ライフサイエンスコーパス: squash

1 stemically infects both tobacco and zucchini squash.

2 , with wild-crop hybrids derived from yellow squash (a cultivar of C. pepo with transgenic resistance

3 ns of two of the three primary domesticates--squash and goosefoot--are now debated, and until recentl

4 s the possible cultivation of Cucurbita pepo squash and little barley (Hordeum pusillum).

5 he determination of chlorfenapyr residues in squash and okra matrices.

6 lized for surveying chlorfenapyr residues in squash and okra samples collected from the market.

7 ence for the early consumption of cultivated squash and peanuts along with two other major food plant

8 ication of the WL1 satellite RNA in zucchini squash and that this phenotype maps to RNA 1.

9 getable" pattern, which consisted largely of squashes and root and leafy vegetables.

10 eafy vegetables [carrots, pechay (bok choy), squash, and kangkong (swamp cabbage)] and 7, 15, or 29 g

11 curbits such as cucumber, melon, watermelon, squash, and pumpkin.

12 Virus-resistant transgenic squash are grown throughout the United States and much o

13 e study of plant food use wherever gourds or squashes are preserved, documents the earliest evidence

14 In a study of residues from gourd and squash artifacts, we recovered starch grains from manioc

15 Squash associated physically with Piwi, and reductions i

16 -barrel fold, and a P1 domain, which forms a squashed beta-barrel consisting of six antiparallel beta

17 stitutions are unable to systemically infect squash, but they revert to a wild-type phenotype in the

18 s, the perikarya of the oligodendrocytes are squashed close together, and it is common to find tight

19 ed in fascicular phloem P-protein plugs from squash (Cucurbita maxima) represent cucurbit members of

20 olus vulgaris), bamboo (Phyllostachys nuda), squash (Cucurbita maxima), castor bean (Ricinus communis

21 Peanut (Arachis sp.), squash (Cucurbita moschata), and cotton (Gossypium barba

22 nhabitants adopted major crop plants such as squash (Cucurbita moschata), peanuts (Arachis sp.), and

23 s cradles of domestication with evidence for squash (Cucurbita pepo) cultivation appearing as early a

24 ified plasma membrane vesicles obtained from squash (Cucurbita pepo) roots and found it to be 3 x 10(

25 annua), chenopod (Chenopodium berlandieri), squash (Cucurbita pepo), and sunflower (Helianthus annuu

26 nce for maize (Zea mays L.) and domesticated squash (Cucurbita spp.) in contexts contemporaneous with

27 ngo, apple, kiwi, lettuce, broccoli, carrot, squash, eggplant, radish, mushroom, cucumber, and tomato

28 In this study, we developed a squash FISH procedure allowing successful detection of s

29 Squash genes (SLW1 and SLW3) induced systemically after

30 eobotanical record of three important crops--squash, goosefoot and sunflower--as well as an extinct m

31 The squashed iGb3 orientation is stabilized by several inter

32 provide evidence for early use of peanut and squash in the human diet and of cotton for industrial pu

33 whole plants and in protoplasts of zucchini squash is analyzed.

34 replicating bipartite geminiviruses such as squash leaf curl to systemically infect the host require

35 the species level were other members of the Squash leaf curl virus (SLCV) clade, which is endemic in

36 movement of bipartite geminiviruses such as squash leaf curl virus (SqLCV) requires the cooperative

37 BR1 and BL1 encoded by the plant pathogenic squash leaf curl virus act in a coordinated manner to fa

38 Thus, squash leaf curl virus appears to recruit the endoplasmi

39 ese studies support and extend our model for squash leaf curl virus movement, showing that BR1 has a

40 roteins encoded by the bipartite geminivirus squash leaf curl virus, was immunolocalized to unique ap

41 ng microscopy, optical tweezers, and a novel squashed-mount embryo preparation, we tracked single dro

42 permatids as detected by GFP fluorescence in squashes of living seminiferous tubules from adult teste

43 and pUBA, respectively, on mitotic metaphase squashes of T1 plants of the cultivated hexaploid oat Av

44 d or extensively tested in the field such as squash, papaya, plum, grape, and sugar beet.

45 mber mosaic virus (CMV) onto young leaves of squash plants and used two aphid species, Aphis gossypii

46 tions from infected source plants to healthy squash plants.

47 eramic presence of a domesticated species of squash, possibly Cucurbita argyrosperma.

48 Further analyses on the testis squash preparation and spermatozoa at a subcellular leve

49 nscriptionally active puffs in such polytene squash preparations after heat shock treatment.

50 we show that mitotic neuroblasts from brain squash preparations from larvae heteroallelic for the tw

51 A mutation, L261F, in the squash protein converts it from a non-selective enzyme i

52 as well as an acid-free polytene chromosome squash protocol that preserves the antigenicity of the h

53 The genus Cucurbita (squashes, pumpkins, gourds) contains numerous domesticat

54 tal function, including armadillo, spaghetti squash, quail, spire, Src64B, and Tec29A.

55 the myosin regulatory light chain Spaghetti squash rather than another potential substrate, Moesin,

56 ol assemblages associated with the maize and squash remains all indicate that these plants were early

57 nd weak larval lethal mutations in spaghetti squash (sqh), which encodes the nonmuscle myosin II regu

58 ntification of Drosophila zucchini (zuc) and squash (squ), which function in germline RNAi processes.

59 A squash technique was developed for log phase Tetrahymena

60 rediction of antioxidant compounds in summer squash tissues collected since 2009-2012.

61 ively, the extended iGb3 headgroup could be "squashed" upon docking of the TCR and accommodated betwe

62 Mutations in eight squashed vulva (sqv) genes in Caenorhabditis elegans cau

63 Mutations in C. elegans sqv (squashed vulva) genes affect both vulval morphogenesis a

64 sqv (squashed vulva) genes comprise a set of eight independen

65 in any of eight Caenorhabditis elegans sqv (squashed vulva) genes, the vulval extracellular space fa

66 We have named these genes sqv-1 to sqv-8 (squashed vulva).

67 ickadee, diaphanous, Cdc42, quail, spaghetti-squash, zipper, and scrambled.