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Regulation of Flowering Time by Histone Acetylation in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00264213openalex-snapshot
A genetic and physiological analysis of late flowering mutants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0092-8674(00)80256-1openalex-snapshot
FCA, a Gene Controlling Flowering Time in Arabidopsis, Encodes a Protein Containing RNA-Binding Domains
inferredcites →https://doi.org/10.1016/s0092-8674(03)00425-2openalex-snapshot
FY Is an RNA 3′ End-Processing Factor that Interacts with FCA to Control the Arabidopsis Floral Transition
inferredcites →https://doi.org/10.1016/s0969-2126(99)80037-9openalex-snapshot
A 30 Å long U-shaped catalytic tunnel in the crystal structure of polyamine oxidase
inferredcites →https://doi.org/10.1042/bj20021587openalex-snapshot
Cloning and characterization of multiple human polyamine oxidase splice variants that code for isoenzymes with different biochemical characteristics
inferredcites →https://doi.org/10.1073/pnas.011347998openalex-snapshot
Blocking histone deacetylation in Arabidopsis induces pleiotropic effects on plant gene regulation and development
inferredcites →https://doi.org/10.1073/pnas.112008599openalex-snapshot
A core–BRAF35 complex containing histone deacetylase mediates repression of neuronal-specific genes
inferredcites →https://doi.org/10.1074/jbc.m007372200openalex-snapshot
Stable Histone Deacetylase Complexes Distinguished by the Presence of SANT Domain Proteins CoREST/kiaa0071 and Mta-L1
inferredcites →https://doi.org/10.1074/jbc.m208992200openalex-snapshot
A Candidate X-linked Mental Retardation Gene Is a Component of a New Family of Histone Deacetylase-containing Complexes
inferredcites →https://doi.org/10.1093/emboj/cdf561openalex-snapshot
Loss of spr‐5 bypasses the requirement for the C.elegans presenilin sel‐12 by derepressing hop‐1
inferredcites →https://doi.org/10.1093/genetics/148.2.885openalex-snapshot
Genetic Interactions Among Late-Flowering Mutants of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.111.2.641openalex-snapshot
Ecotype-Specific Expression of a Flowering Mutant Phenotype in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.004564openalex-snapshot
Different Regulatory Regions Are Required for the Vernalization-Induced Repression of FLOWERING LOCUS C and for the Epigenetic Maintenance of Repression
inferredcites →https://doi.org/10.1105/tpc.010017openalex-snapshot
FPA, a Gene Involved in Floral Induction in Arabidopsis, Encodes a Protein Containing RNA-Recognition Motifs
inferredcites →https://doi.org/10.1105/tpc.011825openalex-snapshot
The Transcriptional Enhancer of the Pea Plastocyanin Gene Associates with the Nuclear Matrix and Regulates Gene Expression through Histone Acetylation
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/10.1105/tpc.13.6.1427openalex-snapshot
FPA, a Gene Involved in Floral Induction in Arabidopsis, Encodes a Protein Containing RNA-Recognition Motifs
inferredcites →https://doi.org/10.1105/tpc.6.1.75openalex-snapshot
Isolation of LUMINIDEPENDENS: a gene involved in the control of flowering time in Arabidopsis.
