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PEP1 regulates perennial flowering in Arabis alpina

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.cell.2006.05.005openalex-snapshot
The Timing of Developmental Transitions in Plants
inferredcites →https://doi.org/10.1016/j.cub.2006.11.052openalex-snapshot
The PHD Finger Protein VRN5 Functions in the Epigenetic Silencing of Arabidopsis FLC
inferredcites →https://doi.org/10.1016/j.cub.2007.10.026openalex-snapshot
Vernalization-Induced Trimethylation of Histone H3 Lysine 27 at FLC Is Not Maintained in Mitotically Quiescent Cells
inferredcites →https://doi.org/10.1016/j.infsof.2005.09.005openalex-snapshot
Engineering a software tool for gene structure prediction in higher organisms
inferredcites →https://doi.org/10.1016/s0092-8674(01)00573-6openalex-snapshot
The VERNALIZATION 2 Gene Mediates the Epigenetic Regulation of Vernalization in Arabidopsis
inferredcites →https://doi.org/10.1016/s1369-5266(01)00229-1openalex-snapshot
Molecular control and variation in the floral transition
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/nature06877openalex-snapshot
Evolution of metal hyperaccumulation required cis-regulatory changes and triplication of HMA4
inferredcites →https://doi.org/10.1038/ng1835openalex-snapshot
The genetic basis for differences in leaf form between Arabidopsis thaliana and its wild relative Cardamine hirsuta
inferredcites →https://doi.org/10.1038/sj.emboj.7601311openalex-snapshot
Silencing by plant Polycomb‐group genes requires dispersed trimethylation of histone H3 at lysine 27
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0700488104openalex-snapshot
Emerging principles of regulatory evolution
inferredcites →https://doi.org/10.1073/pnas.74.12.5463openalex-snapshot
DNA sequencing with chain-terminating inhibitors
inferredcites →https://doi.org/10.1093/aob/mcg120openalex-snapshot
A Morphological and Quantitative Characterization of Early Floral Development in Apple (Malus x domestica Borkh.)
inferredcites →https://doi.org/10.1093/bioinformatics/14.1.68openalex-snapshot
SplitsTree: analyzing and visualizing evolutionary data.
inferredcites →https://doi.org/10.1093/bioinformatics/16.12.1145openalex-snapshot
InterPro—an integrated documentation resource for protein families, domains and functional sites
inferredcites →https://doi.org/10.1093/genetics/162.3.1457openalex-snapshot
Characterization and Effects of the Replicated Flowering Time Gene FLC in Brassica rapa
inferredcites →https://doi.org/10.1093/jexbot/51.352.1769openalex-snapshot
Aspects of seasonality
inferredcites →https://doi.org/10.1093/jexbot/51.352.1781openalex-snapshot
Annuality, perenniality and cell death
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/nar/26.4.1107openalex-snapshot
GeneMark.hmm: new solutions for gene finding
inferredcites →https://doi.org/10.1098/rspb.1998.0410openalex-snapshot
Molecular phylogenetic approach for studying life-history evolution: the ambiguous example of the genus Medicago L.
inferredcites →https://doi.org/10.1101/gad.1493306openalex-snapshot
A PHD finger protein involved in both the vernalization and photoperiod pathways in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.373506openalex-snapshot
The transcription factor FLC confers a flowering response to vernalization by repressing meristem competence and systemic signaling in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.405306openalex-snapshot
Variation in the epigenetic silencing of FLC contributes to natural variation in Arabidopsis vernalization response
inferredcites →https://doi.org/10.1101/gr.10.4.516openalex-snapshot
Ab initio Gene Finding in Drosophila Genomic DNA
inferredcites →https://doi.org/10.1101/gr.8.3.175openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. I. Accuracy Assessment
inferredcites →https://doi.org/10.1101/gr.8.3.186openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
inferredcites →https://doi.org/10.1101/gr.8.3.195openalex-snapshot
Consed: A Graphical Tool for Sequence Finishing
inferredcites →https://doi.org/10.1105/tpc.11.3.445openalex-snapshot
The FLF MADS Box Gene: A Repressor of Flowering in Arabidopsis Regulated by Vernalization and Methylation
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/10.1111/j.1365-294x.2005.02848.xopenalex-snapshot
Three times out of Asia Minor: the phylogeography of Arabis alpina L. (Brassicaceae)
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03739.xopenalex-snapshot
Genetic discontinuity, breeding‐system change and population history of Arabis alpina in the Italian Peninsula and adjacent Alps
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02404.xopenalex-snapshot
