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2 acids in the case of cultivars belonging to Cucurbita maxima and Cucurbita pepo species, while a sli
4 garis), bamboo (Phyllostachys nuda), squash (Cucurbita maxima), castor bean (Ricinus communis), and t
5 dentified and characterized a 50-kD pumpkin (Cucurbita maxima cv Big Max) phloem RNA binding protein
6 n this study, proteins contained in pumpkin (Cucurbita maxima cv Big Max) phloem sap were used as a s
8 ding the phloem filament protein in pumpkin (Cucurbita maxima Duch.) has been isolated and characteri
9 Further analyses (also in Brassica napus and Cucurbita maxima) employing complementary electrophysiol
13 abeled dextrans along with size-fractionated Cucurbita maxima phloem proteins, ranging in size from 1
14 chemical, and functional characterization of Cucurbita maxima phloem serpin-1 (CmPS-1), a novel 42-kD
19 scicular phloem P-protein plugs from squash (Cucurbita maxima) represent cucurbit members of the SEO
20 such complex is based on a phloem RBP named Cucurbita maxima RNA-binding protein 50 (CmRBP50), a mem
21 ission of a florigenic signal from flowering Cucurbita maxima stocks to LD-grown C. moschata scions.
23 otein scaffold by means of hydrogen bonds in Cucurbita maxima trypsin inhibitor-V (CMTI-V), a potato
25 peptide bond) hydrolyzed form of recombinant Cucurbita maxima trypsin inhibitor-V (rCMTI-V*) were cha
27 e prephloem pathway of the symplasmic loader Cucurbita maxima was found to be well coupled with the S
28 of protein kinases within the phloem sap of Cucurbita maxima were investigated to test the hypothesi
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