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A novel R3 MYB transcriptional repressor associated with the loss of floral pigmentation in Iochroma

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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/bf00014672openalex-snapshot

The small, versatilepPZP family ofAgrobacterium binary vectors for plant transformation

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Petunia hybrida: A short description of the action of 91 genes, their origin and their map location

inferredcites →https://doi.org/10.1007/s00239-016-9750-zopenalex-snapshot

Diversification of R2R3-MYB Transcription Factors in the Tomato Family Solanaceae

inferredcites →https://doi.org/10.1016/0092-8674(94)90549-5openalex-snapshot

Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices

inferredcites →https://doi.org/10.1016/j.molp.2015.03.012openalex-snapshot

MYB Transcription Factors as Regulators of Phenylpropanoid Metabolism in Plants

inferredcites →https://doi.org/10.1016/j.phytochem.2016.05.007openalex-snapshot

Evolutionary correlations in flavonoid production across flowers and leaves in the Iochrominae (Solanaceae)

inferredcites →https://doi.org/10.1016/j.plantsci.2007.08.007openalex-snapshot

Molecular characterization of EgMYB1, a putative transcriptional repressor of the lignin biosynthetic pathway

inferredcites →https://doi.org/10.1016/j.tplants.2004.12.011openalex-snapshot

MYB–bHLH–WD40 protein complex and the evolution of cellular diversity

inferredcites →https://doi.org/10.1016/j.tplants.2005.03.002openalex-snapshot

Flavonoids: a colorful model for the regulation and evolution of biochemical pathways

inferredcites →https://doi.org/10.1016/j.tplants.2010.06.005openalex-snapshot

MYB transcription factors in Arabidopsis

inferredcites →https://doi.org/10.1016/s1369-5266(00)00199-0openalex-snapshot

The R2R3-MYB gene family in Arabidopsis thaliana

inferredcites →https://doi.org/10.1017/s0305004100015644openalex-snapshot

A Mathematical Theory of Natural and Artificial Selection, Part V: Selection and Mutation

inferredcites →https://doi.org/10.1038/nbt.1621openalex-snapshot

Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation

inferredcites →https://doi.org/10.1038/srep11037openalex-snapshot

The Evolutionary History of R2R3-MYB Proteins Across 50 Eukaryotes: New Insights Into Subfamily Classification and Expansion

inferredcites →https://doi.org/10.1038/srep45966openalex-snapshot

North Andean origin and diversification of the largest ithomiine butterfly genus

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00005.xopenalex-snapshot

Analysis of flower pigmentation mutants generated by random transposon mutagenesis in Petunia hybrida

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00278.xopenalex-snapshot

Towards functional characterisation of the members of the R2R3‐MYB gene family from Arabidopsis thaliana

inferredcites →https://doi.org/10.1071/fp12195openalex-snapshot

From landing lights to mimicry: the molecular regulation of flower colouration and mechanisms for pigmentation patterning

inferredcites →https://doi.org/10.1074/jbc.272.1.563openalex-snapshot

Differences between Plant and Animal Myb Domains Are Fundamental for DNA Binding Activity, and Chimeric Myb Domains Have Novel DNA Binding Specificities

inferredcites →https://doi.org/10.1086/285406openalex-snapshot

Evolutionary Rates in Partially Self-Fertilizing Species

inferredcites →https://doi.org/10.1086/523358openalex-snapshot

Evolutionary Transitions in Floral Color

inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot

Fast and accurate short read alignment with Burrows–Wheeler transform

inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot

The Sequence Alignment/Map format and SAMtools

inferredcites →https://doi.org/10.1093/emboj/19.22.6150openalex-snapshot

Transcriptional repression by AtMYB4 controls production of UV‐protecting sunscreens in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/ers267openalex-snapshot

