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The axr6 mutants of Arabidopsis thaliana define a gene involved in auxin response and early development
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jmbi.1995.0454openalex-snapshot
ThePS-IAA4/5-like Family of Early Auxin-inducible mRNAs inArabidopsis thaliana
inferredcites →https://doi.org/10.1007/978-94-011-0473-9_25openalex-snapshot
The Induction of Vascular Tissues by Auxin and Cytokinin
inferredcites →https://doi.org/10.1007/bf00208313openalex-snapshot
Studies on the role of the Arabidopsis gene MONOPTEROS in vascular development and plant cell axialization
inferredcites →https://doi.org/10.1007/bf00484337openalex-snapshot
Mutants of Arabidopsis thaliana with altered responses to auxins and gravity
inferredcites →https://doi.org/10.1007/bf00633843openalex-snapshot
A dominant mutation inArabidopsis confers resistance to auxin, ethylene and abscisic acid
inferredcites →https://doi.org/10.1016/0045-6039(87)90448-9openalex-snapshot
Unusual patterns of somatic embryogenesis in the domesticated carrot: developmental effects of exogenous auxins and auxin transport inhibitors
inferredcites →https://doi.org/10.1016/s1360-1385(97)90054-6openalex-snapshot
Down and out in Arabidopsis: the formation of lateral roots
inferredcites →https://doi.org/10.1038/27240openalex-snapshot
Suppression of auxin signal transduction by a MAPK cascade in higher plants
inferredcites →https://doi.org/10.1038/364161a0openalex-snapshot
Arabidopsis auxin-resistance gene AXR1 encodes a protein related to ubiquitin-activating enzyme E1
inferredcites →https://doi.org/10.1038/375676a0openalex-snapshot
Normal differentiation patterns in plants lacking microtubular preprophase bands
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.5010111.xopenalex-snapshot
Characterization of two cDNAs that encode MAP kinase homologues in Arabidopsis thaliana and analysis of the possible role of auxin in activating such kinase activities in cultured cells
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.5010149.xopenalex-snapshot
An Arabidopsis thaliana RFLP mapping set to localize mutations to chromosomal regions
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.7020211.xopenalex-snapshot
The axr4 auxin‐resistant mutants of Arabidopsis thaliana define a gene important for root gravitropism and lateral root initiation
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.10030403.xopenalex-snapshot
Mutations in the AXR3 gene of Arabidopsis result in altered auxin response including ectopic expression from the SAUR‐AC1 promoter
inferredcites →https://doi.org/10.1046/j.1365-313x.1996.9050659.xopenalex-snapshot
Influence of auxin on the establishment of bilateral symmetry in monocots
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00283.xopenalex-snapshot
Cytosolic acidification but not auxin at physiological concentration is an activator of MAP kinases in tobacco cells
inferredcites →https://doi.org/10.1073/pnas.91.1.326openalex-snapshot
Early auxin-induced genes encode short-lived nuclear proteins.
inferredcites →https://doi.org/10.1073/pnas.96.10.5844openalex-snapshot
Activation and repression of transcription by auxin-response factors
inferredcites →https://doi.org/10.1093/emboj/17.5.1405openalex-snapshot
The Arabidopsis gene MONOPTEROS encodes a transcription factor mediating embryo axis formation and vascular development
inferredcites →https://doi.org/10.1093/genetics/138.4.1239openalex-snapshot
The axr2-1 mutation of Arabidopsis thaliana is a gain-of-function mutation that disrupts an early step in auxin response.
inferredcites →https://doi.org/10.1101/gad.12.2.198openalex-snapshot
The TIR1 protein of Arabidopsis functions in auxin response and is related to human SKP2 and yeast Grr1p
inferredcites →https://doi.org/10.1104/pp.110.4.1109openalex-snapshot
Hormonal Studies of fass, an Arabidopsis Mutant That Is Altered in Organ Elongation
inferredcites →https://doi.org/10.1104/pp.117.1.113openalex-snapshot
Indole-3-Acetic Acid Controls Cambial Growth in Scots Pine by Positional Signaling1
inferredcites →https://doi.org/10.1104/pp.94.3.1462openalex-snapshot
The aux1 Mutation of Arabidopsis Confers Both Auxin and Ethylene Resistance
inferredcites →https://doi.org/10.1105/tpc.10.10.1649openalex-snapshot
age Mutants of Arabidopsis Exhibit Altered Auxin-Regulated Gene Expression
inferredcites →https://doi.org/10.1105/tpc.2.11.1071openalex-snapshot
Growth and Development of the axr1 Mutants of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.2.6.513openalex-snapshot
Exploiting the Triple Response of Arabidopsis to Identify Ethylene-Related Mutants
inferredcites →https://doi.org/10.1105/tpc.5.6.621openalex-snapshot
Auxin Polar Transport Is Essential for the Establishment of Bilateral Symmetry during Early Plant Embryogenesis.
