ライフサイエンスコーパス: anthesis

1 h higher lignin content at 25 DPA (Days Post Anthesis).

2 ting heat stress effects on grain set during anthesis.

3 ss-lintless (fl) mutant at -3 and 0 day post-anthesis.

4 nol starts when flowers open and peaks after anthesis.

5 impacts better during grain filling than at anthesis.

6 flower buds and in the anther filaments upon anthesis.

7 ifferent QTLs were detected before and after anthesis.

8 ed pistils, where expression decreased after anthesis.

9 he biological function of jasmonates in rice anthesis.

10 omoter is particularly active at 7 days post anthesis.

11 r MD or N. attenuata, ir-EOBII flowers enter anthesis.

12 ransport to support high water demand during anthesis.

13 g from the stem xylem into the flower during anthesis.

14 ation between disease resistance and days to anthesis.

15 tapetum during meiosis and disappears before anthesis.

16 the formation of bicellular pollen grains at anthesis.

17 otyledons in embryos at around 13 days after anthesis.

18 obacterium were applied 5 d or more prior to anthesis.

19 ning Monsanto event 810) at the beginning of anthesis.

20 to form closed locules roughly 3 d prior to anthesis.

21 t accumulates in the stigma and style before anthesis.

22 nmasking of carotenoids from 31st days after anthesis.

23 ore anthesis, and in all floral organs after anthesis.

24 i2;1 mRNA begins to accumulate just prior to anthesis.

25 ript accumulation in pistils from flowers at anthesis.

26 grees C night with additional heat stress at anthesis; 34 degrees C day/26 degrees C night; and 34 de

27 In the period between anthesis and fertilization, the protein content of ovary

28 ith two wheat cultivars under heat stress at anthesis and grain filling stages.

29 e variation during thermo-sensitive periods (anthesis and grain-filling; TSP) of wheat crop developme

30 ent physiological responses, but its role in anthesis and pollinator attraction traits remains largel

31 N. attenuata, ir-EOBII flowers fail to enter anthesis and prematurely senesce.

32 s in stems until approximately 7 days before anthesis and then down-regulated.

33 ion was observed in sepals and petals before anthesis, and in all floral organs after anthesis.

34 and declined during the next few days after anthesis, and it showed a strong, positive correlation w

35 ther filament, the opening of the stomium at anthesis, and the production of viable pollen.

36 ous groups being detected from 11 days after anthesis, and the proteins from about 14 days.

37 the premeiosis stage of development, or pre-anthesis anthers, however, the heat-mediated increase in

38 emission began to decline on the 2nd d after anthesis, BEAT activity continued to increase and remain

39 ts of both osjar1 alleles stayed open during anthesis because the lodicules, which control flower ope

40 nt levels only during the first 30 min after anthesis (before nectar is depleted in wild populations)

41 ate that a low dosage of CPPU applied in pre-anthesis can improve fruit weight/size without any negat

42 tis vinifera 'Chardonnay') 20 to 100 d after anthesis (DAA) and compared with observations of xylem a

43 In young developing seeds 25 d after anthesis (DAA) that did not exhibit OD, the lipid layer

44 l in leaf was manifested early at 12 d after anthesis (DAA), while global transcriptional and phenoty

45 on in the period between 6 and 42 days after anthesis (daa).

46 s were planted with four water regimes after anthesis: daily irrigation (control; S1), every 2days (S

47 sistently lower than those of simple traits (anthesis date and plant height) and prediction accuracy

48 ed with cessation of leaf and stem growth at anthesis, decreased expression of genes involved in stem

49 Pre-anthesis developing spikes were dipped into a solution o

50 fibers harvested between 17 and 24 day post-anthesis (dpa) represent the greatest expressional dista

51 ccumulation occurred from 25 to 38 days post anthesis (DPA) under our growth conditions.

52 increased in abundance from 10 to 20 d post anthesis (DPA), GhTua1 and GhTua5 transcripts were abund

53 ssessed throughout ripening (30-50 days post-anthesis; dpa) in grafted and self-rooted plants.

54 NTS showed the highest contribution of post-anthesis dry matter translocation to grain yield (averag

55 uring male and female meiosis, and one after anthesis, during fertilization and early embryo developm

56 lopmental stages were identified, one before anthesis, during male and female meiosis, and one after

57 la until floral initiation, then stems until anthesis, followed by panicles until grain maturity, and

58 Hsp101 transcript increased in the tassel at anthesis following a heat stress without an increase in

59 ribution of leaf N and light was analyzed at anthesis for 16 cultivars grown in the field in two cons

60 grees C night with additional heat stress at anthesis) for a suite of traits including five yield com

61 Earlier floral anthesis has been suggested, in turn, to have a role in

62 GBS-SNP) markers to extreme response to post anthesis heat stress conditions.

63 verlap between susceptible monarchs and corn anthesis in the northern than the southern part of the s

64 indicate that, while expressed in nectar at anthesis, it is most strongly expressed in the nectary g

65 nd CYP76C3), are simultaneously expressed at anthesis, mainly in upper anther filaments and in petals

66 However, anthers at anthesis, mature pollen, developing endosperm, and embry

67 nly a low level in the anthers and tassel at anthesis, mature pollen, roots, and leaves.

68 Days to anthesis, maturity, and plant height predictions had hig

69 However, three days after anthesis, mRNA levels began a steep decline, whereas BEA

70 opsis (Arabidopsis thaliana) seeds 13 d post anthesis of three transgenic lines, producing varying le

71 increased as the bud matured, and peaked at anthesis, paralleling changes in BEAT activity.

72 ), which occurred in a study with a rainless anthesis period.

73 other studies had rainfall events during the anthesis period.

74 eduction in node number, height, and days to anthesis (pollen shed).

75 quently increasing the R:FR near the time of anthesis promoted bud n-2 outgrowth and reduced topmost

76 Heat stress at anthesis reduced observed grain numbers per unit area an

77 eatment of unripe melon fruits 20 days after anthesis showed that MEL2 and MEL7 mRNAs are only induce

78 typic variation among wheat genotypes at the anthesis stage.

79 of photosynthates to grains during the post-anthesis stage.

80 est level of expression was observed in post-anthesis styles.

81 iate upregulation of GA3ox1 and GA3ox4 after anthesis suggests that pollination and/or fertilization

82 e amplified from cDNA of fiber 14 days after anthesis, the A and D were found, indicating the presenc

83 es and five developmental stages from floral anthesis to enlarged fruits.

84 aita (Eugenia dysenterica) development, from anthesis to ripening.

85 In addition, time to flowering and time from anthesis to the onset of fruit ripening are increased by

86 the "break of sepals", about one week before anthesis, to study its effects on fruit weight/size and

87 during 14 day intervals, from 10 weeks after anthesis until commercial maturity.

88 ast disintegration in fruits from 30 d after anthesis until ripening, suggesting that CmOr regulates

89 Flowering date (anthesis) varied 91 days from late July to late November

90 Biomass accumulation and N uptake after anthesis were significantly and positively correlated wi

91 ions of up to 200 ppm above-ambient CO(2) at anthesis, when nectar rewards are richest.

92 maximal levels of expression coinciding with anthesis, when stigmas are most receptive to pollen and

93 development (approximately 26-30 days after anthesis), whereas homogalacturonan and pectic (1-->5)-a