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ETTIN patterns the Arabidopsis floral meristem and reproductive organs
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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/bf02525170openalex-snapshot
Effective vectors for transformation, expression of heterologous genes, and assaying transposon excision in transgenic plants
inferredcites →https://doi.org/10.1016/0092-8674(91)90245-topenalex-snapshot
Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: Identification of a class of bipartite nuclear targeting sequence
inferredcites →https://doi.org/10.1016/0092-8674(92)90271-dopenalex-snapshot
Ectopic expression of the floral homeotic gene AGAMOUS in transgenic Arabidopsis plants alters floral organ identity
inferredcites →https://doi.org/10.1016/0092-8674(92)90295-nopenalex-snapshot
LEAFY controls floral meristem identity in Arabidopsis
inferredcites →https://doi.org/10.1016/0092-8674(93)90537-zopenalex-snapshot
The Tousled gene in A. thaliana encodes a protein kinase homolog that is required for leaf and flower development
inferredcites →https://doi.org/10.1016/0092-8674(94)90291-7openalex-snapshot
The ABCs of floral homeotic genes
inferredcites →https://doi.org/10.1016/s0092-8674(00)80239-1openalex-snapshot
The CLAVATA1Gene Encodes a Putative Receptor Kinase That Controls Shoot and Floral Meristem Size in Arabidopsis
inferredcites →https://doi.org/10.1016/s0168-9525(97)01094-9openalex-snapshot
T-DNA insertion mutagenesis in Arabidopsis: going back and forth
inferredcites →https://doi.org/10.1038/377495a0openalex-snapshot
A developmental switch sufficient for flower initiation in diverse plants
inferredcites →https://doi.org/10.1038/377522a0openalex-snapshot
A gene triggering flower formation in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.94.22.11786openalex-snapshot
Protein–protein interactions among the Aux/IAA proteins
inferredcites →https://doi.org/10.1105/tpc.1.1.37openalex-snapshot
Genes Directing Flower Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.2.8.741openalex-snapshot
Function of the apetala-1 Gene during Arabidopsis Floral Development
inferredcites →https://doi.org/10.1105/tpc.2.8.755openalex-snapshot
Early Flower Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.4.8.901openalex-snapshot
LEAFY Interacts with Floral Homeotic Genes to Regulate Arabidopsis Floral Development
inferredcites →https://doi.org/10.1105/tpc.7.5.529openalex-snapshot
UFO: An Arabidopsis Gene Involved in Both Floral Meristem and Floral Organ Development
inferredcites →https://doi.org/10.1105/tpc.9.1.37openalex-snapshot
Photo and hormonal control of meristem identity in the Arabidopsis flower mutants apetala2 and apetala1.
inferredcites →https://doi.org/10.1105/tpc.9.3.335openalex-snapshot
TOUSLED participates in apical tissue formation during gynoecium development in Arabidopsis.
inferredcites →https://doi.org/10.1111/j.1365-313x.1991.00071.xopenalex-snapshot
T‐DNA insertion mutagenesis in Arabidopsis: mutational spectrum
inferredcites →https://doi.org/10.1126/science.276.5320.1865openalex-snapshot
ARF1, a Transcription Factor That Binds to Auxin Response Elements
inferredcites →https://doi.org/10.1139/b89-375openalex-snapshot
Floral development in Arabidopsis thaliana: a comparison of the wild type and the homeotic pistillata mutant
inferredcites →https://doi.org/10.1139/b94-052openalex-snapshot
Floral organ initiation and development in wild-type Arabidopsis thaliana (Brassicaceae) and in the organ identity mutants apetala2-1 and agamous-1
inferredcites →https://doi.org/10.1146/annurev.arplant.46.1.167openalex-snapshot
Floral Meristems to Floral Organs: Genes Controlling Early Events in Arabidopsis Flower Development
inferredcites →https://doi.org/10.1146/annurev.ge.29.120195.000315openalex-snapshot
THE GENETICS OF FLOWER DEVELOPMENT: From Floral Induction to Ovule Morphogenesis
inferredcites →https://doi.org/10.1242/dev.112.1.1openalex-snapshot
Genetic interactions among floral homeotic genes of Arabidopsis
inferredcites →https://doi.org/10.1242/dev.114.3.599openalex-snapshot
Superman, a regulator of floral homeotic genes inArabidopsis
inferredcites →https://doi.org/10.1242/dev.119.2.397openalex-snapshot
CLAVATA1, a regulator of meristem and flower development in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.119.3.721openalex-snapshot
Control of flower development in Arabidopsis thaliana by APETALA1 and interacting genes
inferredcites →https://doi.org/10.1242/dev.121.5.1519openalex-snapshot
