.711openalex-snapshot
Analysis of Natural Allelic Variation at Seed Dormancy Loci of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/genetics/165.4.2181openalex-snapshot
The Genetics of Adaptation: The Roles of Pleiotropy, Stabilizing Selection and Drift in Shaping the Distribution of Bidirectional Fixed Mutational Effects
inferredcites →https://doi.org/10.1093/icb/36.1.44openalex-snapshot
Developmental Integration and the Evolution of Pleiotropy
inferredcites →https://doi.org/10.1093/jxb/erh026openalex-snapshot
Light signals, phytochromes and cross-talk with other environmental cues
inferredcites →https://doi.org/10.1093/jxb/erq098openalex-snapshot
Regulation and function of SOC1, a flowering pathway integrator
inferredcites →https://doi.org/10.1093/jxb/err304openalex-snapshot
Conservation and divergence of four kiwifruit SVP-like MADS-box genes suggest distinct roles in kiwifruit bud dormancy and flowering
inferredcites →https://doi.org/10.1093/jxb/err452openalex-snapshot
The Arabidopsis mutant, fy-1, has an ABA-insensitive germination phenotype
inferredcites →https://doi.org/10.1093/jxb/ers361openalex-snapshot
The inhibitory effect of ABA on floral transition is mediated by ABI5 in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erw436openalex-snapshot
Effects of environmental variation during seed production on seed dormancy and germination
inferredcites →https://doi.org/10.1093/jxb/erx053openalex-snapshot
Influence of differing nitrate and nitrogen availability on flowering control in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/ery140openalex-snapshot
PHYD prevents secondary dormancy establishment of seeds exposed to high temperature and is associated with lower PIL5 accumulation
inferredcites →https://doi.org/10.1093/pcp/pcu214openalex-snapshot
A Flowering Integrator, SOC1, Affects Stomatal Opening in Arabidopsis thaliana
inferredcites →https://doi.org/10.1098/rspb.2013.1043openalex-snapshot
Pleiotropy of FRIGIDA enhances the potential for multivariate adaptation
inferredcites →https://doi.org/10.1101/gad.245993.114openalex-snapshot
Multiple FLC haplotypes defined by independent cis-regulatory variation underpin life history diversity in Arabidopsis thaliana
inferredcites →https://doi.org/10.1101/gad.969002openalex-snapshot
Gibberellin regulates Arabidopsis seed germination via RGL2 , a GAI/RGA -like gene whose expression is up-regulated following imbibition
inferredcites →https://doi.org/10.1101/sqb.2013.77.014449openalex-snapshot
The Molecular Basis of Vernalization in Different Plant Groups
inferredcites →https://doi.org/10.1104/pp.104.039578openalex-snapshot
DELLA Proteins and Gibberellin-Regulated Seed Germination and Floral Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.097048openalex-snapshot
GIGANTEA Regulates Phytochrome A-Mediated Photomorphogenesis Independently of Its Role in the Circadian Clock
inferredcites →https://doi.org/10.1104/pp.108.1.157openalex-snapshot
Effect of Vernalization, Photoperiod, and Light Quality on the Flowering Phenotype of Arabidopsis Plants Containing the FRIGIDA Gene
inferredcites →https://doi.org/10.1104/pp.108.118927openalex-snapshot
Functional Redundancy and New Roles for Genes of the Autonomous Floral-Promotion Pathway
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/10.1104/pp.15.01483openalex-snapshot
Seed Dormancy in Arabidopsis Is Controlled by Alternative Polyadenylation of DOG1
inferredcites →https://doi.org/10.1104/pp.16.01161openalex-snapshot
A Flowering Locus C Homolog Is a Vernalization-Regulated Repressor in Brachypodium and Is Cold Regulated in Wheat
inferredcites →https://doi.org/10.1105/tpc.019331openalex-snapshot
A New Arabidopsis Gene,FLK, Encodes an RNA Binding Protein with K Homology Motifs and Regulates Flowering Time viaFLOWERING LOCUS C [W]
inferredcites →https://doi.org/10.1105/tpc.104.026062openalex-snapshot
A Mechanism Related to the Yeast Transcriptional Regulator Paf1c Is Required for Expression of the Arabidopsis FLC/MAF MADS Box Gene Family[W]
inferredcites →https://doi.org/10.1105/tpc.108.064022openalex-snapshot