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
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/10.1146/annurev.cellbio.15.1.519openalex-snapshot
When to Switch to Flowering
inferredcites →https://doi.org/10.1186/gb-2002-3-8-research0039openalex-snapshot
The SWIRM domain: a conserved module found in chromosomal proteins points to novel chromatin-modifying activities
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Histone Modifications and Transcription in Plants
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Control of Flowering Time
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inferred← citeshttps://doi.org/10.1007/978-3-319-55520-1_18openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-04809-8_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf02899639openalex-snapshot
Characterization of a new mutant allele of theArabidopsis Flowering Locus D (FLD) gene that controls the flowering time by repressingFLC
inferred← citeshttps://doi.org/10.1007/bf03030652openalex-snapshot
Historical perspective on breakthroughs in flowering field
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A 215-bp indel at intron I of BoFLC2 affects flowering time in Brassica oleracea var. capitata during vernalization
inferred← citeshttps://doi.org/10.1007/s00299-007-0336-5openalex-snapshot
The Arabidopsis thaliana AT PRP39-1 gene, encoding a tetratricopeptide repeat protein with similarity to the yeast pre-mRNA processing protein PRP39, affects flowering time
inferred← citeshttps://doi.org/10.1007/s00299-012-1249-5openalex-snapshot
Overexpression of a histone H3K4 demethylase, JMJ15, accelerates flowering time in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-013-1393-6openalex-snapshot
Histone deacetylases and their functions in plants
inferred← citeshttps://doi.org/10.1007/s00299-020-02583-3openalex-snapshot
Systemic acquired resistance specific proteome of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-022-02926-2openalex-snapshot
POWERDRESS positively regulates systemic acquired resistance in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00299-023-03021-wopenalex-snapshot
Overexpression of flowering locus D (FLD) in Indian mustard (Brassica juncea) enhances tolerance to Alternaria brassicae and Sclerotinia sclerotiorum
inferred← citeshttps://doi.org/10.1007/s00299-026-03747-3openalex-snapshot
Epigenetic regulation of floral transition: pathways and players
inferred← citeshttps://doi.org/10.1007/s00344-011-9226-8openalex-snapshot
The Cold Awakening of Doritaenopsis ‘Tinny Tender’ Orchid Flowers: The Role of Leaves in Cold-induced Bud Dormancy Release
inferred← citeshttps://doi.org/10.1007/s00425-008-0885-zopenalex-snapshot
PtFLC homolog from trifoliate orange (Poncirus trifoliata) is regulated by alternative splicing and experiences seasonal fluctuation in expression level
inferred← citeshttps://doi.org/10.1007/s00425-010-1195-9openalex-snapshot
Arabidopsis DDB1a and DDB1b are critical for embryo development
inferred← citeshttps://doi.org/10.1007/s00425-015-2447-5openalex-snapshot
The mitogen-activated protein kinase phosphatase PHS1 regulates flowering in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-017-2652-5openalex-snapshot
Fackel interacts with gibberellic acid signaling and vernalization to mediate flowering in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00438-004-1095-4openalex-snapshot
Large deletions within the first intron in VRN-1 are associated with spring growth habit in barley and wheat
inferred← citeshttps://doi.org/10.1007/s00438-021-01785-yopenalex-snapshot
Genetic dissection of flowering time in flax (Linum usitatissimum L.) through single- and multi-locus genome-wide association studies
inferred← citeshttps://doi.org/10.1007/s10059-011-1022-6openalex-snapshot
FVE, an Arabidopsis Homologue of the Retinoblastoma-Associated Protein That Regulates Flowering Time and Cold Response, Binds to Chromatin as a Large Multiprotein Complex
inferred← citeshttps://doi.org/10.1007/s10265-020-01183-2openalex-snapshot
DORMANCY/AUXIN ASSOCIATED FAMILY PROTEIN 2 of Arabidopsis thaliana is a negative regulator of local and systemic acquired resistance
inferred← citeshttps://doi.org/10.1007/s10265-020-01235-7openalex-snapshot
VrLELP controls flowering time under short-day conditions in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10709-006-0030-5openalex-snapshot
The molecular population genetics of shoot development in Arabidopsis thaliana
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inferred← citeshttps://doi.org/10.1007/s11033-025-10365-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11101-016-9466-0openalex-snapshot