Arabidopsis gynoecium structure in the wild type and in ettin mutants
inferredcites →https://doi.org/10.1242/dev.121.7.2057openalex-snapshot
CLAVATA3 is a specific regulator of shoot and floral meristem development affecting the same processes as CLAVATA1
inferredcites →https://doi.org/10.1242/dev.122.4.1261openalex-snapshot
Mutations in the PERIANTHIA gene of Arabidopsis specifically alter floral organ number and initiation pattern
inferredcites →https://doi.org/10.1385/1-59259-677-0:131openalex-snapshot
In Situ Hybridization with Nonradioactive Probes
inferredcites →https://doi.org/10.2307/2446041openalex-snapshot
Arabidopsis (Brassicaceae) flower development and gynoecium patterning in wild type and ettin mutants
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.3981902openalex-extracted
Uncovering the Genetic Architecture of Replicated Adaptation
inferred← citeshttps://doi.org/10.1002/(sici)1526-968x(200001)26:1<42::aid-gene7>3.0.co;2-jopenalex-snapshot
LEUNIG has multiple functions in gynoecium development in Arabidopsis
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0120openalex-snapshot
Polarity in Floral Development
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0167openalex-snapshot
Floral Architecture: Regulation and Diversity of Floral Shape and Pattern
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0198openalex-snapshot
The Genetic Control of Flower Size and Shape
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0409openalex-snapshot
Gynoecium Patterning in Arabidopsis: A Basic Plan Behind a Complex Structure
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0412openalex-snapshot
A rabidopsisFruit Development
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0609openalex-snapshot
Exploring the Role of the Ovule in Cereal Grain Development and Reproductive Stress Tolerance
inferred← citeshttps://doi.org/10.1002/9781444314557.ch2openalex-snapshot
Gynoecium Patterning in Arabidopsis: A Basic Plan behind a Complex Structure
inferred← citeshttps://doi.org/10.1002/bies.201200126openalex-snapshot
A mathematical basis for plant patterning derived from physico‐chemical phenomena
inferred← citeshttps://doi.org/10.1002/dvg.22728openalex-snapshot
Adaxial–abaxial polarity: The developmental basis of leaf shape diversity
inferred← citeshttps://doi.org/10.1002/pld3.328openalex-snapshot
Targeted mutation of transcription factor genes alters metaxylem vessel size and number in rice roots
inferred← citeshttps://doi.org/10.1002/wdev.193openalex-snapshot
Auxin and cytokinin act during gynoecial patterning and the development of ovules from the meristematic medial domain
inferred← citeshttps://doi.org/10.1006/scdb.2001.0266openalex-snapshot
Developmental programmes in floral organ formation
inferred← citeshttps://doi.org/10.1007/7089_2007_150openalex-snapshot
Signaling in Auxin-Dependent Plant Development
inferred← citeshttps://doi.org/10.1007/978-1-0716-3299-4_5openalex-snapshot
Hormones and Flower Development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-4614-9408-9_13openalex-snapshot
Scanning Electron Microscopy Analysis of Floral Development
inferred← citeshttps://doi.org/10.1007/978-3-642-02301-9_9openalex-snapshot
Floral Organ Initiation and Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8openalex-snapshot
Auxin and Its Role in Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-7091-1526-8_11openalex-snapshot
The Role of Auxin for Reproductive Organ Patterning and Development
inferred← citeshttps://doi.org/10.1007/978-94-010-0377-3_10openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferred← citeshttps://doi.org/10.1007/978-94-010-0377-3_3openalex-snapshot
Protein phosphorylation in the delivery of and response to auxin signals
inferred← citeshttps://doi.org/10.1007/978-94-010-0377-3_5openalex-snapshot
Evolutionary patterns in auxin action
inferred← citeshttps://doi.org/10.1007/978-94-010-0377-3_9openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferred← citeshttps://doi.org/10.1007/978-94-011-4453-7_29openalex-snapshot
Isolation of Developmentally-Regulated Genes in Immature Tomato Fruit: Towards an Understanding of Pre-Ripening Development
inferred← citeshttps://doi.org/10.1007/978-94-017-3522-3_4openalex-snapshot
Control of Plant Organogenesis: Genetic and Biochemical Signals in Plant Organ form and Development
inferred← citeshttps://doi.org/10.1007/978-94-017-3522-3_8openalex-snapshot
Thin Cell Layers and Floral Morphogenesis, Floral Genetics and in Vitro Flowering
inferred← citeshttps://doi.org/10.1007/978-981-95-7033-1_6openalex-snapshot
Reproductive Meristems and Regulatory Genes
