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The Regulation of Floral Colour Change in Pleroma raddianum (DC.) Gardner
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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/tax.12151openalex-snapshot
Systematics of Tibouchina and allies (Melastomataceae: Melastomateae): A new taxonomic classification
inferredcites →https://doi.org/10.1007/978-0-387-84796-2openalex-snapshot
Petunia. Evolutionary, Developmental and Physiological Genetics
inferredcites →https://doi.org/10.1007/bf00020187openalex-snapshot
The phenylalanine ammonia-lyase gene family in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf02670468openalex-snapshot
A simple and efficient method for isolating RNA from pine trees
inferredcites →https://doi.org/10.1007/s00425-005-1509-5openalex-snapshot
Active anthocyanin degradation in Brunfelsia calycina (yesterday–today–tomorrow) flowers
inferredcites →https://doi.org/10.1007/s00606-012-0633-5openalex-snapshot
Tibouchina pulchra (Melastomataceae): reproductive biology of a tree species at two sites of an elevational gradient in the Atlantic rainforest in Brazil
inferredcites →https://doi.org/10.1007/s00709-012-0380-zopenalex-snapshot
R2R3 MYB transcription factors: key regulators of the flavonoid biosynthetic pathway in grapevine
inferredcites →https://doi.org/10.1007/s11103-012-0001-4openalex-snapshot
Transcriptional regulation of tocopherol biosynthesis in tomato
inferredcites →https://doi.org/10.1007/s13258-015-0373-3openalex-snapshot
Overexpressing the wheat dihydroflavonol 4-reductase gene TaDFR increases anthocyanin accumulation in an Arabidopsis dfr mutant
inferredcites →https://doi.org/10.1007/s40415-020-00590-yopenalex-snapshot
Analysis of flavonoids and anthocyanin biosynthesis-related genes expression reveals the mechanism of petal color fading of Malus hupehensis (Rosaceae)
inferredcites →https://doi.org/10.1016/j.foodchem.2016.11.052openalex-snapshot
Spectral and colorimetric characteristics of metal chelates of acylated cyanidin derivatives
inferredcites →https://doi.org/10.1016/j.pbi.2016.06.021openalex-snapshot
Floral colour change as a potential signal to pollinators
inferredcites →https://doi.org/10.1016/j.phytochem.2006.03.013openalex-snapshot
Ferric ions involved in the flower color development of the Himalayan blue poppy, Meconopsis grandis
inferredcites →https://doi.org/10.1016/j.plantsci.2003.08.001openalex-snapshot
Differential expression of three key anthocyanin biosynthetic genes in a color-changing flower, Viola cornuta cv. Yesterday, Today and Tomorrow
inferredcites →https://doi.org/10.1016/j.plantsci.2005.12.003openalex-snapshot
Regulation of anthocyanin biosynthesis involved in the formation of marginal picotee petals in Petunia
inferredcites →https://doi.org/10.1016/j.plantsci.2010.05.011openalex-snapshot
Physiological and molecular changes during opening and senescence of Nicotiana mutabilis flowers
inferredcites →https://doi.org/10.1016/j.plantsci.2015.06.001openalex-snapshot
Phytochrome-interacting factors PIF4 and PIF5 negatively regulate anthocyanin biosynthesis under red light in Arabidopsis seedlings
inferredcites →https://doi.org/10.1016/j.plaphy.2019.02.025openalex-snapshot
Transcriptome and chemical analysis reveal putative genes involved in flower color change in Paeonia ‘Coral Sunset’
inferredcites →https://doi.org/10.1016/j.tetlet.2005.07.146openalex-snapshot
Essential structure of co-pigment for blue sepal-color development of hydrangea
inferredcites →https://doi.org/10.1016/j.tplants.2014.12.001openalex-snapshot
Transcriptional control of flavonoid biosynthesis by MYB–bHLH–WDR complexes
inferredcites →https://doi.org/10.1016/s0022-2836(83)80284-8openalex-snapshot
Studies on transformation of Escherichia coli with plasmids
inferredcites →https://doi.org/10.1016/s0168-9452(01)00557-xopenalex-snapshot
Floral color change in Viola cornuta L. (Violaceae): a model system to study regulation of anthocyanin production
inferredcites →https://doi.org/10.1016/s0308-8146(98)00053-3openalex-snapshot
Colour effects of co-pigmentation of anthocyanins revisited—1. A colorimetric definition using the CIELAB scale
inferredcites →https://doi.org/10.1021/acs.chemrev.5b00507openalex-snapshot
Stabilizing and Modulating Color by Copigmentation: Insights from Theory and Experiment
inferredcites →https://doi.org/10.1021/acs.jafc.5b02368openalex-snapshot
Metal Complex Pigment Involved in the Blue Sepal Color Development of Hydrangea
inferredcites →https://doi.org/10.1023/b:plan.0000009267.76482.ceopenalex-snapshot
Post-transcriptional regulation of expression of the Bronze2 gene of Zea mays L.
