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1 RRP = resorufin phosphate, DUT = Dyomics-647 uridine triphosphate).
3 bstantial levels of 2'-deoxy-2'-spirooxetane uridine triphosphate (8), a potent inhibitor of the HCV
5 ed overflow metabolism allows homeostasis of uridine triphosphate and cytidine triphosphate levels at
7 , epidermal growth factor increased cellular uridine triphosphate and this increase was reversed by i
8 s feedback inhibition (which is dependent on uridine triphosphate) and became more sensitive to activ
9 uridine monophosphate, uridine diphosphate, uridine triphosphate, and their nonphosphate compound-ur
11 onists, such as lysophosphatidic acid (LPA), uridine triphosphate, growth hormone, vascular endotheli
12 ate (ATP) > or = 5'adenosine-diphosphate > 5'uridine-triphosphate > or = 5'uridine-diphosphate, suppo
15 situ terminal deoxynucleotidyl transferase d-uridine triphosphate nick end labeling (TUNEL) assay, DN
22 was mediated by elevations in intracellular uridine triphosphate (UTP) and cytidine triphosphate (CT
23 ate (ADP), adenosine triphosphate (ATP), and uridine triphosphate (UTP) dose dependently increased th
31 phate (2MeSADP) or the P2Y2/P2Y4 R agonist 5'uridine-triphosphate (UTP) were reduced but not abolishe
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