ライフサイエンスコーパス: Lycopersicon esculentum

1 ted a family of CTR1- like genes in tomato ( Lycopersicon esculentum ).

2 S (LeAOS) and HPL (LeHPL) cDNAs from tomato (Lycopersicon esculentum).

3 ges of growing and ripening fruit of tomato (Lycopersicon esculentum).

4 thia, tobacco, alfalfa, soybean, and tomato (Lycopersicon esculentum).

5 ecies like Nicotiana benthamiana and tomato (Lycopersicon esculentum).

6 nase (EC 2.7.1.4) were isolated from tomato (Lycopersicon esculentum).

7 NA extracted from premeiotic tomato flowers (Lycopersicon esculentum).

8 and LHA4, was previously detected in tomato (Lycopersicon esculentum).

9 sociated protein first identified in tomato (Lycopersicon esculentum).

10 red arabinogalactan-protein (AGP) in tomato (Lycopersicon esculentum).

11 f the SW5 resistance gene cluster in tomato (Lycopersicon esculentum).

12 novel gene induced in the Pi-starved tomato (Lycopersicon esculentum).

13 The promoter region of tomato (Lycopersicon esculentum) 3-hydroxy-3-methylglutaryl coen

14 ity to modulate peroxide efflux, and tomato (Lycopersicon esculentum), a nonlegume, showed no respons

15 Silencing tomato (Lycopersicon esculentum) ACRE276 leads to breakdown of C

16 A well-characterized classical tomato (Lycopersicon esculentum) AGP containing a glycosylphosph

17 cco (Nicotiana tabacum) of the major tomato (Lycopersicon esculentum) AGP, LeAGP-1, as an enhanced gr

18 Our analysis of four mutants of tomato (Lycopersicon esculentum) altered in their response to gr

19 BC1 population of the self-compatible tomato Lycopersicon esculentum and its wild self-incompatible r

20 dissection seen between two tomato species, Lycopersicon esculentum and L. pennellii.

21 A sesquidiploid hybrid having two genomes of Lycopersicon esculentum and one of Solanum lycopersicoid

22 thaliana, Nicotiana benthamiana, N. tabacum, Lycopersicon esculentum and others could be used as a ma

23 total folate pools in Arabidopsis thaliana, Lycopersicon esculentum and Pisum sativum tissues.

24 ychus urticae Koch), with cultivated tomato (Lycopersicon esculentum) and an isogenic mutant line (de

25 as isolated from a cDNA library from tomato (Lycopersicon esculentum) and characterized.

26 hibitor protein (XEGIP) precursor in tomato (Lycopersicon esculentum) and its homolog in potato (Sola

27 xperiments with ethylene-insensitive tomato (Lycopersicon esculentum) and petunia (Petunia x hybrida)

28 e devastating late blight disease of tomato (Lycopersicon esculentum) and potato (Solanum tuberosum),

29 rotein gene, viscosity 1 (vis1) from tomato (Lycopersicon esculentum) and provide evidence that it pl

30 F(1) hybrids between the cultivated tomato (Lycopersicon esculentum) and the wild nightshade Solanum

31 directed growth toward nearby tomato plants (Lycopersicon esculentum) and toward extracted tomato-pla

32 al growth in the interaction between tomato (Lycopersicon esculentum) and virulent Xanthomonas campes

33 ponse, the compatible interaction of tomato (Lycopersicon esculentum) and Xanthomonas campestris pv v

34 e pv. tomato (Pst) in the cultivated tomato, Lycopersicon esculentum, and the closely related L. pimp

35 says to investigate the targeting of tomato (Lycopersicon esculentum) AOS (LeAOS) and HPL (LeHPL) to

36 hirsutum was introgressed into a susceptible Lycopersicon esculentum background to create the near-is

37 In contrast, the cultivated tomato (Lycopersicon esculentum) bears flowers with flush or ins

38 protein (LeFolB1) was obtained from tomato (Lycopersicon esculentum) by reverse transcription-PCR.