A Role for Multiple Circadian Clock Genes in the Response to Signals That Break Seed Dormancy inArabidopsis
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.11.5.949openalex-snapshot
FLOWERING LOCUS C Encodes a Novel MADS Domain Protein That Acts as a Repressor of Flowering
inferredcites →https://doi.org/10.1105/tpc.111.088492openalex-snapshot
A Wheat Homolog of MOTHER OF FT AND TFL1 Acts in the Regulation of Germination
inferredcites →https://doi.org/10.1105/tpc.112.100214openalex-snapshot
The Time Required for Dormancy Release in Arabidopsis Is Determined by DELAY OF GERMINATION1 Protein Levels in Freshly Harvested Seeds
inferredcites →https://doi.org/10.1105/tpc.113.121830openalex-snapshot
A Role for Barley CRYPTOCHROME1 in Light Regulation of Grain Dormancy and Germination
inferredcites →https://doi.org/10.1105/tpc.13.4.935openalex-snapshot
Loss of FLOWERING LOCUS C Activity Eliminates the Late-Flowering Phenotype of FRIGIDA and Autonomous Pathway Mutations but Not Responsiveness to Vernalization
inferredcites →https://doi.org/10.1111/evo.13320openalex-snapshot
What affects the predictability of evolutionary constraints using aG-matrix? The relative effects of modular pleiotropy and mutational correlation
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00002.xopenalex-snapshot
ADAPTATION AND THE COST OF COMPLEXITY
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00693.xopenalex-snapshot
COMPENSATING FOR OUR LOAD OF MUTATIONS: FREEZING THE MELTDOWN OF SMALL POPULATIONS
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01882.xopenalex-snapshot
DIVERGENT SELECTION ON FLOWERING TIME CONTRIBUTES TO LOCAL ADAPTATION IN MIMULUS GUTTATUS POPULATIONS
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01785.xopenalex-snapshot
Ecological genetics and genomics of plant defences: evidence and approaches
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04557.xopenalex-snapshot
The earliest stages of adaptation in an experimental plant population: strong selection on QTLS for seed dormancy
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05181.xopenalex-snapshot
DOG1 expression is predicted by the seed‐maturation environment and contributes to geographical variation in germination in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01319.xopenalex-snapshot
Stomatal density, anatomy and nutrient concentrations of Scots pine needles are affected by elevated CO2 and temperature
inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02552.xopenalex-snapshot
The dynamic nature of bud dormancy in trees: environmental control and molecular mechanisms
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02738.xopenalex-snapshot
Gene expression profiles of Arabidopsis Cvi seeds during dormancy cycling indicate a common underlying dormancy control mechanism
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03110.xopenalex-snapshot
mRNA metabolism of flowering‐time regulators in wild‐type Arabidopsis revealed by a nuclear cap binding protein mutant, abh1
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03156.xopenalex-snapshot
Constitutive expression of CIR1 (RVE2) affects several circadian‐regulated processes and seed germination in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01610.xopenalex-snapshot
Cloning and characterization of SOC1 homologs in barley (Hordeum vulgare) and their expression during seed development and in response to vernalization
inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01573.xopenalex-snapshot
Measuring and comparing evolvability and constraint in multivariate characters
inferredcites →https://doi.org/10.1111/j.1462-5822.2007.00938.xopenalex-snapshot
Role of plant stomata in bacterial invasion
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02281.xopenalex-snapshot
Diversification of phytochrome contributions to germination as a function of seed‐maturation environment
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02867.xopenalex-snapshot
Gene expression analysis of light‐modulated germination in tomato seeds