inferredcites →https://doi.org/10.1105/tpc.7.9.1405openalex-snapshot
Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction.
inferredcites →https://doi.org/10.1105/tpc.8.9.1505openalex-snapshot
Hormones act downstream of TTG and GL2 to promote root hair outgrowth during epidermis development in the Arabidopsis root.
inferredcites →https://doi.org/10.1105/tpc.9.7.989openalex-snapshot
Embryogenesis: A New Start in Life.
inferredcites →https://doi.org/10.1126/science.279.5355.1371openalex-snapshot
Changes in Auxin Response from Mutations in an AUX/IAA Gene
inferredcites →https://doi.org/10.1126/science.280.5370.1760openalex-snapshot
The Ubiquitin-Related Protein RUB1 and Auxin Response in Arabidopsis
inferredcites →https://doi.org/10.1126/science.282.5391.1114openalex-snapshot
Auxin-Dependent Cell Expansion Mediated by Overexpressed Auxin-Binding Protein 1
inferredcites →https://doi.org/10.1242/dev.118.2.575openalex-snapshot
The role of the monopteros gene in organising the basal body region of the Arabidopsis embryo
inferredcites →https://doi.org/10.1242/dev.120.10.2967openalex-snapshot
Mutations in the FASS gene uncouple pattern formation and morphogenesis in Arabidopsis development
inferredcites →https://doi.org/10.1242/dev.120.9.2475openalex-snapshot
Embryonic origin of the Arabidopsis primary root and root meristem initials
inferredcites →https://doi.org/10.1242/dev.122.2.481openalex-snapshot
The tangled-1 mutation alters cell division orientations throughout maize leaf development without altering leaf shape
inferredcites →https://doi.org/10.1242/dev.125.5.879openalex-snapshot
Auxin-induced developmental patterns in Brassica juncea embryos
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.126.7.1387openalex-snapshot
The auxin-insensitive bodenlos mutation affects primary root formation and apical-basal patterning in the Arabidopsis embryo
inferredcites →https://doi.org/10.2307/3869805openalex-snapshot
Auxin Polar Transport Is Essential for the Establishment of Bilateral Symmetry during Early Plant Embryogenesis
inferredcites →https://doi.org/10.2307/3870246openalex-snapshot
Hormones Act Downstream of TTG and GL2 to Promote Root Hair Outgrowth during Epidermis Development in the Arabidopsis Root
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Uncovering the Genetic Architecture of Replicated Adaptation
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The Functions of Flavonoids in Legume‐Rhizobia Interactions
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Plant Embryogenesis—The Cellular Design of a Plant
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Polarity inArabidopsisEmbryogenesis
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Polar Signals in Vascular Development
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Vascular Cell Differentiation
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ArabidopsisRoot Development
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Signaling and gene regulatory programs in plant vascular stem cells
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Pattern Formation in Embryos — Interpretation of Positional Information
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Life and Times of the Suspensor — Cell Signaling between the Embryo and Suspensor
inferred← citeshttps://doi.org/10.1007/978-1-4020-2686-7_14openalex-snapshot
Auxin Signal Transduction
inferred← citeshttps://doi.org/10.1007/978-1-4020-2686-7_22openalex-snapshot
The Induction of Vascular Tissues by Auxin
inferred← citeshttps://doi.org/10.1007/978-1-4020-6295-7_13openalex-snapshot
Auxin and Cytokinin Signaling Component Genes and Their Potential for Crop Improvement
inferred← citeshttps://doi.org/10.1007/978-1-4939-6854-1_13openalex-snapshot
The Triple Response Assay and Its Use to Characterize Ethylene Mutants in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-59745-273-1_1openalex-snapshot
Arabidopsis Embryogenesis
inferred← citeshttps://doi.org/10.1007/978-1-59745-289-2_10openalex-snapshot
Examining Protein Stability and Its Relevance for Plant Growth and Development
inferred← citeshttps://doi.org/10.1007/978-3-030-53202-4_7openalex-snapshot
Leaf Development and Vascular Differentiation
inferred← citeshttps://doi.org/10.1007/978-3-642-13145-5_2openalex-snapshot
Root Apical Meristem Pattern: Hormone Circuitry and Transcriptional Networks
inferred← citeshttps://doi.org/10.1007/978-4-431-65958-7_12openalex-snapshot
Pattern Formation during Dicotyledonous Plant Embryogenesis
inferred← citeshttps://doi.org/10.1007/978-94-017-1203-3_11openalex-snapshot
Zygotic Embryogenesis: Developmental Genetics
inferred← citeshttps://doi.org/10.1007/978-94-017-3522-3_3openalex-snapshot
