ライフサイエンスコーパス: hairy root

1 hat cause different diseases, crown gall and hairy root.

2 antly while chrysin glycosides accumulate in hairy roots.

3 ic increase of TIA accumulation in C. roseus hairy roots.

4 ivity from the microsomal fraction of peanut hairy roots.

5 rther enhances both productions in wild-type hairy roots.

6 hpRNA mediated gene silencing in transgenic, hairy roots.

7 or tanshinone production in elicited Danshen hairy roots.

8 ce when over-expressed in transgenic soybean hairy roots.

9 factor was observed in MYB182-overexpressing hairy roots.

10 s of phytoplasma-infected plants, by forming hairy roots.

11 to 4-methyl tryptophan inhibition of CrWRKY1 hairy roots.

12 e-induced root galls per plant, than control hairy roots.

13 s of plants regenerated from the transformed hairy roots.

14 Compared with control roots, CrWRKY1 hairy roots accumulated up to 3-fold higher levels of se

15 Overexpression of MtMATE69 in hairy roots altered Fe homeostasis and hormone levels un

16 and their conjugates in Medicago truncatula hairy roots and anthocyanin-overproducing tobacco (Nicot

17 ocyanin and PA accumulation in M. truncatula hairy roots and Arabidopsis thaliana seeds, respectively

18 ores anthocyanins and PAs in mttt8 plant and hairy roots and further enhances both productions in wil

19 l of its own promoter) is lethal both in pea hairy roots and in transgenic alfalfa plants.

20 Transcriptome analyses of overexpressing hairy roots and knockout mutants of MtMYB5 and MtMYB14 i

21 was found to be located in the cell walls of hairy roots and root border cells.

22 gly induces PA accumulation in M. truncatula hairy roots, and both myb5 and myb14 mutants of M. trunc

23 owever, when complex expression systems like hairy roots are used for production, multiple population

24 Histochemical staining of transgenic hairy roots carrying the promoter-reporter constructs in

25 s silenced using RNA interference in soybean hairy root composite plants, these plants had severely r

26 terference of isoflavone synthase in soybean hairy root composite plants.

27 Transgenic hairy roots containing the Icl and Ms gene promoters fus

28 analysis of par mutants and MtPAR-expressing hairy roots, coupled with yeast one-hybrid analysis, rev

29 Overexpression of MYB182 in hairy root culture and whole poplar plants led to reduce

30 yptamine biosynthesis in Catharanthus roseus hairy root culture eliminates all production of monoterp

31 , and increased nicotine accumulation in the hairy root culture media.

32 A has no detectable effect on transgenic pea hairy root cultures or regenerated alfalfa.

33 Peanut (Arachis hypogaea) hairy root cultures produce a diverse array of prenylate

34 transferase genes in elicitor-treated peanut hairy root cultures.

35 have been targeted at either whole plants or hairy root cultures.

36 lium under N-limited growth conditions using hairy root cultures.

37 n both Agrobacterium rhizogenes-transformed "hairy-root" cultures and greenhouse-grown plant roots, w

38 r composition of condensed tannins (CTs) in 'hairy root' cultures of Lotus corniculatus (bird's foot

39 ast growth rates and biochemical stability, 'hairy root' cultures remain unsurpassed as the choice fo

40 ressed in plant cells, causing crown gall or hairy root disease.

41 related pathogens that cause crown gall and hairy root diseases, which result from integration and e

42 entified as a key player in the formation of hairy roots during the plant-A. rhizogenes interaction.

43 Medicago truncatula hairy roots expressing LaPT1 accumulated isowighteone, a

44 mited to root hairs and root border cells in hairy roots grown on "noninducing" medium, whereas induc

45 NUP1-RNAi hairy roots had reduced NUP1 mRNA accumulation levels, r

46 SPARENT TESTA 2 (TT2) in Medicago trunculata hairy roots induces both proanthocyanidin accumulation a

47 decreased the number of galls in transformed hairy roots inoculated with RKN.

48 Hairy root lines transformed with 35S-ASA2 grew in conce

49 Overexpression of MtMATE66 rendered hairy roots more tolerant to Al(3+) toxicity.

50 ling of mttt8 mutant seeds and M. truncatula hairy roots (mttt8 mutant, mttt8 mutant complemented wit

51 Hairy roots obtained by transformation with Agrobacteriu

52 e accumulation of proanthocyanidins (PAs) in hairy roots of Medicago truncatula.

53 PAR was expressed ectopically in transformed hairy roots of Medicago.

54 ed from Agrobacterium rhizogenes-transformed hairy roots of pokeweed (Phytolacca americana).

55 tants, yucca6 plants do not display short or hairy root phenotypes and lack morphological changes und

56 pression by antisense mRNA in transgenic pea hairy roots prevented the normal separation of root bord

57 ression of CKX genes rendered the transgenic hairy roots resistant to exogenous application of the cy

58 xpression of TSAR1 or TSAR2 in M. truncatula hairy roots resulted in elevated transcript levels of kn

59 the ectopic expression of MYB15 in grapevine hairy roots resulted in increased STS expression and in

60 C2-L3 was ectopically expressed in grapevine hairy roots, showing a reduction in proanthocyanidin con

61 However, hairy root transformation had notable influence on Sphin

62 The effect of hairy root transformation on rhizosphere bacterial commu

63 A hairy-root transformation system was employed to investi

64 Using hairy root transformed soybean composite plants, we have

65 The overexpression of CrWRKY1 in C. roseus hairy roots up-regulated several key TIA pathway genes,

66 Overexpression of CrMAPKK1 in C. roseus hairy roots upregulated TIA pathways genes and increased

67 Using composite plants with transgenic hairy roots, we show that RDN1 and RDN2 orthologs from d

68 Hairy roots will have a continuing role as an experiment