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1 itu topology of NBCe1-A were examined by the substituted cysteine accessibility method.
2 e and function of the TM11 segment using the substituted cysteine accessibility method.
3 connecting the M2 and M3 segments using the substituted cysteine accessibility method.
4 cus pneumoniae PlsY was determined using the substituted cysteine accessibility method.
5 of the beta(1) subunit M2 segment using the substituted cysteine accessibility method.
6 s role in gating were investigated using the substituted cysteine accessibility method.
7 ding-site crevices of these receptors by the substituted cysteine accessibility method.
8 d the secondary structure of M6, we used the substituted cysteine accessibility method.
9 e aqueous channel was investigated using the substituted-cysteine accessibility method.
12 in agreement with our in silico predictions, substituted cysteine accessibility method analysis of he
13 eered cysteine-less hCNT3 protein hCNT3(C-), substituted cysteine accessibility method analysis with
19 id receptors, site-directed mutagenesis, the substituted cysteine accessibility method, and molecular
20 o be pore-lining in the open state using the substituted-cysteine accessibility method, but not for A
21 genetically modified lipid content using the substituted cysteine accessibility method for determinin
24 site crevice based on our application of the substituted-cysteine accessibility method in the dopamin
27 he [(125)I]RTI 82-labeled mutants and by the substituted cysteine accessibility method protection ana
28 o the mutated residues by both a traditional substituted cysteine accessibility method (SCAM) and a n
29 nformation were subequently examined via the substituted cysteine accessibility method (SCAM) in tran
46 beta2gamma2L GABAA receptors, we applied the substituted cysteine accessibility method to alpha1-M1 d
48 191) segment in these processes, we used the substituted cysteine accessibility method to characteriz
49 e- and arginine-scanning mutagenesis and the substituted cysteine accessibility method to determine t
51 Here, we used systematic mutagenesis and the substituted cysteine accessibility method to map the rec
59 correlation with experimental results by the substituted cysteine accessibility method upon addition
60 ned by cysteine-scanning mutagenesis and the substituted cysteine accessibility method using the memb
61 ned by cysteine-scanning mutagenesis and the substituted cysteine accessibility method using the memb
62 scanning mutagenesis in conjunction with the substituted cysteine accessibility method using the memb
67 nopus oocyte expression system and the SCAM (substituted cysteine accessibility method), we found tha
79 ilter of the rho1 GABA receptor, we used the substituted cysteine accessibility method with charged r
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