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TCP Transcription Factors Regulate the Activities of ASYMMETRIC LEAVES1 and miR164, as Well as the Auxin Response, during Differentiation of Leaves inArabidopsis
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Outgoing claims: the papers this work cites, builds on, or argues with.
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A MORPHOGENETIC STUDY OF LANCEOLATE, A LEAF‐SHAPE MUTANT IN THE TOMATO
inferredcites →https://doi.org/10.1002/j.1537-2197.1964.tb06628.xopenalex-snapshot
DOSAGE EFFECTS OF THE LANCEOLATE GENE IN TOMATO
inferredcites →https://doi.org/10.1002/j.1537-2197.1968.tb07481.xopenalex-snapshot
MORPHOGENETIC ASPECTS OF A LEAFLESS MUTANT IN TOMATO I. GENERAL PATTERNS IN DEVELOPMENT
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Genetics of Aux/IAA and ARF action in plant growth and development
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Cell Differentiation and Organ Initiation at the Shoot Apical Meristem
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The BELL1 gene encodes a homeodomain protein involved in pattern formation in the Arabidopsis ovule primordium
inferredcites →https://doi.org/10.1016/j.cell.2005.04.004openalex-snapshot
microRNA-Directed Phasing during Trans-Acting siRNA Biogenesis in Plants
inferredcites →https://doi.org/10.1016/j.cub.2003.09.004openalex-snapshot
The Arabidopsis Heterochronic Gene ZIPPY Is an ARGONAUTE Family Member
inferredcites →https://doi.org/10.1016/j.cub.2005.09.052openalex-snapshot
Patterns of Auxin Transport and Gene Expression during Primordium Development Revealed by Live Imaging of the Arabidopsis Inflorescence Meristem
inferredcites →https://doi.org/10.1016/j.cub.2006.03.035openalex-snapshot
DRB4-Dependent TAS3 trans-Acting siRNAs Control Leaf Morphology through AGO7
inferredcites →https://doi.org/10.1016/j.cub.2006.03.064openalex-snapshot
Specification of Leaf Polarity in Arabidopsis via the trans-Acting siRNA Pathway
inferredcites →https://doi.org/10.1016/j.cub.2006.03.065openalex-snapshot
Regulation of AUXIN RESPONSE FACTOR3 by TAS3 ta-siRNA Affects Developmental Timing and Patterning in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2004.12.001openalex-snapshot
The evolutionary dynamics of plant duplicate genes
inferredcites →https://doi.org/10.1016/j.tplants.2009.11.003openalex-snapshot
TCP genes: a family snapshot ten years later
inferredcites →https://doi.org/10.1016/s0092-8674(00)81051-xopenalex-snapshot
The Making of a Compound Leaf: Genetic Manipulation of Leaf Architecture in Tomato
inferredcites →https://doi.org/10.1016/s0092-8674(00)81439-7openalex-snapshot
The PHANTASTICA Gene Encodes a MYB Transcription Factor Involved in Growth and Dorsoventrality of Lateral Organs in Antirrhinum
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1016/s0960-9822(02)01125-9openalex-snapshot
The Gibberellin Pathway Mediates KNOTTED1-Type Homeobox Function in Plants with Different Body Plans
inferredcites →https://doi.org/10.1023/a:1015207114117openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferredcites →https://doi.org/10.1023/a:1015255030047openalex-snapshot
Genetics of Aux/IAA and ARF action in plant growth and development
inferredcites →https://doi.org/10.1023/b:plan.0000009297.37235.4aopenalex-snapshot
An Arabidopsis thaliana T-DNA mutagenized population (GABI-Kat) for flanking sequence tag-based reverse genetics
inferredcites →https://doi.org/10.1038/35050091openalex-snapshot
Asymmetric leaves1 mediates leaf patterning and stem cell function in Arabidopsis
inferredcites →https://doi.org/10.1038/nature01198openalex-snapshot
Role of duplicate genes in genetic robustness against null mutations
inferredcites →https://doi.org/10.1038/nature01958openalex-snapshot
Control of leaf morphogenesis by microRNAs
inferredcites →https://doi.org/10.1038/ng.189openalex-snapshot
A developmental framework for dissected leaf formation in the Arabidopsis relative Cardamine hirsuta
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/ng2036openalex-snapshot
Regulation of LANCEOLATE by miR319 is required for compound-leaf development in tomato
inferredcites →https://doi.org/10.1038/sj.emboj.7600659openalex-snapshot
Developmental specificity of auxin response by pairs of ARF and Aux/IAA transcriptional regulators
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00868.xopenalex-snapshot
An estrogen receptor‐based transactivator XVE mediates highly inducible gene expression in transgenic plants
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01294.xopenalex-snapshot
DNA binding and dimerization specificity and potential targets for the TCP protein family
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01759.xopenalex-snapshot