Cells: Functional Units of TCLs
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/bf02715857openalex-snapshot
Induced mutation to monocotyledony in periwinkle,Catharanthus roseus, and suppression of mutant phenotype by kinetin
inferred← citeshttps://doi.org/10.1007/pl00014014openalex-snapshot
Cell-Cell Interactions during Vascular Development
inferred← citeshttps://doi.org/10.1007/s00122-019-03290-8openalex-snapshot
Identification and characterization of a new dwarf locus DS-4 encoding an Aux/IAA7 protein in Brassica napus
inferred← citeshttps://doi.org/10.1007/s00299-004-0858-zopenalex-snapshot
Regulated proteolysis and plant development
inferred← citeshttps://doi.org/10.1007/s00299-012-1362-5openalex-snapshot
Polar protein transport between apical and basal cells during tobacco early embryogenesis
inferred← citeshttps://doi.org/10.1007/s00344-014-9423-3openalex-snapshot
Heterologous Expression of BoPAP1 in Tomato Induces Stamen Specific Anthocyanin Accumulation and Enhances Tolerance to a Long-Term Low Temperature Stress
inferred← citeshttps://doi.org/10.1007/s003440000041openalex-snapshot
Maintenance of Asymmetric Cellular Localization of an Auxin Transport Protein through Interaction with the Actin Cytoskeleton
inferred← citeshttps://doi.org/10.1007/s003440010001openalex-snapshot
Foliar and Axial Aspects of Vascular Differentiation: Hypotheses and Evidence
inferred← citeshttps://doi.org/10.1007/s003440010006openalex-snapshot
Regulation of Tracheary Element Differentiation
inferred← citeshttps://doi.org/10.1007/s003440010007openalex-snapshot
Top-Down and Inside-Out: Directionality of Signaling in Vascular and Embryo Development
inferred← citeshttps://doi.org/10.1007/s003440010008openalex-snapshot
Regulation of Vascular Development
inferred← citeshttps://doi.org/10.1007/s003440010029openalex-snapshot
The Role of Auxin in Apical-Basal Pattern Formation During Arabidopsis Embryogenesis
inferred← citeshttps://doi.org/10.1007/s00425-009-0912-8openalex-snapshot
The short-rooted vitamin B6-deficient mutant pdx1 has impaired local auxin biosynthesis
inferred← citeshttps://doi.org/10.1007/s00425-014-2137-8openalex-snapshot
Rapid identification of angulata leaf mutations using next-generation sequencing
inferred← citeshttps://doi.org/10.1007/s00497-003-0165-9openalex-snapshot
Analysis of four maize mutants arrested in early embryogenesis reveals an irregular pattern of cell division
inferred← citeshttps://doi.org/10.1007/s00709-006-0180-4openalex-snapshot
Involvement of gibberellin in tracheary element differentiation and lignification in Zinnia elegans xylogenic culture
inferred← citeshttps://doi.org/10.1007/s00709-007-0246-yopenalex-snapshot
Developmental anatomy of cotyledons and leaves in has mutant of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10535-011-0163-yopenalex-snapshot
Auxin is involved in the regulation of leaf and root development by LAF1 under short day conditions
inferred← citeshttps://doi.org/10.1007/s11103-005-4547-2openalex-snapshot
Lateral Root Initiation or the Birth of a New Meristem
inferred← citeshttps://doi.org/10.1007/s11240-011-9986-7openalex-snapshot
In silico identification and characterization of putative differentially expressed genes involved in common bean (Phaseolus vulgaris L.) seed development
inferred← citeshttps://doi.org/10.1007/s11434-010-3137-0openalex-snapshot
Genetic analysis and gene fine mapping of a rolling leaf mutant (rl 11(t) ) in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1007/s13258-017-0622-8openalex-snapshot
Characterization and comparative expression analysis of CUL1 genes in rice
inferred← citeshttps://doi.org/10.1007/s40011-012-0090-5openalex-snapshot
Abnormal Leaf Morphologies Associated with Primary and Secondary Vein Patterning Defects in Catharanthus roseus: Mid-vein Defect Converts Simple Leaf into Binate Compound Leaf
inferred← citeshttps://doi.org/10.1016/b978-012660570-9/50165-9openalex-snapshot
Auxin Signal Perception and Transduction
inferred← citeshttps://doi.org/10.1016/j.cell.2004.09.018openalex-snapshot
The PLETHORA Genes Mediate Patterning of the Arabidopsis Root Stem Cell Niche
inferred← citeshttps://doi.org/10.1016/j.cj.2026.03.021openalex-snapshot
The pleiotropic gene LVN3 increases rice grain yield by modulating GA signaling to increase sink strength, source supply, and vascular flow
inferred← citeshttps://doi.org/10.1016/j.cub.2006.08.091openalex-snapshot
Vectorial Information for Arabidopsis Planar Polarity Is Mediated by Combined AUX1, EIN2, and GNOM Activity
inferred← citeshttps://doi.org/10.1016/j.cub.2007.05.008openalex-snapshot
FT Protein Acts as a Long-Range Signal in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2015.03.032openalex-snapshot
