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Developmental control of convergent floral pigmentation across evolutionary timescales
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-0-387-28822-2_7openalex-snapshot
The Evolution of Flavonoids and Their Genes
inferredcites →https://doi.org/10.1007/bf00429466openalex-snapshot
Genetic control of the conversion of dihydroflavonols into flavonols and anthocyanins in flowers of Petunia hybrida
inferredcites →https://doi.org/10.1016/bs.ctdb.2016.03.004openalex-snapshot
The Genetic Basis of Pigmentation Differences Within and Between Drosophila Species
inferredcites →https://doi.org/10.1016/j.cell.2008.06.030openalex-snapshot
Evo-Devo and an Expanding Evolutionary Synthesis: A Genetic Theory of Morphological Evolution
inferredcites →https://doi.org/10.1016/j.cub.2011.03.028openalex-snapshot
Gene Duplication in Mimulus Underlies Parallel Floral Evolution via Independent trans-Regulatory Changes
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.semcdb.2008.10.002openalex-snapshot
Development and evolution of insect pigmentation: Genetic mechanisms and the potential consequences of pleiotropy
inferredcites →https://doi.org/10.1016/j.tig.2010.02.002openalex-snapshot
Vertebrate pigmentation: from underlying genes to adaptive function
inferredcites →https://doi.org/10.1016/j.ydbio.2009.04.040openalex-snapshot
The causes of repeated genetic evolution
inferredcites →https://doi.org/10.1038/nrg2063openalex-snapshot
The evolutionary significance of cis-regulatory mutations
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01786.xopenalex-snapshot
Analysis of a chalcone synthase mutant in Ipomoea purpurea reveals a novel function for flavonoids: amelioration of heat stress
inferredcites →https://doi.org/10.1046/j.1365-3059.1999.00318.xopenalex-snapshot
Phytochemical Methods. A Guide to Modern Techniques of Plant Analysis.
inferredcites →https://doi.org/10.1073/pnas.1515294113openalex-snapshot
Competition between anthocyanin and flavonol biosynthesis produces spatial pattern variation of floral pigments between Mimulus species
inferredcites →https://doi.org/10.1080/10635150701313830openalex-snapshot
Within-Species Variation and Measurement Error in Phylogenetic Comparative Methods
inferredcites →https://doi.org/10.1086/590395openalex-snapshot
Morphometrics of the Avian Small Intestine Compared with That of Nonflying Mammals: A Phylogenetic Approach
inferredcites →https://doi.org/10.1093/icb/ict068openalex-snapshot
Phylogenetic Analysis of Gene Expression
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/molbev/msy117openalex-snapshot
Convergent Evolution at the Pathway Level: Predictable Regulatory Changes during Flower Color Transitions
inferredcites →https://doi.org/10.1093/nar/29.9.e45openalex-snapshot
A new mathematical model for relative quantification in real-time RT-PCR
inferredcites →https://doi.org/10.1093/nar/gng073openalex-snapshot
Experimental validation of novel and conventional approaches to quantitative real-time PCR data analysis
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026108openalex-snapshot
Patterns of evolutionary rate variation among genes of the anthocyanin biosynthetic pathway
inferredcites →https://doi.org/10.1104/pp.102.3.925openalex-snapshot
Chalcone Synthase and Flavonol Accumulation in Stigmas and Anthers of Petunia hybrida
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.113.122069openalex-snapshot
A Conserved Network of Transcriptional Activators and Repressors Regulates Anthocyanin Pigmentation in Eudicots
inferredcites →https://doi.org/10.1111/evo.12081openalex-snapshot
THE LOCI OF REPEATED EVOLUTION: A CATALOG OF GENETIC HOTSPOTS OF PHENOTYPIC VARIATION
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00544.xopenalex-snapshot
PERSPECTIVE: EVOLUTIONARY DEVELOPMENTAL BIOLOGY AND THE PROBLEM OF VARIATION
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03114.xopenalex-snapshot
Convergence, constraint and the role of gene expression during adaptive radiation: floral anthocyanins in Aquilegia
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03447.xopenalex-snapshot
Biosynthesis of plant pigments: anthocyanins, betalains and carotenoids
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00761.xopenalex-snapshot
METAMODELS AND PHYLOGENETIC REPLICATION: A SYSTEMATIC APPROACH TO THE EVOLUTION OF DEVELOPMENTAL PATHWAYS
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00804.xopenalex-snapshot
SIZE-CORRECTION AND PRINCIPAL COMPONENTS FOR INTERSPECIFIC COMPARATIVE STUDIES
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/j.1558-5646.2012.01771.xopenalex-snapshot
THE EVOLUTION OF GENES IN BRANCHED METABOLIC PATHWAYS
inferredcites →https://doi.org/10.1111/j.2041-210x.2011.00169.xopenalex-snapshot
phytools: an R package for phylogenetic comparative biology (and other things)
inferredcites →https://doi.org/10.1111/nph.14830openalex-snapshot
A novel R3 MYB transcriptional repressor associated with the loss of floral pigmentation in Iochroma
inferredcites →https://doi.org/10.1126/science.1158997openalex-snapshot
Is Genetic Evolution Predictable?
