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1                                          The solanaceous alkaloids S-(-)-nicotine and hyoscyamine (at
2 acearum' (Lso) is associated with disease in Solanaceous and Apiaceous crops.
3  derived from PROPEP orthologs identified in Solanaceous and Fabaceous plants also induce herbivory-a
4 ated Nicotiana species, nor in various other solanaceous and non-solanacous plants.
5 and R gene homologues were analyzed in three solanaceous crop genera, Lycopersicon (tomato), Solanum
6 zebra chip (ZC) disease are major threats to solanaceous crop production in North America.
7 ity and resilience; for example, grafting of Solanaceous crops couples disease-resistant rootstocks w
8 ompared with closely related seed-propagated solanaceous crops, indicative of the effect of tuber-bas
9 ibacter solanacearum' (Lso) is a pathogen of solanaceous crops.
10 nd trans targets to generate stress-tolerant solanaceous crops.
11 l glycoside, indioside D, that is present in solanaceous foliage.
12 2 were found in syntenous positions in other solanaceous genomes and in some cases also mapped to add
13 and Bs4C-like genes that are present in many solanaceous genomes seem to be as tightly regulated as p
14 ed using a miR165/166 target mimic and three solanaceous hosts: Nicotiana benthamiana, tobacco (N. ta
15 ici (Pst) activates immunity in the non-host solanaceous model plant Nicotiana benthamiana.
16        The impact of these new haplotypes on solanaceous or other crops is not known.
17  Here we analyze EDS1 functions in the model Solanaceous plant Nicotiana benthamiana (Nb).
18 s its use as a source of resistance in other Solanaceous plant species.
19  of three cultivars and one accession of the solanaceous plant, Capsicum annum against moist sand in
20 functional unit that can be transferred from solanaceous plants (lamiids) to Campanulid species.
21  mechanisms for LAP action in the defense of solanaceous plants against stress.
22 olution and function of NRC networks outside solanaceous plants are currently unclear.
23 issue from herbarium samples of three native solanaceous plants collected near potato-growing regions
24                            Transcriptomes of solanaceous plants expressing a plastid-targeted antioxi
25 ivatives and sesquiterpenoid phytoalexins in solanaceous plants following mechanical injury or pathog
26 omonas syringae and that this degradation in Solanaceous plants is dependent on the resistance protei
27                                         Many solanaceous plants secrete acylsugars, which are branche
28 transcriptome databases from Arabidopsis and solanaceous plants, and characterized miR172-mediated re
29 ced in secretory glandular trichomes of many solanaceous plants, including cultivated tomato (Solanum
30                                      Certain solanaceous plants, including tomato, potato and pepper,
31                                           In solanaceous plants, the NRC (NLR required for cell death
32 f pollen rejection in self-incompatible (SI) solanaceous plants, they alone are not sufficient to cau
33 nstituting the major component of exudate in solanaceous plants.
34 th, Manduca sexta (Sphingidae), oviposits on solanaceous plants.
35 ell death in Nicotiana benthamiana and other solanaceous plants.
36  in tobacco and tropane alkaloids in several Solanaceous plants.
37 de Arabidopsis NHP biosynthetic genes in two Solanaceous plants.
38 ns and comprises up to half of the NLRome of solanaceous plants.
39  glycoalkaloids (GAs) are toxins produced by solanaceous plants.
40 r the rapid development of pathogen-tolerant solanaceous plants.
41 nalysis of the genomic sequence encompassing solanaceous R genes revealed the magnitude of transposon
42 ysis and synthesis of all available data for solanaceous R genes suggests a working hypothesis regard
43 tional positions near phenotypically defined solanaceous R genes.
44 it and leaves of Lycium intricatum Boiss., a Solanaceous shrubbery with the potential to become a hig
45  to Colorado potato beetle larvae and to the solanaceous specialist Manduca sexta was verified in no-
46  of rearrangements that distinguish pairs of solanaceous species also indicates that the frequency of
47 e and gene order are conserved between these solanaceous species and that this conservation can be le
48 n sequencing the genomes of tomato and other solanaceous species are discussed.
49 ic defense response may have evolved in some solanaceous species by co-opting the BRI1 receptor and a
50 population size (Ne) were determined for two solanaceous species by examination of S-allele diversity
51 ly proteins and their functions in different solanaceous species confirmed that gene duplication and
52 aling that the inflorescence architecture of Solanaceous species depends on sequential and temporal e
53                Estimates of recent Ne in two solanaceous species differed by an order of magnitude, c
54  family have been isolated from a variety of solanaceous species including Solanum tuberosum (potato)
55 S2), the predominant GS isoform in leaves of Solanaceous species including tobacco (Nicotiana tabacum
56 a along with the previous sequences of three solanaceous species indicate that much of the combined a
57 1 cell death activity is transferable to the Solanaceous species Nicotiana benthamiana and cannot be
58                        We show here that the solanaceous species Nicotiana benthamiana perceives the
59                            Self-incompatible solanaceous species possess the S-RNase and SLF (S-locus
60             We report herein that tobacco, a solanaceous species that does not express a systemin pre
61 aturally occurring pollen-part mutation of a solanaceous species that was shown to be associated with
62    Tomato (Solanum lycopersicum), like other Solanaceous species, accumulates high levels of antioxid
63 derstanding of phenylpropanoid metabolism in Solanaceous species, and evolution of flavonoid decorati
64 SpLFS orthologs in other acylsugar-producing solanaceous species, and VIGS of SpLFS orthologs in Nico
65 ed metabolites produced by trichomes of many solanaceous species, provide protection against biotic a
66 m extensive surveys of S alleles in two wild solanaceous species, Solanum carolinense and Physalis lo
67 irradiation-generated pollen-part mutants of solanaceous species, that duplication, but not deletion,
68 Lepidium (Lepidium sativum), and that of the Solanaceous species, tobacco (Nicotiana tabacum).
69 itions and developmental time points for two Solanaceous species, tomato (Solanum lycopersicum cv 75
70 e event that is shared with tomato and other solanaceous species.
71 ion of flgII-28 is restricted to a number of solanaceous species.
72 n to be phloem mediated in several different solanaceous species.
73 omato diverged from potato and other related solanaceous species.
74 eneral resistance pathways is conserved in a Solanaceous species.
75 e principal route for accumulation of CGA in solanaceous species.
76  distinguish Lycopersicon species from other solanaceous species.
77 lity alleles from natural populations of two solanaceous species.
78 reatening the production of tomato and other solanaceous vegetables in many countries.