ライフサイエンスコーパス: Cucumis

1 n with 2n = 2x = 14 chromosomes in the genus Cucumis.

2 r the origin of these diverse genomes within Cucumis.

3 ecently, after the divergence of Begonia and Cucumis.

4 argely intact during the entire evolution of Cucumis are supported.

5 In the large Cucurbitaceae genus Cucumis, cucumber (C. sativus) is the only species with

6 ic scion-rootstock combinations, though wild Cucumis (e.g. Fian) rootstocks represent an alternative

7 Cucumis karyotype (n = 12) evolved to extant Cucumis genomes by hybridizations and frequent lineage-

8 ies, including melon (Cucumis melo, n = 12), Cucumis hystrix (n = 12) and cucumber (Cucumis sativus,

9 omosomes, and demonstrate that the ancestral Cucumis karyotype (n = 12) evolved to extant Cucumis gen

10 t the partitioned evolutionary plasticity of Cucumis karyotype is primarily located in the centromere

11 hat fruit rinds of yellow casaba muskmelons (Cucumis melo 'Inodorous Group') accumulate naringenin ch

12 The GALACTINOL SYNTHASE promoter of Cucumis melo (CmGAS1p) confers expression only in the mi

13 Charentais melons (Cucumis melo cv Reticulatus) are climacteric and undergo

14 lysis of 35 multiclass pesticides in melons (Cucumis melo inodorus) produced in Ceara-Brazil.

15 Cucumis melo is highly diverse for fruit traits providin

16 s and sensory perception of three muskmelon (Cucumis melo L. reticulatus group) cultivars was evaluat

17 Novel acidic varieties of muskmelon (Cucumis melo L.) are emerging onto the UK market.

18 these candidates in the infection of melon (Cucumis melo L.) plants, using gene expression analysis,

19 In muskmelon (Cucumis melo L.) seeds, a thin, membranous endosperm com

20 esent in the pulp flour of Cantaloupe melon (Cucumis melo L.) were encapsulated in whey protein isola

21 Melon (Cucumis melo L.), being under intensive domestication an

22 talian variety (Scopatizzo) of unripe melon (Cucumis melo L.), known for the sweetness of its fruits.

23 loning of C. melo PH gene (CmPH) from melon, Cucumis melo taking advantage of the novel natural genet

24 se is expressed in the minor veins of melon (Cucumis melo) as part of the symplastic-loading mechanis

25 show the high-resolution structure of melon (Cucumis melo) eIF4E in complex with a melon eIF4G peptid

26 ornaments some commercially important melon (Cucumis melo) fruit and is an important quality trait.

27 e evidence that pectin disassembly in melon (Cucumis melo) may be PG mediated.

28 he C940-fe (fefe) Fe-uptake mutant of melon (Cucumis melo) was characterized, and the fefe mutant was

29 ctinol synthase promoter, cloned from melon (Cucumis melo), directs expression of the gusA gene to th

30 tal framework for trait dissection in melon (Cucumis melo), leveraging a novel pan-genome constructed

31 esistance loci in the non-model crop, melon (Cucumis melo).

32 s the color of many fruits, including melon (Cucumis melo).

33 species, the Asian species, including melon (Cucumis melo, n = 12), Cucumis hystrix (n = 12) and cucu

34 s study analyses the impact of Cucurbita and Cucumis rootstocks on the accumulation of flavor-related

35 enate toxicity was investigated in cucumber (Cucumis sativa L) using 10 contrasting soils.

36 Cucumber (Cucumis sativa) leaves infiltrated with Pseudomonas syri

37 ion of heat-inactivated walls from cucumber (Cucumis sativus cv Burpee Pickler) hypocotyls was induce

38 species Rhodiola rosea, Boehmeria nivea, and Cucumis sativus for their root epidermal cell patterns.

