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1 F, an S-locus F-box gene of Petunia inflata (Solanaceae).
2 h (tolerance) traits in Solanum carolinense (Solanaceae).
3 solanums) of the species-rich genus Solanum (Solanaceae).
4 formance on a novel host, Physalis angulata (Solanaceae).
5 plant families (Asteraceae, Brassicaceae and Solanaceae).
6 ive barriers (IRBs) are related to SI in the Solanaceae.
7 its loss is irreversible in the plant family Solanaceae.
8 psicum and Lycopersicon, both members of the Solanaceae.
9 ry mechanism for chromosome evolution in the Solanaceae.
10 ent that occurred prior to speciation of the Solanaceae.
11 homologues of the tomato kinases from other Solanaceae.
12 he two Rosaceae species as compared with the Solanaceae.
13 sylgalactosides are conserved throughout the Solanaceae.
14 nctional homologs of systemin outside of the Solanaceae.
15 site of tropane alkaloid biosynthesis in the Solanaceae.
16 r gene regulation and pathogen resistance in Solanaceae.
17 mportant tropane alkaloids in species of the Solanaceae.
18 LAP-A) are expressed only in a subset of the Solanaceae.
19 ction and evolution of miR4376 in the family Solanaceae.
20 play a role in MITE siRNA generation in the Solanaceae.
21 cies within the Cucurbitaceae, Fabaceae, and Solanaceae.
23 nach and Chlamydomonas reinhardtii), and non-Solanaceae activase fails to activate Solanaceae Rubisco
24 tology encompass terms relevant to Fabaceae, Solanaceae, additional cereal crops, and poplar (Populus
26 ed by an as yet unidentified receptor in the Solanaceae, although it has an FLS2-dependent virulence
27 Gametophytic SI is well characterized for Solanaceae and although balancing selection is hypothesi
29 g plants from three species of two families, Solanaceae and Fabaceae, results in the accumulation of
31 study of gene expression in tobacco and the Solanaceae and helps to fill a current gap in studies of
33 ll separated from the S-RNase sequences from Solanaceae and Rosaceae, and also from most known "S-lik
34 hat gave rise to the core euasterid families Solanaceae and Rubiaceae had a basic chromosome number o
35 ontaining biological data for species in the Solanaceae and their close relatives, with data types ra
36 es at the self-incompatibility locus ( S) of Solanaceae and their extraordinary spectrum of sequence
38 s also functional in a family other than the Solanaceae, and could be considered for canker control.
39 s tested, even including some members of the Solanaceae, and it is therefore unlikely that Chi2;1 is
41 hree flowering plant families, including the Solanaceae, and this self/non-self recognition mechanism
43 ily, termed TNACS, appears restricted to the Solanaceae, as they are absent from currently sequenced
44 novel Ascomycete PAMP, RcCDI1, recognized by Solanaceae but not by monocots, which activates cell dea
45 ibited PAMP activity, inducing cell death in Solanaceae but not in other families of dicots or monoco
46 emin regulates antiherbivore defenses in the Solanaceae, but in other plant families, peptides with a
47 e trend strengthened when we weighted edible Solanaceae by nicotine concentration (ptrend = 0.004).
48 capable of inducing alkalinization in other Solanaceae cell types (or species), indicating that stru
49 ly associated with consumption of all edible Solanaceae combined (relative risk [RR] = 0.81, 95% conf
50 ealed that transgenic expression of AtEFR in Solanaceae confers elf18 responsiveness and broad-spectr
51 er of genes in tomato (Solanum lycopersicum; Solanaceae) contains genes for terpene synthases (TPSs)
53 ely related to a tobacco (Nicotiana tabacum; Solanaceae) diterpene synthase encoding Z-abienol syntha
54 shared with most Eudicots, and a more recent Solanaceae event that is shared with tomato and other so
58 ynthesized in the glandular trichomes of the Solanaceae family and are implicated in protection again
60 l hundreds of acylsugars produced across the Solanaceae family and even within a single plant, built
61 ted to AtRTE1, we report that members of the Solanaceae family contain two phylogenetically distinct
65 hole genome data for an increasing number of Solanaceae family members including tomato, potato, pepp
66 ypSys gene family to be found outside of the Solanaceae family, and its encoded peptide precursor is
67 f adaptation and phenotypic diversity in the Solanaceae family, other species in the Asterid clade su
68 pepper (Capsicum annuum), all members of the Solanaceae family, using reverse-transcription polymeras
69 g comparative resource for the plants of the Solanaceae family, which includes important crop and mod
70 erated, we investigated the evolution of the Solanaceae family-specific, trichome-localized acylsugar
78 ty (SI) for a population of Lycium parishii (Solanaceae) from Organ Pipe National Monument, Arizona.