A Developmental Framework for Graft Formation and Vascular Reconnection in Arabidopsis thaliana
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Key Divisions in the Early Arabidopsis Embryo Require POL and PLL1 Phosphatases to Establish the Root Stem Cell Organizer and Vascular Axis
inferred← citeshttps://doi.org/10.1016/j.ejcb.2009.11.010openalex-snapshot
Cell–cell communication in Arabidopsis early embryogenesis
inferred← citeshttps://doi.org/10.1016/j.gde.2017.02.009openalex-snapshot
The logic of plant vascular patterning. Polarity, continuity and plasticity in the formation of the veins and of their networks
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Transcriptome and hormonal analysis of grafting process by investigating the homeostasis of a series of metabolic pathways in Torreya grandis cv. Merrillii
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.plantsci.2005.02.010openalex-snapshot
Comparison of ABP1 over-expressing Arabidopsis and under-expressing tobacco with an auxinic herbicide-resistant wild mustard (Brassica kaber) biotype
inferred← citeshttps://doi.org/10.1016/j.plantsci.2005.08.005openalex-snapshot
Isolation of a novel lateral-rootless mutant in rice (Oryza sativa L.) with reduced sensitivity to auxin
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.03.001openalex-snapshot
The physiological mechanism of a drooping leaf2 mutation in rice
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112112openalex-snapshot
The de-ubiquitinase UBQUITIN SPECIFIC PROTEASE 15 (UBP15) interacts with the SCF E3 complex adaptor ARABIDOPSIS SKP1 HOMOLOGUE 1 (ASK1) to regulate petal size and fertility in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109650openalex-snapshot
Blue light and NAA treatment significantly improve rooting on single leaf-bud cutting of Chrysanthemum via upregulated rooting-related genes
inferred← citeshttps://doi.org/10.1016/j.tplants.2009.04.005openalex-snapshot
Linking development to defense: auxin in plant–pathogen interactions
inferred← citeshttps://doi.org/10.1016/j.tplants.2009.05.002openalex-snapshot
Arabidopsis lateral root development: an emerging story
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.07.009openalex-snapshot
The genetic and molecular basis of haploinsufficiency in flowering plants
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Developmental genetics of the angiosperm leaf
inferred← citeshttps://doi.org/10.1016/s0065-2296(05)42003-0openalex-snapshot
Cytoskeletal Regulation of the Plane of Cell Division: An Essential Component of Plant Development and Reproduction
inferred← citeshttps://doi.org/10.1016/s0070-2153(10)91008-9openalex-snapshot
Vascular Pattern Formation in Plants
inferred← citeshttps://doi.org/10.1016/s0074-7696(02)20007-8openalex-snapshot
Vascular development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/s0083-6729(05)72002-1openalex-snapshot
Gravitropic Bending and Plant Hormones
inferred← citeshttps://doi.org/10.1016/s0960-9822(03)00409-3openalex-snapshot
Vascular Patterning: More Than Just Auxin?
inferred← citeshttps://doi.org/10.1016/s1360-1385(00)01725-8openalex-snapshot
Vascular continuity and auxin signals
inferred← citeshttps://doi.org/10.1016/s1360-1385(03)00051-7openalex-snapshot
Dissecting Arabidopsis lateral root development
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Vascular development: tracing signals along veins
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00105-9openalex-snapshot
Non-linear signaling for pattern formation?
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)00135-7openalex-snapshot
Vascular patterning and leaf shape
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)00210-7openalex-snapshot
Cell axiality and polarity in plants — adding pieces to the puzzle
inferred← citeshttps://doi.org/10.1023/a:1010753630573openalex-snapshot
Vascular continuity, cell axialisation and auxin
inferred← citeshttps://doi.org/10.1023/a:1022592511387openalex-snapshot
The effects of auxin on lateral root initiation and root gravitropism in a lateral rootless mutant Lrt1 of rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1023/b:gene.0000003744.39599.6dopenalex-snapshot
New Embryo Lethals in Arabidopsis thaliana: Basic Genetic and Morphological Study
inferred← citeshttps://doi.org/10.1038/nrm1364openalex-snapshot
Signals that control plant vascular cell differentiation
inferred← citeshttps://doi.org/10.1038/s41598-019-40657-9openalex-snapshot
Transcriptomics of cytokinin and auxin metabolism and signaling genes during seed maturation in dormant and non-dormant wheat genotypes
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.01078.xopenalex-snapshot