inferredcites →https://doi.org/10.1111/j.1558-5646.1979.tb04694.xopenalex-snapshot
QUANTITATIVE GENETIC ANALYSIS OF MULTIVARIATE EVOLUTION, APPLIED TO BRAIN:BODY SIZE ALLOMETRY
inferredcites →https://doi.org/10.1111/j.1558-5646.1983.tb00236.xopenalex-snapshot
THE MEASUREMENT OF SELECTION ON CORRELATED CHARACTERS
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb02339.xopenalex-snapshot
PERSPECTIVE: COMPLEX ADAPTATIONS AND THE EVOLUTION OF EVOLVABILITY
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00255.xopenalex-snapshot
GENETIC VARIATION IN PLEIOTROPY: DIFFERENTIAL EPISTASIS AS A SOURCE OF VARIATION IN THE ALLOMETRIC RELATIONSHIP BETWEEN LONG BONE LENGTHS AND BODY WEIGHT
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01828.xopenalex-snapshot
PLEIOTROPY IN THE WILD: THE DORMANCY GENEDOG1EXERTS CASCADING CONTROL ON LIFE CYCLES
inferredcites →https://doi.org/10.1111/mec.12285openalex-snapshot
Paths to selection on life history loci in different natural environments across the native range of A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/mec.15034openalex-snapshot
Seed traits are pleiotropically regulated by the flowering time gene PERPETUAL FLOWERING 1 ( PEP1 ) in the perennial Arabis alpina
inferredcites →https://doi.org/10.1111/nph.13090openalex-snapshot
Seed production temperature regulation of primary dormancy occurs through control of seed coat phenylpropanoid metabolism
inferredcites →https://doi.org/10.1111/nph.13685openalex-snapshot
Multiple paths to similar germination behavior in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/nph.14520openalex-snapshot
Maternal vernalization and vernalization‐pathway genes influence progeny seed germination
inferredcites →https://doi.org/10.1111/nph.14712openalex-snapshot
Interacting effects of genetic variation for seed dormancy and flowering time on phenology, life history, and fitness of experimental Arabidopsis thaliana populations over multiple generations in the field
inferredcites →https://doi.org/10.1111/nph.15029openalex-snapshot
Phenological responses to multiple environmental drivers under climate change: insights from a long‐term observational study and a manipulative field experiment
inferredcites →https://doi.org/10.1111/pce.12286openalex-snapshot
Functional diversity of phytochrome family in the control of light and gibberellin‐mediated germination in A rabidopsis
inferredcites →https://doi.org/10.1111/ppl.12664openalex-snapshot
Nitrogen – essential macronutrient and signal controlling flowering time
inferredcites →https://doi.org/10.1111/tpj.12186openalex-snapshot
Temperature, light and nitrate sensing coordinate A rabidopsis seed dormancy cycling, resulting in winter and summer annual phenotypes
inferredcites →https://doi.org/10.1111/tpj.12735openalex-snapshot
Seed dormancy cycling in A rabidopsis: chromatin remodelling and regulation of DOG 1 in response to seasonal environmental signals
inferredcites →https://doi.org/10.1126/science.1094305openalex-snapshot
The Wheat VRN2 Gene Is a Flowering Repressor Down-Regulated by Vernalization
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.1126038openalex-snapshot
CO/FT Regulatory Module Controls Timing of Flowering and Seasonal Growth Cessation in Trees
inferredcites →https://doi.org/10.1126/science.1165826openalex-snapshot
Effects of Genetic Perturbation on Seasonal Life History Plasticity
inferredcites →https://doi.org/10.1126/science.1209271openalex-snapshot
A Map of Local Adaptation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.285.5433.1579openalex-snapshot
Control of Circadian Rhythms and Photoperiodic Flowering by the Arabidopsis GIGANTEA Gene
inferredcites →https://doi.org/10.1126/science.288.5471.1613openalex-snapshot
Distinct Roles of CONSTANS Target Genes in Reproductive Development of Arabidopsis
inferredcites →https://doi.org/10.1126/science.290.5490.344openalex-snapshot
Molecular Analysis of FRIGIDA , a Major Determinant of Natural Variation in Arabidopsis Flowering Time
inferredcites →https://doi.org/10.1126/science.296.5566.285openalex-snapshot
Arabidopsis , the Rosetta Stone of Flowering Time?
