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1                                              Lotus japonicus has been used for decades as a model leg
2                                              Lotus japonicus is a model species for legume genomics.
3                                              Lotus SYMRK is required for a symbiotic signal transduct
4                                              Lotus valve or CoreValve/EvolutR TAVR platforms.
5 e legume functional genomics, we developed a Lotus japonicus Gene Expression Atlas (LjGEA), which pro
6                           Here we identify a Lotus japonicus gene encoding a predicted ACTIN-RELATED
7                           Here we identify a Lotus japonicus nodulation pectate lyase gene (LjNPL), w
8                           We have isolated a Lotus japonicus cDNA corresponding to a highly abundant,
9 s identified in Medicago truncatula (52) and Lotus japonicus (53), including pseudogenes and non-func
10 subcellular localizations in Arabidopsis and Lotus japonicus.
11 egumes, Medicago truncatula, Glycine max and Lotus japonicus plus two reference plant species, A. tha
12 two other sequenced legumes, Glycine max and Lotus japonicus.
13 receptor5 (nfr5), Nodule inception (nin) and Lotus histidine kinase1 (lhk1) genes identified a previo
14 type, similar to the clv2 mutants of pea and Lotus japonicus.
15 ed between Mesorhizobium loti strain R7A and Lotus japonicus Gifu, rhizobial exopolysaccharide (EPS)
16 nt (396 and 273 mg kg(-1), respectively) and Lotus creticus, the lowest (20 mg kg(-1)).
17 ty to different degrees in Pisum sativum and Lotus japonicus.
18 gume species, namely pea (Pisum sativum) and Lotus japonicus, we show that this motor organ identity
19 odel legume species, Medicago truncatula and Lotus japonicus, and two crop species, Glycine max (soyb
20 odel legume species, Medicago truncatula and Lotus japonicus, as well as data available for Arabidops
21 ssing is observed in Medicago truncatula and Lotus japonicus, implying a conserved mechanism of cell
22 e two model legumes, Medicago truncatula and Lotus japonicus, provide a unique opportunity to address
23 f the model legumes, Medicago truncatula and Lotus japonicus, provides an opportunity for large-scale
24 t epidermal cells of Medicago truncatula and Lotus japonicus.
25 1 (CERK1), in rice, Medicago truncatula, and Lotus japonicus, as well as the non-host of AM fungi, Ar
26 Horse chestnut (HS), Water chestnut (WS) and Lotus stem (LS) by using mild alkali hydrolysis and ultr
27 ater chestnut starch nanoparticles (WSP) and Lotus stem starch nanoparticles (LSP) was found to be 42
28 development of root hairs in the angiosperms Lotus japonicus, Arabidopsis thaliana, and rice (Oryza s
29 a SAPIEN-type valve (n=20,40.0%) or a Boston Lotus valve (n=1, 2.0%).
30 t a subset of these epithelial tubules bound Lotus tetragonolobus and expressed alpha(1) Na(+)/K(+) A
31 crystal structure of the signaling-competent Lotus japonicus NFR5 intracellular domain, comprising th
32 %; P=0.62), or major vascular complications (Lotus, 2.9%; ES3, 2.4%; P=0.69).
33 inate (Medicago truncatula) and determinate (Lotus japonicus) nodulation.
34 edicago truncatula with those of the diploid Lotus japonicus and the polyploid Glycine max.
35 cal trial compared the mechanically expanded Lotus valve with the self-expanding CoreValve/EvolutR TA
36 ed a sensitive ethylene detection system for Lotus japonicus and found that ethylene production incre
37  10 patients who had undergone Redo TAVI for Lotus bioprosthetic valve failure in 5 centers.