inferredcites →https://doi.org/10.1126/science.1176980openalex-snapshot
Intraspecific Polymorphism to Interspecific Divergence: Genetics of Pigmentation in Drosophila
inferredcites →https://doi.org/10.1371/journal.pgen.1003740openalex-snapshot
Recurrent Modification of a Conserved Cis-Regulatory Element Underlies Fruit Fly Pigmentation Diversity
inferredcites →https://doi.org/10.1371/journal.pone.0018230openalex-snapshot
Arctic Mustard Flower Color Polymorphism Controlled by Petal-Specific Downregulation at the Threshold of the Anthocyanin Biosynthetic Pathway
inferredcites →https://doi.org/10.1371/journal.pone.0081173openalex-snapshot
The Genetic Basis of a Rare Flower Color Polymorphism in Mimulus lewisii Provides Insight into the Repeatability of Evolution
inferredcites →https://doi.org/10.1534/genetics.104.034975openalex-snapshot
Neutral Evolution of the Nonbinding Region of the Anthocyanin Regulatory Gene Ipmyb1 in IpomoeaSequence data from this article have been deposited with the EMBL/GenBank Data Libraries under accession nos. AY986823, AY986824, AY986825, AY986826, AY986827, AY986828, AY986829, AY986830, AY986831,…
inferredcites →https://doi.org/10.1534/genetics.109.110411openalex-snapshot
The Evolution of Control and Distribution of Adaptive Mutations in a Metabolic Pathway
inferredcites →https://doi.org/10.1534/genetics.113.156463openalex-snapshot
A Perspective on Micro-Evo-Devo: Progress and Potential
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/10.3732/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.93.8.1140openalex-snapshot
Phylogenetics of the florally diverse Andean clade Iochrominae (Solanaceae)
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/dvdy.123openalex-snapshot
Evo‐devo explores the endless forms most beautiful, from extreme traits to subtle diversities
inferred← citeshttps://doi.org/10.1007/s00606-025-01939-0openalex-snapshot
Comparative and phylogenomic plastome analysis of the Physalideae tribe (Solanaceae)
inferred← citeshttps://doi.org/10.1016/j.cj.2024.02.002openalex-snapshot
Unraveling the regulatory network of flower coloration in soybean: Insights into roles of GmMYBA3 and GmMYBR1
inferred← citeshttps://doi.org/10.1016/j.tree.2021.01.011openalex-snapshot
What Maintains Flower Colour Variation within Populations?
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/molbev/msac044openalex-snapshot
Transcription Factors Evolve Faster Than Their Structural Gene Targets in the Flavonoid Pigment Pathway
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/10.1111/mec.17334openalex-snapshot
The road less taken: Dihydroflavonol 4‐reductase inactivation and delphinidin anthocyanin loss underpins a natural intraspecific flower colour variation
inferred← citeshttps://doi.org/10.1111/nph.16818openalex-snapshot
The spatio‐temporal biosynthesis of floral flavonols is controlled by differential phylogenetic MYB regulators in Freesia hybrida
inferred← citeshttps://doi.org/10.1111/tpj.17188openalex-snapshot
A single nucleotide polymorphism affects protein translation and leads to post‐anthesis color change variation in closely related Lotus species
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