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Auxin response factor 2 (ARF2) plays a major role in regulating auxin-mediated leaf longevity

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What this work says

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

inferredcites →https://doi.org/10.1007/978-94-010-0377-3_10openalex-snapshot

Genetics of Aux/IAA and ARF action in plant growth and development

inferredcites →https://doi.org/10.1007/s11103-005-2271-6openalex-snapshot

Oxidative stress responses during cassava post-harvest physiological deterioration

inferredcites →https://doi.org/10.1016/0076-6879(71)18325-5openalex-snapshot

[57] Pantothenic acid and coenzyme A: Phosphopantothenoylcysteine synthetase from rat liver (pantothenate 4′-phosphate:l-cysteine ligase, EC 6.3.2.5)

inferredcites →https://doi.org/10.1016/0076-6879(87)48036-1openalex-snapshot

[34] Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes

inferredcites →https://doi.org/10.1016/b978-0-12-520920-5.x5001-9openalex-snapshot

Senescence and Aging in Plants

inferredcites →https://doi.org/10.1016/j.pbi.2007.08.014openalex-snapshot

Auxin response factors

inferredcites →https://doi.org/10.1016/s0958-1669(97)80103-6openalex-snapshot

The molecular genetic analysis of leaf senescence

inferredcites →https://doi.org/10.1016/s1360-1385(00)01655-1openalex-snapshot

Molecular aspects of leaf senescence

inferredcites →https://doi.org/10.1023/a:1005934428906openalex-snapshot

A comparison of the expression patterns of several senescence-associated genes in response to stress and hormone treatment

inferredcites →https://doi.org/10.1023/a:1006199932265openalex-snapshot

Diverse range of gene activity during Arabidopsis thaliana leaf senescence includes pathogen-independent induction of defense-related genes

inferredcites →https://doi.org/10.1023/a:1006342412688openalex-snapshot

Identification of a promoter region responsible for the senescence-specific expression of SAG12

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.0000019076.76614.88openalex-snapshot

Oxidative stress responses during cassava post-harvest physiological deterioration

inferredcites →https://doi.org/10.1046/j.1365-313x.1995.8040595.xopenalex-snapshot

Ethylene regulates the timing of leaf senescence in Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.1997.00527.xopenalex-snapshot

Movement and subcellular localization of a tobamovirus in Arabidopsis

inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01908.xopenalex-snapshot

Large‐scale identification of leaf senescence‐associated genes

inferredcites →https://doi.org/10.1046/j.1467-7652.2003.00004.xopenalex-snapshot

The molecular analysis of leaf senescence – a genomics approach

inferredcites →https://doi.org/10.1073/pnas.0505150103openalex-snapshot

Cytokinin-mediated control of leaf longevity by AHK3 through phosphorylation of ARR2 in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.0803996105openalex-snapshot

Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2

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/oxfordjournals.pcp.a078025openalex-snapshot

Effects of Nuclear and Cytoplasmic Genes Altering Chlorophyll Loss on Gas Exchange during Monocarpic Senescence in Soybean

inferredcites →https://doi.org/10.1093/pcp/pch110openalex-snapshot

The Delayed Leaf Senescence Mutants of Arabidopsis, ore1, ore3, and ore9 are Tolerant to Oxidative Stress

inferredcites →https://doi.org/10.1104/pp.106.079293openalex-snapshot

Transcription Analysis of Arabidopsis Membrane Transporters and Hormone Pathways during Developmental and Induced Leaf Senescence

inferredcites →https://doi.org/10.1104/pp.107.4.1075openalex-snapshot

Cytokinin Action Is Coupled to Ethylene in Its Effects on the Inhibition of Root and Hypocotyl Elongation in Arabidopsis thaliana Seedlings

inferredcites →https://doi.org/10.1104/pp.108.133439openalex-snapshot

An Arabidopsis Mitogen-Activated Protein Kinase Cascade, MKK9-MPK6, Plays a Role in Leaf Senescence

inferredcites →https://doi.org/10.1104/pp.124.3.1305openalex-snapshot

Cloning and Characterization of a Receptor-Like Protein Kinase Gene Associated with Senescence

inferredcites →https://doi.org/10.1104/pp.126.2.707openalex-snapshot

Networking Senescence-Regulating Pathways by Using Arabidopsis Enhancer Trap Lines

inferredcites →https://doi.org/10.1104/pp.26.1.189openalex-snapshot

AUXIN IN RELATION TO LEAF BLADE ABSCISSION

inferredcites →https://doi.org/10.1105/tpc.008417openalex-snapshot

The Roles of Auxin Response Factor Domains in Auxin-Responsive Transcription

inferredcites →https://doi.org/10.1105/tpc.010061openalex-snapshot

ORE9, an F-Box Protein That Regulates Leaf Senescence in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.017384openalex-snapshot