Lessons from flower colour evolution on targets of selection

inferredcites →https://doi.org/10.1093/molbev/msr109openalex-snapshot

Gene Loss and Parallel Evolution Contribute to Species Difference in Flower Color

inferredcites →https://doi.org/10.1093/mp/ssp030openalex-snapshot

CPC, a Single-Repeat R3 MYB, Is a Negative Regulator of Anthocyanin Biosynthesis in Arabidopsis

inferredcites →https://doi.org/10.1093/nar/gki458openalex-snapshot

AUGUSTUS: a web server for gene prediction in eukaryotes that allows user-defined constraints

inferredcites →https://doi.org/10.1093/pcp/pcp075openalex-snapshot

Functional Analysis of Transcription Factors in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pct187openalex-snapshot

AtMYB7, a New Player in the Regulation of UV-Sunscreens in Arabidopsis thaliana

inferredcites →https://doi.org/10.1104/pp.112.198267openalex-snapshot

Proteomic Study of Low-Temperature Responses in Strawberry Cultivars (Fragaria×ananassa) That Differ in Cold Tolerance

inferredcites →https://doi.org/10.1104/pp.126.2.485openalex-snapshot

Flavonoid Biosynthesis. A Colorful Model for Genetics, Biochemistry, Cell Biology, and Biotechnology

inferredcites →https://doi.org/10.1105/tpc.105.039255openalex-snapshot

A Small Family of MYB -Regulatory Genes Controls Floral Pigmentation Intensity and Patterning in the Genus Antirrhinum

inferredcites →https://doi.org/10.1105/tpc.106.048694openalex-snapshot

Single Gene–Mediated Shift in Pollinator Attraction in Petunia

inferredcites →https://doi.org/10.1105/tpc.11.6.1105openalex-snapshot

Generation of a Spacing Pattern: The Role of TRIPTYCHON in Trichome Patterning in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.11.8.1433openalex-snapshot

Molecular Analysis of the anthocyanin2 Gene of Petunia and Its Role in the Evolution of Flower Color

inferredcites →https://doi.org/10.1105/tpc.113.122069openalex-snapshot

A Conserved Network of Transcriptional Activators and Repressors Regulates Anthocyanin Pigmentation in Eudicots

inferredcites →https://doi.org/10.1111/j.0908-8857.2004.03297.xopenalex-snapshot

Glacial history and colonization of Europe by the blue tit Parus caeruleus

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02183.xopenalex-snapshot

Comprehensive identification of Arabidopsis thaliana MYB transcription factors interacting with R/B‐like BHLH proteins

inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02280.xopenalex-snapshot

AtMYB32 is required for normal pollen development in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03564.xopenalex-snapshot

MYBL2 is a new regulator of flavonoid biosynthesis in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03565.xopenalex-snapshot

AtMYBL2, a protein with a single MYB domain, acts as a negative regulator of anthocyanin biosynthesis in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04214.xopenalex-snapshot

A single-repeat MYB transcription factor, GmMYB176, regulates CHS8 gene expression and affects isoflavonoid biosynthesis in soybean

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04459.xopenalex-snapshot

Evolutionary and comparative analysis of MYB and bHLH plant transcription factors

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04465.xopenalex-snapshot

Members of an R2R3‐MYB transcription factor family in Petunia are developmentally and environmentally regulated to control complex floral and vegetative pigmentation patterning

inferredcites →https://doi.org/10.1111/j.1469-185x.1924.tb00546.xopenalex-snapshot

A MATHEMATICAL THEORY OF NATURAL AND ARTIFICIAL SELECTION. PART II THE INFLUENCE OF PARTIAL SELF‐FERTILISATION, INBREEDING, ASSORTATIVE MATING, AND SELECTIVE FERTILISATION ON THE COMPOSITION OF MENDELIAN POPULATIONS, AND ON NATURAL SELECTION.

inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01165.xopenalex-snapshot

POPULATION GENETICS, PLEIOTROPY, AND THE PREFERENTIAL FIXATION OF MUTATIONS DURING ADAPTIVE EVOLUTION

inferredcites →https://doi.org/10.1111/nph.13576openalex-snapshot

Widespread flower color convergence in Solanaceae via alternate biochemical pathways

inferredcites →https://doi.org/10.1126/science.277.5329.1113openalex-snapshot

Epidermal Cell Differentiation in Arabidopsis Determined by a Myb Homolog, CPC

inferredcites →https://doi.org/10.1128/jvi.64.4.1590-1597.1990openalex-snapshot

Cap-independent enhancement of translation by a plant potyvirus 5' nontranslated region

inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105248openalex-snapshot

THE GENETICS AND BIOCHEMISTRY OF FLORAL PIGMENTS

inferredcites →https://doi.org/10.1146/annurev.es.12.110181.000531openalex-snapshot

Adaptation and Evolution in Heliconius: A Defense of NeoDarwinism

inferredcites →https://doi.org/10.1186/gb-2009-10-3-r25openalex-snapshot

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

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/10.1186/s12862-016-0675-3openalex-snapshot

Molecular evolution of anthocyanin pigmentation genes following losses of flower color

inferredcites →https://doi.org/10.1186/s12870-014-0249-8openalex-snapshot

Genome-wide identification and characterisation of R2R3-MYB genes in sugar beet (Beta vulgaris)

inferredcites →https://doi.org/10.1242/dev.02139openalex-snapshot

Cell-to-cell movement of the CAPRICE protein in Arabidopsis root epidermal cell differentiation

inferredcites →https://doi.org/10.1385/1-59745-130-4:143openalex-snapshot

Nicotiana (Nicotiana tobaccum, Nicotiana benthamiana)

inferredcites →https://doi.org/10.1534/genetics.112.146852openalex-snapshot

Genetic Dissection of a Major Anthocyanin QTL Contributing to Pollinator-Mediated Reproductive Isolation Between Sister Species ofMimulus

inferredcites →https://doi.org/10.17660/actahortic.2007.745.10openalex-snapshot

SYSTEMATICS OF IOCHROMINAE (SOLANACEAE): PATTERNS IN FLORAL DIVERSITY AND INTERSPECIFIC CROSSABILITY

inferredcites →https://doi.org/10.3389/fpls.2013.00321openalex-snapshot

Flower color as a model system for studies of plant evo-devo

inferredcites →https://doi.org/10.3389/fpls.2014.00133openalex-snapshot

Regulation of cell fate determination by single-repeat R3 MYB transcription factors in Arabidopsis

inferredcites →https://doi.org/10.3732/ajb.1400395openalex-snapshot

Genetic basis for a rare floral mutant in an Andean species of Solanaceae

inferredcites →https://doi.org/10.3732/ajb.1500163openalex-snapshot

Tempo and mode of flower color evolution

inferredcites →https://doi.org/10.3732/ajb.1600350openalex-snapshot

Related allopolyploids display distinct floral pigment profiles and transgressive pigments

inferredcites →https://doi.org/10.3732/ajb.93.8.1140openalex-snapshot

Phylogenetics of the florally diverse Andean clade Iochrominae (Solanaceae)

inferredcites →https://doi.org/10.4161/epi.6.2.13627openalex-snapshot

EAR motif-mediated transcriptional repression in plants

inferredcites →https://doi.org/10.4161/psb.3.12.6254openalex-snapshot

CAPRICEpositively regulates stomatal formation in the Arabidopsis hypocotyl

What points at this work

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

inferred← citeshttps://doi.org/10.1002/tax.12990zenodo-depositor-declared

Morphological trait evolution inSolanum(Solanaceae): Evolutionary lability of key taxonomic characters

inferred← citeshttps://doi.org/10.1002/9781394183913.ch12openalex-snapshot

Insight into the Flavonoids Enrichment in Plants by Genome Engineering

inferred← citeshttps://doi.org/10.1002/ajb2.70106openalex-snapshot

Temperature and the evolution of flower color: A review

inferred← citeshttps://doi.org/10.1002/ajb2.70137openalex-snapshot

Differential expression of flavonoid biosynthetic pathway genes drives the production of transgressive pigments in Nicotiana section Repandae allotetraploids

inferred← citeshttps://doi.org/10.1002/dvdy.82openalex-snapshot

Developmental control of convergent floral pigmentation across evolutionary timescales

