ライフサイエンスコーパス: Cucurbita

1 supporting an allotetraploidization event in Cucurbita.

2 re on 2 major domestication genes in Zea and Cucurbita.

3 maintained mosaic-like landscapes ideal for Cucurbita, and vegetative changes following the megafaun

4 ruck a critical ecological blow against wild Cucurbita, and we take initial steps to consider this hy

5 Cucurbita argyrosperma does not appear until 2,065 cal y

6 f a domesticated species of squash, possibly Cucurbita argyrosperma.

7 orn rootworms and is considered a simplified Cucurbita blossom kairomone odor.

8 on to phenylpropanoid volatile components of Cucurbita blossoms.

9 vailable proteinase of fig-leaf gourd fruit (Cucurbita ficifolia) increased the use value of egg whit

10 Directly, megafauna consumed Cucurbita fruits and dispersed their seeds; wild Cucurbi

11 The Cucurbita genus contains several economically important

12 is systematically incurred with grafting on Cucurbita hybrid rootstocks (heterografting).

13 Cucurbita maxima (pumpkin) phloem sap contains a 31 kDa

14 be system, as eIF5A was recently detected in Cucurbita maxima (pumpkin) phloem sap.

15 acids in the case of cultivars belonging to Cucurbita maxima and Cucurbita pepo species, while a sli

16 dentified and characterized a 50-kD pumpkin (Cucurbita maxima cv Big Max) phloem RNA binding protein

17 n this study, proteins contained in pumpkin (Cucurbita maxima cv Big Max) phloem sap were used as a s

18 2 pumpkin varieties belonging to the species Cucurbita maxima Duch. and Cucurbita pepo L.

19 ding the phloem filament protein in pumpkin (Cucurbita maxima Duch.) has been isolated and characteri

20 Three Cucurbita maxima Hsc70 chaperones were cloned and functi

21 high homology with GA 20-oxidase cDNAs from Cucurbita maxima L. and Arabidopsis thaliana Heynh.

22 abeled dextrans along with size-fractionated Cucurbita maxima phloem proteins, ranging in size from 1

23 chemical, and functional characterization of Cucurbita maxima phloem serpin-1 (CmPS-1), a novel 42-kD

24 such complex is based on a phloem RBP named Cucurbita maxima RNA-binding protein 50 (CmRBP50), a mem

25 ission of a florigenic signal from flowering Cucurbita maxima stocks to LD-grown C. moschata scions.

26 The side chains of Arg50 and Arg52 iin Cucurbita maxima trypsin inhibitor-V (CMTI-V) anchor the

27 otein scaffold by means of hydrogen bonds in Cucurbita maxima trypsin inhibitor-V (CMTI-V), a potato

28 The solution structure of recombinant Cucurbita maxima trypsin inhibitor-V (rCMTI-V), whose N-

29 peptide bond) hydrolyzed form of recombinant Cucurbita maxima trypsin inhibitor-V (rCMTI-V*) were cha

30 CmPP16 from Cucurbita maxima was cloned and the protein was shown to

31 e prephloem pathway of the symplasmic loader Cucurbita maxima was found to be well coupled with the S

32 of protein kinases within the phloem sap of Cucurbita maxima were investigated to test the hypothesi

33 le defense mechanisms in the EFP of pumpkin (Cucurbita maxima) after leaf damage.

34 We conducted studies on pumpkin (Cucurbita maxima) and cucumber (Cucumis sativus) to dete

35 Further analyses (also in Brassica napus and Cucurbita maxima) employing complementary electrophysiol

36 n of mRNA from phloem sap of mature pumpkin (Cucurbita maxima) leaves and stems.

37 preparation using as bait the NCAP, pumpkin (Cucurbita maxima) PHLOEM PROTEIN16 (Cm-PP16).