Partial complementation of embryo defective mutations: a general strategy to elucidate gene function
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.01152.xopenalex-snapshot
The role of auxin‐binding protein 1 in the expansion of tobacco leaf cells
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2003.01909.xopenalex-snapshot
Regulation of Arabidopsis SHY2/IAA3 protein turnover
inferred← citeshttps://doi.org/10.1073/pnas.2016049117openalex-snapshot
HOS15 is a transcriptional corepressor of NPR1-mediated gene activation of plant immunity
inferred← citeshttps://doi.org/10.1079/ivp2002405openalex-snapshot
Pepper (capsicum annuum L.) regenerants obtained by direct somatic embryogenesis fail to develop a shoot
inferred← citeshttps://doi.org/10.1080/15592324.2015.1078956openalex-snapshot
A new temperature-insensitive allele of the ArabidopsisAXR6/CUL1locus derived from a missense mutation in the C-terminal RBX1 binding region
inferred← citeshttps://doi.org/10.1086/382794openalex-snapshot
Vein Pattern Development in Adult Leaves ofArabidopsis thaliana
inferred← citeshttps://doi.org/10.1086/430336openalex-snapshot
Control of Leaf Formation and Somatic Embryogenesis in Cultured Zygotic Embryos ofArabidopsis thalianaby 2,4‐Dichlorophenoxyacetic Acid (2,4‐ d )
inferred← citeshttps://doi.org/10.1093/emboj/20.14.3609openalex-snapshot
Apical–basal pattern formation in Arabidopsis embryogenesis
inferred← citeshttps://doi.org/10.1093/emboj/cdg190openalex-snapshot
The RUB/Nedd8 conjugation pathway is required for early development in Arabidopsis
inferred← citeshttps://doi.org/10.1093/emboj/cdg335openalex-snapshot
Arabidopsis AXR6 encodes CUL1 implicating SCF E3 ligases in auxin regulation of embryogenesis
inferred← citeshttps://doi.org/10.1093/hr/uhae249openalex-snapshot
A telomere-to-telomere gap-free reference genome of Chionanthus retusus provides insights into the molecular mechanism underlying petal shape changes
inferred← citeshttps://doi.org/10.1093/insilicoplants/diab030openalex-snapshot
Polar auxin transport dynamics of primary and secondary vein patterning in dicot leaves
inferred← citeshttps://doi.org/10.1093/jexbot/51.347.971openalex-snapshot
Polarity and signalling in plant embryogenesis
inferred← citeshttps://doi.org/10.1093/jxb/erad272openalex-snapshot
Game of thrones among AUXIN RESPONSE FACTORs—over 30 years of MONOPTEROS research
inferred← citeshttps://doi.org/10.1093/jxb/erg306openalex-snapshot
Interaction between two auxin-resistant mutants and their effects on lateral root formation in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1093/jxb/erw429openalex-snapshot
Overexpression ofAtERF019delays plant growth and senescence and improves drought tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1093/mp/sss064openalex-snapshot
Studies on the Rice LEAF INCLINATION1 (LC1), an IAA–amido Synthetase, Reveal the Effects of Auxin in Leaf Inclination Control
inferred← citeshttps://doi.org/10.1093/pcp/pch051openalex-snapshot
amphivasal vascular bundle 1, a Gain-of-Function Mutation of the IFL1/REV Gene, Is Associated with Alterations in the Polarity of Leaves, Stems and Carpels
inferred← citeshttps://doi.org/10.1093/pcp/pch175openalex-snapshot
Spatial and Temporal Tracing of Vessel Differentiation in Young Arabidopsis Seedlings by the Expression of an Immature Tracheary Element-specific Promoter
inferred← citeshttps://doi.org/10.1093/pcp/pci217openalex-snapshot
Inhibition of Transdifferentiation into Tracheary Elements by Polar Auxin Transport Inhibitors Through Intracellular Auxin Depletion
inferred← citeshttps://doi.org/10.1093/plcell/koac357openalex-snapshot
Analyses of Cullin1 homologs reveal functional redundancy in S-RNase-based self-incompatibility and evolutionary relationships in eudicots
inferred← citeshttps://doi.org/10.1093/plcell/koae125openalex-snapshot
Protein degradation in auxin response
inferred← citeshttps://doi.org/10.1093/plphys/kiac461openalex-snapshot
Large Vascular Bundle Phloem Area 4 enhances grain yield and quality in rice via source–sink–flow
inferred← citeshttps://doi.org/10.1093/plphys/kiae465openalex-snapshot
YELLOW, SERRATED LEAF is essential for cotyledon vein patterning in Arabidopsis
inferred← citeshttps://doi.org/10.1101/850826openalex-snapshot
The TARANI/ UBIQUITIN SPECIFIC PROTEASE 14 destabilizes the AUX/IAA transcriptional repressors and regulates auxin response in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/cshperspect.a039958openalex-snapshot
Of Cells, Strands, and Networks: Auxin and the Patterned Formation of the Vascular System
inferred← citeshttps://doi.org/10.1101/gad.1035402openalex-snapshot
