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1 hat cause different diseases, crown gall and hairy root.
2 ced fewer nodules, in contrast to GmWRI1b-OE hairy roots.
3 antly while chrysin glycosides accumulate in hairy roots.
4 ce when over-expressed in transgenic soybean hairy roots.
5 roots but increased nodulation in GmWRI1b-OE hairy roots.
6 ic increase of TIA accumulation in C. roseus hairy roots.
7 ivity from the microsomal fraction of peanut hairy roots.
8 rther enhances both productions in wild-type hairy roots.
9 hpRNA mediated gene silencing in transgenic, hairy roots.
10 or tanshinone production in elicited Danshen hairy roots.
11 factor was observed in MYB182-overexpressing hairy roots.
12 s of phytoplasma-infected plants, by forming hairy roots.
13 to 4-methyl tryptophan inhibition of CrWRKY1 hairy roots.
14 , and membrane lipids compared to GmWRI1b-OE hairy roots.
15 e-induced root galls per plant, than control hairy roots.
16 s of plants regenerated from the transformed hairy roots.
17 istance in both Arabidopsis and Stylosanthes hairy roots.
18         Compared with control roots, CrWRKY1 hairy roots accumulated up to 3-fold higher levels of se
19                Overexpression of MtMATE69 in hairy roots altered Fe homeostasis and hormone levels un
20  and their conjugates in Medicago truncatula hairy roots and anthocyanin-overproducing tobacco (Nicot
21 ocyanin and PA accumulation in M. truncatula hairy roots and Arabidopsis thaliana seeds, respectively
22 ores anthocyanins and PAs in mttt8 plant and hairy roots and further enhances both productions in wil
23 l of its own promoter) is lethal both in pea hairy roots and in transgenic alfalfa plants.
24     Transcriptome analyses of overexpressing hairy roots and knockout mutants of MtMYB5 and MtMYB14 i
25 was found to be located in the cell walls of hairy roots and root border cells.
26 gly induces PA accumulation in M. truncatula hairy roots, and both myb5 and myb14 mutants of M. trunc
27 owever, when complex expression systems like hairy roots are used for production, multiple population
28 unt for the reduced nodulation in GmLEC2a-OE hairy roots but increased nodulation in GmWRI1b-OE hairy
29         Histochemical staining of transgenic hairy roots carrying the promoter-reporter constructs in
30 n (GmMAP1), were modified in GmPLDa1-altered hairy roots compared with those of GUS roots.
31 s silenced using RNA interference in soybean hairy root composite plants, these plants had severely r
32 terference of isoflavone synthase in soybean hairy root composite plants.
33                                   Transgenic hairy roots containing the Icl and Ms gene promoters fus
34 analysis of par mutants and MtPAR-expressing hairy roots, coupled with yeast one-hybrid analysis, rev
35                  Overexpression of MYB182 in hairy root culture and whole poplar plants led to reduce
36 yptamine biosynthesis in Catharanthus roseus hairy root culture eliminates all production of monoterp
37 , and increased nicotine accumulation in the hairy root culture media.
38 g widely explored agents for the creation of hairy root cultures for the sustainable production of pl
39 A has no detectable effect on transgenic pea hairy root cultures or regenerated alfalfa.
40                    Peanut (Arachis hypogaea) hairy root cultures produce a diverse array of prenylate
41 transferase genes in elicitor-treated peanut hairy root cultures.
42 have been targeted at either whole plants or hairy root cultures.
43 lium under N-limited growth conditions using hairy root cultures.
44 n both Agrobacterium rhizogenes-transformed "hairy-root" cultures and greenhouse-grown plant roots, w
45 r composition of condensed tannins (CTs) in 'hairy root' cultures of Lotus corniculatus (bird's foot
46 ast growth rates and biochemical stability, 'hairy root' cultures remain unsurpassed as the choice fo
47 target promoter induction in Lotus japonicus hairy roots depends on MYCS (MYCORRHIZA SEQUENCE)-elemen
48 onfirmed the importance of RolB and RolC for hairy root development by A. rhizogenes K599.
49 cogenic locus B (rolB), play a major role in hairy root development.
50  through interaction with TPL, to facilitate hairy root development.
51 ins comprise biotrophic pathogens that cause hairy root disease (HRD) on hydroponically grown Solanac
52 ressed in plant cells, causing crown gall or hairy root disease.
53 at are the causative agents of crown gall or hairy root disease.
