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Different cucumber CsYUC genes regulate response to abiotic stresses and flower 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/10.1007/s00299-015-1814-9openalex-snapshot
Silicon improves salt tolerance by increasing root water uptake in Cucumis sativus L.
inferredcites →https://doi.org/10.1007/s00425-011-1552-3openalex-snapshot
Activation of a flavin monooxygenase gene YUCCA7 enhances drought resistance in Arabidopsis
inferredcites →https://doi.org/10.1007/s00425-014-2115-1openalex-snapshot
Endogenous salicylic acid accumulation is required for chilling tolerance in cucumber (Cucumis sativus L.) seedlings
inferredcites →https://doi.org/10.1007/s00438-008-0328-3openalex-snapshot
NARROW LEAF 7 controls leaf shape mediated by auxin in rice
inferredcites →https://doi.org/10.1007/s10142-010-0174-3openalex-snapshot
Auxin-related gene families in abiotic stress response in Sorghum bicolor
inferredcites →https://doi.org/10.1007/s11103-007-9203-6openalex-snapshot
Constitutively wilted 1, a member of the rice YUCCA gene family, is required for maintaining water homeostasis and an appropriate root to shoot ratio
inferredcites →https://doi.org/10.1016/0022-1759(86)90070-0openalex-snapshot
A biotin-avidin-based enzyme immunoassay to quantify three phytohormones: auxin, abscisic acid and zeatin-riboside
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1016/j.gene.2014.06.020openalex-snapshot
Isolation and characterization of three TaYUC10genes from wheat
inferredcites →https://doi.org/10.1016/j.pharmthera.2005.01.001openalex-snapshot
Mammalian flavin-containing monooxygenases: structure/function, genetic polymorphisms and role in drug metabolism
inferredcites →https://doi.org/10.1016/j.plantsci.2013.04.009openalex-snapshot
The role of CORYMBOSA1/BIG and auxin in the growth of Arabidopsis pedicel and internode
inferredcites →https://doi.org/10.1016/j.plaphy.2011.02.022openalex-snapshot
Gene structure and spatiotemporal expression profile of tomato genes encoding YUCCA-like flavin monooxygenases: The ToFZY gene family
inferredcites →https://doi.org/10.1016/j.tplants.2007.06.011openalex-snapshot
Molecular dissection of the role of auxin in fruit initiation
inferredcites →https://doi.org/10.1016/j.tplants.2007.08.009openalex-snapshot
Flavin-containing monooxygenases in plants: looking beyond detox
inferredcites →https://doi.org/10.1016/s1360-1385(01)02101-xopenalex-snapshot
Polar auxin transport: controlling where and how much
inferredcites →https://doi.org/10.1038/ng.475openalex-snapshot
The genome of the cucumber, Cucumis sativus L.
inferredcites →https://doi.org/10.1038/srep08031openalex-snapshot
Transcriptomic analysis reveals the roles of microtubule-related genes and transcription factors in fruit length regulation in cucumber (Cucumis sativus L.)
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/10.1046/j.1365-313x.2001.01173.xopenalex-snapshot
Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth
inferredcites →https://doi.org/10.1073/pnas.0805596105openalex-snapshot
sparse inflorescence1 encodes a monocot-specific YUCCA -like gene required for vegetative and reproductive development in maize
inferredcites →https://doi.org/10.1073/pnas.1000869107openalex-snapshot
Auxins reverse plant male sterility caused by high temperatures
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.95.12.7197openalex-snapshot
High temperature promotes auxin-mediated hypocotyl elongation in Arabidopsis
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1093/jxb/err094openalex-snapshot
YUCCA6 over-expression demonstrates auxin function in delaying leaf senescence in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/ers091openalex-snapshot
The pathway of auxin biosynthesis in plants
inferredcites →https://doi.org/10.1093/jxb/ert080openalex-snapshot
Auxin biosynthesis and storage forms
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/mp/ssr104openalex-snapshot
Auxin Biosynthesis: A Simple Two-Step Pathway Converts Tryptophan to Indole-3-Acetic Acid in Plants
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/pcp/pcn101openalex-snapshot