39 opsis, encodes three CBF homologs, LeCBF1-3 (Lycopersicon esculentum CBF1-3), that are present in tan

40 We isolated two tomato (Lycopersicon esculentum) cDNA clones, tomPRO1 and tomPRO

41 A truncated tomato (Lycopersicon esculentum) cDNA lacking the targeting sequ

42 The tomato (Lycopersicon esculentum) Cf-9 resistance gene encodes th

43 some from the JOINTLESS locus on the tomato (Lycopersicon esculentum) chromosome 11 contained 15 puta

44 Pto kinase of tomato (Lycopersicon esculentum) confers resistance to bacterial

45 Stable transformation of tomato (Lycopersicon esculentum cv Ailsa Craig) plants with a co

46 The tomato (Lycopersicon esculentum cv Ailsa Craig) polygalacturonas

47 olated from auxin-treated, etiolated tomato (Lycopersicon esculentum cv T5) hypocotyls.

48 XETs are encoded by a gene family in tomato (Lycopersicon esculentum cv T5).

49 alent BAC library for the cultivated tomato, Lycopersicon esculentum cv. Heinz 1706.

50 Meloidogyne incognita in transgenic roots of Lycopersicon esculentum cv. Motelle composite plants.

51 st abundant sesquiterpene in the leaf oil of Lycopersicon esculentum cv. VFNT Cherry, with lesser amo

52 roots, and red and green pericarp of tomato (Lycopersicon esculentum, cv VFNT and cv Momotaro).

53 nted by heat-treating mature green tomatoes (Lycopersicon esculentum, cv. Mountain Springs) at 42 deg

54 a mays L.) endoplasmic reticulum and tomato (Lycopersicon esculentum) cytoplasmic Stress70 proteins w

55 leaves of Pisum sativum, Phaseolus vulgaris, Lycopersicon esculentum, Daucus carota sativum, Raphanus

56 abacum) after mechanical damage, and tomato (Lycopersicon esculentum) during drought stress.

57 Tomatoes (Lycopersicon esculentum) express two forms of leucine am

58 zymes was substantially inhibited in tomato (Lycopersicon esculentum) following illumination at 4 deg

59 ellifolium gene bred into cultivated tomato (Lycopersicon esculentum) for resistance to Cladosporium

60 ctanase (EC 3.2.1.23) present during tomato (Lycopersicon esculentum) fruit ripening, was suppressed

61 ession of the HMG1 and HMG2 genes in tomato (Lycopersicon esculentum) fruit using arachidonic acid (A

62 s specifically expressed in ripening tomato (Lycopersicon esculentum) fruit where cell wall disassemb

63 Transgenic tomato (Lycopersicon esculentum) fruits in which endogenous ethy

64 visiae) two-hybrid screen, using the tomato (Lycopersicon esculentum) FTase alpha-subunit (FTA) as ba

65 screen in yeast, we have isolated a tomato (Lycopersicon esculentum) gene encoding a phospholipid hy

66 The epinastic (epi) mutant of tomato (Lycopersicon esculentum) has a dark-grown seedling pheno

67 The cultivated tomato (Lycopersicon esculentum) has a unipinnate compound leaf.

68 Gase cDNA clone, Cel4, isolated from tomato (Lycopersicon esculentum) has been shown to be identical

69 wn to block rapid auxin reactions of tomato (Lycopersicon esculentum) hypocotyls.

70 ) by spinach (Spinacia oleracea) and tomato (Lycopersicon esculentum) in solutions with or without me

71 abidopsis (Arabidopsis thaliana) and tomato (Lycopersicon esculentum) indicate that at least one-thir

72 e family of apoplastic invertases in tomato (Lycopersicon esculentum), is a quantitative trait locus

73 perfect discrimination between the different Lycopersicon esculentum L. cultivars considered.

74 metabolomic expression of different tomato (Lycopersicon esculentum L.) cultivars--Plum, Campari, Gr

75 ed the structure and expression of a tomato (Lycopersicon esculentum L.) phosphate starvation-induced

76 be the tissue-specific regulation of tomato (Lycopersicon esculentum L.) Pi-transporter genes by Pi.

77 I) and II (Inh II) in young, excised tomato (Lycopersicon esculentum L.) plants were investigated.

78 y members, namely tobacco EREBP2 and tomato (Lycopersicon esculentum L.) Pti4/5/6.

79 olation of two coding sequences from tomato (Lycopersicon esculentum L.) which encode phylogeneticall

80 low-water-potential induction of the tomato (Lycopersicon esculentum) le25 promoter were selected.

81 The tomato (Lycopersicon esculentum) Lea-Gal gene under the control

82 MAPKs, we cloned three MAPKs from a tomato (Lycopersicon esculentum) leaf cDNA library, generated me

83 Lycopersicon esculentum leaves, usually considered as a

84 systemin-dependent wound response in tomato (Lycopersicon esculentum) leaves.

