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1 to seed exudates of its host plant alfalfa (Medicago sativa).
2 el legume Medicago truncatula or in alfalfa (Medicago sativa).
3 ngineering PAs in the forage legume alfalfa (Medicago sativa).
4 ing symbiosis with its host legume, alfalfa (Medicago sativa).
5 ing symbiosis with its legume host, alfalfa (Medicago sativa).
6 ntrol of a constitutive promoter in alfalfa (Medicago sativa).
7 mbiotic relationship with the alfalfa plant (Medicago sativa).
8 GS1) gene have been introduced into alfalfa (Medicago sativa).
9 nt CPSase gene (CPAII) derived from alfalfa (Medicago sativa).
10 uction in pea had no such effect in alfalfa (Medicago sativa).
11 apus), and somatic embryogenesis in alfalfa (Medicago sativa).
12 e symbiosis between S. meliloti and its host Medicago sativa.
13 tablishment of symbiosis with its host plant Medicago sativa.
14 ogen fixation when they were inoculated onto Medicago sativa.
15 red to establish a successful symbiosis with Medicago sativa.
16 gen-fixing relationship with its plant host, Medicago sativa.
17 psis thaliana, Saccharomyces cerevisiae, and Medicago sativa.
18 nd symbiotically defective on the host plant Medicago sativa.
19 a nitrogen-fixing symbiosis with the legume Medicago sativa.
20 ified in the genomes of both Glycine max and Medicago sativa.
21 Overexpression of a KNOX1 gene in alfalfa (Medicago sativa), a member of the IRLC, resulted in an i
22 . truncatula is a close relative of alfalfa (Medicago sativa), a widely cultivated crop with limited
23 ven by the constitutive CaMV 35S promoter in Medicago sativa (alfalfa) and Nicotiana tabacum (tobacco
24 nt host plant systems: Ncotiana benthamiana, Medicago sativa (alfalfa) and Nicotiana tabacum NT1 cell
25 between Sinorhizobium meliloti and its host Medicago sativa (alfalfa) depends on several signaling m
27 tween Rhizobium meliloti and its host plant, Medicago sativa (alfalfa), but the precise role of EPS i
32 alcium spiking in M. truncatula and alfalfa (Medicago sativa) also uncovered the possibility of diffe
33 mmunication between the roots of two plants (Medicago sativa and Arabidopsis thaliana) and the bacter
34 bles the bacterium to invade root nodules on Medicago sativa and establish a nitrogen-fixing symbiosi
37 udged them to be symbiotically proficient on Medicago sativa, and concluded that LPS might not have a
39 plants such as pea (Pisum sativum), alfalfa (Medicago sativa), barrel medic (Medicago truncatula), an
40 lignin levels in the forage legume alfalfa (Medicago sativa) by down-regulation of the monolignol bi
42 ly 56-60% identities with C. microcarpa ACS, Medicago sativa chalcone synthase (CHS), and the previou
46 zobium meliloti and its legume host alfalfa (Medicago sativa) depends on the timely expression of nod
47 ide (alfAFP) defensin isolated from seeds of Medicago sativa displays strong activity against the agr
48 these systems, such as Trifolium repens and Medicago sativa, do not contain any substantial amounts
49 abidopsis IRT1 (AtIRT1) under control of the Medicago sativa EARLY NODULIN 12B promoter in our previo
56 e that enhances root respiration in alfalfa (Medicago sativa L.) and also triggers a compensatory inc
62 which was originally isolated from alfalfa (Medicago sativa L.), contains genes that increase compet
63 to the sixth internode in stems of alfalfa (Medicago sativa L.), preceding the deposition of lignin.
66 le cress (Arabidopsis thaliana) and alfalfa (Medicago sativa) leads to strongly reduced lignin levels
67 -1) fresh weight) was engineered in alfalfa (Medicago sativa) leaves by constitutive expression of is
68 ositional changes in two low-lignin alfalfa (Medicago sativa) lines with antisense down-regulation of
69 lux rates by 5% to 545% in roots of alfalfa (Medicago sativa), Medicago truncatula, maize (Zea mays),
71 Xenopus laevis nucleolin (31%), the alfalfa (Medicago sativa) nucleolin homolog (66%), and the yeast
74 aackia amurensis Rupr. & Maxim. and alfalfa (Medicago sativa), produced pseudonodules after treatment
75 long A17 small GTPase MtROP9, orthologous to Medicago sativa Rac1, via an RNA interference silencing
76 symbiosis between Sinorhizobium meliloti and Medicago sativa requires complex physiological adaptatio
77 ssion of MtPAR in the forage legume alfalfa (Medicago sativa) resulted in detectable levels of PA in
78 umol N2 (g dry weight nodule)(-1) h(-1) of a Medicago sativa-Rhizobium consortium by continuously ana
80 rates that the nodule endodermis of alfalfa (Medicago sativa) root nodules contains elevated levels o
82 tial stages of symbiosis with the host plant Medicago sativa, Sinorhizobium meliloti must overcome an
83 s analysis of two alfalfa varieties, Wisfal (Medicago sativa ssp. falcata var. sativa var. Chilean),
85 ion and confer drought tolerance in alfalfa (Medicago sativa), the most important forage legume speci
86 ene TubA1 in situ and in transgenic alfalfa (Medicago sativa) to explore its use as a probe for plant
87 ere used to construct an all-native alfalfa (Medicago sativa) transfer DNA vector that can be used fo
89 were independently downregulated in alfalfa (Medicago sativa) using antisense and/or RNA interference
91 and thereby enhance Al tolerance in alfalfa (Medicago sativa), we produced transgenic plants using no
92 ptake and distribution of silver in alfalfa (Medicago sativa) were quantified and visualized upon hyd
93 eding a single leaf of intact Arabidopsis or Medicago sativa with 10 or 20 mM L-galactono-1,4-lactone
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