Vernalization‐induced repression ofFLOWERING LOCUS Cstimulates flowering inSinapis albaand enhances plant responsiveness to photoperiod
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.1126038openalex-snapshot
CO/FT Regulatory Module Controls Timing of Flowering and Seasonal Growth Cessation in Trees
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092755openalex-snapshot
Regulation and Identity of Florigen: FLOWERING LOCUS T Moves Center Stage
inferredcites →https://doi.org/10.1186/gb-2002-3-12-research0082openalex-snapshot
Apollo: a sequence annotation editor
inferredcites →https://doi.org/10.3732/ajb.93.4.607openalex-snapshot
Brassicaceae phylogeny and trichome evolution

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.543.1.4zenodo-depositor-declared
The new tribe Fourraeeae (Brassicaceae) and two Moroccan Arabis species transferred to the new genus Hurkaea
inferred← citeshttps://doi.org/10.1002/9780470015902.a0002048.pub3openalex-snapshot
Vernalization
inferred← citeshttps://doi.org/10.1002/9780470015902.a0002048.pub4openalex-snapshot
Vernalisation
inferred← citeshttps://doi.org/10.1002/9781118305881.ch10openalex-snapshot
Development in the Wild: Phenotypic Plasticity
inferred← citeshttps://doi.org/10.1002/9781118308240.ch4openalex-snapshot
Vernalization
inferred← citeshttps://doi.org/10.1002/9781119210436.ch11openalex-snapshot
Gibberellins and plant reproduction
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0495openalex-snapshot
Development in the Wild: Phenotypic Plasticity
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0540openalex-snapshot
Gibberellins and Plant Reproduction
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0640openalex-snapshot
Forbidden Fruit: Dominance Relationships and the Control of Shoot Architecture
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0695openalex-snapshot
Contrasting Life History Traits in Monocarpic Versus Polycarpic Plants from a Molecular‐Evolutionary Point of View
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0726openalex-snapshot
Functional Strategies and Life Histories of Grasses Underlying Yield and Resilience
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0759openalex-snapshot
The MADS‐Box Gene Family Involved in the Regulatory Mechanism of Dormancy and Flowering in Rosaceae Fruit Trees
inferred← citeshttps://doi.org/10.1002/ece3.3341openalex-snapshot
Between semelparity and iteroparity: Empirical evidence for a continuum of modes of parity
inferred← citeshttps://doi.org/10.1002/nzc2.70027openalex-snapshot
Orchids Versus Model Plants: A Comparison of Flowering Mechanisms
inferred← citeshttps://doi.org/10.1002/pld3.302openalex-snapshot
Glycerolipid profile differences between perennial and annual stem zones in the perennial model plant Arabis alpina
inferred← citeshttps://doi.org/10.1002/pld3.60openalex-snapshot
Expression of FLOWERING LOCUS C and a frameshift mutation of this gene on chromosome 20 differentiate a summer and winter annual biotype of Camelina sativa
inferred← citeshttps://doi.org/10.1002/tax.615007openalex-snapshot
BrassiBase : Tools and biological resources to study characters and traits in the Brassicaceae—version 1.1
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Genetic regulation of flowering time in annual and perennial plants
inferred← citeshttps://doi.org/10.1007/978-1-4419-1541-2_8openalex-snapshot
Reproductive Development in Populus
inferred← citeshttps://doi.org/10.1007/978-1-4419-7118-0_12openalex-snapshot
Arabidopsis lyrata Genetics
inferred← citeshttps://doi.org/10.1007/978-1-4419-7118-0_23openalex-snapshot
Perspectives on Genetics and Genomics of the Brassicaceae
inferred← citeshttps://doi.org/10.1007/978-1-4419-7118-0_6openalex-snapshot
Comparative Genome Analysis at the Sequence Level in the Brassicaceae
inferred← citeshttps://doi.org/10.1007/978-3-319-25688-7_10openalex-snapshot
Evolution of the Flowering Pathways
inferred← citeshttps://doi.org/10.1007/978-3-319-99070-5_9openalex-snapshot
Flowering Time as a Model Trait to Bridge Proximate and Evolutionary Questions
inferred← citeshttps://doi.org/10.1007/978-3-642-35227-0_5openalex-snapshot
Epigenetic Control of Flowering Time
inferred← citeshttps://doi.org/10.1007/978-3-642-38212-3_13openalex-snapshot
Memory of Temperature in the Seasonal Control of Flowering Time: An Unexplored Link Between Meteorology and Molecular Biology
inferred← citeshttps://doi.org/10.1007/978-3-662-56233-8_2openalex-snapshot
General Themes of Molecular Stress Physiology
inferred← citeshttps://doi.org/10.1007/s00018-011-0673-yopenalex-snapshot
Regulation of flowering time: all roads lead to Rome
inferred← citeshttps://doi.org/10.1007/s00035-017-0196-8openalex-snapshot
The phylogeographic structure of Arabis alpina in the Alps shows consistent patterns across different types of molecular markers and geographic scales
