bionlp-ost-19-SeeDev-bin-dev  

Documents (19) JSON TSV

source DB source ID text size updated at # proj. # Ann. updated_at
SeeDev-binary@ldeleger SeeDev-binary-10318690-2 We reported previously that AGL15 accumulated at its highest levels in the products of double fertil 4.45 KB 2020-02-07 1 303
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SeeDev-binary@ldeleger SeeDev-binary-14701918-2 The mature seed coat, in addition to forming a protective layer around the embryo, can play roles in 596 Bytes 2020-02-07 1 27
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SeeDev-binary@ldeleger SeeDev-binary-14701918-8 Although the defect in mucilage production is readily explained by the putative function of MUM4 as 1.12 KB 2020-02-07 1 46
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SeeDev-binary@ldeleger SeeDev-binary-11573014-2 The pleiotropic effects of lec mutations, represented in Fig. 1, suggest that the LEC genes serve as 438 Bytes 2020-02-07 1 22
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SeeDev-binary@ldeleger SeeDev-binary-15708976-2 Seeds of higher plants consist of three major components, each with a different genotype. The embryo 3.99 KB 2020-02-07 1 304
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SeeDev-binary@ldeleger SeeDev-binary-17204538-3 It has been reported that expression of the ERF genes including AtEBP is regulated by AP2 activity ( 1.71 KB 2020-02-07 1 185
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SeeDev-binary@ldeleger SeeDev-binary-19531597-2 As an outstanding adaptation of terrestrial plants, seed formation favors dispersal of species and a 3.58 KB 2020-02-07 1 251
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SeeDev-binary@ldeleger SeeDev-binary-21123653-7 Early dcl1 mutant embryos lack miR156 and exhibit premature expression of miR156 targets SPL10 and S 5.96 KB 2020-02-07 1 739
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SeeDev-binary@ldeleger SeeDev-binary-21330492-5 Interestingly, after the heart stage, fus3-3 dcl1-15 and lec2-1 dcl1-15 embryos have high levels of 353 Bytes 2020-02-07 1 33
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SeeDev-binary@ldeleger SeeDev-binary-21635767-4 To gain insight into possible relationships in gene coexpression and regulation, we first identified 1.93 KB 2020-02-07 1 141
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