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1  is duplicated in L. japonicus We obtained a L. japonicus Ljein2a Ljein2b double mutant that exhibits
2                Symbiosis between M. loti and L. japonicus requires bacterial synthesis of secreted an
3 d us to establish putative M. truncatula and L. japonicus orthologues.
4  the model legume species, M. truncatula and L. japonicus, and substantially enhanced the knowledgeba
5 ved between the genomes of M. truncatula and L. japonicus, whereas lower levels of conservation were
6           Together with previously described L. japonicus Nck-associated protein1 and 121F-specific p
7         Spot inoculations of NahG-expressing L. japonicus plants confirmed increased nodulation in th
8       The single- and double-copy sense gs52 L. japonicus lines had enhanced nodulation that correlat
9                                           In L. japonicus, two VPY orthologs (LjVPY1 and LjVPY2) were
10 elopment: arbuscule branching is arrested in L. japonicus ram1 mutants, and ectopic expression of RAM
11 s not a factor controlling N-assimilation in L. japonicus roots during stable growth in N-sufficient
12  transcripts and metabolites that changed in L. japonicus plants during the transfer from photorespir
13 erved specialisation in HNG based defence in L. japonicus flowers is discussed in the context of bala
14 s controlled by EIN2, which is duplicated in L. japonicus We obtained a L. japonicus Ljein2a Ljein2b
15 l cells before spreading to the epidermis in L. japonicus While mutant analysis identified redundancy
16                           NahG expression in L. japonicus resulted in a marked reduction of SA levels
17 dule organogenesis, and nitrogen fixation in L. japonicus.
18 ys a negative role in rhizobial infection in L. japonicus.
19 f the GS52 apyrase can enhance nodulation in L. japonicus and points to an important role for this gr
20 with LHK1 to mediate nodule organogenesis in L. japonicus.
21 LjMYB14, was constitutively overexpressed in L. japonicus and induced the expression of at least 12 g
22  The induction of isoflavonoid production in L. japonicus also involves the coordinated down-regulati
23 s localized within distinct motile puncta in L. japonicus root hairs and in Nicotiana benthamiana lea
24 ene was found to be enhanced specifically in L. japonicus nodules, whereas the LjPP2C2 gene was expre
25 in acclimation to tolerate drought stress in L. japonicus.
26  characterization carried out in independent L. japonicus LORE1 insertion lines indicates a positive
27 ormed phenotypic analysis of two independent L. japonicus mutant alleles and investigated the regulat
28 ed NOD FACTOR RECEPTOR1 (LjNFR1) and LjNFR5 (L. japonicus) and LYSM DOMAIN CONTAINING RECEPTOR KINASE
29 o be expressed only in the infected cells of L. japonicus nodules.
30 acterized plant genomes, the TE component of L. japonicus contained several surprises.
31 h symbiotic and non-symbiotic development of L. japonicus, and suggest that regulatory processes cont
32  pollux, and castor pollux double mutants of L. japonicus were rescued by DMI1 alone, while both Lj-C
33                                The nectar of L. japonicus flowers was also found to contain HNGs and
34  induced during late developmental stages of L. japonicus nodule organogenesis and provide important,
35  Mesorhizobium loti, the natural symbiont of L. japonicus.
36  and a decreased rate of nodule formation on L. japonicus.
37 thetic steps form nitrogen-fixing nodules on L. japonicus Gifu after a delay, whereas mutants affecte
38            In addition, previously published L. japonicus Affymetrix data are included in the databas
39  member of a small family of closely related L. japonicus genes.
40  found to be drastically altered in specific L. japonicus lines carrying monogenic-recessive mutation
41                            We show here that L. japonicus contains a small family of four cytokinin r
42 olecular modelling, and the observation that L. japonicus accessions lacking cyanogenic flowers conta
43                    The findings suggest that L. japonicus possesses a voltage-dependent cation efflux
44                                          The L. japonicus arpc1 mutant showed a distorted trichome ph
45                                          The L. japonicus mutant carrying the loss-of-function lhk1-1
46 y described cDNA, LjNOD16, which encodes the L. japonicus late nodulin Nlj16.
47                                 Finally, the L. japonicus genome contains many hundreds, perhaps thou
48 mble the expression pattern observed for the L. japonicus leghemoglobin gene.
49       No other AS genes were detected in the L. japonicus genome.
50                Significantly, several of the L. japonicus Sireviruses have recently amplified and may
51             Therefore, we postulate that the L. japonicus LjNOD70 gene family encodes nodule-specific
52                     As in M. truncatula, the L. japonicus ram1 mutant lines show compromised AM colon
53  subgroups of proteins that were specific to L. japonicus or closely related to known regulators of t
54                        Despite homology with L. japonicus RinRK1 (LjRinRK1), these proteins are funct