ライフサイエンスコーパス: tiller

1 mes participate in systemic invasion of each tiller.

2 -type buds continue growing and develop into tillers.

3 by panicles until grain maturity, and apical tillers.

4 t diverts sucrose (Suc) away from developing tillers.

5 RCS had greater benefit in plants with fewer tillers.

6 older leaves, younger leaves, and secondary tillers.

7 lates less Striga germination, and is highly tillered.

8 ea and developing thicker roots and moderate tillering.

9 SPL4 seriously suppressed bud formation and tillering.

10 results in reduced chlorophyll and increased tillering.

11 rhizomatous growth and with QTLs influencing tillering.

12 Plants grown at phi values of 0.55 and 0.33 tillered 43 and 56%, less compared with plants grown at

13 Reduced tillering allowed testing the transgenic plants under hi

14 This suppression of tiller and lateral branch growth is an important trait s

15 Expression of the genes involved in tiller and leaf angle control was also affected in the m

16 : FA ratio, reduced plant stature, increased tillering and an approx. threefold increase in sugar rel

17 to a quantitative trait locus that regulates tillering and lateral branching in maize and shows evide

18 b1), a major domestication locus controlling tillering and lateral branching.

19 seminal axile roots) and stem-borne tissues (tillers and coleoptile and leaf node axile roots) plus b

20 matic activity, showing reduced formation of tillers and internodes and extensive adventitious root/s

21 Furthermore, triple mutants have more tillers and leaves-phenotypes seen in Corngrass1 mutants

22 The transgenic plants produced more tillers and more seed than wild-type plants.

23 host plant as assessed by immunoblotting of tillers and quantitative PCR.

24 similar to the wild type but produced fewer tillers and seeds.

25 rative genomics reveal that basal branching (tillering) and axillary branching are partially controll

26 evels of PPF resulted in more dry mass, more tillering, and a more advanced Haun stage.

27 rait loci--qSLB1.1--for the exudation of SL, tillering, and induction of Striga germination was detec

28 with respect to flowering, as well as short, tillering, and segregating for yellow kernel color.

29 ce similarity searches identified rice TAC1 (tiller angle control 1) as a putative ortholog, and we t

30 Restoration of a normal tiller angle in fuct-1 by complementation demonstrated t

31 d-type cv Kitaake, fuct-1 displayed a larger tiller angle, shorter internode and panicle lengths, and

32 duced gravitropic response and the increased tiller angle.

33 ead to less compact growth by increasing the tiller angle.

34 Tillers are vegetative branches that develop from axilla

35 of tillering, leading to a larger number of tillers bearing fertile spikes, and increases in seed nu

36 Tillers, branches initiated at the base of grass plants,

37 Tillering (branching) is a major yield component and, th

38 illering in tin is due to early cessation of tiller bud outgrowth during the transition of the shoot

39 The growth of tiller buds in the first leaf axil of wild-type (100M, P

40 branching and the possibility of optimizing tillering by manipulating the timing of internode elonga

41 ant, which produces an exaggerated number of tillers compared to wild-type plants, is caused by a gai

42 Shoot size and tillers correlated positively with roots with irrigation

43 barley Uniculme4 (Cul4) locus cause reduced tillering, deregulation of the number of axillary buds i

44 s known about the molecular genetic bases of tiller development in important Triticeae crops such as

45 Semi-dwarf rice varieties with low tiller formation but high seed production per panicle an

46 water-dependent water uptake and xylem flow; tiller formation; evapotranspiration; simultaneous simul

47 s studies have largely focused on basal bud (tiller) formation but scarcely touched on aerial buds, w

48 enables plants to modify shoot branching or tillering in response to varying light intensities and r

49 The reduced tillering in tin is due to early cessation of tiller bud

50 eaf Zn uptake (r = 0.60, P < 0.01) at active tillering, indicating dependence on remobilization for g

51 e characterize a reduced tillering (tin, for tiller inhibition) mutant of wheat (Triticum aestivum).

52 Genetic manipulation of tillering is a major objective in breeding for improved

53 Tillering is inhibited in sorghum genotypes that lack ph

54 However, tillering is regulated by complex interactions of endoge

55 sed yield was controlled by a higher rate of tillering, leading to a larger number of tillers bearing

56 that tin represents a novel type of reduced tillering mutant associated with precocious internode el

57 erization of naturally occurring and induced tillering mutants in the major crops.

58 associated with major effects on leaf size, tiller number and ABA accumulation in wheat.

59 surpassed a threshold height of 1.1 m, both tiller number and survival of S. scoparium plants were d

60 An application to a rice tiller number data set is given.

61 i regulating ABA accumulation, leaf size and tiller number in the two crops is discussed.

62 nd the knowledge required to achieve optimal tiller number through genetic and agronomic means is sti

63 ught-induced ABA accumulation, leaf size and tiller number were compared between rice and wheat.

64 reased leaf greenness, reduction of leaf and tiller number, and affects yield parameters.

65 ants display shortened internodes, increased tiller number, and upright growth.

66 Plant growth parameters including height, tiller number, leaf area and biomass were generally high

67 Tiller numbers of S. scoparium plants were unaffected by

68 with distinct chromosome constitutions among tillers of the same plant and also between root and shoo

69 me rhizomes are similar to those that become tillers--one QTL appears to influence the number of such

70 e whether individual buds differentiate into tillers or rhizomes.

71 lag hypothesis by measuring both short-term (tiller population growth rates) and long-term (17-year s

72 Tillering produced up to 7000 heads per square meter at

73 ophyte infection increased plant biomass and tiller production by 10-15% in both treatments.

74 Genotype leaf and tiller size, leaf lamina thickness, leaf mass per area (

75 ping population was replicated using a split-tiller technique to control and better estimate the envi

76 Here we characterize a reduced tillering (tin, for tiller inhibition) mutant of wheat (

77 aacetic acid)-extractable soil Zn from early tillering to flowering.

78 eaths, and between the mainstem and axillary tillers) to model the dynamics of canopy development.

79 so inhibit shoot branching, Azucena is a low-tillering variety.

80 d by warming, but the number of reproductive tillers was increasingly suppressed by intensified droug

81 es dark green, semidwarf plants with reduced tillering, whereas RNA interference knockdown results in

82 area and leaf rank for the mainstem and its tillers, which was robust across a range of sowing dates