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Molecular and Structural Characterization of Barley Vernalization Genes
inferred← citeshttps://doi.org/10.1007/s11103-005-2081-xopenalex-snapshot
Dynamic Histone Acetylation of Late Embryonic Genes during Seed Germination
inferred← citeshttps://doi.org/10.1007/s11103-005-8105-8openalex-snapshot
Conservation and Divergence of FCA Function between Arabidopsis and Rice
inferred← citeshttps://doi.org/10.1007/s11103-014-0280-zopenalex-snapshot
Arabidopsis thaliana MSI4/FVE associates with members of a novel family of plant specific PWWP/RRM domain proteins
inferred← citeshttps://doi.org/10.1007/s11103-015-0324-zopenalex-snapshot
CYCLIN-DEPENDENT KINASE G2 regulates salinity stress response and salt mediated flowering in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s11103-019-00935-6openalex-snapshot
Molecular characterization and expression analysis reveal the roles of Cys2/His2 zinc-finger transcription factors during flower development of Brassica rapa subsp. chinensis
inferred← citeshttps://doi.org/10.1007/s11240-012-0156-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11284-011-0835-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11703-011-1084-4openalex-snapshot
Identification of a gene responsible for the 60-day delay in flowering time of Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11738-016-2314-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11816-021-00731-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12298-017-0458-3openalex-snapshot
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Histone modifications in transcriptional activation during plant development
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The brassinosteroid-regulated transcription factors BZR1/BES1 function as a coordinator in multisignal-regulated plant growth
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Plant homologs of mammalian MBT-domain protein-regulated KDM1 histone lysine demethylases do not interact with plant Tudor/PWWP/MBT-domain proteins
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Histone Demethylation Mediated by the Nuclear Amine Oxidase Homolog LSD1
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The Timing of Developmental Transitions in Plants
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A Matrix Protein Silences Transposons and Repeats through Interaction with Retinoblastoma-Associated Proteins
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The Spen Family Protein FPA Controls Alternative Cleavage and Polyadenylation of RNA
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Histone demethylation catalysed by LSD1 is a flavin‐dependent oxidative process
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Expanding the SRI domain family: A common scaffold for binding the phosphorylated C‐terminal domain of RNA polymerase II
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Genome-wide association study of flowering time reveals complex genetic heterogeneity and epistatic interactions in rice
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inferred← citeshttps://doi.org/10.1016/j.jplph.2012.11.007openalex-snapshot
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Proteomic differences in apple spur buds from high and non-cropping trees during floral initiation
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C-TERMINAL DOMAIN PHOSPHATASE-LIKE 1 promotes flowering with TAF15b by repressing the floral repressor gene FLOWERING LOCUS C
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The Arabidopsis RNA-Binding Protein FCA Requires a Lysine-Specific Demethylase 1 Homolog to Downregulate FLC
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Functional Consequences of Splicing of the Antisense Transcript COOLAIR on FLC Transcription
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The Intronic cis Element SE1 Recruits trans-Acting Repressor Complexes to Repress the Expression of ELONGATED UPPERMOST INTERNODE1 in Rice
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Brassinosteroid Signaling Recruits Histone 3 Lysine-27 Demethylation Activity to FLOWERING LOCUS C Chromatin to Inhibit the Floral Transition in Arabidopsis
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Ectopic expression of VRT-A2 underlies the origin of Triticum polonicum and Triticum petropavlovskyi with long outer glumes and grains
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ALFIN-like proteins link histone H3K4me3 to H2A ubiquitination and coordinate diverse chromatin modifications in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2013.10.003openalex-snapshot
