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1 n was found to have tricin (Medicago sativa, Fabaceae).
2 xistence in the Neotropical tree genus Inga (Fabaceae).
3 nts-via a host belonging to tribe Genisteae (Fabaceae).
4 vasion of the forage crop, Trifolium repens (Fabaceae).
5 zontal gene transfer (HGT) from their hosts (Fabaceae).
6 n individuals in the legume genus Lespedeza (Fabaceae).
7 families, viz., Asteraceae, Boraginaceae and Fabaceae.
8 own as forisomes, have evolved solely in the Fabaceae.
9 ntrol of tendrilled leaf development outside Fabaceae.
10 stalloid phloem proteins found solely in the Fabaceae.
11 na unguiculata), was limited even within the Fabaceae.
12 n an ancestor of subfamily Papilionoideae of Fabaceae.
13  and functional evolutionary analyses across Fabaceae.
14 %) (mainly Vachellia tortilis) in the family Fabaceae.
15 ry history of symbiotic nitrogen fixation in Fabaceae.
16 rtion of shorter regions were related to the Fabaceae (a total of ~ 110 kb, 15.4%), some of which wer
17    We examined ploidy variation across Inga (Fabaceae), a characteristic Amazonian tree radiation, us
18 ese predictions for nitrogen-fixing legumes (Fabaceae) across 45 grasslands on six continents.
19  communities of the diverse tree genus Inga (Fabaceae) across a 250-km transect in Amazonian Peru and
20 vans (phenolics), in Pentaclethra macroloba (Fabaceae), an abundant tree in Costa Rican wet forests.
21 families, and further analyses supported the Fabaceae ancestral polyploidy.
22                             For instance, in Fabaceae and Bignoniaceae, leaf parts can be modified in
23 abaceae, including those at the ancestors of Fabaceae and five of the subfamilies, and further analys
24  butterflies are likely to have first fed on Fabaceae and originated in what is now the Americas.
25 ences in six angiosperm families outside the Fabaceae and Poaceae.
26             We grew four nitrogen (N)-fixing Fabaceae and seven diverse non-N-fixing tropical dry for
27 , Violaceae, Cucurbitaceae, and recently the Fabaceae and Solanaceae families.
28           BBIs are known only in the legume (Fabaceae) and cereal (Poaceae) families, but peptides th
29 es in the ancient symbiosis between legumes (Fabaceae) and nitrogen-fixing bacteria, asking how labil
30  its food plants (Crotalaria species: family Fabaceae) and retains them through metamorphosis.
31 tropical tree species, Dicorynia guianensis (Fabaceae) and Sextonia rubra (Lauraceae).
32 s occurs in two taxonomic lineages: legumes (Fabaceae) and the genus Parasponia (Cannabaceae).
33 ies than expected by chance, with Ericaceae, Fabaceae, and Orchidaceae experiencing losses and Amaran
34 n only three plant families (Convolvulaceae, Fabaceae, and Poaceae).
35 y infected species within the Cucurbitaceae, Fabaceae, and Solanaceae.
36 vonoid metabolism and primarily found in the Fabaceae (angiosperms).
37                Prenylated phenolics from the Fabaceae are promising lead compounds for new antibacter
38                                              Fabaceae are the third largest angiosperm family, with 7
39                                 The Legumes (Fabaceae) are an economically and ecologically important
40  detached leaves from plants of the Poaceae, Fabaceae, Asteraceae, Brassicaceae, and Cucurbitaceae th
41 0 NBS-LRR RGHs were analyzed, primarily from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species,
42 es in compound leaf development in ancestral Fabaceae but that the FLO/LFY gene took over this role i
43 ble to interact with most leguminous plants (Fabaceae) but also with the non-legume Parasponia (Canna
44                               Among legumes (Fabaceae) capable of nitrogen-fixing nodulation, several
45                          The genus Caragana (Fabaceae), comprising predominantly xerophytic shrubs, i
46 th economically and ecologically, and global Fabaceae crops are intensively studied in part for their
47 izidine alkaloids from its larval foodplant (Fabaceae, Crotalaria spp.).