inferredcites →https://doi.org/10.1126/science.aar7361openalex-snapshot
Feedback regulation of COOLAIR expression controls seed dormancy and flowering time
inferredcites →https://doi.org/10.1146/annurev-ecolsys-120213-091721openalex-snapshot
Constraints Evolve: Context Dependency of Gene Effects Allows Evolution of Pleiotropy
inferredcites →https://doi.org/10.1146/annurev.ecolsys.110308.120232openalex-snapshot
Abundant Genetic Variation + Strong Selection = Multivariate Genetic Constraints: A Geometric View of Adaptation
inferredcites →https://doi.org/10.1186/1471-2229-6-10openalex-snapshot
FLOWERING LOCUS C-dependent and -independent regulation of the circadian clock by the autonomous and vernalization pathways
inferredcites →https://doi.org/10.1242/dev.01924openalex-snapshot
An allelic series reveals essential roles for FY in plant development in addition to flowering-time control
inferredcites →https://doi.org/10.1242/dev.063511openalex-snapshot
The control of developmental phase transitions in plants
inferredcites →https://doi.org/10.1371/journal.pgen.1003130openalex-snapshot
PEP1 of Arabis alpina Is Encoded by Two Overlapping Genes That Contribute to Natural Genetic Variation in Perennial Flowering
inferredcites →https://doi.org/10.1371/journal.pgen.1006413openalex-snapshot
Bottom-up Assembly of the Phytochrome Network
inferredcites →https://doi.org/10.1371/journal.pgen.1007510openalex-snapshot
Genetic basis and evolution of rapid cycling in railway populations of tetraploid Arabidopsis arenosa
inferredcites →https://doi.org/10.1371/journal.pone.0002733openalex-snapshot
Differential Interactions of the Autonomous Pathway RRM Proteins and Chromatin Regulators in the Silencing of Arabidopsis Targets
inferredcites →https://doi.org/10.1371/journal.pone.0008878openalex-snapshot
Favorable Climate Change Response Explains Non-Native Species' Success in Thoreau's Woods
inferredcites →https://doi.org/10.1371/journal.pone.0022241openalex-snapshot
Identification of the Arabidopsis REDUCED DORMANCY 2 Gene Uncovers a Role for the Polymerase Associated Factor 1 Complex in Seed Dormancy
inferredcites →https://doi.org/10.1371/journal.pone.0099642openalex-snapshot
Identification of a Soybean MOTHER OF FT AND TFL1 Homolog Involved in Regulation of Seed Germination
inferredcites →https://doi.org/10.1371/journal.pone.0127699openalex-snapshot
Investigating the Association between Flowering Time and Defense in the Arabidopsis thaliana-Fusarium oxysporum Interaction
inferredcites →https://doi.org/10.1534/genetics.111.135681openalex-snapshot
On the Pleiotropic Structure of the Genotype–Phenotype Map and the Evolvability of Complex Organisms
inferredcites →https://doi.org/10.1534/genetics.112.143214openalex-snapshot
Gene Functional Trade-Offs and the Evolution of Pleiotropy
inferredcites →https://doi.org/10.1890/0012-9658(2006)87[1445:soefdd]2.0.co;2openalex-snapshot
STRENGTH OF EVIDENCE FOR DENSITY DEPENDENCE IN ABUNDANCE TIME SERIES OF 1198 SPECIES
inferredcites →https://doi.org/10.2503/jjshs1.77.38openalex-snapshot
Isolation and Characterization of a Citrus FT/TFL1 Homologue (CuMFT1), Which Shows Quantitatively Preferential Expression in Citrus Seeds
inferredcites →https://doi.org/10.3389/fpls.2017.00477openalex-snapshot
SVP-like MADS Box Genes Control Dormancy and Budbreak in Apple
inferredcites →https://doi.org/10.3389/fpls.2017.01107openalex-snapshot
BdVRN1 Expression Confers Flowering Competency and Is Negatively Correlated with Freezing Tolerance in Brachypodium distachyon
inferredcites →https://doi.org/10.3389/fpls.2018.01368openalex-snapshot
Modulation of Dormancy and Growth Responses in Reproductive Buds of Temperate Trees
inferredcites →https://doi.org/10.3732/ajb.1200478openalex-snapshot
Temperature‐dependent shifts in phenology contribute to the success of exotic species with climate change
inferredcites →https://doi.org/10.3732/ajb.93.11.1633openalex-snapshot
On the developmental dependence of leaf respiration: responses to short‐ and long‐term changes in growth temperature
inferredcites →https://doi.org/10.4161/psb.5.10.13161openalex-snapshot
MOTHER OFFT ANDTFL1regulates seed germination and fertility relevant to the brassinosteroid signaling pathway
inferredcites →https://doi.org/10.5962/bhl.title.27468openalex-snapshot
The genetical theory of natural selection
inferredcites →https://doi.org/10.7554/elife.05557openalex-snapshot
Flowering time and seed dormancy control use external coincidence to generate life history strategy
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/ajb2.1607openalex-snapshot
Evolutionary divergence of potential drought adaptations between two subspecies of an annual plant: Are trait combinations facilitated, independent, or constrained?
