コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ne nucleotides but is largely independent of uridine nucleotides.
2 2 receptor, is activated by both adenine and uridine nucleotides.
3 the extracellular metabolism of adenine and uridine nucleotides.
4 the pharmacological activities of these two uridine nucleotides.
5 and contains negligible amounts of NADH and uridine nucleotides.
6 brucei RET2 apoenzyme and its complexes with uridine nucleotides.
8 sults demonstrate differential regulation of uridine nucleotide-activated P2Y4-R and P2Y6-R and indic
9 e relative nucleotide selectivities of these uridine nucleotide-activated receptors have not been est
10 ciple was used to develop stacked and folded uridine nucleotide analogs that showed highly quenched f
12 sed the safety and efficacy of sofosbuvir, a uridine nucleotide analogue, in treatment-naive patients
13 their respective specificity for adenine and uridine nucleotides and di- and triphosphates, these res
14 es of being photolabeled by vanadate-trapped uridine nucleotides and immunoreactive with a monoclonal
15 tides containing single 2'-aminocytidine or -uridine nucleotides annealed to DNA or RNA targets under
18 eaves mitochondrial mRNA, inserts or deletes uridine nucleotides at specific positions and re-ligates
19 nusual agonist rank order was revealed, with uridine nucleotides being more potent than adenosine nuc
20 ich most likely explain the observation that uridine nucleotides bind more tightly to epimerase/NADH
21 alyze deamination of cytidine nucleotides to uridine nucleotides (C-to-U) in single-strand DNA substr
22 y binding to specific sites on pyr mRNA in a uridine nucleotide-dependent manner and altering the fol
23 dine nucleotide (pyr) operon by binding in a uridine nucleotide-dependent manner to specific sites on
25 een cloned that are selectively activated by uridine nucleotides, direct demonstration of the release
26 ith the terminal deoxynucleotidyltransferase-uridine nucleotide end-labeling technique on tissue sect
27 ding on the RNA tested and the assay method; uridine nucleotides enhanced RNA binding, but guanosine
29 iptional RNA editing that inserts or deletes uridine nucleotides in many mitochondrial pre-mRNAs.
31 active, abortive complexes designated E.NADH.uridine nucleotide, in which the uridine nucleotide may
32 the charge-transfer band are altered by the uridine nucleotide-induced conformational change in this
33 aracterized by the insertion and deletion of uridine nucleotides into otherwise nontranslatable messe
34 he postulate that NAD+ activation induced by uridine nucleotides is brought about by a conformational
36 ated E.NADH.uridine nucleotide, in which the uridine nucleotide may be UDP-glucose, UDP-galactose, or
37 extracellular interconversion of adenine and uridine nucleotides plays a key role in defining activit
38 ngs to the class of 2'-deoxy-2'-spirooxetane uridine nucleotide prodrugs which are known as inhibitor
39 ressed in C6-2B cells and to account for the uridine nucleotide responses originally identified in th
40 rovided the first indication that a class of uridine nucleotide-responsive receptors might exist.
41 lioma cells and by the recent cloning of two uridine nucleotide-responsive receptors, the P2Y6 recept
42 ne, catalyzes the esterification of modified uridine nucleotides, resulting in the formation of 5-met
43 hermore, the P2Y6 receptor, which displays a uridine nucleotide selectivity essentially identical to
45 ctivity essentially identical to that of the uridine nucleotide-specific receptor in C6-2B cells, was
46 sis was confirmed by our identification of a uridine nucleotide-specific receptor on C6-2B rat glioma
47 le of topo I at the 3' phosphodiester of the uridine nucleotide to generate a covalent enzyme-DNA add
48 owed the intracellular pools of cytidine and uridine nucleotides to be manipulated by the composition
51 ce sites while adapting to both cytidine and uridine nucleotides with nearly equivalent frequencies.
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。