inferred← citeshttps://doi.org/10.1007/978-981-95-7033-1_9openalex-snapshot
Stamen and Anther Development
inferred← citeshttps://doi.org/10.1007/bf02512187openalex-snapshot
Genetic pathways controlling carpel development inArabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/bf03187000openalex-snapshot
Isolation and identification of genes expressed differentially in rice inflorescence meristem with suppression subtractive hybridization
inferred← citeshttps://doi.org/10.1007/s00018-006-6116-5openalex-snapshot
Spatiotemporal asymmetric auxin distribution: a means to coordinate plant development
inferred← citeshttps://doi.org/10.1007/s00018-012-0999-0openalex-snapshot
Floral meristem initiation and emergence in plants
inferred← citeshttps://doi.org/10.1007/s000180050190openalex-snapshot
The ARF family of transcription factors and their role in plant hormone-responsive transcription
inferred← citeshttps://doi.org/10.1007/s00299-013-1433-2openalex-snapshot
Mapping quantitative trait loci for tissue culture response in VCS3M-DH population of Brassica rapa
inferred← citeshttps://doi.org/10.1007/s00344-010-9180-xopenalex-snapshot
The Hormonal Regulation of Flower Development
inferred← citeshttps://doi.org/10.1007/s003440010006openalex-snapshot
Regulation of Tracheary Element Differentiation
inferred← citeshttps://doi.org/10.1007/s00425-003-1100-xopenalex-snapshot
Roles for auxin during morphogenesis of the compound leaves of pea ( Pisum sativum )
inferred← citeshttps://doi.org/10.1007/s00425-005-0088-9openalex-snapshot
Role of auxin in regulating Arabidopsis flower development
inferred← citeshttps://doi.org/10.1007/s00425-005-0151-6openalex-snapshot
Primary metabolic pathways and signal transduction in sunflower (Helianthus annuus L.): comparison of transcriptional profiling in leaves and immature embryos using cDNA microarrays
inferred← citeshttps://doi.org/10.1007/s00425-012-1602-5openalex-snapshot
Inception of maleness: auxin contribution to flower masculinization in the dioecious cactus Opuntia stenopetala
inferred← citeshttps://doi.org/10.1007/s00425-012-1607-0openalex-snapshot
A novel, semi-dominant allele of MONOPTEROS provides insight into leaf initiation and vein pattern formation
inferred← citeshttps://doi.org/10.1007/s00438-004-1057-xopenalex-snapshot
The PIN and LAX families of auxin transport genes in Medicago truncatula
inferred← citeshttps://doi.org/10.1007/s00438-011-0602-7openalex-snapshot
Genome-wide analysis of auxin response factor (ARF) gene family from tomato and analysis of their role in flower and fruit development
inferred← citeshttps://doi.org/10.1007/s00497-004-0231-yopenalex-snapshot
Differentiation and degeneration of cells that play a major role in tobacco anther dehiscence
inferred← citeshttps://doi.org/10.1007/s00497-018-00359-0openalex-snapshot
Control of stem cell activity in the carpel margin meristem (CMM) in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00497-023-00494-3openalex-snapshot
Comparative analysis of floral transition and floral organ formation in two contrasting species: Disocactus speciosus and D. eichlamii (Cactaceae)
inferred← citeshttps://doi.org/10.1007/s004970050158openalex-snapshot
Anther developmental defects in Arabidopsis thaliana male-sterile mutants
inferred← citeshttps://doi.org/10.1007/s00709-013-0572-1openalex-snapshot
The far side of auxin signaling: fundamental cellular activities and their contribution to a defined growth response in plants
inferred← citeshttps://doi.org/10.1007/s10142-015-0437-0openalex-snapshot
Genome-wide identification of auxin response factor (ARF) genes and its tissue-specific prominent expression in Gossypium raimondii
inferred← citeshttps://doi.org/10.1007/s10142-018-0622-zopenalex-snapshot
Identification, characterization, and expression analysis of auxin response factor (ARF) gene family in Brachypodium distachyon
inferred← citeshttps://doi.org/10.1007/s10265-010-0336-3openalex-snapshot
Perspectives on leaf dorsoventral polarity
inferred← citeshttps://doi.org/10.1007/s10265-019-01156-0openalex-snapshot
Hormonal and transcriptional analyses of fruit development and ripening in different varieties of black pepper (Piper nigrum)
inferred← citeshttps://doi.org/10.1007/s10709-024-00214-3openalex-snapshot
Systematic analysis of the ARF gene family in Fagopyrum dibotrys and its potential roles in stress tolerance
inferred← citeshttps://doi.org/10.1007/s11032-025-01606-9openalex-snapshot
Identification of an ovuleless mutant and fine mapping of its causal Ol locus in cucumber (Cucumis sativus L.)