Trp-dependent auxin biosynthesis in Arabidopsis: involvement of cytochrome P450s CYP79B2 and CYP79B3
inferred← citeshttps://doi.org/10.1101/gad.189200openalex-snapshot
A novel two-component hybrid molecule regulates vascular morphogenesis of the Arabidopsis root
inferred← citeshttps://doi.org/10.1101/gad.237302openalex-snapshot
The Arabidopsis HOBBIT gene encodes a CDC27 homolog that links the plant cell cycle to progression of cell differentiation
inferred← citeshttps://doi.org/10.1101/gad.866201openalex-snapshot
ABP1 is required for organized cell elongation and division in Arabidopsis embryogenesis
inferred← citeshttps://doi.org/10.1104/pp.004747openalex-snapshot
Early Embryo Development in Fucus distichus Is Auxin Sensitive
inferred← citeshttps://doi.org/10.1104/pp.010546openalex-snapshot
Auxin and Ethylene Response Interactions during Arabidopsis Root Hair Development Dissected by Auxin Influx Modulators
inferred← citeshttps://doi.org/10.1104/pp.013623openalex-snapshot
Auxin Signaling in Arabidopsis Leaf Vascular Development
inferred← citeshttps://doi.org/10.1104/pp.103.030692openalex-snapshot
Diphtheria Toxin-Mediated Cell Ablation Reveals Interregional Communication during Arabidopsis Seed Development
inferred← citeshttps://doi.org/10.1104/pp.103.031971openalex-snapshot
Regulation of Flower Development in Arabidopsis by SCF Complexes
inferred← citeshttps://doi.org/10.1104/pp.103.034900openalex-snapshot
Interactions between Auxin Transport and the Actin Cytoskeleton in Developmental Polarity of Fucus distichus Embryos in Response to Light and Gravity
inferred← citeshttps://doi.org/10.1104/pp.104.044495openalex-snapshot
AtCAND1, A HEAT-Repeat Protein That Participates in Auxin Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.104.045179openalex-snapshot
Identification of Genes Required for Embryo Development in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.104.053843openalex-snapshot
Auxin-Dependent Cell Division and Cell Elongation. 1-Naphthaleneacetic Acid and 2,4-Dichlorophenoxyacetic Acid Activate Different Pathways
inferred← citeshttps://doi.org/10.1104/pp.104.055756openalex-snapshot
Arabidopsis thickvein Mutation Affects Vein Thickness and Organ Vascularization, and Resides in a Provascular Cell-Specific Spermine Synthase Involved in Vein Definition and in Polar Auxin Transport
inferred← citeshttps://doi.org/10.1104/pp.105.064337openalex-snapshot
Novel Markers of Xylogenesis in Zinnia Are Differentially Regulated by Auxin and Cytokinin
inferred← citeshttps://doi.org/10.1104/pp.105.067140openalex-snapshot
At5PTase13 Modulates Cotyledon Vein Development through Regulating Auxin Homeostasis
inferred← citeshttps://doi.org/10.1104/pp.106.083519openalex-snapshot
Down-Regulation of the 26S Proteasome Subunit RPN9 Inhibits Viral Systemic Transport and Alters Plant Vascular Development
inferred← citeshttps://doi.org/10.1104/pp.106.091439openalex-snapshot
A New CULLIN 1 Mutant Has Altered Responses to Hormones and Light in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.109.141325openalex-snapshot
Truffles Regulate Plant Root Morphogenesis via the Production of Auxin and Ethylene
inferred← citeshttps://doi.org/10.1104/pp.109.152587openalex-snapshot
The Sterol Methyltransferases SMT1, SMT2, and SMT3 Influence Arabidopsis Development through Nonbrassinosteroid Products
inferred← citeshttps://doi.org/10.1104/pp.112.207779openalex-snapshot
incurvata13, a Novel Allele of AUXIN RESISTANT6, Reveals a Specific Role for Auxin and the SCF Complex in Arabidopsis Embryogenesis, Vascular Specification, and Leaf Flatness
inferred← citeshttps://doi.org/10.1104/pp.114.246314openalex-snapshot
The VASCULATURE COMPLEXITY AND CONNECTIVITY Gene Encodes a Plant-Specific Protein Required for Embryo Provasculature Development
inferred← citeshttps://doi.org/10.1104/pp.124.4.1739openalex-snapshot
The rib1 Mutant Is Resistant to Indole-3-Butyric Acid, an Endogenous Auxin in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.125.2.990openalex-snapshot
Chromosaponin I Specifically Interacts with AUX1 Protein in Regulating the Gravitropic Response of Arabidopsis Roots
inferred← citeshttps://doi.org/10.1104/pp.15.01540openalex-snapshot
Novel Vein Patterns in Arabidopsis Induced by Small Molecules
inferred← citeshttps://doi.org/10.1104/pp.20.00689openalex-snapshot
The Ubiquitin-Specific Protease TNI/UBP14 Functions in Ubiquitin Recycling and Affects Auxin Response
inferred← citeshttps://doi.org/10.1105/tpc.005629openalex-snapshot
AtOPT3, a Member of the Oligopeptide Transporter Family, Is Essential for Embryo Development in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.016014openalex-snapshot
Genetic Regulation of Embryonic Pattern Formation
