ライフサイエンスコーパス: fruit development

1 tent of capsaicin and dihydrocapsacin during fruit development.

2 eemed to play the most important role in the fruit development.

3 ver, suggest different roles during leaf and fruit development.

4 es in mitotic activity in the early stage of fruit development.

5 that require ethylene at a certain stage in fruit development.

6 mutants that display abnormal gynoecium and fruit development.

7 ulated lycopene accumulation 2.3-fold during fruit development.

8 lants but little is known about its roles in fruit development.

9 a differential pattern of expression during fruit development.

10 k1 mRNA accumulated to higher levels late in fruit development.

11 cellular soluble acid invertase in plant and fruit development.

12 in various tissues and are regulated during fruit development.

13 life cycle aspects, including flowering and fruit development.

14 nts of the epidermal cell wall during tomato fruit development.

15 nus persica) that has little or no effect on fruit development.

16 NA-seq data derived from different stages of fruit development.

17 gesting that they play a significant role in fruit development.

18 velopment in the flower and controlling late fruit development.

19 roach to control tree size without impairing fruit development.

20 hysical and chemical properties during olive fruit development.

21 the accumulation of these amino acids during fruit development.

22 of fruit ripening during different stages of fruit development.

23 rs indicated climate has an effect on almond fruit development.

24 by approximately 40% and substantially over fruit development.

25 lecular mechanism(s) mediating GA effects on fruit development.

26 ween GA and other hormones may contribute to fruit development.

27 arp throughout tomato (Solanum lycopersicum) fruit development.

28 ion and expression patterns during plant and fruit development.

29 confirmed the leading role of glucosides in fruit development.

30 d genome, is an excellent model for studying fruit development.

31 and decreased with toxicity to fungi during fruit development.

32 ralogs, were determined in leaves and across fruit development.

33 cular insight into fruit set and early stage fruit development.

34 ol phase transition, cauline leaf growth and fruit development.

35 e time points, at one week intervals, during fruit development.

36 coordinate seed, ovary wall, and receptacle fruit development.

37 entity and that they also play a key role in fruit development.

38 lation during climacteric and nonclimacteric fruit development.

39 for auxin-mediated blade outgrowth and early fruit development.

40 which are known to play a role in flower and fruit development.

41 function together in a linear pathway during fruit development.

42 at three distinct time-points in watermelon fruit development.

43 controls carpel number during flower and/or fruit development.

44 define the role of sorbitol distribution in fruit development.

45 he changes of anthocyanin composition during fruit development and between Ruegen F7-4 and YW5AF7 wer

46 Although much is known about fruit development and climacteric ripening, little infor

47 sepal and petal identity (AP1) and in proper fruit development and determinacy (FUL).

48 ed to Verticillium dahliae shed insight into fruit development and disease response, respectively.

49 es accumulate more starch at early stages of fruit development and display enhanced chlorophyll conte

50 t an excellent model system for the study of fruit development and diversity of fruit-bearing palm sp

51 OVATE is expressed early in flower and fruit development and encodes a previously uncharacteriz

52 atterning, an important component of overall fruit development and eventual maturation and ripening.

53 to is the model species of choice for fleshy fruit development and for the Solanaceae family.

54 tinuous pattern of cuticle deposition during fruit development and involving substantial accumulation

55 Response of transcript abundance to fruit development and leaf wounding was determined for a

56 the vitamin C redox state at early stages of fruit development and more than doubled vitamin C conten

57 st, PcSOT2 is mainly expressed only early in fruit development and not in leaves.

58 of ethylene regulatory control during tomato fruit development and provide new insights into the mole

59 Since PGIP gene expression is regulated by fruit development and responds to wounding, fungal infec

60 into the pathways that are essential during fruit development and ripening across species.

61 Fruit development and ripening entail key biological and

62 t softening, and secondary metabolism during fruit development and ripening have been identified in o

63 oints with nine pair-wise comparisons during fruit development and ripening in a normal tomato variet

64 elucidate the flow of events associated with fruit development and ripening in this species.

65 multiple tables containing data on different fruit development and ripening stages in three climacter

66 In the wild-type, fruit development and ripening were accompanied by an in

67 ant physiology and development (specifically fruit development and ripening) and for comparative geno

68 early isogenic single gene mutants impacting fruit development and ripening.

69 n-regulated mutants and wild-type throughout fruit development and ripening.

70 but was essentially absent during subsequent fruit development and ripening.

71 whose behavior is similarly affected during fruit development and ripening.

72 NA sRNAs are differentially expressed during fruit development and ripening.

73 t set did not affect the temporal pattern of fruit development and ripening; neither provitamin A (ca

74 study is to enhance the levels of Put during fruit development and see its implications in ripening a

75 he effect of fruit toxicity on reductions of fruit development and seed survival by vertebrates, inve

76 s, thus providing a simplified framework for fruit development and shape diversity.

77 at apple PGIP may have multiple roles during fruit development and stress response.

