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1 VL5) with its target gene GhCHR from cotton (Gossypium hirsutum).
2 s directly in seed tissues of upland cotton (Gossypium hirsutum).
3 mmon beans (Phaseolus vulgaris), and cotton (Gossypium hirsutum).
4 emic disease resistance in the dicot cotton (Gossypium hirsutum).
5 and DT) of the allopolyploid cotton species, Gossypium hirsutum.
6 ted for 10 of 40 genes examined in ovules of Gossypium hirsutum.
7 with genomic DNA from allotetraploid cotton Gossypium hirsutum.
8 ries were derived from allopolyploid cotton (Gossypium hirsutum; A(T) and D(T) genomes) as well as it
9 dely cultivated cotton is an allotetraploid (Gossypium hirsutum, AADD) that contains GhMYB2A and GhMY
10 Here, we investigated the role of a cotton (Gossypium hirsutum) actin gene in the organization of ac
11 cotton seed proteomes from the allopolyploid Gossypium hirsutum (AD genome) and its model A-genome an
12 characterize genome-wide diversity among 440 Gossypium hirsutum and 219 G. barbadense cultivars and l
16 rm (flowering plant) genes in elite cottons (Gossypium hirsutum and Gossypium barbadense), genetic co
17 loid species of great commercial importance, Gossypium hirsutum and Gossypium barbadense, were domest
18 f homoeologous loci in allopolyploid cotton (Gossypium hirsutum) and in species representing its dipl
19 including wheat (Triticum aestivum), cotton (Gossypium hirsutum), and soybean (Glycine max), have con
21 nomes (A(T) and D(T)) of the allotetraploid, Gossypium hirsutum, as well as the model diploid progeni
22 enomic coding sequences from upland cotton ( Gossypium hirsutum ) BRI1 ( GhBRI1 ) were obtained and c
23 that specific AGPs were produced by cotton (Gossypium hirsutum) calli undergoing SE and that when th
24 ase in Nicotiana or subunit 1 of cottonseed (Gossypium hirsutum) catalase were introduced in the sens
28 al structure of recombinant annexin Gh1 from Gossypium hirsutum (cotton fibre) has been determined an
29 hesis, a family of transgenic cotton plants (Gossypium hirsutum cv. Coker 312 elite) was produced tha
30 nslocation breakpoints, and telosome arms in Gossypium hirsutum cytogenetic stocks by fluorescence in
31 s from several plant sources (mature cotton (Gossypium hirsutum) embryos, roots of cotton seedlings,
39 rough examining the tips of young elongating Gossypium hirsutum (Gh) and G. barbadense (Gb) fibers.
40 virus-induced gene silencing, we identified Gossypium hirsutum GhWRKY59 as an important transcriptio
44 While the widely cultivated cotton species Gossypium hirsutum is generally susceptible, the diploid
48 re isolated from cotton cultivars Coker 312 (Gossypium hirsutum L.) and Sea Island (G. barbadense L.)
49 asing the leaf temperature of intact cotton (Gossypium hirsutum L.) and wheat (Triticum aestivum L.)
54 iased distribution in the tetraploid cotton (Gossypium hirsutum L.) genome that was also linked to di
56 cDNA clone (997 bp in length) from a cotton (Gossypium hirsutum L.) library which putatively encodes
60 CotMYBA, a myb gene which is expressed in Gossypium hirsutum ovules and has some homology to MIXTA
61 synthases of other prokaryotes, Arabidopsis, Gossypium hirsutum, Populus alba x Populus tremula, corn
63 photosynthetic, cotyledon library of cotton (Gossypium hirsutum) seedlings with putative plastid-targ
65 ponses of field and greenhouse-grown cotton (Gossypium hirsutum) source leaves to water-deficit stres
66 ss-1 (Li1) is a monogenic dominant mutant of Gossypium hirsutum (upland cotton) with a phenotype of i
67 s between cultivars of allotetraploid (AADD) Gossypium hirsutum ("Upland" cotton) and Gossypium barba
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