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A comparative transcriptome analysis of a wild purple potato and its red mutant provides insight into the mechanism of anthocyanin transformation
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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/bf01798022openalex-snapshot
The inheritance of colour and other characters int the potato
inferredcites →https://doi.org/10.1007/bf02981517openalex-snapshot
The inheritance of colour in diploid potatoes
inferredcites →https://doi.org/10.1007/bf02981567openalex-snapshot
The inheritance of colour and other characters in the potato
inferredcites →https://doi.org/10.1007/bf02981699openalex-snapshot
The inheritance oe colour in diploid potatoes II. A three-factor linkage group
inferredcites →https://doi.org/10.1007/s00122-003-1395-9openalex-snapshot
An allele of dihydroflavonol 4-reductase associated with the ability to produce red anthocyanin pigments in potato (Solanum tuberosum L.)
inferredcites →https://doi.org/10.1007/s00122-004-1829-zopenalex-snapshot
The potato P locus codes for flavonoid 3′,5′-hydroxylase
inferredcites →https://doi.org/10.1007/s00122-009-1024-3openalex-snapshot
Genetic analysis of pigmented tuber flesh in potato
inferredcites →https://doi.org/10.1007/s00122-009-1100-8openalex-snapshot
The potato R locus codes for dihydroflavonol 4-reductase
inferredcites →https://doi.org/10.1007/s00122-009-1158-3openalex-snapshot
The potato developer (D) locus encodes an R2R3 MYB transcription factor that regulates expression of multiple anthocyanin structural genes in tuber skin
inferredcites →https://doi.org/10.1007/s002990100319openalex-snapshot
Genetic engineering of the anthocyanin biosynthetic pathway with flavonoid-3′,5′-hydroxylase: specific switching of the pathway in petunia
inferredcites →https://doi.org/10.1007/s00438-005-0080-xopenalex-snapshot
A new MADS-box gene (IbMADS10) from sweet potato (Ipomoea batatas (L.) Lam) is involved in the accumulation of anthocyanin
inferredcites →https://doi.org/10.1007/s00438-016-1268-yopenalex-snapshot
Identification of anthocyanin biosynthesis related microRNAs in a distinctive Chinese radish (Raphanus sativus L.) by high-throughput sequencing
inferredcites →https://doi.org/10.1007/s10142-009-0145-8openalex-snapshot
Abscisic acid stimulated ripening and gene expression in berry skins of the Cabernet Sauvignon grape
inferredcites →https://doi.org/10.1007/s11103-004-6910-0openalex-snapshot
Differential combinatorial interactions of cis-acting elements recognized by R2R3-MYB, BZIP, and BHLH factors control light-responsive and tissue-specific activation of phenylpropanoid biosynthesis genes
inferredcites →https://doi.org/10.1007/s11103-014-0231-8openalex-snapshot
Co-modification of class B genes TfDEF and TfGLO in Torenia fournieri Lind. alters both flower morphology and inflorescence architecture
inferredcites →https://doi.org/10.1007/s11816-011-0201-4openalex-snapshot
Increased accumulation of anthocyanins in transgenic potato tubers by overexpressing the 3GT gene
inferredcites →https://doi.org/10.1016/j.fct.2012.12.048openalex-snapshot
Antioxidant, antimicrobial and anti-proliferative activities of Solanum tuberosum L. var. Vitelotte
inferredcites →https://doi.org/10.1016/j.febslet.2013.03.037openalex-snapshot
HY5 regulates anthocyanin biosynthesis by inducing the transcriptional activation of the MYB75/PAP1 transcription factor in Arabidopsis
inferredcites →https://doi.org/10.1016/j.foodchem.2008.05.056openalex-snapshot
Characterisation of anthocyanins in the black soybean (Glycine max L.) by HPLC-DAD-ESI/MS analysis
inferredcites →https://doi.org/10.1016/j.foodchem.2014.12.039openalex-snapshot
Anthocyanins and antioxidant capacities of six Chilean berries by HPLC–HR-ESI-ToF-MS
inferredcites →https://doi.org/10.1016/j.jff.2016.07.026openalex-snapshot
Antimicrobial activity and differentiation of anthocyanin profiles of rabbiteye and highbush blueberries using HPLC–DAD–ESI-MS n and multivariate analysis
inferredcites →https://doi.org/10.1016/j.jplph.2010.07.025openalex-snapshot
Both HY5 and HYH are necessary regulators for low temperature-induced anthocyanin accumulation in Arabidopsis seedlings
inferredcites →https://doi.org/10.1016/j.plantsci.2008.12.015openalex-snapshot
Color recovery in berries of grape (Vitis vinifera L.) ‘Benitaka’, a bud sport of ‘Italia’, is caused by a novel allele at the VvmybA1 locus
inferredcites →https://doi.org/10.1016/j.scienta.2013.11.018openalex-snapshot
Apigenin accumulation and expression analysis of apigenin biosynthesis relative genes in celery
inferredcites →https://doi.org/10.1016/s0031-9422(02)00720-3openalex-snapshot
Monitoring changes in anthocyanin and steroid alkaloid glycoside content in lines of transgenic potato plants using liquid chromatography/mass spectrometry