78 f auxin during tomato (Solanum lycopersicum) fruit development and the function of the PIN and AUX/LA

79 ry interactions among the genes that control fruit development and the mechanism that results in the

80 CsExp1 cross-reacted with expansins in early fruit development and the onset of ripening, but not at

81 vered with paper bags during early stages of fruit development and then removed prior to maturation t

82 on of expansin activity in several stages of fruit development and while characteristic creep activit

83 ne duplicates enriched for sugar metabolism, fruit development, and anthocyanin related genes which m

84 metabolic pathways vary significantly during fruit development, and carbohydrate metabolism (especial

85 genes are present at the earliest stages of fruit development, and continue to be expressed througho

86 seed development and germination, flower and fruit development, and flowering time.

87 mainly involved in flower development, early fruit development, and ripening.

88 em flow of water into fruits declines during fruit development, and the literature indicates a corres

89 tone methylation may play a critical role in fruit development as well as responses to abiotic stress

90 uxin transcriptional regulator during tomato fruit development at the level of transcripts, enzyme ac

91 Hand-pollination restored transgenic fruit development but not the rapid abscission seen in w

92 PcSOT1 is expressed throughout fruit development, but especially when growth and sorbit

93 that ABP1 transcript levels were low during fruit development, but transcripts were detected by RT P

94 robes of 832 EST-unigenes from a subtracted, fruit development, cDNA library of watermelon were utili

95 The total fruit development comprised 37days.

96 interesting model species for studying early fruit development, during which an extremely relevant ph

97 ginating from 22 countries, at two stages of fruit development, for vitamin C content and its relatio

98 d, while CYP78A9 overexpression can uncouple fruit development from fertilization, the cyp78a8 cyp78a

99 In addition to the effect on fruit development, ful cauline leaves are broader than t

100 rgan identity, but whose role in Arabidopsis fruit development had not been previously described.

101 mical defenses and shifts in allocation with fruit development, I quantified variation in toxicity be

102 The terminal step of fruit development in Arabidopsis involves valve separati

103 tion genetic screen for genes that influence fruit development in Arabidopsis, we identified a novel

104 into the current genetic network controlling fruit development in Arabidopsis.

105 pecific cytosines during the early stages of fruit development in both promoters as previously shown

106 s further support to the role of ethylene in fruit development in non-climacteric fruits.

107 ere, we investigated the role of FSM1 during fruit development in tomato and its mode of action.

108 and growth suggest that the early stages of fruit development in tomato are regulated, at least in p

109 the transcription factor BZR1 is involved in fruit development in tomato.

110 ar localization of PHs was determined during fruit development in two sweet and two bitter almond cul

111 The production of ethylene during fruit development in watermelon gives further support to

112 used to evaluate TBG mRNA levels throughout fruit development, in different fruit tissues, and in va

113 ) effects on red raspberry (Rubus idaeus L.) fruit development (including ripening) were studied, wit

114 n appears to affect only the early stages of fruit development, irrespective of allele or genetic bac

115 Here, we report that early fruit development is also dramatically altered by the si

116 Tomato fruit development is characterized by distinct developme

117 ory networks governing this relevant part of fruit development is still missing.

118 s and metabolomics analyses performed during fruit development on the reference cultivar Fantasia, co

119 ene--a pattern of expression not observed in fruit development on the vine.

120 veral expansin genes may contribute to green fruit development, only Exp1 mRNA is present at high lev

121 rations, were applied at three key points of fruit development (pit hardening, initial colour changes

122 eins contribute to GA-mediated gynoecium and fruit development remains to be clarified.

123 volved in carbohydrate metabolism throughout fruit development revealed significant differences in pa

124 hows complicated metabolic activities during fruit development, ripening, synthesis and accumulation

125 the PH proteins is dependent on the stage of fruit development, shifting between apoplast and symplas

126 ld suggest an increase in VTE content across fruit development, the data indicate that in the M82 cul

127 ated different modes of AS in the context of fruit development; the percentage of intron retention (I

128 Early in tomato fruit development there is a transient increase in sucro

129 s of Spd in the leaf, and transiently during fruit development, whereas E8-ySpdSyn expression led to

130 SLW1 RNAs accumulated during floral and fruit development, whereas SLW3 RNAs were not detected d

131 t secretory cavities are formed early during fruit development, whereas the expansion of cavities, an

132 Fruit firmness slowly decreases during fruit development, whereas the solid soluble content/tit

133 ese findings might help the comprehension of fruit development, which in turn, impacts the quality of

134 he fact that auxin regulates many aspects of fruit development, which include fruit formation, expans

135 ditional complexities in GA signaling during fruit development, which may be particularly important t

136 ilencing of SlPIN4 and SlPIN3 did not affect fruit development, which suggested functional redundancy

137 nd TAGL1 have diversified their functions in fruit development: while TAG1 controls placenta and seed

138 quencing was employed to profile early-stage fruit development with five fruit tissue types and five