54  related pathogens that cause crown gall and hairy root diseases, which result from integration and e
55                                   GmLEC2a-OE hairy roots displayed different or even opposite express
56     Double myc1 myc2 loss-of-function tomato hairy roots displayed suppressed constitutive expression
57 fer leads to the formation of crown galls or hairy roots, due to expression of transferred T-DNA gene
58 entified as a key player in the formation of hairy roots during the plant-A. rhizogenes interaction.
59                          Medicago truncatula hairy roots expressing LaPT1 accumulated isowighteone, a
60 ase showed strong expression in the stele of hairy roots for all 4 PRP genes tested, with additional
61       Importantly, we leverage the microbial hairy roots for rapid, reproducible efficacy screening o
62                                              Hairy root formation is mediated through the expression
63 mited to root hairs and root border cells in hairy roots grown on "noninducing" medium, whereas induc
64                                    NUP1-RNAi hairy roots had reduced NUP1 mRNA accumulation levels, r
65 B137 overexpression in transgenic Eucalyptus hairy roots increased xylem lignification, while its dom
66 SPARENT TESTA 2 (TT2) in Medicago trunculata hairy roots induces both proanthocyanidin accumulation a
67 decreased the number of galls in transformed hairy roots inoculated with RKN.
68                                              Hairy root lines transformed with 35S-ASA2 grew in conce
69          Overexpression of MtMATE66 rendered hairy roots more tolerant to Al(3+) toxicity.
70 ling of mttt8 mutant seeds and M. truncatula hairy roots (mttt8 mutant, mttt8 mutant complemented wit
71                            By characterizing hairy root mutants obtained through Clustered Regularly
72                                              Hairy roots obtained by transformation with Agrobacteriu
73 on of these five nodule-induced GLV genes in hairy roots of M. truncatula and application of their sy
74   Furthermore, overexpression of MtMYB134 in hairy roots of M. truncatula enhanced the biosynthesis o
75 e accumulation of proanthocyanidins (PAs) in hairy roots of Medicago truncatula.
76 UC1 correlated with lignin C-unit content in hairy roots of Medicago truncatula.
77 PAR was expressed ectopically in transformed hairy roots of Medicago.
78 ed from Agrobacterium rhizogenes-transformed hairy roots of pokeweed (Phytolacca americana).
79 ucted comparative transcriptomics on soybean hairy roots of the variety Williams 82 and imbibing seed
80  further supported by analysis of transgenic hairy roots overexpressing soybean GmWRI1b-OE and GmLEC2
81 tants, yucca6 plants do not display short or hairy root phenotypes and lack morphological changes und
82 pression by antisense mRNA in transgenic pea hairy roots prevented the normal separation of root bord
83                                   GmLEC2a-OE hairy roots produced fewer nodules, in contrast to GmWRI
84 ression of CKX genes rendered the transgenic hairy roots resistant to exogenous application of the cy
85 xpression of TSAR1 or TSAR2 in M. truncatula hairy roots resulted in elevated transcript levels of kn
86 the ectopic expression of MYB15 in grapevine hairy roots resulted in increased STS expression and in
87 C2-L3 was ectopically expressed in grapevine hairy roots, showing a reduction in proanthocyanidin con
88  GmBIR1 (WT-GmBIR1) using transgenic soybean hairy roots significantly increased soybean susceptibili
89                   Here, we report that plant hairy roots support the growth of fastidious pathogens l
90 re identified and validated using transgenic hairy root system.
91 TL1a using complementation in plant mutants, hairy root transformation and microscopy.
92                                     However, hairy root transformation had notable influence on Sphin
93                                The effect of hairy root transformation on rhizosphere bacterial commu
94                                            A hairy-root transformation system was employed to investi
95 MF phenotypes using Agrobacterium rhizogenes hairy-root transformation.
96                                        Using hairy root transformed soybean composite plants, we have
97 ducing PRP expression in Medicago truncatula hairy root tumors disrupted cortical and vascular patter
98 PRP2 in that it greatly reduced viability of hairy root tumors.
99   The overexpression of CrWRKY1 in C. roseus hairy roots up-regulated several key TIA pathway genes,
100      Overexpression of CrMAPKK1 in C. roseus hairy roots upregulated TIA pathways genes and increased
101 ty labeling in tomato (Solanum lycopersicum) hairy roots, we identified the repressor proteins TOPLES
102       Using composite plants with transgenic hairy roots, we show that RDN1 and RDN2 orthologs from d
103 ed in GmLEC2a-OE but increased in GmWRI1b-OE hairy roots, which may account for the reduced nodulatio
104                                              Hairy roots will have a continuing role as an experiment

 
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