Dominant repression of target genes by chimeric repressors that include the EAR motif, a repression domain, in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01911.xopenalex-snapshot
CUC1 gene activates the expression of SAM‐related genes to induce adventitious shoot formation
inferredcites →https://doi.org/10.1073/pnas.0507782103openalex-snapshot
Buffering of crucial functions by paleologous duplicated genes may contribute cyclicality to angiosperm genome duplication
inferredcites →https://doi.org/10.1073/pnas.0809761106openalex-snapshot
NPY genes and AGC kinases define two key steps in auxin-mediated organogenesis in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0908718106openalex-snapshot
miR319a targeting of TCP4 is critical for petal growth and development in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1530509100openalex-snapshot
Statistical significance for genomewide studies
inferredcites →https://doi.org/10.1101/gad.1402406openalex-snapshot
Control of leaf vascular patterning by polar auxin transport
inferredcites →https://doi.org/10.1101/gad.1415106openalex-snapshot
Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.229402openalex-snapshot
The Arabidopsis BODENLOS gene encodes an auxin response protein inhibiting MONOPTEROS-mediated embryo patterning
inferredcites →https://doi.org/10.1104/pp.107.113787openalex-snapshot
Arabidopsis Genes AS1 , AS2 , and JAG Negatively Regulate Boundary-Specifying Genes to Promote Sepal and Petal Development
inferredcites →https://doi.org/10.1104/pp.109.143875openalex-snapshot
SAUR39, a Small Auxin-Up RNA Gene, Acts as a Negative Regulator of Auxin Synthesis and Transport in Rice
inferredcites →https://doi.org/10.1105/tpc.010283openalex-snapshot
Arabidopsis SHY2/IAA3 Inhibits Auxin-Regulated Gene Expression
inferredcites →https://doi.org/10.1105/tpc.012203openalex-snapshot
The CUP-SHAPED COTYLEDON3 Gene Is Required for Boundary and Shoot Meristem Formation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.013557openalex-snapshot
The Arabidopsis Auxin-Inducible Gene ARGOS Controls Lateral Organ Size
inferredcites →https://doi.org/10.1105/tpc.016014openalex-snapshot
Genetic Regulation of Embryonic Pattern Formation
inferredcites →https://doi.org/10.1105/tpc.105.035477openalex-snapshot
Maize rough sheath2 and Its Arabidopsis Orthologue ASYMMETRIC LEAVES1 Interact with HIRA, a Predicted Histone Chaperone, to Maintain knox Gene Silencing and Determinacy during Organogenesis
inferredcites →https://doi.org/10.1105/tpc.106.042325openalex-snapshot
Histone Deacetylases and ASYMMETRIC LEAVES2 Are Involved in the Establishment of Polarity in Leaves ofArabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.044792openalex-snapshot
TCP Transcription Factors Control the Morphology of Shoot Lateral Organs via Negative Regulation of the Expression of Boundary-Specific Genes inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.045617openalex-snapshot
The Balance between the MIR164A and CUC2 Genes Controls Leaf Margin Serration in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.045716openalex-snapshot
Arabidopsis CUP-SHAPED COTYLEDON3 Regulates Postembryonic Shoot Meristem and Organ Boundary Formation
inferredcites →https://doi.org/10.1105/tpc.106.047472openalex-snapshot
KANADI and Class III HD-Zip Gene Families Regulate Embryo Patterning and Modulate Auxin Flow during Embryogenesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.047761openalex-snapshot
ARF7 and ARF19 Regulate Lateral Root Formation via Direct Activation of LBD/ASL Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.048769openalex-snapshot
TheArabidopsisBEL1-LIKE HOMEODOMAIN Proteins SAW1 and SAW2 Act Redundantly to RegulateKNOXExpression Spatially in Leaf Margins
inferredcites →https://doi.org/10.1105/tpc.107.056127openalex-snapshot
Direct Repression of KNOX Loci by the ASYMMETRIC LEAVES1 Complex of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.057521openalex-snapshot
A Protracted and Dynamic Maturation Schedule Underlies Arabidopsis Leaf Development
inferredcites →https://doi.org/10.1105/tpc.109.065482openalex-snapshot
The NGATHA Distal Organ Development Genes Are Essential for Style Specification in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.065508openalex-snapshot
The NGATHA Genes Direct Style Development in the Arabidopsis Gynoecium
inferredcites →https://doi.org/10.1105/tpc.11.10.1841openalex-snapshot
Multiple Independent Defective Suppressor-mutator Transposon Insertions in Arabidopsis: A Tool for Functional Genomics
inferredcites →https://doi.org/10.1105/tpc.12.3.393openalex-snapshot
Arabidopsis Ethylene-Responsive Element Binding Factors Act as Transcriptional Activators or Repressors of GCC Box–Mediated Gene Expression
inferredcites →https://doi.org/10.1105/tpc.9.11.1963openalex-snapshot
Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements.