Aux/IAA Proteins Contain a Potent Transcriptional Repression Domain

inferredcites →https://doi.org/10.1105/tpc.104.028316openalex-snapshot

Functional Genomic Analysis of the AUXIN RESPONSE FACTOR Gene Family Members in Arabidopsis thaliana : Unique and Overlapping Functions of ARF7 and ARF19

inferredcites →https://doi.org/10.1105/tpc.107.055715openalex-snapshot

FIONA1 Is Essential for Regulating Period Length in the Arabidopsis Circadian Clock

inferredcites →https://doi.org/10.1105/tpc.13.8.1779openalex-snapshot

ORE9, an F-Box Protein That Regulates Leaf Senescence in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.5.5.553openalex-snapshot

Developmental and age-related processes that influence the longevity and senescence of photosynthetic tissues in arabidopsis.

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.9.7.1169openalex-snapshot

Last exit: senescence, abscission, and meristem arrest in Arabidopsis.

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02160.xopenalex-snapshot

Molecular events in senescing Arabidopsis leaves

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02399.xopenalex-snapshot

Comparative transcriptome analysis reveals significant differences in gene expression and signalling pathways between developmental and dark/starvation‐induced senescence in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02426.xopenalex-snapshot

AUXIN RESPONSE FACTOR 2 (ARF2): a pleiotropic developmental regulator

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02432.xopenalex-snapshot

NPH4/ARF7 and ARF19 promote leaf expansion and auxin‐induced lateral root formation

inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02723.xopenalex-snapshot

AtNAP, a NAC family transcription factor, has an important role in leaf senescence

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03317.xopenalex-snapshot

Overexpression of a chromatin architecture‐controlling AT‐hook protein extends leaf longevity and increases the post‐harvest storage life of plants

inferredcites →https://doi.org/10.1111/j.1438-8677.2008.00083.xopenalex-snapshot

A novel upstream regulator of WRKY53 transcription during leaf senescence in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb04243.xopenalex-snapshot

Gene expression during leaf senescence

inferredcites →https://doi.org/10.1126/science.1166386openalex-snapshot

Trifurcate Feed-Forward Regulation of Age-Dependent Cell Death Involving miR164 in Arabidopsis

inferredcites →https://doi.org/10.1126/science.270.5244.1986openalex-snapshot

Inhibition of Leaf Senescence by Autoregulated Production of Cytokinin

inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105316openalex-snapshot

Leaf Senescence

inferredcites →https://doi.org/10.1242/dev.00196openalex-snapshot

TheBLADE-ON-PETIOLE 1gene controls leaf pattern formation through the modulation of meristematic activity inArabidopsis

inferredcites →https://doi.org/10.1242/dev.01955openalex-snapshot

Auxin response factors ARF6 and ARF8 promote jasmonic acid production and flower maturation

inferredcites →https://doi.org/10.1242/dev.02012openalex-snapshot

AUXIN RESPONSE FACTOR1andAUXIN RESPONSE FACTOR2regulate senescence and floral organ abscission inArabidopsis thaliana

inferredcites →https://doi.org/10.1242/dev.02194openalex-snapshot

The AUXIN RESPONSE FACTOR 2 gene of Arabidopsis links auxin signalling, cell division, and the size of seeds and other organs

What points at this work

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

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Integrative Inference of Atore1 Mutant Networks in Hormonal Balance Yields Induces Distinct Novel H2o2-Nacs Signaling in Regulating the Onset of Leaf Senescence in Soybean (Glycine Max L.)

