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1 ance of maximizing adherence to treatment in pharmacogenetic studies.
2 ns of drug metabolism in epidemiological and pharmacogenetic studies.
3 lso report some of the initial findings from pharmacogenetic studies.
4 clinical information collected from ongoing pharmacogenetic studies.
5 ed populations, which can be used for future pharmacogenetic studies.
15 morphisms (SNPs) in clinical association and pharmacogenetic studies has created a need for high-thro
19 rom non-responders via genetic predictors in pharmacogenetics studies have not met their anticipated
27 mine treatment in a prospective double-blind pharmacogenetics study in first-generation Mexican Ameri
28 s: in vivo pharmacokinetics studies, in vivo pharmacogenetic studies, in vivo drug interaction studie
29 NP-drug response association dataset for 650 pharmacogenetic studies involving 257 drugs in this upda
33 etic studies, review the first generation of pharmacogenetic studies of psychotropic drug response, a
34 selective antagonists for further molecular pharmacogenetic studies of the human prostacyclin recept
35 We conducted a multicenter observational and pharmacogenetic study of 200 patients with DLE treated w
36 participated in a prospective, double-blind, pharmacogenetic study of antidepressant response, and 33
37 We conducted a randomized, double-blind, pharmacogenetic study of behavioral therapy and sibutram
40 ed by Genetic Haplotype Markers) study was a pharmacogenetics study of statin efficacy and safety.
42 authors discuss methods issues in executing pharmacogenetic studies, review the first generation of
43 nally, the authors discuss unique aspects of pharmacogenetic studies that may distinguish them from s
44 l, Costa-Mattioli et al. present data from a pharmacogenetic study that places a key regulatory event
45 was performed on data from three genome-wide pharmacogenetic studies (the Genome-Based Therapeutic Dr
46 ssion Network [DeNT] study; N=332), and 3) a pharmacogenetic study (the Genome-Based Therapeutic Drug
48 This is the largest and most comprehensive pharmacogenetics study to date examining clinical respon
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