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1 ng mutation, abh1, in an Arabidopsis nuclear mRNA cap-binding protein.
3 ne encoding the large subunit of the nuclear mRNA cap-binding protein, ABH1 (ABA hypersensitive1).
4 le of cytosolic Ca2+ and pH in regulation of mRNA cap-binding protein activity under O2 deprivation i
5 encodes the Arabidopsis homolog of a nuclear mRNA cap binding protein and functions in a heterodimeri
6 ms of translational control highlighting the mRNA cap-binding proteins and the regulation of GCN4 and
8 complex depends upon the availability of the mRNA cap binding protein, eIF-4E, which is sequestered a
10 ins (4E-BP) 1 and 2, releasing them from the mRNA cap binding protein eIF4E, thereby promoting assemb
11 , in its hypophosphorylated state, binds the mRNA cap-binding protein eIF4E and represses cap-depende
13 ssion of 4E-BP1 and its interaction with the mRNA cap-binding protein eIF4E were enhanced in conjunct
14 essor 4E-BP1, association of 4E-BP1 with the mRNA cap-binding protein eIF4E, and sequestration of cyc
15 protein eIF4E, we characterized the distinct mRNA cap-binding proteins eIF4E and eIFiso4E of maize.
24 t phosphorylation of PHAS-I, an inhibitor of mRNA cap-binding protein, eukaryotic initiation factor (
25 at govern the association of PHAS-I with the mRNA cap-binding protein, eukaryotic initiation factor 4
28 ree-dimensional costructures of cap with two mRNA cap-binding proteins, namely, translational initiat
30 nslation initiation factor 4E (eIF4E) is the mRNA cap-binding protein required for translation of cel
31 initiation factor 4E (eIF4E), the essential mRNA cap-binding protein that controls global translatio
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