inferred← citeshttps://doi.org/10.1007/s11033-011-0991-zopenalex-snapshot
Diversification, phylogeny and evolution of auxin response factor (ARF) family: insights gained from analyzing maize ARF genes
inferred← citeshttps://doi.org/10.1007/s11033-012-1448-8openalex-snapshot
Systematic analysis of plant-specific B3 domain-containing proteins based on the genome resources of 11 sequenced species
inferred← citeshttps://doi.org/10.1007/s11103-004-3473-zopenalex-snapshot
Transcript profiling of transcription factor genes during silique development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-020-01086-9openalex-snapshot
Bulk RNA-Seq analysis to dissect the regulation of stigma position in tomato
inferred← citeshttps://doi.org/10.1007/s11103-024-01503-3openalex-snapshot
Suppression of SlHDT1 expression increases fruit yield and decreases drought and salt tolerance in tomato
inferred← citeshttps://doi.org/10.1007/s11295-016-1055-2openalex-snapshot
Transcriptome analysis of the male-to-hermaphrodite sex reversal induced by low temperature in papaya
inferred← citeshttps://doi.org/10.1007/s12041-014-0462-0openalex-snapshot
Genomewide identification and expression analysis of the ARF gene family in apple
inferred← citeshttps://doi.org/10.1007/s12298-021-01011-4openalex-snapshot
Genome-wide identification of auxin response factor (ARF) family in kiwifruit (Actinidia chinensis) and analysis of their inducible involvements in abiotic stresses
inferred← citeshttps://doi.org/10.1007/s12298-024-01474-1openalex-snapshot
The auxin response factor (ARF) gene family in Cyclocarya paliurus: genome-wide identification and their expression profiling under heat and drought stresses
inferred← citeshttps://doi.org/10.1007/s12374-012-0325-2openalex-snapshot
CLV1 interacts with UFO in modulation of gynoecium development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s12374-013-0097-3openalex-snapshot
Analysis of gradient-like expression of miR167 in Arabidopsis thaliana embryonic tissue
inferred← citeshttps://doi.org/10.1007/s44281-025-00084-5openalex-snapshot
Diverse actions of auxin on fruit development and ripening
inferred← citeshttps://doi.org/10.1016/b978-0-12-380868-4.00001-6openalex-snapshot
Carpel Development
inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00017-3openalex-snapshot
Potential roles of hormonal crosstalk in flower development or plant morphogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-443-15719-6.00015-5openalex-snapshot
Nucleotidyl cyclase activities of TIR1/AFB auxin receptors: new insights into the mechanism of auxin signaling
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.10.004openalex-snapshot
Female reproductive organ formation: A multitasking endeavor
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2008.02.007openalex-snapshot
Evolution of microRNAs and their targets: Are all microRNAs biologically relevant?
