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1  the pentose-phosphate pathway, from potato (Solanum tuberosum).
2 similarity to the SK2 chitinase from potato (Solanum tuberosum).
3 ant architecture and tuberization in potato (Solanum tuberosum).
4 ral crops, has not been developed in potato (Solanum tuberosum).
5 ted by an unidentified resistance in potato (Solanum tuberosum).
6 associated with CENH3 nucleosomes in potato (Solanum tuberosum).
7 abidopsis (Arabidopsis thaliana) and potato (Solanum tuberosum).
8 icum), pepper (Capsicum annuum), and potato (Solanum tuberosum).
9 sicon esculentum) and its homolog in potato (Solanum tuberosum).
10  near-colinear genomes of tomato and potato (Solanum tuberosum).
11 a plumbaginifolia), Arabidopsis, and potato (Solanum tuberosum).
12 psis, bean (Phaseolus vulgaris), and potato (Solanum tuberosum).
13 of Cultivar Groups within the single species Solanum tuberosum.
14  abundant in vegetative meristems of potato (Solanum tuberosum), accumulating specifically in the tun
15 tive, low-activity form of the potato tuber (Solanum tuberosum) AGPase (small subunit homotetramer) r
16 d regulation of the APETALA2 gene in potato (Solanum tuberosum) and demonstrated conservation of MIR3
17 ual reproduction in the crop species potato (Solanum tuberosum) and strawberry (Fragaria spp), where
18 nt pathogenic oomycetes, such as the potato (Solanum tuberosum) and tomato (Lycopersicon esculentum)
19  Arabidopsis (Arabidopsis thaliana), potato (Solanum tuberosum), and white lupin, making them ideal c
20                             Andean potatoes (Solanum tuberosum andigenum) are a staple food for Andea
21    However, application of exogenous potato (Solanum tuberosum) apyrase (ATPase) decreased ROS activi
22 uble E-type ATPases, including potato tuber (Solanum tuberosum) apyrase and parasite ecto-ATPase, are
23 proteins from maize (Zea mays BE2a), potato (Solanum tuberosum BE1), and Escherichia coli (glycogen B
24  sequences encoding prosystemin from potato (Solanum tuberosum), black nightshade (S. nigrum), and be
25 ion (Ds) elements into the nuclei of potato (Solanum tuberosum) cells.
26 fully applied RenSeq to the sequenced potato Solanum tuberosum clone DM, and increased the number of
27 gated using wild-type and transgenic potato (Solanum tuberosum cv Desiree) plants in which urease act
28                           Transgenic potato (Solanum tuberosum cv. Jowon) constitutively overexpressi
29 te dehydrogenase complex (mPDC) from potato (Solanum tuberosum cv. Romano) can be disassociated in 1
30 product (PKIN503) was amplified from potato (Solanum tuberosum) cv. Desiree using oligonucleotide pri
31                            Transformation of Solanum tuberosum, cv. Desiree, with the tomato prosyste
32 usal agent of late blight disease of potato (Solanum tuberosum), depends on multilayered defense resp
33 ement of a specific leaf LOX gene of potato (Solanum tuberosum), designated POTLX-3 (GenBank/EMBL acc
34 ortant crop and model plants such as potato (Solanum tuberosum), eggplant (Solanum melongena), pepper
35 na, tobacco (Nicotiana tabacum), and potato (Solanum tuberosum) failed to produce wiry leaves, sugges
36 ity to petunia (Petunia hybrida) and potato (Solanum tuberosum) FLS.
37 ia were isolated from dormant potato tubers (Solanum tuberosum 'Folva') and their proteome investigat
38 for the high throughput field phenotyping of Solanum tuberosum for differences in stomatal behaviour.
39 ical with a previously characterized potato (Solanum tuberosum) fructokinase.
40                            StBEL5 of potato (Solanum tuberosum) functions as a mobile RNA signal that
41 nchored to 12 chromosomes, using the potato (Solanum tuberosum) genome sequence as a reference.
42                                      Potato (Solanum tuberosum) has the densest genetic linkage map a
43 tomato (Lycopersicon esculentum) and potato (Solanum tuberosum), has evolved an arsenal of protease i
44                                      Potato (Solanum tuberosum) homeobox 1 (POTH1) is a class I homeo
45 erfering RNAs (siRNAs) from Sl ACA10 and its Solanum tuberosum homolog.
46                                      Potato (Solanum tuberosum) is the third most important food crop
47                Tetraploid cultivated potato (Solanum tuberosum) is the World's fourth most important
48                             The potato cDNAs Solanum tuberosum isovaleryl-CoA dehydrogenases 1 and 2
49  cerevisiae) two-hybrid system and a potato (Solanum tuberosum) KNOX protein, designated POTH1, as ba
50 n numerous aspects of development in potato (Solanum tuberosum L).
51 or unintended composition changes in potato (Solanum tuberosum L. cv. Desiree) tubers, which have bee
52 ght on the composition of transgenic potato (Solanum tuberosum L. cv. Desiree) with reduced glycoalka
53                   The gene was introduced to Solanum tuberosum L. cv. Russet Burbank by Agrobacterium
54                            The potato tuber (Solanum tuberosum L.) ADP-glucose pyrophosphorylase (ADP
55                            The potato tuber (Solanum tuberosum L.) ADP-glucose pyrophosphorylase acti
56                                    A potato (Solanum tuberosum L.) AGPase LS down-regulatory mutant (
57 on on growth and tuberization of two potato (Solanum tuberosum L.) cultivars, Kennebec and Superior.
58  from six American and nine European potato (Solanum tuberosum L.) cultivars.