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Ethylene and Senescence Processes

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Ca 2+ , The Miracle Molecule in Plant Hormone Signaling During Abiotic Stress

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mi RNA s in Plant Development

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inferred← citeshttps://doi.org/10.1038/srep33728openalex-snapshot

SlARF2a plays a negative role in mediating axillary shoot formation

inferred← citeshttps://doi.org/10.1073/pnas.1304250110openalex-snapshot

Convergence of auxin and gibberellin signaling on the regulation of the GATA transcription factors GNC and GNL in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1080/07352689.2011.616065openalex-snapshot

The Complex Regulation of Senescence

inferred← citeshttps://doi.org/10.1080/07352689.2026.2739786openalex-snapshot

Deciphering the molecular mechanisms of leaf senescence: from nutrient remobilization to stress tolerance improvement

inferred← citeshttps://doi.org/10.1093/aob/mcz173openalex-snapshot

Plasma membrane receptor-like kinases and transporters are associated with 2,4-D resistance in wild radish

inferred← citeshttps://doi.org/10.1093/dnares/dst027openalex-snapshot

The Auxin Response Factor Transcription Factor Family in Soybean: Genome-Wide Identification and Expression Analyses During Development and Water Stress

inferred← citeshttps://doi.org/10.1093/gbe/evab198openalex-snapshot

The Ancient Salicoid Genome Duplication Event: A Platform for Reconstruction of De Novo Gene Evolution inPopulus trichocarpa

inferred← citeshttps://doi.org/10.1093/jxb/eraf195openalex-snapshot

Does leaf lifespan affect the regulation of photosynthetic function during natural senescence of leaves in various sorghum cultivars?

inferred← citeshttps://doi.org/10.1093/jxb/err094openalex-snapshot

YUCCA6 over-expression demonstrates auxin function in delaying leaf senescence in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/jxb/err390openalex-snapshot

Comparative transcriptomics and proteomics analysis of citrus fruit, to improve understanding of the effect of low temperature on maintaining fruit quality during lengthy post-harvest storage

inferred← citeshttps://doi.org/10.1093/jxb/eru002openalex-snapshot

miRNAs in the crosstalk between phytohormone signalling pathways

inferred← citeshttps://doi.org/10.1093/jxb/eru337openalex-snapshot

Small RNAs as important regulators for the hybrid vigour of super-hybrid rice

inferred← citeshttps://doi.org/10.1093/jxb/erv273openalex-snapshot

Post-translational modifications of hormone-responsive transcription factors: the next level of regulation

inferred← citeshttps://doi.org/10.1093/jxb/erx287openalex-snapshot

New insights into the regulation of leaf senescence in Arabidopsis

inferred← citeshttps://doi.org/10.1093/jxb/erx401openalex-snapshot

Beyond the genetic code in leaf senescence

inferred← citeshttps://doi.org/10.1093/pcp/pcw120openalex-snapshot

ANAC032 Positively Regulates Age-Dependent and Stress-Induced Senescence in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/plphys/kiab014openalex-snapshot

ARF2 represses expression of plant GRF transcription factors in a complementary mechanism to microRNA miR396

inferred← citeshttps://doi.org/10.1093/plphys/kiac497openalex-snapshot

The auxin response factor TaARF15-A1 negatively regulates senescence in common wheat (Triticum aestivumL.)

inferred← citeshttps://doi.org/10.1093/plphys/kiac535openalex-snapshot

Wheat AUXIN RESPONSE FACTOR 15 delays senescence through competitive interaction at the TaNAM1 locus

inferred← citeshttps://doi.org/10.1093/plphys/kiad086openalex-snapshot

Wheat AUXIN RESPONSE FACTOR 15 delays senescence through interaction at the TaNAM1 locus

inferred← citeshttps://doi.org/10.1093/plphys/kiae299openalex-snapshot

Endoplasmic reticulum protein ALTERED MERISTEM PROGRAM 1 negatively regulates senescence in Arabidopsis

inferred← citeshttps://doi.org/10.1093/plphys/kiag122openalex-snapshot

Deciphering vital transcription factors in cytokinin- and ABA-mediated postharvest leaf senescence of Brassica rapa

inferred← citeshttps://doi.org/10.1093/treephys/tpab102openalex-snapshot

The meristem-associated endosymbiontMethylorubrum extorquensDSM13060 reprograms development and stress responses of pine seedlings

inferred← citeshttps://doi.org/10.1101/2022.11.22.517554openalex-snapshot

A single Verticillium dahliae effector determines pathogenicity on tomato by targeting auxin response factors