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.11.082openalex-snapshot
Histone deacetylases HDA6 and HDA9 coordinately regulate valve cell elongation through affecting auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cell.2005.04.004openalex-snapshot
microRNA-Directed Phasing during Trans-Acting siRNA Biogenesis in Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2017.06.053openalex-snapshot
The Evolution of Diverse Floral Morphologies
inferred← citeshttps://doi.org/10.1016/j.cub.2020.09.006openalex-snapshot
Three STIGMA AND STYLE STYLISTs Pattern the Fine Architectures of Apical Gynoecium and Are Critical for Male Gametophyte-Pistil Interaction
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.05.014openalex-snapshot
Plant Development Is Regulated by a Family of Auxin Receptor F Box Proteins
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.01.019openalex-snapshot
A multiscale analysis of early flower development in Arabidopsis provides an integrated view of molecular regulation and growth control
inferred← citeshttps://doi.org/10.1016/j.gde.2017.02.005openalex-snapshot
Gynoecium formation: an intimate and complicated relationship
inferred← citeshttps://doi.org/10.1016/j.gene.2007.01.006openalex-snapshot
Genome-wide analysis of the auxin response factors (ARF) gene family in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.gep.2016.01.001openalex-snapshot
MicroRNA expression profiles in response to drought stress in Sorghum bicolor
inferred← citeshttps://doi.org/10.1016/j.hpj.2017.07.011openalex-snapshot
Expression Analyses of ABCDE Model Genes and Changes in Levels of Endogenous Hormones in Chinese Cabbage Exhibiting Petal-Loss
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.10.011openalex-snapshot
Dioxygenase RhDAO1 regulates floral organ identity by controlling auxin homeostasis in miniature rose (Rosa hybrida)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.06.100openalex-snapshot
AT-HOOK MOTIF NUCLEAR LOCALIZED (AHL) proteins of ancient origin radiate new functions
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115118openalex-snapshot
Genomic identification of ARF transcription factors and expression analysis in Cannabis sativa L
inferred← citeshttps://doi.org/10.1016/j.pbi.2004.07.016openalex-snapshot
Auxin signals — turning genes on and turning cells around
inferred← citeshttps://doi.org/10.1016/j.pbi.2004.09.006openalex-snapshot
Funneling auxin action: specificity in signal transduction
inferred← citeshttps://doi.org/10.1016/j.pbi.2005.11.001openalex-snapshot
Integrating hormone signaling and patterning mechanisms in plant development
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.09.004openalex-snapshot
Developmental cartography: coordination via hormonal and genetic interactions during gynoecium formation
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102262openalex-snapshot
Context-specific functions of transcription factors controlling plant development: From leaves to flowers
inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102732openalex-snapshot
Organ symmetry establishment during gynoecium development
inferred← citeshttps://doi.org/10.1016/j.plantsci.2013.09.004openalex-snapshot
Interactions between Arabidopsis DNA repair genes UVH6, DDB1A, and DDB2 during abiotic stress tolerance and floral development
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.06.051openalex-snapshot
Knockdown of MicroRNA160a/b by STTM leads to root architecture changes via auxin signaling in Solanum tuberosum
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108463openalex-snapshot
OfBFT genes play an essential role in the proliferate flower formation of Osmanthus fragrans
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111720openalex-snapshot
The role of SlGH9-16 cellulase in gynoecium morphogenesis and fruit texture in tomato
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.10.028openalex-snapshot
Shaping a fruit: Developmental pathways that impact growth patterns
inferred← citeshttps://doi.org/10.1016/j.tig.2006.03.003openalex-snapshot
The diversity of RNA silencing pathways in plants
inferred← citeshttps://doi.org/10.1016/j.tig.2007.08.005openalex-snapshot
Packaging the male germline in plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2008.09.006openalex-snapshot
The plant B3 superfamily
inferred← citeshttps://doi.org/10.1016/s0065-2296(06)44009-xopenalex-snapshot
Gene Duplication and Floral Developmental Genetics of Basal Eudicots
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60316-6openalex-snapshot
4 Molecular Genetics of Gynoecium Development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
inferred← citeshttps://doi.org/10.1016/s0092-8674(04)00254-5openalex-snapshot
From Tough Nuts to Touch-Me-Nots
inferred← citeshttps://doi.org/10.1016/s1360-1385(01)02042-8openalex-snapshot
Roles and activities of Aux/IAA proteins in Arabidopsis
inferred← citeshttps://doi.org/10.1016/s1360-1385(98)01244-8openalex-snapshot
Aux/IAA proteins and auxin signal transduction
inferred← citeshttps://doi.org/10.1016/s1360-1385(99)01454-5openalex-snapshot
Piecing together the Arabidopsis gynoecium
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00104-7openalex-snapshot
Vascular development: tracing signals along veins
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00136-9openalex-snapshot
Plant morphogenesis: long-distance coordination and local patterning
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00138-2openalex-snapshot
The role of floral meristems in patterning
inferred← citeshttps://doi.org/10.1016/s1369-5266(98)80047-2openalex-snapshot
Auxin signaling in Arabidopsis flower development?
