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1 d IB) to the polyadenylation factors of CPF (cleavage and polyadenylation factor).
2 ) is associated with gene 3' ends to recruit cleavage and polyadenylation factors.
3 icient processing of EBV pol RNA by cellular cleavage and polyadenylation factors appears to be compe
4   No such interaction of Srb5/Med18 with the cleavage and polyadenylation factor complex, however, co
5 h Glc7p, and multiple components of the CPF (cleavage and polyadenylation factor) complex involved in
6 tem, focusing on the roles played by general cleavage and polyadenylation factors (CPA factors).
7 mponent of two very different complexes: the cleavage and polyadenylation factor CPF and the Set1 met
8 ir 3' ends by the 1-megadalton multiprotein cleavage and polyadenylation factor (CPF).
9 d by expressing a truncated form of the mRNA cleavage and polyadenylation factor CPSF6, the completio
10 er mutation in four independent pedigrees in cleavage and polyadenylation factor I subunit 1 (CLP1).
11 gulatory complex that exploits Pab1p to link cleavage and polyadenylation factors of CFIA and CFIB (c
12  directly by physically interacting with the cleavage and polyadenylation factor or cleavage factor 1
13                                 Depletion of cleavage and polyadenylation factors or of histone pre-m
14 ulation was not inhibited by mutations in 3'-cleavage and polyadenylation factors, Rna14, Rna15 and P
15  and are required for the recruitment of the cleavage and polyadenylation factor Rna15p.
16  the stem-loop binding protein, SR proteins, cleavage and polyadenylation factors, small nucleolar RN
17 ily 3A protein; beta(2) microglobulin; and a cleavage and polyadenylation factor) were identified as

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