inferred← citeshttps://doi.org/10.1002/ajb2.16090openalex-snapshot
The Boechera model system for evolutionary ecology
inferred← citeshttps://doi.org/10.1002/aro2.13openalex-snapshot
Multi‐trait genomic predictions using GBLUP and Bayesian mixture prior model in beef cattle
inferred← citeshttps://doi.org/10.1002/ece3.72961openalex-snapshot
Agrestal Environments and Maternal Genetic Effects Weaken the Ecological Barriers for Crop to Wild Introgression in Sunflower
inferred← citeshttps://doi.org/10.1002/ece3.8232openalex-snapshot
Depicting the phenotypic space of the annual plant Diplotaxis acris in hyperarid deserts
inferred← citeshttps://doi.org/10.1002/njb.05105openalex-snapshot
Distribution under climate change of Anemone coronaria : linking flower colour and seed dispersal
inferred← citeshttps://doi.org/10.1007/s00438-022-01949-4openalex-snapshot
Identification of genetic loci shared between Alzheimer’s disease and hypertension
inferred← citeshttps://doi.org/10.1007/s11104-022-05608-wopenalex-snapshot
Nitrogen as a regulator for flowering time in plant
inferred← citeshttps://doi.org/10.1007/s11105-021-01312-8openalex-snapshot
Overexpression of Polypogon fugax Type I–Like MADS-Box Gene PfAGL28 Affects Flowering Time and Pod Formation in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.1007/s13258-025-01640-zopenalex-snapshot
Transcriptomic analysis revealed that short-day treatment of seedlings promotes flowering in maize (Zea mays L.)
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100464openalex-snapshot
Genome-wide association study (GWAS) of rice (Oryza sativa L.) panicle compactness
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.120545openalex-snapshot
A MADS-box protein GhAGL8 promotes early flowering and increases yield without compromising fiber quality in cotton
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122424openalex-snapshot
Photoperiodic flowering in field crops: Mechanisms and the link to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153784openalex-snapshot
Quantitative genetics of pleiotropy and its potential for plant sciences
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.plantsci.2024.112382openalex-snapshot
Genome-wide association study of rice (Oryza sativa L.) inflorescence architecture
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109763openalex-snapshot
Functional diversity of two apple paralogs MADS5 and MADS35 in regulating flowering and parthenocarpy
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110192openalex-snapshot
From morphology to epigenetics: current understanding of the floral regulation in woody perennials
inferred← citeshttps://doi.org/10.1016/j.pld.2025.05.011openalex-snapshot
Dendrogenomic resilience mechanisms of two endangered Mexican spruces
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101002openalex-snapshot
Dual-extraction modeling: A multi-modal deep-learning architecture for phenotypic prediction and functional gene mining of complex traits
inferred← citeshttps://doi.org/10.1021/acsagscitech.5c00598openalex-snapshot
Evolutionary Genomics of Adaptive Traits in Wheat Landraces: Role of Chromatin Remodeling
inferred← citeshttps://doi.org/10.1038/s41467-020-17896-wopenalex-snapshot
Natural variation at FLM splicing has pleiotropic effects modulating ecological strategies in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41467-025-56884-wopenalex-snapshot
Regulatory variation controlling architectural pleiotropy in maize
inferred← citeshttps://doi.org/10.1038/s41598-023-28049-6openalex-snapshot
HDF1, a novel flowering time regulator identified in a mutant suppressing sensitivity to red light reduced 1 early flowering
inferred← citeshttps://doi.org/10.1038/s42003-025-08673-wopenalex-snapshot
Genomic signatures of adaptation in seed traits in the wild plant Brassica incana
inferred← citeshttps://doi.org/10.1073/pnas.1912451117openalex-snapshot
Functional variants of DOG1 control seed chilling responses and variation in seasonal life-history strategies in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1086/730186openalex-snapshot
Conditionally Deleterious Mutation Load Accumulates in Genomic Islands of Local Adaptation but Can Be Purged with Sufficient Genotypic Redundancy
inferred← citeshttps://doi.org/10.1086/731402openalex-snapshot
Effect of the Seed Bank on Evolutionary Rescue in Small Populations: Univariate and Multivariate Demogenetic Dynamics
inferred← citeshttps://doi.org/10.1093/9780197846032.001.0001openalex-snapshot
Populations of Individuals
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0001openalex-snapshot
Populations of Individuals
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0002openalex-snapshot
Population-based Threshold Models
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0003openalex-snapshot
Origin and Integration of Biological Processes
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0007openalex-snapshot
Developmental Plasticity, Ecology and Evolution
inferred← citeshttps://doi.org/10.1093/9780197846032.003.0008openalex-snapshot
Implications and Anticipations
inferred← citeshttps://doi.org/10.1093/aob/mcae040openalex-snapshot
Local climate and vernalization sensitivity predict the latitudinal patterns of flowering onset in the crop wild relative Linum bienne Mill.