inferredcites →https://doi.org/10.1105/tpc.9.6.841openalex-snapshot
Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03132.xopenalex-snapshot
Expression of the ASYMMETRIC LEAVES2 gene in the adaxial domain of Arabidopsis leaves represses cell proliferation in this domain and is critical for the development of properly expanded leaves
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03796.xopenalex-snapshot
A microRNA–transcription factor module regulates lateral organ size and patterning in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1467-7652.2006.00184.xopenalex-snapshot
Efficient production of male and female sterile plants by expression of a chimeric repressor in Arabidopsis and rice
inferredcites →https://doi.org/10.1126/science.1079354openalex-snapshot
Genetic Control of Surface Curvature
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1164147openalex-snapshot
A Genetic Framework for the Control of Cell Division and Differentiation in the Root Meristem
inferredcites →https://doi.org/10.1126/science.1166168openalex-snapshot
A Conserved Molecular Framework for Compound Leaf Development
inferredcites →https://doi.org/10.1126/science.284.5411.151openalex-snapshot
ROUGH SHEATH2: A Myb Protein That Represses knox Homeobox Genes in Maize Lateral Organ Primordia
inferredcites →https://doi.org/10.1126/science.284.5411.154openalex-snapshot
The Maize rough sheath2 Gene and Leaf Development Programs in Monocot and Dicot Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105356openalex-snapshot
Patterning and Polarity in Seed Plant Shoots
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.031803.093824openalex-snapshot
THE ROLE OF KNOX GENES IN PLANT DEVELOPMENT
inferredcites →https://doi.org/10.1242/dev.01279openalex-snapshot
PETAL LOSS , a trihelix transcription factor gene, regulates perianth architecture in the Arabidopsis flower
inferredcites →https://doi.org/10.1242/dev.01338openalex-snapshot
Compound leaves: equal to the sum of their parts?
inferredcites →https://doi.org/10.1242/dev.01388openalex-snapshot
PIN-FORMED1andPINOIDregulate boundary formation and cotyledon development inArabidopsisembryogenesis
inferredcites →https://doi.org/10.1242/dev.02491openalex-snapshot
Trans-acting siRNA-mediated repression of ETTIN and ARF4 regulates heteroblasty in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.02545openalex-snapshot
ASYMMETRIC LEAVES1 and auxin activities converge to repressBREVIPEDICELLUSexpression and promote leaf development inArabidopsis
inferredcites →https://doi.org/10.1242/dev.02817openalex-snapshot
Redundancy and specialization among plant microRNAs: role of the MIR164 family in developmental robustness
inferredcites →https://doi.org/10.1242/dev.031625openalex-snapshot
The NAC-domain transcription factor GOBLET specifies leaflet boundaries in compound tomato leaves
inferredcites →https://doi.org/10.1242/dev.033811openalex-snapshot
Auxin patternsSolanum lycopersicumleaf morphogenesis
inferredcites →https://doi.org/10.1242/dev.125.15.2857openalex-snapshot
The rough sheath2 gene negatively regulates homeobox gene expression during maize leaf development
inferredcites →https://doi.org/10.1242/dev.126.4.711openalex-snapshot
Control of auxin-regulated root development by the Arabidopsis thaliana SHY2/IAA3 gene
inferredcites →https://doi.org/10.1242/dev.126.8.1563openalex-snapshot
Shoot apical meristem and cotyledon formation during Arabidopsis embryogenesis: interaction among the CUP-SHAPED COTYLEDON and SHOOT MERISTEMLESS genes
inferredcites →https://doi.org/10.1242/dev.127.24.5523openalex-snapshot
Mechanisms that control knox gene expression in the Arabidopsis shoot
inferredcites →https://doi.org/10.1242/dev.128.10.1771openalex-snapshot
The ASYMMETRIC LEAVES2 gene of Arabidopsis thaliana regulates formation of a symmetric lamina, establishment of venation and repression of meristem-related homeobox genes in leaves
inferredcites →https://doi.org/10.1371/journal.pbio.0060230openalex-snapshot
Control of Jasmonate Biosynthesis and Senescence by miR319 Targets
inferredcites →https://doi.org/10.1387/ijdb.041921htopenalex-snapshot
Leaf shape: genetic controls and environmental factors
inferredcites →https://doi.org/10.2307/3870557openalex-snapshot
Aux/IAA Proteins Repress Expression of Reporter Genes Containing Natural and Highly Active Synthetic Auxin Response Elements
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s12033-023-00713-2openalex-snapshot
miRNAs and Their Target Genes Play a Critical Role in Response to Heat Stress in Cynodon dactylon (L.) Pers.
