ライフサイエンスコーパス: tassel

1 hanges in leaf and ear but relatively few in tassel.

2 in an implementation of the software program TASSEL.

3 of expression in cob glumes, husk, silk, and tassel.

4 ue that otherwise would form the base of the tassel.

5 the earliest known cobs, husks, stalks, and tassels.

6 sion of aox1 is detected only in NCS and CMS tassels.

7 wo staminate florets in each spikelet on the tassel and a single pistillate floret in each spikelet o

8 rs through abortion of female carpels in the tassel and arrest of male stamens in the ear.

9 ypes include increased numbers of flowers in tassel and ear spikelets, disrupted rowing in the ear, f

10 antly lack long branches, giving rise to the tassel and familiar corncob.

11 es are few and upright in the wab1 revertant tassel and have an increased branch angle in the dominan

12 In germinal cells, immature tassel and mature pollen, reporter expression increases

13 rly development of maize inflorescences, the tassel and the ear, and has been implicated in the evolu

14 espread sterility in its inflorescences, the tassel and the ear.

15 chitecture of maize inflorescences, the male tassel and the female ear, is defined by a series of rei

16 s in other developing tissues, including the tassels and juvenile leaves.

17 These patterns are consistent across leaf, tassel, and immature ear libraries, but particularly emp

18 e (Zea mays), 94 RNA-seq libraries from ear, tassel, and leaf of the B73 public inbred line were cons

19 d WAB1 reveals a link between leaf shape and tassel architecture, and suggests the ligule is a bounda

20 esis) detect a significant effect of bif2 on tassel architecture.

21 a semidwarfed mutant with fasciated ears and tassels as well as greatly enlarged vegetative and inflo

22 level of Hsp101 transcript increased in the tassel at anthesis following a heat stress without an in

23 esent at only a low level in the anthers and tassel at anthesis, mature pollen, roots, and leaves.

24 In expanding foliar leaves, husk leaves, the tassel at the premeiosis stage of development, or pre-an

25 All mutants showed extremely acute tassel branch angles accompanied by a significant reduct

26 Double mutants display a decrease in tassel branch number and an increase in ear row number,

27 For example, tassel branch number controls pollen abundance and lengt

28 tive trait loci (QTL) for ear row number and tassel branch number in both the nested association mapp

29 y, loss of a single copy of rs1 enhances the tassel branch reduction phenotype, while loss of both co

30 The Mo17 allele is associated with a reduced tassel branch zone and shows lower expression than the B

31 ength, stalk circumference, leaf length, and tassel-branch number in 20 paired families that involved

32 Tassel branches are few and upright in the wab1 revertan

33 ces, consistent with the complete absence of tassel branches in the bif2 knockout mutant.

34 that lg2 mutant plants can have reduced long tassel branches, extra vegetative leaves and extra husk

35 t slower growth rate, later flowering, fewer tassel branches, reduced stature and fertility.

36 gule formation and in the axil of developing tassel branches.

37 elatively high levels of aox2 mRNAs in young tassels but none in ear shoots.

38 This suppression persists during tassel development and does not appear to be released un

39 er of vegetative nodes before it switches to tassel development.

40 heir maize homologs knotted1 (kn1) and thick tassel dwarf1 (td1).

41 protein was most abundant in the developing tassel, ear, silks, endosperm, and embryo.

42 orthern hybridizations of mutant leaf, root, tassel, endosperm and embryo tissues with non-specific S

43 does not affect tumor formation in immature tassel floral tissues, where maize cell proliferation oc

44 The maize fuzzy tassel (fzt) mutant has striking inflorescence defects w

45 elded on average three times as many SNPs as TASSEL-GBS analyses (32 and 64 bp tag lengths) and over

46 version of GBS-SNP-CROP behaved similarly to TASSEL-GBS in terms of the number of SNPs called but had

47 nd largely environment dependent for days to tassel, grain moisture and ear number.

48 al maize (Zea mays) ears are unbranched, and tassels have long branches only at their base.

49 defects, including formation of a feminized tassel, initiation of female reproductive buds at each n

50 The maize (Zea mays) tassel-less1 (tls1) mutant has defects in vegetative and

51 cences, which are programmed to develop into tassels (male) in teosinte, to become ears (female) in m

52 , and (iii) Bt pollen contaminated with corn tassel material applied directly to milkweed leaf discs.

53 ypic syndrome that includes reduced stature, tassel morphology changes and the presence of knots on t

54 howed moderate effects on flowering time and tassel morphology, whereas ZCN3 and ZCN6 did not change

55 e flowering time but still showed effects on tassel morphology.

56 e architectures in which cylindrical micelle tassels of controlled length are grown from specific cry

57 arge number of genes have been identified as tassel-preferred in their expression pattern, both by tr

58 Mutant tassels produce fewer branches and spikelets.

59 Analysis of ear and tassel QTL across biparental families suggests that mult

60 suppression through direct activation of the tassels replace upper ears1 (tru1) gene that encodes an

61 Ectopic expression of ids1 in the tassel, resulting from a failure of regulation by the ta

62 pressed in endosperm, embryo, immature ears, tassel, roots, and seedling shoots at low levels.

63 Double-mutant analysis with anther ear1 and tassel seed2 revealed that the sex of the axillary inflo

64 We identified maize (Zea mays) tassel sheath (tsh) mutants, characterized by the loss o

65 OSA ortholog Zea mays mads16 (Zmm16)/sterile tassel silky ear1 (sts1).

66 lets and the abortion of pistils in both the tassel spikelets and in the secondary florets of ear spi

67 in the primary and secondary florets of the tassel spikelets, and in the secondary florets of ear sp

68 osase mRNA levels between LAG1-O and lag1(+) tassels, suggesting that suppression is post-transcripti

69 TASSEL (Trait Analysis by aSSociation, Evolution and Lin

70 bp tag lengths) and over 18 times as many as TASSEL-UNEAK, with fewer genotyping errors in all cases,

71 ) mutations permit carpel development in the tassel while increasing meristem branching, showing that

72 , these transgenic plants produced a "bushy" tassel with increased lateral branching and spikelet den