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Mechanisms underlying the enhanced biomass and abiotic stress tolerance phenotype of an Arabidopsis MIOX over‐expresser

https://doi.org/10.1002/pld3.165
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Preharvest salicylic acid and acetylsalicylic acid treatments preserve quality and enhance antioxidant systems during postharvest storage of sweet cherry cultivars
inferredcites →https://doi.org/10.1002/pld3.165openalex-snapshot
Mechanisms underlying the enhanced biomass and abiotic stress tolerance phenotype of an Arabidopsis MIOX over‐expresser
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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
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Ascorbic Acid in Plant Growth, Development and Stress Tolerance
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The Role of Ascorbate in Plant Growth and Development
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Auxin and Its Role in Plant Senescence
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The inositol oxygenase gene family of Arabidopsis is involved in the biosynthesis of nucleotide sugar precursors for cell-wall matrix polysaccharides
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inferredcites →https://doi.org/10.1007/s00425-011-1394-zopenalex-snapshot
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Enzymes for lipolysis and fatty acid metabolism in different organelle fractions from rape seed cotyledons
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Feeding on Leaves of the Glucosinolate Transporter Mutant gtr1gtr2 Reduces Fitness of Myzus persicae
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The auxin-induced K+ channel gene Zmk1 in maize functions in coleoptile growth and is required for embryo development
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Functionally redundant LNG3 and LNG4 genes regulate turgor-driven polar cell elongation through activation of XTH17 and XTH24
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Elevating vitamin C content via overexpression of myo-inositol oxygenase and l-gulono-1,4-lactone oxidase in Arabidopsis leads to enhanced biomass and tolerance to abiotic stresses
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Transgenic tomato plants expressing strawberry d-galacturonic acid reductase gene display enhanced tolerance to abiotic stresses
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inferredcites →https://doi.org/10.1016/j.pbi.2010.02.002openalex-snapshot
Regulatory networks of glucosinolates shape Arabidopsis thaliana fitness
inferredcites →https://doi.org/10.1016/j.plantsci.2012.08.003openalex-snapshot
OsMIOX, a myo-inositol oxygenase gene, improves drought tolerance through scavenging of reactive oxygen species in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1016/j.plantsci.2014.01.003openalex-snapshot
Ferulic acid 5-hydroxylase 1 is essential for expression of anthocyanin biosynthesis-associated genes and anthocyanin accumulation under photooxidative stress in Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2007.12.014openalex-snapshot
Structure and function of plant acyl-CoA oxidases
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Differences between seedlings and flowers in anti-ROS based heat responses of Arabidopsis plants deficient in cyclic nucleotide gated channel 2
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Overexpression of the acerola (Malpighia glabra) monodehydroascorbate reductase gene in transgenic tobacco plants results in increased ascorbate levels and enhanced tolerance to salt stress
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KEAP1 and done? Targeting the NRF2 pathway with sulforaphane
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Biochemical dissection of photorespiration
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Direct Antioxidant Activity of Purified Glucoerucin, the Dietary Secondary Metabolite Contained in Rocket ( Eruca sativa Mill.) Seeds and Sprouts
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Gut-Based Antioxidant Enzymes in a Polyphagous and a Graminivorous Grasshopper
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The New Isothiocyanate 4-(Methylthio)Butylisothiocyanate Selectively Affects Cell-Cycle Progression and Apoptosis Induction of Human Leukemia Cells
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L-Gulono-1,4-lactone oxidase expression rescues vitamin C-deficient Arabidopsis (vtc) mutants
inferredcites →https://doi.org/10.1038/30728openalex-snapshot
The biosynthetic pathway of vitamin C in higher plants
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/nbt777openalex-snapshot
Engineering increased vitamin C levels in plants by overexpression of a D-galacturonic acid reductase
inferredcites →https://doi.org/10.1038/nmeth.3279openalex-snapshot