inferred← citeshttps://doi.org/10.1002/evl3.296openalex-snapshot

Plant-associate interactions and diversification across trophic levels

inferred← citeshttps://doi.org/10.1002/jez.b.22804openalex-snapshot

The second biennial meeting of the Pan‐American Society for Evolutionary Developmental Biology

inferred← citeshttps://doi.org/10.1007/978-3-030-29493-9_11openalex-snapshot

The Genetic Basis of Flower Color Differences in Nicotiana tabacum

inferred← citeshttps://doi.org/10.1007/s00299-019-02391-4openalex-snapshot

Repression of anthocyanin biosynthesis by R3-MYB transcription factors in lily (Lilium spp.)

inferred← citeshttps://doi.org/10.1007/s00438-022-01973-4openalex-snapshot

Transcriptome profiling reveals the roles of pigment formation mechanisms in yellow Paeonia delavayi flowers

inferred← citeshttps://doi.org/10.1007/s11105-018-1094-yopenalex-snapshot

The Novel Rose MYB Transcription Factor RhMYB96 Enhances Salt Tolerance in Transgenic Arabidopsis

inferred← citeshttps://doi.org/10.1007/s13205-024-04119-yopenalex-snapshot

In silico analysis of R2R3-MYB transcription factors in the basal eudicot model, Aquilegia coerulea

inferred← citeshttps://doi.org/10.1007/s44281-026-00119-5openalex-snapshot

The R2R3-MYB transcription factor LcMYBC2-L1 represses anthocyanin biosynthesis in Litchi chinensis Sonn.

inferred← citeshttps://doi.org/10.1016/j.biosystems.2023.104938openalex-snapshot

Thermodynamic understanding of flower pigmentation

inferred← citeshttps://doi.org/10.1016/j.cpb.2024.100351openalex-snapshot

Single-repeat MYB transcription factor, OsMYB1R, enhanced phytoalexin sakuranetin accumulation and Magnaporthe oryzae resistance

inferred← citeshttps://doi.org/10.1016/j.cub.2019.12.067openalex-snapshot

Two MYB Proteins in a Self-Organizing Activator-Inhibitor System Produce Spotted Pigmentation Patterns

inferred← citeshttps://doi.org/10.1016/j.cub.2020.01.056openalex-snapshot

Development: Painting Flowers with MYBs

inferred← citeshttps://doi.org/10.1016/j.cub.2026.03.085openalex-snapshot

Gene co-option across scales shapes plant diversity

inferred← citeshttps://doi.org/10.1016/j.gene.2021.146105openalex-snapshot

R3-MYB transcription factor LcMYBx from Litchi chinensis negatively regulates anthocyanin biosynthesis by ectopic expression in tobacco

inferred← citeshttps://doi.org/10.1016/j.hpj.2020.12.001openalex-snapshot

Genome-wide Analysis of MYB Gene Family in Potato Provides Insights into Tissue-specific Regulation of Anthocyanin Biosynthesis

inferred← citeshttps://doi.org/10.1016/j.hpj.2022.01.006openalex-snapshot

Genetic relatedness and association mapping of horticulturally valuable traits for the Ceiba plants using ddRAD sequencing

inferred← citeshttps://doi.org/10.1016/j.hpj.2024.01.002openalex-snapshot

The coordinated interaction or regulation between floral pigments and volatile organic compounds

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110588openalex-snapshot

A novel R3 MYB transcriptional repressor, MaMYBx, finely regulates anthocyanin biosynthesis in grape hyacinth

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110696openalex-snapshot

Functional characterization of SmMYB86, a negative regulator of anthocyanin biosynthesis in eggplant (Solanum melongena L.)

inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113310openalex-snapshot

LsMYB3, an R2R3-MYB repressor without canonical repression motifs, negatively regulates anthocyanin biosynthesis in lettuce

inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.01.024openalex-snapshot

Advance of the negative regulation of anthocyanin biosynthesis by MYB transcription factors

inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.06.018openalex-snapshot

Metabolite and gene expression analysis reveal the molecular mechanism for petal colour variation in six Centaurea cyanus cultivars

inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.05.035openalex-snapshot

Integrated mRNA and small RNA sequencing reveals a regulatory network associated with flower color in oriental hybrid lily

inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112374openalex-snapshot

Research progress in understanding the biosynthesis and regulation of plant anthocyanins

inferred← citeshttps://doi.org/10.1016/j.tplants.2018.12.003openalex-snapshot

MYB Repressors as Regulators of Phenylpropanoid Metabolism in Plants

inferred← citeshttps://doi.org/10.1016/j.tree.2021.01.011openalex-snapshot

What Maintains Flower Colour Variation within Populations?

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.02.002openalex-snapshot

Filtering of target sequence capture individuals facilitates species tree construction in the plant subtribe Iochrominae (Solanaceae)

inferred← citeshttps://doi.org/10.1021/acs.jafc.3c05185openalex-snapshot

SlMYB7, an AtMYB4-Like R2R3-MYB Transcription Factor, Inhibits Anthocyanin Accumulation in Solanum lycopersicum Fruits

inferred← citeshttps://doi.org/10.1038/s41598-024-56117-yopenalex-snapshot

Absence of long-term balancing selection on variation in EuMYB3, an R2R3-MYB gene responsible for the anther-color polymorphism in Erythronium umbilicatum

inferred← citeshttps://doi.org/10.1080/03036758.2022.2034654openalex-snapshot

Flavonoids – flowers, fruit, forage and the future

inferred← citeshttps://doi.org/10.1093/aob/mcac103openalex-snapshot

DhMYB22andDhMYB60regulate pigment intensity and floral organ shape inDendrobiumhybrid

inferred← citeshttps://doi.org/10.1093/botlinnean/boad052openalex-snapshot

Homeologue differential expression in the flavonoid biosynthetic pathway underlies flower colour variation in natural and synthetic polyploids of Nicotiana tabacum (Solanaceae)

inferred← citeshttps://doi.org/10.1093/g3journal/jkaf230openalex-snapshot

MYB regulator of “colorless” flavonols underlies the evolution of red flowers in Iochroma (Solanaceae)

inferred← citeshttps://doi.org/10.1093/hr/uhag065openalex-snapshot

LlR3MYB-mediated flavonoid biosynthesis confers cold stress tolerance in Lilium lancifolium through the LlDREB-LlCHS2 regulatory cascade

inferred← citeshttps://doi.org/10.1093/icb/icz049openalex-snapshot

Computational Modeling of Anthocyanin Pathway Evolution: Biases, Hotspots, and Trade-offs

inferred← citeshttps://doi.org/10.1093/jxb/erac069openalex-snapshot

TRIPTYCHON-LIKE regulates aspects of both fruit flavor and color in citrus

inferred← citeshttps://doi.org/10.1093/jxb/erz121openalex-snapshot

CmMYB#7, an R3 MYB transcription factor, acts as a negative regulator of anthocyanin biosynthesis in chrysanthemum

inferred← citeshttps://doi.org/10.1093/molbev/msy117openalex-snapshot

Convergent Evolution at the Pathway Level: Predictable Regulatory Changes during Flower Color Transitions

inferred← citeshttps://doi.org/10.1093/plcell/koab114openalex-snapshot

Complex evolution of novel red floral color inPetunia

inferred← citeshttps://doi.org/10.1098/rspb.2023.0275openalex-snapshot

Evolutionary walks through flower colour space driven by gene expression inPetuniaand allies (Petunieae)

inferred← citeshttps://doi.org/10.1101/336263openalex-snapshot

Pericarp Pigmentation Correlates with Hormones and Intensifies with Continuation of Bud Sport Generations from ‘Red Delicious’

inferred← citeshttps://doi.org/10.1111/evo.13589openalex-snapshot

Stepwise evolution of floral pigmentation predicted by biochemical pathway structure

inferred← citeshttps://doi.org/10.1111/nph.16565openalex-snapshot

Hongzhi Kong

inferred← citeshttps://doi.org/10.1111/nph.16908openalex-snapshot

R2R3‐MYB genes control petal pigmentation patterning in Clarkia gracilis ssp. sonomensis (Onagraceae)

