ライフサイエンスコーパス: shoot development

1 nt to harmonize internode morphogenesis with shoot development.

2 nsport is an ancient, conserved regulator of shoot development.

3 ll differentiation is essential for root and shoot development.

4 ristem) transcript accumulation during maize shoot development.

5 (BPS1) gene is required for normal root and shoot development.

6 otenoid-derived signal affects both root and shoot development.

7 missible signal that is capable of arresting shoot development.

8 psis UCHs, UCH1, and UCH2, are important for shoot development.

9 y is affected by factors that act throughout shoot development.

10 te a subset of GA-dependent responses during shoot development.

11 h defects but had relatively mild effects on shoot development.

12 ediated protein degradation is essential for shoot development.

13 ferent types of organs at different times in shoot development.

14 by fourfold or more at any one stage during shoot development.

15 rom hormone-dependent to hormone-independent shoot development.

16 tional regulators of phase transition during shoot development.

17 organ cell number and organ size throughout shoot development.

18 pes of leaves produced at different times in shoot development.

19 ients are monitored to control plasticity of shoot development.

20 periodicity in auxin maxima formation during shoot development.

21 ranscriptomics, and confirmed their roles in shoot development.

22 drop in PIN expression are involved in angle shoot development.

23 induce a heterochronic switch from flower to shoot development, a process known as floral meristem re

24 maize, the transition from juvenile to adult shoot development affects a variety of leaf epidermal ce

25 tifies candidate genes involved in rice root/shoot development and defense responses, demonstrating i

26 de-etiolation phenotype, and continuation of shoot development and flowering in the dark.

27 s syndrome develops at a predictable time in shoot development and is tightly associated with the tem

28 croRNA homologous to miR172 increases during shoot development and mediates gl15 mRNA degradation.

29 The effect is evident both on root and shoot development and occurs during the growth period af

30 we show that UV-B induces genes involved in shoot development and organ patterning.

31 or gibberellin (GA) has a profound effect on shoot development and promotes developmental transitions

32 ull mutants have severely disrupted root and shoot development and reduced auxin transport.

33 es a community resource for further study of shoot development and response to internal and environme

34 into the coordinated regulation of tea plant shoot development and secondary metabolism, paving the w

35 dependently recruited into Selaginella angle shoot development and seed plant axillary branching duri

36 e it promotes low levels of H3K27ac early in shoot development and stabilizes the nucleosome at the +

37 6 is expressed at a very high level early in shoot development and then decreases, leading to the ons

38 mote the expression of the juvenile phase of shoot development and to suppress the expression of the

39 ranscriptional data from six stages in maize shoot development are generated.

40 mechanisms regulating bryophyte gametophytic shoot development are largely unknown.

41 ransition (vegetative phase change) early in shoot development, as well as species that remain perman

42 ions as an essential pool of miR156 early in shoot development, but that its effect on leaf identity

43 led multiple defects during maize vegetative shoot development, but these sector phenotypes are not c

44 iana, leaves produced at different stages of shoot development can be distinguished by the distributi

45 nents of variation in gene expression during shoot development can be represented by groups of genes,

46 However, so far the role of AMP1 in shoot development could not be assigned to a specific mo

47 predicted the MYB TFs involved in regulating shoot development (CsMYB2, 98, 107, and 221), epidermal

48 in relation to a possible role for AtZFP1 in shoot development, downstream of photomorphogenic activa

49 and 2 has substantial effects on Arabidopsis shoot development, especially with respect to infloresce

50 ression of cotyledon greening and expansion, shoot development, floral transition, and gene expressio

51 Oligonucleotide array data obtained during shoot development from approximately 8000 Arabidopsis ge

52 free plastids depended on repeatedly forcing shoot development from axillary buds, a process that was

53 terminate flowers, and prolific adventitious shoot development from the rachis or rachillae of the le

54 -binding PpTEL1 protein in the regulation of shoot development, from early ancestors to vascular plan

55 he genetic control of gene expression during shoot development in Arabidopsis thaliana was analyzed b

56 al analysis of gene expression events during shoot development in Arabidopsis was conducted using oli

57 ons that cause a conditional arrest of early shoot development in Arabidopsis.

58 rriers are primary regulators of sporophytic shoot development in flowering plants, the extent of con

59 Shoot development in maize begins when meristematic, non

60 Shoot development in many higher plant species is charac

61 tion from the juvenile to the adult phase of shoot development in plants is accompanied by changes in

62 ys a central role in the temporal control of shoot development in plants.

63 AR1-like genes have been involved in diploid shoot development in vascular plants.

64 164 activity leads to a severe disruption of shoot development, in contrast to the effect of mutation

65 genes that are normally up-regulated during shoot development including CUP-SHAPED COTYLEDON2 that i

66 L27aC that affects multiple aspects of plant shoot development, including leaf patterning, infloresce

67 t from erh1 the mutants also show defects in shoot development, indicating a complex role for the aff

68 ivity to glucose repression of cotyledon and shoot development is phenocopied by ethylene precursor t

69 Shoot development is reiterative: shoot apical meristems

70 Despite its integral role in maize shoot development, little is known about the molecular m

71 As such, repression of a fundamental shoot development pathway is essential for correct root

72 es connected RPL directly to many of the key shoot development pathways, including the development of

73 ings suggest that KAI2 has multiple roles in shoot development, root system development and transcrip

74 allary SAMs and suggest a cyclical model for shoot development: SAMs make leaves which in turn are re

75 x led to a pale-green phenotype with delayed shoot development, smaller chloroplasts, decreased thyla

76 ely, these data show that during Arabidopsis shoot development, the maintenance of optimal proteasome

77 rphological and molecular characteristics of shoot development, this demonstrates that the topless 1

78 rs change in a coordinated fashion, allowing shoot development to be divided into discrete juvenile a

79 ctor gene that was up-regulated during early shoot development was RAP2.6L (At5g13330), a member of t

80 d 21 DAT, where an allometric growth towards shoot development was significant.

81 capable of conferring cytokinin-independent shoot development, were upregulated during incubation on

82 fic meristematic areas fundamental for plant shoot development, which are involved in meristem format

83 ot signaling is used by plants to coordinate shoot development with the conditions experienced by the

84 programs that regulate leaf identity during shoot development with those that specify macrohair init