inferred← citeshttps://doi.org/10.1007/s12042-017-9197-4openalex-snapshot
Phylogeny and Molecular Evolution of miR820 and miR396 microRNA Families in Oryza AA Genomes
inferred← citeshttps://doi.org/10.1007/s12042-020-09274-zopenalex-snapshot
TCP Genes and the Orchestration of Plant Architecture
inferred← citeshttps://doi.org/10.1007/s13205-025-04273-xopenalex-snapshot
Genome-wide identification and expression analysis of the TCP transcription factor family and its response to abiotic stress in rapeseed (Brassica napus L.)
inferred← citeshttps://doi.org/10.1007/s13237-023-00447-1openalex-snapshot
Implications of small RNAs in plant development, abiotic stress response and crop improvement in changing climate
inferred← citeshttps://doi.org/10.1007/s40502-017-0326-8openalex-snapshot
MicroRNAs: potential target for genome editing in plants for traits improvement
inferred← citeshttps://doi.org/10.1016/b978-0-12-800854-6.00009-9openalex-snapshot
TCP Transcription Factors: Evolution, Structure, and Biochemical Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-800854-6.00015-4openalex-snapshot
CUC Transcription Factors: To the Meristem and Beyond
inferred← citeshttps://doi.org/10.1016/b978-0-12-800854-6.00016-6openalex-snapshot
The Role of TCP Transcription Factors in Shaping Flower Structure, Leaf Morphology, and Plant Architecture
inferred← citeshttps://doi.org/10.1016/b978-0-12-802259-7.00021-xopenalex-snapshot
Negative Regulators of Messenger RNA and the Role of microRNA for Plant Genetic Engineering
inferred← citeshttps://doi.org/10.1016/b978-0-12-817112-7.00013-4openalex-snapshot
Regulation of photosynthesis and vegetative growth of plants by small RNAs
inferred← citeshttps://doi.org/10.1016/b978-0-12-818581-0.00003-6openalex-snapshot
Tweaking microRNA-mediated gene regulation for crop improvement
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.02.003openalex-snapshot
Phytohormones and microRNAs as sensors and regulators of leaf senescence: Assigning macro roles to small molecules
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.12.002openalex-snapshot
The molecular path to in vitro shoot regeneration
inferred← citeshttps://doi.org/10.1016/j.cj.2020.07.007openalex-snapshot
Roles of miR319-regulated TCPs in plant development and response to abiotic stress
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2018.11.009openalex-snapshot
Genome-wide identification and expression analysis of StTCP transcription factors of potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.1016/j.cub.2014.09.058openalex-snapshot
Temporal Control of Leaf Complexity by miRNA-Regulated Licensing of Protein Complexes
inferred← citeshttps://doi.org/10.1016/j.cub.2015.05.024openalex-snapshot
Temporal Control of Plant Organ Growth by TCP Transcription Factors
inferred← citeshttps://doi.org/10.1016/j.cub.2016.12.016openalex-snapshot
Plant Stress Tolerance Requires Auxin-Sensitive Aux/IAA Transcriptional Repressors
inferred← citeshttps://doi.org/10.1016/j.gene.2013.08.091openalex-snapshot
Transcriptomic analysis of incised leaf-shape determination in birch
inferred← citeshttps://doi.org/10.1016/j.gene.2019.03.059openalex-snapshot
Genome-wide identification of members of the TCP gene family in switchgrass (Panicum virgatum L.) and analysis of their expression
inferred← citeshttps://doi.org/10.1016/j.hpj.2022.09.005openalex-snapshot
CsIPT1b and CsUGT85A2 delay female corolla opening in cucumber by regulating the content of cytokinins
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.08.002openalex-snapshot
Expression changes of miRNA-regulated genes associated with the formation of the leafy head in cabbage
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.130471openalex-snapshot
Comparative analysis of PLATZ transcription factors in six poplar species and analysis of the role of PtrPLATZ14 in leaf development
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.132544openalex-snapshot
BnaC06.WIP2-BnaA09.STM transcriptional regulatory module promotes leaf lobe formation in Brassica napus
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.118521openalex-snapshot
The overexpression of the BpTCP20 gene enhances cell proliferation and improves tolerance to drought and salt stress in Betula platyphylla
inferred← citeshttps://doi.org/10.1016/j.isci.2019.04.005openalex-snapshot
Arabidopsis Transcription Factor TCP5 Controls Plant Thermomorphogenesis by Positively Regulating PIF4 Activity
inferred← citeshttps://doi.org/10.1016/j.jare.2022.12.010openalex-snapshot
Physiological Control and Genetic Basis of Leaf Curvature and Heading in Brassica rapa L
inferred← citeshttps://doi.org/10.1016/j.jplph.2015.05.006openalex-snapshot
Plant development regulation: Overview and perspectives
inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153224openalex-snapshot
Identification of candidate miRNAs related in storage root development of sweet potato by high throughput sequencing
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.11.005openalex-snapshot
Regulation of plant lateral-organ growth by modulating cell number and size
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.11.013openalex-snapshot
How boundaries control plant development
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.06.018openalex-snapshot
Transcriptional networks in leaf senescence
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.11.006openalex-snapshot
The role of small RNAs in vegetative shoot development