inferred← citeshttps://doi.org/10.1105/tpc.017772openalex-snapshot
The ASK1 and ASK2 Genes Are Essential for Arabidopsis Early Development
inferred← citeshttps://doi.org/10.1105/tpc.021030openalex-snapshot
COTYLEDON VASCULAR PATTERN2–Mediated Inositol (1,4,5) Triphosphate Signal Transduction Is Essential for Closed Venation Patterns of Arabidopsis Foliar Organs
inferred← citeshttps://doi.org/10.1105/tpc.104.161220openalex-snapshot
The Ubiquitin-Proteasome Pathway and Plant Development
inferred← citeshttps://doi.org/10.1105/tpc.105.031302openalex-snapshot
The Evolutionarily Conserved TOUGH Protein Is Required for Proper Development ofArabidopsis thaliana
inferred← citeshttps://doi.org/10.1105/tpc.105.033415openalex-snapshot
The Tomato Aux / IAA Transcription Factor IAA9 Is Involved in Fruit Development and Leaf Morphogenesis
inferred← citeshttps://doi.org/10.1105/tpc.105.034975openalex-snapshot
The RPN1 Subunit of the 26S Proteasome in Arabidopsis Is Essential for Embryogenesis
inferred← citeshttps://doi.org/10.1105/tpc.105.036889openalex-snapshot
Interactions between the Cell Cycle and Embryonic Patterning in Arabidopsis Uncovered by a Mutation in DNA Polymerase ε
inferred← citeshttps://doi.org/10.1105/tpc.109.065508openalex-snapshot
The NGATHA Genes Direct Style Development in the Arabidopsis Gynoecium
inferred← citeshttps://doi.org/10.1105/tpc.112.105486openalex-snapshot
The Arabidopsis F-Box Protein CORONATINE INSENSITIVE1 Is Stabilized by SCFCOI1 and Degraded via the 26S Proteasome Pathway
inferred← citeshttps://doi.org/10.1105/tpc.13.5.1047openalex-snapshot
Identification of Arabidopsis Histone Deacetylase HDA6 Mutants That Affect Transgene Expression
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2009.01997.xopenalex-snapshot
Auxin transport‐feedback models of patterning in plants
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2004.02023.xopenalex-snapshot
Interallelic complementation at the Arabidopsis CRE1 locus uncovers independent pathways for the proliferation of vascular initials and canonical cytokinin signalling
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2004.02254.xopenalex-snapshot
The IAA1 protein is encoded by AXR5 and is a substrate of SCFTIR1
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2005.02394.xopenalex-snapshot
Point mutations in Arabidopsis Cullin1 reveal its essential role in jasmonate response
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2005.02449.xopenalex-snapshot
Characterization of a novel temperature‐sensitive allele of the CUL1/AXR6 subunit of SCF ubiquitin‐ligases
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2005.02455.xopenalex-snapshot
Cell adhesion inArabidopsis thalianais mediated by ECTOPICALLY PARTING CELLS 1 – a glycosyltransferase (GT64) related to the animal exostosins
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2005.02467.xopenalex-snapshot
Arabidopsis CUL3A and CUL3B genes are essential for normal embryogenesis
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2005.02526.xopenalex-snapshot
hca: an Arabidopsis mutant exhibiting unusual cambial activity and altered vascular patterning
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2006.02977.xopenalex-snapshot
Dynamics of MONOPTEROS and PIN‐FORMED1 expression during leaf vein pattern formation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2009.03920.xopenalex-snapshot
CVP2‐ and CVL1‐mediated phosphoinositide signaling as a regulator of the ARF GAP SFC/VAN3 in establishment of foliar vein patterns
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2010.04112.xopenalex-snapshot
The ubiquitin‐proteasome system regulates plant hormone signaling
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2010.04143.xopenalex-snapshot
Embryogenesis – the humble beginnings of plant life
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2010.04250.xopenalex-snapshot
COE1, an LRR-RLK responsible for commissural vein pattern formation in rice
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2010.04416.xopenalex-snapshot
OsPUB15 , an E3 ubiquitin ligase, functions to reduce cellular oxidative stress during seedling establishment
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04513.xopenalex-snapshot
Auxin stimulates DWARF4 expression and brassinosteroid biosynthesis in Arabidopsis
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04785.xopenalex-snapshot
The Arabidopsis APC4 subunit of the anaphase‐promoting complex/cyclosome (APC/C) is critical for both female gametogenesis and embryogenesis
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2005.00475.xopenalex-snapshot
Auxin and the developing root of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01191.xopenalex-snapshot
