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Systems analyses of key metabolic modules of floral and extrafloral nectaries of cotton

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What this work says

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

inferredcites →https://doi.org/10.1002/j.1537-2197.1975.tb14124.xopenalex-snapshot
ULTRASTRUCTURE OF THE SUBGLANDULAR CELLS FROM THE FOLIAR NECTARIES OF COTTON IN RELATION TO THE DISTRIBUTION OF PLASMODESMATA AND THE SYMPLASTIC TRANSPORT OF NECTAR
inferredcites →https://doi.org/10.1002/j.1537-2197.1979.tb06309.xopenalex-snapshot
ULTRASTRUCTURE OF NECTARIES IN RELATION TO NECTAR SECRETION
inferredcites →https://doi.org/10.1002/j.1537-2197.1983.tb10850.xopenalex-snapshot
NECTAR PRODUCTION PATTERNS IN IPOMOPSIS AGGREGATA (POLEMONIACEAE)
inferredcites →https://doi.org/10.1002/pld3.120openalex-snapshot
An integrated transcriptomics and metabolomics analysis of the Cucurbita pepo nectary implicates key modules of primary metabolism involved in nectar synthesis and secretion
inferredcites →https://doi.org/10.1006/anbo.2000.1342openalex-snapshot
The Effect of Herbivory on Temporal and Spatial Dynamics of Foliar Nectar Production in Cotton and Castor
inferredcites →https://doi.org/10.1007/978-1-4020-5937-7openalex-snapshot
Nectaries and Nectar
inferredcites →https://doi.org/10.1007/978-3-662-04064-5_2openalex-snapshot
Nitrate Reduction and signalling
inferredcites →https://doi.org/10.1007/s00114-005-0062-1openalex-snapshot
A novel role for proline in plant floral nectars
inferredcites →https://doi.org/10.1007/s00442-002-1168-1openalex-snapshot
Behavioral mechanisms underlie an ant-plant mutualism
inferredcites →https://doi.org/10.1007/s00497-009-0112-5openalex-snapshot
Arabidopsis thaliana as a model for functional nectary analysis
inferredcites →https://doi.org/10.1007/s00606-003-0282-9openalex-snapshot
A major function of the tobacco floral nectary is defense against microbial attack
inferredcites →https://doi.org/10.1007/s00606-018-1531-2openalex-snapshot
Structure and ultrastructure of floral nectaries of two Opuntia species (Cactaceae) in relation to their floral visitors
inferredcites →https://doi.org/10.1007/s00709-004-0051-9openalex-snapshot
Nectar production and transportation in the nectaries of the female Cucumis sativus L. flower during anthesis
inferredcites →https://doi.org/10.1007/s00709-018-1216-2openalex-snapshot
Nectar trichome structure of aquatic bladderworts from the section Utricularia (Lentibulariaceae) with observation of flower visitors and pollinators
inferredcites →https://doi.org/10.1007/s00709-018-1269-2openalex-snapshot
Micromorphological and histochemical attributes of flowers and floral reward in Linaria vulgaris (Plantaginaceae)
inferredcites →https://doi.org/10.1007/s00709-018-1274-5openalex-snapshot
Floral nectary and osmophore of Epipactis helleborine (L.) Crantz (Orchidaceae)
inferredcites →https://doi.org/10.1007/s10886-018-01044-2openalex-snapshot
Effects of Non-Protein Amino Acids in Nectar on Bee Survival and Behavior
inferredcites →https://doi.org/10.1007/s11103-008-9361-1openalex-snapshot
Identification, cloning and characterization of a GDSL lipase secreted into the nectar of Jacaranda mimosifolia
inferredcites →https://doi.org/10.1007/s13361-017-1699-7openalex-snapshot
Overlapping MALDI-Mass Spectrometry Imaging for In-Parallel MS and MS/MS Data Acquisition without Sacrificing Spatial Resolution
inferredcites →https://doi.org/10.1016/j.cub.2009.03.015openalex-snapshot
Communal Nutrition in Ants
inferredcites →https://doi.org/10.1016/j.febslet.2007.04.047openalex-snapshot
Nitrate transporters and peptide transporters
inferredcites →https://doi.org/10.1016/j.flora.2012.06.005openalex-snapshot
Functional genomics of nectar production in the Brassicaceae
inferredcites →https://doi.org/10.1016/j.flora.2017.04.001openalex-snapshot
Ultrastructural and histochemical analysis of glandular trichomes of Marrubium vulgare L. (Lamiaceae)
inferredcites →https://doi.org/10.1016/j.heliyon.2018.e00541openalex-snapshot
Foliar secretory structures in Ekebergia capensis (Meliaceae)
inferredcites →https://doi.org/10.1016/j.jinsphys.2014.05.025openalex-snapshot
Amino acid and carbohydrate tradeoffs by honey bee nectar foragers and their implications for plant–pollinator interactions
inferredcites →https://doi.org/10.1016/j.jplph.2011.03.007openalex-snapshot
Expression and substrate specificity of betaine/proline transporters suggest a novel choline transport mechanism in sugar beet
inferredcites →https://doi.org/10.1016/j.molp.2015.12.019openalex-snapshot
A Role for GIBBERELLIN 2-OXIDASE6 and Gibberellins in Regulating Nectar Production