85 injected fluorescent cationic liposomes and Lycopersicon esculentum lectin and by CD31 (PECAM) immun

86 ascularly administered, fluorescence-labeled Lycopersicon esculentum lectin in frozen tumor sections.

87 vascularity, assessed in whole mounts after Lycopersicon esculentum lectin staining, increased in bo

88 r nitrate to mark EC borders or biotinylated Lycopersicon esculentum lectin to label the EC surface a

89 l transferase-mediated nick end labeling and Lycopersicon esculentum lectin.

90 ed farnesyl-protein transferase from tomato (Lycopersicon esculentum, LeFTase) to analyze its biochem

91 We have isolated three tomato (Lycopersicon esculentum, M.) cDNAs (LeRab 1A, B, and C)

92 As in Arabidopsis and tomato (Lycopersicon esculentum), maize shoots failed to initiat

93 expansin genes has been observed in tomato (Lycopersicon esculentum) meristems, expanding tissues, a

94 lase (AGP) in developing pericarp of tomato (Lycopersicon esculentum Mill) has been investigated by i

95 cklebur (Xanthium strumarium L.) and tomato (Lycopersicon esculentum Mill), but 0.1 cubic centimeter

96 iosynthesis of RFOs, was cloned from tomato (Lycopersicon esculentum Mill. cv Moneymaker) seeds, and

97 Seedlings of Lycopersicon esculentum Mill. cv Rutgers emit a pulse of

98 oding profilin from pollen grains of tomato (Lycopersicon esculentum Mill. cv. Moneymaker).

99 Plants of tomato (Lycopersicon esculentum Mill. cv. T5) were transformed w

100 t size between large, domesticated tomatoes (Lycopersicon esculentum Mill.) and their small-fruited w

101 Tomato (Lycopersicon esculentum Mill.) endo-beta-1,4-glucanase C

102 of the mannan-rich cell walls of the tomato (Lycopersicon esculentum Mill.) endosperm during germinat

103 The dumpy (dpy) mutant of tomato (Lycopersicon esculentum Mill.) exhibits short stature, r

104 om total RNA of the ethylene-treated tomato (Lycopersicon esculentum Mill.) flower abscission zone by

105 lactosidase II, a protein present in tomato (Lycopersicon esculentum Mill.) fruit during ripening and

106 ctanase (EC 3.2.1.23) present during tomato (Lycopersicon esculentum Mill.) fruit ripening, a family

107 hosphorylase (AGP) was purified from tomato (Lycopersicon esculentum Mill.) fruit to apparent homogen

108 istant diageotropica (dgt) mutant of tomato (Lycopersicon esculentum Mill.) in a range of auxin- and

109 istant diageotropica (dgt) mutant of tomato (Lycopersicon esculentum Mill.) includes reduced gravitro

110 ene in gravitropism by hypocotyls of tomato (Lycopersicon esculentum Mill.) indicate that gravitropis

111 Transgenic tomato (Lycopersicon esculentum Mill.) plants expressing a const

112 Tomato (Lycopersicon esculentum Mill.) plants, which normally do

113 tation, suspension-cultured cells of tomato (Lycopersicon esculentum Mill.) secrete phosphodiesterase

114 expansin genes that are expressed in tomato (Lycopersicon esculentum Mill.) seeds during germination.

115 rellin (GA)-deficient (gib-1) mutant tomato (Lycopersicon esculentum Mill.) seeds is dependent upon e

116 in the micropylar tissues of imbibed tomato (Lycopersicon esculentum Mill.) seeds prior to radicle em

117 Radicle protrusion from tomato (Lycopersicon esculentum Mill.) seeds to complete germina

118 genes were expressed in germinating tomato (Lycopersicon esculentum Mill.) seeds, one of which (LeEX

119 nalysis were used to detect specific tomato (Lycopersicon esculentum Mill.) transcripts in dodder gro

120 coding sequence in transgenic tomato plants (Lycopersicon esculentum Mill.) under the control of a co

121 is induced early after infection of tomato (Lycopersicon esculentum Mill.) with root-knot nematodes

122 omonas campestris pv. vesicatoria in tomato (Lycopersicon esculentum Mill.).

123 d cDNA clone (pLE16) from cultivated tomato (Lycopersicon esculentum Mill.).

