ライフサイエンスコーパス: Helianthus

1 actinoporin family produced by Stichodactyla helianthus.

2 isolated from the sea anemone Stichodactyla helianthus.

3 as data collected across scales in the genus Helianthus.

4 epresenting 14 taxa from the sunflower genus Helianthus, 91 phenotypic traits measured in common gard

5 population and evolutionary biology both in Helianthus and other angiosperms.

6 nform the genetics of species differences in Helianthus and suggest an approach for the simultaneous

7 clear discordance in wild annual sunflowers (Helianthus), and to test alternative explanations for su

8 etic and synteny analysis indicated that the Helianthus annnus CCO (HaCCO) genes were conserved in di

9 pollen phospholipase activity in sunflower (Helianthus annus), we serendipitously discovered that em

10 ia faba, nonlegume dicots Brassica napus and Helianthus annus, and nonlegume cereals Hordeum vulgare

11 traits distinguishing two annual sunflowers, Helianthus annuus and H. debilis ssp. cucumerifolius.

12 ids between two species of Texas sunflowers (Helianthus annuus and H. debilis) that form a natural hy

13 ackcross between two wild annual sunflowers, Helianthus annuus and H. petiolaris, interpret different

14 tion between the sympatric sunflower species Helianthus annuus and H. petiolaris.

15 pathogen, we analyzed transgenic sunflower (Helianthus annuus cv SMF3) plants constitutively express

16 g that a frameshift mutation in one paralog, Helianthus annuus FT 1 (HaFT1), underlies a major QTL fo

17 ran herbivore, we hydroponically manipulated Helianthus annuus host plants' tissue-sodium concentrati

18 f the thermally induced VPs in the leaves of Helianthus annuus L. seedlings in situ.

19 mance trials of oilseed sunflower varieties (Helianthus annuus L.) conducted since 1978 across the Gr

20 Genetic diversity in modern sunflower (Helianthus annuus L.) cultivars (elite oilseed inbred li

21 e now debated, and until recently sunflower (Helianthus annuus L.) has been considered the only undis

22 , we immersed marked, decapitated sunflower (Helianthus annuus L.) hypocotyl sections in buffered aux

23 Sunflower (Helianthus annuus L.) production is challenged by differ

24 To date, the domestication of sunflower (Helianthus annuus L.) stands as the only counterexample

25 the most devastating diseases of sunflower (Helianthus annuus L.), affecting global production.

26 g seedlings of cocklebur, tomato, sunflower (Helianthus annuus L.), and soybean (Glycine max [L.] Mer

27 amics of transposable elements in sunflower (Helianthus annuus L.), especially given its large genome

28 tion (GWA) analyses in cultivated sunflower (Helianthus annuus L.).

29 Rf1 is used for commercial hybrid sunflower (Helianthus annuus L., 2n = 34) seed production worldwide

30 The domesticated sunflower, Helianthus annuus L., is a global oil crop that has prom

31 nucleus) of the first leaf of the sunflower, Helianthus annuus L., is influenced by the quality and t

32 Here, we report the 3D NMR structure of the Helianthus annuus PawS1 (preproalbumin with sunflower tr

33 ylem anatomy and resistance to cavitation in Helianthus annuus plants grown under three CO(2) regimes

34 Brassica napus and Helianthus annuus pollen were the variables situated nea

35 gene expression between two wild (non-weedy) Helianthus annuus populations from Utah and Kansas and f

36 Heiser hypothesized that Helianthus annuus ssp. texanus was derived by the introd

37 xylem (Populus angustifolia, P. tremuloides, Helianthus annuus stems, and Aesculus hippocastanum peti

38 lder (Iva annua var. macrocarpa), sunflower (Helianthus annuus var. macrocarpus), and 2 cultivated va

39 the leaf surface of the heterobaric species Helianthus annuus was covered by 4-mm-diameter patches o

40 rypsin-inhibitory loops exist in sunflowers (Helianthus annuus) and frogs.