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.05.006openalex-snapshot
TCP factors: new kids on the signaling block
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.10.003openalex-snapshot
Control of cell proliferation by microRNAs in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.08.002openalex-snapshot
Molecular cartography of leaf development — role of transcription factors
inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102647openalex-snapshot
Diversity and development of domatia: Symbiotic plant structures to host mutualistic ants or mites
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102872openalex-snapshot
The coupling of local and global growth patterns governs leaf morphogenesis
inferred← citeshttps://doi.org/10.1016/j.pbi.2026.102915openalex-snapshot
How to grow a leaf: Generating, maintaining, and modulating flatness
inferred← citeshttps://doi.org/10.1016/j.plantsci.2013.10.019openalex-snapshot
BLADE-ON-PETIOLE genes: Setting boundaries in development and defense
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.10.009openalex-snapshot
miR393 inhibits in vitro shoot regeneration in Arabidopsis thaliana via repressing TIR1
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.08.006openalex-snapshot
A hidden link between leaf development and senescence
inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110681openalex-snapshot
Roles of CsBRC1-like in leaf and lateral branch development in cucumber
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113000openalex-snapshot
A series of BrGA1 allelic mutations impair gibberellin biosynthesis to affect heading in Chinese cabbage
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.03.020openalex-snapshot
Soybean TCP transcription factors: Evolution, classification, protein interaction and stress and hormone responsiveness
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.02.015openalex-snapshot
The regulatory effects of MeTCP4 on cold stress tolerance in Arabidopsis thaliana: A transcriptome analysis
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.01.049openalex-snapshot
Flowering under enhanced ionising radiation conditions and its regulation through epigenetic mechanisms
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107906openalex-snapshot
Identification and characterization of long noncoding RNAs in two contrasting olive (Olea europaea L.) genotypes subjected to aluminum toxicity
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108094openalex-snapshot
Construction of transcription factor mutagenesis population in tomato using a pooled CRISPR/Cas9 plasmid library
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110508openalex-snapshot
miR164-targets involved in plant biological processes and stress response: A review
inferred← citeshttps://doi.org/10.1016/j.scienta.2015.10.027openalex-snapshot
Evidence for the biological function of miR403 in tomato development
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111055openalex-snapshot
Unravelling new roles of a tomato SIN3 homolog in leaf polarity mediated by auxin signaling and leaf growth-related transcription factors
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112306openalex-snapshot
LfiTCP15;2 regulates plant height of Lagerstroemia indica by influencing the growth of stem cells
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112362openalex-snapshot
Integrated transcriptomics and metabolomics analyses provide insights into the mechanisms of capitulum architecture in Argyranthemum frutescens (Asteraceae)
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114974openalex-snapshot
SlTCP24 regulates tomato leaf morphology, fruit quality, and productivity via the auxin signaling pathway
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.03.001openalex-snapshot
MicroRNA networks and developmental plasticity in plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.01.005openalex-snapshot
TCP three-way handshake: linking developmental processes with plant immunity
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.09.009openalex-snapshot
Small RNAs: Big Impact on Plant Development
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.08.019openalex-snapshot
Is auxin enough? Cytokinins and margin patterning in simple leaves
inferred← citeshttps://doi.org/10.1016/j.tplants.2026.05.014openalex-snapshot
Bilateral symmetry genes: If they exist, how would we know?
inferred← citeshttps://doi.org/10.1016/j.virusres.2012.11.003openalex-snapshot
Gene expression responses to Rice tungro spherical virus in susceptible and resistant near-isogenic rice plants
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100309openalex-snapshot
Arabidopsis transcription factor TCP4 represses chlorophyll biosynthesis to prevent petal greening
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.102095openalex-snapshot
The ZmMIR319A–ZmTCP5/44 module bifurcates into two pathways to coordinately regulate leaf angle and thermotolerance in maize
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c00478openalex-snapshot
Epigenomic Regulatory Mechanism in Vegetative Phase Transition of Malus hupehensis
inferred← citeshttps://doi.org/10.1038/cr.2014.145openalex-snapshot
The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
inferred← citeshttps://doi.org/10.1038/s41438-020-0241-4openalex-snapshot
A CIN-like TCP transcription factor (LsTCP4) having retrotransposon insertion associates with a shift from Salinas type to Empire type in crisphead lettuce (Lactuca sativa L.)