38 formed from fucose-specific isolectin A from Lotus tetragonolobus cross-linked with difucosyllacto-N-
39 Boeing 787 Dreamliner; lightweight cars from Lotus, Ferrari and TVR; and high-speed trains, speedboat
40                Here we show that CASTOR from Lotus japonicus is a highly selective Ca(2+) channel who
41 e the characterization of a gene family from Lotus japonicus that encodes a novel class of plant PITP
42 'symbiosis receptor-like kinase') genes from Lotus and pea, which are required for both fungal and ba
43 e clamp records of an ortholog of GmN70 from Lotus japonicus also showed anion currents with a simila
44  a type III sucrose transporter homolog from Lotus japonicus, is expressed in nodules and its transpo
45              Although the DMI1 homologs from Lotus japonicus, CASTOR and POLLUX, were recently report
46                       Gene order in Glycine, Lotus, and Medicago differs from the usual gene order fo
47                      Comparisons of Glycine, Lotus and Medicago confirm the organization of legume ch
48 NN and the previously identified genes HAR1 (Lotus japonicus) and NARK (Glycine max) are orthologs ba
49 nters into a symbiosis with the legume host, Lotus japonicus, which results in the formation of novel
50                                           In Lotus japonicus, a LysM receptor kinase, EPR3, distingui
51                                           In Lotus japonicus, two symbiotic cation channels, CASTOR a
52   Overexpression of the GS52 ecto-apyrase in Lotus japonicus increased the level of rhizobial infecti
53 d in regulating isoflavonoid biosynthesis in Lotus (Lotus japonicus).
54 ve gain-of-function CNGC mutation (brush) in Lotus japonicus resulting in a leaky tetrameric channel.
55 e found that P. palmivora induces disease in Lotus japonicus and used this interaction to identify ce
56 tified and sequenced and their expression in Lotus japonicus characterised.
57 n of many genes required for AM formation in Lotus japonicus.
58 ntial for infection thread (IT) formation in Lotus japonicus.
59  and also sufficient for nodule formation in Lotus japonicus.
60                 We have identified a gene in Lotus japonicus, Epr3, encoding a receptor-like kinase t
61 TOR and POLLUX, the twin homologous genes in Lotus japonicus that encode putative ion channel protein
62 bial suppression of plant innate immunity in Lotus japonicus.
63 tion as well as target promoter induction in Lotus japonicus hairy roots depends on MYCS (MYCORRHIZA
64 n AM colonisation and rhizobial infection in Lotus japonicus.
65 ociated with Nod factor receptor 5 (NFR5) in Lotus japonicus.
66 sense inhibition of LNP blocks nodulation in Lotus japonicus.
67 olved in both infection and organogenesis in Lotus japonicus.
68 g IPD3 in Arabidopsis and knocking it out in Lotus was strongest in plants not exposed to AMF, which
69 ces similar to MtDHDPS2 and 3 are present in Lotus japonicus and Glycine max, suggesting the existenc
70   While the kinase domain of NF receptors in Lotus japonicus suffices for nodule organogenesis, their
71  that VTL8, the closest homologue of SEN1 in Lotus japonicus, is the main route for delivering iron t
72 ene, LjNOD70, associated with late stages in Lotus japonicus nodule development and/or functioning wa
73 s in lateral root formation and symbiosis in Lotus japonicus.
74  Recommendations for performing Redo TAVI in Lotus are made, based on these findings.
75                                 Redo TAVI in Lotus requires an understanding of unique design charact
76 f 16S rRNA gene amplicons, we reveal that in Lotus, distinctive nodule- and root-inhabiting communiti
77 ateral root developmental program is used in Lotus for nodule organogenesis.
78 action is unclear and the function of VPY in Lotus japonicus has not been studied.
79 e cauliflower mosaic virus 35S promoter into Lotus corniculatus, which is nodulated by R. loti.
80 rmined the structure of the Lotus japonicus (Lotus) exopolysaccharide receptor 3 (EPR3) ectodomain.
81 (LjNPP2C1 and LjPP2C2) from the model legume Lotus japonicus that encode protein phosphatase type 2C
82  the symbiosome membrane of the model legume Lotus japonicus were analyzed by patch-clamp recording.
83 utamine (Gln) synthetase in the model legume Lotus japonicus were investigated.
84                          In the model legume Lotus japonicus, one of these LegCYC genes has been show
85 ts during nodule organogenesis in the legume Lotus japonicus were identified using mRNA differential
86 regulated in mycorrhizal roots of the legume Lotus japonicus, expression of a unique GRAS protein par
87 olic responses to waterlogging of the legume Lotus japonicus, it was previously suggested that, durin
88 s in a determinate symbiosis with the legume Lotus japonicus.
89 with endogenous SYMRK in roots of the legume Lotus japonicus.
90 bility to elicit nodules on its host legume, Lotus japonicus.
91  development of nodules in the model legume, Lotus japonicus.