79 -MiS22) and found abundant MiS insertions in Solanaceae genomic DNA and expressed sequence tags (EST)
81 he results suggest that domestication of the Solanaceae has been driven by mutations in a very limite
82 gender dimorphism in North American Lycium (Solanaceae) has evolved in polyploid, self-compatible ta
83 uctive barriers between even closely related Solanaceae have precluded a genetic dissection, we captu
84 omato species (Solanum section Lycopersicon (Solanaceae)) have been described as polymorphic for mati
86 sized in the roots of specific genera of the Solanaceae in a multistep pathway that is only partially
87 olanum lycopersicum) is a model organism for Solanaceae in both molecular and agronomic research.
88 gene duplicate function have occurred in the Solanaceae, in that individual gene roles are distinct,
89 d portions of the plant in contrast with the Solanaceae, in which tropane alkaloid biosynthesis occur
92 c self-incompatibility (SI) possessed by the Solanaceae is controlled by a highly polymorphic locus c
93 rd distinct type of cyclotide precursor, and Solanaceae is the fourth phylogenetically disparate plan
97 The potentially protective effect of edible Solanaceae largely occurred in men and women who had nev
98 We identified 22 families of MITEs in the Solanaceae (MiS1-MiS22) and found abundant MiS insertion
100 rescences of tomato and related nightshades (Solanaceae), new lateral inflorescence branches develop
101 Across a phylogeny of 56 wild species of Solanaceae (nightshades), we show here that the repeated
102 nces obtained by RT-PCR from five species of Solanaceae now reveal a picture of conspicuous inter-spe
103 bacco (Nicotiana tabacum) is a member of the Solanaceae, one of the agronomically most important grou
104 is of TFs has been made from a member of the Solanaceae, one of the most important families of vascul
105 ly prior to or after the radiation of either Solanaceae or Rubiaceae as has been recently suggested.
109 tobacco) fails to activate Rubisco from non-Solanaceae plants (e.g. spinach and Chlamydomonas reinha
112 mato plants and many of its relatives in the Solanaceae produce a mixture of O-acyl sugars that contr
113 lanum lycopersicum) and other species in the Solanaceae produce and secrete a mixture of O-acylsugars
114 sicum) and many other species throughout the Solanaceae produce and secrete mixtures of sugar esters
115 mes of many plants in the nightshade family (Solanaceae) produce O-acylsugars, and in cultivated and
118 te 2006, interest and participation from the Solanaceae research community has been strong and growin
119 ) was formed as an umbrella organization for Solanaceae research in over 30 countries to address impo
120 air of congeners from each of five genera in Solanaceae reveals extensive transgeneric evolution of L
128 neralist Trichoplusia ni and the facultative Solanaceae-specialist Manduca sexta, was significantly i
129 notable differences between tobacco and non-Solanaceae species in TF family size and evidence for bo
132 the whole-genome triplication identified in Solanaceae species such as tomato, the genome includes s
133 SGN currently houses map and marker data for Solanaceae species, a large expressed sequence tag colle
134 ly from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species, but also from representatives of oth
135 se/oxygenase (Rubisco, EC 4.1.1.39) from non-Solanaceae species, including the green alga Chlamydomon
139 owever, that in the nightshade plant family (Solanaceae), species with functional self-incompatibilit
141 ato and feeds on several wild species in the Solanaceae, such as S. eleagnifolium and S. rostratum Du
142 ited resistance in both the Brassicaceae and Solanaceae suggests that this trait may be more widely d
143 hat allow plants to avoid inbreeding--in the Solanaceae (the nightshade family) is controlled by a po
144 umbers fall within the range observed in the Solanaceae, the only other family with RNase-based incom
148 a positional candidate gene approach in the Solanaceae, these genes were genetically mapped in peppe
152 ns of red flower color in the tomato family, Solanaceae, using large-scale data mining and new sequen
153 nt genomes, indicating that evolution of the Solanaceae was not associated with the gain or loss of T
154 in the ground cherry, Physalis crassifolia (Solanaceae), was surveyed in a natural population occurr
155 ion of these early Eocene fossils shows that Solanaceae were well diversified long before final Gondw
157 ter to the well-documented phenomenon in the Solanaceae where SC accompanying polyploidization is fre
159 es similar biology with other members of the Solanaceae, yet has features unique within the family, s
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