ライフサイエンスコーパス: Solanum tuberosum

1 psis, bean (Phaseolus vulgaris), and potato (Solanum tuberosum).

2 the pentose-phosphate pathway, from potato (Solanum tuberosum).

3 similarity to the SK2 chitinase from potato (Solanum tuberosum).

4 noncanonical AIM motif in ATG3 from potato (Solanum tuberosum).

5 ant architecture and tuberization in potato (Solanum tuberosum).

6 ral crops, has not been developed in potato (Solanum tuberosum).

7 ted by an unidentified resistance in potato (Solanum tuberosum).

8 associated with CENH3 nucleosomes in potato (Solanum tuberosum).

9 abidopsis (Arabidopsis thaliana) and potato (Solanum tuberosum).

10 icum), pepper (Capsicum annuum), and potato (Solanum tuberosum).

11 ted from a segregating population of potato (Solanum tuberosum).

12 sicon esculentum) and its homolog in potato (Solanum tuberosum).

13 near-colinear genomes of tomato and potato (Solanum tuberosum).

14 a plumbaginifolia), Arabidopsis, and potato (Solanum tuberosum).

15 of Cultivar Groups within the single species Solanum tuberosum.

16 loid species, such as the tetraploid potato, Solanum tuberosum (2n = 4x = 48).

17 abundant in vegetative meristems of potato (Solanum tuberosum), accumulating specifically in the tun

18 tive, low-activity form of the potato tuber (Solanum tuberosum) AGPase (small subunit homotetramer) r

19 d regulation of the APETALA2 gene in potato (Solanum tuberosum) and demonstrated conservation of MIR3

20 ual reproduction in the crop species potato (Solanum tuberosum) and strawberry (Fragaria spp), where

21 quantify all expressed PPOs in potato tuber (Solanum tuberosum) and to purify and characterize the ma

22 nt pathogenic oomycetes, such as the potato (Solanum tuberosum) and tomato (Lycopersicon esculentum)

23 Potato (Solanum tuberosum) and tomato (Solanum lycopersicon) cro

24 S-locus remnants of self-compatible potato (Solanum tuberosum) and tomato (Solanum lycopersicum).

25 Arabidopsis (Arabidopsis thaliana), potato (Solanum tuberosum), and white lupin, making them ideal c

26 Andean potatoes (Solanum tuberosum andigenum) are a staple food for Andea

27 However, application of exogenous potato (Solanum tuberosum) apyrase (ATPase) decreased ROS activi

28 uble E-type ATPases, including potato tuber (Solanum tuberosum) apyrase and parasite ecto-ATPase, are

29 uting and maintaining the quality of potato, Solanum tuberosum 'Asterix', during cold storage.

30 proteins from maize (Zea mays BE2a), potato (Solanum tuberosum BE1), and Escherichia coli (glycogen B

31 sequences encoding prosystemin from potato (Solanum tuberosum), black nightshade (S. nigrum), and be

32 ion (Ds) elements into the nuclei of potato (Solanum tuberosum) cells.

33 fully applied RenSeq to the sequenced potato Solanum tuberosum clone DM, and increased the number of

34 gated using wild-type and transgenic potato (Solanum tuberosum cv Desiree) plants in which urease act

35 Here, we show that host potato plants (Solanum tuberosum cv. Desiree) selectively allocate carb

36 Transgenic potato (Solanum tuberosum cv. Jowon) constitutively overexpressi

37 te dehydrogenase complex (mPDC) from potato (Solanum tuberosum cv. Romano) can be disassociated in 1

38 product (PKIN503) was amplified from potato (Solanum tuberosum) cv. Desiree using oligonucleotide pri

39 Transformation of Solanum tuberosum, cv. Desiree, with the tomato prosyste

40 The potato (Solanum tuberosum) cyst nematode Globodera pallida induc

41 usal agent of late blight disease of potato (Solanum tuberosum), depends on multilayered defense resp

42 ement of a specific leaf LOX gene of potato (Solanum tuberosum), designated POTLX-3 (GenBank/EMBL acc

43 ortant crop and model plants such as potato (Solanum tuberosum), eggplant (Solanum melongena), pepper

44 d species, such as the autotetraploid potato Solanum tuberosum, face a variety of challenges during m

45 na, tobacco (Nicotiana tabacum), and potato (Solanum tuberosum) failed to produce wiry leaves, sugges

46 ity to petunia (Petunia hybrida) and potato (Solanum tuberosum) FLS.

47 ia were isolated from dormant potato tubers (Solanum tuberosum 'Folva') and their proteome investigat

48 for the high throughput field phenotyping of Solanum tuberosum for differences in stomatal behaviour.

49 ical with a previously characterized potato (Solanum tuberosum) fructokinase.

50 StBEL5 of potato (Solanum tuberosum) functions as a mobile RNA signal that

51 nchored to 12 chromosomes, using the potato (Solanum tuberosum) genome sequence as a reference.

52 raploid potatoes originated from the diploid Solanum tuberosum group Stenotomum.

