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1 ective preferences (e.g., I prefer apples to melons).
2 diversity capture and mapping resolution in melon.
3 , respectively, compared with the unmodified melon.
4 endelian traits to a candidate-gene level in melon.
5 reciprocal inversion between C. hystrix and melon.
6 of the potential of GWA for trait mapping in melon.
7 acidic varieties with a standard Galia-type melon.
8 rimitive acidic varieties and modern dessert melons.
9 rences between acidic varieties and standard melons.
10 3-carotenone were detected in orange-fleshed melons.
11 causes significant losses in the cultivated melon, a key member of the economically important family
14 mosomes (AK1-AK12) of an ancestor similar to melon and C. hystrix had strikingly different evolutiona
16 age values obtained were similar to those of melon and cucumber, but the phenolic contents were much
17 on the milk-clotting activity of kiwi fruit, melon and ginger extracts was evaluated, as well as the
18 propose this flexibility is modulated by the melon and implemented to accommodate dynamic spatial rel
20 arative analyses of the genomes of cucumber, melon and watermelon, we uncovered conserved syntenic lo
23 d to LeExp1 were also identified in ripening melons and strawberries, suggesting that they are a comm
24 ess the organoleptic impact of the different melons and the sensory data were correlated with the che
25 ined by objective states of the world (e.g., melons are bigger than apples), whereas value-based deci
26 and fruity flavours (peach/apricot, Muscat, melon, banana and strawberry) while the remainder were d
27 majority of the remaining species, including melon (C. melo) and the sister species of cucumber, C. h
29 pening-related genes we have screened a ripe melon cDNA library and isolated two novel cDNA clones (M
31 tivated and wild cucumbers, and the syntenic melon chromosome I suggested that the paracentric invers
35 erting enzyme (ACE) inhibitory activity of a melon concentrate rich in superoxide dismutase (SOD-MC)
37 omes based on different genetic distances to melon, cucumber, and watermelon in the Benincaseae tribe
38 synthase is expressed in the minor veins of melon (Cucumis melo) as part of the symplastic-loading m
39 ere we show the high-resolution structure of melon (Cucumis melo) eIF4E in complex with a melon eIF4G
42 a galactinol synthase promoter, cloned from melon (Cucumis melo), directs expression of the gusA gen
45 the analysis of 35 multiclass pesticides in melons (Cucumis melo inodorus) produced in Ceara-Brazil.
46 based cloning of C. melo PH gene (CmPH) from melon, Cucumis melo taking advantage of the novel natura
47 ptive antecedent to the development of sweet melon cultigens in Central Asia over 1,000 years ago.
48 f AVRFOM2 will not only be helpful to select melon cultivars to avoid melon Fusarium wilt, but also t
51 melon (Cucumis melo) eIF4E in complex with a melon eIF4G peptide and propose the first eIF4E-eIF4G st
53 ost abundant compounds in FGE3, while bitter melon extracts contained only small amounts of mainly ph
54 hose obtained using commercial rennet, while melon extracts produced a fragile gel and low curd yield
57 onal studies of chemosensory proteins in the melon fly and for making more detailed comparisons to ot
59 s involved in chemosensory perception in the melon fly, Bactrocera cucurbitae (Diptera: Tephritidae)
64 h quality losses were isolated in rocket and melon fresh-cut produce and their expression levels anal
66 n reported that PG activity is absent during melon fruit ripening, a mechanism for PG-independent pec
67 racted from tomato seeds, cotton fibers, and melon fruit showed pH optima of 6, 6, and 8, respectivel
68 tein levels and carotenoid metabolic flux in melon fruit, as shown by carotenoid and immunoblot analy
69 examined in transgenic antisense ACC oxidase melon fruit, three distinct patterns of mRNA accumulatio
70 Wounding and ethylene treatment of unripe melon fruits 20 days after anthesis showed that MEL2 and
72 e helpful to select melon cultivars to avoid melon Fusarium wilt, but also to monitor how quickly a F
74 ay in part explain the increased size of the melon genome compared with the close relative cucumber.
75 romosomes are largely retained in the modern melon genome, while have undergone different degrees of
77 rotenoid and immunoblot analyses of selected melon genotypes and by using chemical pathway inhibitors
78 he control of the polymerization process for melon ("graphitic carbon nitride"), with the aim of impr
80 'Chardonnay', 'Gamay noir', 'Aligote', and 'Melon', have microsatellite genotypes consistent with th
82 Ripening-associated pectin disassembly in melon is characterized by a decrease in molecular mass a
85 e of recent whole-genome duplications in the melon lineage since the ancient eudicot triplication, an
86 C-SAW analysis allowed the discrimination of melon maturity stage based on six measured peaks, whose
87 es of two genotypes of Charentais cantaloupe melons (medium shelf-life and long shelf-life), harveste
89 vitro model to assess the efficacy of bitter melon (Momordica charantia) extract (BME) as an anticanc
90 (Trigonella foenum-graecum) seeds and bitter melon (Momordica charantia) fruit were extracted sequent
92 degrees C storage temperatures for fresh-cut melon over 14days reveals that storage at 0 degrees C is
95 c acid is the major phenolic compound in the melon peels by 33.45mg/100g, followed by apigenin-7-glyc
96 l retention capacities) and color shows that melon peels have properties that may be useful in indust
97 quantification of the phenolic compounds of melon peels were performed by high performance liquid ch
101 ees C) is critical for maintaining fresh-cut melon quality, but often reaches 10 degrees C during tra
102 ylamide gel electrophoresis of proteins from melons revealed that several mRNAs increased in amount d
106 ble patterns (e.g., those observed in Korean melons, silk gourds, ribbed pumpkins, striped cavern tom
107 igation was performed on kiwi, pineapple and melon, subjected to minimal processing, packaging, cold
111 iation of a cyanamide surface-functionalized melon-type carbon nitride ((NCN)CNx) and a molecular nic
113 osome synteny among cucumber, C. hystrix and melon using integrated and complementary approaches.
114 igh beta-carotene accumulation in golden SNP melons was found to be due to a reduced further metaboli
116 valuate the inhibitory effect of wild bitter melons (WBM; Momordica charantia Linn. var. abbreviata S
117 genome sequencing of a set of strains of the melon wilt fungus Fusarium oxysporum f. sp. melonis (Fom
118 genome sequencing of a set of strains of the melon wilt fungus Fusarium oxysporum f.sp. melonis (Fom)
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