38 Biochemical analysis of pumpkin (Cucurbita maxima) phloem sap led to the characterization

39 scicular phloem P-protein plugs from squash (Cucurbita maxima) represent cucurbit members of the SEO

40 Furthermore, phloem exudates of pumpkin (Cucurbita maxima) were analyzed.

41 garis), bamboo (Phyllostachys nuda), squash (Cucurbita maxima), castor bean (Ricinus communis), and t

42 dioxide (SC-CO(2)) extraction from pumpkin (Cucurbita moschata Duch.) is described.

43 Cucurbita moschata FLOWERING LOCUS T-LIKE 2 (hereafter F

44 of Phaseolus and Inga feuillei, the flesh of Cucurbita moschata fruits, and the nuts of Arachis was r

45 es, while a slight increase was recorded for Cucurbita moschata species.

46 The earlier identification of Cucurbita moschata specimens is not confirmed.

47 ds on physicochemical properties of pumpkin (Cucurbita moschata) samples.

48 Peanut (Arachis sp.), squash (Cucurbita moschata), and cotton (Gossypium barbadense) m

49 ts adopted major crop plants such as squash (Cucurbita moschata), peanuts (Arachis sp.), and cotton (

50 Cucurbita moschata, a cucurbit species responsive to ind

51 ered chlordane or DDx (DDT + metabolites) by Cucurbita pepo (zucchini), Zea mays (corn), Solanum lyco

52 nd attractiveness of one of its host plants (Cucurbita pepo cv. Dixie) for two aphid vectors, Myzus p

53 We compared fitness components of wild Cucurbita pepo from Arkansas, USA, with wild-crop hybrid

54 Cucurbita pepo is the earliest documented domesticate in

55 ng to the species Cucurbita maxima Duch. and Cucurbita pepo L.

56 cular markers in Solanum lycopersicum L. and Cucurbita pepo L.

57 accumulation by Glycine max L. (soybean) and Cucurbita pepo L. (zucchini) was investigated.

58 chloroethylene (p,p'-DDE; DDT metabolite) by Cucurbita pepo L. (zucchini), Glycine max L. (soybean),

59 Monomeric actin from zucchini (Cucurbita pepo L.) hypocotyl tissue was purified to elec

60 Zucchini (Cucurbita pepo L.) was planted in soil with 0 or 1228 mu

61 on garden experiments with plants from three Cucurbita pepo populations exposed to three virus treatm

62 cultivars belonging to Cucurbita maxima and Cucurbita pepo species, while a slight increase was reco

63 eri), as well as the possible cultivation of Cucurbita pepo squash and little barley (Hordeum pusillu

64 volatile emissions of its host (wild gourd, Cucurbita pepo ssp. texana) in ways that enhance both ve

65 compartment also was identified in pumpkin (Cucurbita pepo) and transformed Arabidopsis cells.

66 s of domestication with evidence for squash (Cucurbita pepo) cultivation appearing as early as 8,000

67 oxidase (GLO) were transported into pumpkin (Cucurbita pepo) glyoxysomes with no apparent differences

68 to reconstitute protein import into pumpkin (Cucurbita pepo) glyoxysomes, a class of peroxisome found

69 asma membrane vesicles obtained from squash (Cucurbita pepo) roots and found it to be 3 x 10(-7) +/-1

70 chenopod (Chenopodium berlandieri), squash (Cucurbita pepo), and sunflower (Helianthus annuus).

71 ) on a range of plant responses in zucchini (Cucurbita pepo).

72 analyze complete plastid genomes of 91 total Cucurbita samples, comprising ancient (n = 19), modern w

73 maize (Zea mays L.) and domesticated squash (Cucurbita spp.) in contexts contemporaneous with and str

74 The genus Cucurbita (squashes, pumpkins, gourds) contains numerous

75 In the genus Cucurbita, these filaments are composed of two major pro

76 rbita fruits and dispersed their seeds; wild Cucurbita were likely left without mutualistic dispersal

77 es and stability of oil bodies from pumpkin (Cucurbita) were determined with a view to patterning oil

78 egafaunal extinctions severely impacted wild Cucurbita, whereas their domestic counterparts adapted t