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3 pecies is relatively poor, especially in the carboxyl-terminal portion, and, unlike other J chains, t
4 ptor by a two-domain mechanism: the ligand's carboxyl-terminal portion binds the receptor's extracell
5 60 is an integral thylakoid protein, and its carboxyl-terminal portion is distantly related to prokar
6 n cDNA library as target, indicated that the carboxyl terminal portion of hlj1, a member of the human
7 ng a microspecificity determinant within the carboxyl terminal portion of the third intracellular loo
8 he role of two distinct basic regions in the carboxyl terminal portion of the third intracellular loo
9 ous studies have demonstrated that while the carboxyl-terminal portion of 7B2 (residues 155-186) regu
11 etitive antagonism of agonist binding by the carboxyl-terminal portion of Agouti protein and down-reg
12 eat domain of O-GlcNAc transferase binds the carboxyl-terminal portion of an HCF-1 proteolytic repeat
14 Similarly, replacement of the nonconserved carboxyl-terminal portion of ECII resulted in a receptor
15 ervariable sequence of 21 amino acids in the carboxyl-terminal portion of ECL2 plays a critical role
16 yses of a putative coiled coil region in the carboxyl-terminal portion of HEXIM1 revealed that the pr
17 port establishes for the first time that the carboxyl-terminal portion of HPV L1 interacts with hepar
18 ompassing amphipathic alpha-helices within a carboxyl-terminal portion of micro1 were necessary for e
19 study, the data demonstrate that within the carboxyl-terminal portion of mouse TG, T3 is formed de n
20 n (PTHrP) receptor (rP1R) interacts with the carboxyl-terminal portion of PTH-(1-34) or PTHrP-(1-36).
21 esponding to a 15-amino acid sequence in the carboxyl-terminal portion of rat Tg (Arg(689)-Lys(703)),
22 e identified a heparin-binding region in the carboxyl-terminal portion of rat Tg and have studied its
24 Rather, the responses are specific for the carboxyl-terminal portion of RP3 that is derived from th
26 glutamic acid residue (Glu(302/303)) in the carboxyl-terminal portion of the AAA+ protein, torsinA.
27 ntified by its physical association with the carboxyl-terminal portion of the adenomatous polyposis c
29 on of the B domain of a v.1 protein, and the carboxyl-terminal portion of the B domain and the C doma
34 rived amino acids distributed throughout the carboxyl-terminal portion of the protein are required fo
36 olase but not transferase activity, i.e. the carboxyl-terminal portion of the transferase can exist a
40 g activity of the amino-terminal but not the carboxyl-terminal portion of Tmod1 is enhanced several t
41 to confirm that two different domains in the carboxyl-terminal portion of TRIP8b--the tetratricopepid
43 tigate the multimerization potentials of the carboxyl-terminal portions of AbrB, Abh, and SpoVT we ut
47 s counterpart, with a higher homology in the carboxyl-terminal portion, which contains two RNA recogn
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