ライフサイエンスコーパス: solanaceous

1 The solanaceous alkaloids S-(-)-nicotine and hyoscyamine (at

2 derived from PROPEP orthologs identified in Solanaceous and Fabaceous plants also induce herbivory-a

3 ated Nicotiana species, nor in various other solanaceous and non-solanacous plants.

4 and R gene homologues were analyzed in three solanaceous crop genera, Lycopersicon (tomato), Solanum

5 l glycoside, indioside D, that is present in solanaceous foliage.

6 2 were found in syntenous positions in other solanaceous genomes and in some cases also mapped to add

7 and Bs4C-like genes that are present in many solanaceous genomes seem to be as tightly regulated as p

8 ed using a miR165/166 target mimic and three solanaceous hosts: Nicotiana benthamiana, tobacco (N. ta

9 ici (Pst) activates immunity in the non-host solanaceous model plant Nicotiana benthamiana.

10 s its use as a source of resistance in other Solanaceous plant species.

11 of three cultivars and one accession of the solanaceous plant, Capsicum annum against moist sand in

12 mechanisms for LAP action in the defense of solanaceous plants against stress.

13 ivatives and sesquiterpenoid phytoalexins in solanaceous plants following mechanical injury or pathog

14 omonas syringae and that this degradation in Solanaceous plants is dependent on the resistance protei

15 transcriptome databases from Arabidopsis and solanaceous plants, and characterized miR172-mediated re

16 ced in secretory glandular trichomes of many solanaceous plants, including cultivated tomato (Solanum

17 Certain solanaceous plants, including tomato, potato and pepper,

18 f pollen rejection in self-incompatible (SI) solanaceous plants, they alone are not sufficient to cau

19 nstituting the major component of exudate in solanaceous plants.

20 ell death in Nicotiana benthamiana and other solanaceous plants.

21 in tobacco and tropane alkaloids in several Solanaceous plants.

22 nalysis of the genomic sequence encompassing solanaceous R genes revealed the magnitude of transposon

23 ysis and synthesis of all available data for solanaceous R genes suggests a working hypothesis regard

24 tional positions near phenotypically defined solanaceous R genes.

25 it and leaves of Lycium intricatum Boiss., a Solanaceous shrubbery with the potential to become a hig

26 to Colorado potato beetle larvae and to the solanaceous specialist Manduca sexta was verified in no-

27 of rearrangements that distinguish pairs of solanaceous species also indicates that the frequency of

28 e and gene order are conserved between these solanaceous species and that this conservation can be le

29 n sequencing the genomes of tomato and other solanaceous species are discussed.

30 ic defense response may have evolved in some solanaceous species by co-opting the BRI1 receptor and a

31 population size (Ne) were determined for two solanaceous species by examination of S-allele diversity

32 ly proteins and their functions in different solanaceous species confirmed that gene duplication and

33 aling that the inflorescence architecture of Solanaceous species depends on sequential and temporal e

34 Estimates of recent Ne in two solanaceous species differed by an order of magnitude, c

35 family have been isolated from a variety of solanaceous species including Solanum tuberosum (potato)

36 S2), the predominant GS isoform in leaves of Solanaceous species including tobacco (Nicotiana tabacum

37 a along with the previous sequences of three solanaceous species indicate that much of the combined a

38 We show here that the solanaceous species Nicotiana benthamiana perceives the

39 Self-incompatible solanaceous species possess the S-RNase and SLF (S-locus

40 We report herein that tobacco, a solanaceous species that does not express a systemin pre

41 aturally occurring pollen-part mutation of a solanaceous species that was shown to be associated with

42 Tomato (Solanum lycopersicum), like other Solanaceous species, accumulates high levels of antioxid

43 derstanding of phenylpropanoid metabolism in Solanaceous species, and evolution of flavonoid decorati

44 m extensive surveys of S alleles in two wild solanaceous species, Solanum carolinense and Physalis lo

45 irradiation-generated pollen-part mutants of solanaceous species, that duplication, but not deletion,

46 Lepidium (Lepidium sativum), and that of the Solanaceous species, tobacco (Nicotiana tabacum).

47 ion of flgII-28 is restricted to a number of solanaceous species.

48 n to be phloem mediated in several different solanaceous species.

49 omato diverged from potato and other related solanaceous species.

50 e event that is shared with tomato and other solanaceous species.

51 eneral resistance pathways is conserved in a Solanaceous species.

52 e principal route for accumulation of CGA in solanaceous species.

53 distinguish Lycopersicon species from other solanaceous species.

54 lity alleles from natural populations of two solanaceous species.