ライフサイエンスコーパス: radish

1 llowing fertilization are largely unknown in radish.

2 rlying embryogenesis and seed development in radish.

3 ts than their acylated counterparts from red radish.

4 latory networks remain largely unexplored in radish.

5 of Cr-responsive miRNAs and their targets in radish.

6 roles of miRNAs in response to Cr stress in radish.

7 ined deletion interval and is unlikely to be radish.

8 vels were found in red cabbage (857 pg/g DW) radish (536 pg/g DW) and broccoli (439 pg/g DW).

9 lied as a biofertilizer to improve growth of radishes, a model crop plant, by up to approximately 1,4

10 luable for the incorporation of red cabbage, radish and broccoli germinated seeds into the diet to pr

11 ds in all edible seeds, showing red cabbage, radish and broccoli the highest contents (21.6, 20.4 and

12 were independent of PFAA chain length, while radish and celery RCFs showed a slight decrease with inc

13 eae species including broccoli, cauliflower, radish and rapeseed.

14 Radish and ryegrass roots generally accumulated higher a

15 ne of the AuNPs accumulated in the shoots of radishes and pumpkins.

16 bolting and flowering regulatory networks in radish, and facilitate dissecting the molecular mechanis

17 ocyanate, associated with typical rocket and radish aroma.

18 s study, three cDNA libraries from ovules of radish before and after fertilization were sequenced usi

19 AA), in selected edible seeds of mung beans, radish, broccoli and sunflower.

20 ions of S in various spinach, leek, lettuce, radish, Brussels sprouts, zucchini and chard samples wer

21 Consideration of uptake from air into radish bulbs was relevant for PCBs.

22 series of Brassicaceae family members (i.e. radish, cabbage, broccoli, and cauliflower).

23 Within an aphid-parasitoid-radish community, we created a fully factorial manipulat

24 ortholog floral expression levels, retained radish duplicates diverged primarily via maintenance of

25 n identification of DEGs profiles related to radish embryogenesis and seed development.

26 iRNA and mRNA may play a pivotal role in the radish embryogenesis process.

27 -like kinase (SERK ) known to be involved in radish embryogenesis were differentially expressed.

28 y DeltaH, whole seeds of crambe (6295.1J/g), radish forage (6182.7 J/g), and physic nut (6420.0 J/g)

29 e the quality of sunflower, soybean, crambe, radish forage and physic nut, by measuring chemical comp

30 Here, we have identified the radish gene by positional cloning and comparative sequen

31 , which was used as a source of nitrogen for radish grown in a second hydroponics experiment.

32 Cs in broccoli, white cabbage, garden cress, radish, horseradish and papaya.

33 ve been as necessary for the success of wild radish in new environments.

34 The Drosophila memory mutant radish is specifically deficient in anesthesia-resistant

35 d samples (pomegranate flower, organic pear, radish leaf, lamb meat, etc.), and good results were obt

36 In this study, two small RNA libraries from radish leaves at vegetative and reproductive stages were

37 spholipase A2 gene, previously identified as radish, maps 95 kb outside the behaviorally determined d

38 Radish microgreens constitute a good source of bioactive

39 d concentrations and antioxidant capacity of radish microgreens during storage.

40 Radish microgreens in bags of 29.5 pmol s(-1) m(-2) Pa(-

41 light exposure accelerated deterioration of radish microgreens, while dark storage maintained qualit

42 lettuce, broccoli, carrot, squash, eggplant, radish, mushroom, cucumber, and tomato).

43 training and corrected the memory defect of radish mutants, but did not improve memory produced by s

44 ppetitive LTM is completely disrupted by the radish mutation that apparently represents a distinct me

45 y treatment with anti-IgY labeled with horse radish peroxidase (Anti-IgY-HRP).

