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Spermidine application affects the adventitious root formation and root morphology of apple rootstock by altering the hormonal profile and regulating the gene expression pattern
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A Rapid and effective method for RNA extraction from different tissues of grapevine and other woody plants
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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
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Levels of indole-3-acetic acid in intact and decapitated coleoptiles as determined by a specific and highly sensitive solid-phase enzyme immunoassay
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The key players of the primary root growth and development also function in lateral roots in Arabidopsis
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Expression of the pea S -adenosylmethionine decarboxylase gene is involved in developmental and environmental responses
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Phylogenetic analysis of IDD gene family and characterization of its expression in response to flower induction in Malus
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Genome-wide identification, characterization and expression analysis of novel long non-coding RNAs that mediate IBA-induced adventitious root formation in apple rootstocks
inferredcites →https://doi.org/10.1016/j.crvi.2008.04.002openalex-snapshot
Anatomical and biochemical changes during adventitious rooting of apple rootstocks MM 106 cultured in vitro
inferredcites →https://doi.org/10.1016/j.plantsci.2009.09.009openalex-snapshot
Involvement of the ARRO-1 gene in adventitious root formation in apple
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Effect of exogenous indole-3-butanoic acid (IBA) application on the morphology, hormone status, and gene expression of developing lateral roots in Malus hupehensis
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Fast and efficient separation of cytokinins from auxin and abscisic acid and their purification using mixed-mode solid-phase extraction
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Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
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Morpho-funcional Gradients in Superficial and Deep Tissues along Tobacco Stem: Polyamine Levels, Biosynthesis and Oxidation, and Organogenesis in vitro
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Proteome Analyses Using iTRAQ Labeling Reveal Critical Mechanisms in Alternate Bearing Malus prunifolia
inferredcites →https://doi.org/10.1023/a:1000304922507openalex-snapshot
Regeneration of roots, shoots and embryos: physiological, biochemical and molecular aspects
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Polar auxin transport – old questions and new concepts?
inferredcites →https://doi.org/10.1023/a:1025895731017openalex-snapshot
Involvement of polyamines in root development
inferredcites →https://doi.org/10.1038/35104500openalex-snapshot
Auxin regulates SCFTIR1-dependent degradation of AUX/IAA proteins
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Cloning, Sequencing, and Heterologous Expression of the Murine Peroxisomal Flavoprotein, N1-Acetylated Polyamine Oxidase
inferredcites →https://doi.org/10.1080/07352689.2015.1090831openalex-snapshot
Physiological and Molecular Regulation of Adventitious Root Formation
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Auxin and cytokinin control formation of the quiescent centre in the adventitious root apex of arabidopsis
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Overaccumulation of Higher Polyamines in Ripening Transgenic Tomato Fruit Revives Metabolic Memory, Upregulates Anabolism-Related Genes, and Positively Impacts Nutritional Quality
inferredcites →https://doi.org/10.1093/jxb/erf077openalex-snapshot
A trans-zeatin riboside in root xylem sap negatively regulates adventitious root formation on cucumber hypocotyls
inferredcites →https://doi.org/10.1093/jxb/eri102openalex-snapshot
Expression of arginine decarboxylase and ornithine decarboxylase genes in apple cells and stressed shoots
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a086045openalex-snapshot
Auxin Transport Inhibitors and the Rooting of Hypocotyl Cuttings from Etiolated Mung-bean Vigna radiata (L.) Wilczek Seedlings
inferredcites →https://doi.org/10.1093/pcp/pci183openalex-snapshot
A PIN1 Family Gene, OsPIN1, involved in Auxin-dependent Adventitious Root Emergence and Tillering in Rice
inferredcites →https://doi.org/10.1093/treephys/16.5.515openalex-snapshot
Changes in the concentrations of auxins and polyamines during rooting of in-vitro-propagated walnut shoots
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A pathway for lateral root formation in Arabidopsis thaliana.
