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1 ieved greater discriminability at the longer deadlines.
2 made in the weeks immediately preceding the deadlines.
3 e assessed the association between the PDUFA deadlines and the timing of FDA drug approval by constru
4 21; P = .02), and those with near-regulatory deadline approval (IRR = 1.90; 95% CI, 1.19-3.05; P = .0
5 peutics, and accelerated and near-regulatory deadline approval were statistically significantly assoc
7 re still faced with offers having very short deadlines, compelling them to accept or reject offers wi
8 ite a Prefatory Chapter, but as the delivery deadline draws closer one begins to think, "Oh my God!
10 tal Task Force recently extended to 2035 the deadline for achieving the goal of a 5,000-km(2) 5-y ave
17 escription Drug User Fee Act (PDUFA) imposes deadlines for the completion of drug reviews by the Food
18 r of shapes on each trial and, under a timed deadline, guessed which one concealed a smiling face.
24 esent study, we examined late responses in a deadline reaction time task, in which the subject become
25 e whose expression increased as the response deadline shortened and the task became more difficult.
26 hat were annotated after the CAFA submission deadline showed that overall MS-kNN accuracy was higher
28 It was absent, however, when the response deadline was relaxed and the strategic need for biasing
30 hether drugs approved immediately before the deadlines were associated with a higher rate of postmark
33 approved in the 2 months before their PDUFA deadlines were more likely to be withdrawn for safety re
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