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1 phological diversities between maize ear and tassel.
2 hanges in leaf and ear but relatively few in tassel.
3 in an implementation of the software program TASSEL.
4 of expression in cob glumes, husk, silk, and tassel.
5 ue that otherwise would form the base of the tassel.
6 the earliest known cobs, husks, stalks, and tassels.
7 sion of aox1 is detected only in NCS and CMS tassels.
8 wers initiated in ears and in all flowers in tassels.
9 , MLMM, FarmCPU, and BLINK), three models in TASSEL 5 (SMR, GLM, and MLM), and three models in rMVP (
11 wo staminate florets in each spikelet on the tassel and a single pistillate floret in each spikelet o
13 ypes include increased numbers of flowers in tassel and ear spikelets, disrupted rowing in the ear, f
15 es are few and upright in the wab1 revertant tassel and have an increased branch angle in the dominan
17 rly development of maize inflorescences, the tassel and the ear, and has been implicated in the evolu
19 chitecture of maize inflorescences, the male tassel and the female ear, is defined by a series of rei
20 ucted molecular ontogenies from 40 B73 maize tassels and 47 BTx623 sorghum panicles and separated the
22 These patterns are consistent across leaf, tassel, and immature ear libraries, but particularly emp
23 e (Zea mays), 94 RNA-seq libraries from ear, tassel, and leaf of the B73 public inbred line were cons
25 entially expressed genes determining ear and tassel architecture within the 3D genome context is larg
27 d WAB1 reveals a link between leaf shape and tassel architecture, and suggests the ligule is a bounda
30 a semidwarfed mutant with fasciated ears and tassels as well as greatly enlarged vegetative and inflo
31 level of Hsp101 transcript increased in the tassel at anthesis following a heat stress without an in
32 esent at only a low level in the anthers and tassel at anthesis, mature pollen, roots, and leaves.
33 In expanding foliar leaves, husk leaves, the tassel at the premeiosis stage of development, or pre-an
35 nt, necrotic upper tips1 (nut1), that mimics tassel blasting and drought stress and reveals the genet
36 and sterility, a stress condition known as "tassel blasting." We identified a mutant, necrotic upper
40 tive trait loci (QTL) for ear row number and tassel branch number in both the nested association mapp
42 y, loss of a single copy of rs1 enhances the tassel branch reduction phenotype, while loss of both co
43 The Mo17 allele is associated with a reduced tassel branch zone and shows lower expression than the B
44 ength, stalk circumference, leaf length, and tassel-branch number in 20 paired families that involved
47 that lg2 mutant plants can have reduced long tassel branches, extra vegetative leaves and extra husk
50 cis-regulatory control of pleiotropy between tassel branching and leaf angle across maize diversity.
51 flowering result in leaf wilting, necrosis, tassel browning, and sterility, a stress condition known
53 , a 12-band Sentinel-2 composite and derived tasselled cap components, and a Sentinel-1 VV-polarisati
59 orthern hybridizations of mutant leaf, root, tassel, endosperm and embryo tissues with non-specific S
61 ted plants (n = 780) that was phenotyped for tassel fertility, plants containing F187 were completely
62 ned for recombinants and then phenotyped for tassel fertility, resulting in a final map-based cloning
63 does not affect tumor formation in immature tassel floral tissues, where maize cell proliferation oc
64 naling, resulting in short plants and normal tassel floret development in the presence of excess GA.
69 elded on average three times as many SNPs as TASSEL-GBS analyses (32 and 64 bp tag lengths) and over
70 version of GBS-SNP-CROP behaved similarly to TASSEL-GBS in terms of the number of SNPs called but had
74 and has fewer branches and spikelets in the tassel, indicating that ba2 functions in reproductive AM
76 defects, including formation of a feminized tassel, initiation of female reproductive buds at each n
78 cences, which are programmed to develop into tassels (male) in teosinte, to become ears (female) in m
79 , and (iii) Bt pollen contaminated with corn tassel material applied directly to milkweed leaf discs.
80 ypic syndrome that includes reduced stature, tassel morphology changes and the presence of knots on t
81 howed moderate effects on flowering time and tassel morphology, whereas ZCN3 and ZCN6 did not change
83 e architectures in which cylindrical micelle tassels of controlled length are grown from specific cry
85 arge number of genes have been identified as tassel-preferred in their expression pattern, both by tr
86 n regions (OCRs) in developing maize ear and tassel primordia using ATAC-seq and characterize combina
90 suppression through direct activation of the tassels replace upper ears1 (tru1) gene that encodes an
93 Double-mutant analysis with anther ear1 and tassel seed2 revealed that the sex of the axillary inflo
99 lets and the abortion of pistils in both the tassel spikelets and in the secondary florets of ear spi
100 in the primary and secondary florets of the tassel spikelets, and in the secondary florets of ear sp
102 osase mRNA levels between LAG1-O and lag1(+) tassels, suggesting that suppression is post-transcripti
104 measurement errors for five maize (Zea mays) tassel traits collected using an image-based phenotyping
105 ssociation studies (GWASs) conducted on five tassel traits that had been phenotyped both manually (i.
106 bp tag lengths) and over 18 times as many as TASSEL-UNEAK, with fewer genotyping errors in all cases,
107 S-SNP-CROP versions significantly outperform TASSEL-UNEAK; and v.4.0 resolves the issue of non-overla
108 ) mutations permit carpel development in the tassel while increasing meristem branching, showing that
109 generally active in young leaves, silks, and tassels, while largely inactive in seeds and roots.
110 , these transgenic plants produced a "bushy" tassel with increased lateral branching and spikelet den