53 Potato (Solanum tuberosum) has the densest genetic linkage map a

54 tomato (Lycopersicon esculentum) and potato (Solanum tuberosum), has evolved an arsenal of protease i

55 Potato (Solanum tuberosum) homeobox 1 (POTH1) is a class I homeo

56 erfering RNAs (siRNAs) from Sl ACA10 and its Solanum tuberosum homolog.

57 Hydroalcoholic extracts from Solanum tuberosum, Ipomoea batatas, S. lycocarpum, and f

58 Potato (Solanum tuberosum) is a significant non-grain food crop

59 Potato (Solanum tuberosum) is the fourth largest food crop in th

60 Potato (Solanum tuberosum) is the third crucial global crop faci

61 Potato (Solanum tuberosum) is the third most important food crop

62 Tetraploid cultivated potato (Solanum tuberosum) is the World's fourth most important

63 The potato cDNAs Solanum tuberosum isovaleryl-CoA dehydrogenases 1 and 2

64 cerevisiae) two-hybrid system and a potato (Solanum tuberosum) KNOX protein, designated POTH1, as ba

65 n numerous aspects of development in potato (Solanum tuberosum L).

66 tion between AMF and potato virus Y (PVY) in Solanum tuberosum L.

67 or unintended composition changes in potato (Solanum tuberosum L. cv. Desiree) tubers, which have bee

68 ght on the composition of transgenic potato (Solanum tuberosum L. cv. Desiree) with reduced glycoalka

69 The gene was introduced to Solanum tuberosum L. cv. Russet Burbank by Agrobacterium

70 The potato tuber (Solanum tuberosum L.) ADP-glucose pyrophosphorylase (ADP

71 The potato tuber (Solanum tuberosum L.) ADP-glucose pyrophosphorylase acti

72 A potato (Solanum tuberosum L.) AGPase LS down-regulatory mutant (

73 e and biochemical responses of three potato (Solanum tuberosum L.) cultivars to drought and aphid (My

74 on on growth and tuberization of two potato (Solanum tuberosum L.) cultivars, Kennebec and Superior.

75 from six American and nine European potato (Solanum tuberosum L.) cultivars.

76 amino-acid-residue epitope tag to a potato (Solanum tuberosum L.) HMGR isoform and expressed this no

77 Potato (Solanum tuberosum L.) is cultivated for its tubers, whic

78 tuberization in the major crop plant potato (Solanum tuberosum L.) is of importance to secure yield e

79 Potato (Solanum tuberosum L.) is the most important tuber crop w

80 Potato (Solanum tuberosum L.) is the world's most important non-

81 The growth and tuberization of potatoes (Solanum tuberosum L.) maintained for 6 weeks under four

82 Potato (Solanum tuberosum L.) single-node explants undergoing in

83 ress conditions were correlated with potato (Solanum tuberosum L.) tuber protein synthesis.

84 heterotetrameric ADP-Glc PPase from potato (Solanum tuberosum L.) tuber, the homologous residue is p

85 in the heterotetrameric enzyme from potato (Solanum tuberosum L.) tubers.

86 eristems isolated from field-grown potatoes (Solanum tuberosum L.) was determined during a 7-month st

87 clonal propagation of the cultivated potato (Solanum tuberosum L.)(1,2) dictate a slow, non-accumulat

88 omes of six accessions of cultivated potato (Solanum tuberosum L.), a vegetatively propagated autotet

89 far for the extent of LD, cultivated potato (Solanum tuberosum L.), an outcrossing species, is a high

90 us carota var. sativa Hoffm.), sweet potato (Solanum tuberosum L.), cucumber (Cucumis sativus L.), to

91 Cultivated potatoes (Solanum tuberosum L.), domesticated from wild Solanum sp

92 temperature on the RS contents of potatoes (Solanum tuberosum L.).

93 (Momordica charantia Descourt.), and potato (Solanum tuberosum L.).

94 ter chestnut (Eleocharis dulcis L.), potato (Solanum tuberosum L.; Bintje), and carrot (Daucus carota

95 ryl coenzyme A reductase (HMGR) from potato (Solanum tuberosum) L. tubers.

96 he Ca(2+) biosensor apoaequorin into potato (Solanum tuberosum, Lcv. Desiree).

97 espiration was altered in transgenic potato (Solanum tuberosum) lines by overexpression of the altern

98 ghum bicolor), Arabidopsis thaliana, potato (Solanum tuberosum), Medicago truncatula, and poplar (Pop

99 Immunoblot analysis of potato (Solanum tuberosum) mitochondria demonstrated that PSD is

100 Potato (Solanum tuberosum) multicystatin (PMC) is a crystalline

101 Potato (Solanum tuberosum) multicystatin (PMC) is a unique cysta

102 Here we report that the potato (Solanum tuberosum) NLR gene RB undergoes AS of its intro

103 ly cultivar amongst those tested with a pure Solanum tuberosum origin and A cooking type.

104 from sugar beet (Beta vulgaris) and potato (Solanum tuberosum) pectin in vitro.