inferredcites →https://doi.org/10.1034/j.1399-3054.2000.100212.xopenalex-snapshot
Sugars enhance the expression of gibberellin‐induced genes in developing petunia flowers
inferredcites →https://doi.org/10.1038/436791aopenalex-snapshot
Structure of the blue cornflower pigment
inferredcites →https://doi.org/10.1038/nbt.1506openalex-snapshot
Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors
inferredcites →https://doi.org/10.1039/b800165kopenalex-snapshot
Blue flower color development by anthocyanins: from chemical structure to cell physiology
inferredcites →https://doi.org/10.1093/jxb/erq008openalex-snapshot
Metabolic networking in Brunfelsia calycina petals after flower opening
inferredcites →https://doi.org/10.1093/jxb/erq442openalex-snapshot
Recent advances in the transcriptional regulation of the flavonoid biosynthetic pathway
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/nar/25.17.3389openalex-snapshot
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
inferredcites →https://doi.org/10.1093/nar/30.9.e36openalex-snapshot
Relative expression software tool (REST(C)) for group-wise comparison and statistical analysis of relative expression results in real-time PCR
inferredcites →https://doi.org/10.1093/nar/gkp045openalex-snapshot
Amplification efficiency: linking baseline and bias in the analysis of quantitative PCR data
inferredcites →https://doi.org/10.1093/pcp/pcg033openalex-snapshot
Sepal Color Variation of Hydrangea macrophylla and Vacuolar pH Measured with a Proton-Selective Microelectrode
inferredcites →https://doi.org/10.1093/pcp/pci192openalex-snapshot
The Star-type Color Pattern in Petunia hybrida ‘Red Star’ Flowers is Induced by Sequence-Specific Degradation of Chalcone Synthase RNA
inferredcites →https://doi.org/10.1101/gad.1476406openalex-snapshot
A diverse and evolutionarily fluid set of microRNAs in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.109.147280openalex-snapshot
Uncovering Small RNA-Mediated Responses to Phosphate Deficiency in Arabidopsis by Deep Sequencing
inferredcites →https://doi.org/10.1104/pp.113.3.729openalex-snapshot
Cinnamate-4-Hydroxylase Expression in Arabidopsis (Regulation in Response to Development and the Environment)
inferredcites →https://doi.org/10.1104/pp.113.4.1437openalex-snapshot
Characterization of Flavonol Synthase and Leucoanthocyanidin Dioxygenase Genes in Arabidopsis (Further Evidence for Differential Regulation of "Early" and "Late" Genes)
inferredcites →https://doi.org/10.1104/pp.17.01384openalex-snapshot
Phytochromes and Phytochrome Interacting Factors
inferredcites →https://doi.org/10.1105/tpc.111.084525openalex-snapshot
Negative Regulation of Anthocyanin Biosynthesis in Arabidopsis by a miR156-Targeted SPL Transcription Factor
inferredcites →https://doi.org/10.1105/tpc.113.119644openalex-snapshot
Arabidopsis Kelch Repeat F-Box Proteins Regulate Phenylpropanoid Biosynthesis via Controlling the Turnover of Phenylalanine Ammonia-Lyase
inferredcites →https://doi.org/10.1105/tpc.15.00608openalex-snapshot
Functionally Similar WRKY Proteins Regulate Vacuolar Acidification in Petunia and Hair Development in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.16.00130openalex-snapshot
MYB75 Phosphorylation by MPK4 Is Required for Light-Induced Anthocyanin Accumulation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1751-1097.1999.tb01944.xopenalex-snapshot
Environmental Significance of Anthocyanins in Plant Stress Responses
inferredcites →https://doi.org/10.1111/nph.12620openalex-snapshot
Complexity and robustness of the flavonoid transcriptional regulatory network revealed by comprehensive analyses of MYB –b HLH – WDR complexes and their targets in A rabidopsis seed
inferredcites →https://doi.org/10.1111/nph.13038openalex-snapshot
In planta anthocyanin degradation by a vacuolar class III peroxidase in Brunfelsia calycina flowers
inferredcites →https://doi.org/10.1111/tpj.12153openalex-snapshot
Light and the E3 ubiquitin ligase COP 1/ SPA control the protein stability of the MYB transcription factors PAP 1 and PAP 2 involved in anthocyanin accumulation in Arabidopsis
inferredcites →https://doi.org/10.1128/jb.62.3.293-300.1951openalex-snapshot
STUDIES ON LYSOGENESIS I
inferredcites →https://doi.org/10.1128/mcb.8.5.1985openalex-snapshot
Transcriptional regulation of the Arabidopsis thaliana chalcone synthase gene.