inferred← citeshttps://doi.org/10.1038/s41438-021-00538-7openalex-snapshot
CsTCPs regulate shoot tip development and catechin biosynthesis in tea plant (Camellia sinensis)
inferred← citeshttps://doi.org/10.1038/s41467-023-41416-1openalex-snapshot
Arabidopsis TCP4 transcription factor inhibits high temperature-induced homeotic conversion of ovules
inferred← citeshttps://doi.org/10.1038/s41477-021-00965-3openalex-snapshot
Active suppression of leaflet emergence as a mechanism of simple leaf development
inferred← citeshttps://doi.org/10.1038/s41598-017-10609-2openalex-snapshot
Genome-wide identification and characterization of TCP transcription factor genes in upland cotton (Gossypium hirsutum)
inferred← citeshttps://doi.org/10.1038/s41598-019-45003-7openalex-snapshot
Identification of a binding protein for sesamin and characterization of its roles in plant growth
inferred← citeshttps://doi.org/10.1038/s41598-024-83985-1openalex-snapshot
Regulation of meristem and hormone function revealed through analysis of directly-regulated SHOOT MERISTEMLESS target genes
inferred← citeshttps://doi.org/10.1038/s42003-020-01274-9openalex-snapshot
The genetic framework of shoot regeneration in Arabidopsis comprises master regulators and conditional fine-tuning factors
inferred← citeshttps://doi.org/10.1038/srep11093openalex-snapshot
High-throughput sequencing of small RNAs and anatomical characteristics associated with leaf development in celery
inferred← citeshttps://doi.org/10.1038/srep17617openalex-snapshot
An integrated network of Arabidopsis growth regulators and its use for gene prioritization
inferred← citeshttps://doi.org/10.1038/srep32795openalex-snapshot
Genome-wide Identification of TCP Family Transcription Factors from Populus euphratica and Their Involvement in Leaf Shape Regulation
inferred← citeshttps://doi.org/10.1039/c3mb70128jopenalex-snapshot
The intrinsically disordered C-terminal region of Arabidopsis thaliana TCP8 transcription factor acts both as a transactivation and self-assembly domain
inferred← citeshttps://doi.org/10.1042/bst20190441openalex-snapshot
Crop reproductive meristems in the genomic era: a brief overview
inferred← citeshttps://doi.org/10.1071/fp23320openalex-snapshot
Identification of cysteine-rich receptor-like kinase gene family in potato: revealed StCRLK9 in response to heat, salt and drought stresses
inferred← citeshttps://doi.org/10.1073/pnas.1713288114openalex-snapshot
Ancient polymorphisms and divergence hitchhiking contribute to genomic islands of divergence within a poplar species complex
inferred← citeshttps://doi.org/10.1073/pnas.2019698117openalex-snapshot
Upregulation of a KN1 homolog by transposon insertion promotes leafy head development in lettuce
inferred← citeshttps://doi.org/10.1073/pnas.2303836120openalex-snapshot
Dynamics of cis -regulatory sequences and transcriptional divergence of duplicated genes in soybean
inferred← citeshttps://doi.org/10.1074/jbc.m111.256271openalex-snapshot
Determinants of the DNA Binding Specificity of Class I and Class II TCP Transcription Factors
inferred← citeshttps://doi.org/10.1080/15592324.2015.1044192openalex-snapshot
TheArabidopsis thalianaTCP transcription factors: A broadening horizon beyond development
inferred← citeshttps://doi.org/10.1080/15592324.2015.1071002openalex-snapshot
Dysfunctional mitochondria regulate the size of root apical meristem and leaf development in Arabidopsis
inferred← citeshttps://doi.org/10.1080/15592324.2021.1994248openalex-snapshot
Genome-wide identification and expression pattern analysis of the TCP transcription factor family in Ginkgo biloba
inferred← citeshttps://doi.org/10.1093/aob/mcx152openalex-snapshot
To be serrate or pinnate: diverse leaf forms of yarrows (Achillea) are linked to differential expression patterns of NAM genes
inferred← citeshttps://doi.org/10.1093/g3journal/jkab097openalex-snapshot
High-resolution genetic dissection of the major QTL for tipburn resistance in lettuce,Lactuca sativa
inferred← citeshttps://doi.org/10.1093/gbe/evx174openalex-snapshot
Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
inferred← citeshttps://doi.org/10.1093/hr/uhaf032openalex-snapshot
Wo interacts with SlTCP25 to regulate type I trichome branching in tomato
inferred← citeshttps://doi.org/10.1093/hr/uhaf095openalex-snapshot
CmARF3 – CmTCP7 module regulates flowering time in chrysanthemum ( Chrysanthemum morifolium )
inferred← citeshttps://doi.org/10.1093/hr/uhaf281openalex-snapshot