inferred← citeshttps://doi.org/10.1101/2025.03.24.644839openalex-snapshot

Chemical Inhibition of Splicing-Related Protein Kinases Reveals Phosphorylation-Driven Regulation of RNA Alternative Splicing in Arabidopsis Seedlings

inferred← citeshttps://doi.org/10.1104/pp.111.182899openalex-snapshot

A Soybean Dual-Specificity Kinase, GmSARK, and Its Arabidopsis Homolog, AtSARK, Regulate Leaf Senescence through Synergistic Actions of Auxin and Ethylene

inferred← citeshttps://doi.org/10.1104/pp.111.189829openalex-snapshot

Regulatory Functions of SnRK1 in Stress-Responsive Gene Expression and in Plant Growth and Development

inferred← citeshttps://doi.org/10.1104/pp.15.01112openalex-snapshot

SENESCENCE-SUPPRESSED PROTEIN PHOSPHATASE Directly Interacts with the Cytoplasmic Domain of SENESCENCE-ASSOCIATED RECEPTOR-LIKE KINASE and Negatively Regulates Leaf Senescence in Arabidopsis

inferred← citeshttps://doi.org/10.1104/pp.15.01929openalex-snapshot

Programming of Plant Leaf Senescence with Temporal and Inter-Organellar Coordination of Transcriptome in Arabidopsis1

inferred← citeshttps://doi.org/10.1104/pp.16.01410openalex-snapshot

Forever Young: The Role of Ubiquitin Receptor DA1 and E3 Ligase BIG BROTHER in Controlling Leaf Growth and Development

inferred← citeshttps://doi.org/10.1105/tpc.113.117838openalex-snapshot

Arabidopsis WRKY57 Functions as a Node of Convergence for Jasmonic Acid– and Auxin-Mediated Signaling in Jasmonic Acid–Induced Leaf Senescence

inferred← citeshttps://doi.org/10.1105/tpc.18.00471openalex-snapshot

Developmental Genetics of Corolla Tube Formation: Role of the tasiRNA- ARF Pathway and a Conceptual Model

inferred← citeshttps://doi.org/10.1111/j.1744-7348.2011.00497.xopenalex-snapshot

Interactions between flowering and senescence regulation and the influence of low temperature in Arabidopsis and crop plants

inferred← citeshttps://doi.org/10.1111/j.1744-7909.2012.01136.xopenalex-snapshot

Gene Network Analysis and Functional Studies of Senescence‐associated Genes Reveal Novel Regulators of Arabidopsis Leaf SenescenceF

inferred← citeshttps://doi.org/10.1111/jipb.12005openalex-snapshot

Regulation of Leaf Senescence and Crop Genetic ImprovementF

inferred← citeshttps://doi.org/10.1111/jipb.13392openalex-snapshot

Advances in structure and function of auxin response factor in plants

inferred← citeshttps://doi.org/10.1111/jpi.12188openalex-snapshot

INDOLE ‐3‐ ACETIC ACID INDUCIBLE 17 positively modulates natural leaf senescence through melatonin‐mediated pathway in Arabidopsis

inferred← citeshttps://doi.org/10.1111/nph.13196openalex-snapshot

Identification of CROWN ROOTLESS 1‐regulated genes in rice reveals specific and conserved elements of postembryonic root formation

inferred← citeshttps://doi.org/10.1111/nph.15291openalex-snapshot

ORESARA15, a PLATZ transcription factor, mediates leaf growth and senescence in Arabidopsis

inferred← citeshttps://doi.org/10.1111/nph.15501openalex-snapshot

Natural allelic variation of GVS 1 confers diversity in the regulation of leaf senescence in Arabidopsis

inferred← citeshttps://doi.org/10.1111/plb.12373openalex-snapshot

A transcriptome‐wide study on the micro RNA ‐ and the Argonaute 1‐enriched small RNA ‐mediated regulatory networks involved in plant leaf senescence

inferred← citeshttps://doi.org/10.1111/plb.12672openalex-snapshot

Plant organ senescence – regulation by manifold pathways

inferred← citeshttps://doi.org/10.1111/ppl.13068openalex-snapshot

A novel microRNA, SlymiR208, promotes leaf senescence via regulating cytokinin biosynthesis in tomato

