ライフサイエンスコーパス: Gossypium hirsutum

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 t GhCIPK6 homologous genes in upland cotton (Gossypium hirsutum).

6 and DT) of the allopolyploid cotton species, Gossypium hirsutum.

7 ted for 10 of 40 genes examined in ovules of Gossypium hirsutum.

8 with genomic DNA from allotetraploid cotton Gossypium hirsutum.

9 ries were derived from allopolyploid cotton (Gossypium hirsutum; A(T) and D(T) genomes) as well as it

10 dely cultivated cotton is an allotetraploid (Gossypium hirsutum, AADD) that contains GhMYB2A and GhMY

11 susceptible (Coker 312) and tolerant (Mac7) Gossypium hirsutum accessions identified several unique

12 Here, we investigated the role of a cotton (Gossypium hirsutum) actin gene in the organization of ac

13 cotton seed proteomes from the allopolyploid Gossypium hirsutum (AD genome) and its model A-genome an

14 g the existing Gossypium arboreum (A(2)) and Gossypium hirsutum ((AD)(1)) genomes, we showed that all

15 pic variation in hydraulic traits of cotton (Gossypium hirsutum), an economically important species f

16 characterize genome-wide diversity among 440 Gossypium hirsutum and 219 G. barbadense cultivars and l

17 motor kinesins, Kinesin-13A, from the cotton Gossypium hirsutum and Arabidopsis thaliana.

18 Gossypium hirsutum and G. barbadense, are the two cultiv

19 o independently domesticated cotton species, Gossypium hirsutum and G. barbadense.

20 o allotetraploid (AD-genome) cotton species, Gossypium hirsutum and G. mustelinum, relative to their

21 2,569 and 8851 non-reference genes lost from Gossypium hirsutum and Gossypium barbadense reference ge

22 Allotetraploid cotton species (Gossypium hirsutum and Gossypium barbadense) have long b

23 rm (flowering plant) genes in elite cottons (Gossypium hirsutum and Gossypium barbadense), genetic co

24 loid species of great commercial importance, Gossypium hirsutum and Gossypium barbadense, were domest

25 f homoeologous loci in allopolyploid cotton (Gossypium hirsutum) and in species representing its dipl

26 s (CNTs) on fiber-producing species (cotton, Gossypium hirsutum) and ornamental species (vinca, Catha

27 ptomes between wild and domesticated cotton (Gossypium hirsutum) and their reciprocal F(1) hybrids, r

28 including wheat (Triticum aestivum), cotton (Gossypium hirsutum), and soybean (Glycine max), have con

29 , including two currently unexamined species Gossypium hirsutum, and Zostera marina, were characteriz

30 The fibers of cotton (Gossypium hirsutum) are single-cell trichomes that under

31 nomes (A(T) and D(T)) of the allotetraploid, Gossypium hirsutum, as well as the model diploid progeni

32 enomic coding sequences from upland cotton ( Gossypium hirsutum ) BRI1 ( GhBRI1 ) were obtained and c

33 f fiber development in allotetraploid cotton Gossypium hirsutum by sequencing 376 genomes and 2,215 t

34 that specific AGPs were produced by cotton (Gossypium hirsutum) calli undergoing SE and that when th

35 ase in Nicotiana or subunit 1 of cottonseed (Gossypium hirsutum) catalase were introduced in the sens

36 We have characterized two cotton (Gossypium hirsutum) cDNA clones and identified one rice

37 Gossypium hirsutum contributes the most production of co

38 Domestication of upland cotton (Gossypium hirsutum) converted it from a lanky photoperio

39 al structure of recombinant annexin Gh1 from Gossypium hirsutum (cotton fibre) has been determined an

40 iva (arugula), Triticum aestivum (wheat) and Gossypium hirsutum (cotton) leaves and arugula protoplas

41 hesis, a family of transgenic cotton plants (Gossypium hirsutum cv. Coker 312 elite) was produced tha

42 nslocation breakpoints, and telosome arms in Gossypium hirsutum cytogenetic stocks by fluorescence in

43 elucidating gene function in Upland cotton (Gossypium hirsutum) due to its complex allotetraploid ge

44 s from several plant sources (mature cotton (Gossypium hirsutum) embryos, roots of cotton seedlings,

45 encoding annexin was isolated from a cotton (Gossypium hirsutum) fiber cDNA library.