inferred← citeshttps://doi.org/10.1007/s00122-010-1376-8openalex-snapshot
A survey of EMS-induced biennial Beta vulgaris mutants reveals a novel bolting locus which is unlinked to the bolting gene B
inferred← citeshttps://doi.org/10.1007/s00122-017-2916-2openalex-snapshot
Deciphering the complex nature of bolting time regulation in Beta vulgaris
inferred← citeshttps://doi.org/10.1007/s00299-013-1489-zopenalex-snapshot
The Vaccinium corymbosum FLOWERING LOCUS T-like gene (VcFT): a flowering activator reverses photoperiodic and chilling requirements in blueberry
inferred← citeshttps://doi.org/10.1007/s10682-012-9597-8openalex-snapshot
An outlier locus relevant in habitat-mediated selection in an alpine plant across independent regional replicates
inferred← citeshttps://doi.org/10.1007/s10725-012-9767-2openalex-snapshot
Characterizing developmental and inducible differentiation between juvenile and adult plants of Aechmea fasciata treated with ethylene by transcriptomic analysis
inferred← citeshttps://doi.org/10.1007/s10725-018-0371-yopenalex-snapshot
Comparative transcriptome discovery and elucidation of the mechanism of long noncoding RNAs during vernalization in Brassica rapa
inferred← citeshttps://doi.org/10.1007/s11103-010-9621-8openalex-snapshot
Low temperatures impact dormancy status, flowering competence, and transcript profiles in crown buds of leafy spurge
inferred← citeshttps://doi.org/10.1007/s11103-011-9864-zopenalex-snapshot
MicroRNAs in trees
inferred← citeshttps://doi.org/10.1007/s11103-018-0727-8openalex-snapshot
Developmental transcriptome analysis of floral transition in Rosa odorata var. gigantea
inferred← citeshttps://doi.org/10.1007/s11105-011-0310-9openalex-snapshot
In Silico and Quantitative Analyses of the Putative FLC-like Homologue in Coffee (Coffea arabica L.)
inferred← citeshttps://doi.org/10.1007/s11105-020-01237-8openalex-snapshot
Exploring Flowering Genes in Isabgol (Plantago ovata Forsk.) Through Transcriptome Analysis
inferred← citeshttps://doi.org/10.1007/s11120-012-9760-7openalex-snapshot
Thermal energy dissipation and xanthophyll cycles beyond the Arabidopsis model
inferred← citeshttps://doi.org/10.1007/s11240-015-0855-7openalex-snapshot
Heat mediated silencing of MdTFL1 genes in apple (Malus × domestica)
inferred← citeshttps://doi.org/10.1007/s11427-018-9457-1openalex-snapshot
Plant Morphogenesis 123: a renaissance in modern botany?
inferred← citeshttps://doi.org/10.1007/s12374-021-09300-xopenalex-snapshot
Influence of Climate Change on Flowering Time
inferred← citeshttps://doi.org/10.1007/s13205-025-04458-4openalex-snapshot
Transcriptomic revealing of the mechanism of flowering in a stay green mutant Andrographis paniculata with lack of flowering on apical tip
inferred← citeshttps://doi.org/10.1007/s13562-018-0483-5openalex-snapshot
Species-specific genes account for the differences in floral transition between continuous-flowering and once-flowering roses
inferred← citeshttps://doi.org/10.1007/s13580-019-00218-5openalex-snapshot
Current understanding of flowering pathways in plants: focusing on the vernalization pathway in Arabidopsis and several vegetable crop plants
inferred← citeshttps://doi.org/10.1016/b978-0-08-100068-7.00007-0openalex-snapshot
Regulation framework for flowering
inferred← citeshttps://doi.org/10.1016/b978-0-12-381466-1.00025-0openalex-snapshot
Control of flowering
inferred← citeshttps://doi.org/10.1016/b978-0-12-800854-6.00018-xopenalex-snapshot
The Multifaceted Roles of miR156-targeted SPL Transcription Factors in Plant Developmental Transitions
inferred← citeshttps://doi.org/10.1016/b978-0-12-813187-9.00018-4openalex-snapshot
Plant Senescence and Agriculture
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Field Guide to Plant Model Systems
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Reciprocal conversion between annual and polycarpic perennial flowering behavior in the Brassicaceae
inferred← citeshttps://doi.org/10.1016/j.cell.2024.05.054openalex-snapshot
Timing is everything: How plants optimize reproduction in a variable environment
inferred← citeshttps://doi.org/10.1016/j.cels.2018.10.011openalex-snapshot
Temperature Sensing Is Distributed throughout the Regulatory Network that Controls FLC Epigenetic Silencing in Vernalization
inferred← citeshttps://doi.org/10.1016/j.cub.2013.07.027openalex-snapshot
Remembering the Prolonged Cold of Winter
inferred← citeshttps://doi.org/10.1016/j.cub.2020.01.003openalex-snapshot
Life History Variation as a Model for Understanding Trade-Offs in Plant–Environment Interactions
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.05.021openalex-snapshot
Developmental Genetics and New Sequencing Technologies: The Rise of Nonmodel Organisms