Epigenetic memory of environmental organisms: A reflection of lifetime stressor exposures
inferred← citeshttps://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
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Epigenetic control of plant development by Polycomb-group proteins
inferred← citeshttps://doi.org/10.1016/j.pbi.2005.11.010openalex-snapshot
Chromatin modifiers that control plant development
inferred← citeshttps://doi.org/10.1016/j.pbi.2008.09.005openalex-snapshot
Flowering time regulation produces much fruit
inferred← citeshttps://doi.org/10.1016/j.plantsci.2009.08.015openalex-snapshot
Arabidopsis cytoplasmic N-acetyltransferase, as the ortholog of RimL in E. coli, controls flowering time via the autonomous pathway
inferred← citeshttps://doi.org/10.1016/j.plantsci.2012.01.007openalex-snapshot
Evaluating the potential of SHI expression as a compacting tool for ornamental plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111926openalex-snapshot
Epigenetic insight into floral transition and seed development in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108630openalex-snapshot
WRKY transcription factors modulate flowering time and response to environmental changes
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108842openalex-snapshot
Multilayered regulation and implication of flowering time in plants
inferred← citeshttps://doi.org/10.1016/j.pmpp.2019.04.005openalex-snapshot
RSI1/FLD is a positive regulator for defense against necrotrophic pathogens
inferred← citeshttps://doi.org/10.1016/j.rsci.2025.10.006openalex-snapshot
Jumonji C Domain-Containing Protein OsJMJ712 Integrates Epigenetic Regulation and Circadian Clock to Fine-Tune Flowering in Rice
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Unveiling the genetic control of repeat flowering in blueberry with a novel continuous quantitative phenotyping approach
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Chromatin, photoperiod and the Arabidopsis circadian clock: A question of time
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The impact of chromatin regulation on the floral transition
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Keeping plants in shape: Polycomb-group genes and histone methylation
inferred← citeshttps://doi.org/10.1016/j.semcdb.2013.02.009openalex-snapshot
Chromatin remodeling and alternative splicing: Pre- and post-transcriptional regulation of the Arabidopsis circadian clock
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Role of chromatin modification in flowering-time control
inferred← citeshttps://doi.org/10.1016/j.tplants.2004.12.012openalex-snapshot
Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters
inferred← citeshttps://doi.org/10.1016/j.tplants.2005.05.003openalex-snapshot
Regulation of meristem activity by chromatin remodelling
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Role of plant RNA-binding proteins in development, stress response and genome organization
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100497openalex-snapshot
Pistachio genomes provide insights into nut tree domestication and ZW sex chromosome evolution
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.11.012openalex-snapshot
C2H2 zinc finger-SET histone methyltransferase is a plant-specific chromatin modifier
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.06.035openalex-snapshot
Antagonistic interactions between Arabidopsis K-homology domain genes uncover PEPPER as a positive regulator of the central floral repressor FLOWERING LOCUS C
inferred← citeshttps://doi.org/10.1016/s0065-2296(08)00805-7openalex-snapshot
Chapter 5 Roles of Circadian Clock and Histone Methylation in the Control of Floral Repressors
inferred← citeshttps://doi.org/10.1016/s1016-8478(23)14010-6openalex-snapshot
Functional Conservation and Divergence of FVE Genes that Control Flowering Time and Cold Response in Rice and Arabidopsis
inferred← citeshttps://doi.org/10.1016/s1874-6047(06)80010-7openalex-snapshot
8 Demethylation pathways for histone methyllysine residues
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c15939openalex-snapshot
Mutation in BrEPCR1 Led to Early Flowering in Chinese Cabbage
inferred← citeshttps://doi.org/10.1021/bi701969kopenalex-snapshot
Characterization of a Lysine-Specific Histone Demethylase from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/emboj.2010.198openalex-snapshot
Growth habit determination by the balance of histone methylation activities in Arabidopsis