inferredcites →https://doi.org/10.1016/j.plantsci.2007.05.008openalex-snapshot
Transient starch metabolism in ornamental tobacco floral nectaries regulates nectar composition and release
inferredcites →https://doi.org/10.1016/j.plantsci.2017.04.012openalex-snapshot
Review: Nectar biology: From molecules to ecosystems
inferredcites →https://doi.org/10.1016/j.tplants.2004.05.008openalex-snapshot
Is the nectar redox cycle a floral defense against microbial attack?
inferredcites →https://doi.org/10.1016/j.tplants.2011.01.003openalex-snapshot
Nectar: generation, regulation and ecological functions
inferredcites →https://doi.org/10.1016/s1044-0305(99)00047-1openalex-snapshot
An integrated method for spectrum extraction and compound identification from gas chromatography/mass spectrometry data
inferredcites →https://doi.org/10.1021/jf60193a038openalex-snapshot
Amino acid composition of cotton nectar
inferredcites →https://doi.org/10.1023/a:1006363508648openalex-snapshot
Nectarin I is a novel, soluble germin-like protein expressed in the nectar of Nicotiana sp.
inferredcites →https://doi.org/10.1038/nature13082openalex-snapshot
Nectar secretion requires sucrose phosphate synthases and the sugar transporter SWEET9
inferredcites →https://doi.org/10.1051/apido:19810203openalex-snapshot
AMINO ACIDS IN THE FLORAL NECTAR OF COTTON
inferredcites →https://doi.org/10.1071/bi9710647openalex-snapshot
Nectar Production in Abutilon I. Movement of Nectar Through the Cuticle
inferredcites →https://doi.org/10.1071/bi9710665openalex-snapshot
Nectar Production in Abutilon III. Sugar Secretion
inferredcites →https://doi.org/10.1071/bt17086openalex-snapshot
Floral nectaries of Heliocarpus popayanensis and Luehea divaricata (Malvaceae-Grewioideae): structure and ultrastructure
inferredcites →https://doi.org/10.1071/ea01063openalex-snapshot
Cotton pollination by honeybees
inferredcites →https://doi.org/10.1071/ea97144openalex-snapshot
Can mid infrared diffuse reflectance analysis replace soil extractions?
inferredcites →https://doi.org/10.1074/jbc.m006461200openalex-snapshot
Tobacco Nectarin I
inferredcites →https://doi.org/10.1085/jgp.56.6.768openalex-snapshot
The Effects of Amino Acids on the Labellar Hair Chemosensory Cells of the Fly
inferredcites →https://doi.org/10.1086/337008openalex-snapshot
A Comparison of the Amino Acid Complements of Floral and Extrafloral Nectars
inferredcites →https://doi.org/10.1086/377060openalex-snapshot
Floral Nectary Fine Structure and Development inGlycine maxL. (Fabaceae)
inferredcites →https://doi.org/10.1093/aesa/65.4.857openalex-snapshot
Evaluating Responses of Honey Bees1 to Sugar Solutions Using an Artificial-Flower Feeder2
inferredcites →https://doi.org/10.1093/aob/mcp122openalex-snapshot
Ecology and evolution of plant–pollinator interactions
inferredcites →https://doi.org/10.1093/aob/mcp302openalex-snapshot
On the mechanisms of nectar secretion: revisited
inferredcites →https://doi.org/10.1093/aob/mcq028openalex-snapshot
Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture
inferredcites →https://doi.org/10.1093/aob/mcw012openalex-snapshot
How do secretory products cross the plant cell wall to be released? A new hypothesis involving cyclic mechanical actions of the protoplast
inferredcites →https://doi.org/10.1093/botlinnean/boy016openalex-snapshot
Diversity of floral nectary secretions and structure, and implications for their evolution in Anacardiaceae
inferredcites →https://doi.org/10.1093/jxb/34.2.103openalex-snapshot
The Extrafloral Nectaries of Cotton
inferredcites →https://doi.org/10.1093/jxb/34.8.1066openalex-snapshot
The Extrafloral Nectaries of Cotton
inferredcites →https://doi.org/10.1093/jxb/erp309openalex-snapshot
CELL WALL INVERTASE 4 is required for nectar production in Arabidopsis
inferredcites →https://doi.org/10.1098/rspb.2004.2900openalex-snapshot
A selection mosaic in the facultative mutualism between ants and wild cotton
inferredcites →https://doi.org/10.1104/pp.102.017236openalex-snapshot
AraCyc: A Biochemical Pathway Database for Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.051268openalex-snapshot
Tonoplast Intrinsic Proteins AtTIP2;1 and AtTIP2;3 Facilitate NH3 Transport into the Vacuole
inferredcites →https://doi.org/10.1104/pp.106.089326openalex-snapshot
Tobacco Nectaries Express a Novel NADPH Oxidase Implicated in the Defense of Floral Reproductive Tissues against Microorganisms
inferredcites →https://doi.org/10.1105/tpc.108.060244openalex-snapshot
Mutation of the Arabidopsis NRT1.5 Nitrate Transporter Causes Defective Root-to-Shoot Nitrate Transport