41 report that leaf water washes of sunflower (Helianthus annuus) and jimson weed (Datura metel), but n

42 synteny analysis with the annual sunflower (Helianthus annuus) and lettuce (Lactuca sativa) genomes.

43 with experiments performed with sunflower ( Helianthus annuus) and wheat ( Triticum aestivum) cultiv

44 The common sunflower (Helianthus annuus) contains the unusual gene PawS1 (Prep

45 lupin (Lupin angustifolius), and sunflower (Helianthus annuus) grew well at 100 microm Mn.

46 ohistoric data demonstrating that sunflower (Helianthus annuus) had entered the repertoire of Mexican

47 capacity in sun- and shade-grown sunflower (Helianthus annuus) leaves underlies its previously obser

48 ve (i.e., landrace), and improved sunflower (Helianthus annuus) lines.

49 ntained the rbcL gene from either sunflower (Helianthus annuus) or the cyanobacterium Synechococcus P

50 nspired by the traditional use of sunflower (Helianthus annuus) preparations for analgesic purposes,

51 We grew 33 sunflower (Helianthus annuus) strains (n = 5) that varied in their

52 Sunflower (Helianthus annuus), a moderately salt-tolerant crop, exh

53 bis sativa), Pumpkin (Cucurbita), Sunflower (Helianthus annuus), and Safflower (Carthamus tinctorius)

54 ), tomato (Solanum lycopersicum), sunflower (Helianthus annuus), Catharanthus roseus, maize (Zea mays

55 n: acacia (Robinia pseudoacacia), sunflower (Helianthus annuus), linden (Tilia cordata), basil (Ocimu

56 ach is demonstrated on leaves of sunflowers (Helianthus annuus), soy beans (Glycine max), and corn (Z

57 ion and modern improvement of the sunflower (Helianthus annuus).

58 eloping seeds of two genotypes of sunflower (Helianthus annuus).

59 ri), squash (Cucurbita pepo), and sunflower (Helianthus annuus).

60 Helianthus annuus, a highly outcrossing species, is mark

61 a in Tradescantia pallida, Lactuca serriola, Helianthus annuus, and Oenothera caespitosa.

62 The studies primarily used wild Helianthus annuus, but also included a commercial and ea

63 class of sesquiterpenes isolated mostly from Helianthus annuus, commonly known as sunflower.

64 al adaptation in three species of sunflower: Helianthus annuus, Helianthus argophyllus, and Helianthu

65 encing 1,506 wild sunflowers from 3 species (Helianthus annuus, Helianthus petiolaris and Helianthus

66 originating from the wild sunflower species Helianthus annuus, is able to restore the widely used PE

67 For instance, in Allium cepa, Helianthus annuus, or Andropogon gerardi, more than 35%

68 ommunis, Arabidopsis [Arabidopsis thaliana], Helianthus annuus, Solanum lycopersicum, and Beta vulgar

69 ion at 128 EST-based microsatellites in wild Helianthus annuus, using populations from the species' t

70 es with bundle sheath extensions, sunflower [Helianthus annuus] and dwarf bean [Phaseolus vulgaris];

71 is Nutt., Helianthus deserticola Heiser, and Helianthus anomalus Blake).

72 resource-use strategies in a desert annual (Helianthus anomalus) distributed along a gradient of pos

73 es of parental species chromosomal blocks in Helianthus anomalus, a wild sunflower species derived vi

74 age maps for three hybrid sunflower species, Helianthus anomalus, H. deserticola, and H. paradoxus, a

75 Helianthus annuus, Helianthus petiolaris and Helianthus argophyllus), we identify 37 large (1-100 Mbp

76 ree species of sunflower: Helianthus annuus, Helianthus argophyllus, and Helianthus petiolaris, which

77 s and subsequent introgression of genes from Helianthus debilis ssp. cucumerifolius into H. annuus.