inferred← citeshttps://doi.org/10.1038/ncb1329openalex-snapshot
Prevention of early flowering by expression of FLOWERING LOCUS C requires methylation of histone H3 K36
inferred← citeshttps://doi.org/10.1038/ncomms3186openalex-snapshot
Two FLX family members are non-redundantly required to establish the vernalization requirement in Arabidopsis
inferred← citeshttps://doi.org/10.1038/ncomms9326openalex-snapshot
A transposable element in a NAC gene is associated with drought tolerance in maize seedlings
inferred← citeshttps://doi.org/10.1038/ng.3712openalex-snapshot
A cis cold memory element and a trans epigenome reader mediate Polycomb silencing of FLC by vernalization in Arabidopsis
inferred← citeshttps://doi.org/10.1038/ng1295openalex-snapshot
Regulation of flowering time by FVE, a retinoblastoma-associated protein
inferred← citeshttps://doi.org/10.1038/ng1298openalex-snapshot
A genetic link between cold responses and flowering time through FVE in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/nrg2218openalex-snapshot
Histone lysine demethylases: emerging roles in development, physiology and disease
inferred← citeshttps://doi.org/10.1038/s41467-019-09386-5openalex-snapshot
Primed histone demethylation regulates shoot regenerative competency
inferred← citeshttps://doi.org/10.1038/s41467-025-60209-2openalex-snapshot
A naturally occurring SNP modulates thermotolerance divergence among grapevines
inferred← citeshttps://doi.org/10.1038/s41467-025-61328-6openalex-snapshot
Natural variation in histone demethylase GmLDL2 confers flowering time divergence for geographical expansion in soybean
inferred← citeshttps://doi.org/10.1038/s41477-021-00868-3openalex-snapshot
Chromatin-based mechanisms to coordinate convergent overlapping transcription
inferred← citeshttps://doi.org/10.1038/s41540-019-0106-3openalex-snapshot
Hierarchical graphical model reveals HFR1 bridging circadian rhythm and flower development in Arabidopsis thaliana
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/sj.cr.7310059openalex-snapshot
Arabidopsis thaliana histone deacetylase 1 (AtHD1) is localized in euchromatic regions and demonstrates histone deacetylase activity in vitro
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601647openalex-snapshot
SKB1‐mediated symmetric dimethylation of histone H4R3 controls flowering time in Arabidopsis
inferred← citeshttps://doi.org/10.1038/sj.embor.7401111openalex-snapshot
Regulation of flowering time by the protein arginine methyltransferase AtPRMT10
inferred← citeshttps://doi.org/10.1038/srep30641openalex-snapshot
Comparative proteomic analysis of the shoot apical meristem in maize between a ZmCCT-associated near-isogenic line and its recurrent parent
inferred← citeshttps://doi.org/10.1038/srep42593openalex-snapshot
Chilling Affects Phytohormone and Post-Embryonic Development Pathways during Bud Break and Fruit Set in Apple (Malus domestica Borkh.)
inferred← citeshttps://doi.org/10.1042/bst0320565openalex-snapshot
RNA processing and Arabidopsis flowering time control
inferred← citeshttps://doi.org/10.1051/jbio/2017004openalex-snapshot
Réciprocité entre transcription active et méthylation des histones
inferred← citeshttps://doi.org/10.1071/ar05155openalex-snapshot
Flowering time control: gene network modelling and the link to quantitative genetics
inferred← citeshttps://doi.org/10.1071/fp04245openalex-snapshot
Components of the Arabidopsis autonomous floral promotion pathway, FCA and FY, are conserved in monocots
inferred← citeshttps://doi.org/10.1073/pnas.0404552101openalex-snapshot
Regulation of flowering time in Arabidopsis by K homology domain proteins
inferred← citeshttps://doi.org/10.1073/pnas.0406232101openalex-snapshot
Epistatic interaction between Arabidopsis FRI and FLC flowering time genes generates a latitudinal cline in a life history trait
inferred← citeshttps://doi.org/10.1073/pnas.0409474102openalex-snapshot
Quantitative trait locus mapping and DNA array hybridization identify an FLM deletion as a cause for natural flowering-time variation
inferred← citeshttps://doi.org/10.1073/pnas.0502600102openalex-snapshot
The elongata mutants identify a functional Elongator complex in plants with a role in cell proliferation during organ growth
inferred← citeshttps://doi.org/10.1073/pnas.0611459104openalex-snapshot
Small RNA-mediated chromatin silencing directed to the 3′ region of the Arabidopsis gene encoding the developmental regulator, FLC
inferred← citeshttps://doi.org/10.1073/pnas.1014030108openalex-snapshot
Involvement of KDM1C histone demethylase–OTLD1 otubain-like histone deubiquitinase complexes in plant gene repression