inferredcites →https://doi.org/10.1111/1365-2745.12170openalex-snapshot
Beyond nectar sweetness: the hidden ecological role of non‐protein amino acids in nectar
inferredcites →https://doi.org/10.1111/j.1365-2656.2004.00789.xopenalex-snapshot
Preferences for sugars and amino acids and their conditionality in a diverse nectar‐feeding ant community
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02016.xopenalex-snapshot
mapman : a user‐driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04875.xopenalex-snapshot
Knockdown of MYB305 disrupts nectary starch metabolism and floral nectar production
inferredcites →https://doi.org/10.1111/j.1442-9993.2004.01380.xopenalex-snapshot
Sugar and amino acid composition of ant‐attended nectar and honeydew sources from an Australian rainforest
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02823.xopenalex-snapshot
The importance of cytosolic glutamine synthetase in nitrogen assimilation and recycling
inferredcites →https://doi.org/10.1111/j.1756-1051.1986.tb00462.xopenalex-snapshot
Development of trichomes in the Abutilon nectary gland
inferredcites →https://doi.org/10.1111/j.2006.0030-1299.14487.xopenalex-snapshot
What shapes amino acid and sugar composition in Mediterranean floral nectars?
inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
inferredcites →https://doi.org/10.1111/tpj.12184openalex-snapshot
PIN6 is required for nectary auxin response and short stamen development
inferredcites →https://doi.org/10.1146/annurev-ecolsys-110316-022919openalex-snapshot
Pollinator Diversity: Distribution, Ecological Function, and Conservation
inferredcites →https://doi.org/10.1146/annurev.es.08.110177.002203openalex-snapshot
Extrafloral Nectaries and Protection by Pugnacious Bodyguards
inferredcites →https://doi.org/10.1186/1471-2105-10-421openalex-snapshot
BLAST+: architecture and applications
inferredcites →https://doi.org/10.1186/1471-2229-9-92openalex-snapshot
Uncovering the Arabidopsis thaliana nectary transcriptome: investigation of differential gene expression in floral nectariferous tissues
inferredcites →https://doi.org/10.1186/gb-2010-11-10-r106openalex-snapshot
Differential expression analysis for sequence count data
inferredcites →https://doi.org/10.1186/s12859-014-0430-yopenalex-snapshot
Predicting protein functions using incomplete hierarchical labels
inferredcites →https://doi.org/10.1186/s12870-016-0960-8openalex-snapshot
Comparative RNA-seq based transcriptomic analysis of bud dormancy in grape
inferredcites →https://doi.org/10.1371/journal.pone.0008782openalex-snapshot
Identification of Differential Gene Expression in Brassica rapa Nectaries through Expressed Sequence Tag Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0046598openalex-snapshot
Increased Host Investment in Extrafloral Nectar (EFN) Improves the Efficiency of a Mutualistic Defensive Service
inferredcites →https://doi.org/10.1590/0102-33062016abb0444openalex-snapshot
How does the nectar of stomata-free nectaries cross the cuticle?
inferredcites →https://doi.org/10.18474/0749-8004-20.4.422openalex-snapshot
ANALYSIS OF LIPIDS IN COTTON EXTRAFLORAL NECTAR1
inferredcites →https://doi.org/10.1890/03-0422openalex-snapshot
HOW TO BE SWEET? EXTRAFLORAL NECTAR ALLOCATION BY GOSSYPIUM HIRSUTUM FITS OPTIMAL DEFENSE THEORY PREDICTIONS
inferredcites →https://doi.org/10.2134/agronj1972.00021962006400030033xopenalex-snapshot
Amounts and Kinds of Sugars in the Nectars of Cotton (Gossypium spp.) and the Time of Their Secretion1,2
inferredcites →https://doi.org/10.2307/2388328openalex-snapshot
Ant Preferences for Passiflora Nectar Mimics That Contain Amino Acids
inferredcites →https://doi.org/10.2307/2398800openalex-snapshot
Floral Rewards: Alternatives to Pollen and Nectar
inferredcites →https://doi.org/10.3389/fpls.2018.00259openalex-snapshot
RNAi-Mediated Downregulation of Inositol Pentakisphosphate Kinase (IPK1) in Wheat Grains Decreases Phytic Acid Levels and Increases Fe and Zn Accumulation

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

inferred← citeshttps://doi.org/10.1007/s10681-021-02799-8openalex-snapshot
Identification of simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) that are associated with the nectariless trait of Gossypium hirsutum L
inferred← citeshttps://doi.org/10.1007/s11829-021-09837-1openalex-snapshot
Indirect plant defenses: volatile organic compounds and extrafloral nectar
inferred← citeshttps://doi.org/10.1111/pbi.13366openalex-snapshot
Genetic and evolution analysis of extrafloral nectary in cotton
inferred← citeshttps://doi.org/10.1111/tpj.14814openalex-snapshot
Outstanding questions in flower metabolism
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