78 l wild species (Helianthus petiolaris Nutt., Helianthus deserticola Heiser, and Helianthus anomalus B

79 ndicating that the evolution of larger GS in Helianthus diploids may be more permissible in habitats

80 gically significant and demonstrate that for Helianthus, g(night) can be regulated.

81 The Helianthus GS database presented here and corresponding

82 ide, ShK, from the sea anemone Stichodactyla helianthus inhibited Kv1.3 potently and also blocked Kv1

83 ShK toxin from the sea anemone Stichodactyla helianthus is a 35-residue protein that binds to the Kv1

84 l blocker from the sea anemone Stichodactyla helianthus, is a 35 residue polypeptide cross-linked by

85 nd StnII) from the sea anemone Stichodactyla helianthus, it is shown that actinoporin isoforms can po

86 Stichodactyla helianthus neurotoxin (ShK) is an immunomodulatory pepti

87 ent Kv1.3-blocking sea anemone Stichodactyla helianthus peptide (ShK) suppressed proliferation of T(E

88 unflowers from 3 species (Helianthus annuus, Helianthus petiolaris and Helianthus argophyllus), we id

89 a joint SSR/RAPD genetic linkage map of the Helianthus petiolaris genome and used it, along with an

90 the introgression of chromosomal segments of Helianthus petiolaris into H. annuus in three natural hy

91 H. annuus and three additional wild species (Helianthus petiolaris Nutt., Helianthus deserticola Heis

92 lianthus annuus, Helianthus argophyllus, and Helianthus petiolaris, which each harbour a large number

93 ic evolution in independent dune ecotypes of Helianthus petiolaris.

94 are not redundant in function and that wild Helianthus represents a rich source of variation for the

95 osphotyrosine extension of the Stichodactyla helianthus ShK toxin, is a potent and selective blocker

96 We investigated the response of Helianthus species nighttime conductance (g(night)) and

97 emonstrated that different clades of diploid Helianthus species showed evolutionary patterns of GS co

98 generated a comprehensive GS database for 49 Helianthus species using flow cytometric approaches.

99 ogenetic analysis of GS evolution in diploid Helianthus species.

100 Helianthus sunflowers consist of c. 50 species native to

101 rgence time between the Parthenium genus and Helianthus (sunflowers) was approximately 15.1 million y

102 ide toxin from the sea anemone Stichodactyla helianthus that inhibits the voltage-gated potassium ion

103 leaf economic strategy across 28 species of Helianthus (the sunflowers).

104 haracterized a large family of Stichodactyla helianthus toxin (ShK)-related peptides in parasitic wor

105 emory B cells is suppressed by Stichodactyla helianthus toxin but not TRAM-34.

106 ot by the potent Kv1.3 blocker Stichodactyla helianthus toxin, whereas the proliferation of class-swi

107 Kv1.3, whereas margatoxin and Stichodactyla helianthus toxin, which are more selective Kv1.3 inhibit

108 Across datasets in Helianthus, trait relationships are highly variable, ind

109 Jerusalem artichoke tubers (Helianthus tuberosus L.) undergo enzymatic browning when

110 The Jerusalem artichoke (Helianthus tuberosus) xenobiotic inducible cytochrome P4

111 ShK, a peptide isolated from Stichodactyla helianthus venom, blocks the voltage-gated potassium cha

112 rom greenhouse crosses of the rare sunflower Helianthus verticillatus Small.

113 from the Caribbean Sea anemone Stichodactyla helianthus, was encapsulated with OVA into liposomes (Lp

114 ted cells and rendered them refractory to S. helianthus, whereas chronically activated T(EM) cell lin

115 de produced by the sea anemone Stichodactyla helianthus, which blocks the potassium channels Kv1.1 an

116 inhibitor from the sea anemone Stichodactyla helianthus with high biomedical and biotechnological pot