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1 mation of both stem-born roots and base-born adventitious roots.
2 ot growth and a proliferation of lateral and adventitious roots.
3  of root cells and promoted the emergence of adventitious roots.
4 on of root hairs, lateral root primordia and adventitious roots.
5  of shoot-borne roots, which are also called adventitious roots.
6 ously reported growth angle response of bean adventitious roots.
7 ooting that acts early in the development of adventitious roots.
8  of the centrally important, nodal system of adventitious roots.
9 n and the Nr mutation reducing the number of adventitious roots.
10 rs, which attach to supports via tendrils or adventitious roots.
11  cutting and played a key regulatory role in adventitious rooting.
12 sponse mutants of both species have enhanced adventitious rooting.
13 ental factors control the complex process of adventitious rooting.
14 wer senescence and fruit ripening, inhibited adventitious root and seedling root hair formation, prem
15 ted hypocotyls in light-grown plants, excess adventitious rooting and incomplete leaf vascularization
16  have overlapping expression profiles during adventitious rooting and that they regulate each other's
17      Unexpectedly, large woody rhizomes with adventitious roots and aerial branch systems identified
18 oot growth angle, longer primary roots, more adventitious roots and greater nutrient uptake efficienc
19 s supported by supplemental Arg induction of adventitious roots and increased NO accumulation in arga
20                                   Developing adventitious roots and lateral root primordia also conta
21 physiognomy with vertical crown development, adventitious roots and massive root mounds, leading to m
22 t neoplastic activity by producing calli and adventitious roots and shoots.
23 link between the gene expression patterns of adventitious roots and the growth phenotype, suggesting
24 ly revert the stimulatory effect of auxin on adventitious rooting, and auxin can further increase the
25 ted in reduced lateral rooting and increased adventitious rooting apically in the hypocotyl.
26 e and auxin signaling pathways in regulating adventitious rooting appears to be more complex.
27                                              Adventitious root (AR) formation is critically important
28                                              Adventitious root (AR) growth is vital for mass propagat
29                           Rice stems develop adventitious root (AR) primordia at each node that slowl
30  light, etiolated Arabidopsis seedlings form adventitious roots (AR) along the hypocotyl.
31                                              Adventitious roots are plant roots that form from any no
32 Clonal propagation of plants by induction of adventitious roots (ARs) from stem cuttings is a requisi
33 nins appear to act independently to suppress adventitious rooting, as cytokinin mutants are strigolac
34 , and mechanisms regulating lateral root and adventitious root branching in the plant models Arabidop
35 g that strigolactones restrain the number of adventitious roots by inhibiting the very first formativ
36 acid) IAA conversion resulted in an expanded adventitious root competence zone and delineated the con
37 rpenoids in the culture medium, fast-growing adventitious root cultures may hold promise as a sustain
38                                              Adventitious root cultures were developed from Tripteryg
39 ids accumulating in the medium of T. regelii adventitious root cultures, facilitated by searching the
40                                              Adventitious roots develop from aerial parts of the plan
41 eltaDDKPtRR13 expression appeared to disrupt adventitious root development 24 h after shoot excision,
42  case studies to summarize the physiology of adventitious root development in response to flooding (c
43 onditions, it is important to understand the adventitious root development of crops both in normal an
44 xin, and vascularization pathways leading to adventitious root development.
45                                              Adventitious roots emerge from aerial plant tissues, and
46  hypocotyl above the point of excision where adventitious roots emerge.
47  including a drastic decrease in lateral and adventitious root formation and a decrease in leaf cell
48 CC treatment and the epi mutation increasing adventitious root formation and the Nr mutation reducing
49  auxin and its interaction with cytokinin in adventitious root formation and the regenerative propert
50                                              Adventitious root formation at the base of plant cutting
51 t the plant hormone strigolactone suppresses adventitious root formation in Arabidopsis (Arabidopsis
52                 We examined excision-induced adventitious root formation in auxin influx and efflux m
53 13 acting downstream of cytokinin to repress adventitious root formation in intact plants, and that r
54 tect the induction of gene expression during adventitious root formation in loblolly pine (Pinus taed
55  associated with the developmental stages of adventitious root formation in the model tree poplar (Po
56 nts were conducted to determine if normal or adventitious root formation is affected by ethylene inse
57 derstanding the regulation and physiology of adventitious root formation is critical for breeding pro
58                                              Adventitious root formation is essential for the propaga
59 normally added to culture medium, to achieve adventitious root formation on in vitro papaya plantlets
60 minocyclopropane-1-carboxylic acid increased adventitious root formation on vegetative stem cuttings
61 lied auxin (indole-3-butyric acid) increased adventitious root formation on vegetative stem cuttings
62                  In contrast, the process of adventitious root formation shows the opposite response
63 uxin transport from the shoot apex abolishes adventitious root formation under these conditions.