Reporters for sensitive and quantitative measurement of auxin response
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/nprot.2012.016openalex-snapshot
Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
inferredcites →https://doi.org/10.1038/s41467-018-03884-8openalex-snapshot
BRI1 and BAK1 interact with G proteins and regulate sugar-responsive growth and development in Arabidopsis
inferredcites →https://doi.org/10.1038/srep31854openalex-snapshot
Glucose enhances indolic glucosinolate biosynthesis without reducing primary sulfur assimilation
inferredcites →https://doi.org/10.1042/ebc20160016openalex-snapshot
Photosynthesis
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1071/fp15119openalex-snapshot
Exogenous salicylic acid-triggered changes in the glutathione transferases and peroxidases are key factors in the successful salt stress acclimation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1071/fp16172openalex-snapshot
Moderate to severe water limitation differentially affects the phenome and ionome of Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0308095100openalex-snapshot
Expression of an active tobacco mitogen-activated protein kinase kinase kinase enhances freezing tolerance in transgenic maize
inferredcites →https://doi.org/10.1073/pnas.0510864103openalex-snapshot
l -Tartaric acid synthesis from vitamin C in higher plants
inferredcites →https://doi.org/10.1073/pnas.0604882103openalex-snapshot
Overexpressing a NAM, ATAF, and CUC (NAC) transcription factor enhances drought resistance and salt tolerance in rice
inferredcites →https://doi.org/10.1073/pnas.1612635113openalex-snapshot
Arabidopsis thaliana GH3.5 acyl acid amido synthetase mediates metabolic crosstalk in auxin and salicylic acid homeostasis
inferredcites →https://doi.org/10.1073/pnas.93.23.13404openalex-snapshot
Constitutive expression of the cold-regulated Arabidopsis thaliana COR15a gene affects both chloroplast and protoplast freezing tolerance
inferredcites →https://doi.org/10.1073/pnas.95.24.14570openalex-snapshot
Mode of action of the COR15a gene on the freezing tolerance of Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m006796200openalex-snapshot
High Resolution X-ray Crystallography Shows That Ascorbate Is a Cofactor for Myrosinase and Substitutes for the Function of the Catalytic Base
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GDP-Mannose 3′,5′-Epimerase Forms GDP-L-gulose, a Putative Intermediate for the de Novo Biosynthesis of Vitamin C in Plants
inferredcites →https://doi.org/10.1074/jbc.m400071200openalex-snapshot
Characterization and Metabolic Function of a Peroxisomal Sarcosine and Pipecolate Oxidase from Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m513054200openalex-snapshot
Plant Sulfite Oxidase as Novel Producer of H2O2
inferredcites →https://doi.org/10.1080/15216540500138402openalex-snapshot
Purification and Characterization of Two Small Heat Shock Proteins from Anabaena sp. PCC 7120
inferredcites →https://doi.org/10.1089/ars.2012.5097openalex-snapshot
Vitamin C and the Abscisic Acid-Insensitive 4 Transcription Factor Are Important Determinants of Aphid Resistance in Arabidopsis
inferredcites →https://doi.org/10.1093/aob/mct067openalex-snapshot
Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany
inferredcites →https://doi.org/10.1093/genetics/154.2.847openalex-snapshot
Identification of Ascorbic Acid-Deficient Arabidopsis thaliana Mutants
inferredcites →https://doi.org/10.1093/jxb/erl010openalex-snapshot
Modulation of plant morphology, root architecture, and cell structure by low vitamin C in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/err126openalex-snapshot
Hydraulic conductance as well as nitrogen accumulation plays a role in the higher rate of leaf photosynthesis of the most productive variety of rice in Japan
inferredcites →https://doi.org/10.1093/jxb/ers297openalex-snapshot
Ascorbate as seen through plant evolution: the rise of a successful molecule?
inferredcites →https://doi.org/10.1093/jxb/ers330openalex-snapshot
The role of l-ascorbic acid recycling in responding to environmental stress and in promoting plant growth
inferredcites →https://doi.org/10.1093/jxb/ert080openalex-snapshot
Auxin biosynthesis and storage forms
inferredcites →https://doi.org/10.1093/jxb/ert140openalex-snapshot
Identification of Arabidopsis VTC3 as a putative and unique dual function protein kinase::protein phosphatase involved in the regulation of the ascorbic acid pool in plants
inferredcites →https://doi.org/10.1093/jxb/ert348openalex-snapshot
Jasmonic acid and glucose synergistically modulate the accumulation of glucosinolates in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/ert420openalex-snapshot
DELLA proteins modulateArabidopsisdefences induced in response to caterpillar herbivory
inferredcites →https://doi.org/10.1093/mp/sss100openalex-snapshot