inferred← citeshttps://doi.org/10.1093/evolut/qpaf049openalex-snapshot
Evidence of landscape-driven repeated adaptation among 13 Eucalyptus species
inferred← citeshttps://doi.org/10.1093/g3journal/jkad300openalex-snapshot
Allelic combinations of Hd1, Hd16, and Ghd7 exhibit pleiotropic effects on agronomic traits in rice
inferred← citeshttps://doi.org/10.1093/g3journal/jkaf230openalex-snapshot
MYB regulator of “colorless” flavonols underlies the evolution of red flowers in Iochroma (Solanaceae)
inferred← citeshttps://doi.org/10.1093/jxb/erab166openalex-snapshot
Correlation and co-localization of QTL for stomatal density, canopy temperature, and productivity with and without drought stress in Setaria
inferred← citeshttps://doi.org/10.1093/molbev/msac203openalex-snapshot
A Pleiotropic Flowering Time QTL Exhibits Gene-by-Environment Interaction for Fitness in a Perennial Grass
inferred← citeshttps://doi.org/10.1093/nar/gkae963openalex-snapshot
Uncoupling FRUITFULL’s functions through modification of a protein motif identified by co-ortholog analysis
inferred← citeshttps://doi.org/10.1093/plcell/koaf151openalex-snapshot
Advancing ecological and evolutionary research in Arabidopsis: Extending insights into model and nonmodel plants
inferred← citeshttps://doi.org/10.1093/plphys/kiac522openalex-snapshot
Expression inheritance and constraints on cis- and trans-regulatory mutations underlying lotus color variation
inferred← citeshttps://doi.org/10.1093/plphys/kiae109openalex-snapshot
Flowering time: From physiology, through genetics to mechanism
inferred← citeshttps://doi.org/10.1093/plphys/kiae440openalex-snapshot
Vernalization or devernalization? A question about VRT2
inferred← citeshttps://doi.org/10.1101/2022.01.02.474722openalex-snapshot
Local climate and vernalization requirements explain the latitudinal patterns of flowering initiation in the crop wild relative Linum bienne
inferred← citeshttps://doi.org/10.1101/2022.02.24.481758openalex-snapshot
QTL analysis reveals an oligogenic architecture of a rapidly adapting trait during the European invasion of common ragweed
inferred← citeshttps://doi.org/10.1101/2022.02.26.482116openalex-snapshot
A pleiotropic flowering time QTL exhibits gene-by-environmental interaction for fitness in a perennial grass
inferred← citeshttps://doi.org/10.1101/2023.02.17.528989openalex-snapshot
Repeatability of adaptation in sunflowers: genomic regions harbouring inversions also drive adaptation in species lacking an inversion
inferred← citeshttps://doi.org/10.1101/2023.03.16.532996openalex-snapshot
Conditionally deleterious mutation load accumulates in genomic islands but can be purged with sufficient genotypic redundancy
inferred← citeshttps://doi.org/10.1101/2024.06.14.599000openalex-snapshot
Cryptic Variation in Adaptive Phenotypes Revealed by Panspecific flc Mutants
inferred← citeshttps://doi.org/10.1101/2025.04.01.646560openalex-snapshot
Canonical Wnt/β-catenin signalling regulates inducible aging and regeneration loss in hydra
inferred← citeshttps://doi.org/10.1104/pp.20.00873openalex-snapshot
Key Traits and Genes Associate with Salinity Tolerance Independent from Vigor in Cultivated Sunflower
inferred← citeshttps://doi.org/10.1111/1365-2745.13981openalex-snapshot
Spatiotemporal dynamics of genetic variation at the quantitative and molecular levels within a natural Arabidopsis thaliana population
inferred← citeshttps://doi.org/10.1111/age.13282openalex-snapshot
Pleiotropic architectures of porcine immune and growth trait pairs revealed by a self‐product‐based transcriptome method
inferred← citeshttps://doi.org/10.1111/eva.13453openalex-snapshot
Quantitative trait loci mapping reveals an oligogenic architecture of a rapidly adapting trait during the European invasion of common ragweed
inferred← citeshttps://doi.org/10.1111/jeb.14011openalex-snapshot
Negotiating mutualism: A locus for exploitation by rhizobia has a broad effect size distribution and context‐dependent effects on legume hosts
inferred← citeshttps://doi.org/10.1111/mec.16180openalex-snapshot
Genetic trade‐offs underlie divergent life history strategies for local adaptation in white clover