64                                      Reduced adventitious root formation was also observed in ethylen
65 ateral root formation and a positive role in adventitious root formation with modulation of auxin tra
66  signaling were involved in PtrXB38-mediated adventitious root formation.
67 uded dwarfing, excessive shoot branching and adventitious root formation.
68 d lateral root growth as well as lateral and adventitious root formation.
69 transport and local IAA accumulation driving adventitious root formation.
70  linked to local IAA accumulation leading to adventitious root formation.
71 ranscription factor of the AP2 family during adventitious root formation.
72 f PtAIL1 expression, which led to a delay in adventitious root formation.
73 actones, cytokinins, and auxin in regulating adventitious root formation.
74 can survive flash floods by the emergence of adventitious roots from the stem.
75  is a developmental process that regenerates adventitious roots from wounded tissues.
76 -L-tryptophan-OMe as a competent enhancer of adventitious rooting in a number of recalcitrant woody p
77 ntiation occurs, flooded roots (aerenchyma), adventitious rooting in hypocotyls, and leaf abscission
78 sulted in increased formation of lateral and adventitious roots in Arabidopsis (Arabidopsis thaliana)
79 and auxin can further increase the number of adventitious roots in max mutants.
80  of ethylene in the formation of lateral and adventitious roots in tomato (Solanum lycopersicum) usin
81 ng a small molecule named Hypocotyl Specific Adventitious Root INducer (HYSPARIN) that strongly induc
82 three GH3 genes are required for fine-tuning adventitious root initiation in the Arabidopsis thaliana
83 is (Arabidopsis thaliana) seedlings in which adventitious root initiation was induced by excising roo
84  by a cyclin B1 reporter (pCYCB1;1:GUS), and adventitious root initiation.
85                  We propose a model in which adventitious rooting is an adaptive developmental respon
86                                              Adventitious rooting is an essential but sometimes rate-
87 uggest that the promotive effect of auxin on adventitious rooting is influenced by ethylene responsiv
88 ominance, inhibit root elongation, stimulate adventitious rooting, mediate root gravitropism, and sti
89 ominance, reduced root elongation, increased adventitious rooting, no root gravitropism, and ectopic
90 tions and cell-specific ion distributions in adventitious roots of barley (Hordeum vulgare).
91 nce Charles Darwin first discovered that the adventitious roots of English ivy (Hedera helix) exude a
92 ation of mechanical interlocking between the adventitious roots of English ivy and the surface of sub
93           Integrity of grafts and absence of adventitious roots on scions were assessed using plants
94 phogenesis, and emergence of new lateral and adventitious root organs, much more remains to be done.
95 ssion, an early marker for the initiation of adventitious root primordia in Arabidopsis, is enhanced
96                 Epidermal cells that overlie adventitious root primordia undergo cell death to facili
97 g the auxin-induced formation of lateral and adventitious root primordia.
98 reprogram certain pericycle cells to produce adventitious roots proximal to the wound site.
99 tion of tillers and internodes and extensive adventitious root/shoot formation on nodes.
100     An ABCB19 overexpression line forms more adventitious roots than the wild type in intact seedling
101 -type plants, but NR cuttings produced fewer adventitious roots than wild-type cuttings.
102 elow-ground root mass but fewer above-ground adventitious roots than wild-type Pearson plants.
103 oot system is composed of several classes of adventitious roots that include crown roots and brace ro
104                In spite of the importance of adventitious rooting, the mechanism behind this developm
105             Recent work shows that different adventitious root types are regulated differently, and h
106  in vitro plantlets were not able to produce adventitious roots, when IBA (2 mg L(-1)) was added to t
107  microRNA miR167, are positive regulators of adventitious rooting, whereas ARF17, a target of miR160,
108 al cells close to the wound site can produce adventitious roots, whereas cells distal from the wound
109 IL1 were able to grow an increased number of adventitious roots, whereas RNA interference mediated th

 
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