Overexpression of Arabidopsis YUCCA6 in Potato Results in High-Auxin Developmental Phenotypes and Enhanced Resistance to Water Deficit
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029285openalex-snapshot
Molecular Characterization and Physiological Role of a Glyoxysome-Bound Ascorbate Peroxidase from Spinach
inferredcites →https://doi.org/10.1093/pcp/pcn114openalex-snapshot
A Putative Peroxisomal Polyamine Oxidase, AtPAO4, is Involved in Polyamine Catabolism in Arabidopsis thaliana
inferredcites →https://doi.org/10.1094/mpmi-23-3-0340openalex-snapshot
Ascorbic Acid Deficiency in Arabidopsis Induces Constitutive Priming That is Dependent on Hydrogen Peroxide, Salicylic Acid, and the NPR1 Gene
inferredcites →https://doi.org/10.1098/rsos.160592openalex-snapshot
MultispeQ Beta: a tool for large-scale plant phenotyping connected to the open PhotosynQ network
inferredcites →https://doi.org/10.1104/pp.103.033936openalex-snapshot
myo-Inositol Oxygenase Offers a Possible Entry Point into Plant Ascorbate Biosynthesis
inferredcites →https://doi.org/10.1104/pp.103.034736openalex-snapshot
Comprehensive Comparison of Auxin-Regulated and Brassinosteroid-Regulated Genes in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.042820openalex-snapshot
Role of Hsp17.4-CII as Coregulator and Cytoplasmic Retention Factor of Tomato Heat Stress Transcription Factor HsfA2
inferredcites →https://doi.org/10.1104/pp.104.045542openalex-snapshot
Characterization of the Arabidopsis Lysine-Rich Arabinogalactan-Protein AtAGP17 Mutant (rat1) That Results in a Decreased Efficiency of Agrobacterium Transformation
inferredcites →https://doi.org/10.1104/pp.105.063743openalex-snapshot
Genome-Wide Identification and Testing of Superior Reference Genes for Transcript Normalization in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.065896openalex-snapshot
Genome-Wide Analysis of Hydrogen Peroxide-Regulated Gene Expression in Arabidopsis Reveals a High Light-Induced Transcriptional Cluster Involved in Anthocyanin Biosynthesis
inferredcites →https://doi.org/10.1104/pp.105.067686openalex-snapshot
Ascorbic Acid Deficiency Activates Cell Death and Disease Resistance Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.078204openalex-snapshot
Reactive Oxygen Species and Reactive Nitrogen Species in Peroxisomes. Production, Scavenging, and Role in Cell Signaling
inferredcites →https://doi.org/10.1104/pp.108.125757openalex-snapshot
Subclade of Flavin-Monooxygenases Involved in Aliphatic Glucosinolate Biosynthesis
inferredcites →https://doi.org/10.1104/pp.108.135129openalex-snapshot
VTC4 Is a Bifunctional Enzyme That Affects Myoinositol and Ascorbate Biosynthesis in Plants
inferredcites →https://doi.org/10.1104/pp.109.149286openalex-snapshot
A Complex Interplay of Three R2R3 MYB Transcription Factors Determines the Profile of Aliphatic Glucosinolates in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.167569openalex-snapshot
Ascorbate and Glutathione: The Heart of the Redox Hub
inferredcites →https://doi.org/10.1104/pp.110.171918openalex-snapshot
The Physiological Role of Ascorbate as Photosystem II Electron Donor: Protection against Photoinactivation in Heat-Stressed Leaves
inferredcites →https://doi.org/10.1104/pp.111.174169openalex-snapshot
Intronic T-DNA Insertion Renders Arabidopsisopr3a Conditional Jasmonic Acid-Producing Mutant
inferredcites →https://doi.org/10.1104/pp.111.178681openalex-snapshot
Small Heat Shock Protein Hsp17.8 Functions as an AKR2A Cofactor in the Targeting of Chloroplast Outer Membrane Proteins in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.112.196428openalex-snapshot
Auxin Activates the Plasma Membrane H+-ATPase by Phosphorylation during Hypocotyl Elongation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.219006openalex-snapshot
Improving Photosynthesis
inferredcites →https://doi.org/10.1104/pp.113.227801openalex-snapshot
Monoubiquitination of Histone 2B at the Disease Resistance Gene Locus Regulates Its Expression and Impacts Immune Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.114.245399openalex-snapshot
Disordered Cold Regulated15 Proteins Protect Chloroplast Membranes during Freezing through Binding and Folding, But Do Not Stabilize Chloroplast Enzymes in Vivo
inferredcites →https://doi.org/10.1104/pp.16.00536openalex-snapshot
Class I and II small heat-shock proteins protect protein translation factors during heat stress
inferredcites →https://doi.org/10.1104/pp.16.00725openalex-snapshot
Ethylene- and shade-induced hypocotyl elongation share transcriptome patterns and functional regulators
inferredcites →https://doi.org/10.1105/tpc.010011openalex-snapshot
Growth Stage–Based Phenotypic Analysis of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.010261openalex-snapshot
The Arabidopsis Epithiospecifier Protein Promotes the Hydrolysis of Glucosinolates to Nitriles and Influences Trichoplusia ni Herbivory
inferredcites →https://doi.org/10.1105/tpc.010538openalex-snapshot
