ライフサイエンスコーパス: shoot apex

1 tivating SFT in the leaves and AP1/MC at the shoot apex.

2 xamined, with the highest levels seen in the shoot apex.

3 ne the development of organ primordia at the shoot apex.

4 7 reversibly arrests leaf development at the shoot apex.

5 fic transcriptomes of the Populus vegetative shoot apex.

6 one straddling concentric domains around the shoot apex.

7 genesis driven by lateral inhibitions at the shoot apex.

8 , and develop a mass of callus tissue at the shoot apex.

9 ds to cell division plane orientation at the shoot apex.

10 key regulator of stem cell activation at the shoot apex.

11 ively kills epidermal and niche cells in the shoot apex.

12 ignaling control cell differentiation at the shoot apex.

13 otic stress with cell differentiation at the shoot apex.

14 flowers at the periphery of the reproductive shoot apex.

15 ains patterned at a fixed distance below the shoot apex.

16 ported to axillary mersitems rather than the shoot apex.

17 nd the MADS-Box gene APETALA1(AP1)/MC at the shoot apex.

18 monal effects with KNOX gene function at the shoot apex.

19 ctive signals transmitted from leaves to the shoot apex.

20 ion phloem and traffic cell to cell into the shoot apex.

21 ein in sections through the maize (Zea mays) shoot apex.

22 w of symplastic tracers from the leaf to the shoot apex.

23 loral stimulus that moves from leaves to the shoot apex.

24 have no detectable AtZFP1 expression in the shoot apex.

25 ranscripts from the body of the plant to the shoot apex.

26 tive to reproductive phase transition of the shoot apex.

27 ends on a group of meristematic cells in the shoot apex.

28 insects and diseases that attack the growing shoot apex.

29 and leaf tissue, rather than leaves, at the shoot apex.

30 Inhibition of auxin transport from the shoot apex abolishes adventitious root formation under t

31 vels in proliferative tissues, including the shoot apex and developing inflorescences.

32 we show that VRN2 is enriched in the hypoxic shoot apex and emerging leaves of Arabidopsis, where it

33 oral variation in the level of miR156 in the shoot apex and leaf-to-leaf variation in miR156 expressi

34 e for the severe alterations observed in the shoot apex and reproductive organs under salinity condit

35 ids inhibit auxin transport primarily at the shoot apex and root tip and appear to modulate vesicular

36 The stem cell pools at the shoot apex and root tip give rise to all the above- and

37 umber and size of the stem cell pools at the shoot apex and root tip.

38 This induction of Adh/GUS in shoot apex and roots is due, at least in part, to mechan

39 hat promoter activity is associated with the shoot apex and the base of leaf petioles throughout the

40 We sampled sRNAs from the seedling shoot apex and the developing ear, two rapidly growing t

41 e in the rapidly growing regions such as the shoot apex and the secondary meristem producing axillary

42 Auxin is synthesized in the shoot apex and transported through the stem, but the mol

43 th gene expression and cell mechanics at the shoot apex and, by extension, in the epidermis of any th

44 tage, dramatically increases the size of the shoot apex and, like xtc1 and xtc2, produces enlarged le

45 whole plant senescence, especially when the shoot apexes are senescent, is not clear.

46 ue to deficiencies in auxin transport in the shoot apex, as judged by altered expression of PIN1, the

47 Expression of LEAFY and AGAMOUS-LIKE8 in the shoot apex at the time of floral determination is also c

48 do not clearly alter node distance, from the shoot apex, at which axillary shoot meristems initiate b

49 factor FD, which is already expressed at the shoot apex before floral induction.

50 fference in the development of the main stem shoot apex between tin and the wild type.

51 red for high levels of FLC expression in the shoot apex, but it is not required for FLC expression in

52 incipient and emergent leaf primordia at the shoot apex, but not in the vegetative meristem or stem.

53 n regulates rhythmic organ production at the shoot apex, but the spatio-temporal dynamics of auxin gr

54 es are restricted to separate domains of the shoot apex by different mechanisms.

55 Meristems derived from the shoot apex can develop into either shoots or flowers.

56 Presently, we lack a lineage map of the shoot apex cells in woody perennials - a crucial gap con

57 also be observed in plants "rejuvenated" via shoot apex culture.

58 Here, we show that leafy shoot apex decapitation releases apical dominance throug

59 The link between delayed shoot apex development and the induction of cold toleran

60 s for two family members were highest in the shoot apex, dry seeds (hmg1), and bark (hmg3) which are

61 the depletion of AP2 and AP2-LIKE TFs at the shoot apex during floral transition and demonstrate that

62 Our observations indicate that the shoot apex exerts long-distance control on the growth of

63 In the shoot apex, expansin transcripts are abundant in the eme

64 nt regeneration procedure was developed from shoot apex explants and used to downregulate expression

65 a threshold level of dlf1 is required in the shoot apex for proper timing of the floral transition.