inferred← citeshttps://doi.org/10.1111/ppl.70165openalex-snapshot

Auxin biodynamics and its integral role in enhancing plant resilience to environmental cues

inferred← citeshttps://doi.org/10.1111/ppl.70315openalex-snapshot

Crosstalk Between Auxin Signalling and Growth Regulating Factor 5: Implications for Chloroplast Division and Leaf Development

inferred← citeshttps://doi.org/10.1111/tpj.12567openalex-snapshot

Post‐transcriptional control of GRF transcription factors by micro RNA miR396 and GIF co‐activator affects leaf size and longevity

inferred← citeshttps://doi.org/10.1111/tpj.17043openalex-snapshot

Incomplete filling in the basal region of maize endosperm: timing of development of starch synthesis and cell vitality

inferred← citeshttps://doi.org/10.1134/s1022795422020053openalex-snapshot

Molecular and Genetic Aspects of Potato Response to Late Blight Infection

inferred← citeshttps://doi.org/10.1145/3208955.3208964openalex-snapshot

Cloning and Expression Analysis of Auxin Response Factor 8 (ARF8) Gene from Lettuce (Lactuca Sativa L.)

inferred← citeshttps://doi.org/10.1146/annurev-arplant-050718-095859openalex-snapshot

Leaf Senescence: Systems and Dynamics Aspects

inferred← citeshttps://doi.org/10.1155/2018/7658910openalex-snapshot

Genome-Wide Identification, Phylogeny, and Expression Analysis of ARF Genes Involved in Vegetative Organs Development in Switchgrass

inferred← citeshttps://doi.org/10.1159/000354334openalex-snapshot

The Role of Hormones in the Aging of Plants - A Mini-Review

inferred← citeshttps://doi.org/10.11606/d.11.2011.tde-09022011-165431openalex-snapshot

Influência de diferentes doses de Fósforo e Potássio nos aspectos morfológicos, fisiológicos e na produtividade de plantas de soja tratadas com ácido 2,3,5 - triiodobenzóico

inferred← citeshttps://doi.org/10.11606/d.41.2020.tde-29102019-141830openalex-snapshot

Predição in silico do papel de ScRAV1 sobre os genes de parede celular e fatores de transcrição durante a formação do aerênquima na raiz de cana-de-açúcar

inferred← citeshttps://doi.org/10.1186/1471-2164-13-371openalex-snapshot

High-throughput sequencing of small RNAs and analysis of differentially expressed microRNAs associated with pistil development in Japanese apricot

inferred← citeshttps://doi.org/10.1186/1471-2164-13-421openalex-snapshot

Identification of miRNAs and their targets from Brassica napus by high-throughput sequencing and degradome analysis

inferred← citeshttps://doi.org/10.1186/1756-0500-7-218openalex-snapshot

Genome-wide identification and transcriptional profiling analysis of auxin response-related gene families in cucumber

inferred← citeshttps://doi.org/10.1186/s12864-021-07504-6openalex-snapshot

Characterization of cotton ARF factors and the role of GhARF2b in fiber development

inferred← citeshttps://doi.org/10.1186/s12870-015-0656-5openalex-snapshot

Identification of miRNAs associated with dark-induced senescence in Arabidopsis

inferred← citeshttps://doi.org/10.1186/s12870-018-1559-zopenalex-snapshot

Genome-wide identification, molecular evolution, and expression analysis of auxin response factor (ARF) gene family in Brachypodium distachyon L

inferred← citeshttps://doi.org/10.1186/s12870-019-1767-1openalex-snapshot

Characterization of S40-like proteins and their roles in response to environmental cues and leaf senescence in rice

inferred← citeshttps://doi.org/10.1186/s12870-021-03018-1openalex-snapshot

Impact of water deficit on the development and senescence of tomato roots grown under various soil textures of Shaanxi, China

inferred← citeshttps://doi.org/10.1186/s12870-021-03283-0openalex-snapshot

Genome and transcriptome-based characterization of high energy carbon-ion beam irradiation induced delayed flower senescence mutant in Lotus japonicus

inferred← citeshttps://doi.org/10.1186/s12870-022-03539-3openalex-snapshot

miR390 family of Cymbidium goeringii is involved in the development of reproductive organs in transgenic Arabidopsis