inferred← citeshttps://doi.org/10.1016/j.fcr.2013.04.018openalex-snapshot
Evaluating an interspecific Helianthus annuus×Helianthus tuberosus population for use in a perennial sunflower breeding program
inferred← citeshttps://doi.org/10.1016/j.fmre.2024.11.003openalex-snapshot
Towards the generation of polycarpic perennial rapeseeds
inferred← citeshttps://doi.org/10.1016/j.gde.2010.04.007openalex-snapshot
Patterning and evolution of floral structures — marking time
inferred← citeshttps://doi.org/10.1016/j.gde.2013.10.006openalex-snapshot
The spectrum of mutations controlling complex traits and the genetics of fitness in plants
inferred← citeshttps://doi.org/10.1016/j.gde.2022.102016openalex-snapshot
Distinct responses to autumn and spring temperatures by the key flowering-time regulator FLOWERING LOCUS C
inferred← citeshttps://doi.org/10.1016/j.indcrop.2016.09.034openalex-snapshot
Camelina uses, genetics, genomics, production, and management
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110829openalex-snapshot
A reduced vernalization requirement is a key component of the early-bolting trait in globe artichoke (Cynara cardunculus var. scolymus)
inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.07.019openalex-snapshot
Diversity of plant life cycles is generated by dynamic epigenetic regulation in response to vernalization
inferred← citeshttps://doi.org/10.1016/j.jtbi.2011.09.034openalex-snapshot
Effects of causal networks on the structure and stability of resource allocation trait correlations
inferred← citeshttps://doi.org/10.1016/j.jtbi.2012.02.009openalex-snapshot
A stochastic model of chromatin modification: Cell population coding of winter memory in plants
inferred← citeshttps://doi.org/10.1016/j.mgene.2013.10.004openalex-snapshot
Complete Arabis alpina chloroplast genome sequence and insight into its polymorphism
inferred← citeshttps://doi.org/10.1016/j.mocell.2024.100114openalex-snapshot
C-TERMINAL DOMAIN PHOSPHATASE-LIKE 1 promotes flowering with TAF15b by repressing the floral repressor gene FLOWERING LOCUS C
inferred← citeshttps://doi.org/10.1016/j.molp.2023.12.011openalex-snapshot
Perenniality: From model plants to applications in agriculture
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.01.001openalex-snapshot
Evolutionary genetics of plant adaptation: insights from new model systems
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Genomic studies of adaptive evolution in outcrossing Arabidopsis species
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Bloom and bust: understanding the nature and regulation of the end of flowering
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Digital paradigm for Polycomb epigenetic switching and memory
inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102831openalex-snapshot
Non-coding regulation in seasonal flowering control – Insights from FLC
inferred← citeshttps://doi.org/10.1016/j.plantsci.2010.12.001openalex-snapshot
Make hay when the sun shines: The role of MADS-box genes in temperature-dependant seasonal flowering responses
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.06.011openalex-snapshot
Timing is everything in plant development. The central role of floral repressors
inferred← citeshttps://doi.org/10.1016/j.plantsci.2012.03.002openalex-snapshot
Manipulating plant architecture with members of the CETS gene family
inferred← citeshttps://doi.org/10.1016/j.plantsci.2013.02.006openalex-snapshot
Constraints to obtaining consistent annual yields in perennials. II: Environment and fruit load affect induction of flowering
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111479openalex-snapshot
Expression of coffee florigen CaFT1 reveals a sustained floral induction window associated with asynchronous flowering in tropical perennials
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111810openalex-snapshot
Warm temperature during floral bud transition turns off EjTFL1 gene expression and promotes flowering in Loquat (Eriobotrya japonica Lindl.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112743openalex-snapshot
Vernalization reveals distinct roles of FLOWERING LOCUS T homologs in floral transition of perennial Taraxacum koksaghyz
inferred← citeshttps://doi.org/10.1016/j.ppees.2014.06.001openalex-snapshot
Phylogenetic signatures of adaptation: The Arabis hirsuta species aggregate (Brassicaceae) revisited
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.110972openalex-snapshot
Models for a molecular calendar of bud-break in fruit trees
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113401openalex-snapshot
Investigation of endogenous phytohormones and critical flowering genes during flower development in Iris germanica