inferred← citeshttps://doi.org/10.1111/mec.70180openalex-snapshot
Identifying the Degree of Gene Reuse During Repeated Adaptation
inferred← citeshttps://doi.org/10.1111/nph.16205openalex-snapshot
Evolutionary processes from the perspective of flowering time diversity
inferred← citeshttps://doi.org/10.1111/nph.18769openalex-snapshot
Environment‐specific selection alters flowering‐time plasticity and results in pervasive pleiotropic responses in maize
inferred← citeshttps://doi.org/10.1111/nph.20375openalex-snapshot
Historic rewiring of grass flowering time pathways and implications for crop improvement under climate change
inferred← citeshttps://doi.org/10.1111/nph.70861openalex-snapshot
Genetic architecture of flowering time and perenniality: implications for the origin of wild rice Oryza nivara
inferred← citeshttps://doi.org/10.1111/nph.71539openalex-snapshot
Nondefense functions of plant specialized metabolites: ecological phenomena, molecular mechanisms, and evolutionary implications
inferred← citeshttps://doi.org/10.1111/pbi.14362openalex-snapshot
A genome‐wide association study uncovers a ZmRap2.7‐ZCN9/ZCN10 module to regulate ABA signalling and seed vigour in maize
inferred← citeshttps://doi.org/10.1111/pbi.70007openalex-snapshot
Introgression of dwarfing allele dw1 reduced seed dormancy and increased pre‐harvest sprouting susceptibility in grain sorghum converted lines
inferred← citeshttps://doi.org/10.1111/pce.14557openalex-snapshot
Combined genome‐wide association study and epistasis analysis reveal multifaceted genetic architectures of plant height in Asian cultivated rice
inferred← citeshttps://doi.org/10.1111/tpj.15118openalex-snapshot
Flowering time gene or jack of all trades?
inferred← citeshttps://doi.org/10.1126/science.adw3673openalex-snapshot
Can wild plant adaptations help crops tolerate heat?
inferred← citeshttps://doi.org/10.1146/annurev-arplant-063025-111942openalex-snapshot
Plant Phenotypic Plasticity: From Molecular Mechanisms to Breeding and Climate Change Adaptation
inferred← citeshttps://doi.org/10.1186/s12864-026-13036-8openalex-snapshot
Genetic architecture and candidate loci associated with growth and yield-related traits in sweet fig banana (Musa acuminata cv Sotoumon, AA)
inferred← citeshttps://doi.org/10.1186/s12870-021-02889-8openalex-snapshot
Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.1186/s12870-026-08272-9openalex-snapshot
Brachypodium HISTONE DEACETYLASE 19.1 promotes yield, flowering, and freezing tolerance at the expense of drought tolerance
inferred← citeshttps://doi.org/10.1186/s12870-026-09500-yopenalex-snapshot
Genomic early growth mechanisms of two endangered Mexican spruces
inferred← citeshttps://doi.org/10.1186/s13059-025-03770-9openalex-snapshot
Antagonistic effects of selection on alleles associated with seed size and seed dormancy in wheat
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003226openalex-snapshot
Species-wide gene editing of a flowering regulator reveals hidden phenotypic variation
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003536openalex-snapshot
Divergent and stabilizing selection shape the phenotypic space of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.15244/pjoes/186652openalex-snapshot
Molecular Mechanisms Underlying Triple and Single-Capsule Sesame (Sesamum Indicum L.) Varieties and Their Antioxidant Enzyme Activities
inferred← citeshttps://doi.org/10.2174/1389202923666211223115214openalex-snapshot
Identification of Potential Pleiotropic Genes for Immune and Skeletal Diseases Using Multivariate MetaCCA Analysis
inferred← citeshttps://doi.org/10.22541/au.160460109.97406017/v1openalex-snapshot
QTL x environment interactions for panicle traits in switchgrass ( Panicum virgatum )
inferred← citeshttps://doi.org/10.3389/fevo.2026.1750171openalex-snapshot
Molecular evolution of floral development genes in spiral gingers with divergent pollination syndromes
inferred← citeshttps://doi.org/10.3389/fgene.2020.602526openalex-snapshot
How Well Can Multivariate and Univariate GWAS Distinguish Between True and Spurious Pleiotropy?