46 Cotton (Gossypium hirsutum) fibers are single-celled seed coat h

47 We used cotton (Gossypium hirsutum) fibers that underwent robust elongat

48 In cotton (Gossypium hirsutum) fibers, cortical microtubules underg

49 Developing cotton (Gossypium hirsutum) fibers, cultured in vitro with their

50 in, GhKCH1, has been identified from cotton (Gossypium hirsutum) fibers.

51 s], tobacco [Nicotiana tabacum], and cotton [Gossypium hirsutum]) from warm regions.

52 rough examining the tips of young elongating Gossypium hirsutum (Gh) and G. barbadense (Gb) fibers.

53 However, the role of D53 in cotton (Gossypium hirsutum, Gh) fiber development remains unclea

54 virus-induced gene silencing, we identified Gossypium hirsutum GhWRKY59 as an important transcriptio

55 Gossypium hirsutum has proven difficult to sequence owin

56 Upland cotton (Gossypium hirsutum) has long been an important economic

57 Gossypium hirsutum is a predominant source of natural pl

58 Gossypium hirsutum is an allotetraploid cotton species p

59 While the widely cultivated cotton species Gossypium hirsutum is generally susceptible, the diploid

60 ses of 32 789 high-quality ESTs derived from Gossypium hirsutum L.

61 Here we sequenced the allotetraploid Gossypium hirsutum L. acc.

62 ginseng C.A. Meyer), fiber length in cotton (Gossypium hirsutum L. and G. barbadense L.) and grain yi

63 Cotton (Gossypium hirsutum L. cv Acala SJ-1) fibers were also an

64 After polyploidization, Gossypium hirsutum L. evolved to produce a higher fiber

65 re isolated from cotton cultivars Coker 312 (Gossypium hirsutum L.) and Sea Island (G. barbadense L.)

66 asing the leaf temperature of intact cotton (Gossypium hirsutum L.) and wheat (Triticum aestivum L.)

67 ured in vivo during the expansion of cotton (Gossypium hirsutum L.) cotyledons.

68 Cotton (Gossypium hirsutum L.) fibers are single-celled trichome

69 We have characterized cotton (Gossypium hirsutum L.) genes encoding type 1 metallothio

70 Two homologous cotton (Gossypium hirsutum L.) genes, GhCTL1 and GhCTL2, encode

71 iased distribution in the tetraploid cotton (Gossypium hirsutum L.) genome that was also linked to di

72 Cotton (Gossypium hirsutum L.) is a key allopolyploid crop with

73 m irrigation termination periods for cotton (Gossypium hirsutum L.) is crucial for efficient utilizat

74 chitinase and 1,3-beta-glucanase in cotton (Gossypium hirsutum L.) leaves.

75 cDNA clone (997 bp in length) from a cotton (Gossypium hirsutum L.) library which putatively encodes

76 American cotton (Gossypium hirsutum L.), transformed with Bacillus thurin

77 the elongating fiber cells of Upland cotton (Gossypium hirsutum L.).

78 radiation hybrid" (WWRH) panel from cotton (Gossypium hirsutum L.).

79 to variation in the P x Zn supply of cotton (Gossypium hirsutum L.).

80 CotMYBA, a myb gene which is expressed in Gossypium hirsutum ovules and has some homology to MIXTA

81 synthases of other prokaryotes, Arabidopsis, Gossypium hirsutum, Populus alba x Populus tremula, corn

82 Cotton (Gossypium hirsutum) provides the world's dominant renewa

83 photosynthetic, cotyledon library of cotton (Gossypium hirsutum) seedlings with putative plastid-targ

84 NAEs in vitro and in vivo in imbibed cotton (Gossypium hirsutum) seeds.

85 ponses of field and greenhouse-grown cotton (Gossypium hirsutum) source leaves to water-deficit stres

86 ss-1 (Li1) is a monogenic dominant mutant of Gossypium hirsutum (upland cotton) with a phenotype of i

87 s between cultivars of allotetraploid (AADD) Gossypium hirsutum ("Upland" cotton) and Gossypium barba

88 A silencing vector for cotton (Gossypium hirsutum) was developed from the geminivirus C

89 The role of Gossypium hirsutum WRINKLED1 (GhWRI1) in seed-oil accumu