inferred← citeshttps://doi.org/10.1073/pnas.1103959108openalex-snapshot
Derepression of ethylene-stabilized transcription factors (EIN3/EIL1) mediates jasmonate and ethylene signaling synergy in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.1217022110openalex-snapshot
Ordered changes in histone modifications at the core of the Arabidopsis circadian clock
inferred← citeshttps://doi.org/10.1073/pnas.1406635111openalex-snapshot
Antisense-mediated FLC transcriptional repression requires the P-TEFb transcription elongation factor
inferred← citeshttps://doi.org/10.1073/pnas.1521599113openalex-snapshot
Chloroplast retrograde signal regulates flowering
inferred← citeshttps://doi.org/10.1073/pnas.1618618114openalex-snapshot
POWERDRESS and HDA9 interact and promote histone H3 deacetylation at specific genomic sites in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.1704211114openalex-snapshot
Ploidy-dependent changes in the epigenome of symbiotic cells correlate with specific patterns of gene expression
inferred← citeshttps://doi.org/10.1080/09168451.2014.932670openalex-snapshot
VASCULAR PLANT ONE-ZINC FINGER1 and VOZ2 repress the FLOWERING LOCUS C clade members to control flowering time in Arabidopsis
inferred← citeshttps://doi.org/10.1080/11263501003718570openalex-snapshot
Plastic, inquisitive roots and intelligent plants in the light of some new vistas in plant biology
inferred← citeshttps://doi.org/10.1080/15592324.2015.1027851openalex-snapshot
Dynamics of H3K27me3 methylation and demethylation in plant development
inferred← citeshttps://doi.org/10.1086/421856openalex-snapshot
Differences in Developmental Programming and Node Number at Flowering in the 5‐Azacytidine‐Induced Early Flowering Flax Lines and Their Controls
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780195335903.003.0006openalex-snapshot
Integration of Photoperiodic Timing and Vernalization in Arabidopsis
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.001.0001openalex-snapshot
Understanding Flowers and Flowering
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0001openalex-snapshot
The Evolution of Flowers
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0002openalex-snapshot
Historical Interpretations of Flower Induction and Flower Development
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0003openalex-snapshot
Flower Induction inArabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0004openalex-snapshot
The Autonomous Pathways for Floral Inhibition and Induction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0005openalex-snapshot
The Photoperiodic Pathway of Floral Induction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0006openalex-snapshot
The Vernalization Pathway of Floral Induction and the Role of Gibberellin
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0007openalex-snapshot
Integrating theArabidopsis thalianaFlower Induction Pathways and Assessing the Extent to Which the Model Is Ubiquitous
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0008openalex-snapshot
Changes at the Shoot Apical Meristem in Response to Floral Induction
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0009openalex-snapshot
Development of the Floral Organs
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0010openalex-snapshot
The ABC Model in Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0011openalex-snapshot
Function and Development of Gametophytes
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0012openalex-snapshot
Preventing Self-fertilization
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0013openalex-snapshot
Why Are Flowers Different? Pollination Syndromes—The Theory
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0014openalex-snapshot
Changing Floral Shape and Structure
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0015openalex-snapshot
Colouring the Flower
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0016openalex-snapshot
Enhancing Flower Colour
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0017openalex-snapshot
Are Flowers under Selective Pressure to Increase Pollinator Attention?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0018openalex-snapshot
Do Pollinators Discriminate between Different Floral Forms?
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198565970.003.0019openalex-snapshot
Pollination Syndromes—The Evidence
inferred← citeshttps://doi.org/10.1093/aob/mcp063openalex-snapshot
The molecular biology of seasonal flowering-responses in Arabidopsis and the cereals
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