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1 orylated amino acid sites are followed by an asterisk (*).
2 = x/x between the two results marked by the asterisk).
3 nd beta-d-Galp to C-4 of the fourth glucose (asterisked above) of the octasaccharide, forming a branc
4 or groove residues C5 and A6 (indicated with asterisks), also corroborated by enzyme digestion studie
5 aK's tryptophan fluorescence (denoted by the asterisk) and expels bound peptide occurs in the second
6 ed a button to indicate whether a subsequent asterisk appeared on the same (congruent) or opposite (i
7 and Arg69*-Asp101, residues labeled with an asterisk are from the neighboring subunit) in the TtCM x
11 es containing the AG*G*C sequence, where the asterisks denote the sites of platination, with differen
13 u-Asp-LeuAla-Val-Glu-Phe, K(i) = 0.3 nM, the asterisk denotes the hydroxyethylene transition-state is
14 platin 5'-d(G*pC)/5'-d(G*pC) ICLs, where the asterisk denotes the platinated nucleoside, to examine t
15 e receptor (nAChR) subtype alpha6beta2* (the asterisk denotes the possible presence of additional sub
16 in the peripheral nervous system (where the asterisk denotes the possible presence of additional sub
17 PrfA and PrfA-dependent virulence genes; the asterisk distinguishes the mutation from inactivation or
19 preference for alpha6-containing [alpha6(*) (asterisks indicate the possible presence of additional s
20 s and lateral to the breast 83 +/- 20* ohms (asterisk indicates p < 0.01 vs. on the breast by analysi
22 ct, 5'-CCTCGTCC-3'/3'-GGAGCAGG-5', where the asterisk indicates the [Pt(en)ACRAMTU)](3+) fragment.
23 )-CC-1065 to the two 5'-AGTTA(asterisk) (the asterisk indicates the covalent bonding site) drug modif
24 V-1 protease specificity site AETF*YCDG (the asterisk indicates the location scissile bond) during pr
25 hromaffin cells is the alpha3beta4* subtype (asterisk indicates the possible presence of additional s
28 icotinic acetylcholine receptors (nAChR; the asterisk (*) indicates known or possible presence of oth
30 ne of the more interesting properties of the asterisks is that they remain monomeric in water despite
31 bored a second-site mutation (denoted by the asterisk) of alanine to glutamate at position 193, a pro
32 3, Glu-Leu-Asp-LeuAla-Val-Glu-Phe (where the asterisk represents the hydroxyethylene tansition-state
33 inated with a site-directed (indicated by an asterisk) (S366A) mutant purified intact toxin (Pta*) or
34 eactivity of (+)-CC-1065 to the two 5'-AGTTA(asterisk) (the asterisk indicates the covalent bonding s
35 strand cross-link at the position denoted by asterisks, was determined in solution by high-resolution
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