Leaf Vitamin C Contents Modulate Plant Defense Transcripts and Regulate Genes That Control Development through Hormone Signaling[W]
inferredcites →https://doi.org/10.1105/tpc.104.022699openalex-snapshot
Isolation and Functional Analysis of Arabidopsis Stress-Inducible NAC Transcription Factors That Bind to a Drought-Responsivecis-Element in theearly responsive to dehydration stress 1Promoter[W]
inferredcites →https://doi.org/10.1105/tpc.106.049965openalex-snapshot
Signaling from an Altered Cell Wall to the Nucleus Mediates Sugar-Responsive Growth and Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.110.082792openalex-snapshot
Disruption of LACCASE4 and 17 Results in Tissue-Specific Alterations to Lignification of Arabidopsis thaliana Stems
inferredcites →https://doi.org/10.1105/tpc.111.090100openalex-snapshot
The Transcription Factor ABI4 Is Required for the Ascorbic Acid–Dependent Regulation of Growth and Regulation of Jasmonate-Dependent Defense Signaling Pathways in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.117770openalex-snapshot
LACCASE Is Necessary and Nonredundant with PEROXIDASE for Lignin Polymerization during Vascular Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.118927openalex-snapshot
The Protein Phosphatase RCF2 and Its Interacting Partner NAC019 Are Critical for Heat Stress–Responsive Gene Regulation and Thermotolerance in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.7.1499openalex-snapshot
Growth Stage-Based Phenotypic Analysis of Arabidopsis: A Model for High Throughput Functional Genomics in Plants
inferredcites →https://doi.org/10.1105/tpc.16.00130openalex-snapshot
MYB75 Phosphorylation by MPK4 Is Required for Light-Induced Anthocyanin Accumulation in Arabidopsis
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A guide to using MapMan to visualize and compare Omics data in plants: a case study in the crop species, Maize
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A lysine‐rich arabinogalactan protein in Arabidopsis is essential for plant growth and development, including cell division and expansion
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03039.xopenalex-snapshot
SA‐inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA‐responsive PDF1.2 transcription
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03101.xopenalex-snapshot
Identification of a flavin‐monooxygenase as the S ‐oxygenating enzyme in aliphatic glucosinolate biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03133.xopenalex-snapshot
The R2R3‐MYB transcription factor HAG1/MYB28 is a regulator of methionine‐derived glucosinolate biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03266.xopenalex-snapshot
Two genes in Arabidopsis thaliana encoding GDP‐ l ‐galactose phosphorylase are required for ascorbate biosynthesis and seedling viability
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03373.xopenalex-snapshot
Regulation of the anthocyanin biosynthetic pathway by the TTG1/bHLH/Myb transcriptional complex in Arabidopsis seedlings
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Enhanced tolerance to ozone and drought stresses in transgenic tobacco overexpressing dehydroascorbate reductase in cytosol
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02295.xopenalex-snapshot
HAG2/MYB76 and HAG3/MYB29 exert a specific and coordinated control on the regulation of aliphatic glucosinolate biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02981.xopenalex-snapshot
Myo‐inositol oxygenase genes are involved in the development of syncytia induced by Heterodera schachtii in Arabidopsis roots
inferredcites →https://doi.org/10.1111/nph.12535openalex-snapshot
Myo‐inositol oxygenase is important for the removal of excess myo‐inositol from syncytia induced by H eterodera schachtii in A rabidopsis roots
inferredcites →https://doi.org/10.1111/nph.13612openalex-snapshot
CML 10, a variant of calmodulin, modulates ascorbic acid synthesis
inferredcites →https://doi.org/10.1111/pce.12409openalex-snapshot
Peroxisomal APX knockdown triggers antioxidant mechanisms favourable for coping with high photorespiratory H 2 O 2 induced by CAT deficiency in rice
inferredcites →https://doi.org/10.1111/plb.12898openalex-snapshot
The Myo‐inositol pathway does not contribute to ascorbic acid synthesis
inferredcites →https://doi.org/10.1111/tpj.13039openalex-snapshot
Ultra‐fast alterations in mRNA levels uncover multiple players in light stress acclimation in plants
inferredcites →https://doi.org/10.1126/science.1080585openalex-snapshot
Role of the Arabidopsis Glucose Sensor HXK1 in Nutrient, Light, and Hormonal Signaling
inferredcites →https://doi.org/10.1126/science.291.5502.306openalex-snapshot
A Role for Flavin Monooxygenase-Like Enzymes in Auxin Biosynthesis
inferredcites →https://doi.org/10.1146/annurev.phyto.050908.135202openalex-snapshot
Salicylic Acid, a Multifaceted Hormone to Combat Disease