39 Helix-Loop-Helix (bHLH) transcription factor Cucumis sativus Irregular Vasculature Patterning (CsIVP)

40 Cucumis sativus L. is a freshly consumed garden vegetabl

41 Cucumber, Cucumis sativus L. is the only taxon with 2n = 2x = 14 c

42 tification and characterization in cucumber (Cucumis sativus L.) have been hindered by the lack of a

43 Cucumber (Cucumis sativus L.) is a rich source of vitamins, minera

44 Immature fruit color (IFC) of cucumber (Cucumis sativus L.) is an important marketability trait

45 Cucumber (Cucumis sativus L.) is an important vegetable crop that

46 Sex determination in cucumber (Cucumis sativus L.) is controlled largely by three genes

47 Two cucumber ( Cucumis sativus L.) proteins, PCI6 (PABP-CT-interacting)

48 ed by exogenous glutathione (GSH), cucumber (Cucumis sativus L.) seedlings were exposed to HT with or

49 specific regions of the lamina of cucumber (Cucumis sativus L.) was mapped using carboxyfluorescein

50 Cucumber (Cucumis sativus L.), a major horticultural crop, in the

51 eet potato (Solanum tuberosum L.), cucumber (Cucumis sativus L.), tomato (Solanum lycopersicum L.), g

52 s were detected in phloem sap from cucumber (Cucumis sativus) and lupin (Lupinus albus).

53 effluent water of aquaculture in a cucumber (Cucumis sativus) cultivation system.

54 he four FRO genes in the melon and cucumber (Cucumis sativus) genomes was Fe-regulated, and one was C

55 ic and metabolite responses of two cucumber (Cucumis sativus) genotypes to chelicerate spider mites (

56 d greenhouse study, we studied in cucumbers (Cucumis sativus) how changes in soil nitrogen and phosph

57 model, we assessed the ability of cucumber (Cucumis sativus) hypocotyl walls to undergo creep (long-

58 he growth, physiology and yield of cucumber (Cucumis sativus) in West Texas.

59 The Gy14 cucumber (Cucumis sativus) is resistant to oomyceteous downy milde

60 Cucumber (Cucumis sativus) originated in tropical areas and is ver

61 vivo phloem transport velocity in cucumber (Cucumis sativus) plants during early seedling developmen

62 Experiments using cucumber (Cucumis sativus) plants show that the shoot growth enhan

63 n this study, hydroponically grown cucumber (Cucumis sativus) plants were aerially treated either wit

64 evaluated in hydroponically grown cucumber (Cucumis sativus) plants.

65 een IAA and OGA activity in intact cucumber (Cucumis sativus) seedlings.

66 on pumpkin (Cucurbita maxima) and cucumber (Cucumis sativus) to determine the origin and composition

67 Cucumber (Cucumis sativus) was grown under an artificial sunlight

68 alcohol dehydrogenases (CADs) from cucumber (Cucumis sativus) with low activity toward p-coumaraldehy

69 he 1685-kb mitochondrial genome of cucumber (Cucumis sativus).

70 s, Syzygium cumini, Solanum lycopersicum and Cucumis sativus).

71 nsis, the monotypic sister genus to Begonia, Cucumis sativus, Arabidopsis thaliana, and Zea mays.

72 Cucumber (Cucumis sativus, Cs) tendrils are slender vegetative org

73 cDNA library from RNA of senescing cucumber (Cucumis sativus, L.) cotyledons.

74 ination and sugar responses of the cucumber (Cucumis sativus, L.) malate synthase (Ms) gene.

75 12), Cucumis hystrix (n = 12) and cucumber (Cucumis sativus, n = 7), had highly shuffled genomes cau

76 onogalactosyldiacylglycerol synthase gene of Cucumis sativus, which encodes a galactosyltransferase,

77 ion of fine-scale genome structures of eight Cucumis species from both African-origin and Asian-origi

78 ecific events underlying the origin of these Cucumis species.

79 Plants in the genus Cucumis, specifically melon and cucumber, exhibit patern

80 represent extant karyotypes with the genus, Cucumis, using highly customizable comparative oligo-pai