66 in maize by the isolation and culture of the shoot apex from an adult phase plant: an 'adult' meriste

67 r bud outgrowth during the transition of the shoot apex from the vegetative to the reproductive stage

68 ts is a consequence of the transition of the shoot apex from vegetative to reproductive growth in res

69 In darkness, shoot apex growth is repressed, but it becomes rapidly a

70 PGP1 and PGP19 colocalized with PIN1 in the shoot apex in Arabidopsis thaliana and with PIN1 and PIN

71 F4 promote organogenesis at the reproductive shoot apex in parallel with MP via histone-deacetylation

72 ocious germination, primordia develop at the shoot apex in the mode characteristic of postgerminative

73 meristem identity genes at the centre of the shoot apex in two ways; first by delaying their upregula

74 AGL15 protein accumulates transiently in the shoot apex in young Arabidopsis and Brassica seedlings a

75 otein 1), is expressed at high levels in the shoot apex, including the apical meristem, developing le

76 d spatial pattern of IAA localization in the shoot apex indicates a change in IAA source during leaf

77 chastic model of primordia initiation at the shoot apex, integrating locality and stochasticity in th

78 Adh/GUS expression in the shoot apex is also highly induced by root penetration of

79 , we show that the activity of miR172 at the shoot apex is encoded by 3 MIR172 genes, is critical for

80 Auxin produced by an active primary shoot apex is transported down the main stem and inhibit

81 ristem, a small dome-shaped structure at the shoot apex, is responsible for the initiation of all pos

82 vealed that Fv SOC1 activates Fv TFL1 in the shoot apex, leading to the repression of flowering in st

83 f the Blec4 promoter in the epidermis of the shoot apex makes it particularly suitable for geneticall

84 a finely resolved time course, comparing the shoot apex (meristem and leaf primordia) and the cotyled

85 al hypoxia induces Adh/GUS expression in the shoot apex, no apex staining was observed in the spacefl

86 not AmMAR2 prevented floral induction at the shoot apex of A. alpina, strongly enhancing the effect o

87 ne FLOWERING LOCUS C (FLC) is reduced in the shoot apex of atu2af65b, due to both increased intron re

88 At the shoot apex of plants is a small region known as the shoo

89 C introns was significantly increased in the shoot apex of the srpkii mutant.

90 development, axillary buds are inhibited by shoot apex-produced auxin, a mechanism known as apical d

91 of SVP contributes to the rise in GA at the shoot apex, promoting rapid induction of flowering.

92 ots, silk, developing or mature kernels, the shoot apex, prop roots, or pollen.

93 velopmental decision to flower occurs in the shoot apex, requiring the transmission of flowering info

94 MES17 was expressed at the highest levels in shoot apex, stem, and root of Arabidopsis.

95 as root tips, lateral root primordia and the shoot apex, supporting a role for FTase in the control o

96 rophilic molecules are likely to move to the shoot apex symplastically via the phloem and/or via cell

97 The new shoot apex that differentiated at the injection site con

98 Because flowers form at a distant site, the shoot apex, these data suggest that FT primarily control

99 ied effect on the rate of progression of the shoot apex through different developmental phases.

100 s able to translocate from the leaves to the shoot apex through the phloem.

101 ressed unique transcripts were identified in shoot apex tissue between fast- and slow-developing RILs

102 nd the ld mutation converts the reproductive shoot apex to a more vegetative state, a phenotype that

103 globular-to-heart transition but permit the shoot apex to develop to an unusually advanced stage lat

104 of branching involves dichotomy of a parent shoot apex to form two new daughter apices.

105 leaf that elicits the transformation of the shoot apex to reproductive development.

106 f the phytohormone auxin that flows from the shoot apex to the tip of the root.

107 y transported from sites of synthesis in the shoot apex to their sites of action in the basal regions

108 wnregulate auxin transport from the seedling shoot apex towards the root system, rather than a failur

109 In the shoot apex, VRN2 differentially modulates flowering time

110 ene expression atlas of the vegetative maize shoot apex, we show here that distinct sets of genes gov

111 ge 1 in which the scutellum, coleoptile, and shoot apex were clearly defined.

112 rceived in the leaves and transmitted to the shoot apex, where the vegetative shoot apical meristem i

113 in the pre-mRNA splicing of FLC and ABI5 in shoot apex, whereby AtU2AF65b is involved in ABA-mediate

114 id-chloroplast transition takes place at the shoot apex, which consists of the shoot apical meristem

115 o the divisions occurring in the Arabidopsis shoot apex, which contains domains with anisotropic curv

116 2 is expressed in the endosperm, embryo, and shoot apex, which explains the pleiotropic nature of the

117 Maize leaves are initiated from the shoot apex with an inherent leaf dorsoventral polarity;

118 assess the status of individual cells in the shoot apex with regard to the transition between embryon

119 e single-cell transcriptomic analyses of the shoot apex yield insight into the processes of stem-cell