ライフサイエンスコーパス: adventitious root

1 ot growth and a proliferation of lateral and adventitious roots.

2 of root cells and promoted the emergence of adventitious roots.

3 on of root hairs, lateral root primordia and adventitious roots.

4 ously reported growth angle response of bean adventitious roots.

5 of shoot-borne roots, which are also called adventitious roots.

6 ooting that acts early in the development of adventitious roots.

7 of the centrally important, nodal system of adventitious roots.

8 n and the Nr mutation reducing the number of adventitious roots.

9 sponse mutants of both species have enhanced adventitious rooting.

10 ental factors control the complex process of adventitious rooting.

11 wer senescence and fruit ripening, inhibited adventitious root and seedling root hair formation, prem

12 ted hypocotyls in light-grown plants, excess adventitious rooting and incomplete leaf vascularization

13 have overlapping expression profiles during adventitious rooting and that they regulate each other's

14 Unexpectedly, large woody rhizomes with adventitious roots and aerial branch systems identified

15 s supported by supplemental Arg induction of adventitious roots and increased NO accumulation in arga

16 Developing adventitious roots and lateral root primordia also conta

17 physiognomy with vertical crown development, adventitious roots and massive root mounds, leading to m

18 t neoplastic activity by producing calli and adventitious roots and shoots.

19 ly revert the stimulatory effect of auxin on adventitious rooting, and auxin can further increase the

20 e and auxin signaling pathways in regulating adventitious rooting appears to be more complex.

21 Rice stems develop adventitious root (AR) primordia at each node that slowl

22 Adventitious roots are plant roots that form from any no

23 nins appear to act independently to suppress adventitious rooting, as cytokinin mutants are strigolac

24 , and mechanisms regulating lateral root and adventitious root branching in the plant models Arabidop

25 g that strigolactones restrain the number of adventitious roots by inhibiting the very first formativ

26 rpenoids in the culture medium, fast-growing adventitious root cultures may hold promise as a sustain

27 Adventitious root cultures were developed from Tripteryg

28 ids accumulating in the medium of T. regelii adventitious root cultures, facilitated by searching the

29 eltaDDKPtRR13 expression appeared to disrupt adventitious root development 24 h after shoot excision,

30 case studies to summarize the physiology of adventitious root development in response to flooding (c

31 onditions, it is important to understand the adventitious root development of crops both in normal an

32 xin, and vascularization pathways leading to adventitious root development.

33 Adventitious roots emerge from aerial plant tissues, and

34 hypocotyl above the point of excision where adventitious roots emerge.

35 including a drastic decrease in lateral and adventitious root formation and a decrease in leaf cell

36 CC treatment and the epi mutation increasing adventitious root formation and the Nr mutation reducing

37 Adventitious root formation at the base of plant cutting

38 t the plant hormone strigolactone suppresses adventitious root formation in Arabidopsis (Arabidopsis

39 We examined excision-induced adventitious root formation in auxin influx and efflux m

40 13 acting downstream of cytokinin to repress adventitious root formation in intact plants, and that r

41 tect the induction of gene expression during adventitious root formation in loblolly pine (Pinus taed

42 associated with the developmental stages of adventitious root formation in the model tree poplar (Po

43 nts were conducted to determine if normal or adventitious root formation is affected by ethylene inse

44 derstanding the regulation and physiology of adventitious root formation is critical for breeding pro

45 Adventitious root formation is essential for the propaga

46 minocyclopropane-1-carboxylic acid increased adventitious root formation on vegetative stem cuttings

47 lied auxin (indole-3-butyric acid) increased adventitious root formation on vegetative stem cuttings

48 In contrast, the process of adventitious root formation shows the opposite response

49 uxin transport from the shoot apex abolishes adventitious root formation under these conditions.

50 Reduced adventitious root formation was also observed in ethylen

51 ateral root formation and a positive role in adventitious root formation with modulation of auxin tra

52 d lateral root growth as well as lateral and adventitious root formation.

53 transport and local IAA accumulation driving adventitious root formation.

54 linked to local IAA accumulation leading to adventitious root formation.

55 ranscription factor of the AP2 family during adventitious root formation.

56 f PtAIL1 expression, which led to a delay in adventitious root formation.

57 actones, cytokinins, and auxin in regulating adventitious root formation.

58 can survive flash floods by the emergence of adventitious roots from the stem.

59 ntiation occurs, flooded roots (aerenchyma), adventitious rooting in hypocotyls, and leaf abscission

60 sulted in increased formation of lateral and adventitious roots in Arabidopsis (Arabidopsis thaliana)

61 and auxin can further increase the number of adventitious roots in max mutants.

62 of ethylene in the formation of lateral and adventitious roots in tomato (Solanum lycopersicum) usin

63 three GH3 genes are required for fine-tuning adventitious root initiation in the Arabidopsis thaliana

64 is (Arabidopsis thaliana) seedlings in which adventitious root initiation was induced by excising roo

65 by a cyclin B1 reporter (pCYCB1;1:GUS), and adventitious root initiation.

66 We propose a model in which adventitious rooting is an adaptive developmental respon

67 Adventitious rooting is an essential but sometimes rate-

68 uggest that the promotive effect of auxin on adventitious rooting is influenced by ethylene responsiv

69 ominance, inhibit root elongation, stimulate adventitious rooting, mediate root gravitropism, and sti

70 ominance, reduced root elongation, increased adventitious rooting, no root gravitropism, and ectopic

71 tions and cell-specific ion distributions in adventitious roots of barley (Hordeum vulgare).

72 nce Charles Darwin first discovered that the adventitious roots of English ivy (Hedera helix) exude a

73 ation of mechanical interlocking between the adventitious roots of English ivy and the surface of sub

74 Integrity of grafts and absence of adventitious roots on scions were assessed using plants

75 phogenesis, and emergence of new lateral and adventitious root organs, much more remains to be done.

76 ssion, an early marker for the initiation of adventitious root primordia in Arabidopsis, is enhanced

77 Epidermal cells that overlie adventitious root primordia undergo cell death to facili

78 g the auxin-induced formation of lateral and adventitious root primordia.

79 tion of tillers and internodes and extensive adventitious root/shoot formation on nodes.

80 An ABCB19 overexpression line forms more adventitious roots than the wild type in intact seedling

81 -type plants, but NR cuttings produced fewer adventitious roots than wild-type cuttings.

82 elow-ground root mass but fewer above-ground adventitious roots than wild-type Pearson plants.

83 oot system is composed of several classes of adventitious roots that include crown roots and brace ro

84 In spite of the importance of adventitious rooting, the mechanism behind this developm

85 Recent work shows that different adventitious root types are regulated differently, and h

86 microRNA miR167, are positive regulators of adventitious rooting, whereas ARF17, a target of miR160,

87 IL1 were able to grow an increased number of adventitious roots, whereas RNA interference mediated th