inferred← citeshttps://doi.org/10.1016/s1369-5266(98)80269-0openalex-snapshot
Molecular mechanisms of auxin action
inferred← citeshttps://doi.org/10.1016/s1673-8527(09)60021-7openalex-snapshot
The many roles of small RNAs in leaf development
inferred← citeshttps://doi.org/10.1017/qpb.2023.13openalex-snapshot
A blast from the past: Understanding stem cell specification in plant roots using laser ablation
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr1openalex-snapshot
Author comment: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R0/PR1
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr10openalex-snapshot
Decision: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R1/PR10
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr11openalex-snapshot
Author comment: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R2/PR11
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr12openalex-snapshot
Recommendation: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R2/PR12
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr13openalex-snapshot
Decision: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R2/PR13
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr2openalex-snapshot
Review: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R0/PR2
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr3openalex-snapshot
Review: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R0/PR3
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr4openalex-snapshot
Recommendation: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R0/PR4
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr5openalex-snapshot
Decision: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R0/PR5
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr6openalex-snapshot
Author comment: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R1/PR6
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr7openalex-snapshot
Review: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R1/PR7
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr8openalex-snapshot
Review: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R1/PR8
inferred← citeshttps://doi.org/10.1017/qpb.2023.13.pr9openalex-snapshot
Recommendation: A blast from the past: Understanding stem cell specification in plant roots using laser ablation — R1/PR9
inferred← citeshttps://doi.org/10.1023/a:1015207114117openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferred← citeshttps://doi.org/10.1023/a:1015242627321openalex-snapshot
Evolutionary patterns in auxin action
inferred← citeshttps://doi.org/10.1023/a:1015246828230openalex-snapshot
Protein phosphorylation in the delivery of and response to auxin signals
inferred← citeshttps://doi.org/10.1023/a:1015255030047openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferred← citeshttps://doi.org/10.1023/a:1019818110761openalex-snapshot
OsARF1, an auxin response factor from rice, is auxin-regulated and classifies as a primary auxin responsive gene
inferred← citeshttps://doi.org/10.1038/msb.2011.39openalex-snapshot
The auxin signalling network translates dynamic input into robust patterning at the shoot apex
inferred← citeshttps://doi.org/10.1038/s41438-018-0068-4openalex-snapshot
Auxin regulates anthocyanin biosynthesis through the Aux/IAA–ARF signaling pathway in apple
inferred← citeshttps://doi.org/10.1038/s41438-019-0205-8openalex-snapshot
Auxin regulation involved in gynoecium morphogenesis of papaya flowers
inferred← citeshttps://doi.org/10.1038/s41467-018-06772-3openalex-snapshot
Architecture of gene regulatory networks controlling flower development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s41467-024-47325-1openalex-snapshot
Two orthogonal differentiation gradients locally coordinate fruit morphogenesis
inferred← citeshttps://doi.org/10.1038/s41477-019-0498-5openalex-snapshot
Developmental mechanisms involved in the diversification of flowers
inferred← citeshttps://doi.org/10.1038/s41477-025-01973-3openalex-snapshot
Comparative mutant analyses reveal a novel mechanism of ARF regulation in land plants
inferred← citeshttps://doi.org/10.1038/s41598-017-11327-5openalex-snapshot
Genome-wide identification and co-expression network analysis provide insights into the roles of auxin response factor gene family in chickpea
inferred← citeshttps://doi.org/10.1038/s41598-018-31634-9openalex-snapshot
Auxin sensing is a property of an unstructured domain in the Auxin Response Factor ETTIN of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1038/s42003-024-05786-6openalex-snapshot
Reciprocal expression of MADS-box genes and DNA methylation reconfiguration initiate bisexual cones in spruce
inferred← citeshttps://doi.org/10.1038/sj.emboj.7600659openalex-snapshot
Developmental specificity of auxin response by pairs of ARF and Aux/IAA transcriptional regulators
