ライフサイエンスコーパス: Fabaceae

1 xistence in the Neotropical tree genus Inga (Fabaceae).

2 n individuals in the legume genus Lespedeza (Fabaceae).

3 n was found to have tricin (Medicago sativa, Fabaceae).

4 families, viz., Asteraceae, Boraginaceae and Fabaceae.

5 own as forisomes, have evolved solely in the Fabaceae.

6 ntrol of tendrilled leaf development outside Fabaceae.

7 stalloid phloem proteins found solely in the Fabaceae.

8 na unguiculata), was limited even within the Fabaceae.

9 communities of the diverse tree genus Inga (Fabaceae) across a 250-km transect in Amazonian Peru and

10 vans (phenolics), in Pentaclethra macroloba (Fabaceae), an abundant tree in Costa Rican wet forests.

11 For instance, in Fabaceae and Bignoniaceae, leaf parts can be modified in

12 ences in six angiosperm families outside the Fabaceae and Poaceae.

13 , Violaceae, Cucurbitaceae, and recently the Fabaceae and Solanaceae families.

14 BBIs are known only in the legume (Fabaceae) and cereal (Poaceae) families, but peptides th

15 es in the ancient symbiosis between legumes (Fabaceae) and nitrogen-fixing bacteria, asking how labil

16 its food plants (Crotalaria species: family Fabaceae) and retains them through metamorphosis.

17 y infected species within the Cucurbitaceae, Fabaceae, and Solanaceae.

18 vonoid metabolism and primarily found in the Fabaceae (angiosperms).

19 Prenylated phenolics from the Fabaceae are promising lead compounds for new antibacter

20 The Legumes (Fabaceae) are an economically and ecologically important

21 detached leaves from plants of the Poaceae, Fabaceae, Asteraceae, Brassicaceae, and Cucurbitaceae th

22 0 NBS-LRR RGHs were analyzed, primarily from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species,

23 es in compound leaf development in ancestral Fabaceae but that the FLO/LFY gene took over this role i

24 ble to interact with most leguminous plants (Fabaceae) but also with the non-legume Parasponia (Canna

25 izidine alkaloids from its larval foodplant (Fabaceae, Crotalaria spp.).

26 plants within the Rubiaceae, Violaceae, and Fabaceae families and share the CCK motif with trypsin-i

27 lycopsamine and heliotrine type PAs and the Fabaceae family contained senecionine and monocrotaline

28 spite its low abundance (2.9%), DNA from the Fabaceae family was detected in 94.7% of the sand flies.

29 Four species, all from the Fabaceae family, exhibited little or no wound-inducible

30 ic conserved class of DHDPS genes within the Fabaceae family.

31 eference of L. longipalpis for plants in the Fabaceae family.

32 of the terpene synthase (TPS) family and two Fabaceae GLSs that belong to the TPS-g clade have been r

33 our databases to represent the Brassicaceae, Fabaceae, Gramineae and Solanaceae families.

34 The majority of compound-leafed Fabaceae have expression of KNOX1 proteins associated wi

35 The legume plant family (Fabaceae) is a potential source of antimicrobial phytoch

36 d isoflavonoids are mainly restricted to the Fabaceae, it is tempting to speculate that this branch o

37 d clades, Sapindales, Apiales, Papaveraceae, Fabaceae, Lepidium, Solanum) were analysed using maximum

38 nt the first molecular characterization of a Fabaceae non-forisome P-protein and the first evidence t

39 Legumes (Fabaceae or Leguminosae) are unique among cultivated pla

40 LO/LFY to leaf complexity in a member of the Fabaceae outside of the IRLC was examined by reducing ex

41 ecently, SEO genes discovered in various non-Fabaceae plants were proposed to encode the common phloe

42 hree species of two families, Solanaceae and Fabaceae, results in the accumulation of proteinase inhi

43 of the ontology encompass terms relevant to Fabaceae, Solanaceae, additional cereal crops, and popla

44 prising > 216 000 world-wide observations of Fabaceae, spanning three orders of magnitude in seed siz

45 The Fabaceae-specific subgroup 1 contains genes encoding for

46 However, in a large subclade of the Fabaceae, the inverted repeat-lacking clade (IRLC), of w

47 The Fabaceae, the third largest family of plants and the sou

48 We have found that, in Crotalaria (Fabaceae), this reprogramming is associated with the bio

49 urvey of KNOX1 protein expression across the Fabaceae was undertaken.

50 nd lineages-through-time plots of Australian Fabaceae, we compared the southwest Australia Floristic

51 An exception to this trend is found in the Fabaceae, where pea (Pisum sativum) uses UNIFOLIATA, an

52 phid Megoura viciae feeds exclusively on the Fabaceae, whereas the currant-lettuce aphid Nasonovia ri

53 utionary origin of 4-Cl-IAA synthesis in the Fabaceae, which may provide an ideal model system to fur