46 ys, the detection limits obtained from horse radish peroxidase (HRP) and bisphenol A assays were 12.5

47 nanoparticles were functionalized with horse radish peroxidase (HRP) based on aminopropyl triethoxy s

48 Horse radish peroxidase (HRP) is one of the most common enzyme

49 ne serum albumin, primary antibody and Horse Radish Peroxidase (HRP) tagged secondary antibody on the

50 tilized for covalent immobilization of horse radish peroxidase (HRP), via glutaraldehyde (Glu), for d

51 groups, alginate-g-pyrrole, through a horse-radish peroxidase (HRP)-activated cross-linking of the p

52 a simplicifilia B4-isolectin (GSA-IB4) horse radish peroxidase (HRP)-conjugate for identification of

53 re, we show that wheat germ agglutinin horse radish peroxidase (WGA-HRP) chemically conjugated to gol

54 ed out using isoeugenol polymerised by horse radish peroxidase in aqueous solution.

55 A probe strand, labeled with horse radish peroxidase, was then hybridized to the target.

56 In comparison with the natural horse radish peroxidase, WC NR exhibits excellent robustness o

57 fluorescence, Alexa-fluorophores, and horse radish peroxidase-based bead assays, enabling multiplexe

58 Radish plants (Raphanus sativus) were grown hydroponical

59 rrelations between six floral traits in wild radish plants are unchanged, showing that pleiotropy gen

60 After 5 weeks of growth, the radish plants were harvested and cryosectioned, and sect

61 The Radish protein has recently been reported to bind to Rac

62 The Radish protein is highly expressed in the mushroom bodie

63 rials in terrestrial plants, including rice, radish, pumpkin, and perennial ryegrass.

64 nological traits (measured as Q(ST)) of wild radish (Raphanus raphanistrum) across populations from t

65 We sequenced the genome of wild radish (Raphanus raphanistrum), a Brassicaceae species t

66 racted from spinach (Spinacia oleracea), red radish (Raphanus sativus L), winter jasmine (Jasminum nu

67 rawberry (Fragaria x ananassa Duch.) and red radish (Raphanus sativus L.) by intermolecular co-pigmen

68 The radish (Raphanus sativus L.) is an important root vegeta

69 Like a homologous protein cloned from radish (Raphanus sativus) and named pheophorbidase, MES1

70 experimental observations of damping-off of radish (Raphanus sativus) caused by the fungal pathogen

71 GalAT assay reaction products made using radish (Raphanus sativus) microsomal membranes or solubi

72 whereas structurally similar MtDef2 and the radish (Raphanus sativus) seed defensin Rs-AFP2 fail to

73 ared the uptake of PFAAs in greenhouse-grown radish (Raphanus sativus), celery (Apium graveolens var.

74 ng plant growth inhibition were observed for radish (Raphanus sativus), perennial ryegrass (Lolium pe

75 ngal protein Rs-Afp1 [a knottin protein from radish (Raphanus sativus), rmsd of 2.7 A].

76 f a self-incompatible invasive species, wild radish (Raphanus sativus).

77 antically meaningful combinations like "tiny radish" relative to non-meaningful combinations, such as

78 st for perfluorooctanoate (PFOA; 67 ng/g) in radish root, perfluorobutanoate (PFBA; 232 ng/g) in cele

79 study, the metabolite profiling analysis of radish roots exposed to lead (Pb) and cadmium (Cd) stres

80 ipts from our previous transcriptome work in radish roots.

81 aling appears independent of the function of Radish (Rsh), a protein long implicated in ARM, suggesti

82 broccoli and from 45% to 118% of increase in radish sprouts after MeJA priming and treatments.

83 Sango radish sprouts are exceptional dietary sources of heath-

84 Radish sprouts exhibited the highest ability to produce

85 Sunflower and radish sprouts were the most rich in phenolic compounds.

86 d feasible treatment to produce broccoli and radish sprouts with enhanced levels of health-promoting

87 )N KNO3 as nutrient and those grown from the radish "tea" was readily discernible.

88 to ferment in water for 2 weeks to create a radish "tea", which was used as a source of nitrogen for

89 have been the key adaptations enabling wild radish to become a major agricultural weed.

90 tegration data demonstrated that exposure of radish to Pb stress resulted in profound biochemical cha

91 fy Cr-responsive miRNAs and their targets in radish, two sRNA libraries derived from Cr-free (CK) and

92 on, 3-butenyl isothiocyanate was detected in radish varieties.

93 Radish was grown in contaminated soil (maximum concentra

94 h a reduction in virulence of Xcc to Chinese Radish when assayed by leaf spraying but not by leaf ino