ライフサイエンスコーパス: shoot development

1 ristem) transcript accumulation during maize shoot development.

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

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

4 missible signal that is capable of arresting shoot development.

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

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

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

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

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

10 ediated protein degradation is essential for shoot development.

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

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

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

14 tional regulators of phase transition during shoot development.

15 organ cell number and organ size throughout shoot development.

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

17 ll differentiation is essential for root and shoot development.

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

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

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

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

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

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

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

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

26 6 is expressed at a very high level early in shoot development and then decreases, leading to the ons

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

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

29 mechanisms regulating bryophyte gametophytic shoot development are largely unknown.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45 Shoot development in many higher plant species is charac

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

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

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

49 164 activity leads to a severe disruption of shoot development, in contrast to the effect of mutation

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

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

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

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

54 Shoot development is reiterative: shoot apical meristems

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

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

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

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

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

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

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

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

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

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

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