inferred← citeshttps://doi.org/10.1186/s12870-022-03930-0openalex-snapshot

Combined transcriptome and metabolome analysis revealed pathways involved in improved salt tolerance of Gossypium hirsutum L. seedlings in response to exogenous melatonin application

inferred← citeshttps://doi.org/10.1186/s12915-015-0180-yopenalex-snapshot

ZLL/AGO10 maintains shoot meristem stem cells during Arabidopsis embryogenesis by down-regulating ARF2-mediated auxin response

inferred← citeshttps://doi.org/10.1186/s13059-017-1235-xopenalex-snapshot

Histone H3 lysine 36 methylation affects temperature-induced alternative splicing and flowering in plants

inferred← citeshttps://doi.org/10.1186/s40529-016-0120-3openalex-snapshot

Leaf senescence induced by EGY1 defection was partially restored by glucose in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1186/s43897-021-00006-9openalex-snapshot

Leaf senescence: progression, regulation, and application

inferred← citeshttps://doi.org/10.1242/jcs.109116openalex-snapshot

Plant leaf senescence and death – regulation by multiple layers of control and implications for aging in general

inferred← citeshttps://doi.org/10.1360/ssv-2019-0157openalex-snapshot

Auxin and leaf senescence regulation

inferred← citeshttps://doi.org/10.1371/journal.pgen.1005903openalex-snapshot

AUXIN RESPONSE FACTOR 2 Intersects Hormonal Signals in the Regulation of Tomato Fruit Ripening

inferred← citeshttps://doi.org/10.1371/journal.pone.0018094openalex-snapshot

Relationship between Symptoms and Gene Expression Induced by the Infection of Three Strains of Rice dwarf virus

inferred← citeshttps://doi.org/10.1371/journal.pone.0042839openalex-snapshot

Selection and Validation of Endogenous Reference Genes for qRT-PCR Analysis in Leafy Spurge (Euphorbia esula)

inferred← citeshttps://doi.org/10.1371/journal.pone.0047810openalex-snapshot

Identification of Differentially-Expressed Genes Associated with Pistil Abortion in Japanese Apricot by Genome-Wide Transcriptional Analysis

inferred← citeshttps://doi.org/10.1371/journal.pone.0056570openalex-snapshot

Regulation of Wheat Seed Dormancy by After-Ripening Is Mediated by Specific Transcriptional Switches That Induce Changes in Seed Hormone Metabolism and Signaling

inferred← citeshttps://doi.org/10.1371/journal.pone.0069847openalex-snapshot

Gene Expression Profiles Deciphering Leaf Senescence Variation between Early- and Late-Senescence Cotton Lines

inferred← citeshttps://doi.org/10.1371/journal.pone.0084203openalex-snapshot

Characterization of the Tomato ARF Gene Family Uncovers a Multi-Levels Post-Transcriptional Regulation Including Alternative Splicing

inferred← citeshttps://doi.org/10.1371/journal.pone.0098465openalex-snapshot

Transcriptome Analysis of Shade-Induced Inhibition on Leaf Size in Relay Intercropped Soybean

inferred← citeshttps://doi.org/10.1371/journal.pone.0121902openalex-snapshot

Fusarium oxysporum Triggers Tissue-Specific Transcriptional Reprogramming in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1371/journal.pone.0193517openalex-snapshot

Auxin Response Factors (ARFs) are potential mediators of auxin action in tomato response to biotic and abiotic stress (Solanum lycopersicum)

inferred← citeshttps://doi.org/10.1371/journal.pone.0199716openalex-snapshot

QTL analysis reveals quantitative resistant loci for Phytophthora infestans and Tecia solanivora in tetraploid potato (Solanum tuberosum L.)

