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1 tropism changes or reduced susceptibility to vicriviroc.
3 rn associated with reduced susceptibility to vicriviroc, although numerous changes were observed in t
10 -1-infected, treatment-experienced patients, vicriviroc demonstrated potent virologic suppression thr
12 y inhibitors maraviroc, AD101, CMPD 167, and vicriviroc dramatically increases receptor stability.
13 ses that exhibited reduced susceptibility to vicriviroc, envelope clones were phenotypically and geno
14 evel (log(10) copies/mL) were greater in the vicriviroc groups (-0.87 and -1.51 [5 mg], -1.15 and -1.
16 a double-blind, randomized phase 2 study of vicriviroc in treatment-experienced, human immunodeficie
19 ximal responses for aplaviroc, maraviroc and vicriviroc suggests that these modulators have minimal e
22 rom a phase IIb study of the CCR5 antagonist vicriviroc (VCV) and identified one individual with HIV-
26 ected individual who developed resistance to vicriviroc (VCV), an investigational CCR5 antagonist, du
27 antagonist resistance during treatment with vicriviroc (VCV), an investigational small-molecule CCR5
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