Arabidopsis Transcriptome Analysis under Drought, Cold, High-Salinity and ABA Treatment Conditions using a Tiling Array
inferredcites →https://doi.org/10.1101/cshperspect.a001628openalex-snapshot
Distinct and Dynamic Auxin Activities During Reproductive Development
inferredcites →https://doi.org/10.1101/gad.1415106openalex-snapshot
Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.187849.112openalex-snapshot
Linking photoreceptor excitation to changes in plant architecture
inferredcites →https://doi.org/10.1101/gad.219502openalex-snapshot
FLOOZY of petunia is a flavin mono-oxygenase-like protein required for the specification of leaf and flower architecture
inferredcites →https://doi.org/10.1101/gad.905201openalex-snapshot
BIG: a calossin-like protein required for polar auxin transport in Arabidopsis
inferredcites →https://doi.org/10.1101/gr.849004openalex-snapshot
WebLogo: A Sequence Logo Generator: Figure 1
inferredcites →https://doi.org/10.1104/pp.102.010579openalex-snapshot
Mutations in the Gravity Persistence Signal Loci in Arabidopsis Disrupt the Perception and/or Signal Transduction of Gravitropic Stimuli
inferredcites →https://doi.org/10.1104/pp.105.063495openalex-snapshot
Interaction of Auxin and ERECTA in Elaborating Arabidopsis Inflorescence Architecture Revealed by the Activation Tagging of a New Member of the YUCCA Family Putative Flavin Monooxygenases
inferredcites →https://doi.org/10.1104/pp.106.091561openalex-snapshot
Auxin Biosynthesis by the YUCCA Genes in Rice
inferredcites →https://doi.org/10.1104/pp.110.3.933openalex-snapshot
Gravitropic Response of Inflorescence Stems in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.99.4.1271openalex-snapshot
The Acid Growth Theory of auxin-induced cell elongation is alive and well.
inferredcites →https://doi.org/10.1105/tpc.007542openalex-snapshot
Auxin Acts in Xylem-Associated or Medullary Cells to Mediate Apical Dominance
inferredcites →https://doi.org/10.1105/tpc.107.053009openalex-snapshot
Auxin Synthesized by the YUCCA Flavin Monooxygenases Is Essential for Embryogenesis and Leaf Formation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.107854openalex-snapshot
Transcription Repressor HANABA TARANU Controls Flower Development by Integrating the Actions of Multiple Hormones, Floral Organ Specification Genes, and GATA3 Family Genes inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.2.11.1071openalex-snapshot
Growth and Development of the axr1 Mutants of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03983.xopenalex-snapshot
Hormonal regulation of temperature‐induced growth in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04866.xopenalex-snapshot
Alternative splicing of the auxin biosynthesis gene YUCCA4 determines its subcellular compartmentation
inferredcites →https://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
inferredcites →https://doi.org/10.1111/jipb.12150openalex-snapshot
Auxin Biosynthesis by the YUCCA6 Flavin Monooxygenase Gene in Woodland Strawberry
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-arplant-042809-112308openalex-snapshot
Auxin Biosynthesis and Its Role in Plant Development
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103805openalex-snapshot
Auxin: The Looping Star in Plant Development
inferredcites →https://doi.org/10.1371/journal.pgen.1002594openalex-snapshot
PIF4–Mediated Activation of YUCCA8 Expression Integrates Temperature into the Auxin Pathway in Regulating Arabidopsis Hypocotyl Growth
inferredcites →https://doi.org/10.17660/actahortic.2010.871.52openalex-snapshot
EFFECT OF DIFFERENT LEVELS OF SHADING ON YIELD AND FRUIT QUALITY OF CUCUMBER (CUCUMIS SATIVUS)
inferredcites →https://doi.org/10.3389/fpls.2014.00333openalex-snapshot
Auxin polar transport in stamen formation and development: how many actors?
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Knockout of Slmtc Impacts Tomato Seed Size and Reduces Resistance to Salt Stress in Tomato
inferred← citeshttps://doi.org/10.1007/978-3-030-54478-2_6openalex-snapshot
Functional Correlation of Auxin and Serotonin in Plants: Possible Receptor Surrogacy?
inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_7openalex-snapshot
Recent Insights into Auxin-Mediated Molecular Cross Talk Events Associated with Regulation of Root Growth and Architecture During Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-78521-5_3openalex-snapshot
Auxins and Plant Response to Adverse Environmental Conditions
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Regulating Plant Growth and Defense: Multifaceted Roles of Auxin in Plants
inferred← citeshttps://doi.org/10.1007/s00425-020-03467-2openalex-snapshot
Salicylic acid regulates adventitious root formation via competitive inhibition of the auxin conjugation enzyme CsGH3.5 in cucumber hypocotyls
inferred← citeshttps://doi.org/10.1007/s00425-024-04398-yopenalex-snapshot
Identification of microRNAs and their target genes associated with chasmogamous and cleistogamous flower development in Viola prionantha
inferred← citeshttps://doi.org/10.1007/s00425-026-05093-wopenalex-snapshot
Integrated analysis of auxin-related gene families and WGCNA reveals regulatory mechanisms underlying reproductive organ development in pear
inferred← citeshttps://doi.org/10.1007/s11738-026-03928-3openalex-snapshot
Transcriptional and biochemical responses of wheat seedlings to trimethylamine N-oxide under drought stress
inferred← citeshttps://doi.org/10.1007/s40415-023-00922-8openalex-snapshot
Treatment with auxin and paclobutrazol mediates ROS regulation, antioxidant defence system and cell wall response in salt treated soybean
inferred← citeshttps://doi.org/10.1016/b978-0-12-822849-4.00002-4openalex-snapshot
Role of phytohormones as master regulators during the abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-323-95375-7.00004-5openalex-snapshot
Hormonal crosstalk in abiotic stress responses
inferred← citeshttps://doi.org/10.1016/b978-0-443-18927-2.00009-1openalex-snapshot
Plant growth coordination during stress conditions: Role of phytohormones
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110285openalex-snapshot
Gamma-aminobutyric acid enhances tolerance to iron deficiency by stimulating auxin signaling in cucumber (Cucumis sativusL.)
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104038openalex-snapshot
Mild cadmium stress induces auxin synthesis and accumulation, while severe cadmium stress causes its rapid depletion in barley root tip
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.02.001openalex-snapshot
Genome-wide identification of apple auxin receptor family genes and functional characterization of MdAFB1
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.143712openalex-snapshot
Overexpression of auxin synthesis gene PagYUC6a in poplar (Populus alba × P. glandulosa) enhances salt tolerance
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.113290openalex-snapshot
Systematical characterization of YUCCA gene family in five cotton species, and potential functions of YUCCA22 gene in drought resistance of cotton
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121764openalex-snapshot
HSF-HSP-GST coordinated network underlies ginger's adaptation to combined high-temperature and strong-light stress: Insights from multi-omics integration
inferred← citeshttps://doi.org/10.1016/j.ocsci.2022.07.001openalex-snapshot
Genome-wide identification and expression profiling of the YUCCA gene family in Brassica napus
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112228openalex-snapshot
The knockout of SlMTC impacts tomato seed size and reduces resistance to salt stress in tomato
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102902openalex-snapshot
YUCCA gene expression modulates Cercospora leaf spot (CLS) resistance, Leaf regeneration: A comparative analysis of sugar content and root yield in different Sugar beet (Beta vulgaris L.)
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Current progress in genetic and genomics-aided breeding for stress resistance in cucumber (Cucumis sativus L.)
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.05.011openalex-snapshot
Out of Shape During Stress: A Key Role for Auxin
inferred← citeshttps://doi.org/10.1038/s41438-020-00354-5openalex-snapshot
The curvature of cucumber fruits is associated with spatial variation in auxin accumulation and expression of a YUCCA biosynthesis gene
inferred← citeshttps://doi.org/10.1038/s41598-020-66483-yopenalex-snapshot
Genome-wide identification and expression profiling of the YUCCA gene family in Malus domestica
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A comparative UHPLC-Q/TOF–MS-based eco-metabolomics approach reveals temperature adaptation of four Nepenthes species
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OsWNK9 regulates the expression of key transcription factors, phytohormonal, and transporters genes to improve salinity stress tolerance in rice
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The CsHEC1-CsOVATE module contributes to fruit neck length variation via modulating auxin biosynthesis in cucumber
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Ameliorative effect of indole-3-acetic acid- and siderophore-producing Leclercia adecarboxylata MO1 on cucumber plants under zinc stress
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Auxin biosynthesis: spatial regulation and adaptation to stress
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VvFHY3 links auxin and endoplasmic reticulum stress to regulate grape anthocyanin biosynthesis at high temperatures
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A cytochrome P450 gene, GmSUR2 a , confers submergence tolerance and improves yield in soybean by modulating auxin homeostasis
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Preface by A. S. Crafts
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Impact of Climate Change on Regulation of Genes Involved in Sex Determination and Fruit Production in Cucumber
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CsPHYB–CsPIF3/4 Regulates Hypocotyl Elongation by Coordinating the Auxin and Gibberellin Biosynthetic Pathways in Cucumber (Cucumis sativus L.)
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Identification of Quantitative Trait Loci Controlling High-Temperature Tolerance in Cucumber (Cucumis sativus L.) Seedlings
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