59  amino-acid-residue epitope tag to a potato (Solanum tuberosum L.) HMGR isoform and expressed this no
60     The growth and tuberization of potatoes (Solanum tuberosum L.) maintained for 6 weeks under four
61                                      Potato (Solanum tuberosum L.) single-node explants undergoing in
62 ress conditions were correlated with potato (Solanum tuberosum L.) tuber protein synthesis.
63  heterotetrameric ADP-Glc PPase from potato (Solanum tuberosum L.) tuber, the homologous residue is p
64  in the heterotetrameric enzyme from potato (Solanum tuberosum L.) tubers.
65 eristems isolated from field-grown potatoes (Solanum tuberosum L.) was determined during a 7-month st
66 omes of six accessions of cultivated potato (Solanum tuberosum L.), a vegetatively propagated autotet
67 far for the extent of LD, cultivated potato (Solanum tuberosum L.), an outcrossing species, is a high
68                         Cultivated potatoes (Solanum tuberosum L.), domesticated from wild Solanum sp
69  temperature on the RS contents of potatoes (Solanum tuberosum L.).
70 (Momordica charantia Descourt.), and potato (Solanum tuberosum L.).
71 ter chestnut (Eleocharis dulcis L.), potato (Solanum tuberosum L.; Bintje), and carrot (Daucus carota
72 ryl coenzyme A reductase (HMGR) from potato (Solanum tuberosum) L. tubers.
73 espiration was altered in transgenic potato (Solanum tuberosum) lines by overexpression of the altern
74 ghum bicolor), Arabidopsis thaliana, potato (Solanum tuberosum), Medicago truncatula, and poplar (Pop
75               Immunoblot analysis of potato (Solanum tuberosum) mitochondria demonstrated that PSD is
76                                      Potato (Solanum tuberosum) multicystatin (PMC) is a crystalline
77                                      Potato (Solanum tuberosum) multicystatin (PMC) is a unique cysta
78 ly cultivar amongst those tested with a pure Solanum tuberosum origin and A cooking type.
79  from sugar beet (Beta vulgaris) and potato (Solanum tuberosum) pectin in vitro.
80 a (Petunia hybrida; PhpreproHypSys), potato (Solanum tuberosum; PhpreproHypSys), and sweet potato (Ip
81 eds of marker-free and backbone-free potato (Solanum tuberosum) plants displaying reduced expression
82  endodermis, bark, specialized organs (e.g., Solanum tuberosum (potato) tubers), and seed coats.
83 m a variety of solanaceous species including Solanum tuberosum (potato), S. demissum, S. chacoense, L
84 fficient for tight direct binding of potato (Solanum tuberosum) REMORIN 1.3 (StREM1.3) to the PM.
85                   Here, we show that potato (Solanum tuberosum) resistance protein R3a relocates from
86                     We have used the potato (Solanum tuberosum) Rx protein, which confers resistance
87                       The cultivated potato (Solanum tuberosum) shares similar biology with other mem
88     TIF1 contains sequence similarity to the Solanum tuberosum single strand-specific transcription f
89                        In cultivated potato (Solanum tuberosum), six PP2A catalytic subunits (StPP2Ac
90         Recently, a maize (Zea mays)/potato (Solanum tuberosum) small subunit mosaic, MP [Mos(1-198)]
91  of these cDNAs is highly polymorphic within Solanum tuberosum ssp. tuberosum, containing mainly a si
92                                   In potato (Solanum tuberosum), StBEL5 and its Knox protein partner
93 nalyses, we previously identified in potato (Solanum tuberosum) StRGGA, coding for an Arginine Glycin
94                                   In potato (Solanum tuberosum subsp. andigena), the BEL1-like transc
95 CLAVATA2-like receptor (StCLV2) from potato (Solanum tuberosum) than its nonglycosylated forms.
96  cysteine-rich peptide isolated from potato (Solanum tuberosum) that was classified as a member of th
97                                   In potato (Solanum tuberosum), the BEL1 transcription factor St BEL
98                                   In potato (Solanum tuberosum), the BELL1 transcription factor StBEL
99 accessions, and S. lycopersicum/S. pennellii/Solanum tuberosum (three-way polymorphic) are included.
100 ymbiont infection by exposing potato plants (Solanum tuberosum) to psyllids infected with "Candidatus
101  and Rx1, which confer resistance in potato (Solanum tuberosum) to the cyst nematode Globodera pallid
102 denosylmethionine decarboxylase from potato, Solanum tuberosum, to 2.3 A resolution.
103 ystem and mosaic AGPases composed of potato (Solanum tuberosum) tuber and maize (Zea mays) endosperm
104 e effects on starch synthesis in the potato (Solanum tuberosum) tuber and seeds of important cereals.
105 all subunits of the heterotetrameric potato (Solanum tuberosum) tuber enzyme.
106                                      Potato (Solanum tuberosum) tuber, a swollen underground stem, is
107  those in other tissues, such as the potato (Solanum tuberosum) tuber, are heat stable.
108                                   In potato (Solanum tuberosum), tuber integrity is dependent on sube
109                                   In potato (Solanum tuberosum), tubers develop from underground stol
110                       The cultivated potato, Solanum tuberosum, ultimately traces its origin to Andea
111 gulate the expression of fumarase in potato (Solanum tuberosum) under the control of the tuber-specif
112 g variation in primary metabolism in potato (Solanum tuberosum), we have profiled primary metabolite
113  of important crop species including potato (Solanum tuberosum) which is grown for its underground st
114 evidence concerning the early use of potato (Solanum tuberosum) within its botanical locus of origin
115          We identified eight putative StYUC (Solanum tuberosum YUCCA) genes whose deduced amino acid

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