ライフサイエンスコーパス: Helianthus

1 isolated from the sea anemone Stichodactyla helianthus.

2 as data collected across scales in the genus Helianthus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 Stichodactyla helianthus neurotoxin (ShK) is an immunomodulatory pepti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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