Pattern formation in the vascular system of monocot and dicot plant species
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2007.02239.xopenalex-snapshot
The cellular and molecular biology of conifer embryogenesis
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2009.07194.xopenalex-snapshot
Plant oxylipins: COI1/JAZs/MYC2 as the core jasmonic acid‐signalling module
inferred← citeshttps://doi.org/10.1111/j.1744-7909.2010.01007.xopenalex-snapshot
Allelic Analyses of theArabidopsis YUC1Locus Reveal Residues and Domains Essential for the Functions of YUC Family of Flavin Monooxygenases
inferred← citeshttps://doi.org/10.1111/tpj.13032openalex-snapshot
Small‐molecule auxin inhibitors that target YUCCA are powerful tools for studying auxin function
inferred← citeshttps://doi.org/10.1111/tpj.14939openalex-snapshot
Generation of a fertile ask1 mutant uncovers a comprehensive set of SCF‐mediated intracellular functions
inferred← citeshttps://doi.org/10.1111/tpj.15299openalex-snapshot
grasviq : an image analysis framework for automatically quantifying vein number and morphology in grass leaves
inferred← citeshttps://doi.org/10.1126/science.1059776openalex-snapshot
Interactions of the COP9 Signalosome with the E3 Ubiquitin Ligase SCF TIR1 in Mediating Auxin Response
inferred← citeshttps://doi.org/10.1139/b07-029openalex-snapshot
From genes to patterns: Auxin distribution and auxin-dependent gene regulation in plant pattern formation
inferred← citeshttps://doi.org/10.1146/annurev-arplant-043015-112122openalex-snapshot
Transcriptional Responses to the Auxin Hormone
inferred← citeshttps://doi.org/10.1146/annurev.arplant.53.100301.135227openalex-snapshot
M OLECULAR G ENETICS OF A UXIN S IGNALING
inferred← citeshttps://doi.org/10.1146/annurev.arplant.53.100301.135245openalex-snapshot
V ASCULAR T ISSUE D IFFERENTIATION AND P ATTERN F ORMATION IN P LANTS
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.21.122303.114753openalex-snapshot
REGULATION OF ROOT APICAL MERISTEM DEVELOPMENT
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.22.011105.102609openalex-snapshot
Embryonic Patterning in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.23.090506.123214openalex-snapshot
Auxin Receptors and Plant Development: A New Signaling Paradigm
inferred← citeshttps://doi.org/10.1146/annurev.genet.38.072902.092231openalex-snapshot
Mechanisms of Pattern Formation in Plant Embryogenesis
inferred← citeshttps://doi.org/10.11606/t.41.2008.tde-28012009-101737openalex-snapshot
Sinalização no ganho de competência para a conversão de meristemas apicais radiculares de Catasetum fimbriatum em gemas caulinares
inferred← citeshttps://doi.org/10.1186/s12864-016-3182-4openalex-snapshot
Analysis of transcriptome in hickory (Carya cathayensis), and uncover the dynamics in the hormonal signaling pathway during graft process
inferred← citeshttps://doi.org/10.1199/tab.0043openalex-snapshot
Arabidopsis thaliana: A Model for the Study of Root and Shoot Gravitropism
inferred← citeshttps://doi.org/10.1199/tab.0126openalex-snapshot
Embryogenesis: Pattern Formation from a Single Cell
inferred← citeshttps://doi.org/10.1199/tab.0175openalex-snapshot
Composition, Roles, and Regulation of Cullin-Based Ubiquitin E3 Ligases
inferred← citeshttps://doi.org/10.1242/dev.00243openalex-snapshot
The RADICLELESS1 gene is required for vascular pattern formation in rice
inferred← citeshttps://doi.org/10.1242/dev.00441openalex-snapshot
Isolation ofCOV1, a gene involved in the regulation of vascular patterning in the stem ofArabidopsis
inferred← citeshttps://doi.org/10.1242/dev.00689openalex-snapshot
The FORKED genes are essential for distal vein meeting inArabidopsis
inferred← citeshttps://doi.org/10.1242/dev.00925openalex-snapshot
Overlapping and non-redundant functions of the Arabidopsis auxin response factors MONOPTEROS and NONPHOTOTROPIC HYPOCOTYL 4
inferred← citeshttps://doi.org/10.1242/dev.01716openalex-snapshot
VAN3 ARF–GAP-mediated vesicle transport is involved in leaf vascular network formation
inferred← citeshttps://doi.org/10.1242/dev.019349openalex-snapshot
ACAULIS5 controls Arabidopsis xylem specification through the prevention of premature cell death
inferred← citeshttps://doi.org/10.1242/dev.01952openalex-snapshot
Surge and destroy: the role of auxin in plant embryogenesis
inferred← citeshttps://doi.org/10.1242/dev.025932openalex-snapshot
A gain-of-function mutation inIAA18altersArabidopsisembryonic apical patterning
inferred← citeshttps://doi.org/10.1242/dev.127.15.3205openalex-snapshot
The SCARFACE gene is required for cotyledon and leaf vein patterning
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