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.05.007openalex-snapshot
Evolution and functional diversification of FLOWERING LOCUS T/TERMINAL FLOWER 1 family genes in plants
inferred← citeshttps://doi.org/10.1016/j.tig.2011.04.001openalex-snapshot
Evolutionary genetics of plant adaptation
inferred← citeshttps://doi.org/10.1016/j.tig.2018.07.006openalex-snapshot
Epigenetic Environmental Memories in Plants: Establishment, Maintenance, and Reprogramming
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Cabbage family affairs: the evolutionary history of Brassicaceae
inferred← citeshttps://doi.org/10.1016/j.tplants.2016.01.024openalex-snapshot
Turnip Time Travels: Age Estimates in Brassicaceae
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.09.016openalex-snapshot
Class VIIIb APETALA2 Ethylene Response Factors in Plant Development
inferred← citeshttps://doi.org/10.1016/j.tplants.2021.08.007openalex-snapshot
Towards understanding the biological foundations of perenniality
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100566openalex-snapshot
The central role of stem cells in determining plant longevity variation
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101963openalex-snapshot
Deciphering the genetic mechanism of perenniality in rice potentiates sustainable agricultural production
inferred← citeshttps://doi.org/10.1016/j.ygeno.2019.05.008openalex-snapshot
Identification of Arabis alpina genomic regions associated with climatic variables along an elevation gradient through whole genome scan
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.01.029openalex-snapshot
Differential SPL gene expression patterns reveal candidate genes underlying flowering time and architectural differences in Mimulus and Arabidopsis
inferred← citeshttps://doi.org/10.1016/s0070-2153(10)91011-9openalex-snapshot
Comparative Analysis of Flowering in Annual and Perennial Plants
inferred← citeshttps://doi.org/10.1017/9781139939867.014openalex-snapshot
The Evolution of Senescence in Annual Plants
inferred← citeshttps://doi.org/10.1017/cbo9781107323933.013openalex-snapshot
Supplementary online material
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Plant research accelerates along the (bio)informatics superhighway
inferred← citeshttps://doi.org/10.1038/hortres.2016.53openalex-snapshot
Overexpression of blueberry FLOWERING LOCUS T is associated with changes in the expression of phytohormone-related genes in blueberry plants
inferred← citeshttps://doi.org/10.1038/ismej.2016.109openalex-snapshot
Root microbiota dynamics of perennial Arabis alpina are dependent on soil residence time but independent of flowering time
inferred← citeshttps://doi.org/10.1038/nature22010openalex-snapshot
The plant perceptron connects environment to development
inferred← citeshttps://doi.org/10.1038/nbt.2515openalex-snapshot
Mutation identification by direct comparison of whole-genome sequencing data from mutant and wild-type individuals using k-mers
inferred← citeshttps://doi.org/10.1038/ncomms3303openalex-snapshot
Forecasting flowering phenology under climate warming by modelling the regulatory dynamics of flowering-time genes
inferred← citeshttps://doi.org/10.1038/ncomms5457openalex-snapshot
Evolutionary conservation of cold-induced antisense RNAs of FLOWERING LOCUS C in Arabidopsis thaliana perennial relatives
inferred← citeshttps://doi.org/10.1038/nplants.2014.23openalex-snapshot
Genome expansion of Arabis alpina linked with retrotransposition and reduced symmetric DNA methylation
inferred← citeshttps://doi.org/10.1038/nrg3291openalex-snapshot
The genetic basis of flowering responses to seasonal cues
inferred← citeshttps://doi.org/10.1038/nrg3883openalex-snapshot
Beyond the thale: comparative genomics and genetics of Arabidopsis relatives
inferred← citeshttps://doi.org/10.1038/s41422-024-01001-7openalex-snapshot
Perenniality: the tale of three MADS-box genes
inferred← citeshttps://doi.org/10.1038/s41438-021-00610-2openalex-snapshot
Morphological, phenological, and transcriptional analyses provide insight into the diverse flowering traits of a mutant of the relic woody plant Liriodendron chinense
inferred← citeshttps://doi.org/10.1038/s41467-018-03067-5openalex-snapshot
Genetic control of meristem arrest and life span in Arabidopsis by a FRUITFULL-APETALA2 pathway
inferred← citeshttps://doi.org/10.1038/s41467-020-15896-4openalex-snapshot
Repressive chromatin modification underpins the long-term expression trend of a perennial flowering gene in nature
inferred← citeshttps://doi.org/10.1038/s41467-026-76142-xopenalex-snapshot
CmDREBa regulates the perennial growth habit of chrysanthemum in response to prolonged chilling
inferred← citeshttps://doi.org/10.1038/s41477-022-01102-4openalex-snapshot