inferredcites →https://doi.org/10.1017/bjn20061928openalex-snapshot
Anthocyanin-rich purple potato flake extract has antioxidant capacity and improves antioxidant potential in rats
inferredcites →https://doi.org/10.1021/jf0302207openalex-snapshot
Analysis of Grape and Wine Anthocyanins by HPLC-MS
inferredcites →https://doi.org/10.1021/jf034482kopenalex-snapshot
Antioxidant Capacity Manipulation in Transgenic Potato Tuber by Changes in Phenolic Compounds Content
inferredcites →https://doi.org/10.1021/jf3055455openalex-snapshot
Characterization and Quantitation of Anthocyanins in Purple-Fleshed Sweet Potatoes Cultivated in Korea by HPLC-DAD and HPLC-ESI-QTOF-MS/MS
inferredcites →https://doi.org/10.1093/emboj/16.4.726openalex-snapshot
Rapid stimulation of a soybean protein‐serine kinase that phosphorylates a novel bZIP DNA‐binding protein, G/HBF‐1, during the induction of early transcription‐dependent defenses
inferredcites →https://doi.org/10.1093/jxb/erv549openalex-snapshot
Network analysis of the metabolome and transcriptome reveals novel regulation of potato pigmentation
inferredcites →https://doi.org/10.1093/jxb/erw014openalex-snapshot
Functional diversification of the potato R2R3 MYB anthocyanin activators AN1, MYBA1, and MYB113 and their interaction with basic helix-loop-helix cofactors
inferredcites →https://doi.org/10.1093/molbev/msu298openalex-snapshot
Ecological Transition Predictably Associated with Gene Degeneration
inferredcites →https://doi.org/10.1093/pcp/pcu013openalex-snapshot
A Role for PacMYBA in ABA-Regulated Anthocyanin Biosynthesis in Red-Colored Sweet Cherry cv. Hong Deng (Prunus avium L.)
inferredcites →https://doi.org/10.1101/gad.176826.111openalex-snapshot
Pioneer transcription factors: establishing competence for gene expression
inferredcites →https://doi.org/10.1104/pp.106.093203openalex-snapshot
The Grapevine Transcription Factor VvMYBPA1 Regulates Proanthocyanidin Synthesis during Fruit Development
inferredcites →https://doi.org/10.1104/pp.107.103788openalex-snapshot
Phosphate Starvation Root Architecture and Anthocyanin Accumulation Responses Are Modulated by the Gibberellin-DELLA Signaling Pathway in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.158279openalex-snapshot
A SQUAMOSA MADS Box Gene Involved in the Regulation of Anthocyanin Accumulation in Bilberry Fruits
inferredcites →https://doi.org/10.1104/pp.114.253674openalex-snapshot
The MYB182 Protein Down-Regulates Proanthocyanidin and Anthocyanin Biosynthesis in Poplar by Repressing Both Structural and Regulatory Flavonoid Genes
inferredcites →https://doi.org/10.1105/tpc.5.10.1253openalex-snapshot
Control of Pigment Biosynthesis Genes during Petal Development
inferredcites →https://doi.org/10.1105/tpc.7.7.1071openalex-snapshot
Genetics and Biochemistry of Anthocyanin Biosynthesis.
inferredcites →https://doi.org/10.1111/1755-0998.12504openalex-snapshot
De novo assembly and characterization of leaf and floral transcriptomes of the hybridizing bromeliad species (Pitcairnia spp.) adapted to Neotropical Inselbergs
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04426.xopenalex-snapshot
Genome‐wide mapping of the HY5 ‐mediated genenetworks in Arabidopsis that involve both transcriptional and post‐transcriptional regulation
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.0001l.xopenalex-snapshot
The MADS-Box Family of Transcription Factors
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.tb20430.xopenalex-snapshot
The MADS-Box Family of Transcription Factors
inferredcites →https://doi.org/10.1111/j.1467-7652.2008.00362.xopenalex-snapshot
Engineered native pathways for high kaempferol and caffeoylquinate production in potato
inferredcites →https://doi.org/10.1111/j.1744-7909.2011.01042.xopenalex-snapshot
Brassinosteroid Enhances Jasmonate‐Induced Anthocyanin Accumulation in Arabidopsis Seedlings
inferredcites →https://doi.org/10.1111/jipb.12136openalex-snapshot
Cloning and characterization of a potato StAN11 gene involved in anthocyanin biosynthesis regulation
inferredcites →https://doi.org/10.1111/nph.12723openalex-snapshot
Flower development of Phalaenopsis orchid involves functionally divergent SEPALLATA ‐like genes
inferredcites →https://doi.org/10.1111/ppl.12265openalex-snapshot
Anthocyanin synthesis in native and wound periderms of potato
inferredcites →https://doi.org/10.1111/tpj.12653openalex-snapshot
High AN 1 variability and interaction with basic helix‐loop‐helix co‐factors related to anthocyanin biosynthesis in potato leaves
inferredcites →https://doi.org/10.1146/annurev.arplant.54.031902.134938openalex-snapshot
Lignin Biosynthesis
inferredcites →https://doi.org/10.1186/1471-2229-7-1openalex-snapshot
Identification of amino acid residues involved in substrate specificity of plant acyl-ACP thioesterases using a bioinformatics-guided approach.
