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1 synthesized with a short 16-amino acids-long carboxyl-terminal extension.
2 y and two additional residues present in the carboxyl-terminal extension.
3 that the site of interaction was within the carboxyl-terminal extension.
4 t this growth response is independent of the carboxyl-terminal extension.
5 unlike Cdc42, Chp contains unique amino- and carboxyl-terminal extensions.
7 tner protein using both the ETS domain and a carboxyl-terminal extension and provides a view of an ex
8 ly autophosphorylate, predominantly on their carboxyl-terminal extensions, and this autophosphorylati
9 eta-Myc) or the INR beta subunit without the carboxyl-terminal extension (betaDelta) were constructed
10 xpressing cytochrome oxidase subunits with a carboxyl terminal extension containing a biotinylation s
12 cDNA was modified to encode an 11-amino acid carboxyl-terminal extension containing the immunodominan
13 esponse elements (PRE), and a short flexible carboxyl terminal extension (CTE) that interacts with th
14 ing domain plus the intrinsically disordered carboxyl-terminal extension (CTE) of the DNA binding dom
15 e nuclear receptors NGFI-B and ROR utilize a carboxyl-terminal extension (CTE) of the zinc finger DNA
21 tains a highly phosphorylated 123-amino acid carboxyl-terminal extension not present in CKI alpha, is
22 nd other members of this subfamily contain a carboxyl-terminal extension not present in the ExoIII/Ap
23 (murine and human, respectively) amino acid carboxyl-terminal extension not seen in any other chemok
24 out 60% larger than the bacterial protein; a carboxyl-terminal extension of 230 amino acids contains
25 nfluenza virus hemagglutinin, HA+8, having a carboxyl-terminal extension of 8 amino acids that includ
28 in part through autophosphorylation of their carboxyl-terminal extensions, resulting in down-regulati
29 of synaptojanin 1, termed SJ170, contains a carboxyl-terminal extension that harbors interaction mot
30 tal and betaDelta cells, suggesting that the carboxyl-terminal extension, through its interaction wit
31 ent of the critical cysteine residues in the carboxyl-terminal extension unique to this isoform, Rubi
32 e is synthesized as a precursor containing a carboxyl-terminal extension whose correct processing is
33 ng domain of the ABC family, MetN contains a carboxyl-terminal extension with a ferredoxin-like fold
34 ng aspartic proteases in that they possess a carboxyl-terminal extension with a predicted transmembra
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