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105248openalex-snapshot
THE GENETICS AND BIOCHEMISTRY OF FLORAL PIGMENTS
inferredcites →https://doi.org/10.1186/1471-2229-10-4openalex-snapshot
Validation of reference genes for quantitative real-time PCR during leaf and flower development in Petunia hybrida
inferredcites →https://doi.org/10.1186/s12870-019-1886-8openalex-snapshot
Differences in flavonoid pathway metabolites and transcripts affect yellow petal colouration in the aquatic plant Nelumbo nucifera
inferredcites →https://doi.org/10.1371/journal.pone.0072364openalex-snapshot
The Flavonoid Pathway Regulates the Petal Colors of Cotton Flower
inferredcites →https://doi.org/10.1371/journal.pone.0218336openalex-snapshot
Ectopic expression of tea MYB genes alter spatial flavonoid accumulation in alfalfa (Medicago sativa)
inferredcites →https://doi.org/10.1590/s0100-40422007000800040openalex-snapshot
Utilização do índice de retenção linear para caracterização de compostos voláteis em café solúvel utilizando GC-MS e coluna HP-Innowax
inferredcites →https://doi.org/10.2183/pjab.85.187openalex-snapshot
Synchrony between flower opening and petal-color change from red to blue in morning glory, Ipomoea tricolor cv. Heavenly Blue
inferredcites →https://doi.org/10.3389/fpls.2014.00096openalex-snapshot
Leaf metabolite profile of the Brazilian resurrection plant Barbacenia purpurea Hook. (Velloziaceae) shows two time-dependent responses during desiccation and recovering
inferredcites →https://doi.org/10.3389/fpls.2015.00261openalex-snapshot
Recent advances on the development and regulation of flower color in ornamental plants
inferredcites →https://doi.org/10.3389/fpls.2015.00362openalex-snapshot
Trees as huge flowers and flowers as oversized floral guides: the role of floral color change and retention of old flowers in Tibouchina pulchra
inferredcites →https://doi.org/10.3389/fpls.2015.01205openalex-snapshot
Extensive Transcriptome Changes Underlying the Flower Color Intensity Variation in Paeonia ostii
inferredcites →https://doi.org/10.3389/fpls.2016.00963openalex-snapshot
Transcriptome Profiling of Light-Regulated Anthocyanin Biosynthesis in the Pericarp of Litchi
inferredcites →https://doi.org/10.3389/fpls.2017.01645openalex-snapshot
Allelic Variation and Transcriptional Isoforms of Wheat TaMYC1 Gene Regulating Anthocyanin Synthesis in Pericarp
inferredcites →https://doi.org/10.3389/fpls.2017.01787openalex-snapshot
High Ambient Temperature Represses Anthocyanin Biosynthesis through Degradation of HY5
inferredcites →https://doi.org/10.3390/molecules23040827openalex-snapshot
Metabolomic Profiling of the White, Violet, and Red Flowers of Rhododendron schlippenbachii Maxim.
inferredcites →https://doi.org/10.3390/molecules23071698openalex-snapshot
Change of Petals′ Color and Chemical Components in Oenothera Flowers during Senescence
inferredcites →https://doi.org/10.3390/molecules24040718openalex-snapshot
Acylated Flavonoid Glycosides are the Main Pigments that Determine the Flower Colour of the Brazilian Native Tree Tibouchina pulchra (Cham.) Cogn.
inferredcites →https://doi.org/10.4161/15592316.2014.970440openalex-snapshot
COP1/SPA ubiquitin ligase complexes repress anthocyanin accumulation under low light and high light conditions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.684.1.1zenodo-depositor-declared
Unravelling the Mexican Magnolia dealbata (Magnoliaceae) species complex
inferred← citeshttps://doi.org/10.1007/978-3-030-99742-7_21openalex-snapshot
Systematics and Taxonomy of the Tribe Melastomateae
inferred← citeshttps://doi.org/10.1093/hr/uhae326openalex-snapshot
SoNAC72-SoMYB44/SobHLH130 module contributes to flower color fading via regulating anthocyanin biosynthesis by directly binding to the SoUFGT1 promoter in lilac (Syringa oblata)
inferred← citeshttps://doi.org/10.1111/ppl.13921openalex-snapshot
Metabolome and transcriptome analyses of anthocyanin biosynthesis reveal key metabolites and candidate genes in purple wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.3389/fpls.2025.1509120openalex-snapshot
Integrated transcriptomic and metabolomic analyses reveal the molecular mechanism of flower color differentiation in Orychophragmus violaceus
inferred← citeshttps://doi.org/10.3390/agriculture12050635openalex-snapshot
Comparative Analysis of the Effects of Internal Factors on the Floral Color of Four Chrysanthemum Cultivars of Different Colors
inferred← citeshttps://doi.org/10.3390/ijms23158357openalex-snapshot
Response of Anthocyanin Accumulation in Pepper (Capsicum annuum) Fruit to Light Days
inferred← citeshttps://doi.org/10.3390/plants14142185openalex-snapshot
Molecular Control of Flower Colour Change in Angiosperms
inferred← citeshttps://doi.org/10.48130/opr-0024-0019openalex-snapshot
Anthocyanin contents and molecular changes in rose petals during the post-anthesis color transition
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