inferred← citeshttps://doi.org/10.1038/srep33728openalex-snapshot
SlARF2a plays a negative role in mediating axillary shoot formation
inferred← citeshttps://doi.org/10.1042/bst0320611openalex-snapshot
A key factor of translation reinitiation, ribosomal protein L24, is involved in gynoecium development in Arabidopsis
inferred← citeshttps://doi.org/10.1042/bst0380571openalex-snapshot
Cell–cell interactions during patterning of theArabidopsisanther
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00359.xopenalex-snapshot
Identification of genes expressed during earlyArabidopsiscarpel development by mRNA differential display: characterisation ofATCEL2, a novel endo‐1,4‐β‐D‐glucanase gene
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00538.xopenalex-snapshot
Dimerization and DNA binding of auxin response factors
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2000.00691.xopenalex-snapshot
Arabidopsis thaliana SHAGGY‐related protein kinases (AtSK11 and 12) function in perianth and gynoecium development
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2002.01450.xopenalex-snapshot
Down‐regulation of DR12, an auxin‐response‐factor homolog, in the tomato results in a pleiotropic phenotype including dark green and blotchy ripening fruit
inferred← citeshttps://doi.org/10.1055/s-2006-923969openalex-snapshot
Noise Yields Order - Auxin, Actin, and Polar Patterning
inferred← citeshttps://doi.org/10.1063/1.4966727openalex-snapshot
Identification of ARF and AUX/IAA gene families in Rafflesia cantleyi
inferred← citeshttps://doi.org/10.1071/fp19215openalex-snapshot
Improved reproductive growth of euhalophyte Suaeda salsa under salinity is correlated with altered phytohormone biosynthesis and signal transduction
inferred← citeshttps://doi.org/10.1073/pnas.0504029102openalex-snapshot
A database analysis method identifies an endogenous trans-acting short-interfering RNA that targets the Arabidopsis ARF2, ARF3 , and ARF4 genes
inferred← citeshttps://doi.org/10.1073/pnas.1214774109openalex-snapshot
Arabidopsis ribosomal proteins control developmental programs through translational regulation of auxin response factors
inferred← citeshttps://doi.org/10.1073/pnas.1217343109openalex-snapshot
Non-cell-autonomous regulation of crucifer self-incompatibility by Auxin Response Factor ARF3
inferred← citeshttps://doi.org/10.1073/pnas.2018615118openalex-snapshot
ARABIDOPSIS THALIANA HOMEOBOX GENE 1 controls plant architecture by locally restricting environmental responses
inferred← citeshttps://doi.org/10.1073/pnas.2524858123openalex-snapshot
Spatiotemporal transcriptome atlas reveals the dynamic cellular and molecular characteristics of ovule development in gymnosperms
inferred← citeshttps://doi.org/10.1073/pnas.2537963123openalex-snapshot
Mutational analyses of an instability domain reveal its conserved role in the regulation of class-B ARF levels in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.94.22.11786openalex-snapshot
Protein–protein interactions among the Aux/IAA proteins
inferred← citeshttps://doi.org/10.1074/jbc.m102783200openalex-snapshot
Conformational Dynamics Underlie the Activity of the Auxin-binding Protein, Nt-abp1
inferred← citeshttps://doi.org/10.1080/01140671.2020.1779756openalex-snapshot
Genome‐wide analysis of auxin response factor (ARF) genes and functional identification of MdARF2 reveals the involvement in the regulation of anthocyanin accumulation in apple
inferred← citeshttps://doi.org/10.1080/07352689.2014.917531openalex-snapshot
Patterns and Polarity in Floral Meristem and Floral Organ Initiation
inferred← citeshttps://doi.org/10.1080/15592324.2018.1467690openalex-snapshot
AUXIN RESPONSE FACTOR3 plays distinct role during early flower development
inferred← citeshttps://doi.org/10.1080/15592324.2020.1771937openalex-snapshot
Immediate targets of ETTIN suggest a key role for pectin methylesterase inhibitors in the control of Arabidopsis gynecium development
inferred← citeshttps://doi.org/10.1080/15592324.2021.1905335openalex-snapshot
Arabidopsis cysteine-rich receptor-like protein kinase CRK33 affects stomatal density and drought tolerance
inferred← citeshttps://doi.org/10.1086/314213openalex-snapshot
Developmental Instability as a Means of Assessing Stress in Plants: A Case Study Using Electromagnetic Fields and Soybeans
inferred← citeshttps://doi.org/10.1086/324178openalex-snapshot
CRABS CLAWandSPATULAGenes Regulate Growth and Pattern Formation during Gynoecium Development inArabidopsis thaliana
inferred← citeshttps://doi.org/10.1086/504928openalex-snapshot
Developmental Basis of an Anatomical Novelty: Heteroarthrocarpy inCakile lanceolataandErucaria erucarioides(Brassicaceae)
inferred← citeshttps://doi.org/10.1093/aob/mcf007openalex-snapshot
Expression Pattern of Aux/IAA Genes in the iaa3/shy2-1D Mutant of Arabidopsis thaliana (L.)