inferred← citeshttps://doi.org/10.1111/nph.17397openalex-snapshot

Repressors of anthocyanin biosynthesis

inferred← citeshttps://doi.org/10.1111/nph.19341openalex-snapshot

Multiple mechanisms explain loss of anthocyanins from betalain‐pigmented Caryophyllales, including repeated wholesale loss of a key anthocyanidin synthesis enzyme

inferred← citeshttps://doi.org/10.1111/nph.19736openalex-snapshot

Isoform‐resolved genome annotation enables mapping of tissue‐specific betalain regulation in amaranth

inferred← citeshttps://doi.org/10.1111/nph.19866openalex-snapshot

Painted flowers: Eluta generates pigment patterning in Antirrhinum

inferred← citeshttps://doi.org/10.1111/pbi.12902openalex-snapshot

Linkage and association mapping reveals the genetic basis of brown fibre (Gossypium hirsutum)

inferred← citeshttps://doi.org/10.1186/s12870-018-1595-8openalex-snapshot

Anthocyanin accumulation correlates with hormones in the fruit skin of ‘Red Delicious’ and its four generation bud sport mutants

inferred← citeshttps://doi.org/10.1186/s12870-020-2324-7openalex-snapshot

Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.1186/s12870-024-05316-wopenalex-snapshot

Genetic factors explaining anthocyanin pigmentation differences

inferred← citeshttps://doi.org/10.1186/s40104-019-0392-zopenalex-snapshot

Identification of single nucleotide polymorphisms of PIK3R1 and DUSP1 genes and their genetic associations with milk production traits in dairy cows

inferred← citeshttps://doi.org/10.1371/journal.pgen.1007993openalex-snapshot

Regulation of anthocyanin accumulation via MYB75/HAT1/TPL-mediated transcriptional repression

inferred← citeshttps://doi.org/10.1371/journal.pone.0232986openalex-snapshot

Identification of a new R3 MYB type repressor and functional characterization of the members of the MBW transcriptional complex involved in anthocyanin biosynthesis in eggplant (S. melongena L.)

inferred← citeshttps://doi.org/10.17660/actahortic.2024.1405.14openalex-snapshot

Analysis of R2R3-MYB transcription factor family in Ficus carica L. identified FcMYB57 as a negative regulator in anthocyanin biosynthesis

inferred← citeshttps://doi.org/10.2503/hortj.qh-142openalex-snapshot

Mechanisms by Which High Temperatures Suppress Anthocyanin Coloration in Flowers and Fruits, and Discovery of Floricultural Crops that Exhibit High-temperature-tolerant Flower Pigmentation

inferred← citeshttps://doi.org/10.32942/x2759xopenalex-snapshot

Evolutionary walks through flower color space driven by gene expression in Petunia and allies (Petunieae)

inferred← citeshttps://doi.org/10.3389/fpls.2018.00830openalex-snapshot

The atroviolacea Gene Encodes an R3-MYB Protein Repressing Anthocyanin Synthesis in Tomato Plants

inferred← citeshttps://doi.org/10.3389/fpls.2021.633227openalex-snapshot

Evolution of the Subgroup 6 R2R3-MYB Genes and Their Contribution to Floral Color in the Perianth-Bearing Piperales

inferred← citeshttps://doi.org/10.3389/fpls.2021.633979openalex-snapshot

Changes at a Critical Branchpoint in the Anthocyanin Biosynthetic Pathway Underlie the Blue to Orange Flower Color Transition in Lysimachia arvensis

inferred← citeshttps://doi.org/10.3389/fpls.2021.747131openalex-snapshot

Comprehensive Transcriptome and Metabolic Profiling of Petal Color Development in Lycoris sprengeri

inferred← citeshttps://doi.org/10.3389/fpls.2022.1000469openalex-snapshot

Whole genome and transcriptome reveal flavone accumulation in Scutellaria baicalensis roots

