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1 ine 3'-phosphate 5'-phosphosulfate (A3P5PS), adenosine 3'-phosphate 5'-phosphate (A3P5P), and adenosi
2 d by the P2Y1 receptor-specific antagonists, adenosine 3'-phosphate 5'-phosphosulfate (A3P5PS), adeno
5 talyzes transfer of the 5'-sulfuryl group of adenosine 3'-phosphate 5'-phosphosulfate (PAPS) to the 3
6 group donor for SULT-catalyzed sulfation is adenosine 3'-phosphate 5'-phosphosulfate (PAPS), whereas
7 SK) catalyzes the ATP-dependent synthesis of adenosine 3'-phosphate 5'-phosphosulfate (PAPS), which i
10 h a similar affinity for its two substrates, adenosine 3'-phosphate 5'-phosphosulfate and heparan sul
14 s affect the binding to the donor substrate, adenosine 3'-phosphate 5'-phosphosulfate, and an accepto
15 H) structure reveals ordered binding for the adenosine 3'-phosphate 5'-pyrophosphate moiety of CoASH,
16 be crucial for antagonist activity, because adenosine-3' -phosphate-5'- phosphate (A3P5P) and adenos
18 o-2'-deoxyuridine-3'-pyrophosphate (P'-->5') adenosine 3'-phosphate] has been determined at 1.7 A res
19 idine 3'-pyrophosphate, P' --> 5'-ester with adenosine 3'-phosphate (pdUppAp), binds to RNase A with
20 itor 5'-phosphothymidine(3',5')pyrophosphate adenosine 3'-phosphate (pTppAp) with bovine pancreatic r
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