124 ) subunits of the SnRK1 complex from tomato (Lycopersicon esculentum Mill.).

125 equence were constructed and introduced into Lycopersicon esculentum (Mill cv. Ailsa Craig) and Nicot

126 Two tomato (Lycopersicon esculentum) mutants with dark testae displa

127 regulation of ethylene responses in tomato (Lycopersicon esculentum) occurs at the level of hormone

128 s the potato (Solanum tuberosum) and tomato (Lycopersicon esculentum) pathogen Phytophthora infestans

129 2,152-fold, respectively, from ripe tomato (Lycopersicon esculentum) pericarp.

130 tion and characterization of a novel tomato (Lycopersicon esculentum) phosphate starvation-induced ge

131 respectively), an EGase cloned from tomato (Lycopersicon esculentum) pistils, than to any other repo

132 enerated transgenic Arabidopsis thaliana and Lycopersicon esculentum plants that are highly resistant

133 Here we demonstrate that fruit from tomato (Lycopersicon esculentum) plants expressing Arabidopsis (

134 ns and confers disease resistance in tomato (Lycopersicon esculentum) plants in the absence of avrPto

135 stemin-mediated defense signaling in tomato (Lycopersicon esculentum) plants is analogous to the cyto

136 It has been shown that tomato (Lycopersicon esculentum) plants respond to flame woundin

137 nse to wounding in leaves of excised tomato (Lycopersicon esculentum) plants was inhibited by NO dono

138 tion of other wound-related genes in tomato (Lycopersicon esculentum) plants.

139 ecently reported on the cloning of a tomato (Lycopersicon esculentum) polygalacturonase (PG) cDNA, TA

140 e hydrolysis of cell wall pectins by tomato (Lycopersicon esculentum) polygalacturonase (PG) in vitro

141 The tomato (Lycopersicon esculentum) protein, termed XEG inhibitor p

142 The tomato (Lycopersicon esculentum) resistance gene Pto confers res

143 A subtractive tomato (Lycopersicon esculentum) root cDNA library enriched in g

144 array consisting of 1,280 genes from tomato (Lycopersicon esculentum) roots for expression profiling

145 eta-mannanase genes are expressed in tomato (Lycopersicon esculentum) seeds (LeMAN1 and LeMAN2) and f

146 d in the micropylar endosperm cap of tomato (Lycopersicon esculentum) seeds just before radicle emerg

147 as active in the alkalinization response in Lycopersicon esculentum suspension-cultured cells.

148 rization of a JA-deficient mutant of tomato (Lycopersicon esculentum) that lacks local and systemic e

149 matrix-localized protein (MFP1) from tomato (Lycopersicon esculentum) that preferentially binds to MA

150 s thaliana), pea (Pisum sativum), or tomato (Lycopersicon esculentum) tissues, no reduction of the pt

151 otein gene family were isolated from tomato (Lycopersicon esculentum) to characterize their role in d

152 in kinase that confers resistance in tomato (Lycopersicon esculentum) to Pseudomonas syringae pv toma

153 Here, we report the characterization of a Lycopersicon esculentum (tomato) cDNA whose predicted am

154 intravital injection of fluorescein-labeled Lycopersicon esculentum (tomato) lectin.

155 zation of two genes (LeARG1 and LeARG2) from Lycopersicon esculentum (tomato) that encode arginase.

156 berosum (potato), S. demissum, S. chacoense, Lycopersicon esculentum (tomato), and L. hirsutum.

157 pression libraries for cDNAs from the plant, Lycopersicon esculentum (tomato), and the invertebrate a

158 , Ricinus communis agglutinin-1 [RCA-1], and Lycopersicon esculentum, tomato lectin (TL), which recog

159 Pti4 is a tomato (Lycopersicon esculentum) transcription factor that belon

160 Tomato (Lycopersicon esculentum var. Better Boy) plants were tra

161 which cold acclimate, as well as in tomato (Lycopersicon esculentum var. Bonny Best, Castle Mart, Mi

162 the genetic background of cultivated tomato (Lycopersicon esculentum) was used to study factors affec

163 n of a novel AOS-encoding cDNA (LeAOS3) from Lycopersicon esculentum whose predicted amino acid seque

164 PME gene (designated as pmeu1) from tomato (Lycopersicon esculentum) with an expression that is high

165 The tomato (Lycopersicon esculentum) yg-2 and Nicotiana plumbaginifo