ライフサイエンスコーパス: Helianthus annuus

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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