Phylogenomics of the genus Glycine sheds light on polyploid evolution and life-strategy transition
inferred← citeshttps://doi.org/10.1038/s41576-026-00979-7openalex-snapshot
Molecular integration of seasonal temperature signals in flowering time control
inferred← citeshttps://doi.org/10.1038/s41598-017-05850-8openalex-snapshot
Comparative transcriptome analysis of the floral transition in Rosa chinensis ‘Old Blush’ and R. odorata var. gigantea
inferred← citeshttps://doi.org/10.1038/s41598-017-13606-7openalex-snapshot
Comparative analysis of molecular and physiological traits between perennial Arabis alpina Pajares and annual Arabidopsis thaliana Sy-0
inferred← citeshttps://doi.org/10.1038/s41598-017-18084-5openalex-snapshot
A Global View of Transcriptome Dynamics During Male Floral Bud Development in Populus tomentosa
inferred← citeshttps://doi.org/10.1038/s41598-020-72566-7openalex-snapshot
Duration of cold exposure defines the rate of reactivation of a perennial FLC orthologue via H3K27me3 accumulation
inferred← citeshttps://doi.org/10.1038/s41598-025-12414-8openalex-snapshot
Community phylogenetic diversity drives flowering synchrony among coexisting plant species even under drought conditions
inferred← citeshttps://doi.org/10.1038/s42003-021-02152-8openalex-snapshot
Wolfberry genomes and the evolution of Lycium (Solanaceae)
inferred← citeshttps://doi.org/10.1038/srep09729openalex-snapshot
Genome-wide transcriptome profiling provides insights into floral bud development of summer-flowering Camellia azalea
inferred← citeshttps://doi.org/10.1071/cp16468openalex-snapshot
The role of FLOWERING LOCUS C in vernalization of Brassica: the importance of vernalization research in the face of climate change
inferred← citeshttps://doi.org/10.1071/fp09170openalex-snapshot
Seasonal flowering and evolution: the heritage from Charles Darwin
inferred← citeshttps://doi.org/10.1073/pnas.0914293107openalex-snapshot
Robust control of the seasonal expression of the Arabidopsis FLC gene in a fluctuating environment
inferred← citeshttps://doi.org/10.1073/pnas.1104713108openalex-snapshot
FLOWERING LOCUS T duplication coordinates reproductive and vegetative growth in perennial poplar
inferred← citeshttps://doi.org/10.1073/pnas.1419791112openalex-snapshot
Heterochrony underpins natural variation in Cardamine hirsuta leaf form
inferred← citeshttps://doi.org/10.1073/pnas.1618075114openalex-snapshot
Divergence of regulatory networks governed by the orthologous transcription factors FLC and PEP1 in Brassicaceae species
inferred← citeshttps://doi.org/10.1073/pnas.1819440116openalex-snapshot
Genetic and molecular analysis of trichome development in Arabis alpina
inferred← citeshttps://doi.org/10.1073/pnas.2109204118openalex-snapshot
Transposition and duplication of MADS-domain transcription factor genes in annual and perennial Arabis species modulates flowering
inferred← citeshttps://doi.org/10.1073/pnas.2204355119openalex-snapshot
Winter warming post floral initiation delays flowering via bud dormancy activation and affects yield in a winter annual crop
inferred← citeshttps://doi.org/10.1080/0028825x.2010.548070openalex-snapshot
Phase change and flowering in Pachycladon exile and isolation of LEAFY and TERMINAL FLOWER1 homologues
inferred← citeshttps://doi.org/10.1080/07352689.2014.917533openalex-snapshot
MicroRNA-target Interactions: Important Signaling Modules Regulating Flowering Time in Diverse Plant Species
inferred← citeshttps://doi.org/10.1080/07388551.2019.1709795openalex-snapshot
CRISPR/Cas9 genome editing throughin plantatransformation
inferred← citeshttps://doi.org/10.1080/21541264.2020.1803031openalex-snapshot
The contribution of transposable elements to transcriptional novelty in plants: theFLCaffair
inferred← citeshttps://doi.org/10.1093/aob/mcad136openalex-snapshot
Melica as an emerging model system for comparative studies in temperate Pooideae grasses
inferred← citeshttps://doi.org/10.1093/aob/mcr134openalex-snapshot
The importance of Anatolian mountains as the cradle of global diversity in Arabis alpina, a key arctic–alpine species
inferred← citeshttps://doi.org/10.1093/aob/mcr157openalex-snapshot
Sporophytic self-incompatibility genes and mating system variation in Arabis alpina
inferred← citeshttps://doi.org/10.1093/aob/mcr175openalex-snapshot
Breeding crop plants with deep roots: their role in sustainable carbon, nutrient and water sequestration
inferred← citeshttps://doi.org/10.1093/aob/mcr180openalex-snapshot
Plant sexual reproduction during climate change: gene function in natura studied by ecological and evolutionary systems biology
inferred← citeshttps://doi.org/10.1093/aob/mcs161openalex-snapshot
Congratulations, you have been carefully chosen to represent an important developmental regulator!