inferredcites →https://doi.org/10.1104/pp.103.028662openalex-snapshot
Brassinosteroids Promote Root Growth in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.165126openalex-snapshot
SHORT-ROOT Regulates Primary, Lateral, and Adventitious Root Development in Arabidopsis
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Expression of Ornithine Decarboxylase Is Transiently Increased by Pollination, 2,4-Dichlorophenoxyacetic Acid, and Gibberellic Acid in Tomato Ovaries1
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Transcription Factors WOX11/12 Directly Activate WOX5/7 to Promote Root Primordia Initiation and Organogenesis
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Hormonal Characterization of a Nonrooting Naphthalene-Acetic Acid Tolerant Tobacco Mutant by an Immunoenzymic Method
inferredcites →https://doi.org/10.1104/pp.89.2.439openalex-snapshot
Relationship between Indole-3-Acetic Acid Levels in Apple (Malus pumila Mill) Rootstocks Cultured in Vitro and Adventitious Root Formation in the Presence of Indole-3-Butyric Acid
inferredcites →https://doi.org/10.1105/tpc.010354openalex-snapshot
AUX1 Promotes Lateral Root Formation by Facilitating Indole-3-Acetic Acid Distribution between Sink and Source Tissues in the Arabidopsis Seedling
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.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.112.099119openalex-snapshot
Auxin Controls Arabidopsis Adventitious Root Initiation by Regulating Jasmonic Acid Homeostasis
inferredcites →https://doi.org/10.1105/tpc.114.122887openalex-snapshot
WOX11 and 12 Are Involved in the First-Step Cell Fate Transition during de Novo Root Organogenesis in Arabidopsis
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.2011.04698.xopenalex-snapshot
OsIAA23‐mediated auxin signaling defines postembryonic maintenance of QC in rice
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02704.xopenalex-snapshot
Molecular physiology of adventitious root formation in Petunia hybrida cuttings: involvement of wound response and primary metabolism
inferredcites →https://doi.org/10.1126/science.273.5277.948openalex-snapshot
Arabidopsis AUX1 Gene: A Permease-Like Regulator of Root Gravitropism
inferredcites →https://doi.org/10.1186/s12864-016-2484-xopenalex-snapshot
Transcriptome analysis reveals the effects of sugar metabolism and auxin and cytokinin signaling pathways on root growth and development of grafted apple
inferredcites →https://doi.org/10.1186/s12870-015-0615-1openalex-snapshot
Jasmonates act positively in adventitious root formation in petunia cuttings
inferredcites →https://doi.org/10.1186/s12870-017-1208-yopenalex-snapshot
Polyamines in the life of Arabidopsis: profiling the expression of S-adenosylmethionine decarboxylase (SAMDC) gene family during its life cycle
inferredcites →https://doi.org/10.1371/journal.pone.0108709openalex-snapshot
Molecular Cloning, Characterization and Expression Analysis of the SAMS Gene during Adventitious Root Development in IBA-Induced Tetraploid Black Locust
inferredcites →https://doi.org/10.1371/journal.pone.0132969openalex-snapshot
De Novo Characterization of the Mung Bean Transcriptome and Transcriptomic Analysis of Adventitious Rooting in Seedlings Using RNA-Seq
inferredcites →https://doi.org/10.3389/fpls.2014.00495openalex-snapshot
Hypocotyl adventitious root organogenesis differs from lateral root development
inferredcites →https://doi.org/10.3390/ijms19030667openalex-snapshot
iTRAQ-Based Proteomic Analysis Reveals Potential Regulation Networks of IBA-Induced Adventitious Root Formation in Apple
inferredcites →https://doi.org/10.3390/ijms19082201openalex-snapshot
Transcriptome Analysis Reveals Multiple Hormones, Wounding and Sugar Signaling Pathways Mediate Adventitious Root Formation in Apple Rootstock
inferredcites →https://doi.org/10.5352/jls.2015.25.4.390openalex-snapshot
Effect of Gibberellin on the Adventitious Root Formation from the Leaves-derived Calli in Persicaria perfoliata
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/s00344-021-10527-8openalex-snapshot
Nitrate Application Induces Adventitious Root Growth by Regulating Gene Expression Patterns in Apple Rootstocks
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inferred← citeshttps://doi.org/10.1007/s13205-025-04671-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s44281-023-00020-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.hpj.2022.11.001openalex-snapshot
Identification of the HAK gene family reveals their critical response to potassium regulation during adventitious root formation in apple rootstock
inferred← citeshttps://doi.org/10.1016/j.hpj.2025.04.021openalex-snapshot
The interplay of malic acid and hormone signaling in adventitious root formation in MdWOX11-overexpressed transgenic apple microshoots
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Physiological and molecular mechanisms of cytokinin involvement in nitrate-mediated adventitious root formation in apples
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Transcriptome analysis reveals the promotive effect of potassium by hormones and sugar signaling pathways during adventitious roots formation in the apple rootstock
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Additional file 1 of Uncovering early transcriptional regulation during adventitious root formation in Medicago sativa
inferred← citeshttps://doi.org/10.6084/m9.figshare.26580320openalex-snapshot
Additional file 2 of Uncovering early transcriptional regulation during adventitious root formation in Medicago sativa
inferred← citeshttps://doi.org/10.6084/m9.figshare.26580323openalex-snapshot
Additional file 3 of Uncovering early transcriptional regulation during adventitious root formation in Medicago sativa
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Additional file 4 of Uncovering early transcriptional regulation during adventitious root formation in Medicago sativa
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