inferredcites →https://doi.org/10.1186/1471-2229-7-46openalex-snapshot
Transcriptional control of anthocyanin biosynthetic genes in extreme phenotypes for berry pigmentation of naturally occurring grapevines
inferredcites →https://doi.org/10.1271/bbb.60097openalex-snapshot
Red Potato Extract Protects from D -Galactosamine-induced Liver Injury in Rats
inferredcites →https://doi.org/10.1371/journal.pone.0109093openalex-snapshot
Arabidopsis CAPRICE (MYB) and GLABRA3 (bHLH) Control Tomato (Solanum lycopersicum) Anthocyanin Biosynthesis
inferredcites →https://doi.org/10.1371/journal.pone.0129148openalex-snapshot
Comparative Transcriptome Analysis of White and Purple Potato to Identify Genes Involved in Anthocyanin Biosynthesis
inferredcites →https://doi.org/10.1534/genetics.110.117606openalex-snapshot
Miniature Inverted-Repeat Transposable Elements ofStowawayAre Active in Potato
inferredcites →https://doi.org/10.21273/hortsci.42.7.1733openalex-snapshot
Anthocyanin, Carotenoid Content, and Antioxidant Values in Native South American Potato Cultivars
inferredcites →https://doi.org/10.4161/psb.6.5.14343openalex-snapshot
Gibberellins negatively regulate low temperature-induced anthocyanin accumulation in a HY5/HYH-dependent manner
inferredcites →https://doi.org/10.4314/ajb.v4i10.15203openalex-snapshot
cDNA cloning and expression of anthocyanin biosynthetic genes in wild potato ( Solanum pinnatisectum )
inferredcites →https://doi.org/10.5897/ajb06.066openalex-snapshot
cDNA cloning and expression of anthocyaninbiosynthetic genes in wild potato (Solanumpinnatisectum)
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112630openalex-snapshot
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Systematic analysis of potato MYB family genes and their potential functions in anthocyanin biosynthesis
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Phenotypic and molecular analyses in diploid and tetraploid genotypes of Solanum tuberosum L. reveal promising genotypes and candidate genes associated with phenolic compounds, ascorbic acid contents, and antioxidant activity
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Discovery of Anthocyanin Biosynthetic Pathway in Cosmos caudatus Kunth. Using Omics Analysis
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Additional file 1 of Genome-wide identification, evolutionary and functional analyses of KFB family members in potato
inferred← citeshttps://doi.org/10.6084/m9.figshare.19695830openalex-snapshot
Additional file 2 of Genome-wide identification, evolutionary and functional analyses of KFB family members in potato
inferred← citeshttps://doi.org/10.6084/m9.figshare.19695833openalex-snapshot
Additional file 3 of Genome-wide identification, evolutionary and functional analyses of KFB family members in potato
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Investigation of Carotenoid Content in the Color Change of Potato Mutant Produced by Gamma Irradiation
inferred← citeshttps://doi.org/10.7287/peerj.15349v0.1/reviews/1openalex-snapshot
Peer Review #1 of "A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15349v0.1/reviews/2openalex-snapshot
Peer Review #2 of "A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15349v0.1/reviews/3openalex-snapshot
Peer Review #3 of "A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15349v0.2/reviews/2openalex-snapshot
Peer Review #2 of "A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15349v0.2/reviews/3openalex-snapshot
Peer Review #3 of "A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.15349v0.3/reviews/3openalex-snapshot
Peer Review #3 of "A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis (v0.3)"
inferred← citeshttps://doi.org/10.7717/peerj.15349openalex-snapshot
A comparative analysis of small RNA sequencing data in tubers of purple potato and its red mutant reveals small RNA regulation in anthocyanin biosynthesis
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