48                     Species from Poaceae and Fabaceae exhibited a consistent trend of increased LMWOA
49  plants within the Rubiaceae, Violaceae, and Fabaceae families and share the CCK motif with trypsin-i
50  lycopsamine and heliotrine type PAs and the Fabaceae family contained senecionine and monocrotaline
51 spite its low abundance (2.9%), DNA from the Fabaceae family was detected in 94.7% of the sand flies.
52                   Four species, all from the Fabaceae family, exhibited little or no wound-inducible
53      Medicago, a genus in the Leguminosae or Fabaceae family, includes the most globally significant
54    The Prosopis koelziana genus, part of the Fabaceae family, plays a crucial role in the ecology and
55 eference of L. longipalpis for plants in the Fabaceae family.
56 ic conserved class of DHDPS genes within the Fabaceae family.
57 interesting source of nutrients, part of the Fabaceae family.
58 of the terpene synthase (TPS) family and two Fabaceae GLSs that belong to the TPS-g clade have been r
59 our databases to represent the Brassicaceae, Fabaceae, Gramineae and Solanaceae families.
60 A release followed the order: Brassicaceae > Fabaceae > Poaceae.
61              The majority of compound-leafed Fabaceae have expression of KNOX1 proteins associated wi
62 tion/whole-genome triplication events across Fabaceae, including those at the ancestors of Fabaceae a
63                                             (Fabaceae) is a medicinal and ornamental plant, widely us
64                                             (Fabaceae) is a medicinal plant traditionally used for it
65                     The legume plant family (Fabaceae) is a potential source of antimicrobial phytoch
66 d isoflavonoids are mainly restricted to the Fabaceae, it is tempting to speculate that this branch o
67                                    ex Hayne (Fabaceae), known as jatoba-do-cerrado, has significant e
68                 However, two plant lineages, Fabaceae (legumes) and Caryophyllales, have TyrA enzymes
69 d clades, Sapindales, Apiales, Papaveraceae, Fabaceae, Lepidium, Solanum) were analysed using maximum
70 ree growth and survival for coexisting Inga (Fabaceae, Mimosoideae) congeners, we tested two mechanis
71 nt the first molecular characterization of a Fabaceae non-forisome P-protein and the first evidence t
72                                     Legumes (Fabaceae or Leguminosae) are unique among cultivated pla
73 s including the Brassicaceae, Solanaceae and Fabaceae, our work in eudicots supports an earlier singu
74 LO/LFY to leaf complexity in a member of the Fabaceae outside of the IRLC was examined by reducing ex
75  However, resolution of the intrasubfamilial Fabaceae phylogeny and divergence times has remained elu
76 ecently, SEO genes discovered in various non-Fabaceae plants were proposed to encode the common phloe
77 diversification history of the legume family Fabaceae, plastomes have undergone many rearrangements,
78 evolution of keel flowers in Papilionoideae (Fabaceae) provides a suitable system to test this hypoth
79 hree species of two families, Solanaceae and Fabaceae, results in the accumulation of proteinase inhi
80  of the ontology encompass terms relevant to Fabaceae, Solanaceae, additional cereal crops, and popla
81 prising > 216 000 world-wide observations of Fabaceae, spanning three orders of magnitude in seed siz
82 riptomes by phylogenomic analyses with other Fabaceae species, estimating the divergence time of exta
83                                          The Fabaceae-specific subgroup 1 contains genes encoding for
84 ips among subfamilies of the Leguminosae (or Fabaceae), the third largest angiosperm family.
85          However, in a large subclade of the Fabaceae, the inverted repeat-lacking clade (IRLC), of w
86                                          The Fabaceae, the third largest family of plants and the sou
87           We have found that, in Crotalaria (Fabaceae), this reprogramming is associated with the bio
88                                         100, Fabaceae) using ultraperformance liquid chromatography-m
89 n of rhizobial nitrogen-fixing nodulation in Fabaceae was probed by ancestral character reconstructio
90 urvey of KNOX1 protein expression across the Fabaceae was undertaken.
91 nd lineages-through-time plots of Australian Fabaceae, we compared the southwest Australia Floristic
92   An exception to this trend is found in the Fabaceae, where pea (Pisum sativum) uses UNIFOLIATA, an
93 phid Megoura viciae feeds exclusively on the Fabaceae, whereas the currant-lettuce aphid Nasonovia ri
94 utionary origin of 4-Cl-IAA synthesis in the Fabaceae, which may provide an ideal model system to fur