ライフサイエンスコーパス: Spinacia oleracea

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

1 re distinct from a plastidic PGM of spinach (Spinacia oleracea).

2 s in grana thylakoid membranes from spinach (Spinacia oleracea).

3 na benthamiana, Nicotiana tabacum MD609, and Spinacia oleracea.

4 report the draft genome sequence of spinach (Spinacia oleracea, 2n=12), which contains 25,495 protein

5 oris, a methylotrophic yeast, using spinach (Spinacia oleracea) and corn (Zea maize) cDNAs.

6 In contrast, the rrn operon in spinach (Spinacia oleracea) and mustard chloroplasts is transcrib

7 (Cd), zinc (Zn), and nickel (Ni) by spinach (Spinacia oleracea) and tomato (Lycopersicon esculentum)

8 feminization pathway in cultivated spinach (Spinacia oleracea), and investigated how this pathway ma

9 ng complex II (LHCII; isolated from spinach [Spinacia oleracea]) and the plant lipids monogalcatosyld

10 ensis (Portulacaceae) with Silene dioica and Spinacia oleracea as the outgroups.

11 gly, only some of them, such as the spinach (Spinacia oleracea) betaine aldehyde dehydrogenase (SoBAD

12 , we demonstrate that living spinach plants (Spinacia oleracea) can be engineered to serve as self-po

13 angiosperms and in isolated intact spinach (Spinacia oleracea) chloroplasts undergoes light-/dark-in

14 ), soybean (Glycine max Merr.), and spinach (Spinacia oleracea) contained only a single polypeptide c

15 Expression of six Hsp70s in spinach (Spinacia oleracea cv Longstanding Bloomsdale) leaves gro

16 abelled palmitoyl-ACP prepared from spinach (Spinacia oleracea), delta(4)-acyl-ACP desaturase activit

17 dominant in the long-day (LD) plant spinach (Spinacia oleracea; GA53, GA44, GA19, GA20, GA1, GA8, and

18 iated with photosystem II (PSII) on spinach (Spinacia oleracea) grana membranes were examined using c

19 Previous work with spinach (Spinacia oleracea) has shown that the level of gibberell

20 ll proteins between grana in intact spinach (Spinacia oleracea L.) and Arabidopsis chloroplasts.

21 The extremely labile recombinant spinach (Spinacia oleracea L.) enzyme was stabilized by DL-alpha-

22 Spinach (Spinacia oleracea L.) is a long-day (LD) rosette plant i

23 Spinach (Spinacia oleracea L.) is an economically important green

24 Spinach (Spinacia oleracea L.) is often used as a base vegetable

25 ation by osmotic stress in darkened spinach (Spinacia oleracea L.) leaves.

26 concentrations were determined for spinach (Spinacia oleracea L.) over a 24 h period to determine if

27 e investigated in the rosette plant spinach (Spinacia oleracea L.) under long-day (LD) conditions.

28 curcas was analysed and compared to spinach (Spinacia oleracea L.) using a ICP-AES.

29 sly linked with cold acclimation in spinach (Spinacia oleracea L.), was characterized and found to en

30 astic in pea (Pisum sativum L.) and spinach (Spinacia oleracea L.), which lack DMSP.

31 e stresses affect CMO expression, a spinach (Spinacia oleracea L., Chenopodiaceae) probe was used to

32 ctose-2,6-bisphosphatase was isolated from a Spinacia oleracea leaf library and used to express a rec

33 (18)O(2)]Acetate was incubated with spinach (Spinacia oleracea) leaves and the (18)O content in fatty

34 th reduced thioredoxin f and m from spinach (Spinacia oleracea) leaves reduced and activated the enzy

35 atural pigments were extracted from spinach (Spinacia oleracea), red radish (Raphanus sativus L), win

36 n (ACP) synthase III (KAS III) from spinach (Spinacia oleracea; So KAS III) was used to isolate two c

37 Structural comparison with SoPIP2;1 from Spinacia oleracea species provides new insights into the

38 Circular dichroism studies of Cab and the Spinacia oleracea (spinach) beta-class carbonic anhydras

39 Spinach (Spinacia oleracea) TRX f has an apparent dissociation co

40 ive chromosome from chloroplasts of spinach (Spinacia oleracea) was analyzed by two-dimensional gel e

41 ), tobacco (Nicotiana tabacum), and spinach (Spinacia oleracea) with a resolution of approximately 7

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。