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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
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
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
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
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
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.
43 tomato (Lycopersicon esculentum) and potato (Solanum tuberosum), has evolved an arsenal of protease i
49 cerevisiae) two-hybrid system and a potato (Solanum tuberosum) KNOX protein, designated POTH1, as ba
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
57 on on growth and tuberization of two potato (Solanum tuberosum L.) cultivars, Kennebec and Superior.
59 amino-acid-residue epitope tag to a potato (Solanum tuberosum L.) HMGR isoform and expressed this no
63 heterotetrameric ADP-Glc PPase from potato (Solanum tuberosum L.) tuber, the homologous residue is p
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
71 ter chestnut (Eleocharis dulcis L.), potato (Solanum tuberosum L.; Bintje), and carrot (Daucus carota
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
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
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.
88 TIF1 contains sequence similarity to the Solanum tuberosum single strand-specific transcription f
91 of these cDNAs is highly polymorphic within Solanum tuberosum ssp. tuberosum, containing mainly a si
93 nalyses, we previously identified in potato (Solanum tuberosum) StRGGA, coding for an Arginine Glycin
96 cysteine-rich peptide isolated from potato (Solanum tuberosum) that was classified as a member of th
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
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.
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
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