inferredcites →https://doi.org/10.1155/2008/619832openalex-snapshot
Blast2GO: A Comprehensive Suite for Functional Analysis in Plant Genomics
inferredcites →https://doi.org/10.1155/2012/580342openalex-snapshot
Role of Ascorbate in the Regulation of theArabidopsis thalianaRoot Growth by Phosphate Availability
inferredcites →https://doi.org/10.1155/2013/795964openalex-snapshot
L-Ascorbic Acid: A Multifunctional Molecule Supporting Plant Growth and Development
inferredcites →https://doi.org/10.1186/1471-2105-7-179openalex-snapshot
AtRTPrimer: database for Arabidopsis genome-wide homogeneous and specific RT-PCR primer-pairs
inferredcites →https://doi.org/10.1186/1471-2105-7-535openalex-snapshot
PageMan: An interactive ontology tool to generate, display, and annotate overview graphs for profiling experiments
inferredcites →https://doi.org/10.1186/1471-2229-13-1openalex-snapshot
The bHLH transcription factor SPATULA regulates root growth by controlling the size of the root meristem
inferredcites →https://doi.org/10.1186/1471-2229-13-109openalex-snapshot
Copper-containing amine oxidases contribute to terminal polyamine oxidation in peroxisomes and apoplast of Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2229-13-47openalex-snapshot
Overexpression of the transcription factor RAP2.6 leads to enhanced callose deposition in syncytia and enhanced resistance against the beet cyst nematode Heterodera schachtiiin Arabidopsis roots
inferredcites →https://doi.org/10.1186/gb-2013-14-4-r36openalex-snapshot
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
inferredcites →https://doi.org/10.1371/journal.pone.0001322openalex-snapshot
A Systems Biology Approach Identifies a R2R3 MYB Gene Subfamily with Distinct and Overlapping Functions in Regulation of Aliphatic Glucosinolates
inferredcites →https://doi.org/10.1373/clinchem.2008.112797openalex-snapshot
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
inferredcites →https://doi.org/10.3389/fphys.2015.00397openalex-snapshot
Vitamin C in Health and Disease: Its Role in the Metabolism of Cells and Redox State in the Brain
inferredcites →https://doi.org/10.3389/fpls.2012.00069openalex-snapshot
myo-Inositol oxygenase is required for responses to low energy conditions in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2012.00109openalex-snapshot
The CELLULOSE SYNTHASE-LIKE A and CELLULOSE SYNTHASE-LIKE C families: recent advances and future perspectives
inferredcites →https://doi.org/10.3389/fpls.2016.00187openalex-snapshot
Global Plant Stress Signaling: Reactive Oxygen Species at the Cross-Road
inferredcites →https://doi.org/10.3389/fpls.2016.01292openalex-snapshot
Two Novel Flavin-Containing Monooxygenases Involved in Biosynthesis of Aliphatic Glucosinolates
inferredcites →https://doi.org/10.3389/fpls.2017.02230openalex-snapshot
UDP-Glucose: A Potential Signaling Molecule in Plants?
inferredcites →https://doi.org/10.3390/toxins2040593openalex-snapshot
Biological Profile of Erucin: A New Promising Anticancer Agent from Cruciferous Vegetables
inferredcites →https://doi.org/10.3791/55425openalex-snapshot
A Straightforward Method for Glucosinolate Extraction and Analysis with High-pressure Liquid Chromatography (HPLC)
inferredcites →https://doi.org/10.3791/55425-vopenalex-snapshot
A Straightforward Method for Glucosinolate Extraction and Analysis with High-pressure Liquid Chromatography (HPLC)
inferredcites →https://doi.org/10.3945/ajcn.114.089284openalex-snapshot
Processed foods: contributions to nutrition
inferredcites →https://doi.org/10.7554/elife.00260openalex-snapshot
Sugar promotes vegetative phase change in Arabidopsis thaliana by repressing the expression of MIR156A and MIR156C

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/10.1016/j.plantsci.2025.112729openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.03.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107787openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113196openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/jxb/eraf542openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2021.02.24.432757openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2024.02.22.578673openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.17032openalex-snapshot
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inferred← citeshttps://doi.org/10.15835/nbha48312000openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2023.1157435openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2026.1725249openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/genes11121449openalex-snapshot
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inferred← citeshttps://doi.org/10.56369/tsaes.3375openalex-snapshot
ELECTRICAL CONDUCTIVITY OF NUTRIENT SOLUTION AND THEIR EFFECT ON BIOACTIVE COMPOUNDS AND YIELD OF BELL PEPPER (Capsicum annuum L.)
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