Published in Arch Biochem Biophys on October 15, 2002
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Biochemical and structural characterization of benzenoid carboxyl methyltransferases involved in floral scent production in Stephanotis floribunda and Nicotiana suaveolens. Plant Physiol (2004) 1.02
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Understanding in vivo benzenoid metabolism in petunia petal tissue. Plant Physiol (2004) 2.01
The shikimate pathway and aromatic amino Acid biosynthesis in plants. Annu Rev Plant Biol (2012) 1.94
Two terpene synthases are responsible for the major sesquiterpenes emitted from the flowers of kiwifruit (Actinidia deliciosa). J Exp Bot (2009) 1.69
A conifer genomics resource of 200,000 spruce (Picea spp.) ESTs and 6,464 high-quality, sequence-finished full-length cDNAs for Sitka spruce (Picea sitchensis). BMC Genomics (2008) 1.55
Regulation of methylbenzoate emission after pollination in snapdragon and petunia flowers. Plant Cell (2003) 1.54
Plant phenylacetaldehyde synthase is a bifunctional homotetrameric enzyme that catalyzes phenylalanine decarboxylation and oxidation. J Biol Chem (2006) 1.48
Intensity and the ratios of compounds in the scent of snapdragon flowers affect scent discrimination by honeybees (Apis mellifera). J Comp Physiol A Neuroethol Sens Neural Behav Physiol (2004) 1.43
Eugenol and isoeugenol, characteristic aromatic constituents of spices, are biosynthesized via reduction of a coniferyl alcohol ester. Proc Natl Acad Sci U S A (2006) 1.41
Formation of monoterpenes in Antirrhinum majus and Clarkia breweri flowers involves heterodimeric geranyl diphosphate synthases. Plant Cell (2004) 1.31
Characterization of a petunia acetyltransferase involved in the biosynthesis of the floral volatile isoeugenol. Plant J (2007) 1.24
Reduction of benzenoid synthesis in petunia flowers reveals multiple pathways to benzoic acid and enhancement in auxin transport. Plant Cell (2006) 1.16
RNAi suppression of Arogenate Dehydratase1 reveals that phenylalanine is synthesized predominantly via the arogenate pathway in petunia petals. Plant Cell (2010) 1.16
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Two nearly identical terpene synthases catalyze the formation of nerolidol and linalool in snapdragon flowers. Plant J (2008) 1.14
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The multiple phenylpropene synthases in both Clarkia breweri and Petunia hybrida represent two distinct protein lineages. Plant J (2008) 1.12
Interlinking showy traits: co-engineering of scent and colour biosynthesis in flowers. Plant Biotechnol J (2008) 1.07
Contribution of CoA ligases to benzenoid biosynthesis in petunia flowers. Plant Cell (2012) 1.02
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Involvement of snapdragon benzaldehyde dehydrogenase in benzoic acid biosynthesis. Plant J (2009) 1.02
Cuticle characteristics and volatile emissions of petals in Antirrhinum majus. Physiol Plant (2003) 0.98
Prephenate aminotransferase directs plant phenylalanine biosynthesis via arogenate. Nat Chem Biol (2010) 0.98
An important role of a BAHD acyl transferase-like protein in plant innate immunity. Plant J (2008) 0.97
The small subunit of snapdragon geranyl diphosphate synthase modifies the chain length specificity of tobacco geranylgeranyl diphosphate synthase in planta. Plant Cell (2009) 0.97
Completion of the core β-oxidative pathway of benzoic acid biosynthesis in plants. Proc Natl Acad Sci U S A (2012) 0.97
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Generation of phenylpropanoid pathway-derived volatiles in transgenic plants: rose alcohol acetyltransferase produces phenylethyl acetate and benzyl acetate in petunia flowers. Plant Mol Biol (2006) 0.93
Scent engineering: toward the goal of controlling how flowers smell. Trends Biotechnol (2007) 0.91
Functional identification of valerena-1,10-diene synthase, a terpene synthase catalyzing a unique chemical cascade in the biosynthesis of biologically active sesquiterpenes in Valeriana officinalis. J Biol Chem (2012) 0.90
Cytosolic monoterpene biosynthesis is supported by plastid-generated geranyl diphosphate substrate in transgenic tomato fruits. Plant J (2013) 0.89
The lack of floral synthesis and emission of isoeugenol in Petunia axillaris subsp. parodii is due to a mutation in the isoeugenol synthase gene. Plant J (2009) 0.89
Evolution of Cinnamate/p-coumarate carboxyl methyltransferases and their role in the biosynthesis of methylcinnamate. Plant Cell (2007) 0.88
Developmental changes in the metabolic network of snapdragon flowers. PLoS One (2012) 0.86
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Whole plastome sequencing reveals deep plastid divergence and cytonuclear discordance between closely related balsam poplars, Populus balsamifera and P. trichocarpa (Salicaceae). New Phytol (2014) 0.82
Metabolomics of plant volatiles. Methods Mol Biol (2009) 0.82
Enhancer substances: selegiline and R-(-)-1-(benzofuran-2-yl)-2-propylaminopentane [(-)-BPAP] enhance the neurotrophic factor synthesis on cultured mouse astrocytes. Life Sci (2003) 0.81
Profiling hydroxycinnamoyl-coenzyme A thioesters: unlocking the back door of phenylpropanoid metabolism. Anal Biochem (2011) 0.80
A kinetic model describes metabolic response to perturbations and distribution of flux control in the benzenoid network of Petunia hybrida. Plant J (2010) 0.80
The floral volatile, methyl benzoate, from snapdragon (Antirrhinum majus) triggers phytotoxic effects in Arabidopsis thaliana. Planta (2007) 0.79
A survey of oxidative paracatalytic reactions catalyzed by enzymes that generate carbanionic intermediates: implications for ROS production, cancer etiology, and neurodegenerative diseases. Adv Enzymol Relat Areas Mol Biol (2011) 0.77
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Plant metabolism. Editorial. Mol Plant (2010) 0.76
Synthesis of the food flavoring methyl benzoate by genetically engineered Saccharomyces cerevisiae. J Biotechnol (2006) 0.76
The monolignol pathway contributes to the biosynthesis of volatile phenylpropenes in flowers. New Phytol (2014) 0.76
The fate of (-)1-(benzofuran-2-yl)-2-propylaminopentane . HCl, (-)-BPAP, in rats, a potent enhancer of the impulse-evoked release of catecholamines and serotonin in the brain. Eur J Drug Metab Pharmacokinet (2002) 0.75
Molecular mechanisms of cold-induced CYP1A activation in rat liver microsomes. J Physiol Biochem (2011) 0.75
Quantification of plant volatiles. Methods Mol Biol (2014) 0.75
The L-DOPA-sparing effect of R-(-)-1-(benzofuran-2-yl)-2-propylaminopentane hydrochloride [(-)-BPAP] in reserpine-pretreated rats. Life Sci (2003) 0.75