92                    In Papilionoideae legume, Lotus japonicus, the development of dorsal-ventral (DV)
93                 Studies in the model legumes Lotus japonicus and Medicago truncatula showed that rhiz
94 t to the other completely sequenced legumes, Lotus and Medicago.
95 mporal changes in the cytoskeleton of living Lotus japonicus root hairs, which precede root-hair defo
96 gulating isoflavonoid biosynthesis in Lotus (Lotus japonicus).
97                                     Medicago-Lotus comparisons also indicate similar and largely homo
98 s, and compare these results to the AM model Lotus japonicus and its ipd3 knockout mutant cyclops-4.
99 e in the primary end point within 12 months (Lotus, 15.5%; ES3, 18.6%; P=0.69) and 24 months (Lotus,
100 s, 15.5%; ES3, 18.6%; P=0.69) and 24 months (Lotus, 21.9%; ES3, 26.4%; P=0.49).
101 s with no difference in all-cause mortality (Lotus, 1.9%; ES3, 1.8%; P=0.87), rate of disabling strok
102                                       Native Lotus seed (NLS) starch was independently subjected to t
103 m japonicum, which nodulates soybean and not Lotus spp.
104 rtion line, we identify two novel alleles of Lotus japonicus REDUCED ARBUSCULAR MYCORRHIZA1 (RAM1) en
105  The availability of a significant amount of Lotus japonicus genome sequence has permitted for the fi
106 ds in high-turgor cells in the phloem cap of Lotus japonicus, suggesting that storage of defensive co
107 ed tannins (CTs) in 'hairy root' cultures of Lotus corniculatus (bird's foot trefoil) using genetic m
108 his by exploring the phenotypic diversity of Lotus japonicus accessions that uncouple nodule organoge
109 m in nitrogen (N) fixing nodules (Fix(+)) of Lotus japonicus, as well as the link of S-metabolism to
110                    Three clonal genotypes of Lotus corniculatus L.
111 tenotic Aortic Valve Through Implantation of Lotus Valve System-Randomized Clinical Evaluation) rando
112 tenotic Aortic Valve Through Implantation of Lotus Valve System: Evaluation of Safety and Performance
113                        Flowers and leaves of Lotus japonicus contain alpha-, beta-, and gamma-hydroxy
114 l methanesulfonate mutagenized population of Lotus japonicus for mutants defective in IT formation an
115 tin and nodulation (Nod) factor receptors of Lotus japonicus initiate differential signaling of immun
116 -based expression studies and a selection of Lotus japonicus mutants uncoupling different symbiosis s
117 way genes in a sliding developmental zone of Lotus japonicus roots.
118 ale genome duplication in either Medicago or Lotus but instead a duplication predating speciation.
119 led at our center, and 202 patients received Lotus and 335 ES3.
120 significantly higher with the repositionable Lotus device.
121 ower with the repositionable and retrievable Lotus valve compared with the ES3.
122 d 24-month outcomes of the Boston Scientific Lotus valve (Lotus) and the balloon-expandable Edwards S
123  Medicago truncatula, Glycine max (soybean), Lotus japonicus, Phaseolus vulgaris (common bean), Cicer
124 diversification of the streptophyte-specific Lotus japonicus ROOTHAIRLESS LIKE (LRL) transcription fa
125 S3, 1.8%; P=0.87), rate of disabling stroke (Lotus, 1.5%; ES3, 2.1%; P=0.62), or major vascular compl
126                            Here we show that Lotus japonicus and Medicago truncatula possess very sim
127                            Here we show that Lotus japonicus SMAX1 is specifically degraded in the pr
128                                          The Lotus and Medicago genomes share a minimum of 10 large-s
129                                          The Lotus frame posts prevent full apposition of the Redo pr
130                                          The Lotus japonicus SYMBIOSIS RECEPTOR-LIKE KINASE (SYMRK) i
131                                          The Lotus japonicus T-DNA insertion line T90, carrying a pro
132                                          The Lotus leaflets extend from the frame inflow, with a Neos
133                                          The Lotus locking mechanism prevents overexpansion of the fr
134                                          The Lotus mechanically expanded THV has unique design charac
135                                          The Lotus valve, designed to improve upon earlier devices, i
136 while implantation of the Redo THV above the Lotus inflow leads to inadequate apposition of the Lotus
137 rough light-induced photodegradation and the Lotus effect are presented.