inferred← citeshttps://doi.org/10.15252/embj.2022110988openalex-snapshot

ARF2‐PIF5 interaction controls transcriptional reprogramming in the ABS3‐mediated plant senescence pathway

inferred← citeshttps://doi.org/10.15252/embr.201948967openalex-snapshot

Transcription factor CDF4 promotes leaf senescence and floral organ abscission by regulating abscisic acid and reactive oxygen species pathways in Arabidopsis

inferred← citeshttps://doi.org/10.15835/nsb12310823openalex-snapshot

Computational study of environmental stress-related transcription factor binding sites in the promoter regions of maize auxin response factor (ARF) gene family

inferred← citeshttps://doi.org/10.18174/583852openalex-snapshot

Functional analysis of effector proteins of the vascular wilt fungus Verticillium dahliae

inferred← citeshttps://doi.org/10.18699/vj21.020openalex-snapshot

Genetic aspects of potato resistance to phytophthorosis

inferred← citeshttps://doi.org/10.20944/preprints202306.0225.v1openalex-snapshot

Age-Dependent Molecular and Metabolic Rewiring Leading to Wound-Induced Blackening in Cut Carrots

inferred← citeshttps://doi.org/10.20944/preprints202306.0225.v2openalex-snapshot

Age-Dependent Molecular and Metabolic Rewiring Leading to Wound-Induced Blackening in Cut Carrots

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1935977/v1openalex-snapshot

Molecular Cloning, Characterization and Expression Analysis of Auxin Response Factor GhARF2 Gene in Upland Cotton (Gossypium hirsutum L.)

inferred← citeshttps://doi.org/10.2135/cropsci2013.12.0854openalex-snapshot

Identification and Gene Mapping of an early senescence leaf 4 Mutant of Rice

inferred← citeshttps://doi.org/10.22541/au.164243975.52189346/v1openalex-snapshot

Heterogeneous light delayed leaf senescence and ensure yield in maize

inferred← citeshttps://doi.org/10.23860/thesis-almeida-robert-2014openalex-snapshot

INVESTIGATION OF GENES CONTRIBUTING TO WHOLE PLANT SENESCENCE IN SOYBEAN (GLYCINE MAX)

inferred← citeshttps://doi.org/10.2478/johr-2025-0019openalex-snapshot

Molecular Perspective on the Mechanisms Regulating Leaf Senescence in Plants Under Water Stress

inferred← citeshttps://doi.org/10.29252/pgr.6.1.115openalex-snapshot

Upstream Regulatory Elements, Potential Targets and Expression Patterns of Three Drought Responsive miRNAs in Two Grapevine Cultivars

inferred← citeshttps://doi.org/10.32615/ps.2019.021openalex-snapshot

Shading of mature leaves systemically regulates photosynthesis and leaf area of new developing leaves via hormones

inferred← citeshttps://doi.org/10.3389/fpls.2014.00650openalex-snapshot

The roles of ethylene and transcription factors in the regulation of onset of leaf senescence

inferred← citeshttps://doi.org/10.3389/fpls.2014.00683openalex-snapshot

Assessing the transcriptional regulation of L-cysteine desulfhydrase 1 in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.3389/fpls.2014.00782openalex-snapshot

Overexpression of AtGRDP2, a novel glycine-rich domain protein, accelerates plant growth and improves stress tolerance

inferred← citeshttps://doi.org/10.3389/fpls.2015.00742openalex-snapshot

The auxin response factor gene family in banana: genome-wide identification and expression analyses during development, ripening, and abiotic stress

inferred← citeshttps://doi.org/10.3389/fpls.2015.01060openalex-snapshot

Behavior of Leaf Meristems and Their Modification

inferred← citeshttps://doi.org/10.3389/fpls.2017.01370openalex-snapshot

Uncovering Male Fertility Transition Responsive miRNA in a Wheat Photo-Thermosensitive Genic Male Sterile Line by Deep Sequencing and Degradome Analysis

inferred← citeshttps://doi.org/10.3389/fpls.2018.00372openalex-snapshot

Two TPL-Binding Motifs of ARF2 Are Involved in Repression of Auxin Responses

inferred← citeshttps://doi.org/10.3389/fpls.2018.00824openalex-snapshot

The Making of Leaves: How Small RNA Networks Modulate Leaf Development

inferred← citeshttps://doi.org/10.3389/fpls.2018.01103openalex-snapshot

SiSTL2 Is Required for Cell Cycle, Leaf Organ Development, Chloroplast Biogenesis, and Has Effects on C4 Photosynthesis in Setaria italica (L.) P. Beauv.

inferred← citeshttps://doi.org/10.3389/fpls.2018.01395openalex-snapshot

Characterization and Expression Patterns of Auxin Response Factors in Wheat

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