inferred← citeshttps://doi.org/10.3389/fpls.2022.869582openalex-snapshot

The Common Bean V Gene Encodes Flavonoid 3′5′ Hydroxylase: A Major Mutational Target for Flavonoid Diversity in Angiosperms

inferred← citeshttps://doi.org/10.3389/fpls.2024.1310634openalex-snapshot

Cloned genes and genetic regulation of anthocyanin biosynthesis in maize, a comparative review

inferred← citeshttps://doi.org/10.3390/biom9040135openalex-snapshot

LcNAC13 Physically Interacts with LcR1MYB1 to Coregulate Anthocyanin Biosynthesis-Related Genes during Litchi Fruit Ripening

inferred← citeshttps://doi.org/10.3390/genes10080559openalex-snapshot

Assessing Anthocyanin Biosynthesis in Solanaceae as a Model Pathway for Secondary Metabolism

inferred← citeshttps://doi.org/10.3390/genes15040511openalex-snapshot

An R2R3-MYB Transcriptional Factor LuMYB314 Associated with the Loss of Petal Pigmentation in Flax (Linum usitatissimum L.)

inferred← citeshttps://doi.org/10.3390/horticulturae11020190openalex-snapshot

Unveiling CcR2R3-MYB: A Key Regulator of Leaf Pigmentation in Cymbidium Orchids

inferred← citeshttps://doi.org/10.3390/horticulturae11091097openalex-snapshot

Transcriptomics and Metabolomics Revealed Genes Associated with the Formation of Different Fruit Colors in Fragaria pentaphylla

inferred← citeshttps://doi.org/10.3390/ijms22063103openalex-snapshot

MYB-Mediated Regulation of Anthocyanin Biosynthesis

inferred← citeshttps://doi.org/10.3390/ijms22168752openalex-snapshot

Anthocyanin Biosynthesis Genes as Model Genes for Genome Editing in Plants

inferred← citeshttps://doi.org/10.3390/ijms22179544openalex-snapshot

Recent Advanced Metabolic and Genetic Engineering of Phenylpropanoid Biosynthetic Pathways

inferred← citeshttps://doi.org/10.3390/ijms222312769openalex-snapshot

Comparative Transcriptome Analysis Revealed Two Alternative Splicing bHLHs Account for Flower Color Alteration in Chrysanthemum

inferred← citeshttps://doi.org/10.3390/ijms23063382openalex-snapshot

The R3-Type MYB Transcription Factor BrMYBL2.1 Negatively Regulates Anthocyanin Biosynthesis in Chinese Cabbage (Brassica rapa L.) by Repressing MYB–bHLH–WD40 Complex Activity

inferred← citeshttps://doi.org/10.3390/ijms24032566openalex-snapshot

A MYB Transcription Factor Atlas Provides Insights into the Evolution of Environmental Adaptations in Plants

inferred← citeshttps://doi.org/10.3390/plants14111680openalex-snapshot

A Fragment Insertion of AgDFR Results in a White Flower Phenotype in Arundina graminifolia (Orchidaceae)

inferred← citeshttps://doi.org/10.48130/opr-0024-0028openalex-snapshot

Alternative splicing of activator CcbHLH1 gene accounts for anthocyanin absence in white cornflower

inferred← citeshttps://doi.org/10.55730/1300-011x.3086openalex-snapshot

The molecular regulators, pathways, and environmental impacts of white flowers

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050010openalex-snapshot

Additional file 10 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050016openalex-snapshot

Additional file 11 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050025openalex-snapshot

Additional file 12 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050028openalex-snapshot

Additional file 1 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050034openalex-snapshot

Additional file 2 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050043openalex-snapshot

Additional file 3 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050052openalex-snapshot

Additional file 4 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050058openalex-snapshot

Additional file 5 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050061openalex-snapshot

Additional file 6 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050067openalex-snapshot

Additional file 7 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050070openalex-snapshot

Additional file 8 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.12050076openalex-snapshot

Additional file 9 of Annotation of genes involved in high level of dihydromyricetin production in vine tea (Ampelopsis grossedentata) by transcriptome analysis

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