inferred← citeshttps://doi.org/10.3389/fgene.2022.954015openalex-snapshot
Structural changes and adaptative evolutionary constraints in FLOWERING LOCUS T and TERMINAL FLOWER1-like genes of flowering plants
inferred← citeshttps://doi.org/10.3389/fpls.2021.627258openalex-snapshot
The Diverse Roles of FLOWERING LOCUS C in Annual and Perennial Brassicaceae Species
inferred← citeshttps://doi.org/10.3389/frfst.2024.1372770openalex-snapshot
Seed storage allergens tackled via next-generation research assistant
inferred← citeshttps://doi.org/10.3390/horticulturae11010102openalex-snapshot
Floral Regulation: The Significant Virtue of Horticultural Flowering Plants
inferred← citeshttps://doi.org/10.3390/ijms23126632openalex-snapshot
DNA Demethylation Induces Tree Peony Flowering with a Low Deformity Rate Compared to Gibberellin by Inducing PsFT Expression under Forcing Culture Conditions
inferred← citeshttps://doi.org/10.3390/ijms27156761openalex-snapshot
Genome-Wide Identification and Expression Profiling of the DOG1-like Genes in Radish (Raphanus sativus L.)
inferred← citeshttps://doi.org/10.3390/plants10112475openalex-snapshot
SNP- and Haplotype-Based GWAS of Flowering-Related Traits in Brassica napus
inferred← citeshttps://doi.org/10.3390/plants11223072openalex-snapshot
Novel Single-Nucleotide Variants for Morpho-Physiological Traits Involved in Enhancing Drought Stress Tolerance in Barley
inferred← citeshttps://doi.org/10.3390/plants12234020openalex-snapshot
Unlocking Nature’s Clock: CRISPR Technology in Flowering Time Engineering
inferred← citeshttps://doi.org/10.3390/plants15030456openalex-snapshot
Biotic and Abiotic Drivers of Phenotypic Diversity in the Genus Lupinus (Fabaceae)
inferred← citeshttps://doi.org/10.3390/plants9010114openalex-snapshot
HD-ZIP I Transcription Factor (PtHB13) Negatively Regulates Citrus Flowering through Binding to FLOWERING LOCUS C Promoter
inferred← citeshttps://doi.org/10.3390/plants9040480openalex-snapshot
Delay of Germination-1 (DOG1): A Key to Understanding Seed Dormancy
inferred← citeshttps://doi.org/10.48130/seedbio-0026-0007openalex-snapshot
Beyond flowering: the pleiotropic functions of key flowering-time genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140317openalex-snapshot
Additional file 1 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140320openalex-snapshot
Additional file 2 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140323openalex-snapshot
Additional file 3 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140326openalex-snapshot
Additional file 4 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140332openalex-snapshot
Additional file 5 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140335openalex-snapshot
Additional file 6 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.6084/m9.figshare.14140338openalex-snapshot
Additional file 7 of Gene co-expression analysis of tomato seed maturation reveals tissue-specific regulatory networks and hubs associated with the acquisition of desiccation tolerance and seed vigour
inferred← citeshttps://doi.org/10.70675/4e9f89a2z568dz48aez8405za9b9078e6d8fopenalex-snapshot
Implication des cytokinines dans la formation de l'haustorium chez la plante parasite Phelipanche ramosa
inferred← citeshttps://doi.org/10.70675/f0d6bb10zbbddz494cz91fczab0385dfa919openalex-snapshot
Contrôle génétique et moléculaire de la qualité germinative chez la tomate : rôle du développement de la graine et influence de la température
inferred← citeshttps://doi.org/10.7554/elife.57671openalex-snapshot
Natural variation in autumn expression is the major adaptive determinant distinguishing Arabidopsis FLC haplotypes
inferred← citeshttps://doi.org/10.7554/elife.66873openalex-snapshot
Genome-wide association study in quinoa reveals selection pattern typical for crops with a short breeding history
inferred← citeshttps://doi.org/10.7554/elife.88604openalex-snapshot
Repeatability of adaptation in sunflowers reveals that genomic regions harbouring inversions also drive adaptation in species lacking an inversion
inferred← citeshttps://doi.org/10.7554/elife.88604.1openalex-snapshot
Repeatability of adaptation in sunflowers: genomic regions harbouring inversions also drive adaptation in species lacking an inversion
inferred← citeshttps://doi.org/10.7554/elife.88604.2openalex-snapshot
Repeatability of adaptation in sunflowers: genomic regions harbouring inversions also drive adaptation in species lacking an inversion
inferred← citeshttps://doi.org/10.7554/elife.88604.3openalex-snapshot
Repeatability of adaptation in sunflowers reveals that genomic regions harbouring inversions also drive adaptation in species lacking an inversion
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.