inferred← citeshttps://doi.org/10.1093/aob/mct055openalex-snapshot
Genetic changes in flowering and morphology in response to adaptation to a high-latitude environment in Arabidopsis lyrata
inferred← citeshttps://doi.org/10.1093/aob/mct165openalex-snapshot
A world-wide perspective on crucifer speciation and evolution: phylogenetics, biogeography and trait evolution in tribe Arabideae
inferred← citeshttps://doi.org/10.1093/aob/mct211openalex-snapshot
Identification of transcription factors potentially involved in the juvenile to adult phase transition in Citrus
inferred← citeshttps://doi.org/10.1093/aob/mcz035openalex-snapshot
Inflorescence shoot elongation, but not flower primordia formation, is photoperiodically regulated in Arabidopsis lyrata
inferred← citeshttps://doi.org/10.1093/icb/icu030openalex-snapshot
Mechanisms Underlying Epigenetic Regulation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/eraa216openalex-snapshot
Gene regulatory networks controlled by FLOWERING LOCUS C that confer variation in seasonal flowering and life history
inferred← citeshttps://doi.org/10.1093/jxb/eraa543openalex-snapshot
Insights into the evo-devo of plant reproduction using next-generation sequencing approaches
inferred← citeshttps://doi.org/10.1093/jxb/erab375openalex-snapshot
Molecular responses to chilling in a warming climate and their impacts on plant reproductive development and yield
inferred← citeshttps://doi.org/10.1093/jxb/erac395openalex-snapshot
Functional variation in the non-coding genome: molecular implications for food security
inferred← citeshttps://doi.org/10.1093/jxb/erad435openalex-snapshot
Epigenetic regulation and epigenetic memory resetting during plant rejuvenation
inferred← citeshttps://doi.org/10.1093/jxb/erae223openalex-snapshot
Beyond floral initiation: the role of flower bud dormancy in flowering time control of annual plants
inferred← citeshttps://doi.org/10.1093/jxb/eraf261openalex-snapshot
Seasons and shape: inflorescences from autumn to summer
inferred← citeshttps://doi.org/10.1093/jxb/err192openalex-snapshot
Reproductive competence from an annual and a perennial perspective
inferred← citeshttps://doi.org/10.1093/jxb/ers157openalex-snapshot
Vernalization-mediated chromatin changes
inferred← citeshttps://doi.org/10.1093/jxb/ert047openalex-snapshot
PFRU, a single dominant locus regulates the balance between sexual and asexual plant reproduction in cultivated strawberry
inferred← citeshttps://doi.org/10.1093/jxb/ert233openalex-snapshot
The regulation of seasonal flowering in the Rosaceae
inferred← citeshttps://doi.org/10.1093/jxb/eru246openalex-snapshot
Regulation of flowering time by the miR156-mediated age pathway
inferred← citeshttps://doi.org/10.1093/jxb/erw326openalex-snapshot
Identification of successive flowering phases highlights a new genetic control of the flowering pattern in strawberry
inferred← citeshttps://doi.org/10.1093/jxb/erw431openalex-snapshot
Post-translational modifications of FLOWERING LOCUS C modulate its activity
inferred← citeshttps://doi.org/10.1093/jxb/erx270openalex-snapshot
Fine-tuning timing: natural variation informs the mechanistic basis of the switch to flowering in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/ery423openalex-snapshot
PERPETUAL FLOWERING2 coordinates the vernalization response and perennial flowering in Arabis alpina
inferred← citeshttps://doi.org/10.1093/jxb/erz125openalex-snapshot
A role for TOR signaling at every stage of plant life
inferred← citeshttps://doi.org/10.1093/molbev/msag212openalex-snapshot
Adaptation to seasonal drought in Arabis alpina is linked to the demographic history and climatic changes since the last glacial maximum
inferred← citeshttps://doi.org/10.1093/molbev/msv110openalex-snapshot
Evolution ofCONSTANSRegulation and Function after Gene Duplication Produced a Photoperiodic Flowering Switch in the Brassicaceae
inferred← citeshttps://doi.org/10.1093/mp/ssp031openalex-snapshot
From Decision to Commitment: The Molecular Memory of Flowering
inferred← citeshttps://doi.org/10.1093/pcp/pcs181openalex-snapshot
FT-Like NFT1 Gene May Play a Role in Flower Transition Induced by Heat Accumulation in Narcissus tazetta var. chinensis
inferred← citeshttps://doi.org/10.1093/plcell/koab304openalex-snapshot
The two clock proteins CCA1 and LHY activate VIN3 transcription during vernalization through the vernalization-responsive cis-element
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/plcell/koag018openalex-snapshot