138 ortic valve replacement with the ES3 and the Lotus were associated with similar 30-day, 12-month, and
139 women [50.8%]) were randomized to either the Lotus valve group (n = 607) or CoreValve/EvolutR group (
140 re available for 581 patients (95.7%) in the Lotus valve group and 285 patients (93.4%) in the CoreVa
141 % vs 1.8%; P = .007) were more common in the Lotus valve group than in the CoreValve/EvolutR group.
142 ate for all-cause mortality was 50.9% in the Lotus valve group vs 52.8% in the CoreValve/EvolutR grou
143                     Previous analysis of the Lotus histidine kinase1 (Lhk1) cytokinin receptor gene h
144 ognition, we determined the structure of the Lotus japonicus (Lotus) exopolysaccharide receptor 3 (EP
145 s of the Medicago truncatula ortholog of the Lotus japonicus and pea (Pisum sativum) NIN gene.
146                      Database studies of the Lotus japonicus genome have revealed the presence of 24
147 e applied this methodology to mutants of the Lotus japonicus GRAS transcription factor RAM1 and the O
148 cess we conducted a detailed analysis of the Lotus japonicus hypernodulating mutants, har1-1, 2 and 3
149 here the characterization of a member of the Lotus japonicus nitrate transporter1/peptide transporter
150 inflow leads to inadequate apposition of the Lotus leaflets.
151 ceptor-like kinase (LRR-RLK) ortholog of the Lotus RINRK1, that mediates NF signaling.
152                   The design features of the Lotus valve and their relevance to Redo TAVI were review
153 nstrates the safety and effectiveness of the Lotus valve in patients with severe aortic stenosis who
154 at, at 5 years, the clinical outcomes of the Lotus valve were comparable to those of the CoreValve/Ev
155 lycan, as might be inferred from work on the Lotus japonicus MtLYK10 ortholog, LjEPR3.
156 ller proportion of patients who received the Lotus valve experienced valve malpositioning (0% vs 2.6%
157                       Here, we show that the Lotus japonicus Ckx3 cytokinin oxidase/dehydrogenase gen
158                       Here, we show that the Lotus japonicus Nod factor receptor 5 (NFR5) and Nod fac
159  those of the CoreValve/EvolutR and that the Lotus valve was safe and effective.
160 for aberrant nodulation phenotypes using the Lotus japonicus LORE1 insertion mutant collection.
161 her with the CoreValve/EvolutR than with the Lotus valve (1.9% vs 0%; P = .31); however, the proporti
162 plantation was significantly higher with the Lotus valve compared with the ES3 valve (36.1% versus 14
163 he CoreValve/EvolutR group compared with the Lotus valve group (23.1% vs 7.8%; P = .006).
164                            Compared with the Lotus valve group, the CoreValve/EvolutR group had a sig
165  Disabling stroke was less frequent with the Lotus valve vs CoreValve/EvolutR (cumulative event rates
166 ar iron transporter family and homologous to Lotus japonicus SEN1 (LjSEN1), which is essential for ni
167 ydroxylase (NahG) in both stably transformed Lotus japonicus and composite Medicago truncatula plants
168                                   Transgenic Lotus japonicus plants were constructed constitutively e
169 ssion in the nodule parenchyma of transgenic Lotus corniculatus plants.
170 he pattern observed in nodules of transgenic Lotus corniculatus plants.
171 , sulla (Hedysarum coronarium), big trefoil (Lotus pedunculatus), and salad burnet (Sanguisorba minor
172 ifolium pratense L.), and birdsfoot trefoil (Lotus corniculatus L.).
173 different forage species: birdsfoot trefoil (Lotus corniculatus), sulla (Hedysarum coronarium), big t
174 mpare unigene sets from Medicago truncatula, Lotus japonicus, and soybean (Glycine max and Glycine so
175 of transcript data from Medicago truncatula, Lotus japonicus, Glycine max and Arabidopsis thaliana.
176 (Nicotiana benthamiana, Medicago truncatula, Lotus japonicus, Oryza sativa) and captured the altered
177  forward genetic approach, we identified two Lotus japonicus mutants defective in AM-specific paralog
178 mbrane-associated protein interactomes using Lotus japonicus symbiotically active receptor kinases as
179 tcomes of the Boston Scientific Lotus valve (Lotus) and the balloon-expandable Edwards Sapien 3 (ES3)
180 ass were determined in sections stained with Lotus tetragonolobus lectin.

 
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