ライフサイエンスコーパス: calli

1 significantly altered in the Osarid3 mutant calli.

2 s cytokinin levels are decreased, in Osarid3 calli.

3 leaves, reproductive tissues and embryogenic calli.

4 d to more frequent transposition of Tos17 in calli.

5 ole in promoting Tos17 transposition in rice calli.

6 mutant seeds compared with that in wild-type calli.

7 RBR3, but not RBR1, RNA in embryogenic maize calli.

8 tion procedure was used to obtain transgenic calli.

9 ce chromosomal DNA isolated from transformed calli.

10 eaves of plants regenerated from transformed calli.

11 unction was detected in hygromycin-resistant calli.

12 blishment of putative transgenic embryogenic calli.

13 ans exhibit neoplastic activity by producing calli and adventitious roots and shoots.

14 tire root including root hairs and root tip, calli and at various developmental stages in trichomes a

15 We show that ectopic expression of ZmIPT2 in calli and in planta created phenotypes consistent with C

16 bably because mass production of embryogenic calli and longer callus growth periods were required to

17 growth performance of mannitol-accumulating calli and mature leaves was due to other stress-protecti

18 nalysis of paromomycin-resistant embryogenic calli and of plants regenerated from these calli, confir

19 Transgenic calli and plant roots overexpressing Alfin1 showed enhan

20 Calli and pollen transformed with the 5' distal 268 bp f

21 ater stress and salinity was evaluated using calli and T(2) plants transformed with (+mtlD) or withou

22 Overexpression of DNG701 in both rice calli and transgenic plants substantially reduced DNA me

23 Transformed colonies ('calli') appear in approximately 4 weeks; they are subcul

24 In most of these calli, beta-glucuronidase was detected histochemically.

25 The membranes of most transgenic plants and calli bound muscarinic ligands with appropriate affiniti

26 c calli and of plants regenerated from these calli, confirmed the stable integration of bombarded DNA

27 s studied via feeding experiments using rice calli cultures to gain further insight into the key step

28 Tos17 showed less transposition in calli derived from dng701 knockout mutant seeds compared

29 on the transformation of compact embryogenic calli derived from immature embryos using visual and che

30 l explants required auxin and cytokinin, dgt calli did not show the typical concentration-dependent s

31 With Hyg treatment, rice calli exhibited cell death, and rice seedlings showed se

32 Cl than vector-transformed controls, whereas calli expressing Alfin1 in the antisense orientation wer

33 diated transformation of friable embryogenic calli (FEC) is the most widely used method to generate t

34 bited cell division and developed transgenic calli, followed by formation of transgenic shoots at low

35 Incubation of fresh calli from a fragrant rice variety (Aychade) and a non-f

36 cCer in organ-specific cell differentiation, calli from gcs-1 mutants formed roots and leaves on medi

37 g GlcCer proliferated in a manner similar to calli from wild-type plants.

38 Undifferentiated calli generated from gcs-1 seedlings and lacking GlcCer

39 tivity continued in undifferentiated tobacco calli in the absence of Ca(2+) oscillations.

40 However, gcs-1 calli, in contrast to wild-type calli, were unable to de

41 ion profiles were generated from embryogenic calli induced to undergo embryo maturation and germinati

42 As calli of both varieties still maintained very low levels

43 rpenes and oxygenated volatiles emitted from calli of both varieties were greatly and conversely affe

44 Membranes of untransformed plants and calli or those transformed with vector alone did not bin

45 Calli overexpressing Alfin1 were more resistant to growt

46 RepA-containing transgenic maize calli remained embryogenic, were readily regenerable, an

47 The established calli represented the most interesting miniaturised arom

48 using both transient and stably transformed calli revealed that Kiddo contributed some 20% of the to

49 to form particular tissues: undifferentiated calli, shoot structures, root structures, or a whole pla

50 Heat treatment of calli suggested that 1-pyrroline might be enzymatically

51 The presence of labelled 2AP in calli supplemented with [U-(13)C]glucose, sodium acetate

52 expression of Zeama;KRP;1 in maize embryonic calli that ectopically expressed the wheat dwarf virus R

53 Growth of selected calli to sufficient quantities for antigen screening may

54 were produced by cotton (Gossypium hirsutum) calli undergoing SE and that when these AGPs were isolat

55 Growth of +mtlD calli was not affected by stress.

56 Fresh weight of -mtlD calli was reduced by 40% in the presence of polyethylene

57 Calli were exposed to -1.0 MPa of polyethylene glycol 8,

58 When rice calli were fed with increasing levels of 1-pyrroline, 2A

59 when Bbm and Wus2 were expressed, transgenic calli were recovered from over 40% of the starting expla

60 n a parallel experiment, when wild type rice calli were transformed with the same binary vector, neit

61 wever, gcs-1 calli, in contrast to wild-type calli, were unable to develop organs on differentiation

62 f mainly beta-carotene in roots and nongreen calli, whereas carotenoids remained unchanged in leaves.

63 f EBE promotes cell proliferation in growing calli, while the opposite is observed in EBE-RNAi lines.

64 Earlier studies of calli with a higher-than-normal cytokinin content indica

65 Up to 20% of bombarded embryos produced calli with the recombined loxP sites under our experimen

66 Protoplasts from BGL-1 lines divide and form calli without exogenous hormones.