Epigenetic reprogramming drives the annual growth–dormancy cycle in Populus
inferred← citeshttps://doi.org/10.1093/plphys/kiab194openalex-snapshot
Integrated dominance mechanisms regulate reproductive architecture inArabidopsis thalianaandBrassica napus
inferred← citeshttps://doi.org/10.1093/plphys/kiab206openalex-snapshot
Light signals generated by vegetation shade facilitate acclimation to low light in shade-avoider plants
inferred← citeshttps://doi.org/10.1093/plphys/kiac111openalex-snapshot
Flowering time runs hot and cold
inferred← citeshttps://doi.org/10.1093/plphys/kiad597openalex-snapshot
Molecular epigenetic understanding of winter memory in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiae109openalex-snapshot
Flowering time: From physiology, through genetics to mechanism
inferred← citeshttps://doi.org/10.1093/pnasnexus/pgad141openalex-snapshot
Plant-on-chip: Core morphogenesis processes in the tiny plant Wolffia australiana
inferred← citeshttps://doi.org/10.1093/treephys/tpaa061openalex-snapshot
Unisexual flower initiation in the monoecious Quercus suber L.: a molecular approach
inferred← citeshttps://doi.org/10.1093/treephys/tpz111openalex-snapshot
Functional and expressional analyses of appleFLC-like in relation to dormancy progress and flower bud development
inferred← citeshttps://doi.org/10.1094/pdis-06-25-1183-pdnopenalex-snapshot
First Report of Powdery Mildew on Arabis paniculata Caused by Erysiphe cruciferarum in China
inferred← citeshttps://doi.org/10.1098/rspb.2023.1401openalex-snapshot
Adaptation of perennial flowering phenology across the European range of Arabis alpina
inferred← citeshttps://doi.org/10.1098/rstb.2010.0128openalex-snapshot
Genetic and physiological bases for phenological responses to current and predicted climates
inferred← citeshttps://doi.org/10.1098/rstb.2010.0145openalex-snapshot
Toward a synthetic understanding of the role of phenology in ecology and evolution
inferred← citeshttps://doi.org/10.1101/070847openalex-snapshot
Population dynamics of Arabis alpina in the French Alps: evidence for demographic compensation?
inferred← citeshttps://doi.org/10.1101/2020.09.14.296632openalex-snapshot
Light quality signals generated by vegetation shade facilitate acclimation to reduced light quantity in shade-avoider plants
inferred← citeshttps://doi.org/10.1101/2023.05.26.542514openalex-snapshot
Epigenetic and transcriptional landscape of heat-stress memory in woodland strawberry ( Fragaria vesca )
inferred← citeshttps://doi.org/10.1101/2025.09.01.673603openalex-snapshot
Mining genes underlying perennial-to-annual transitions in Oryza with comparative genomics
inferred← citeshttps://doi.org/10.1101/414938openalex-snapshot
Carbohydrate activity regulation of floral quantity during the juvenile phase in black pepper ( Piper nigrum L.)
inferred← citeshttps://doi.org/10.1101/562868openalex-snapshot
Flowering behaviour in Arabis alpina ensures the maintenance of a perennating dormant bud bank
inferred← citeshttps://doi.org/10.1101/cshperspect.a019471openalex-snapshot
Epigenetic Regulation in Plant Responses to the Environment
inferred← citeshttps://doi.org/10.1101/cshperspect.a034652openalex-snapshot
Plant Inflorescence Architecture: The Formation, Activity, and Fate of Axillary Meristems
inferred← citeshttps://doi.org/10.1101/gad.333245.119openalex-snapshot
Noncoding SNPs influence a distinct phase of Polycomb silencing to destabilize long-term epigenetic memory at Arabidopsis FLC
inferred← citeshttps://doi.org/10.1104/pp.112.196659openalex-snapshot
Mutation inTERMINAL FLOWER1Reverses the Photoperiodic Requirement for Flowering in the Wild StrawberryFragaria vesca
inferred← citeshttps://doi.org/10.1104/pp.15.00496openalex-snapshot
Flowering Locus C’s Lessons: Conserved Chromatin Switches Underpinning Developmental Timing and Adaptation
inferred← citeshttps://doi.org/10.1104/pp.15.01875openalex-snapshot
Habitat-Associated Life History and Stress-Tolerance Variation in Arabidopsis arenosa
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1104/pp.16.01322openalex-snapshot
Winter Memory throughout the Plant Kingdom: Different Paths to Flowering
inferred← citeshttps://doi.org/10.1104/pp.17.01754openalex-snapshot
Extended Vernalization Regulates Inflorescence Fate in Arabis alpina by Stably Silencing PERPETUAL FLOWERING1
inferred← citeshttps://doi.org/10.1104/pp.19.00021openalex-snapshot
Gibberellins Act Downstream of Arabis PERPETUAL FLOWERING1 to Accelerate Floral Induction during Vernalization
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