Integrated single-nucleus transcriptomic and metabolomic insights into bud-to-leaf development and metabolite synthesis in tea plant
inferred← citeshttps://doi.org/10.1093/jxb/eraa056openalex-snapshot
Dynamic regulation of anthocyanin biosynthesis at different light intensities by the BT2-TCP46-MYB1 module in apple
inferred← citeshttps://doi.org/10.1093/jxb/eraa569openalex-snapshot
TCP5 controls leaf margin development by regulating KNOX and BEL-like transcription factors in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erac156openalex-snapshot
Physiological and genetic control of transpiration efficiency in African rice, Oryza glaberrima Steud
inferred← citeshttps://doi.org/10.1093/jxb/erad402openalex-snapshot
Arabidopsis transcription factor TCP13 promotes shade avoidance syndrome-like responses by directly targeting a subset of shade-responsive gene promoters
inferred← citeshttps://doi.org/10.1093/jxb/eraf203openalex-snapshot
An overview of low-oxygen sensing and flooding responses of tomato
inferred← citeshttps://doi.org/10.1093/jxb/err305openalex-snapshot
The class I protein AtTCP15 modulates plant development through a pathway that overlaps with the one affected by CIN-like TCP proteins
inferred← citeshttps://doi.org/10.1093/jxb/ert337openalex-snapshot
Analysis of functional redundancies within the Arabidopsis TCP transcription factor family
inferred← citeshttps://doi.org/10.1093/jxb/eru002openalex-snapshot
miRNAs in the crosstalk between phytohormone signalling pathways
inferred← citeshttps://doi.org/10.1093/jxb/eru327openalex-snapshot
Flower opening and closure: an update
inferred← citeshttps://doi.org/10.1093/jxb/eru399openalex-snapshot
Protein import into plant mitochondria: signals, machinery, processing, and regulation
inferred← citeshttps://doi.org/10.1093/jxb/erv015openalex-snapshot
The tarani mutation alters surface curvature in Arabidopsis leaves by perturbing the patterns of surface expansion and cell division
inferred← citeshttps://doi.org/10.1093/jxb/erv103openalex-snapshot
Genome-wide analysis reveals dynamic changes in expression of microRNAs during vascular cambium development in Chinese fir, Cunninghamia lanceolata
inferred← citeshttps://doi.org/10.1093/jxb/erv238openalex-snapshot
Identification of jasmonic acid-associated microRNAs and characterization of the regulatory roles of the miR319/TCP4 module under root-knot nematode stress in tomato
inferred← citeshttps://doi.org/10.1093/jxb/erv444openalex-snapshot
Gene networks controlling petal organogenesis
inferred← citeshttps://doi.org/10.1093/jxb/erw273openalex-snapshot
Genome-wide identification and characterization ofTCPgenes involved in ovule development ofPhalaenopsis equestris
inferred← citeshttps://doi.org/10.1093/jxb/erw419openalex-snapshot
RABBIT EARS regulates the transcription of TCP4 during petal development in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erx345openalex-snapshot
Genetic redundancy of senescence-associated transcription factors in Arabidopsis
inferred← citeshttps://doi.org/10.1093/mp/sss160openalex-snapshot
Addressing the Role of microRNAs in Reprogramming Leaf Growth during Drought Stress in Brachypodium distachyon
inferred← citeshttps://doi.org/10.1093/mp/ssu084openalex-snapshot
Repression of Cell Proliferation by miR319-Regulated TCP4
inferred← citeshttps://doi.org/10.1093/pcp/pcaa083openalex-snapshot
De Novo Shoot Regeneration Controlled by HEN1 and TCP3/4 in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcr062openalex-snapshot
Isoquinoline Alkaloid Biosynthesis is Regulated by a Unique bHLH-Type Transcription Factor in Coptis japonica
inferred← citeshttps://doi.org/10.1093/pcp/pcs057openalex-snapshot
Interactions of CUP-SHAPED COTYLEDON and SPATULA Genes Control Carpel Margin Development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/pcp/pcs080openalex-snapshot
Regulation of Leaf Morphology by MicroRNA394 and its Target LEAF CURLING RESPONSIVENESS
inferred← citeshttps://doi.org/10.1093/pcp/pcs118openalex-snapshot
Transcriptome-Wide Characterization of miRNA-Directed and Non-miRNA-Directed Endonucleolytic Cleavage Using Degradome Analysis Under Low Ambient Temperature in Phalaenopsis aphrodite subsp. formosana
inferred← citeshttps://doi.org/10.1093/pcp/pcw081openalex-snapshot
Generation of Novel Floral Traits Using a Combination of Floral Organ-Specific Promoters and a Chimeric Repressor inTorenia fournieriLind.