inferred← citeshttps://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferred← citeshttps://doi.org/10.1093/aob/mcr115openalex-snapshot
Correlation between number and position of floral organs in Arabidopsis
inferred← citeshttps://doi.org/10.1093/aob/mcy218openalex-snapshot
TaARF4 genes are linked to root growth and plant height in wheat
inferred← citeshttps://doi.org/10.1093/aobpla/plaa051openalex-snapshot
Irregular adaxial–abaxial polarity rearrangement contributes to the monosymmetric-to-asymmetric transformation of Canna indica stamen
inferred← citeshttps://doi.org/10.1093/genetics/156.3.1379openalex-snapshot
Quantitative Trait Loci for Floral Morphology in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/hr/uhad110openalex-snapshot
Combined genome-wide association studies and expression quantitative trait locus analysis uncovers a genetic regulatory network of floral organ number in a tree peony (Paeonia suffruticosa Andrews) breeding population
inferred← citeshttps://doi.org/10.1093/jxb/eraa050openalex-snapshot
Gynoecium size and ovule number are interconnected traits that impact seed yield
inferred← citeshttps://doi.org/10.1093/jxb/erab110openalex-snapshot
Cell identity specification in plants: lessons from flower development
inferred← citeshttps://doi.org/10.1093/jxb/erad135openalex-snapshot
An evo-devo view of the gynoecium
inferred← citeshttps://doi.org/10.1093/jxb/erae136openalex-snapshot
Molecular and genetic regulation of petal number variation
inferred← citeshttps://doi.org/10.1093/jxb/eraf535openalex-snapshot
Auxin and cytokinin regulate growth dynamics underlying carpel initiation in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erf082openalex-snapshot
Regulation of fruit dehiscence in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erh075openalex-snapshot
Changes in gene expression during meristem activation processes in Solanum tuberosum with a focus on the regulation of an auxin response factor gene*
inferred← citeshttps://doi.org/10.1093/jxb/erl188openalex-snapshot
Patterning the female side of Arabidopsis: the importance of hormones
inferred← citeshttps://doi.org/10.1093/jxb/erm215openalex-snapshot
The conserved cysteine-rich domain of a tesmin/TSO1-like protein binds zinc in vitro and TSO1 is required for both male and female fertility in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/jxb/erp230openalex-snapshot
Genome-wide analysis of the auxin-responsive transcriptome downstream of iaa1 and its expression analysis reveal the diversity and complexity of auxin-regulated gene expression
inferred← citeshttps://doi.org/10.1093/jxb/erq015openalex-snapshot
Regulation of tissue-specific expression of SPATULA, a bHLH gene involved in carpel development, seedling germination, and lateral organ growth in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/err127openalex-snapshot
Auxin regulation of Arabidopsis flower development involves members of the AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) family
inferred← citeshttps://doi.org/10.1093/jxb/ert099openalex-snapshot
Auxin and the Arabidopsis thaliana gynoecium
inferred← citeshttps://doi.org/10.1093/jxb/ert190openalex-snapshot
Genome-wide transcriptomic analysis of the sporophyte of the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1093/jxb/ert479openalex-snapshot
Role of the FUL–SHP network in the evolution of fruit morphology and function
inferred← citeshttps://doi.org/10.1093/jxb/eru233openalex-snapshot
The (r)evolution of gene regulatory networks controlling Arabidopsis plant reproduction: a two-decade history
inferred← citeshttps://doi.org/10.1093/jxb/erv256openalex-snapshot
The importance of localized auxin production for morphogenesis of reproductive organs and embryos inArabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erv444openalex-snapshot
Gene networks controlling petal organogenesis
inferred← citeshttps://doi.org/10.1093/jxb/erx237openalex-snapshot
Auxin Response Factors: output control in auxin biology
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