105 a (Petunia hybrida; PhpreproHypSys), potato (Solanum tuberosum; PhpreproHypSys), and sweet potato (Ip

106 eds of marker-free and backbone-free potato (Solanum tuberosum) plants displaying reduced expression

107 ycopersicum (tomato), Solanum pennellii, and Solanum tuberosum (potato) - using herbarium samples fro

108 s study identified three BiP homologs in the Solanum tuberosum (potato) genome using phylogenetic, am

109 date this system in Arabidopsis thaliana and Solanum tuberosum (potato) grown hydroponically and in s

110 As a proof-of-concept, we generated Solanum tuberosum (potato) macro-chloroplast lines overe

111 endodermis, bark, specialized organs (e.g., Solanum tuberosum (potato) tubers), and seed coats.

112 m a variety of solanaceous species including Solanum tuberosum (potato), S. demissum, S. chacoense, L

113 produced here incorporated differing potato (Solanum tuberosum) rbcL-rbcS operons that either encoded

114 In cultivated tetraploid potato (Solanum tuberosum), reduction to diploidy (dihaploidy) a

115 ty to this phenomenon, we analyzed potatoes (Solanum tuberosum) regenerated from either protoplasts o

116 fficient for tight direct binding of potato (Solanum tuberosum) REMORIN 1.3 (StREM1.3) to the PM.

117 Here, we show that potato (Solanum tuberosum) resistance protein R3a relocates from

118 We have used the potato (Solanum tuberosum) Rx protein, which confers resistance

119 The cultivated potato (Solanum tuberosum) shares similar biology with other mem

120 TIF1 contains sequence similarity to the Solanum tuberosum single strand-specific transcription f

121 In cultivated potato (Solanum tuberosum), six PP2A catalytic subunits (StPP2Ac

122 Recently, a maize (Zea mays)/potato (Solanum tuberosum) small subunit mosaic, MP [Mos(1-198)]

123 eld, but stimulates aerial tubers in potato (Solanum tuberosum ssp andigena) under short-day (SD) pho

124 ar phenotypes of GERMIN3 transgenic lines in Solanum tuberosum ssp.

125 of these cDNAs is highly polymorphic within Solanum tuberosum ssp. tuberosum, containing mainly a si

126 In potato (Solanum tuberosum), StBEL5 and its Knox protein partner

127 nalyses, we previously identified in potato (Solanum tuberosum) StRGGA, coding for an Arginine Glycin

128 In potato (Solanum tuberosum subsp. andigena), the BEL1-like transc

129 spp.), cassava (Manihot esculenta), potato (Solanum tuberosum), sweet potato (Ipomoea batatas), and

130 CLAVATA2-like receptor (StCLV2) from potato (Solanum tuberosum) than its nonglycosylated forms.

131 cysteine-rich peptide isolated from potato (Solanum tuberosum) that was classified as a member of th

132 In potato (Solanum tuberosum), the BEL1 transcription factor St BEL

133 In potato (Solanum tuberosum), the BELL1 transcription factor StBEL

134 Potato (Solanum tuberosum), the third most important food crop g

135 accessions, and S. lycopersicum/S. pennellii/Solanum tuberosum (three-way polymorphic) are included.

136 ymbiont infection by exposing potato plants (Solanum tuberosum) to psyllids infected with "Candidatus

137 and Rx1, which confer resistance in potato (Solanum tuberosum) to the cyst nematode Globodera pallid

138 denosylmethionine decarboxylase from potato, Solanum tuberosum, to 2.3 A resolution.

139 ystem and mosaic AGPases composed of potato (Solanum tuberosum) tuber and maize (Zea mays) endosperm

140 e effects on starch synthesis in the potato (Solanum tuberosum) tuber and seeds of important cereals.

141 all subunits of the heterotetrameric potato (Solanum tuberosum) tuber enzyme.

142 effect of reduced N availability on potato (Solanum tuberosum) tuber yield and quality traits using

143 Potato (Solanum tuberosum) tuber, a swollen underground stem, is

144 those in other tissues, such as the potato (Solanum tuberosum) tuber, are heat stable.

145 In potato (Solanum tuberosum), tuber integrity is dependent on sube

146 Wound tissue in potato (Solanum tuberosum) tubers, and all higher plants, is com

147 In potato (Solanum tuberosum), tubers develop from underground stol

148 The cultivated potato, Solanum tuberosum, ultimately traces its origin to Andea

149 gulate the expression of fumarase in potato (Solanum tuberosum) under the control of the tuber-specif

150 develop high-resolution DHS maps in potato (Solanum tuberosum) using chromatin isolated from tubers

151 g variation in primary metabolism in potato (Solanum tuberosum), we have profiled primary metabolite

152 of important crop species including potato (Solanum tuberosum) which is grown for its underground st

153 evidence concerning the early use of potato (Solanum tuberosum) within its botanical locus of origin

154 We identified eight putative StYUC (Solanum tuberosum YUCCA) genes whose deduced amino acid