inferred← citeshttps://doi.org/10.1093/pcp/pcx023openalex-snapshot
Hormone Distribution and Transcriptome Profiles in Bamboo Shoots Provide Insights on Bamboo Stem Emergence and Growth
inferred← citeshttps://doi.org/10.1093/pcp/pcz179openalex-snapshot
Integrated mRNA, MicroRNA Transcriptome and Degradome Analyses Provide Insights into Stamen Development in Moso Bamboo
inferred← citeshttps://doi.org/10.1093/pcp/pcz233openalex-snapshot
The AtHB1 Transcription Factor Controls the miR164-CUC2 Regulatory Node to Modulate Leaf Development
inferred← citeshttps://doi.org/10.1093/plcell/koae107openalex-snapshot
Arabidopsis transcription factor TCP4 controls the identity of the apical gynoecium
inferred← citeshttps://doi.org/10.1093/plcell/koag020openalex-snapshot
The Arabidopsis transcription factor TCP4 controls seed size by repressing the MINI3-SHB1-IKU pathway
inferred← citeshttps://doi.org/10.1093/plcell/koag198openalex-snapshot
VvNUP96–VvTCP15 coupling regulates growth and salt tolerance via a VvmiR319c– VvTCP4 module in grapevine
inferred← citeshttps://doi.org/10.1093/plphys/kiab053openalex-snapshot
TCP transcription factors suppress cotyledon trichomes by impeding a cell differentiation-regulating complex
inferred← citeshttps://doi.org/10.1101/2020.08.19.257550openalex-snapshot
Collaboration of multiple pathways in making a compound leaf
inferred← citeshttps://doi.org/10.1101/2021.01.28.428559openalex-snapshot
MicroRNA775 targets a β-(1,3)-galactosyltransferase to regulate growth and development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/2021.11.28.470237openalex-snapshot
High-throughput phenotyping reveals a link between transpiration efficiency and transpiration restriction under high evaporative demand and new loci controlling water use-related traits in African rice, Oryza glaberrima Steud
inferred← citeshttps://doi.org/10.1101/2022.11.01.514736openalex-snapshot
Cell growth rates coordinate across the width of the leaf to remain flat
inferred← citeshttps://doi.org/10.1101/2024.09.07.611804openalex-snapshot
MIR319C activation by CUP-SHAPED COTYLEDON2 delays cell proliferation-to-differentiation transition in Arabidopsis leaf primordia
inferred← citeshttps://doi.org/10.1101/747790openalex-snapshot
Specific Regulation of TCP genes by miR319
inferred← citeshttps://doi.org/10.1104/pp.111.188789openalex-snapshot
Transcriptional Regulation of ArabidopsisMIR168aandARGONAUTE1Homeostasis in Abscisic Acid and Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1104/pp.112.200303openalex-snapshot
Arabidopsis Class I and Class II TCP Transcription Factors Regulate Jasmonic Acid Metabolism and Leaf Development Antagonistically
inferred← citeshttps://doi.org/10.1104/pp.112.208702openalex-snapshot
Constitutive Expression of a miR319 Gene Alters Plant Development and Enhances Salt and Drought Tolerance in Transgenic Creeping Bentgrass
inferred← citeshttps://doi.org/10.1104/pp.113.215673openalex-snapshot
The Cotton Transcription Factor TCP14 Functions in Auxin-Mediated Epidermal Cell Differentiation and Elongation
inferred← citeshttps://doi.org/10.1104/pp.113.218115openalex-snapshot
A Regulatory Cascade Involving Class II ETHYLENE RESPONSE FACTOR Transcriptional Repressors Operates in the Progression of Leaf Senescence
inferred← citeshttps://doi.org/10.1104/pp.114.237495openalex-snapshot
A Functional Antagonistic Relationship between Auxin and Mitochondrial Retrograde Signaling Regulates Alternative Oxidase1a Expression in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.15.00899openalex-snapshot
Constitutive Expression of Rice MicroRNA528 Alters Plant Development and Enhances Tolerance to Salinity Stress and Nitrogen Starvation in Creeping Bentgrass
inferred← citeshttps://doi.org/10.1104/pp.15.01181openalex-snapshot
Distinct Regulatory Changes Underlying Differential Expression of TEOSINTE BRANCHED1-CYCLOIDEA-PROLIFERATING CELL FACTOR Genes Associated with Petal Variations in Zygomorphic Flowers of Petrocosmea spp. of the Family Gesneriaceae
inferred← citeshttps://doi.org/10.1104/pp.16.00209openalex-snapshot
Integration of Hormonal and Nutritional Cues Orchestrates Progressive Corolla Opening
inferred← citeshttps://doi.org/10.1104/pp.16.00332openalex-snapshot
Regulation of microRNA-mediated developmental changes by the SWR1 chromatin remodeling complex in Arabidopsis thaliana
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